Advanced search options

Advanced Search Options 🞨

Browse by author name (“Author name starts with…”).

Find ETDs with:

in
/  
in
/  
in
/  
in

Written in Published in Earliest date Latest date

Sorted by

Results per page:

Sorted by: relevance · author · university · dateNew search

You searched for subject:(Familial risk). Showing records 1 – 30 of 46 total matches.

[1] [2]

Search Limiters

Last 2 Years | English Only

▼ Search Limiters


University of Adelaide

1. Gilson, Amaya. Potential futures: an ethnography of a familial cancer counselling and genetic testing unit.

Degree: 2015, University of Adelaide

 In current Western biomedicine, an accepted and shared belief is that human beings are made up of ‘genes’ and ‘genetic mutations’ which people can inherit… (more)

Subjects/Keywords: familial cancer; genetic risk; medical anthropology; ethnography

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Gilson, A. (2015). Potential futures: an ethnography of a familial cancer counselling and genetic testing unit. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/100455

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Gilson, Amaya. “Potential futures: an ethnography of a familial cancer counselling and genetic testing unit.” 2015. Thesis, University of Adelaide. Accessed April 22, 2021. http://hdl.handle.net/2440/100455.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Gilson, Amaya. “Potential futures: an ethnography of a familial cancer counselling and genetic testing unit.” 2015. Web. 22 Apr 2021.

Vancouver:

Gilson A. Potential futures: an ethnography of a familial cancer counselling and genetic testing unit. [Internet] [Thesis]. University of Adelaide; 2015. [cited 2021 Apr 22]. Available from: http://hdl.handle.net/2440/100455.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Gilson A. Potential futures: an ethnography of a familial cancer counselling and genetic testing unit. [Thesis]. University of Adelaide; 2015. Available from: http://hdl.handle.net/2440/100455

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

2. Al Frouh, Fadi. Analyse des facteurs de risque de maladie thromboembolique veineuse (MTEV) chez les femmes sous contraception oestroprogestative : Analysis of the risk factors of venous thromboembolic disease (VTE) in women with oestroprogestative contraception.

Degree: Docteur es, Pathologie humaine. Génétique humaine, 2017, Aix Marseille Université

L'objectif de notre première étude était d'identifier les déterminants génétiques et environnementaux du risque de maladie thromboembolique veineuse (MTEV) chez les femmes sous contraceptifs oraux… (more)

Subjects/Keywords: Thrombophilie; Thrombose veineuse; Polymorphisme; Risque familial; Contraception; Thrombophilia; Venous Thrombosis; Polymorphism; Familial risk; Contraception

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Al Frouh, F. (2017). Analyse des facteurs de risque de maladie thromboembolique veineuse (MTEV) chez les femmes sous contraception oestroprogestative : Analysis of the risk factors of venous thromboembolic disease (VTE) in women with oestroprogestative contraception. (Doctoral Dissertation). Aix Marseille Université. Retrieved from http://www.theses.fr/2017AIXM0663

Chicago Manual of Style (16th Edition):

Al Frouh, Fadi. “Analyse des facteurs de risque de maladie thromboembolique veineuse (MTEV) chez les femmes sous contraception oestroprogestative : Analysis of the risk factors of venous thromboembolic disease (VTE) in women with oestroprogestative contraception.” 2017. Doctoral Dissertation, Aix Marseille Université. Accessed April 22, 2021. http://www.theses.fr/2017AIXM0663.

MLA Handbook (7th Edition):

Al Frouh, Fadi. “Analyse des facteurs de risque de maladie thromboembolique veineuse (MTEV) chez les femmes sous contraception oestroprogestative : Analysis of the risk factors of venous thromboembolic disease (VTE) in women with oestroprogestative contraception.” 2017. Web. 22 Apr 2021.

Vancouver:

Al Frouh F. Analyse des facteurs de risque de maladie thromboembolique veineuse (MTEV) chez les femmes sous contraception oestroprogestative : Analysis of the risk factors of venous thromboembolic disease (VTE) in women with oestroprogestative contraception. [Internet] [Doctoral dissertation]. Aix Marseille Université 2017. [cited 2021 Apr 22]. Available from: http://www.theses.fr/2017AIXM0663.

Council of Science Editors:

Al Frouh F. Analyse des facteurs de risque de maladie thromboembolique veineuse (MTEV) chez les femmes sous contraception oestroprogestative : Analysis of the risk factors of venous thromboembolic disease (VTE) in women with oestroprogestative contraception. [Doctoral Dissertation]. Aix Marseille Université 2017. Available from: http://www.theses.fr/2017AIXM0663


Universiteit Utrecht

3. Collin, G. The Connectomic Blueprint of Schizophrenia.

Degree: 2015, Universiteit Utrecht

 The foundation for the studies comprising this thesis is the notion that schizophrenia's symptoms stem from faulty integration of neural information due to disruptions in… (more)

Subjects/Keywords: Schizophrenia; Connectome; Brain Network; Familial risk; Diffusion Imaging; White matter

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Collin, G. (2015). The Connectomic Blueprint of Schizophrenia. (Doctoral Dissertation). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/321058

Chicago Manual of Style (16th Edition):

Collin, G. “The Connectomic Blueprint of Schizophrenia.” 2015. Doctoral Dissertation, Universiteit Utrecht. Accessed April 22, 2021. http://dspace.library.uu.nl:8080/handle/1874/321058.

MLA Handbook (7th Edition):

Collin, G. “The Connectomic Blueprint of Schizophrenia.” 2015. Web. 22 Apr 2021.

Vancouver:

Collin G. The Connectomic Blueprint of Schizophrenia. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2015. [cited 2021 Apr 22]. Available from: http://dspace.library.uu.nl:8080/handle/1874/321058.

Council of Science Editors:

Collin G. The Connectomic Blueprint of Schizophrenia. [Doctoral Dissertation]. Universiteit Utrecht; 2015. Available from: http://dspace.library.uu.nl:8080/handle/1874/321058


University of Toronto

4. Rodrigues, Michelle. Familial Risk and Sibling Mentalization: Links with Preschoolers' Internalizing Problems.

Degree: 2016, University of Toronto

The current study explored whether older sibling mentalization moderated the relationship between familial risk for internalizing symptoms and the development of future internalizing problems in… (more)

Subjects/Keywords: Familial Risk; Internalizing Problems; Internal state talk; Protective Factors; Siblings; 0620

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Rodrigues, M. (2016). Familial Risk and Sibling Mentalization: Links with Preschoolers' Internalizing Problems. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/80353

Chicago Manual of Style (16th Edition):

Rodrigues, Michelle. “Familial Risk and Sibling Mentalization: Links with Preschoolers' Internalizing Problems.” 2016. Masters Thesis, University of Toronto. Accessed April 22, 2021. http://hdl.handle.net/1807/80353.

MLA Handbook (7th Edition):

Rodrigues, Michelle. “Familial Risk and Sibling Mentalization: Links with Preschoolers' Internalizing Problems.” 2016. Web. 22 Apr 2021.

Vancouver:

Rodrigues M. Familial Risk and Sibling Mentalization: Links with Preschoolers' Internalizing Problems. [Internet] [Masters thesis]. University of Toronto; 2016. [cited 2021 Apr 22]. Available from: http://hdl.handle.net/1807/80353.

Council of Science Editors:

Rodrigues M. Familial Risk and Sibling Mentalization: Links with Preschoolers' Internalizing Problems. [Masters Thesis]. University of Toronto; 2016. Available from: http://hdl.handle.net/1807/80353

5. Kryski, Katie R. Biological and Contextual Correlates of Cortisol Reactivity in Early Childhood.

Degree: 2014, University of Western Ontario

 Purpose: Individual differences in early-emerging vulnerability to mood and anxiety disorders have been linked to genetic and environmental influences, with psychophysiological reactivity potentially mediating this… (more)

Subjects/Keywords: Cortisol; familial risk; parenting; life stress; 5-HTTLPR; BDNF

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Kryski, K. R. (2014). Biological and Contextual Correlates of Cortisol Reactivity in Early Childhood. (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/2219

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Kryski, Katie R. “Biological and Contextual Correlates of Cortisol Reactivity in Early Childhood.” 2014. Thesis, University of Western Ontario. Accessed April 22, 2021. https://ir.lib.uwo.ca/etd/2219.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Kryski, Katie R. “Biological and Contextual Correlates of Cortisol Reactivity in Early Childhood.” 2014. Web. 22 Apr 2021.

Vancouver:

Kryski KR. Biological and Contextual Correlates of Cortisol Reactivity in Early Childhood. [Internet] [Thesis]. University of Western Ontario; 2014. [cited 2021 Apr 22]. Available from: https://ir.lib.uwo.ca/etd/2219.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Kryski KR. Biological and Contextual Correlates of Cortisol Reactivity in Early Childhood. [Thesis]. University of Western Ontario; 2014. Available from: https://ir.lib.uwo.ca/etd/2219

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Ohio University

6. Sur, Bonita. Examining Perceived Susceptibility of Illness and Health Protective Behaviors Among Emerging Adults with Familial Risk for Type 2 Diabetes.

Degree: MS, Clinical Psychology (Arts and Sciences), 2015, Ohio University

 Type 2 Diabetes Mellitus (T2DM) is a lifelong chronic illness influenced by both genetic and behavioral risk factors. Although children of parents with T2DM are… (more)

Subjects/Keywords: Clinical Psychology; type 2 diabetes; perceived susceptibility; perceived risk; health protective behaviors; familial risk

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Sur, B. (2015). Examining Perceived Susceptibility of Illness and Health Protective Behaviors Among Emerging Adults with Familial Risk for Type 2 Diabetes. (Masters Thesis). Ohio University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1439811016

Chicago Manual of Style (16th Edition):

Sur, Bonita. “Examining Perceived Susceptibility of Illness and Health Protective Behaviors Among Emerging Adults with Familial Risk for Type 2 Diabetes.” 2015. Masters Thesis, Ohio University. Accessed April 22, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1439811016.

MLA Handbook (7th Edition):

Sur, Bonita. “Examining Perceived Susceptibility of Illness and Health Protective Behaviors Among Emerging Adults with Familial Risk for Type 2 Diabetes.” 2015. Web. 22 Apr 2021.

Vancouver:

Sur B. Examining Perceived Susceptibility of Illness and Health Protective Behaviors Among Emerging Adults with Familial Risk for Type 2 Diabetes. [Internet] [Masters thesis]. Ohio University; 2015. [cited 2021 Apr 22]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1439811016.

Council of Science Editors:

Sur B. Examining Perceived Susceptibility of Illness and Health Protective Behaviors Among Emerging Adults with Familial Risk for Type 2 Diabetes. [Masters Thesis]. Ohio University; 2015. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1439811016


University of Lund

7. Lindgren, Magnus. Familial Risks of Heart Failure in Sweden.

Degree: 2020, University of Lund

 Introduction: Despite major advances, the incidence rate and mortality of heart failure (HF) remains high, with a five-year survival of approximately 50%. At the time… (more)

Subjects/Keywords: Cardiac and Cardiovascular Systems; Hjärtsvikt; genetik; Epidemiologi; familjära risker; Heart failure; Genetics; Epidemiology; Familial risk

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Lindgren, M. (2020). Familial Risks of Heart Failure in Sweden. (Doctoral Dissertation). University of Lund. Retrieved from https://lup.lub.lu.se/record/a32fb4ac-7101-478d-96c2-c2791f626863 ; https://portal.research.lu.se/ws/files/76828016/Magnus_Lindgren_web.pdf

Chicago Manual of Style (16th Edition):

Lindgren, Magnus. “Familial Risks of Heart Failure in Sweden.” 2020. Doctoral Dissertation, University of Lund. Accessed April 22, 2021. https://lup.lub.lu.se/record/a32fb4ac-7101-478d-96c2-c2791f626863 ; https://portal.research.lu.se/ws/files/76828016/Magnus_Lindgren_web.pdf.

MLA Handbook (7th Edition):

Lindgren, Magnus. “Familial Risks of Heart Failure in Sweden.” 2020. Web. 22 Apr 2021.

Vancouver:

Lindgren M. Familial Risks of Heart Failure in Sweden. [Internet] [Doctoral dissertation]. University of Lund; 2020. [cited 2021 Apr 22]. Available from: https://lup.lub.lu.se/record/a32fb4ac-7101-478d-96c2-c2791f626863 ; https://portal.research.lu.se/ws/files/76828016/Magnus_Lindgren_web.pdf.

Council of Science Editors:

Lindgren M. Familial Risks of Heart Failure in Sweden. [Doctoral Dissertation]. University of Lund; 2020. Available from: https://lup.lub.lu.se/record/a32fb4ac-7101-478d-96c2-c2791f626863 ; https://portal.research.lu.se/ws/files/76828016/Magnus_Lindgren_web.pdf


University of Lund

8. Akrawi, Delshad. Epidemiology of kidney failure and glomerulonephritis in Sweden. Hereditary and non-hereditary factors.

Degree: 2018, University of Lund

 AbstractBackground: Kidney disease is recognised as an important worldwide health burden. Kidney failure is the result of acute and chronic kidney disease and is associated… (more)

Subjects/Keywords: Medical and Health Sciences; kidney failure; glomerulonephritis; epidemiological study; Familial relative risk

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Akrawi, D. (2018). Epidemiology of kidney failure and glomerulonephritis in Sweden. Hereditary and non-hereditary factors. (Doctoral Dissertation). University of Lund. Retrieved from https://lup.lub.lu.se/record/0e18ad06-3e74-47cc-ada7-be3fb1dd0b41 ; https://portal.research.lu.se/ws/files/42070035/Delshad_Akrawi_HELA.pdf

Chicago Manual of Style (16th Edition):

Akrawi, Delshad. “Epidemiology of kidney failure and glomerulonephritis in Sweden. Hereditary and non-hereditary factors.” 2018. Doctoral Dissertation, University of Lund. Accessed April 22, 2021. https://lup.lub.lu.se/record/0e18ad06-3e74-47cc-ada7-be3fb1dd0b41 ; https://portal.research.lu.se/ws/files/42070035/Delshad_Akrawi_HELA.pdf.

MLA Handbook (7th Edition):

Akrawi, Delshad. “Epidemiology of kidney failure and glomerulonephritis in Sweden. Hereditary and non-hereditary factors.” 2018. Web. 22 Apr 2021.

Vancouver:

Akrawi D. Epidemiology of kidney failure and glomerulonephritis in Sweden. Hereditary and non-hereditary factors. [Internet] [Doctoral dissertation]. University of Lund; 2018. [cited 2021 Apr 22]. Available from: https://lup.lub.lu.se/record/0e18ad06-3e74-47cc-ada7-be3fb1dd0b41 ; https://portal.research.lu.se/ws/files/42070035/Delshad_Akrawi_HELA.pdf.

Council of Science Editors:

Akrawi D. Epidemiology of kidney failure and glomerulonephritis in Sweden. Hereditary and non-hereditary factors. [Doctoral Dissertation]. University of Lund; 2018. Available from: https://lup.lub.lu.se/record/0e18ad06-3e74-47cc-ada7-be3fb1dd0b41 ; https://portal.research.lu.se/ws/files/42070035/Delshad_Akrawi_HELA.pdf


University of Washington

9. Oshima, Emiko. Familial communication patterns in a cohort of men with metastatic prostate cancer: A cross-sectional exploratory analysis using data from the GENTleMEN Study.

Degree: 2020, University of Washington

 Background – A notable subset of men with metastatic prostate cancer (mPC) may carry an inherited germline mutation in a key cancer risk gene such… (more)

Subjects/Keywords: BRCA; familial communication; hereditary breast and ovarian cancer; hereditary cancer risk; prostate cancer; risk communication; Public health; Genetics; Public health genetics

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Oshima, E. (2020). Familial communication patterns in a cohort of men with metastatic prostate cancer: A cross-sectional exploratory analysis using data from the GENTleMEN Study. (Thesis). University of Washington. Retrieved from http://hdl.handle.net/1773/46171

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Oshima, Emiko. “Familial communication patterns in a cohort of men with metastatic prostate cancer: A cross-sectional exploratory analysis using data from the GENTleMEN Study.” 2020. Thesis, University of Washington. Accessed April 22, 2021. http://hdl.handle.net/1773/46171.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Oshima, Emiko. “Familial communication patterns in a cohort of men with metastatic prostate cancer: A cross-sectional exploratory analysis using data from the GENTleMEN Study.” 2020. Web. 22 Apr 2021.

Vancouver:

Oshima E. Familial communication patterns in a cohort of men with metastatic prostate cancer: A cross-sectional exploratory analysis using data from the GENTleMEN Study. [Internet] [Thesis]. University of Washington; 2020. [cited 2021 Apr 22]. Available from: http://hdl.handle.net/1773/46171.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Oshima E. Familial communication patterns in a cohort of men with metastatic prostate cancer: A cross-sectional exploratory analysis using data from the GENTleMEN Study. [Thesis]. University of Washington; 2020. Available from: http://hdl.handle.net/1773/46171

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Edinburgh

10. Bois, Catherine Linnea. Structural brain imaging in individuals at high familial risk of schizophrenia.

Degree: PhD, 2016, University of Edinburgh

 Schizophrenia is often a debilitating psychiatric disorder, characterised by both positive and negative symptoms, and cognitive and psychosocial impairments. The established disorder has been associated… (more)

Subjects/Keywords: 616.89; schizophrenia; familial vulnerability; Edinburgh High Risk Study; HR[ill] group; high risk; brain structural alterations

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Bois, C. L. (2016). Structural brain imaging in individuals at high familial risk of schizophrenia. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/22045

Chicago Manual of Style (16th Edition):

Bois, Catherine Linnea. “Structural brain imaging in individuals at high familial risk of schizophrenia.” 2016. Doctoral Dissertation, University of Edinburgh. Accessed April 22, 2021. http://hdl.handle.net/1842/22045.

MLA Handbook (7th Edition):

Bois, Catherine Linnea. “Structural brain imaging in individuals at high familial risk of schizophrenia.” 2016. Web. 22 Apr 2021.

Vancouver:

Bois CL. Structural brain imaging in individuals at high familial risk of schizophrenia. [Internet] [Doctoral dissertation]. University of Edinburgh; 2016. [cited 2021 Apr 22]. Available from: http://hdl.handle.net/1842/22045.

Council of Science Editors:

Bois CL. Structural brain imaging in individuals at high familial risk of schizophrenia. [Doctoral Dissertation]. University of Edinburgh; 2016. Available from: http://hdl.handle.net/1842/22045

11. Bubien, Virginie. Identification de nouveaux gènes de prédisposition héréditaire au cancer du sein par génotypage tumoral et séquençage de nouvelle génération : Identification of new breast cancer susceptibility genes by tumor single nucleotide polymorphism array and next generation sequencing.

Degree: Docteur es, Génétique, 2016, Bordeaux

5 à 10% des cancers du sein sont héréditaires mais parmi ceux-ci seulement la moitié est expliquée par une altération constitutionnelle d’un gène de prédisposition… (more)

Subjects/Keywords: Cancer du sein familial; ATM; Puces SNP; NGS; Risque de cancer du sein; Familial breast cancer; ATM; SNP array; NGS; Breast cancer risk

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Bubien, V. (2016). Identification de nouveaux gènes de prédisposition héréditaire au cancer du sein par génotypage tumoral et séquençage de nouvelle génération : Identification of new breast cancer susceptibility genes by tumor single nucleotide polymorphism array and next generation sequencing. (Doctoral Dissertation). Bordeaux. Retrieved from http://www.theses.fr/2016BORD0393

Chicago Manual of Style (16th Edition):

Bubien, Virginie. “Identification de nouveaux gènes de prédisposition héréditaire au cancer du sein par génotypage tumoral et séquençage de nouvelle génération : Identification of new breast cancer susceptibility genes by tumor single nucleotide polymorphism array and next generation sequencing.” 2016. Doctoral Dissertation, Bordeaux. Accessed April 22, 2021. http://www.theses.fr/2016BORD0393.

MLA Handbook (7th Edition):

Bubien, Virginie. “Identification de nouveaux gènes de prédisposition héréditaire au cancer du sein par génotypage tumoral et séquençage de nouvelle génération : Identification of new breast cancer susceptibility genes by tumor single nucleotide polymorphism array and next generation sequencing.” 2016. Web. 22 Apr 2021.

Vancouver:

Bubien V. Identification de nouveaux gènes de prédisposition héréditaire au cancer du sein par génotypage tumoral et séquençage de nouvelle génération : Identification of new breast cancer susceptibility genes by tumor single nucleotide polymorphism array and next generation sequencing. [Internet] [Doctoral dissertation]. Bordeaux; 2016. [cited 2021 Apr 22]. Available from: http://www.theses.fr/2016BORD0393.

Council of Science Editors:

Bubien V. Identification de nouveaux gènes de prédisposition héréditaire au cancer du sein par génotypage tumoral et séquençage de nouvelle génération : Identification of new breast cancer susceptibility genes by tumor single nucleotide polymorphism array and next generation sequencing. [Doctoral Dissertation]. Bordeaux; 2016. Available from: http://www.theses.fr/2016BORD0393


Linköping University

12. Tahir, Hassaan. Familial Aggregation of Severe Preeclampsia.

Degree: Statistics, 2011, Linköping University

  It has been proved from several studies that the genetic influence has been the most significant factor for having preeclampsia (PE). Still there are… (more)

Subjects/Keywords: Preeclampsia; Diagnosis; Onset; Analysis; Relative Risk; Binomial regression; History; Familial aggregation; Reoccurrence; Genetic effect; Comparison; Insignificant; Gestational length; Preeclamptic pregnancy

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Tahir, H. (2011). Familial Aggregation of Severe Preeclampsia. (Thesis). Linköping University. Retrieved from http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-73266

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Tahir, Hassaan. “Familial Aggregation of Severe Preeclampsia.” 2011. Thesis, Linköping University. Accessed April 22, 2021. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-73266.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Tahir, Hassaan. “Familial Aggregation of Severe Preeclampsia.” 2011. Web. 22 Apr 2021.

Vancouver:

Tahir H. Familial Aggregation of Severe Preeclampsia. [Internet] [Thesis]. Linköping University; 2011. [cited 2021 Apr 22]. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-73266.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Tahir H. Familial Aggregation of Severe Preeclampsia. [Thesis]. Linköping University; 2011. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-73266

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

13. Esch, Adrianus. Febrile seizures Familial risk factors, outcome and preventive use of antipyretic drugs.

Degree: 1997, Erasmus University Medical Center

 textabstractFebrile seizures (FS) occur in early childhood during a febrile illness. A typical or simple FS is characterized by a sudden loss of consciousness with… (more)

Subjects/Keywords: familial risk factors; febrile seizures; outcome; prevention

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Esch, A. (1997). Febrile seizures Familial risk factors, outcome and preventive use of antipyretic drugs. (Doctoral Dissertation). Erasmus University Medical Center. Retrieved from http://hdl.handle.net/1765/18142

Chicago Manual of Style (16th Edition):

Esch, Adrianus. “Febrile seizures Familial risk factors, outcome and preventive use of antipyretic drugs.” 1997. Doctoral Dissertation, Erasmus University Medical Center. Accessed April 22, 2021. http://hdl.handle.net/1765/18142.

MLA Handbook (7th Edition):

Esch, Adrianus. “Febrile seizures Familial risk factors, outcome and preventive use of antipyretic drugs.” 1997. Web. 22 Apr 2021.

Vancouver:

Esch A. Febrile seizures Familial risk factors, outcome and preventive use of antipyretic drugs. [Internet] [Doctoral dissertation]. Erasmus University Medical Center; 1997. [cited 2021 Apr 22]. Available from: http://hdl.handle.net/1765/18142.

Council of Science Editors:

Esch A. Febrile seizures Familial risk factors, outcome and preventive use of antipyretic drugs. [Doctoral Dissertation]. Erasmus University Medical Center; 1997. Available from: http://hdl.handle.net/1765/18142

14. Chang, Xiao. Large-scale brain connectivity in schizophrenia in relation to auditory verbal hallucinations and familial liability.

Degree: 2019, University Utrecht

 The research in this thesis aims to assess functional and structural connectivity in schizophrenia using MRI techniques, and to contribute new evidence to elucidate connectivity… (more)

Subjects/Keywords: Schizophrenia; auditory hallucinations; familial risk; neuroimaging; fMRI; DTI; connectivity

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Chang, X. (2019). Large-scale brain connectivity in schizophrenia in relation to auditory verbal hallucinations and familial liability. (Doctoral Dissertation). University Utrecht. Retrieved from https://dspace.library.uu.nl/handle/1874/384541 ; URN:NBN:NL:UI:10-1874-384541 ; urn:isbn:978-94-6375-515-3 ; URN:NBN:NL:UI:10-1874-384541 ; https://dspace.library.uu.nl/handle/1874/384541

Chicago Manual of Style (16th Edition):

Chang, Xiao. “Large-scale brain connectivity in schizophrenia in relation to auditory verbal hallucinations and familial liability.” 2019. Doctoral Dissertation, University Utrecht. Accessed April 22, 2021. https://dspace.library.uu.nl/handle/1874/384541 ; URN:NBN:NL:UI:10-1874-384541 ; urn:isbn:978-94-6375-515-3 ; URN:NBN:NL:UI:10-1874-384541 ; https://dspace.library.uu.nl/handle/1874/384541.

MLA Handbook (7th Edition):

Chang, Xiao. “Large-scale brain connectivity in schizophrenia in relation to auditory verbal hallucinations and familial liability.” 2019. Web. 22 Apr 2021.

Vancouver:

Chang X. Large-scale brain connectivity in schizophrenia in relation to auditory verbal hallucinations and familial liability. [Internet] [Doctoral dissertation]. University Utrecht; 2019. [cited 2021 Apr 22]. Available from: https://dspace.library.uu.nl/handle/1874/384541 ; URN:NBN:NL:UI:10-1874-384541 ; urn:isbn:978-94-6375-515-3 ; URN:NBN:NL:UI:10-1874-384541 ; https://dspace.library.uu.nl/handle/1874/384541.

Council of Science Editors:

Chang X. Large-scale brain connectivity in schizophrenia in relation to auditory verbal hallucinations and familial liability. [Doctoral Dissertation]. University Utrecht; 2019. Available from: https://dspace.library.uu.nl/handle/1874/384541 ; URN:NBN:NL:UI:10-1874-384541 ; urn:isbn:978-94-6375-515-3 ; URN:NBN:NL:UI:10-1874-384541 ; https://dspace.library.uu.nl/handle/1874/384541

15. Middeldorp, Janneke Willemijn. Genetics and tumor genomics in familial colorectal cancer.

Degree: 2010, Department of Pathology, Faculty of Medicine / Leiden University Medical Center (LUMC), Leiden University

 Colorectal cancer (CRC) is one of the most common cancers in the Western world and in about 30% hereditary factors play a role. Although several… (more)

Subjects/Keywords: Colorectal cancer; copy-neutral LOH; Familial; Genetics; Risk loci; Colorectal cancer; copy-neutral LOH; Familial; Genetics; Risk loci

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Middeldorp, J. W. (2010). Genetics and tumor genomics in familial colorectal cancer. (Doctoral Dissertation). Department of Pathology, Faculty of Medicine / Leiden University Medical Center (LUMC), Leiden University. Retrieved from http://hdl.handle.net/1887/16041

Chicago Manual of Style (16th Edition):

Middeldorp, Janneke Willemijn. “Genetics and tumor genomics in familial colorectal cancer.” 2010. Doctoral Dissertation, Department of Pathology, Faculty of Medicine / Leiden University Medical Center (LUMC), Leiden University. Accessed April 22, 2021. http://hdl.handle.net/1887/16041.

MLA Handbook (7th Edition):

Middeldorp, Janneke Willemijn. “Genetics and tumor genomics in familial colorectal cancer.” 2010. Web. 22 Apr 2021.

Vancouver:

Middeldorp JW. Genetics and tumor genomics in familial colorectal cancer. [Internet] [Doctoral dissertation]. Department of Pathology, Faculty of Medicine / Leiden University Medical Center (LUMC), Leiden University; 2010. [cited 2021 Apr 22]. Available from: http://hdl.handle.net/1887/16041.

Council of Science Editors:

Middeldorp JW. Genetics and tumor genomics in familial colorectal cancer. [Doctoral Dissertation]. Department of Pathology, Faculty of Medicine / Leiden University Medical Center (LUMC), Leiden University; 2010. Available from: http://hdl.handle.net/1887/16041


University of Oulu

16. Lieslehto, J. (Johannes). Early adversity, psychosis risk and brain response to faces.

Degree: 2018, University of Oulu

Abstract Schizophrenia and other psychotic disorders are severe and disabling mental disorders that break out during early adulthood, often when a person is in his/her… (more)

Subjects/Keywords: birth cohort study; early adulthood; early adversity; familial psychosis risk; functional magnetic resonance imaging (fMRI); polygenic risk score (PRS); perinnöllinen psykoosiriski; polygeeninen riskipiste (PRS); syntymäkohortti; toiminnallinen magneettikuvantaminen (fMRI); varhaiset vastoinkäymiset

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Lieslehto, J. (. (2018). Early adversity, psychosis risk and brain response to faces. (Doctoral Dissertation). University of Oulu. Retrieved from http://urn.fi/urn:isbn:9789526220659

Chicago Manual of Style (16th Edition):

Lieslehto, J (Johannes). “Early adversity, psychosis risk and brain response to faces.” 2018. Doctoral Dissertation, University of Oulu. Accessed April 22, 2021. http://urn.fi/urn:isbn:9789526220659.

MLA Handbook (7th Edition):

Lieslehto, J (Johannes). “Early adversity, psychosis risk and brain response to faces.” 2018. Web. 22 Apr 2021.

Vancouver:

Lieslehto J(. Early adversity, psychosis risk and brain response to faces. [Internet] [Doctoral dissertation]. University of Oulu; 2018. [cited 2021 Apr 22]. Available from: http://urn.fi/urn:isbn:9789526220659.

Council of Science Editors:

Lieslehto J(. Early adversity, psychosis risk and brain response to faces. [Doctoral Dissertation]. University of Oulu; 2018. Available from: http://urn.fi/urn:isbn:9789526220659


University of North Texas

17. Boneau, Rebecca Dunnan. This is Your Brain on Football: Making Sense of Parents' Decision to Allow Their Child to Play Tackle Football.

Degree: 2018, University of North Texas

 Parents make decisions on behalf of their children on a daily basis. Some parents in the United States face the unique decision of whether or… (more)

Subjects/Keywords: sensemaking theory; parental decision-making; parental risk assessment, familial identity; football; Football for children  – Health aspects.; Youth league football  – Health aspects.; Football players  – Health risk assessment.; Parents.; Decision making.

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Boneau, R. D. (2018). This is Your Brain on Football: Making Sense of Parents' Decision to Allow Their Child to Play Tackle Football. (Thesis). University of North Texas. Retrieved from https://digital.library.unt.edu/ark:/67531/metadc1157613/

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Boneau, Rebecca Dunnan. “This is Your Brain on Football: Making Sense of Parents' Decision to Allow Their Child to Play Tackle Football.” 2018. Thesis, University of North Texas. Accessed April 22, 2021. https://digital.library.unt.edu/ark:/67531/metadc1157613/.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Boneau, Rebecca Dunnan. “This is Your Brain on Football: Making Sense of Parents' Decision to Allow Their Child to Play Tackle Football.” 2018. Web. 22 Apr 2021.

Vancouver:

Boneau RD. This is Your Brain on Football: Making Sense of Parents' Decision to Allow Their Child to Play Tackle Football. [Internet] [Thesis]. University of North Texas; 2018. [cited 2021 Apr 22]. Available from: https://digital.library.unt.edu/ark:/67531/metadc1157613/.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Boneau RD. This is Your Brain on Football: Making Sense of Parents' Decision to Allow Their Child to Play Tackle Football. [Thesis]. University of North Texas; 2018. Available from: https://digital.library.unt.edu/ark:/67531/metadc1157613/

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Lund

18. Magnusson, Susanne. Genetic factors in childhood cancer. Associations between tumors in childhood and adulthood, and prevalence of germline TP53 mutations.

Degree: 2012, University of Lund

 The etiology of childhood cancer is largely unknown. Approximately 1-10% of all childhood tumors are associated with known cancer predisposition syndromes. However, the contribution may… (more)

Subjects/Keywords: Cancer and Oncology; Childhood cancer; hereditary factors; breast cancer; survival; hereditary breast and ovarian cancer; hereditary non-polyposis colorectal cancer; familial malignant melanoma; BRCA1; BRCA2; mismatch repair; CDKN2A; familial risk; multiple childhood tumors; Li-Fraumeni syndrome; TP53; adrenocortical carcinoma; choroid plexus tumors; rhabdomyosarcoma

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Magnusson, S. (2012). Genetic factors in childhood cancer. Associations between tumors in childhood and adulthood, and prevalence of germline TP53 mutations. (Doctoral Dissertation). University of Lund. Retrieved from https://lup.lub.lu.se/record/2364386 ; https://portal.research.lu.se/ws/files/3867820/2364415.pdf

Chicago Manual of Style (16th Edition):

Magnusson, Susanne. “Genetic factors in childhood cancer. Associations between tumors in childhood and adulthood, and prevalence of germline TP53 mutations.” 2012. Doctoral Dissertation, University of Lund. Accessed April 22, 2021. https://lup.lub.lu.se/record/2364386 ; https://portal.research.lu.se/ws/files/3867820/2364415.pdf.

MLA Handbook (7th Edition):

Magnusson, Susanne. “Genetic factors in childhood cancer. Associations between tumors in childhood and adulthood, and prevalence of germline TP53 mutations.” 2012. Web. 22 Apr 2021.

Vancouver:

Magnusson S. Genetic factors in childhood cancer. Associations between tumors in childhood and adulthood, and prevalence of germline TP53 mutations. [Internet] [Doctoral dissertation]. University of Lund; 2012. [cited 2021 Apr 22]. Available from: https://lup.lub.lu.se/record/2364386 ; https://portal.research.lu.se/ws/files/3867820/2364415.pdf.

Council of Science Editors:

Magnusson S. Genetic factors in childhood cancer. Associations between tumors in childhood and adulthood, and prevalence of germline TP53 mutations. [Doctoral Dissertation]. University of Lund; 2012. Available from: https://lup.lub.lu.se/record/2364386 ; https://portal.research.lu.se/ws/files/3867820/2364415.pdf

19. Ghaleb, Youmna. Hypercholestérolémie familiale : recherche de nouveaux gènes et étude des formes polygéniques : Familial hypercholesterolemia : research of new genes and study of polygenic forms.

Degree: Docteur es, Développement, 2017, Sorbonne Paris Cité; Université Saint-Joseph (Beyrouth)

L’hypercholestérolémie familiale à transmission autosomique dominante (ADH), caractérisée par une élévation des taux plasmatiques en cholestérol total et LDL-C, est due à des altérations de… (more)

Subjects/Keywords: LRP6; Score génétique; Phénocopies; Mutation libanaise; GRS; Familial hypercholesterolemia; Cardiovascular diseases; Genetic studies; LRP6; Polygenic hypercholesterolemia; Genetic risk score; Phenocopy; Lebanese mutation; GRS

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Ghaleb, Y. (2017). Hypercholestérolémie familiale : recherche de nouveaux gènes et étude des formes polygéniques : Familial hypercholesterolemia : research of new genes and study of polygenic forms. (Doctoral Dissertation). Sorbonne Paris Cité; Université Saint-Joseph (Beyrouth). Retrieved from http://www.theses.fr/2017USPCC270

Chicago Manual of Style (16th Edition):

Ghaleb, Youmna. “Hypercholestérolémie familiale : recherche de nouveaux gènes et étude des formes polygéniques : Familial hypercholesterolemia : research of new genes and study of polygenic forms.” 2017. Doctoral Dissertation, Sorbonne Paris Cité; Université Saint-Joseph (Beyrouth). Accessed April 22, 2021. http://www.theses.fr/2017USPCC270.

MLA Handbook (7th Edition):

Ghaleb, Youmna. “Hypercholestérolémie familiale : recherche de nouveaux gènes et étude des formes polygéniques : Familial hypercholesterolemia : research of new genes and study of polygenic forms.” 2017. Web. 22 Apr 2021.

Vancouver:

Ghaleb Y. Hypercholestérolémie familiale : recherche de nouveaux gènes et étude des formes polygéniques : Familial hypercholesterolemia : research of new genes and study of polygenic forms. [Internet] [Doctoral dissertation]. Sorbonne Paris Cité; Université Saint-Joseph (Beyrouth); 2017. [cited 2021 Apr 22]. Available from: http://www.theses.fr/2017USPCC270.

Council of Science Editors:

Ghaleb Y. Hypercholestérolémie familiale : recherche de nouveaux gènes et étude des formes polygéniques : Familial hypercholesterolemia : research of new genes and study of polygenic forms. [Doctoral Dissertation]. Sorbonne Paris Cité; Université Saint-Joseph (Beyrouth); 2017. Available from: http://www.theses.fr/2017USPCC270

20. Rullier, Laetitia. Approche psychosociale du risque de malnutrition dans la démence : intrication des facteurs de vulnérabilité des personnes âgées vivant à domicile et de leur proche aidant : Psychosocial approach of risk of malnutrition in dementia : association of vulnerability factors between community-dwelling elderly and family caregivers.

Degree: Docteur es, Psychologie, 2011, Université de Bordeaux Segalen

Ce travail a pour objectif d’étudier, selon une approche psychosociale, les facteurs de vulnérabilité associés au risque de malnutrition au sein du binôme personne âgée… (more)

Subjects/Keywords: Démence; Risque de malnutrition; Facteurs de vulnérabilité psychosociaux; Binôme personne âgée démente/aidant familial; Domicile; Dementia; Risk of malnutrition; Psychosocial factors; Caregiving dyad; Community

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Rullier, L. (2011). Approche psychosociale du risque de malnutrition dans la démence : intrication des facteurs de vulnérabilité des personnes âgées vivant à domicile et de leur proche aidant : Psychosocial approach of risk of malnutrition in dementia : association of vulnerability factors between community-dwelling elderly and family caregivers. (Doctoral Dissertation). Université de Bordeaux Segalen. Retrieved from http://www.theses.fr/2011BOR21869

Chicago Manual of Style (16th Edition):

Rullier, Laetitia. “Approche psychosociale du risque de malnutrition dans la démence : intrication des facteurs de vulnérabilité des personnes âgées vivant à domicile et de leur proche aidant : Psychosocial approach of risk of malnutrition in dementia : association of vulnerability factors between community-dwelling elderly and family caregivers.” 2011. Doctoral Dissertation, Université de Bordeaux Segalen. Accessed April 22, 2021. http://www.theses.fr/2011BOR21869.

MLA Handbook (7th Edition):

Rullier, Laetitia. “Approche psychosociale du risque de malnutrition dans la démence : intrication des facteurs de vulnérabilité des personnes âgées vivant à domicile et de leur proche aidant : Psychosocial approach of risk of malnutrition in dementia : association of vulnerability factors between community-dwelling elderly and family caregivers.” 2011. Web. 22 Apr 2021.

Vancouver:

Rullier L. Approche psychosociale du risque de malnutrition dans la démence : intrication des facteurs de vulnérabilité des personnes âgées vivant à domicile et de leur proche aidant : Psychosocial approach of risk of malnutrition in dementia : association of vulnerability factors between community-dwelling elderly and family caregivers. [Internet] [Doctoral dissertation]. Université de Bordeaux Segalen; 2011. [cited 2021 Apr 22]. Available from: http://www.theses.fr/2011BOR21869.

Council of Science Editors:

Rullier L. Approche psychosociale du risque de malnutrition dans la démence : intrication des facteurs de vulnérabilité des personnes âgées vivant à domicile et de leur proche aidant : Psychosocial approach of risk of malnutrition in dementia : association of vulnerability factors between community-dwelling elderly and family caregivers. [Doctoral Dissertation]. Université de Bordeaux Segalen; 2011. Available from: http://www.theses.fr/2011BOR21869

21. Aissaoui, Souria. Elaboration d'un outil pour l'évaluation et l'amélioration de la qualité de la prise de décision lors du Comité d'Onco-Génétique multidisciplinaire dans le cadre de prédisposition héréditaire au cancer colorectal. : une expérience française : Elaboration of a tool for Assessment and Improvement of Quality of Decision-making at the multidisciplinary oncogenetic committee for colorectal cancer predisposition : a French Experience.

Degree: Docteur es, Pathologie humaine. Conseil en génétique, 2013, Aix Marseille Université

Les maladies les plus fréquentes prédisposant au cancer colorectal sont le Syndrome de Lynch et la Polypose Adénomateuse Familiale. Les gènes du système MMR, le… (more)

Subjects/Keywords: Évaluation du risque, cancer colorectal, diagnostic génétique, décision multidisciplinaire, prise en charge familiale; Risk assessment, colorectal cancer, genetic diagnosis, multidisciplinary decision-making, familial cancer management

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Aissaoui, S. (2013). Elaboration d'un outil pour l'évaluation et l'amélioration de la qualité de la prise de décision lors du Comité d'Onco-Génétique multidisciplinaire dans le cadre de prédisposition héréditaire au cancer colorectal. : une expérience française : Elaboration of a tool for Assessment and Improvement of Quality of Decision-making at the multidisciplinary oncogenetic committee for colorectal cancer predisposition : a French Experience. (Doctoral Dissertation). Aix Marseille Université. Retrieved from http://www.theses.fr/2013AIXM5020

Chicago Manual of Style (16th Edition):

Aissaoui, Souria. “Elaboration d'un outil pour l'évaluation et l'amélioration de la qualité de la prise de décision lors du Comité d'Onco-Génétique multidisciplinaire dans le cadre de prédisposition héréditaire au cancer colorectal. : une expérience française : Elaboration of a tool for Assessment and Improvement of Quality of Decision-making at the multidisciplinary oncogenetic committee for colorectal cancer predisposition : a French Experience.” 2013. Doctoral Dissertation, Aix Marseille Université. Accessed April 22, 2021. http://www.theses.fr/2013AIXM5020.

MLA Handbook (7th Edition):

Aissaoui, Souria. “Elaboration d'un outil pour l'évaluation et l'amélioration de la qualité de la prise de décision lors du Comité d'Onco-Génétique multidisciplinaire dans le cadre de prédisposition héréditaire au cancer colorectal. : une expérience française : Elaboration of a tool for Assessment and Improvement of Quality of Decision-making at the multidisciplinary oncogenetic committee for colorectal cancer predisposition : a French Experience.” 2013. Web. 22 Apr 2021.

Vancouver:

Aissaoui S. Elaboration d'un outil pour l'évaluation et l'amélioration de la qualité de la prise de décision lors du Comité d'Onco-Génétique multidisciplinaire dans le cadre de prédisposition héréditaire au cancer colorectal. : une expérience française : Elaboration of a tool for Assessment and Improvement of Quality of Decision-making at the multidisciplinary oncogenetic committee for colorectal cancer predisposition : a French Experience. [Internet] [Doctoral dissertation]. Aix Marseille Université 2013. [cited 2021 Apr 22]. Available from: http://www.theses.fr/2013AIXM5020.

Council of Science Editors:

Aissaoui S. Elaboration d'un outil pour l'évaluation et l'amélioration de la qualité de la prise de décision lors du Comité d'Onco-Génétique multidisciplinaire dans le cadre de prédisposition héréditaire au cancer colorectal. : une expérience française : Elaboration of a tool for Assessment and Improvement of Quality of Decision-making at the multidisciplinary oncogenetic committee for colorectal cancer predisposition : a French Experience. [Doctoral Dissertation]. Aix Marseille Université 2013. Available from: http://www.theses.fr/2013AIXM5020

22. Collin, G. The Connectomic Blueprint of Schizophrenia.

Degree: 2015, University Utrecht

 The foundation for the studies comprising this thesis is the notion that schizophrenia's symptoms stem from faulty integration of neural information due to disruptions in… (more)

Subjects/Keywords: Schizophrenia; Connectome; Brain Network; Familial risk; Diffusion Imaging; White matter

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Collin, G. (2015). The Connectomic Blueprint of Schizophrenia. (Doctoral Dissertation). University Utrecht. Retrieved from http://dspace.library.uu.nl/handle/1874/321058 ; URN:NBN:NL:UI:10-1874-321058 ; urn:isbn:978-94-6295-362-8 ; URN:NBN:NL:UI:10-1874-321058 ; http://dspace.library.uu.nl/handle/1874/321058

Chicago Manual of Style (16th Edition):

Collin, G. “The Connectomic Blueprint of Schizophrenia.” 2015. Doctoral Dissertation, University Utrecht. Accessed April 22, 2021. http://dspace.library.uu.nl/handle/1874/321058 ; URN:NBN:NL:UI:10-1874-321058 ; urn:isbn:978-94-6295-362-8 ; URN:NBN:NL:UI:10-1874-321058 ; http://dspace.library.uu.nl/handle/1874/321058.

MLA Handbook (7th Edition):

Collin, G. “The Connectomic Blueprint of Schizophrenia.” 2015. Web. 22 Apr 2021.

Vancouver:

Collin G. The Connectomic Blueprint of Schizophrenia. [Internet] [Doctoral dissertation]. University Utrecht; 2015. [cited 2021 Apr 22]. Available from: http://dspace.library.uu.nl/handle/1874/321058 ; URN:NBN:NL:UI:10-1874-321058 ; urn:isbn:978-94-6295-362-8 ; URN:NBN:NL:UI:10-1874-321058 ; http://dspace.library.uu.nl/handle/1874/321058.

Council of Science Editors:

Collin G. The Connectomic Blueprint of Schizophrenia. [Doctoral Dissertation]. University Utrecht; 2015. Available from: http://dspace.library.uu.nl/handle/1874/321058 ; URN:NBN:NL:UI:10-1874-321058 ; urn:isbn:978-94-6295-362-8 ; URN:NBN:NL:UI:10-1874-321058 ; http://dspace.library.uu.nl/handle/1874/321058


Freie Universität Berlin

23. Wackerhagen, Carolin. Limbisch-kortikale Dysbalance als intermediärer Phänotyp der Depression - Untersuchung einer Gruppe mit familiärem Depressionsrisiko.

Degree: 2019, Freie Universität Berlin

 Hintergrund: Eine etabliertes neurobiologisches Modell der Depression erklärt die Tendenz, negative emotionale Reize intensiver zu verarbeiten, anhand eines limbisch-kortikalen Ungleichgewichts: limbische und ventral-präfrontale Regionen, darunter… (more)

Subjects/Keywords: Amygdala; Depression; Connectivity; Endophenotype; Functional Connectivity; Intermediate phenotype; limbic-cortical imbalance; Familial risk; 600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit::610 Medizin und Gesundheit

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Wackerhagen, C. (2019). Limbisch-kortikale Dysbalance als intermediärer Phänotyp der Depression - Untersuchung einer Gruppe mit familiärem Depressionsrisiko. (Thesis). Freie Universität Berlin. Retrieved from http://dx.doi.org/10.17169/refubium-25994

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Wackerhagen, Carolin. “Limbisch-kortikale Dysbalance als intermediärer Phänotyp der Depression - Untersuchung einer Gruppe mit familiärem Depressionsrisiko.” 2019. Thesis, Freie Universität Berlin. Accessed April 22, 2021. http://dx.doi.org/10.17169/refubium-25994.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Wackerhagen, Carolin. “Limbisch-kortikale Dysbalance als intermediärer Phänotyp der Depression - Untersuchung einer Gruppe mit familiärem Depressionsrisiko.” 2019. Web. 22 Apr 2021.

Vancouver:

Wackerhagen C. Limbisch-kortikale Dysbalance als intermediärer Phänotyp der Depression - Untersuchung einer Gruppe mit familiärem Depressionsrisiko. [Internet] [Thesis]. Freie Universität Berlin; 2019. [cited 2021 Apr 22]. Available from: http://dx.doi.org/10.17169/refubium-25994.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Wackerhagen C. Limbisch-kortikale Dysbalance als intermediärer Phänotyp der Depression - Untersuchung einer Gruppe mit familiärem Depressionsrisiko. [Thesis]. Freie Universität Berlin; 2019. Available from: http://dx.doi.org/10.17169/refubium-25994

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

24. Collin, G. The Connectomic Blueprint of Schizophrenia.

Degree: 2015, University Utrecht

 The foundation for the studies comprising this thesis is the notion that schizophrenia's symptoms stem from faulty integration of neural information due to disruptions in… (more)

Subjects/Keywords: Schizophrenia; Connectome; Brain Network; Familial risk; Diffusion Imaging; White matter

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Collin, G. (2015). The Connectomic Blueprint of Schizophrenia. (Doctoral Dissertation). University Utrecht. Retrieved from https://dspace.library.uu.nl/handle/1874/321058 ; URN:NBN:NL:UI:10-1874-321058 ; urn:isbn:978-94-6295-362-8 ; URN:NBN:NL:UI:10-1874-321058 ; https://dspace.library.uu.nl/handle/1874/321058

Chicago Manual of Style (16th Edition):

Collin, G. “The Connectomic Blueprint of Schizophrenia.” 2015. Doctoral Dissertation, University Utrecht. Accessed April 22, 2021. https://dspace.library.uu.nl/handle/1874/321058 ; URN:NBN:NL:UI:10-1874-321058 ; urn:isbn:978-94-6295-362-8 ; URN:NBN:NL:UI:10-1874-321058 ; https://dspace.library.uu.nl/handle/1874/321058.

MLA Handbook (7th Edition):

Collin, G. “The Connectomic Blueprint of Schizophrenia.” 2015. Web. 22 Apr 2021.

Vancouver:

Collin G. The Connectomic Blueprint of Schizophrenia. [Internet] [Doctoral dissertation]. University Utrecht; 2015. [cited 2021 Apr 22]. Available from: https://dspace.library.uu.nl/handle/1874/321058 ; URN:NBN:NL:UI:10-1874-321058 ; urn:isbn:978-94-6295-362-8 ; URN:NBN:NL:UI:10-1874-321058 ; https://dspace.library.uu.nl/handle/1874/321058.

Council of Science Editors:

Collin G. The Connectomic Blueprint of Schizophrenia. [Doctoral Dissertation]. University Utrecht; 2015. Available from: https://dspace.library.uu.nl/handle/1874/321058 ; URN:NBN:NL:UI:10-1874-321058 ; urn:isbn:978-94-6295-362-8 ; URN:NBN:NL:UI:10-1874-321058 ; https://dspace.library.uu.nl/handle/1874/321058

25. Wansa, Charlotte Ruth. The long-term effects of phonological awareness intervention for two populations of at-risk children : a review of the literature.

Degree: MA, Communication Sciences and Disorders, 2012, University of Texas – Austin

 The primary purpose of the present review was to determine why conflicting findings have been reported regarding the long-term effects of phonological awareness training for… (more)

Subjects/Keywords: Low-SES; Familial risk; Reading impairment; Phonological awareness; Intervention

…17 EVALUATING THE EVIDENCE: CHILDREN WITH FAMILIAL RISK FOR READING IMPAIRMENT… …19 Description of Interventions Involving Children with Familial Risk for Reading… …21 Levels of Evidence for Interventions Reviewed for Children with Familial Risk for… …21 Results of Interventions Reviewed for Children with Familial Risk for Reading Impairment… …24 Summary of Findings for Interventions Reviewed for Children with Familial Risk for… 

Page 1 Page 2 Page 3 Page 4 Page 5 Page 6 Page 7

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Wansa, C. R. (2012). The long-term effects of phonological awareness intervention for two populations of at-risk children : a review of the literature. (Masters Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/ETD-UT-2012-05-5346

Chicago Manual of Style (16th Edition):

Wansa, Charlotte Ruth. “The long-term effects of phonological awareness intervention for two populations of at-risk children : a review of the literature.” 2012. Masters Thesis, University of Texas – Austin. Accessed April 22, 2021. http://hdl.handle.net/2152/ETD-UT-2012-05-5346.

MLA Handbook (7th Edition):

Wansa, Charlotte Ruth. “The long-term effects of phonological awareness intervention for two populations of at-risk children : a review of the literature.” 2012. Web. 22 Apr 2021.

Vancouver:

Wansa CR. The long-term effects of phonological awareness intervention for two populations of at-risk children : a review of the literature. [Internet] [Masters thesis]. University of Texas – Austin; 2012. [cited 2021 Apr 22]. Available from: http://hdl.handle.net/2152/ETD-UT-2012-05-5346.

Council of Science Editors:

Wansa CR. The long-term effects of phonological awareness intervention for two populations of at-risk children : a review of the literature. [Masters Thesis]. University of Texas – Austin; 2012. Available from: http://hdl.handle.net/2152/ETD-UT-2012-05-5346


Leiden University

26. Hilbers, F.S.M. The genetic etiology of familial breast cancer: Assessing the role of rare genetic variation using next generation sequencing.

Degree: 2020, Leiden University

  A family history of breast cancer is one of the most important risk factors for the disease. Over the last decades many genetic loci… (more)

Subjects/Keywords: Breast Cancer; Hereditary; Familial; Next-generation sequencing (NGS); Risk; Predisposition; Functional analysis

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Hilbers, F. S. M. (2020). The genetic etiology of familial breast cancer: Assessing the role of rare genetic variation using next generation sequencing. (Doctoral Dissertation). Leiden University. Retrieved from http://hdl.handle.net/1887/123226

Chicago Manual of Style (16th Edition):

Hilbers, F S M. “The genetic etiology of familial breast cancer: Assessing the role of rare genetic variation using next generation sequencing.” 2020. Doctoral Dissertation, Leiden University. Accessed April 22, 2021. http://hdl.handle.net/1887/123226.

MLA Handbook (7th Edition):

Hilbers, F S M. “The genetic etiology of familial breast cancer: Assessing the role of rare genetic variation using next generation sequencing.” 2020. Web. 22 Apr 2021.

Vancouver:

Hilbers FSM. The genetic etiology of familial breast cancer: Assessing the role of rare genetic variation using next generation sequencing. [Internet] [Doctoral dissertation]. Leiden University; 2020. [cited 2021 Apr 22]. Available from: http://hdl.handle.net/1887/123226.

Council of Science Editors:

Hilbers FSM. The genetic etiology of familial breast cancer: Assessing the role of rare genetic variation using next generation sequencing. [Doctoral Dissertation]. Leiden University; 2020. Available from: http://hdl.handle.net/1887/123226


University of Oulu

27. Uimari, O. (Outi). Epidemiological and familial risk factors of uterine leiomyoma development.

Degree: 2017, University of Oulu

Abstract Uterine leiomyomas are the most common benign tumours in females. They are myometrial neoplasms, may present single or multiple, and may be located in… (more)

Subjects/Keywords: cardiovascular risk; endometriosis; epidemiology; familial; glucose metabolism; lipid metabolism; natural history; population-based birth cohort studies; subfertility; uterine leiomyoma/fibroids; alentunut hedelmällisyys; endometrioosi; epidemiologia; familiaalinen; glukoosimetabolia; kardiovaskulaaririski; kohdun leiomyooma; lipidimetabolia; taudinkulku; väestopohjaiset syntymäkohorttitutkimukset; Bcl-2; CD34; FH; HLRCC

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Uimari, O. (. (2017). Epidemiological and familial risk factors of uterine leiomyoma development. (Doctoral Dissertation). University of Oulu. Retrieved from http://urn.fi/urn:isbn:9789526214870

Chicago Manual of Style (16th Edition):

Uimari, O (Outi). “Epidemiological and familial risk factors of uterine leiomyoma development.” 2017. Doctoral Dissertation, University of Oulu. Accessed April 22, 2021. http://urn.fi/urn:isbn:9789526214870.

MLA Handbook (7th Edition):

Uimari, O (Outi). “Epidemiological and familial risk factors of uterine leiomyoma development.” 2017. Web. 22 Apr 2021.

Vancouver:

Uimari O(. Epidemiological and familial risk factors of uterine leiomyoma development. [Internet] [Doctoral dissertation]. University of Oulu; 2017. [cited 2021 Apr 22]. Available from: http://urn.fi/urn:isbn:9789526214870.

Council of Science Editors:

Uimari O(. Epidemiological and familial risk factors of uterine leiomyoma development. [Doctoral Dissertation]. University of Oulu; 2017. Available from: http://urn.fi/urn:isbn:9789526214870

28. Bamimore, Mary A. Resolving the Genetic Etiology of Hypercholesterolemia in Familial Combined Hyperlipidemia.

Degree: 2013, University of Western Ontario

 Hypercholesterolemia is a classical risk factor for cardiovascular disease development. The genetic etiology of hypercholesterolemia in familial combined hyperlipidemia (FCH), one of the most common… (more)

Subjects/Keywords: Hypercholesterolemia; Familial Combined Hyperlipidemia; Rare Variants; Genetic risk scores; Genomics; Cardiovascular Disease; Genetics and Genomics

…4.2.1 List of LDL-C genetic risk score in Mutation Negative Familial Hypercholesterolemia… …1.5 Familial Combined Hyperlipidemia… …51 1.7.2 Using genotyping to compare Genetic risk score in case-control cohorts .. 52 1.8… …55 1.9.2 Study II- Understanding hypercholesterolemia in Mutation Negative Familial… …59 2.1.1 Familial Combined Hyperlipidemia patients (Fredrickson Type 2B Phenotype)… 

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Bamimore, M. A. (2013). Resolving the Genetic Etiology of Hypercholesterolemia in Familial Combined Hyperlipidemia. (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/1511

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Bamimore, Mary A. “Resolving the Genetic Etiology of Hypercholesterolemia in Familial Combined Hyperlipidemia.” 2013. Thesis, University of Western Ontario. Accessed April 22, 2021. https://ir.lib.uwo.ca/etd/1511.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Bamimore, Mary A. “Resolving the Genetic Etiology of Hypercholesterolemia in Familial Combined Hyperlipidemia.” 2013. Web. 22 Apr 2021.

Vancouver:

Bamimore MA. Resolving the Genetic Etiology of Hypercholesterolemia in Familial Combined Hyperlipidemia. [Internet] [Thesis]. University of Western Ontario; 2013. [cited 2021 Apr 22]. Available from: https://ir.lib.uwo.ca/etd/1511.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Bamimore MA. Resolving the Genetic Etiology of Hypercholesterolemia in Familial Combined Hyperlipidemia. [Thesis]. University of Western Ontario; 2013. Available from: https://ir.lib.uwo.ca/etd/1511

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Otago

29. Coufal, Nicole Jessica. DNA Copy Number Variation and BRCAx Hereditary Breast Cancer .

Degree: University of Otago

 Breast cancer is the second most deadly cancer for New Zealand (NZ) women aged between 25-75 years. Breast cancer generally exhibits familial aggregation, consistent with… (more)

Subjects/Keywords: non-BRCA1/2; Breast cancer; Copy Number Variation; CNV; deletion; familial; hereditary; risk; genome wide; cancer

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Coufal, N. J. (n.d.). DNA Copy Number Variation and BRCAx Hereditary Breast Cancer . (Masters Thesis). University of Otago. Retrieved from http://hdl.handle.net/10523/4934

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Chicago Manual of Style (16th Edition):

Coufal, Nicole Jessica. “DNA Copy Number Variation and BRCAx Hereditary Breast Cancer .” Masters Thesis, University of Otago. Accessed April 22, 2021. http://hdl.handle.net/10523/4934.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

MLA Handbook (7th Edition):

Coufal, Nicole Jessica. “DNA Copy Number Variation and BRCAx Hereditary Breast Cancer .” Web. 22 Apr 2021.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Vancouver:

Coufal NJ. DNA Copy Number Variation and BRCAx Hereditary Breast Cancer . [Internet] [Masters thesis]. University of Otago; [cited 2021 Apr 22]. Available from: http://hdl.handle.net/10523/4934.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Council of Science Editors:

Coufal NJ. DNA Copy Number Variation and BRCAx Hereditary Breast Cancer . [Masters Thesis]. University of Otago; Available from: http://hdl.handle.net/10523/4934

Note: this citation may be lacking information needed for this citation format:
No year of publication.


University of Queensland

30. Read, Jazlyn. Familial melanoma risk genes in Queensland.

Degree: School of Medicine, 2016, University of Queensland

Subjects/Keywords: Cancer; Familial; Genetic; Hereditary cancer; Melanoma; Melanoma genetics; Polygenic inheritance; Skin - Cancer; Risk allele; 1112 Oncology and Carcinogenesis

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Read, J. (2016). Familial melanoma risk genes in Queensland. (Thesis). University of Queensland. Retrieved from http://espace.library.uq.edu.au/view/UQ:393147

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Read, Jazlyn. “Familial melanoma risk genes in Queensland.” 2016. Thesis, University of Queensland. Accessed April 22, 2021. http://espace.library.uq.edu.au/view/UQ:393147.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Read, Jazlyn. “Familial melanoma risk genes in Queensland.” 2016. Web. 22 Apr 2021.

Vancouver:

Read J. Familial melanoma risk genes in Queensland. [Internet] [Thesis]. University of Queensland; 2016. [cited 2021 Apr 22]. Available from: http://espace.library.uq.edu.au/view/UQ:393147.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Read J. Familial melanoma risk genes in Queensland. [Thesis]. University of Queensland; 2016. Available from: http://espace.library.uq.edu.au/view/UQ:393147

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

[1] [2]

.