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You searched for subject:(genetic testing). Showing records 1 – 30 of 285 total matches.

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1. Wilson, Miel Mason. At the Roots: Genealogy, Genetics, and Race in American Popular Culture.

Degree: PhD, American Studies, 2015, Brown University

 The growing interest in genealogy for African Americans is one expression of a longstanding desire to find answers to questions about ancestors, family, and heritage… (more)

Subjects/Keywords: genetic ancestry testing

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APA (6th Edition):

Wilson, M. M. (2015). At the Roots: Genealogy, Genetics, and Race in American Popular Culture. (Doctoral Dissertation). Brown University. Retrieved from https://repository.library.brown.edu/studio/item/bdr:419442/

Chicago Manual of Style (16th Edition):

Wilson, Miel Mason. “At the Roots: Genealogy, Genetics, and Race in American Popular Culture.” 2015. Doctoral Dissertation, Brown University. Accessed September 28, 2020. https://repository.library.brown.edu/studio/item/bdr:419442/.

MLA Handbook (7th Edition):

Wilson, Miel Mason. “At the Roots: Genealogy, Genetics, and Race in American Popular Culture.” 2015. Web. 28 Sep 2020.

Vancouver:

Wilson MM. At the Roots: Genealogy, Genetics, and Race in American Popular Culture. [Internet] [Doctoral dissertation]. Brown University; 2015. [cited 2020 Sep 28]. Available from: https://repository.library.brown.edu/studio/item/bdr:419442/.

Council of Science Editors:

Wilson MM. At the Roots: Genealogy, Genetics, and Race in American Popular Culture. [Doctoral Dissertation]. Brown University; 2015. Available from: https://repository.library.brown.edu/studio/item/bdr:419442/


University of South Carolina

2. Alfonso, Andrew Todd. Evaluating Changes in Patient Anxiety Regarding Classic Cancer Genetic Testing Versus Expanded Multiplex Cancer Genetic Testing.

Degree: MS, Genetic Counseling, 2015, University of South Carolina

  Multiplex cancer genetic testing by next generation sequencing (NGS) offers genetic counselors and patients new options for testing multiple genes beyond BRCA1 and BRCA2,… (more)

Subjects/Keywords: Medicine and Health Sciences; cancer genetic testing; genetic testing; expanded multiplex cancer genetic testing

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APA (6th Edition):

Alfonso, A. T. (2015). Evaluating Changes in Patient Anxiety Regarding Classic Cancer Genetic Testing Versus Expanded Multiplex Cancer Genetic Testing. (Masters Thesis). University of South Carolina. Retrieved from https://scholarcommons.sc.edu/etd/4532

Chicago Manual of Style (16th Edition):

Alfonso, Andrew Todd. “Evaluating Changes in Patient Anxiety Regarding Classic Cancer Genetic Testing Versus Expanded Multiplex Cancer Genetic Testing.” 2015. Masters Thesis, University of South Carolina. Accessed September 28, 2020. https://scholarcommons.sc.edu/etd/4532.

MLA Handbook (7th Edition):

Alfonso, Andrew Todd. “Evaluating Changes in Patient Anxiety Regarding Classic Cancer Genetic Testing Versus Expanded Multiplex Cancer Genetic Testing.” 2015. Web. 28 Sep 2020.

Vancouver:

Alfonso AT. Evaluating Changes in Patient Anxiety Regarding Classic Cancer Genetic Testing Versus Expanded Multiplex Cancer Genetic Testing. [Internet] [Masters thesis]. University of South Carolina; 2015. [cited 2020 Sep 28]. Available from: https://scholarcommons.sc.edu/etd/4532.

Council of Science Editors:

Alfonso AT. Evaluating Changes in Patient Anxiety Regarding Classic Cancer Genetic Testing Versus Expanded Multiplex Cancer Genetic Testing. [Masters Thesis]. University of South Carolina; 2015. Available from: https://scholarcommons.sc.edu/etd/4532


University of Newcastle

3. Cornell, Paige. Women's experiences of non-invasive prenatal testing.

Degree: 2020, University of Newcastle

Masters Coursework - Master of Clinical Psychology (MClinPsych)

While the uptake of non-invasive prenatal testing (NIPT) continues to increase, the provision of pre-test genetic counseling… (more)

Subjects/Keywords: genetic counseling; decision making; genetic testing

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APA (6th Edition):

Cornell, P. (2020). Women's experiences of non-invasive prenatal testing. (Thesis). University of Newcastle. Retrieved from http://hdl.handle.net/1959.13/1412442

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):

Cornell, Paige. “Women's experiences of non-invasive prenatal testing.” 2020. Thesis, University of Newcastle. Accessed September 28, 2020. http://hdl.handle.net/1959.13/1412442.

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

MLA Handbook (7th Edition):

Cornell, Paige. “Women's experiences of non-invasive prenatal testing.” 2020. Web. 28 Sep 2020.

Vancouver:

Cornell P. Women's experiences of non-invasive prenatal testing. [Internet] [Thesis]. University of Newcastle; 2020. [cited 2020 Sep 28]. Available from: http://hdl.handle.net/1959.13/1412442.

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

Council of Science Editors:

Cornell P. Women's experiences of non-invasive prenatal testing. [Thesis]. University of Newcastle; 2020. Available from: http://hdl.handle.net/1959.13/1412442

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


Universiteit Utrecht

4. Buijs, J. In context assessment of biology teachers’ content knowledge about the genome in relation to genetic testing.

Degree: 2013, Universiteit Utrecht

 Developments in genomics have led educational researchers to advocate for more genomics in high school biology education and a concept context approach instead of more… (more)

Subjects/Keywords: genetic testing; Biology; teacher

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APA (6th Edition):

Buijs, J. (2013). In context assessment of biology teachers’ content knowledge about the genome in relation to genetic testing. (Masters Thesis). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/280703

Chicago Manual of Style (16th Edition):

Buijs, J. “In context assessment of biology teachers’ content knowledge about the genome in relation to genetic testing.” 2013. Masters Thesis, Universiteit Utrecht. Accessed September 28, 2020. http://dspace.library.uu.nl:8080/handle/1874/280703.

MLA Handbook (7th Edition):

Buijs, J. “In context assessment of biology teachers’ content knowledge about the genome in relation to genetic testing.” 2013. Web. 28 Sep 2020.

Vancouver:

Buijs J. In context assessment of biology teachers’ content knowledge about the genome in relation to genetic testing. [Internet] [Masters thesis]. Universiteit Utrecht; 2013. [cited 2020 Sep 28]. Available from: http://dspace.library.uu.nl:8080/handle/1874/280703.

Council of Science Editors:

Buijs J. In context assessment of biology teachers’ content knowledge about the genome in relation to genetic testing. [Masters Thesis]. Universiteit Utrecht; 2013. Available from: http://dspace.library.uu.nl:8080/handle/1874/280703


Boston University

5. Thomas, Melissa. Counseling following direct to consumer genetic testing for Alzheimer's disease.

Degree: MS, Physician Assistant Program, 2019, Boston University

 Direct to consumer (DTC) personal genetic testing (PGT) is a popular choice for individuals in the United States who are interested in learning more about… (more)

Subjects/Keywords: Genetics; Alzheimer's disease; Genetic testing

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APA (6th Edition):

Thomas, M. (2019). Counseling following direct to consumer genetic testing for Alzheimer's disease. (Masters Thesis). Boston University. Retrieved from http://hdl.handle.net/2144/38736

Chicago Manual of Style (16th Edition):

Thomas, Melissa. “Counseling following direct to consumer genetic testing for Alzheimer's disease.” 2019. Masters Thesis, Boston University. Accessed September 28, 2020. http://hdl.handle.net/2144/38736.

MLA Handbook (7th Edition):

Thomas, Melissa. “Counseling following direct to consumer genetic testing for Alzheimer's disease.” 2019. Web. 28 Sep 2020.

Vancouver:

Thomas M. Counseling following direct to consumer genetic testing for Alzheimer's disease. [Internet] [Masters thesis]. Boston University; 2019. [cited 2020 Sep 28]. Available from: http://hdl.handle.net/2144/38736.

Council of Science Editors:

Thomas M. Counseling following direct to consumer genetic testing for Alzheimer's disease. [Masters Thesis]. Boston University; 2019. Available from: http://hdl.handle.net/2144/38736


University of Limerick

6. Quigley, Stephen James. Knowledge is wealth: investigating psychosocial distress and ameliorating knowledge deficiencies in parents of children identified, through newborn screening in Ireland, as carrying an altered cystic fibrosis gene.

Degree: 2014, University of Limerick

peer-reviewed

Cystic Fibrosis is an inherited disease affecting mainly the lungs and digestive system. In Ireland, the incidence of cystic fibrosis is 1 in 1,461… (more)

Subjects/Keywords: cystic fibrosis; CF; genetic testing

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APA (6th Edition):

Quigley, S. J. (2014). Knowledge is wealth: investigating psychosocial distress and ameliorating knowledge deficiencies in parents of children identified, through newborn screening in Ireland, as carrying an altered cystic fibrosis gene. (Thesis). University of Limerick. Retrieved from http://hdl.handle.net/10344/4318

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):

Quigley, Stephen James. “Knowledge is wealth: investigating psychosocial distress and ameliorating knowledge deficiencies in parents of children identified, through newborn screening in Ireland, as carrying an altered cystic fibrosis gene.” 2014. Thesis, University of Limerick. Accessed September 28, 2020. http://hdl.handle.net/10344/4318.

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

MLA Handbook (7th Edition):

Quigley, Stephen James. “Knowledge is wealth: investigating psychosocial distress and ameliorating knowledge deficiencies in parents of children identified, through newborn screening in Ireland, as carrying an altered cystic fibrosis gene.” 2014. Web. 28 Sep 2020.

Vancouver:

Quigley SJ. Knowledge is wealth: investigating psychosocial distress and ameliorating knowledge deficiencies in parents of children identified, through newborn screening in Ireland, as carrying an altered cystic fibrosis gene. [Internet] [Thesis]. University of Limerick; 2014. [cited 2020 Sep 28]. Available from: http://hdl.handle.net/10344/4318.

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

Council of Science Editors:

Quigley SJ. Knowledge is wealth: investigating psychosocial distress and ameliorating knowledge deficiencies in parents of children identified, through newborn screening in Ireland, as carrying an altered cystic fibrosis gene. [Thesis]. University of Limerick; 2014. Available from: http://hdl.handle.net/10344/4318

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


Brandeis University

7. Hunter, Whitney. Utilization of Genetic Testing Among Children with Autism Spectrum Disorders.

Degree: 2011, Brandeis University

 Autism spectrum disorders (ASDs) which include autistic disorder, Asperger disorder and pervasive developmental disorder-not otherwise specified (PDD-NOS) have gained significant attention because of an apparent… (more)

Subjects/Keywords: Genetic Testing; Autism Spectrum Disorders; Predictors of Genetic Testing

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

APA (6th Edition):

Hunter, W. (2011). Utilization of Genetic Testing Among Children with Autism Spectrum Disorders. (Thesis). Brandeis University. Retrieved from http://hdl.handle.net/10192/24421

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):

Hunter, Whitney. “Utilization of Genetic Testing Among Children with Autism Spectrum Disorders.” 2011. Thesis, Brandeis University. Accessed September 28, 2020. http://hdl.handle.net/10192/24421.

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

MLA Handbook (7th Edition):

Hunter, Whitney. “Utilization of Genetic Testing Among Children with Autism Spectrum Disorders.” 2011. Web. 28 Sep 2020.

Vancouver:

Hunter W. Utilization of Genetic Testing Among Children with Autism Spectrum Disorders. [Internet] [Thesis]. Brandeis University; 2011. [cited 2020 Sep 28]. Available from: http://hdl.handle.net/10192/24421.

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

Council of Science Editors:

Hunter W. Utilization of Genetic Testing Among Children with Autism Spectrum Disorders. [Thesis]. Brandeis University; 2011. Available from: http://hdl.handle.net/10192/24421

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


Duquesne University

8. Minor, Jessica L. A Revised Model for Informed Consent in Predictive Genetic Testing.

Degree: PhD, Health Care Ethics, 2013, Duquesne University

 This dissertation develops a revised model of informed consent for PGT. The need for this model arises from distinguishing characteristics of PGT, which make it… (more)

Subjects/Keywords: Genetics; Genetic testing; Informed consent; Medical ethics; Predictive genetic testing

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APA (6th Edition):

Minor, J. L. (2013). A Revised Model for Informed Consent in Predictive Genetic Testing. (Doctoral Dissertation). Duquesne University. Retrieved from https://dsc.duq.edu/etd/936

Chicago Manual of Style (16th Edition):

Minor, Jessica L. “A Revised Model for Informed Consent in Predictive Genetic Testing.” 2013. Doctoral Dissertation, Duquesne University. Accessed September 28, 2020. https://dsc.duq.edu/etd/936.

MLA Handbook (7th Edition):

Minor, Jessica L. “A Revised Model for Informed Consent in Predictive Genetic Testing.” 2013. Web. 28 Sep 2020.

Vancouver:

Minor JL. A Revised Model for Informed Consent in Predictive Genetic Testing. [Internet] [Doctoral dissertation]. Duquesne University; 2013. [cited 2020 Sep 28]. Available from: https://dsc.duq.edu/etd/936.

Council of Science Editors:

Minor JL. A Revised Model for Informed Consent in Predictive Genetic Testing. [Doctoral Dissertation]. Duquesne University; 2013. Available from: https://dsc.duq.edu/etd/936


University of South Carolina

9. Bettinelli, Audra Lea. Assessing Genetics Providers' Perspectives of and Experiences with DTC Genetic Testing: Creation of an Educational Module.

Degree: MS, Genetic Counseling, 2012, University of South Carolina

  Purpose: Direct-to-consumer genetic testing exemplifies the evolution of the medical genetics field towards more encompassing genomic medicine and the implementation of personalized medicine. This… (more)

Subjects/Keywords: Genetics and Genomics; Life Sciences; Direct-to-Consumer Genetic Testing; Genetic counseling; Genetic Testing; genomic testing; Health education; personal genome testing

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

APA (6th Edition):

Bettinelli, A. L. (2012). Assessing Genetics Providers' Perspectives of and Experiences with DTC Genetic Testing: Creation of an Educational Module. (Masters Thesis). University of South Carolina. Retrieved from https://scholarcommons.sc.edu/etd/1250

Chicago Manual of Style (16th Edition):

Bettinelli, Audra Lea. “Assessing Genetics Providers' Perspectives of and Experiences with DTC Genetic Testing: Creation of an Educational Module.” 2012. Masters Thesis, University of South Carolina. Accessed September 28, 2020. https://scholarcommons.sc.edu/etd/1250.

MLA Handbook (7th Edition):

Bettinelli, Audra Lea. “Assessing Genetics Providers' Perspectives of and Experiences with DTC Genetic Testing: Creation of an Educational Module.” 2012. Web. 28 Sep 2020.

Vancouver:

Bettinelli AL. Assessing Genetics Providers' Perspectives of and Experiences with DTC Genetic Testing: Creation of an Educational Module. [Internet] [Masters thesis]. University of South Carolina; 2012. [cited 2020 Sep 28]. Available from: https://scholarcommons.sc.edu/etd/1250.

Council of Science Editors:

Bettinelli AL. Assessing Genetics Providers' Perspectives of and Experiences with DTC Genetic Testing: Creation of an Educational Module. [Masters Thesis]. University of South Carolina; 2012. Available from: https://scholarcommons.sc.edu/etd/1250


Texas A&M University

10. Xu, Lei. Autism Genetic Testing: Psychological Factors Associated with the Test Decisions Among Parents of Children with Autism Spectrum Disorders (ASDs) in Taiwan.

Degree: PhD, Health Education, 2014, Texas A&M University

 Autism spectrum disorders (ASDs) are a group of highly inheritable disorders. Genetic testing for ASD is anticipated to be offered in Taiwan in the near… (more)

Subjects/Keywords: Autism genetic testing; attitudes; intention; emotions

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

APA (6th Edition):

Xu, L. (2014). Autism Genetic Testing: Psychological Factors Associated with the Test Decisions Among Parents of Children with Autism Spectrum Disorders (ASDs) in Taiwan. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/153431

Chicago Manual of Style (16th Edition):

Xu, Lei. “Autism Genetic Testing: Psychological Factors Associated with the Test Decisions Among Parents of Children with Autism Spectrum Disorders (ASDs) in Taiwan.” 2014. Doctoral Dissertation, Texas A&M University. Accessed September 28, 2020. http://hdl.handle.net/1969.1/153431.

MLA Handbook (7th Edition):

Xu, Lei. “Autism Genetic Testing: Psychological Factors Associated with the Test Decisions Among Parents of Children with Autism Spectrum Disorders (ASDs) in Taiwan.” 2014. Web. 28 Sep 2020.

Vancouver:

Xu L. Autism Genetic Testing: Psychological Factors Associated with the Test Decisions Among Parents of Children with Autism Spectrum Disorders (ASDs) in Taiwan. [Internet] [Doctoral dissertation]. Texas A&M University; 2014. [cited 2020 Sep 28]. Available from: http://hdl.handle.net/1969.1/153431.

Council of Science Editors:

Xu L. Autism Genetic Testing: Psychological Factors Associated with the Test Decisions Among Parents of Children with Autism Spectrum Disorders (ASDs) in Taiwan. [Doctoral Dissertation]. Texas A&M University; 2014. Available from: http://hdl.handle.net/1969.1/153431


University of Cincinnati

11. Strike, Brian J. The Clinical Utility of Comprehensive Genetic Testing for Individuals with Congenital Sensorineural Hearing Loss.

Degree: MS, Allied Health Sciences : Genetic Counseling, 2008, University of Cincinnati

 Sensorineural hearing loss (SNHL) is an etiologically heterogeneous condition with numerous environmental causes and more than 120 identified causative genes. The purpose of this study… (more)

Subjects/Keywords: Genetics; Sensorineural Hearing Loss; genetic testing

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APA (6th Edition):

Strike, B. J. (2008). The Clinical Utility of Comprehensive Genetic Testing for Individuals with Congenital Sensorineural Hearing Loss. (Masters Thesis). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1212164935

Chicago Manual of Style (16th Edition):

Strike, Brian J. “The Clinical Utility of Comprehensive Genetic Testing for Individuals with Congenital Sensorineural Hearing Loss.” 2008. Masters Thesis, University of Cincinnati. Accessed September 28, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1212164935.

MLA Handbook (7th Edition):

Strike, Brian J. “The Clinical Utility of Comprehensive Genetic Testing for Individuals with Congenital Sensorineural Hearing Loss.” 2008. Web. 28 Sep 2020.

Vancouver:

Strike BJ. The Clinical Utility of Comprehensive Genetic Testing for Individuals with Congenital Sensorineural Hearing Loss. [Internet] [Masters thesis]. University of Cincinnati; 2008. [cited 2020 Sep 28]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1212164935.

Council of Science Editors:

Strike BJ. The Clinical Utility of Comprehensive Genetic Testing for Individuals with Congenital Sensorineural Hearing Loss. [Masters Thesis]. University of Cincinnati; 2008. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1212164935


University of Iowa

12. Sloan-Heggen, Christina Marie. Precision health and deafness–optimizing genetic diagnosis.

Degree: PhD, Molecular Physiology and Biophysics, 2018, University of Iowa

  Deafness is the most common sensory deficit in humans. In the United States 1-2 in a thousand babies is born with significant deafness, well… (more)

Subjects/Keywords: Deafness; Genetics; Genetic testing; Precision healthcare; Biophysics

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APA (6th Edition):

Sloan-Heggen, C. M. (2018). Precision health and deafness–optimizing genetic diagnosis. (Doctoral Dissertation). University of Iowa. Retrieved from https://ir.uiowa.edu/etd/6287

Chicago Manual of Style (16th Edition):

Sloan-Heggen, Christina Marie. “Precision health and deafness–optimizing genetic diagnosis.” 2018. Doctoral Dissertation, University of Iowa. Accessed September 28, 2020. https://ir.uiowa.edu/etd/6287.

MLA Handbook (7th Edition):

Sloan-Heggen, Christina Marie. “Precision health and deafness–optimizing genetic diagnosis.” 2018. Web. 28 Sep 2020.

Vancouver:

Sloan-Heggen CM. Precision health and deafness–optimizing genetic diagnosis. [Internet] [Doctoral dissertation]. University of Iowa; 2018. [cited 2020 Sep 28]. Available from: https://ir.uiowa.edu/etd/6287.

Council of Science Editors:

Sloan-Heggen CM. Precision health and deafness–optimizing genetic diagnosis. [Doctoral Dissertation]. University of Iowa; 2018. Available from: https://ir.uiowa.edu/etd/6287


Brandeis University

13. Fayer, Shawn. The Psychosocial Implications of a Hereditary Colorectal Cancer Syndrome Diagnosis in Emerging Adulthood.

Degree: 2016, Brandeis University

 Lynch syndrome (LS), attenuated familial adenomatous polyposis (AFAP), and MUTYH-associated polyposis (MAP), are hereditary colorectal cancer syndromes with increased susceptibility for multiple cancers in adulthood.… (more)

Subjects/Keywords: Genetic testing; emerging adulthood; Lynch syndrome; AFAP

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APA (6th Edition):

Fayer, S. (2016). The Psychosocial Implications of a Hereditary Colorectal Cancer Syndrome Diagnosis in Emerging Adulthood. (Thesis). Brandeis University. Retrieved from http://hdl.handle.net/10192/32091

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):

Fayer, Shawn. “The Psychosocial Implications of a Hereditary Colorectal Cancer Syndrome Diagnosis in Emerging Adulthood.” 2016. Thesis, Brandeis University. Accessed September 28, 2020. http://hdl.handle.net/10192/32091.

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

MLA Handbook (7th Edition):

Fayer, Shawn. “The Psychosocial Implications of a Hereditary Colorectal Cancer Syndrome Diagnosis in Emerging Adulthood.” 2016. Web. 28 Sep 2020.

Vancouver:

Fayer S. The Psychosocial Implications of a Hereditary Colorectal Cancer Syndrome Diagnosis in Emerging Adulthood. [Internet] [Thesis]. Brandeis University; 2016. [cited 2020 Sep 28]. Available from: http://hdl.handle.net/10192/32091.

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

Council of Science Editors:

Fayer S. The Psychosocial Implications of a Hereditary Colorectal Cancer Syndrome Diagnosis in Emerging Adulthood. [Thesis]. Brandeis University; 2016. Available from: http://hdl.handle.net/10192/32091

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


Brandeis University

14. Lei, Qian (Lorraine). An Exploration of the Involvement of Genetic Counselors in the Delivery of Aneuploidy Screening and Testing.

Degree: 2018, Brandeis University

 There is a current shortage of certified clinical genetic counselors to keep up the publics’ growing demand for genetic counseling services. This is especially a… (more)

Subjects/Keywords: Genetic Counseling; prenatal; Noninvasive prenatal testing; cffDNA

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APA (6th Edition):

Lei, Q. (. (2018). An Exploration of the Involvement of Genetic Counselors in the Delivery of Aneuploidy Screening and Testing. (Thesis). Brandeis University. Retrieved from http://hdl.handle.net/10192/35661

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):

Lei, Qian (Lorraine). “An Exploration of the Involvement of Genetic Counselors in the Delivery of Aneuploidy Screening and Testing.” 2018. Thesis, Brandeis University. Accessed September 28, 2020. http://hdl.handle.net/10192/35661.

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

MLA Handbook (7th Edition):

Lei, Qian (Lorraine). “An Exploration of the Involvement of Genetic Counselors in the Delivery of Aneuploidy Screening and Testing.” 2018. Web. 28 Sep 2020.

Vancouver:

Lei Q(. An Exploration of the Involvement of Genetic Counselors in the Delivery of Aneuploidy Screening and Testing. [Internet] [Thesis]. Brandeis University; 2018. [cited 2020 Sep 28]. Available from: http://hdl.handle.net/10192/35661.

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

Council of Science Editors:

Lei Q(. An Exploration of the Involvement of Genetic Counselors in the Delivery of Aneuploidy Screening and Testing. [Thesis]. Brandeis University; 2018. Available from: http://hdl.handle.net/10192/35661

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


University of Toronto

15. Nielsen, Daiva Elena. Disclosure of Genetic Information for Personalized Nutrition and Change in Dietary Intake.

Degree: PhD, 2014, University of Toronto

 Background: Personal genetic information has become increasingly accessible as a result of consumer genetic tests. Proponents claim that the information may motivate positive behavioural changes… (more)

Subjects/Keywords: Genetic testing; Health Behaviour; Nutrigenomics; Nutrition; 0570

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APA (6th Edition):

Nielsen, D. E. (2014). Disclosure of Genetic Information for Personalized Nutrition and Change in Dietary Intake. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/68408

Chicago Manual of Style (16th Edition):

Nielsen, Daiva Elena. “Disclosure of Genetic Information for Personalized Nutrition and Change in Dietary Intake.” 2014. Doctoral Dissertation, University of Toronto. Accessed September 28, 2020. http://hdl.handle.net/1807/68408.

MLA Handbook (7th Edition):

Nielsen, Daiva Elena. “Disclosure of Genetic Information for Personalized Nutrition and Change in Dietary Intake.” 2014. Web. 28 Sep 2020.

Vancouver:

Nielsen DE. Disclosure of Genetic Information for Personalized Nutrition and Change in Dietary Intake. [Internet] [Doctoral dissertation]. University of Toronto; 2014. [cited 2020 Sep 28]. Available from: http://hdl.handle.net/1807/68408.

Council of Science Editors:

Nielsen DE. Disclosure of Genetic Information for Personalized Nutrition and Change in Dietary Intake. [Doctoral Dissertation]. University of Toronto; 2014. Available from: http://hdl.handle.net/1807/68408


University of Melbourne

16. VEARS, DANYA. Genetic carrier testing in children: perspectives of parents and genetic health professionals.

Degree: 2015, University of Melbourne

 Parents are generally considered best placed to make decisions on behalf of their children. However, in some instances, parents’ decisions are called into question. In… (more)

Subjects/Keywords: genetic counselling; children; carrier testing; ethics

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APA (6th Edition):

VEARS, D. (2015). Genetic carrier testing in children: perspectives of parents and genetic health professionals. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/55297

Chicago Manual of Style (16th Edition):

VEARS, DANYA. “Genetic carrier testing in children: perspectives of parents and genetic health professionals.” 2015. Doctoral Dissertation, University of Melbourne. Accessed September 28, 2020. http://hdl.handle.net/11343/55297.

MLA Handbook (7th Edition):

VEARS, DANYA. “Genetic carrier testing in children: perspectives of parents and genetic health professionals.” 2015. Web. 28 Sep 2020.

Vancouver:

VEARS D. Genetic carrier testing in children: perspectives of parents and genetic health professionals. [Internet] [Doctoral dissertation]. University of Melbourne; 2015. [cited 2020 Sep 28]. Available from: http://hdl.handle.net/11343/55297.

Council of Science Editors:

VEARS D. Genetic carrier testing in children: perspectives of parents and genetic health professionals. [Doctoral Dissertation]. University of Melbourne; 2015. Available from: http://hdl.handle.net/11343/55297


University of Melbourne

17. Erlichster, Michael. Improving application of human leukocyte antigen genotyping in precision medicine.

Degree: 2018, University of Melbourne

 Variation in the human leukocyte antigen (HLA) genes has been extensively associated with predisposition to autoimmune disease and adverse drug reaction. Translation of these associations… (more)

Subjects/Keywords: human leukocyte antigen; genetic testing; precision medicine

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APA (6th Edition):

Erlichster, M. (2018). Improving application of human leukocyte antigen genotyping in precision medicine. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/218155

Chicago Manual of Style (16th Edition):

Erlichster, Michael. “Improving application of human leukocyte antigen genotyping in precision medicine.” 2018. Doctoral Dissertation, University of Melbourne. Accessed September 28, 2020. http://hdl.handle.net/11343/218155.

MLA Handbook (7th Edition):

Erlichster, Michael. “Improving application of human leukocyte antigen genotyping in precision medicine.” 2018. Web. 28 Sep 2020.

Vancouver:

Erlichster M. Improving application of human leukocyte antigen genotyping in precision medicine. [Internet] [Doctoral dissertation]. University of Melbourne; 2018. [cited 2020 Sep 28]. Available from: http://hdl.handle.net/11343/218155.

Council of Science Editors:

Erlichster M. Improving application of human leukocyte antigen genotyping in precision medicine. [Doctoral Dissertation]. University of Melbourne; 2018. Available from: http://hdl.handle.net/11343/218155


Texas Medical Center

18. Copeland, Allison. ATTITUDES AND PRACTICES OF GENETIC COUNSELORS IN PROVIDING PREDICTIVE TESTING TO MINORS AT RISK FOR LI-FRAUMENI SYNDROME.

Degree: MS, 2013, Texas Medical Center

  Li- Fraumeni Syndrome (LFS) is a rare autosomal dominant hereditary cancer syndrome caused by mutations in the TP53 gene that predisposes individuals to a… (more)

Subjects/Keywords: Li-Fraumeni syndrome; predictive testing; genetic testing; minors; genetic counseling; Medicine and Health Sciences

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APA (6th Edition):

Copeland, A. (2013). ATTITUDES AND PRACTICES OF GENETIC COUNSELORS IN PROVIDING PREDICTIVE TESTING TO MINORS AT RISK FOR LI-FRAUMENI SYNDROME. (Thesis). Texas Medical Center. Retrieved from https://digitalcommons.library.tmc.edu/utgsbs_dissertations/363

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):

Copeland, Allison. “ATTITUDES AND PRACTICES OF GENETIC COUNSELORS IN PROVIDING PREDICTIVE TESTING TO MINORS AT RISK FOR LI-FRAUMENI SYNDROME.” 2013. Thesis, Texas Medical Center. Accessed September 28, 2020. https://digitalcommons.library.tmc.edu/utgsbs_dissertations/363.

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

MLA Handbook (7th Edition):

Copeland, Allison. “ATTITUDES AND PRACTICES OF GENETIC COUNSELORS IN PROVIDING PREDICTIVE TESTING TO MINORS AT RISK FOR LI-FRAUMENI SYNDROME.” 2013. Web. 28 Sep 2020.

Vancouver:

Copeland A. ATTITUDES AND PRACTICES OF GENETIC COUNSELORS IN PROVIDING PREDICTIVE TESTING TO MINORS AT RISK FOR LI-FRAUMENI SYNDROME. [Internet] [Thesis]. Texas Medical Center; 2013. [cited 2020 Sep 28]. Available from: https://digitalcommons.library.tmc.edu/utgsbs_dissertations/363.

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

Council of Science Editors:

Copeland A. ATTITUDES AND PRACTICES OF GENETIC COUNSELORS IN PROVIDING PREDICTIVE TESTING TO MINORS AT RISK FOR LI-FRAUMENI SYNDROME. [Thesis]. Texas Medical Center; 2013. Available from: https://digitalcommons.library.tmc.edu/utgsbs_dissertations/363

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


Universiteit Utrecht

19. Klous, P.M. Implementation of routine predictive genetic testing for cardiovascular disease. Clinical application and ethical aspects.

Degree: 2013, Universiteit Utrecht

 Cardiovascular diseases are the leading cause of death worldwide and are caused by a combination of genetic and environmental influences. Hence they have a great… (more)

Subjects/Keywords: Cardiovascular disease; Genetic testing; Genetic screening; p4 medicine; ethics; genetics; diagnostics

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

APA (6th Edition):

Klous, P. M. (2013). Implementation of routine predictive genetic testing for cardiovascular disease. Clinical application and ethical aspects. (Masters Thesis). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/279024

Chicago Manual of Style (16th Edition):

Klous, P M. “Implementation of routine predictive genetic testing for cardiovascular disease. Clinical application and ethical aspects.” 2013. Masters Thesis, Universiteit Utrecht. Accessed September 28, 2020. http://dspace.library.uu.nl:8080/handle/1874/279024.

MLA Handbook (7th Edition):

Klous, P M. “Implementation of routine predictive genetic testing for cardiovascular disease. Clinical application and ethical aspects.” 2013. Web. 28 Sep 2020.

Vancouver:

Klous PM. Implementation of routine predictive genetic testing for cardiovascular disease. Clinical application and ethical aspects. [Internet] [Masters thesis]. Universiteit Utrecht; 2013. [cited 2020 Sep 28]. Available from: http://dspace.library.uu.nl:8080/handle/1874/279024.

Council of Science Editors:

Klous PM. Implementation of routine predictive genetic testing for cardiovascular disease. Clinical application and ethical aspects. [Masters Thesis]. Universiteit Utrecht; 2013. Available from: http://dspace.library.uu.nl:8080/handle/1874/279024


University of Cincinnati

20. Somers, Allyson. Provision of cardiovascular genetic counseling services: current practice and future directions.

Degree: MS, Medicine: Genetic Counseling, 2013, University of Cincinnati

 Cardiovascular genetic counseling has emerged as a specialty critical to the care of patients with heritable cardiovascular disease. Although there is an increasing demand for… (more)

Subjects/Keywords: Genetics; Cardiac genetics; Cardiac genetic counseling; Cardiovascular genetic testing

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

APA (6th Edition):

Somers, A. (2013). Provision of cardiovascular genetic counseling services: current practice and future directions. (Masters Thesis). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1367924189

Chicago Manual of Style (16th Edition):

Somers, Allyson. “Provision of cardiovascular genetic counseling services: current practice and future directions.” 2013. Masters Thesis, University of Cincinnati. Accessed September 28, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1367924189.

MLA Handbook (7th Edition):

Somers, Allyson. “Provision of cardiovascular genetic counseling services: current practice and future directions.” 2013. Web. 28 Sep 2020.

Vancouver:

Somers A. Provision of cardiovascular genetic counseling services: current practice and future directions. [Internet] [Masters thesis]. University of Cincinnati; 2013. [cited 2020 Sep 28]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1367924189.

Council of Science Editors:

Somers A. Provision of cardiovascular genetic counseling services: current practice and future directions. [Masters Thesis]. University of Cincinnati; 2013. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1367924189


University of Cincinnati

21. Prochniak, Carolyn F. Barriers to and Motivations for Referral to Cancer Genetics Clinics.

Degree: MS, Allied Health Sciences : Genetic Counseling, 2010, University of Cincinnati

 Although it is well known that under-referral of colon cancer patients to cancer genetics clinics has been a chronic problem, no study has yet to… (more)

Subjects/Keywords: Oncology; genetic counseling; hereditary colorectal cancer; genetic testing; referral; risk assessment

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

APA (6th Edition):

Prochniak, C. F. (2010). Barriers to and Motivations for Referral to Cancer Genetics Clinics. (Masters Thesis). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1276976540

Chicago Manual of Style (16th Edition):

Prochniak, Carolyn F. “Barriers to and Motivations for Referral to Cancer Genetics Clinics.” 2010. Masters Thesis, University of Cincinnati. Accessed September 28, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1276976540.

MLA Handbook (7th Edition):

Prochniak, Carolyn F. “Barriers to and Motivations for Referral to Cancer Genetics Clinics.” 2010. Web. 28 Sep 2020.

Vancouver:

Prochniak CF. Barriers to and Motivations for Referral to Cancer Genetics Clinics. [Internet] [Masters thesis]. University of Cincinnati; 2010. [cited 2020 Sep 28]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1276976540.

Council of Science Editors:

Prochniak CF. Barriers to and Motivations for Referral to Cancer Genetics Clinics. [Masters Thesis]. University of Cincinnati; 2010. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1276976540


Texas Medical Center

22. Rock, Katherine. Attitudes About Predictive MEN1 Genetic Testing in Minors.

Degree: MS, 2012, Texas Medical Center

  Multiple Endocrine Neoplasia type 1 (MEN1) is a hereditary cancer syndrome characterized by tumors of the endocrine system. Tumors most commonly develop in the… (more)

Subjects/Keywords: MEN1; Genetic Testing; Minors; Endocrine; Genetic Counseling; Medicine and Health Sciences

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

APA (6th Edition):

Rock, K. (2012). Attitudes About Predictive MEN1 Genetic Testing in Minors. (Thesis). Texas Medical Center. Retrieved from https://digitalcommons.library.tmc.edu/utgsbs_dissertations/270

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):

Rock, Katherine. “Attitudes About Predictive MEN1 Genetic Testing in Minors.” 2012. Thesis, Texas Medical Center. Accessed September 28, 2020. https://digitalcommons.library.tmc.edu/utgsbs_dissertations/270.

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

MLA Handbook (7th Edition):

Rock, Katherine. “Attitudes About Predictive MEN1 Genetic Testing in Minors.” 2012. Web. 28 Sep 2020.

Vancouver:

Rock K. Attitudes About Predictive MEN1 Genetic Testing in Minors. [Internet] [Thesis]. Texas Medical Center; 2012. [cited 2020 Sep 28]. Available from: https://digitalcommons.library.tmc.edu/utgsbs_dissertations/270.

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

Council of Science Editors:

Rock K. Attitudes About Predictive MEN1 Genetic Testing in Minors. [Thesis]. Texas Medical Center; 2012. Available from: https://digitalcommons.library.tmc.edu/utgsbs_dissertations/270

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


University of Otago

23. Johnston, Ebony Nicole. Nature and Nurture: Are We Missing a Third Option? .

Degree: 2013, University of Otago

 In light of my own situation, I have been drawn to question whether all experiences can be explained in terms solely of nature and nurture.… (more)

Subjects/Keywords: nature; nuture; chaos; emergence; genetic testing; genetic modification; cloning

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APA (6th Edition):

Johnston, E. N. (2013). Nature and Nurture: Are We Missing a Third Option? . (Masters Thesis). University of Otago. Retrieved from http://hdl.handle.net/10523/4157

Chicago Manual of Style (16th Edition):

Johnston, Ebony Nicole. “Nature and Nurture: Are We Missing a Third Option? .” 2013. Masters Thesis, University of Otago. Accessed September 28, 2020. http://hdl.handle.net/10523/4157.

MLA Handbook (7th Edition):

Johnston, Ebony Nicole. “Nature and Nurture: Are We Missing a Third Option? .” 2013. Web. 28 Sep 2020.

Vancouver:

Johnston EN. Nature and Nurture: Are We Missing a Third Option? . [Internet] [Masters thesis]. University of Otago; 2013. [cited 2020 Sep 28]. Available from: http://hdl.handle.net/10523/4157.

Council of Science Editors:

Johnston EN. Nature and Nurture: Are We Missing a Third Option? . [Masters Thesis]. University of Otago; 2013. Available from: http://hdl.handle.net/10523/4157


University of New South Wales

24. Szot, Justin Oliver. Identifying the Genetic Causes of Congenital Heart Disease.

Degree: Biotechnology & Biomolecular Sciences, 2017, University of New South Wales

 Congenital heart diseases (CHDs), structural abnormalities of the heart that arises during embryonic development, are the most common inborn malformations, affecting up to 1% of… (more)

Subjects/Keywords: Genetic Variation; Congenital Heart Disease; Exome; Genetic Testing; CHD Gene List

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APA (6th Edition):

Szot, J. O. (2017). Identifying the Genetic Causes of Congenital Heart Disease. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/59724

Chicago Manual of Style (16th Edition):

Szot, Justin Oliver. “Identifying the Genetic Causes of Congenital Heart Disease.” 2017. Doctoral Dissertation, University of New South Wales. Accessed September 28, 2020. http://handle.unsw.edu.au/1959.4/59724.

MLA Handbook (7th Edition):

Szot, Justin Oliver. “Identifying the Genetic Causes of Congenital Heart Disease.” 2017. Web. 28 Sep 2020.

Vancouver:

Szot JO. Identifying the Genetic Causes of Congenital Heart Disease. [Internet] [Doctoral dissertation]. University of New South Wales; 2017. [cited 2020 Sep 28]. Available from: http://handle.unsw.edu.au/1959.4/59724.

Council of Science Editors:

Szot JO. Identifying the Genetic Causes of Congenital Heart Disease. [Doctoral Dissertation]. University of New South Wales; 2017. Available from: http://handle.unsw.edu.au/1959.4/59724


University of Plymouth

25. Lewis, Celine. The effect of psychosocial information resources on the psychological impact of genetic testing for patients.

Degree: PhD, 2011, University of Plymouth

 The effect of psychosocial information resources on the psychological impact of genetic testing for patients Background: The genetic testing process has been shown to have… (more)

Subjects/Keywords: 615.5; genetic testing, genetic counselling, education, patient information, psychosocial, mixed methods

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APA (6th Edition):

Lewis, C. (2011). The effect of psychosocial information resources on the psychological impact of genetic testing for patients. (Doctoral Dissertation). University of Plymouth. Retrieved from http://hdl.handle.net/10026.1/543

Chicago Manual of Style (16th Edition):

Lewis, Celine. “The effect of psychosocial information resources on the psychological impact of genetic testing for patients.” 2011. Doctoral Dissertation, University of Plymouth. Accessed September 28, 2020. http://hdl.handle.net/10026.1/543.

MLA Handbook (7th Edition):

Lewis, Celine. “The effect of psychosocial information resources on the psychological impact of genetic testing for patients.” 2011. Web. 28 Sep 2020.

Vancouver:

Lewis C. The effect of psychosocial information resources on the psychological impact of genetic testing for patients. [Internet] [Doctoral dissertation]. University of Plymouth; 2011. [cited 2020 Sep 28]. Available from: http://hdl.handle.net/10026.1/543.

Council of Science Editors:

Lewis C. The effect of psychosocial information resources on the psychological impact of genetic testing for patients. [Doctoral Dissertation]. University of Plymouth; 2011. Available from: http://hdl.handle.net/10026.1/543


Princeton University

26. Kilbride, Madison Korinne. Ethical Issues In Genetic Testing .

Degree: PhD, 2017, Princeton University

Genetic testing raises a host of ethical dilemmas—for the patient diagnosed with a genetic disorder, for her medical team, and even for the insurance company… (more)

Subjects/Keywords: duty to warn; ethics; Genetic testing; pre-implantation genetic diagnosis

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APA (6th Edition):

Kilbride, M. K. (2017). Ethical Issues In Genetic Testing . (Doctoral Dissertation). Princeton University. Retrieved from http://arks.princeton.edu/ark:/88435/dsp01w9505313n

Chicago Manual of Style (16th Edition):

Kilbride, Madison Korinne. “Ethical Issues In Genetic Testing .” 2017. Doctoral Dissertation, Princeton University. Accessed September 28, 2020. http://arks.princeton.edu/ark:/88435/dsp01w9505313n.

MLA Handbook (7th Edition):

Kilbride, Madison Korinne. “Ethical Issues In Genetic Testing .” 2017. Web. 28 Sep 2020.

Vancouver:

Kilbride MK. Ethical Issues In Genetic Testing . [Internet] [Doctoral dissertation]. Princeton University; 2017. [cited 2020 Sep 28]. Available from: http://arks.princeton.edu/ark:/88435/dsp01w9505313n.

Council of Science Editors:

Kilbride MK. Ethical Issues In Genetic Testing . [Doctoral Dissertation]. Princeton University; 2017. Available from: http://arks.princeton.edu/ark:/88435/dsp01w9505313n


Brandeis University

27. Delaney, Christine. The Impact of Genetic Testing for Rett Syndrome: An Assessment of Parents' Experiences.

Degree: 2011, Brandeis University

 Rett syndrome (RTT) is an X-linked disorder diagnosed either clinically or with genetic testing. Approximately 60% of girls with RTT have had genetic testing, most… (more)

Subjects/Keywords: genetic diagnosis; clinical diagnosis; genetic testing; parents; Rett syndrome

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APA (6th Edition):

Delaney, C. (2011). The Impact of Genetic Testing for Rett Syndrome: An Assessment of Parents' Experiences. (Thesis). Brandeis University. Retrieved from http://hdl.handle.net/10192/24398

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):

Delaney, Christine. “The Impact of Genetic Testing for Rett Syndrome: An Assessment of Parents' Experiences.” 2011. Thesis, Brandeis University. Accessed September 28, 2020. http://hdl.handle.net/10192/24398.

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

MLA Handbook (7th Edition):

Delaney, Christine. “The Impact of Genetic Testing for Rett Syndrome: An Assessment of Parents' Experiences.” 2011. Web. 28 Sep 2020.

Vancouver:

Delaney C. The Impact of Genetic Testing for Rett Syndrome: An Assessment of Parents' Experiences. [Internet] [Thesis]. Brandeis University; 2011. [cited 2020 Sep 28]. Available from: http://hdl.handle.net/10192/24398.

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

Council of Science Editors:

Delaney C. The Impact of Genetic Testing for Rett Syndrome: An Assessment of Parents' Experiences. [Thesis]. Brandeis University; 2011. Available from: http://hdl.handle.net/10192/24398

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


Brandeis University

28. Tripi, Kelly Schooping. Should All Patients with Breast Cancer be Offered Genetic Testing? Reactions to the ASBrS Consensus Guideline on Genetic Testing for Hereditary Breast Cancer.

Degree: 2020, Brandeis University

 The increase in genetic testing availability, coupled with the increase in demand for genetic counselors has led some groups to evaluate who is offered genetic(more)

Subjects/Keywords: ASBrS; hereditary breast cancer; genetic testing; guidelines; genetic counseling

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APA (6th Edition):

Tripi, K. S. (2020). Should All Patients with Breast Cancer be Offered Genetic Testing? Reactions to the ASBrS Consensus Guideline on Genetic Testing for Hereditary Breast Cancer. (Thesis). Brandeis University. Retrieved from http://hdl.handle.net/10192/37510

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):

Tripi, Kelly Schooping. “Should All Patients with Breast Cancer be Offered Genetic Testing? Reactions to the ASBrS Consensus Guideline on Genetic Testing for Hereditary Breast Cancer.” 2020. Thesis, Brandeis University. Accessed September 28, 2020. http://hdl.handle.net/10192/37510.

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

MLA Handbook (7th Edition):

Tripi, Kelly Schooping. “Should All Patients with Breast Cancer be Offered Genetic Testing? Reactions to the ASBrS Consensus Guideline on Genetic Testing for Hereditary Breast Cancer.” 2020. Web. 28 Sep 2020.

Vancouver:

Tripi KS. Should All Patients with Breast Cancer be Offered Genetic Testing? Reactions to the ASBrS Consensus Guideline on Genetic Testing for Hereditary Breast Cancer. [Internet] [Thesis]. Brandeis University; 2020. [cited 2020 Sep 28]. Available from: http://hdl.handle.net/10192/37510.

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

Council of Science Editors:

Tripi KS. Should All Patients with Breast Cancer be Offered Genetic Testing? Reactions to the ASBrS Consensus Guideline on Genetic Testing for Hereditary Breast Cancer. [Thesis]. Brandeis University; 2020. Available from: http://hdl.handle.net/10192/37510

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


University of Georgia

29. Ramakrishnan, Sharavanan. Direct-to-consumer advertisement of predictive genetic tests.

Degree: 2014, University of Georgia

 Advertising of predictive genetic tests (PGTs) is being used by biotech companies as a promotional strategy to influence consumers. Opponents, including regulators and genetic experts… (more)

Subjects/Keywords: Predictive genetic tests; DTC advertising; Consumer behavior; Information processing; Genetic testing.

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APA (6th Edition):

Ramakrishnan, S. (2014). Direct-to-consumer advertisement of predictive genetic tests. (Thesis). University of Georgia. Retrieved from http://hdl.handle.net/10724/26987

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):

Ramakrishnan, Sharavanan. “Direct-to-consumer advertisement of predictive genetic tests.” 2014. Thesis, University of Georgia. Accessed September 28, 2020. http://hdl.handle.net/10724/26987.

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

MLA Handbook (7th Edition):

Ramakrishnan, Sharavanan. “Direct-to-consumer advertisement of predictive genetic tests.” 2014. Web. 28 Sep 2020.

Vancouver:

Ramakrishnan S. Direct-to-consumer advertisement of predictive genetic tests. [Internet] [Thesis]. University of Georgia; 2014. [cited 2020 Sep 28]. Available from: http://hdl.handle.net/10724/26987.

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

Council of Science Editors:

Ramakrishnan S. Direct-to-consumer advertisement of predictive genetic tests. [Thesis]. University of Georgia; 2014. Available from: http://hdl.handle.net/10724/26987

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


University of Minnesota

30. Movva, Venkata. Automatic Test Suite Generation for Scientific MATLAB Code.

Degree: MS, Computer Science, 2015, University of Minnesota

 Software testing is the process of finding code faults by applying tests and comparing results from the code to an oracle. Mutation testing is one… (more)

Subjects/Keywords: Genetic algorithm; Mutation testing; oracle; Scientific code; Testing Test suite; unit testing

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APA (6th Edition):

Movva, V. (2015). Automatic Test Suite Generation for Scientific MATLAB Code. (Masters Thesis). University of Minnesota. Retrieved from http://hdl.handle.net/11299/174817

Chicago Manual of Style (16th Edition):

Movva, Venkata. “Automatic Test Suite Generation for Scientific MATLAB Code.” 2015. Masters Thesis, University of Minnesota. Accessed September 28, 2020. http://hdl.handle.net/11299/174817.

MLA Handbook (7th Edition):

Movva, Venkata. “Automatic Test Suite Generation for Scientific MATLAB Code.” 2015. Web. 28 Sep 2020.

Vancouver:

Movva V. Automatic Test Suite Generation for Scientific MATLAB Code. [Internet] [Masters thesis]. University of Minnesota; 2015. [cited 2020 Sep 28]. Available from: http://hdl.handle.net/11299/174817.

Council of Science Editors:

Movva V. Automatic Test Suite Generation for Scientific MATLAB Code. [Masters Thesis]. University of Minnesota; 2015. Available from: http://hdl.handle.net/11299/174817

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