检索结果 - Andrew D. Skol

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  1. 1
    The genetics of breast cancer risk in the post-genome era: thoughts on study design to move past BRCA and towards clinical relevance

    The genetics of breast cancer risk in the post-genome era: thoughts on study design to move past BRCA and towards clinical relevance 由 Andrew D. Skol, Mark M. Sasaki, Kenan Onel

    出版 2016
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  2. 2
    QTLRel: an R Package for Genome-wide Association Studies in which Relatedness is a Concern

    QTLRel: an R Package for Genome-wide Association Studies in which Relatedness is a Concern 由 Riyan Cheng, Mark Abney, Abraham A. Palmer, Andrew D. Skol

    出版 2011
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  3. 3
    Optimal designs for two‐stage genome‐wide association studies

    Optimal designs for two‐stage genome‐wide association studies 由 Andrew D. Skol, Laura J. Scott, Gonçalo R. Abecasis, Michael Boehnke

    出版 2007
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  4. 4
    Evaluation of genetic variability in the dopamine receptor D2 in relation to behavioral inhibition and impulsivity/sensation seeking: An exploratory study with d-amphetamine in healthy participants.

    Evaluation of genetic variability in the dopamine receptor D2 in relation to behavioral inhibition and impulsivity/sensation seeking: An exploratory study with d-amphetamine in hea... 由 Ajna Hamidovic, Andrea Dlugos, Andrew D. Skol, Abraham A. Palmer, Harriet de Wit

    出版 2009
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  5. 5
    Genome-Wide Association Studies and the Problem of Relatedness Among Advanced Intercross Lines and Other Highly Recombinant Populations

    Genome-Wide Association Studies and the Problem of Relatedness Among Advanced Intercross Lines and Other Highly Recombinant Populations 由 Riyan Cheng, Jackie E. Lim, Kaitlin E. Samocha, Greta Sokoloff, Mark Abney, Andrew D. Skol, Abraham A. Palmer

    出版 2010
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  6. 6
    Enrichment of inflammatory bowel disease and colorectal cancer risk variants in colon expression quantitative trait loci

    Enrichment of inflammatory bowel disease and colorectal cancer risk variants in colon expression quantitative trait loci 由 Imge Hulur, Eric R. Gamazon, Andrew D. Skol, Rosa M. Xicola, Xavier Llor, Kenan Onel, Nathan A. Ellis, Sonia S. Kupfer

    出版 2015
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  7. 7
    Genetic Heterogeneity in Colorectal Cancer Associations Between African and European Americans

    Genetic Heterogeneity in Colorectal Cancer Associations Between African and European Americans 由 Sonia S. Kupfer, Jeffrey R. Anderson, Stanley Hooker, Andrew D. Skol, Rick A. Kittles, Temitope O. Keku, Robert S. Sandler, Nathan A. Ellis

    出版 2010
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  8. 8
    Trait-stratified genome-wide association study identifies novel and diverse genetic associations with serologic and cytokine phenotypes in systemic lupus erythematosus

    Trait-stratified genome-wide association study identifies novel and diverse genetic associations with serologic and cytokine phenotypes in systemic lupus erythematosus 由 Silvia N. Kariuki, Beverly S. Franek, Akaash Kumar, Jasmine Arrington, Rachel A. Mikolaitis, Tammy O. Utset, Meenakshi Jolly, Mary K. Crow, Andrew D. Skol, Timothy B. Niewold

    出版 2010
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  9. 9
    Integration of genomics and transcriptomics predicts diabetic retinopathy susceptibility genes

    Integration of genomics and transcriptomics predicts diabetic retinopathy susceptibility genes 由 Andrew D. Skol, Segun Jung, Ana Marija Sokovic, Siquan Chen, Sarah Fazal, Olukayode Sosina, Poulami P Borkar, Amy Lin, Maria Sverdlov, Dingcai Cao, Anand Swaroop, Ionut Bebu, Barbara E. Stranger, Michael A. Grassi

    出版 2020
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  10. 10
    Interaction of prenatal exposure to cigarettes and MAOA genotype in pathways to youth antisocial behavior

    Interaction of prenatal exposure to cigarettes and MAOA genotype in pathways to youth antisocial behavior 由 Lauren S. Wakschlag, Emily O. Kistner, Daniel S. Pine, Gretchen Biesecker, Kate E. Pickett, Andrew D. Skol, Vanja Dukić, James Blair, Bennett Leventhal, Nancy J. Cox, James Burns, Kristen Kasza, R. J. Wright, Edwin H. Cook

    出版 2009
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  11. 11
    Genetic changes associated with relapse in favorable histology Wilms tumor: A Children’s Oncology Group AREN03B2 study

    Genetic changes associated with relapse in favorable histology Wilms tumor: A Children’s Oncology Group AREN03B2 study 由 Samantha Gadd, Vicki Huff, Andrew D. Skol, Lindsay A. Renfro, Conrad V. Fernandez, Elizabeth A. Mullen, Corbin D. Jones, Katherine A. Hoadley, Kai Lee Yap, Nilsa C. Ramirez, Sheena M. Aris, Quy H. Phung, Elizabeth J. Perlman

    出版 2022
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  12. 12
    Genome-wide association study to identify novel loci associated with therapy-related myeloid leukemia susceptibility

    Genome-wide association study to identify novel loci associated with therapy-related myeloid leukemia susceptibility 由 Jeffrey A. Knight, Andrew D. Skol, Abhijit Shinde, Darcie Hastings, Richard A. Walgren, Jin Shao, Thelma R. Tennant, Mekhala Banerjee, James M. Allan, Michelle M. Le Beau, Richard A. Larson, Timothy A. Graubert, Nancy J. Cox, Kenan Onel

    出版 2009
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  13. 13
    Genetic analysis of the pathogenic molecular sub-phenotype interferon-alpha identifies multiple novel loci involved in systemic lupus erythematosus

    Genetic analysis of the pathogenic molecular sub-phenotype interferon-alpha identifies multiple novel loci involved in systemic lupus erythematosus 由 Silvia N. Kariuki, Yogita Ghodke‐Puranik, J.M. Dorschner, Beverly S Chrabot, Jennifer A. Kelly, Betty P. Tsao, Robert P. Kimberly, Marta E. Alarcón‐Riquelme, Chaim O. Jacob, Lindsey A. Criswell, Kathy L. Sivils, Carl D. Langefeld, John B. Harley, Andrew D. Skol, Timothy B. Niewold

    出版 2014
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  14. 14
    Variants at 6q21 implicate PRDM1 in the etiology of therapy-induced second malignancies after Hodgkin's lymphoma

    Variants at 6q21 implicate PRDM1 in the etiology of therapy-induced second malignancies after Hodgkin's lymphoma 由 Timothy Best, Dalin Li, Andrew D. Skol, Tomas Kirchhoff, Sarah A. Jackson, Yutaka Yasui, Ravi Bhatia, Louise C. Strong, Susan M. Domchek, Katherine L. Nathanson, Olufunmilayo I. Olopade, R. Stephanie Huang, Thomas M. Mack, David V. Conti, Kenneth Offit, Wendy Cozen, Leslie L. Robison, Kenan Onel

    出版 2011
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  15. 15
    A variant at 9p21.3 functionally implicates CDKN2B in paediatric B-cell precursor acute lymphoblastic leukaemia aetiology

    A variant at 9p21.3 functionally implicates CDKN2B in paediatric B-cell precursor acute lymphoblastic leukaemia aetiology 由 Eric A. Hungate, Sapana Vora, Eric R. Gamazon, Takaya Moriyama, Timothy Best, Imge Hulur, Young‐Hee Lee, Tiffany‐Jane Evans, Eva Ellinghaus, Martin Stanulla, Jérémie Rudant, Laurent Orsi, Jacqueline Clavel, Elizabeth Milne, Rodney J. Scott, Ching‐Hon Pui, Nancy J. Cox, Mignon L. Loh, Jun J. Yang, Andrew D. Skol, Kenan Onel

    出版 2016
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  16. 16
    Genetic Variation Near the Hepatocyte Nuclear Factor-4α Gene Predicts Susceptibility to Type 2 Diabetes

    Genetic Variation Near the Hepatocyte Nuclear Factor-4α Gene Predicts Susceptibility to Type 2 Diabetes 由 Kaisa Silander, Karen L. Mohlke, Laura J. Scott, Erin C. Peck, Pablo E. Hollstein, Andrew D. Skol, Anne Jackson, Panos Deloukas, Sarah Hunt, George Stavrides, Peter S. Chines, Michael R. Erdos, Narisu Narisu, Karen N. Conneely, Chun Li, Tasha E. Fingerlin, Sharanjeet K. Dhanjal, Timo T. Valle, Richard N. Bergman, Jaakko Tuomilehto, Richard M. Watanabe, Michael Boehnke, Francis S. Collins

    出版 2004
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  17. 17
    Chromatin conformation, gene transcription, and nucleosome remodeling as an emergent system

    Chromatin conformation, gene transcription, and nucleosome remodeling as an emergent system 由 Luay M. Almassalha, Marcelo A. Carignano, Emily M. Pujadas-Liwag, Wing Shun Li, Ruyi Gong, Nicolas Acosta, Cody Dunton, Paola Carrillo Gonzalez, Lucas Carter, Rivaan Kakkaramadam, Martin Kröger, Kyle L. MacQuarrie, Jane Frederick, I Chae Ye, Patrick Su, Tiffany Kuo, Karla I. Medina, Josh Pritchard, Andrew D. Skol, Rikkert J. Nap, Masato T. Kanemaki, Vinayak P. Dravid, Igal Szleifer, Vadim Backman

    出版 2025
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  18. 18
    A genome-wide meta-analysis of nodular sclerosing Hodgkin lymphoma identifies risk loci at 6p21.32

    A genome-wide meta-analysis of nodular sclerosing Hodgkin lymphoma identifies risk loci at 6p21.32 由 Wendy Cozen, Dalin Li, Timothy Best, David J. Van Den Berg, Pierre‐Antoine Gourraud, Victoria K. Cortessis, Andrew D. Skol, Thomas M. Mack, Sally L. Glaser, Lawrence M. Weiss, Bharat N. Nathwani, Ravi Bhatia, Fredrick R. Schumacher, Christopher K. Edlund, Amie E. Hwang, Susan L. Slager, Zachary S. Fredericksen, Louise C. Strong, Thomas M. Habermann, Brian K. Link, James R. Cerhan, Leslie L. Robison, David V. Conti, Kenan Onel

    出版 2011
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  19. 19
    Screening of 134 Single Nucleotide Polymorphisms (SNPs) Previously Associated With Type 2 Diabetes Replicates Association With 12 SNPs in Nine Genes

    Screening of 134 Single Nucleotide Polymorphisms (SNPs) Previously Associated With Type 2 Diabetes Replicates Association With 12 SNPs in Nine Genes 由 Cristen J. Willer, Lori L. Bonnycastle, Karen N. Conneely, William L. Duren, Anne Jackson, Laura J. Scott, Narisu Narisu, Peter S. Chines, Andrew D. Skol, Heather M. Stringham, John R. Petrie, Michael R. Erdos, Amy J. Swift, Sareena T. Enloe, Andrew G. Sprau, E. O’Brian Smith, Maurine Tong, Kimberly F. Doheny, Elizabeth Pugh, Richard M. Watanabe, Thomas A. Buchanan, Timo T. Valle, Richard N. Bergman, Jaakko Tuomilehto, Karen L. Mohlke, Francis S. Collins, Michael Boehnke

    出版 2006
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  20. 20
    The impact of sex on gene expression across human tissues

    The impact of sex on gene expression across human tissues 由 Meritxell Oliva, Manuel Muñoz-Aguirre, Sarah Kim-Hellmuth, Valentin Wucher, Ariel DH Gewirtz, Daniel J. Cotter, Princy Parsana, Silva Kasela, Brunilda Balliu, Ana Viñuela, Stephane E. Castel, Pejman Mohammadi, François Aguet, Yuxin Zou, Ekaterina Khramtsova, Andrew D. Skol, Diego Garrido-Martín, Ferrán Reverter, Andrew Brown, Patrick Evans, Eric R. Gamazon, A. J. Payne, Rodrigo Bonazzola, Alvaro Barbeira, Andrew R. Hamel, Ángel Martínez-Pérez, José Manuel Soria, Consortium GTEx, Brandon L. Pierce, Matthew Stephens, Eleazar Eskin, Emmanouil T. Dermitzakis, Ayellet V. Segrè, Hae Kyung Im, Barbara E. Engelhardt, Kristin Ardlie, Stephen B. Montgomery, Alexis Battle, Tuuli Lappalainen, Roderic Guigó, Barbara E. Stranger

    出版 2021
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