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You searched for subject:(eQTL). Showing records 1 – 30 of 71 total matches.

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University of Georgia

1. Sprolden, Tracy Lashonda. Double eQTL mapping method to improve identification of trans eQTLs and construct intermediate gene networks.

Degree: 2014, University of Georgia

 A double eQTL mapping method for identifying trans eQTLs that reduces multiple testing and increases the statistical power of eQTL mapping is described. The first… (more)

Subjects/Keywords: Single nucleotide polymorphism (SNP); Expression quantitative trait loci (eQTL); Microarray; Cis eQTL; Trans eQTL

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

APA (6th Edition):

Sprolden, T. L. (2014). Double eQTL mapping method to improve identification of trans eQTLs and construct intermediate gene networks. (Thesis). University of Georgia. Retrieved from http://hdl.handle.net/10724/28916

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):

Sprolden, Tracy Lashonda. “Double eQTL mapping method to improve identification of trans eQTLs and construct intermediate gene networks.” 2014. Thesis, University of Georgia. Accessed October 21, 2020. http://hdl.handle.net/10724/28916.

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

MLA Handbook (7th Edition):

Sprolden, Tracy Lashonda. “Double eQTL mapping method to improve identification of trans eQTLs and construct intermediate gene networks.” 2014. Web. 21 Oct 2020.

Vancouver:

Sprolden TL. Double eQTL mapping method to improve identification of trans eQTLs and construct intermediate gene networks. [Internet] [Thesis]. University of Georgia; 2014. [cited 2020 Oct 21]. Available from: http://hdl.handle.net/10724/28916.

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

Council of Science Editors:

Sprolden TL. Double eQTL mapping method to improve identification of trans eQTLs and construct intermediate gene networks. [Thesis]. University of Georgia; 2014. Available from: http://hdl.handle.net/10724/28916

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


Cornell University

2. Gao, Chuan. Controlling For Hidden Factors In High Dimensional Eqtl Studies.

Degree: PhD, Computational Biology, 2012, Cornell University

 Finding genetic variants that regulate gene expression now plays a central role in the analysis of mechanism in biological systems. This will also increasingly be… (more)

Subjects/Keywords: Gene expression; hidden factor; eQTL

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APA (6th Edition):

Gao, C. (2012). Controlling For Hidden Factors In High Dimensional Eqtl Studies. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/31374

Chicago Manual of Style (16th Edition):

Gao, Chuan. “Controlling For Hidden Factors In High Dimensional Eqtl Studies.” 2012. Doctoral Dissertation, Cornell University. Accessed October 21, 2020. http://hdl.handle.net/1813/31374.

MLA Handbook (7th Edition):

Gao, Chuan. “Controlling For Hidden Factors In High Dimensional Eqtl Studies.” 2012. Web. 21 Oct 2020.

Vancouver:

Gao C. Controlling For Hidden Factors In High Dimensional Eqtl Studies. [Internet] [Doctoral dissertation]. Cornell University; 2012. [cited 2020 Oct 21]. Available from: http://hdl.handle.net/1813/31374.

Council of Science Editors:

Gao C. Controlling For Hidden Factors In High Dimensional Eqtl Studies. [Doctoral Dissertation]. Cornell University; 2012. Available from: http://hdl.handle.net/1813/31374


Texas A&M University

3. Feng, Shuo. A Likelihood Based Framework for Data Integration with Application to eQTL Mapping.

Degree: PhD, Statistics, 2014, Texas A&M University

 We develop a new way of thinking about and integrating gene expression data (continuous) and genomic information data (binary) by jointly compressing the two data… (more)

Subjects/Keywords: Data integration; eQTL; GWAS; CCA

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APA (6th Edition):

Feng, S. (2014). A Likelihood Based Framework for Data Integration with Application to eQTL Mapping. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/153318

Chicago Manual of Style (16th Edition):

Feng, Shuo. “A Likelihood Based Framework for Data Integration with Application to eQTL Mapping.” 2014. Doctoral Dissertation, Texas A&M University. Accessed October 21, 2020. http://hdl.handle.net/1969.1/153318.

MLA Handbook (7th Edition):

Feng, Shuo. “A Likelihood Based Framework for Data Integration with Application to eQTL Mapping.” 2014. Web. 21 Oct 2020.

Vancouver:

Feng S. A Likelihood Based Framework for Data Integration with Application to eQTL Mapping. [Internet] [Doctoral dissertation]. Texas A&M University; 2014. [cited 2020 Oct 21]. Available from: http://hdl.handle.net/1969.1/153318.

Council of Science Editors:

Feng S. A Likelihood Based Framework for Data Integration with Application to eQTL Mapping. [Doctoral Dissertation]. Texas A&M University; 2014. Available from: http://hdl.handle.net/1969.1/153318


University of California – San Francisco

4. Song, Yi. Investigating host genes involved in HIV control by a novel computational method to combine GWAS with eQTL.

Degree: Biological and Medical Informatics, 2012, University of California – San Francisco

 Acquired immunodeficiency syndrome (AIDS) is one of the most deadly diseases worldwide. AIDS was first reported in 1981, with its disease causing virus discovered and… (more)

Subjects/Keywords: Bioinformatics; control; eQTL; GWAS; HIV

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APA (6th Edition):

Song, Y. (2012). Investigating host genes involved in HIV control by a novel computational method to combine GWAS with eQTL. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/12x6k23n

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):

Song, Yi. “Investigating host genes involved in HIV control by a novel computational method to combine GWAS with eQTL.” 2012. Thesis, University of California – San Francisco. Accessed October 21, 2020. http://www.escholarship.org/uc/item/12x6k23n.

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

MLA Handbook (7th Edition):

Song, Yi. “Investigating host genes involved in HIV control by a novel computational method to combine GWAS with eQTL.” 2012. Web. 21 Oct 2020.

Vancouver:

Song Y. Investigating host genes involved in HIV control by a novel computational method to combine GWAS with eQTL. [Internet] [Thesis]. University of California – San Francisco; 2012. [cited 2020 Oct 21]. Available from: http://www.escholarship.org/uc/item/12x6k23n.

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

Council of Science Editors:

Song Y. Investigating host genes involved in HIV control by a novel computational method to combine GWAS with eQTL. [Thesis]. University of California – San Francisco; 2012. Available from: http://www.escholarship.org/uc/item/12x6k23n

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


University of Oxford

5. Burnham, Katie. Functional genomics of the sepsis response.

Degree: PhD, 2017, University of Oxford

 Sepsis is defined as a dysregulated immune response to infection causing organ dysfunction, and is a major area of unmet clinical need. Although conventionally considered… (more)

Subjects/Keywords: Genetics; eQTL; sepsis; transcriptomics

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APA (6th Edition):

Burnham, K. (2017). Functional genomics of the sepsis response. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:cb98af40-1b66-4966-a643-ae8dfec2c122 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.757767

Chicago Manual of Style (16th Edition):

Burnham, Katie. “Functional genomics of the sepsis response.” 2017. Doctoral Dissertation, University of Oxford. Accessed October 21, 2020. http://ora.ox.ac.uk/objects/uuid:cb98af40-1b66-4966-a643-ae8dfec2c122 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.757767.

MLA Handbook (7th Edition):

Burnham, Katie. “Functional genomics of the sepsis response.” 2017. Web. 21 Oct 2020.

Vancouver:

Burnham K. Functional genomics of the sepsis response. [Internet] [Doctoral dissertation]. University of Oxford; 2017. [cited 2020 Oct 21]. Available from: http://ora.ox.ac.uk/objects/uuid:cb98af40-1b66-4966-a643-ae8dfec2c122 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.757767.

Council of Science Editors:

Burnham K. Functional genomics of the sepsis response. [Doctoral Dissertation]. University of Oxford; 2017. Available from: http://ora.ox.ac.uk/objects/uuid:cb98af40-1b66-4966-a643-ae8dfec2c122 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.757767


University of Edinburgh

6. Moody, Jonathan. Genetic diversity in the processing and transcriptomic diversity in the targeting of microRNAs.

Degree: PhD, 2017, University of Edinburgh

 MicroRNAs are short RNA molecules that are central to the regulation of many cellular and developmental pathways. They are processed in several stages from structured… (more)

Subjects/Keywords: 572.8; microRNA; RNA; eQTL; QTL

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APA (6th Edition):

Moody, J. (2017). Genetic diversity in the processing and transcriptomic diversity in the targeting of microRNAs. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/25409

Chicago Manual of Style (16th Edition):

Moody, Jonathan. “Genetic diversity in the processing and transcriptomic diversity in the targeting of microRNAs.” 2017. Doctoral Dissertation, University of Edinburgh. Accessed October 21, 2020. http://hdl.handle.net/1842/25409.

MLA Handbook (7th Edition):

Moody, Jonathan. “Genetic diversity in the processing and transcriptomic diversity in the targeting of microRNAs.” 2017. Web. 21 Oct 2020.

Vancouver:

Moody J. Genetic diversity in the processing and transcriptomic diversity in the targeting of microRNAs. [Internet] [Doctoral dissertation]. University of Edinburgh; 2017. [cited 2020 Oct 21]. Available from: http://hdl.handle.net/1842/25409.

Council of Science Editors:

Moody J. Genetic diversity in the processing and transcriptomic diversity in the targeting of microRNAs. [Doctoral Dissertation]. University of Edinburgh; 2017. Available from: http://hdl.handle.net/1842/25409


Vanderbilt University

7. Fish, Alexandra Elizabeth. Leveraging gene expression and local ancestry to investigate regulatory epistasis in humans.

Degree: PhD, Human Genetics, 2017, Vanderbilt University

 Epistasis is a phenomenon wherein the effect of a genetic variant on a phenotype is dependent on the genomic context. Better understanding epistastic relationships between… (more)

Subjects/Keywords: epistasis; gene expression; admixed populations; eQTL; PheWAS

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APA (6th Edition):

Fish, A. E. (2017). Leveraging gene expression and local ancestry to investigate regulatory epistasis in humans. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/11250

Chicago Manual of Style (16th Edition):

Fish, Alexandra Elizabeth. “Leveraging gene expression and local ancestry to investigate regulatory epistasis in humans.” 2017. Doctoral Dissertation, Vanderbilt University. Accessed October 21, 2020. http://hdl.handle.net/1803/11250.

MLA Handbook (7th Edition):

Fish, Alexandra Elizabeth. “Leveraging gene expression and local ancestry to investigate regulatory epistasis in humans.” 2017. Web. 21 Oct 2020.

Vancouver:

Fish AE. Leveraging gene expression and local ancestry to investigate regulatory epistasis in humans. [Internet] [Doctoral dissertation]. Vanderbilt University; 2017. [cited 2020 Oct 21]. Available from: http://hdl.handle.net/1803/11250.

Council of Science Editors:

Fish AE. Leveraging gene expression and local ancestry to investigate regulatory epistasis in humans. [Doctoral Dissertation]. Vanderbilt University; 2017. Available from: http://hdl.handle.net/1803/11250


Vanderbilt University

8. Wiley, Laura Katherine. Discovery and Replication of Pathway-Based Trans-Expression Quantitative Trait Loci.

Degree: MS, Biomedical Informatics, 2014, Vanderbilt University

 A logical mechanism by which SNPs affect the pathophysiology of disease is through altering the expression of genes. Several studies have explored how SNPs alter… (more)

Subjects/Keywords: trans-eQTL; SPIA; KEGG; gene expression

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APA (6th Edition):

Wiley, L. K. (2014). Discovery and Replication of Pathway-Based Trans-Expression Quantitative Trait Loci. (Thesis). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/13081

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):

Wiley, Laura Katherine. “Discovery and Replication of Pathway-Based Trans-Expression Quantitative Trait Loci.” 2014. Thesis, Vanderbilt University. Accessed October 21, 2020. http://hdl.handle.net/1803/13081.

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

MLA Handbook (7th Edition):

Wiley, Laura Katherine. “Discovery and Replication of Pathway-Based Trans-Expression Quantitative Trait Loci.” 2014. Web. 21 Oct 2020.

Vancouver:

Wiley LK. Discovery and Replication of Pathway-Based Trans-Expression Quantitative Trait Loci. [Internet] [Thesis]. Vanderbilt University; 2014. [cited 2020 Oct 21]. Available from: http://hdl.handle.net/1803/13081.

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

Council of Science Editors:

Wiley LK. Discovery and Replication of Pathway-Based Trans-Expression Quantitative Trait Loci. [Thesis]. Vanderbilt University; 2014. Available from: http://hdl.handle.net/1803/13081

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


Penn State University

9. Wang, Ningtao. A Block Mixture Model To Map Eqtls For Gene Clustering.

Degree: 2015, Penn State University

 To study how genes function in a cellular and physiological process, a general procedure is to classify gene expression profiles into categories based on their… (more)

Subjects/Keywords: block mixture model; eQTL; gene cluster

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APA (6th Edition):

Wang, N. (2015). A Block Mixture Model To Map Eqtls For Gene Clustering. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/26198

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):

Wang, Ningtao. “A Block Mixture Model To Map Eqtls For Gene Clustering.” 2015. Thesis, Penn State University. Accessed October 21, 2020. https://submit-etda.libraries.psu.edu/catalog/26198.

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

MLA Handbook (7th Edition):

Wang, Ningtao. “A Block Mixture Model To Map Eqtls For Gene Clustering.” 2015. Web. 21 Oct 2020.

Vancouver:

Wang N. A Block Mixture Model To Map Eqtls For Gene Clustering. [Internet] [Thesis]. Penn State University; 2015. [cited 2020 Oct 21]. Available from: https://submit-etda.libraries.psu.edu/catalog/26198.

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

Council of Science Editors:

Wang N. A Block Mixture Model To Map Eqtls For Gene Clustering. [Thesis]. Penn State University; 2015. Available from: https://submit-etda.libraries.psu.edu/catalog/26198

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


North Carolina State University

10. Duarte, Christine Woods. A New Method for Genetic Network Reconstruction in Expression QTL Data Sets.

Degree: PhD, Bioinformatics, 2009, North Carolina State University

 Expression QTL (or eQTL) studies involve the collection of microarray gene expression data and genetic marker data from segregating individuals in a population in order… (more)

Subjects/Keywords: eQTL; Bayesian networks; genetic networks; QTL

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APA (6th Edition):

Duarte, C. W. (2009). A New Method for Genetic Network Reconstruction in Expression QTL Data Sets. (Doctoral Dissertation). North Carolina State University. Retrieved from http://www.lib.ncsu.edu/resolver/1840.16/4410

Chicago Manual of Style (16th Edition):

Duarte, Christine Woods. “A New Method for Genetic Network Reconstruction in Expression QTL Data Sets.” 2009. Doctoral Dissertation, North Carolina State University. Accessed October 21, 2020. http://www.lib.ncsu.edu/resolver/1840.16/4410.

MLA Handbook (7th Edition):

Duarte, Christine Woods. “A New Method for Genetic Network Reconstruction in Expression QTL Data Sets.” 2009. Web. 21 Oct 2020.

Vancouver:

Duarte CW. A New Method for Genetic Network Reconstruction in Expression QTL Data Sets. [Internet] [Doctoral dissertation]. North Carolina State University; 2009. [cited 2020 Oct 21]. Available from: http://www.lib.ncsu.edu/resolver/1840.16/4410.

Council of Science Editors:

Duarte CW. A New Method for Genetic Network Reconstruction in Expression QTL Data Sets. [Doctoral Dissertation]. North Carolina State University; 2009. Available from: http://www.lib.ncsu.edu/resolver/1840.16/4410


University of Adelaide

11. Walker, K. Ryan. Regulation of candidate genes in black point formation in barley.

Degree: 2012, University of Adelaide

 Black point of barley refers to discolouration of the embryo end of the grain. Downgrading of malting barley to feed grade due to black point… (more)

Subjects/Keywords: Black point; barley; environment; eQTL; peroxidase

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APA (6th Edition):

Walker, K. R. (2012). Regulation of candidate genes in black point formation in barley. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/80033

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):

Walker, K Ryan. “Regulation of candidate genes in black point formation in barley.” 2012. Thesis, University of Adelaide. Accessed October 21, 2020. http://hdl.handle.net/2440/80033.

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

MLA Handbook (7th Edition):

Walker, K Ryan. “Regulation of candidate genes in black point formation in barley.” 2012. Web. 21 Oct 2020.

Vancouver:

Walker KR. Regulation of candidate genes in black point formation in barley. [Internet] [Thesis]. University of Adelaide; 2012. [cited 2020 Oct 21]. Available from: http://hdl.handle.net/2440/80033.

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

Council of Science Editors:

Walker KR. Regulation of candidate genes in black point formation in barley. [Thesis]. University of Adelaide; 2012. Available from: http://hdl.handle.net/2440/80033

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

12. Zeng, Biao. Blood eQTL detection in structured populations and its application to interpretation of genetic association studies.

Degree: PhD, Biology, 2018, Georgia Tech

 Expression QTL (eQTL) detection has emerged as an important tool for unravelling the relationship between genetic risk factors and disease or clinical phenotypes. Most studies… (more)

Subjects/Keywords: eQTL; GWAS

…LIST OF TABLES Table 1.1 eQTL studies in human tissues since 2004 14 Table 1.2… …Sharing of cis-eQTL among expression platforms. 101 Table 5.1 Genomic inflation factor for… …viii LIST OF FIGURES Figure 1.1 Diagram of eQTL and eQTL detection 2 Figure 1.2… …Breakthrough eQTL studies in human tissues 8 Figure 2.1 Schematic of multi-site regulation of gene… …Figure 2.3 False multiple eQTL detection due to unimputed variants Figure 2.4 The signal… 

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APA (6th Edition):

Zeng, B. (2018). Blood eQTL detection in structured populations and its application to interpretation of genetic association studies. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/60787

Chicago Manual of Style (16th Edition):

Zeng, Biao. “Blood eQTL detection in structured populations and its application to interpretation of genetic association studies.” 2018. Doctoral Dissertation, Georgia Tech. Accessed October 21, 2020. http://hdl.handle.net/1853/60787.

MLA Handbook (7th Edition):

Zeng, Biao. “Blood eQTL detection in structured populations and its application to interpretation of genetic association studies.” 2018. Web. 21 Oct 2020.

Vancouver:

Zeng B. Blood eQTL detection in structured populations and its application to interpretation of genetic association studies. [Internet] [Doctoral dissertation]. Georgia Tech; 2018. [cited 2020 Oct 21]. Available from: http://hdl.handle.net/1853/60787.

Council of Science Editors:

Zeng B. Blood eQTL detection in structured populations and its application to interpretation of genetic association studies. [Doctoral Dissertation]. Georgia Tech; 2018. Available from: http://hdl.handle.net/1853/60787

13. Maroilley, Tatiana. Génétique et Génomique de la capacité immunitaire chez le porc : approches eQTL et étude de biomarqueurs sanguins : Genetics and Genomics of the immune capacities in pigs : eQTL approach and study of blood biomarkers.

Degree: Docteur es, Sciences de la vie et de la santé, 2017, Université Paris-Saclay (ComUE)

 Une meilleure compréhension des mécanismes de résistance aux agents pathogènes couplée à une caractérisation de la capacité immune devient un axe de recherche prioritaire en… (more)

Subjects/Keywords: Génétique; Immunité; Porc; Eqtl; Biomarqueurs sanguins; Génomique; Genetics; Immunity; Swine; Eqtl; Blood biomarkers; Genomics; 571.9

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APA (6th Edition):

Maroilley, T. (2017). Génétique et Génomique de la capacité immunitaire chez le porc : approches eQTL et étude de biomarqueurs sanguins : Genetics and Genomics of the immune capacities in pigs : eQTL approach and study of blood biomarkers. (Doctoral Dissertation). Université Paris-Saclay (ComUE). Retrieved from http://www.theses.fr/2017SACLV097

Chicago Manual of Style (16th Edition):

Maroilley, Tatiana. “Génétique et Génomique de la capacité immunitaire chez le porc : approches eQTL et étude de biomarqueurs sanguins : Genetics and Genomics of the immune capacities in pigs : eQTL approach and study of blood biomarkers.” 2017. Doctoral Dissertation, Université Paris-Saclay (ComUE). Accessed October 21, 2020. http://www.theses.fr/2017SACLV097.

MLA Handbook (7th Edition):

Maroilley, Tatiana. “Génétique et Génomique de la capacité immunitaire chez le porc : approches eQTL et étude de biomarqueurs sanguins : Genetics and Genomics of the immune capacities in pigs : eQTL approach and study of blood biomarkers.” 2017. Web. 21 Oct 2020.

Vancouver:

Maroilley T. Génétique et Génomique de la capacité immunitaire chez le porc : approches eQTL et étude de biomarqueurs sanguins : Genetics and Genomics of the immune capacities in pigs : eQTL approach and study of blood biomarkers. [Internet] [Doctoral dissertation]. Université Paris-Saclay (ComUE); 2017. [cited 2020 Oct 21]. Available from: http://www.theses.fr/2017SACLV097.

Council of Science Editors:

Maroilley T. Génétique et Génomique de la capacité immunitaire chez le porc : approches eQTL et étude de biomarqueurs sanguins : Genetics and Genomics of the immune capacities in pigs : eQTL approach and study of blood biomarkers. [Doctoral Dissertation]. Université Paris-Saclay (ComUE); 2017. Available from: http://www.theses.fr/2017SACLV097


Université Paris-Sud – Paris XI

14. Rotival, Maxime. Approches intégrées du génome et du transcriptome dans les maladies complexes humaines : Integrated approaches of genome and transcriptome in the study of human complex diseases.

Degree: Docteur es, Génétique statistique, 2011, Université Paris-Sud – Paris XI

Cette thèse a pour objet l'étude du lien génotype-transcriptome et de son influence sur le développement des maladies multifactorielles. Les apports de ce travail sont… (more)

Subjects/Keywords: Génomique; Transcriptome; Maladies Complexes; EQTL; Statistique; Cardiovasculaire; EQTL; Statistique; Cardiovascular; Genomics; Transcriptome; Complex Diseases

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APA (6th Edition):

Rotival, M. (2011). Approches intégrées du génome et du transcriptome dans les maladies complexes humaines : Integrated approaches of genome and transcriptome in the study of human complex diseases. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2011PA11T035

Chicago Manual of Style (16th Edition):

Rotival, Maxime. “Approches intégrées du génome et du transcriptome dans les maladies complexes humaines : Integrated approaches of genome and transcriptome in the study of human complex diseases.” 2011. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed October 21, 2020. http://www.theses.fr/2011PA11T035.

MLA Handbook (7th Edition):

Rotival, Maxime. “Approches intégrées du génome et du transcriptome dans les maladies complexes humaines : Integrated approaches of genome and transcriptome in the study of human complex diseases.” 2011. Web. 21 Oct 2020.

Vancouver:

Rotival M. Approches intégrées du génome et du transcriptome dans les maladies complexes humaines : Integrated approaches of genome and transcriptome in the study of human complex diseases. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2011. [cited 2020 Oct 21]. Available from: http://www.theses.fr/2011PA11T035.

Council of Science Editors:

Rotival M. Approches intégrées du génome et du transcriptome dans les maladies complexes humaines : Integrated approaches of genome and transcriptome in the study of human complex diseases. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2011. Available from: http://www.theses.fr/2011PA11T035

15. Silva, Carolina Malcher Amorim de Carvalho. Investigação do papel de SNVs (single nucleotide variants) na etiologia da fissura lábio-palatina não sindrômica.

Degree: Mestrado, Biologia (Genética), 2013, University of São Paulo

Fissura de lábio com ou sem fissura de palato não-sindrômica (FL/P NS) é uma malformação craniofacial frequente, com modelo de herança multifatorial, onde fatores de… (more)

Subjects/Keywords: 8q24; 8q24; Association studies; Célula-tronco mesenquimal; eQTL; eQTL; Estudos de associação; IRF6; IRF6; Mesenchymal stem cell

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

APA (6th Edition):

Silva, C. M. A. d. C. (2013). Investigação do papel de SNVs (single nucleotide variants) na etiologia da fissura lábio-palatina não sindrômica. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/41/41131/tde-23072013-140648/ ;

Chicago Manual of Style (16th Edition):

Silva, Carolina Malcher Amorim de Carvalho. “Investigação do papel de SNVs (single nucleotide variants) na etiologia da fissura lábio-palatina não sindrômica.” 2013. Masters Thesis, University of São Paulo. Accessed October 21, 2020. http://www.teses.usp.br/teses/disponiveis/41/41131/tde-23072013-140648/ ;.

MLA Handbook (7th Edition):

Silva, Carolina Malcher Amorim de Carvalho. “Investigação do papel de SNVs (single nucleotide variants) na etiologia da fissura lábio-palatina não sindrômica.” 2013. Web. 21 Oct 2020.

Vancouver:

Silva CMAdC. Investigação do papel de SNVs (single nucleotide variants) na etiologia da fissura lábio-palatina não sindrômica. [Internet] [Masters thesis]. University of São Paulo; 2013. [cited 2020 Oct 21]. Available from: http://www.teses.usp.br/teses/disponiveis/41/41131/tde-23072013-140648/ ;.

Council of Science Editors:

Silva CMAdC. Investigação do papel de SNVs (single nucleotide variants) na etiologia da fissura lábio-palatina não sindrômica. [Masters Thesis]. University of São Paulo; 2013. Available from: http://www.teses.usp.br/teses/disponiveis/41/41131/tde-23072013-140648/ ;

16. Ackermann, Marit. Discovering genetic interactions based on natural genetic variation.

Degree: 2012, Technische Universität Dortmund

 Complex traits can be attributed to the effect of two or more genes and their interaction with each other as well as the environment. Unraveling… (more)

Subjects/Keywords: Allel-Inkompatibilität; Epistase; eQTL; Genetische Interaktion; Random forests; 310

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APA (6th Edition):

Ackermann, M. (2012). Discovering genetic interactions based on natural genetic variation. (Thesis). Technische Universität Dortmund. Retrieved from http://hdl.handle.net/2003/29657

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):

Ackermann, Marit. “Discovering genetic interactions based on natural genetic variation.” 2012. Thesis, Technische Universität Dortmund. Accessed October 21, 2020. http://hdl.handle.net/2003/29657.

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

MLA Handbook (7th Edition):

Ackermann, Marit. “Discovering genetic interactions based on natural genetic variation.” 2012. Web. 21 Oct 2020.

Vancouver:

Ackermann M. Discovering genetic interactions based on natural genetic variation. [Internet] [Thesis]. Technische Universität Dortmund; 2012. [cited 2020 Oct 21]. Available from: http://hdl.handle.net/2003/29657.

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

Council of Science Editors:

Ackermann M. Discovering genetic interactions based on natural genetic variation. [Thesis]. Technische Universität Dortmund; 2012. Available from: http://hdl.handle.net/2003/29657

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


Cornell University

17. Kremling, Karl. Regulators of expression in Zea mays.

Degree: PhD, Plant Breeding, 2018, Cornell University

 To assess the impact of regulatory variation on a genomic scale, a large scale gene expression resource was created from seven tissues profiled using 3’… (more)

Subjects/Keywords: GWAS; eQTL; transcriptome; Genetics; Gene regulation; Gene expression; Agriculture; Plant sciences

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APA (6th Edition):

Kremling, K. (2018). Regulators of expression in Zea mays. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/59415

Chicago Manual of Style (16th Edition):

Kremling, Karl. “Regulators of expression in Zea mays.” 2018. Doctoral Dissertation, Cornell University. Accessed October 21, 2020. http://hdl.handle.net/1813/59415.

MLA Handbook (7th Edition):

Kremling, Karl. “Regulators of expression in Zea mays.” 2018. Web. 21 Oct 2020.

Vancouver:

Kremling K. Regulators of expression in Zea mays. [Internet] [Doctoral dissertation]. Cornell University; 2018. [cited 2020 Oct 21]. Available from: http://hdl.handle.net/1813/59415.

Council of Science Editors:

Kremling K. Regulators of expression in Zea mays. [Doctoral Dissertation]. Cornell University; 2018. Available from: http://hdl.handle.net/1813/59415


Penn State University

18. Gosik, Kirk D. STATISTICAL MODELS FOR HIGH DIMENSIONAL SCREENING OF GENETIC AND EPIGENETIC EFFECTS.

Degree: 2017, Penn State University

 Knowledge about how changes in gene expression are encoded by expression quantitative trait loci (eQTLs) is a key to construct the genotype-phenotype map for complex… (more)

Subjects/Keywords: variable-selection; gene-expression; eQTL; genetic-architecture; epigenetics

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APA (6th Edition):

Gosik, K. D. (2017). STATISTICAL MODELS FOR HIGH DIMENSIONAL SCREENING OF GENETIC AND EPIGENETIC EFFECTS. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/14022kdg139

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):

Gosik, Kirk D. “STATISTICAL MODELS FOR HIGH DIMENSIONAL SCREENING OF GENETIC AND EPIGENETIC EFFECTS.” 2017. Thesis, Penn State University. Accessed October 21, 2020. https://submit-etda.libraries.psu.edu/catalog/14022kdg139.

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

MLA Handbook (7th Edition):

Gosik, Kirk D. “STATISTICAL MODELS FOR HIGH DIMENSIONAL SCREENING OF GENETIC AND EPIGENETIC EFFECTS.” 2017. Web. 21 Oct 2020.

Vancouver:

Gosik KD. STATISTICAL MODELS FOR HIGH DIMENSIONAL SCREENING OF GENETIC AND EPIGENETIC EFFECTS. [Internet] [Thesis]. Penn State University; 2017. [cited 2020 Oct 21]. Available from: https://submit-etda.libraries.psu.edu/catalog/14022kdg139.

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

Council of Science Editors:

Gosik KD. STATISTICAL MODELS FOR HIGH DIMENSIONAL SCREENING OF GENETIC AND EPIGENETIC EFFECTS. [Thesis]. Penn State University; 2017. Available from: https://submit-etda.libraries.psu.edu/catalog/14022kdg139

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

19. Ackermann, Marit. Discovering genetic interactions based on natural genetic variation.

Degree: 2012, Technische Universität Dortmund

 Complex traits can be attributed to the effect of two or more genes and their interaction with each other as well as the environment. Unraveling… (more)

Subjects/Keywords: Allel-Inkompatibilität; Epistase; eQTL; Genetische Interaktion; Random forests; 310

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

APA (6th Edition):

Ackermann, M. (2012). Discovering genetic interactions based on natural genetic variation. (Doctoral Dissertation). Technische Universität Dortmund. Retrieved from http://dx.doi.org/10.17877/DE290R-10762

Chicago Manual of Style (16th Edition):

Ackermann, Marit. “Discovering genetic interactions based on natural genetic variation.” 2012. Doctoral Dissertation, Technische Universität Dortmund. Accessed October 21, 2020. http://dx.doi.org/10.17877/DE290R-10762.

MLA Handbook (7th Edition):

Ackermann, Marit. “Discovering genetic interactions based on natural genetic variation.” 2012. Web. 21 Oct 2020.

Vancouver:

Ackermann M. Discovering genetic interactions based on natural genetic variation. [Internet] [Doctoral dissertation]. Technische Universität Dortmund; 2012. [cited 2020 Oct 21]. Available from: http://dx.doi.org/10.17877/DE290R-10762.

Council of Science Editors:

Ackermann M. Discovering genetic interactions based on natural genetic variation. [Doctoral Dissertation]. Technische Universität Dortmund; 2012. Available from: http://dx.doi.org/10.17877/DE290R-10762


Harvard University

20. Sathirapongsasuti, Jarupon Fah. Post-Genomic Approaches to Personalized Medicine: Applications in Exome Sequencing, Microbiome, and COPD.

Degree: PhD, Biostatistics, 2013, Harvard University

 Since the completion of the sequencing of the human genome at the turn of the century, genomics has revolutionized the study of biology and medicine… (more)

Subjects/Keywords: Bioinformatics; Genetics; Statistics; COPD; eQTL; Exome sequencing; Integrative genomics; Microbiome; Network

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APA (6th Edition):

Sathirapongsasuti, J. F. (2013). Post-Genomic Approaches to Personalized Medicine: Applications in Exome Sequencing, Microbiome, and COPD. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:12274187

Chicago Manual of Style (16th Edition):

Sathirapongsasuti, Jarupon Fah. “Post-Genomic Approaches to Personalized Medicine: Applications in Exome Sequencing, Microbiome, and COPD.” 2013. Doctoral Dissertation, Harvard University. Accessed October 21, 2020. http://nrs.harvard.edu/urn-3:HUL.InstRepos:12274187.

MLA Handbook (7th Edition):

Sathirapongsasuti, Jarupon Fah. “Post-Genomic Approaches to Personalized Medicine: Applications in Exome Sequencing, Microbiome, and COPD.” 2013. Web. 21 Oct 2020.

Vancouver:

Sathirapongsasuti JF. Post-Genomic Approaches to Personalized Medicine: Applications in Exome Sequencing, Microbiome, and COPD. [Internet] [Doctoral dissertation]. Harvard University; 2013. [cited 2020 Oct 21]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:12274187.

Council of Science Editors:

Sathirapongsasuti JF. Post-Genomic Approaches to Personalized Medicine: Applications in Exome Sequencing, Microbiome, and COPD. [Doctoral Dissertation]. Harvard University; 2013. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:12274187


University of Manchester

21. Mcallister, Kate. Investigation of Genetic Susceptibility to Rheumatoid Arthritis.

Degree: 2014, University of Manchester

 RA is a chronic and disabling disease with no known cure. The disease has a strong genetic component and modern genetic studies have successfully identified… (more)

Subjects/Keywords: Rheumatoid arthritis; Genetics; ChIP; eQTL; ANKRD55; functional characterisation; novel

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APA (6th Edition):

Mcallister, K. (2014). Investigation of Genetic Susceptibility to Rheumatoid Arthritis. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:234236

Chicago Manual of Style (16th Edition):

Mcallister, Kate. “Investigation of Genetic Susceptibility to Rheumatoid Arthritis.” 2014. Doctoral Dissertation, University of Manchester. Accessed October 21, 2020. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:234236.

MLA Handbook (7th Edition):

Mcallister, Kate. “Investigation of Genetic Susceptibility to Rheumatoid Arthritis.” 2014. Web. 21 Oct 2020.

Vancouver:

Mcallister K. Investigation of Genetic Susceptibility to Rheumatoid Arthritis. [Internet] [Doctoral dissertation]. University of Manchester; 2014. [cited 2020 Oct 21]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:234236.

Council of Science Editors:

Mcallister K. Investigation of Genetic Susceptibility to Rheumatoid Arthritis. [Doctoral Dissertation]. University of Manchester; 2014. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:234236


University of Cambridge

22. Kreuzhuber, Roman. The effect of non-coding variants on gene transcription in human blood cell types.

Degree: PhD, 2019, University of Cambridge

 To understand complex genetic diseases it is necessary to study DNA, its transcription, translation and regulation thereof. In a mechanistic view diseases can be caused… (more)

Subjects/Keywords: eQTL; genomics; deep learning; kipoi; blood cells; colocalisation

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APA (6th Edition):

Kreuzhuber, R. (2019). The effect of non-coding variants on gene transcription in human blood cell types. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/292016

Chicago Manual of Style (16th Edition):

Kreuzhuber, Roman. “The effect of non-coding variants on gene transcription in human blood cell types.” 2019. Doctoral Dissertation, University of Cambridge. Accessed October 21, 2020. https://www.repository.cam.ac.uk/handle/1810/292016.

MLA Handbook (7th Edition):

Kreuzhuber, Roman. “The effect of non-coding variants on gene transcription in human blood cell types.” 2019. Web. 21 Oct 2020.

Vancouver:

Kreuzhuber R. The effect of non-coding variants on gene transcription in human blood cell types. [Internet] [Doctoral dissertation]. University of Cambridge; 2019. [cited 2020 Oct 21]. Available from: https://www.repository.cam.ac.uk/handle/1810/292016.

Council of Science Editors:

Kreuzhuber R. The effect of non-coding variants on gene transcription in human blood cell types. [Doctoral Dissertation]. University of Cambridge; 2019. Available from: https://www.repository.cam.ac.uk/handle/1810/292016


University of California – San Francisco

23. Hackett, Christopher Sultan. Genomic exploration of the peripheral nervous system: Identification of candidate genes for neuroblastoma, hearing loss, and other aspects of neuron biology and tumorigenesis.

Degree: Biomedical Sciences, 2010, University of California – San Francisco

 Neuroblastoma is a deadly tumor derived from neuronal tissue for which the molecular drivers remain a mystery. Here we have applied classical genetics, analysis of… (more)

Subjects/Keywords: Biology, Genetics; eQTL; mouse models; quantitative traits; Sleeping Beauty; transposons

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APA (6th Edition):

Hackett, C. S. (2010). Genomic exploration of the peripheral nervous system: Identification of candidate genes for neuroblastoma, hearing loss, and other aspects of neuron biology and tumorigenesis. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/1cx4w7m3

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):

Hackett, Christopher Sultan. “Genomic exploration of the peripheral nervous system: Identification of candidate genes for neuroblastoma, hearing loss, and other aspects of neuron biology and tumorigenesis.” 2010. Thesis, University of California – San Francisco. Accessed October 21, 2020. http://www.escholarship.org/uc/item/1cx4w7m3.

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

MLA Handbook (7th Edition):

Hackett, Christopher Sultan. “Genomic exploration of the peripheral nervous system: Identification of candidate genes for neuroblastoma, hearing loss, and other aspects of neuron biology and tumorigenesis.” 2010. Web. 21 Oct 2020.

Vancouver:

Hackett CS. Genomic exploration of the peripheral nervous system: Identification of candidate genes for neuroblastoma, hearing loss, and other aspects of neuron biology and tumorigenesis. [Internet] [Thesis]. University of California – San Francisco; 2010. [cited 2020 Oct 21]. Available from: http://www.escholarship.org/uc/item/1cx4w7m3.

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

Council of Science Editors:

Hackett CS. Genomic exploration of the peripheral nervous system: Identification of candidate genes for neuroblastoma, hearing loss, and other aspects of neuron biology and tumorigenesis. [Thesis]. University of California – San Francisco; 2010. Available from: http://www.escholarship.org/uc/item/1cx4w7m3

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


University of Manchester

24. Duffus, Kate. Investigation of genetic susceptibility to Rheumatoid Arthritis.

Degree: PhD, 2014, University of Manchester

 RA is a chronic and disabling disease with no known cure. The disease has a strong genetic component and modern genetic studies have successfully identified… (more)

Subjects/Keywords: novel; functional characterisation; ANKRD55; Rheumatoid arthritis; ChIP; Genetics; eQTL

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APA (6th Edition):

Duffus, K. (2014). Investigation of genetic susceptibility to Rheumatoid Arthritis. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/investigation-of-genetic-susceptibility-to-rheumatoid-arthritis(edf01c7b-3c46-4c75-8751-6f117291c027).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.764290

Chicago Manual of Style (16th Edition):

Duffus, Kate. “Investigation of genetic susceptibility to Rheumatoid Arthritis.” 2014. Doctoral Dissertation, University of Manchester. Accessed October 21, 2020. https://www.research.manchester.ac.uk/portal/en/theses/investigation-of-genetic-susceptibility-to-rheumatoid-arthritis(edf01c7b-3c46-4c75-8751-6f117291c027).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.764290.

MLA Handbook (7th Edition):

Duffus, Kate. “Investigation of genetic susceptibility to Rheumatoid Arthritis.” 2014. Web. 21 Oct 2020.

Vancouver:

Duffus K. Investigation of genetic susceptibility to Rheumatoid Arthritis. [Internet] [Doctoral dissertation]. University of Manchester; 2014. [cited 2020 Oct 21]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/investigation-of-genetic-susceptibility-to-rheumatoid-arthritis(edf01c7b-3c46-4c75-8751-6f117291c027).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.764290.

Council of Science Editors:

Duffus K. Investigation of genetic susceptibility to Rheumatoid Arthritis. [Doctoral Dissertation]. University of Manchester; 2014. Available from: https://www.research.manchester.ac.uk/portal/en/theses/investigation-of-genetic-susceptibility-to-rheumatoid-arthritis(edf01c7b-3c46-4c75-8751-6f117291c027).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.764290


Iowa State University

25. Cheng, Ye. Identification of QTL that Interact with Myostatin Genotype in C57BL/6 x M16i Mice.

Degree: 2011, Iowa State University

 Myostatin, or GDF8, regulates skeletal muscle growth and adipose development in mice, cattle and humans. Individuals with non-functional myostatin mutation exhibit excessive muscle growth, decrease… (more)

Subjects/Keywords: Epistasis; eQTL; Mice; Myostatin; QTL mapping; Animal Sciences

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APA (6th Edition):

Cheng, Y. (2011). Identification of QTL that Interact with Myostatin Genotype in C57BL/6 x M16i Mice. (Thesis). Iowa State University. Retrieved from https://lib.dr.iastate.edu/etd/11933

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):

Cheng, Ye. “Identification of QTL that Interact with Myostatin Genotype in C57BL/6 x M16i Mice.” 2011. Thesis, Iowa State University. Accessed October 21, 2020. https://lib.dr.iastate.edu/etd/11933.

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

MLA Handbook (7th Edition):

Cheng, Ye. “Identification of QTL that Interact with Myostatin Genotype in C57BL/6 x M16i Mice.” 2011. Web. 21 Oct 2020.

Vancouver:

Cheng Y. Identification of QTL that Interact with Myostatin Genotype in C57BL/6 x M16i Mice. [Internet] [Thesis]. Iowa State University; 2011. [cited 2020 Oct 21]. Available from: https://lib.dr.iastate.edu/etd/11933.

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

Council of Science Editors:

Cheng Y. Identification of QTL that Interact with Myostatin Genotype in C57BL/6 x M16i Mice. [Thesis]. Iowa State University; 2011. Available from: https://lib.dr.iastate.edu/etd/11933

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


University of Notre Dame

26. Joseph M Gonzales. Genetic Analysis of Gene Expression and the Underlying Polymorphisms in Plasmodium Falciparum</h1>.

Degree: Biological Sciences, 2008, University of Notre Dame

  The malaria parasite, Plasmodium falciparum, continues to infect millions of people and kills over a million children annually. Multiple drug resistant (MDR) parasite strains… (more)

Subjects/Keywords: eQTL; microarray; malaria; genomics

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APA (6th Edition):

Gonzales, J. M. (2008). Genetic Analysis of Gene Expression and the Underlying Polymorphisms in Plasmodium Falciparum</h1>. (Thesis). University of Notre Dame. Retrieved from https://curate.nd.edu/show/6h440r9856r

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):

Gonzales, Joseph M. “Genetic Analysis of Gene Expression and the Underlying Polymorphisms in Plasmodium Falciparum</h1>.” 2008. Thesis, University of Notre Dame. Accessed October 21, 2020. https://curate.nd.edu/show/6h440r9856r.

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

MLA Handbook (7th Edition):

Gonzales, Joseph M. “Genetic Analysis of Gene Expression and the Underlying Polymorphisms in Plasmodium Falciparum</h1>.” 2008. Web. 21 Oct 2020.

Vancouver:

Gonzales JM. Genetic Analysis of Gene Expression and the Underlying Polymorphisms in Plasmodium Falciparum</h1>. [Internet] [Thesis]. University of Notre Dame; 2008. [cited 2020 Oct 21]. Available from: https://curate.nd.edu/show/6h440r9856r.

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

Council of Science Editors:

Gonzales JM. Genetic Analysis of Gene Expression and the Underlying Polymorphisms in Plasmodium Falciparum</h1>. [Thesis]. University of Notre Dame; 2008. Available from: https://curate.nd.edu/show/6h440r9856r

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


University of Cambridge

27. Kreuzhuber, Roman. The effect of non-coding variants on gene transcription in human blood cell types.

Degree: PhD, 2019, University of Cambridge

 To understand complex genetic diseases it is necessary to study DNA, its transcription, translation and regulation thereof. In a mechanistic view diseases can be caused… (more)

Subjects/Keywords: eQTL; genomics; deep learning; kipoi; blood cells; colocalisation

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APA (6th Edition):

Kreuzhuber, R. (2019). The effect of non-coding variants on gene transcription in human blood cell types. (Doctoral Dissertation). University of Cambridge. Retrieved from https://doi.org/10.17863/CAM.39170 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.774753

Chicago Manual of Style (16th Edition):

Kreuzhuber, Roman. “The effect of non-coding variants on gene transcription in human blood cell types.” 2019. Doctoral Dissertation, University of Cambridge. Accessed October 21, 2020. https://doi.org/10.17863/CAM.39170 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.774753.

MLA Handbook (7th Edition):

Kreuzhuber, Roman. “The effect of non-coding variants on gene transcription in human blood cell types.” 2019. Web. 21 Oct 2020.

Vancouver:

Kreuzhuber R. The effect of non-coding variants on gene transcription in human blood cell types. [Internet] [Doctoral dissertation]. University of Cambridge; 2019. [cited 2020 Oct 21]. Available from: https://doi.org/10.17863/CAM.39170 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.774753.

Council of Science Editors:

Kreuzhuber R. The effect of non-coding variants on gene transcription in human blood cell types. [Doctoral Dissertation]. University of Cambridge; 2019. Available from: https://doi.org/10.17863/CAM.39170 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.774753

28. Costantino, Félicie. Recherche de nouveaux facteurs génétiques de susceptibilité à la spondyloarthrite grâce à une approche associant études familiales et génomique fonctionnelle : Identification of new genetic factors of susceptibility to spondyloarthritis by combining famillial studies and functional genomics.

Degree: Docteur es, Génétique humaine, 2014, Université Paris Descartes – Paris V

La spondyloarthrite (SpA) est un rhumatisme inflammatoire chronique fréquent et invalidant. Plus d’une vingtaine de locus de susceptibilité à la maladie ont été identifiés à… (more)

Subjects/Keywords: Spondylarthrite; Génétique; Étude de liaison; Association intra-familiale; Transcriptomique; Cellules dendritiques; EQTL; Spondyloarthritis; Genetics; Linkage analysis; Family-based association; Transcriptomics; Dendritic cells; EQTL; 576.5

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APA (6th Edition):

Costantino, F. (2014). Recherche de nouveaux facteurs génétiques de susceptibilité à la spondyloarthrite grâce à une approche associant études familiales et génomique fonctionnelle : Identification of new genetic factors of susceptibility to spondyloarthritis by combining famillial studies and functional genomics. (Doctoral Dissertation). Université Paris Descartes – Paris V. Retrieved from http://www.theses.fr/2014PA05T056

Chicago Manual of Style (16th Edition):

Costantino, Félicie. “Recherche de nouveaux facteurs génétiques de susceptibilité à la spondyloarthrite grâce à une approche associant études familiales et génomique fonctionnelle : Identification of new genetic factors of susceptibility to spondyloarthritis by combining famillial studies and functional genomics.” 2014. Doctoral Dissertation, Université Paris Descartes – Paris V. Accessed October 21, 2020. http://www.theses.fr/2014PA05T056.

MLA Handbook (7th Edition):

Costantino, Félicie. “Recherche de nouveaux facteurs génétiques de susceptibilité à la spondyloarthrite grâce à une approche associant études familiales et génomique fonctionnelle : Identification of new genetic factors of susceptibility to spondyloarthritis by combining famillial studies and functional genomics.” 2014. Web. 21 Oct 2020.

Vancouver:

Costantino F. Recherche de nouveaux facteurs génétiques de susceptibilité à la spondyloarthrite grâce à une approche associant études familiales et génomique fonctionnelle : Identification of new genetic factors of susceptibility to spondyloarthritis by combining famillial studies and functional genomics. [Internet] [Doctoral dissertation]. Université Paris Descartes – Paris V; 2014. [cited 2020 Oct 21]. Available from: http://www.theses.fr/2014PA05T056.

Council of Science Editors:

Costantino F. Recherche de nouveaux facteurs génétiques de susceptibilité à la spondyloarthrite grâce à une approche associant études familiales et génomique fonctionnelle : Identification of new genetic factors of susceptibility to spondyloarthritis by combining famillial studies and functional genomics. [Doctoral Dissertation]. Université Paris Descartes – Paris V; 2014. Available from: http://www.theses.fr/2014PA05T056


Cornell University

29. Hansen, Joyanna. Vitamin D: Genetic And Environmental Predictors Of Status And Associations With Pulmonary Outcomes.

Degree: PhD, Nutrition, 2013, Cornell University

 Vitamin D, a pleiotropic hormone essential for calcium homeostasis, has generated widespread interest due to associations with numerous health outcomes. Cross-sectional studies of vitamin D… (more)

Subjects/Keywords: Vitamin D; Nutrition; Genetics; COPD; Epidemiology; FEV1; 25-Hydroxyvitamin D; eQTL; SGPP2; GC; supplements

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

APA (6th Edition):

Hansen, J. (2013). Vitamin D: Genetic And Environmental Predictors Of Status And Associations With Pulmonary Outcomes. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/34263

Chicago Manual of Style (16th Edition):

Hansen, Joyanna. “Vitamin D: Genetic And Environmental Predictors Of Status And Associations With Pulmonary Outcomes.” 2013. Doctoral Dissertation, Cornell University. Accessed October 21, 2020. http://hdl.handle.net/1813/34263.

MLA Handbook (7th Edition):

Hansen, Joyanna. “Vitamin D: Genetic And Environmental Predictors Of Status And Associations With Pulmonary Outcomes.” 2013. Web. 21 Oct 2020.

Vancouver:

Hansen J. Vitamin D: Genetic And Environmental Predictors Of Status And Associations With Pulmonary Outcomes. [Internet] [Doctoral dissertation]. Cornell University; 2013. [cited 2020 Oct 21]. Available from: http://hdl.handle.net/1813/34263.

Council of Science Editors:

Hansen J. Vitamin D: Genetic And Environmental Predictors Of Status And Associations With Pulmonary Outcomes. [Doctoral Dissertation]. Cornell University; 2013. Available from: http://hdl.handle.net/1813/34263


Vanderbilt University

30. O'Brien, Timothy Daniel. Investigating the Genetic Influences of the Germline and Somatic Genomes in Three Subtypes of Lung Cancer.

Degree: PhD, Human Genetics, 2017, Vanderbilt University

 Lung cancer is classified into two main types: small cell lung cancer (SCLC) and non-small cell lung cancer (NSCLC). NSCLC has several subtypes, but the… (more)

Subjects/Keywords: RNA-Seq; WES; somatic mutations; differential expression; enhancer; eQTL; lung cancer subtypes; GWAS

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

APA (6th Edition):

O'Brien, T. D. (2017). Investigating the Genetic Influences of the Germline and Somatic Genomes in Three Subtypes of Lung Cancer. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/12384

Chicago Manual of Style (16th Edition):

O'Brien, Timothy Daniel. “Investigating the Genetic Influences of the Germline and Somatic Genomes in Three Subtypes of Lung Cancer.” 2017. Doctoral Dissertation, Vanderbilt University. Accessed October 21, 2020. http://hdl.handle.net/1803/12384.

MLA Handbook (7th Edition):

O'Brien, Timothy Daniel. “Investigating the Genetic Influences of the Germline and Somatic Genomes in Three Subtypes of Lung Cancer.” 2017. Web. 21 Oct 2020.

Vancouver:

O'Brien TD. Investigating the Genetic Influences of the Germline and Somatic Genomes in Three Subtypes of Lung Cancer. [Internet] [Doctoral dissertation]. Vanderbilt University; 2017. [cited 2020 Oct 21]. Available from: http://hdl.handle.net/1803/12384.

Council of Science Editors:

O'Brien TD. Investigating the Genetic Influences of the Germline and Somatic Genomes in Three Subtypes of Lung Cancer. [Doctoral Dissertation]. Vanderbilt University; 2017. Available from: http://hdl.handle.net/1803/12384

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