Five Years of GWAS Discovery

Visscher, Peter M., Brown, Matthew A., McCarthy, Mark I., Yang, Jian·2012·The American Journal of Human Genetics
DOI 10.1016/j.ajhg.2011.11.029

Cited by (1,006)

Items 201–300 of 1,006

  1. Progress and promise in understanding the genetic basis of common diseases
    Price, Alkes L., Spencer, Chris C. A., Donnelly, Peter · 2015 · Proceedings of the Royal Society B: Biological Sciences
  2. Edgotype: a fundamental link between genotype and phenotype
    Nidhi Sahni, S. Stephen Yi, Quan Zhong, Noor Jailkhani, Benoît Charloteaux, Michael E. Cusick, Marc Vidal · 2013 · Current Opinion in Genetics & Development
  3. Explaining additional genetic variation in complex traits
    Matthew R. Robinson, Naomi R. Wray, Peter M. Visscher · 2014 · Trends in Genetics
  4. From genome-wide association studies to disease mechanisms: celiac disease as a model for autoimmune diseases
    Vinod Kumar, Cisca Wijmenga, Sebo Withoff · 2012 · Seminars in Immunopathology
  5. The Genetics of Complex Cholestatic Disorders
    Gideon Morris Hirschfield, Roger William Chapman, Tom H. Karlsen, Frank Lammert, Konstantinos N. Lazaridis, Andrew L. Mason · 2013 · Gastroenterology
  6. Unifying immunology with informatics and multiscale biology
    Brian A. Kidd, Lauren A Peters, Eric E. Schadt, Joel T. Dudley · 2014 · Nature Immunology
  7. Informatics and Data Analytics to Support Exposome-Based Discovery for Public Health
    Arjun Kumar Manrai, Yuxia Cui, Pierre R. Bushel, Molly A. Hall, Spyros Karakitsios, Carolyn J. Mattingly, Marylyn DeRiggi Ritchie, Charles Schmitt, Dimosthenis Andreas Sarigiannis, Duncan C. Thomas et al. · 2017 · Annual Review of Public Health
  8. Genetic–epigenetic interactions in cis: a major focus in the post-GWAS era
    Catherine Do, Alyssa Shearer, Masako Suzuki, Mary Beth Terry, Joel E. Gelernter, John M. Greally, Benjamin Tycko · 2017 · Genome biology
  9. The genetic basis of major depressive disorder
    Jonathan Flint C · 2023 · Molecular Psychiatry
  10. Twin-sibling study and meta-analysis on the heritability of maximal oxygen consumption
    Nienke M. Schutte, Ineke Nederend, James J. Hudziak, Meike Bartels, Eco J. C. de Geus · 2016 · Physiological Genomics
  11. Phenome-wide analysis of genome-wide polygenic scores
    Eva M. L. Krapohl, Jack Euesden, Delilah Zabaneh, Jean‐Baptiste Pingault, Kaili Rimfeld, Sophie von Stumm, Philip S. Dale, Gerome D. Breen, Paul F. O’Reilly, Robert J. Plomin · 2015 · Molecular Psychiatry
  12. Common DNA Markers Can Account for More Than Half of the Genetic Influence on Cognitive Abilities
    Plomin, Robert, Haworth, Claire M. A., Meaburn, Emma L., Price, Thomas S., Wellcome Trust Case Control Consortium 2, Davis, Oliver S. P. · 2013 · Psychological Science
  13. VAAST 2.0: Improved Variant Classification and Disease‐Gene Identification Using a Conservation‐Controlled Amino Acid Substitution Matrix
    Hao Hu, Chad Daniel Huff, Barry Moore, Steven D. Flygare, Martin G. Reese, Mark D. Yandell · 2013 · Genetic Epidemiology
  14. CUBIC: an atlas of genetic architecture promises directed maize improvement
    Haijun Liu, Xiaqing Wang, Yingjie Xiao, Jingyun Luo, Feng Qiao, Wenyu Yang, Ruyang Zhang, Yijiang Meng, Jiamin Sun, Shijuan Yan et al. · 2020 · Genome biology
  15. Response and Toxicity to Cytarabine Therapy in Leukemia and Lymphoma: From Dose Puzzle to Pharmacogenomic Biomarkers
    Raffaele Di Francia, Stefania Crisci, Angela De Monaco, Concetta Cafiero, Agnese Re, Giancarla Iaccarino, Rosaria De Filippi, Ferdinando Frigeri, Gaetano Corazzelli, Alessandra Micera et al. · 2021 · Cancers
  16. Age-related macular degeneration: genome-wide association studies to translation
    James R. Black, Simon J. Clark · 2015 · Genetics in Medicine
  17. Single-cell RNA-seq of mouse dopaminergic neurons informs candidate gene selection for sporadic Parkinson disease
    Hook, Paul W., McClymont, Sarah A., Cannon, Gabrielle H., Law, William D., Morton, A. Jennifer, Goff, Loyal A., McCallion, Andrew S. · 2018 · The American Journal of Human Genetics
  18. Genetic basis of myasthenia gravis – A comprehensive review
    Nili Avidan, Rozen Le Panse, Sonia Berrih‐Aknin, Ariel Miller · 2013 · Journal of Autoimmunity
  19. Genetics of ankylosing spondylitis
    Philip Cameron Robinson, Matthew Arthur Brown · 2013 · Molecular Immunology
  20. Accurate and Scalable Construction of Polygenic Scores in Large Biobank Data Sets
    Sheng Yang, Xiang Zhou · 2020 · The American Journal of Human Genetics
  21. Understanding Language from a Genomic Perspective
    Sarah A. Graham, Simon E. Fisher · 2015 · Annual Review of Genetics
  22. Genetics and educational attainment
    David A. Cesarini, Peter M. Visscher · 2017 · npj Science of Learning
  23. Wild GWAS—association mapping in natural populations
    Anna W. Santure, Dany Garant · 2018 · Molecular Ecology Resources
  24. Low-pass sequencing increases the power of GWAS and decreases measurement error of polygenic risk scores compared to genotyping arrays
    Jeremiah H. Li, Chase A. Mazur, Tomaz Berisa, Joseph K. Pickrell · 2021 · Genome Research
  25. Genetics of Migraine: Insights into the Molecular Basis of Migraine Disorders
    Heidi G. E. Sutherland, Lyn Robyn Griffiths · 2017 · Headache The Journal of Head and Face Pain
  26. Bioinformatics in translational drug discovery
    Sarah K. Wooller, Graeme Benstead-Hume, Xiangrong Chen, Yusuf Ali, Frances M. G. Pearl · 2017 · Bioscience Reports
  27. Polygenic risk scores and breast cancer risk prediction
    Eleanor Roberts, Sacha Jon Howell, D. Gareth Evans · 2023 · The Breast
  28. MR-Base: a platform for systematic causal inference across the phenome using billions of genetic associations
    Gibran Hemani, Jie Zheng, Kaitlin Hazel Wade, Charles Laurin, Benjamin Elsworth, Stephen Burgess, Jack Bowden, Ryan Langdon, Vanessa Y. Tan, James Yarmolinsky et al. · 2016 · bioRxiv (Cold Spring Harbor Laboratory)
  29. A Genome-Wide Association Study of Behavioral Disinhibition
    M. McGue, Yi-Wei Zhang, Michael B. Miller, S. Basu, S. Vrieze, Brian M. Hicks, S. Malone, W. Oetting, W. Iacono · 2013 · Behavior Genetics
  30. Genetic and epigenetic control of metabolic health
    Robert Wolfgang Schwenk, Heike Vogel, Annette Schürmann · 2013 · Molecular Metabolism
  31. TIGAR: An Improved Bayesian Tool for Transcriptomic Data Imputation Enhances Gene Mapping of Complex Traits
    Sini Nagpal, Xiaoran Meng, Michael P. Epstein, Lam C. Tsoi, Matthew T. Patrick, Greg C. Gibson, Philip L. De Jager, David Alan Bennett, Aliza P. Wingo, Thomas S. Wingo et al. · 2019 · The American Journal of Human Genetics
  32. Genome-wide association studies: assessing trait characteristics in model and crop plants
    Saleh Alseekh, D. Kostova, Mustafa Bulut, Alisdair Robert Fernie · 2021 · Cellular and Molecular Life Sciences
  33. Statistical colocalization of genetic risk variants for related autoimmune diseases in the context of common controls
    Mary D Fortune, Hui Guo, Oliver S. Burren, Ellen C. Schofield, Neil M Walker, Maria Ban, Stephen J. Sawcer, John Bowes, Jane Worthington, Anne C Barton et al. · 2015 · Nature Genetics
  34. Genetics and Genomics for the Prevention and Treatment of Cardiovascular Disease: Update
    Santhi K. Ganesh, Donna K. Arnett, Themistocles L. Assimes, Craig T. Basson, Aravinda Chakravarti, Patrick T. Ellinor, Mary B. Engler, Elizabeth Goldmuntz, David M. Herrington, Ray E. Hershberger et al. · 2013 · Circulation
  35. Genome-wide association of multiple complex traits in outbred mice by ultra-low-coverage sequencing
    Jérôme Nicod, Robert W Davies, Na Cai, Carl Hassett, Leo Goodstadt, Cormac Cosgrove, Benjamin K. Yee, Vikte Lionikaite, Rebecca E. McIntyre, Carol Ann Remme et al. · 2016 · Nature Genetics
  36. Genetic prediction of complex traits with polygenic scores: a statistical review
    Ying Ma, Xiang Zhou · 2021 · Trends in Genetics
  37. Mergeomics: multidimensional data integration to identify pathogenic perturbations to biological systems
    Le Shu, Yuqi Zhao, Zeyneb Kurt, Sean Byars, Taru Tukiainen, Johannes Kettunen, Luz D. Orozco, Matteo A. Pellegrini, Aldons Jake Lusis, Samuli Ripatti et al. · 2016 · BMC Genomics
  38. Combined Linkage and Association Mapping Reveals QTL and Candidate Genes for Plant and Ear Height in Maize
    Xiaopeng Li, Zijian Zhou, Junqiang Ding, Yabin Wu, Bo Zhou, Ruixia Wang, Jinliang Ma, Shiwei Wang, Xuecai Zhang, Zongliang Xia et al. · 2016 · Frontiers in Plant Science
  39. 17q21 asthma-risk variants switch CTCF binding and regulate IL-2 production by T cells
    Schmiedel, Benjamin Joachim, Seumois, Grégory, Samaniego-Castruita, Daniela, Cayford, Justin, Schulten, Veronique, Chavez, Lukas, Ay, Ferhat, Sette, Alessandro, Peters, Bjoern, Vijayanand, Pandurangan · 2016 · Nature Communications
  40. Applications of Population Genetics to Animal Breeding, from Wright, Fisher and Lush to Genomic Prediction
    William George Hill · 2014 · Genetics
  41. Rejection odds and rejection ratios: A proposal for statistical practice in testing hypotheses
    Bayarri, M.J., Benjamin, Daniel J., Berger, James O., Sellke, Thomas M. · 2016 · Journal of Mathematical Psychology
  42. Characterizing the genetic basis of bacterial phenotypes using genome-wide association studies: a new direction for bacteriology
    Timothy D. Read, Ruth C. Massey · 2014 · Genome Medicine
  43. Osteoporosis and Bone Mass Disorders: From Gene Pathways to Treatments
    Fernando Rivadeneira, Outi Mäkitie · 2016 · Trends in Endocrinology and Metabolism
  44. Improved methods for multi-trait fine mapping of pleiotropic risk loci
    Gleb Kichaev, Megan Roytman, Ruth Johnson, Eleazar Eskin, Sara Lindström, Peter Kraft, Bogdan Paşaniuc · 2016 · Bioinformatics
  45. The Genetic Basis of Metabolic Disease
    Inês Barroso, Mark I. McCarthy · 2019 · Cell
  46. Erratum: Predicting educational achievement from DNA
    Saskia Selzam, Eva M. L. Krapohl, Sophie von Stumm, Paul F. O’Reilly, Kaili Rimfeld, Yulia V. Kovas, Philip S. Dale, J J Lee, Robert J. Plomin · 2017 · Molecular Psychiatry
  47. Towards precision medicine: advances in computational approaches for the analysis of human variants
    Peterson, Thomas A., Doughty, Emily, Kann, Maricel G. · 2013 · Journal of Molecular Biology
  48. Quantifying Missing Heritability at Known GWAS Loci
    Alexander Gusev, Gaurav Bhatia, Noah Zaitlen, Bjarni Jóhann Vilhjálmsson, Dorothée Diogo, Eli A. Stahl, Peter K. Gregersen, Jane Worthington, Lars Klareskog, Soumya Raychaudhuri et al. · 2013 · PLoS Genetics
  49. Genomic Prediction for Quantitative Traits Is Improved by Mapping Variants to Gene Ontology Categories in Drosophila melanogaster
    Stefan McKinnon Edwards, Izel Fourie Sørensen, Pernille Merete Sarup, Trudy F. C. Mackay, Peter Borgen Sørensen · 2016 · Genetics
  50. PWAS: proteome-wide association study—linking genes and phenotypes by functional variation in proteins
    Nadav Brandes, Nathan Linial, Michal Linial B · 2020 · Genome biology
  51. The Power of Meta-Analysis in Genome-Wide Association Studies
    Orestis A. Panagiotou, Cristen J. Willer, Joel N. Hirschhorn, John P. A. Ioannidis · 2013 · Annual Review of Genomics and Human Genetics
  52. The MassARRAY® System for Targeted SNP Genotyping
    Justine A. Ellis, Benjamin Ong · 2016 · Methods in molecular biology
  53. Whole-genome and whole-exome sequencing in neurological diseases
    Jia Nee Foo, Jianjun Liu, Eng‐King Tan · 2012 · Nature Reviews Neurology
  54. Estimation and partitioning of (co)heritability of inflammatory bowel disease from GWAS and immunochip data
    Guo‐Bo Chen, Sang Lee, Marie‐Jo Brion, Grant W. Montgomery, Naomi R. Wray, Graham L Radford‐Smith, Peter M. Visscher · 2014 · Human Molecular Genetics
  55. Multivariate simulation framework reveals performance of multi-trait GWAS methods
    Heather F. Porter, Paul F. O’Reilly · 2017 · Scientific Reports
  56. Accuracy of genotype imputation in Nelore cattle
    Roberto Carvalheiro, Solomon Antwi Boison, Haroldo Henrique de Rezende Neves, Mehdi Sargolzaei, Flávio Schramm Schenkel, Yuri Tani Utsunomiya, Ana M. Pérez O’Brien, Johann Sölkner, John Colin McEwan, Curtis P. Van Tassell et al. · 2014 · Genetics Selection Evolution
  57. Recent advances in understanding the genetic architecture of type 2 diabetes
    Karen L. Mohlke, Michael Boehnke · 2015 · Human Molecular Genetics
  58. Population genomics of parallel hybrid zones in the mimetic butterflies, H. melpomene and H. erato
    Nicola J. Nadeau, Mayté Ruiz, Patricio A. Salazar, Brian A. Counterman, Jose Alejandro Medina, Humberto Ortiz‐Zuazaga, Anna Morrison, W. Owen McMillan, Chris D. Jiggins, Riccardo Papa · 2014 · Genome Research
  59. Abstract
    Burgess, S · 2018 · Apollo (University of Cambridge)
  60. Genome-wide association study identifies the SERPINB gene cluster as a susceptibility locus for food allergy
    Ingo Marenholz, Sarah Grosche, Birgit Kalb, Franz Rüschendorf, Katharina Blümchen, Rupert Schlags, Neda Harandi, Mareike Price, Gesine Hansen, Jürgen Seidenberg et al. · 2017 · Nature Communications
  61. Forensically relevant SNaPshot® assays for human DNA SNP analysis: a review
    Bhavik Mehta, R. Daniel, C. Phillips, D. McNevin · 2016 · Zeitschrift für Rechtsmedizin
  62. Polycystic Ovary Syndrome: An Evolutionary Adaptation to Lifestyle and the Environment
    Parker, Jim, O’Brien, Claire, Hawrelak, Jason, Gersh, Felice L. · 2022 · International Journal of Environmental Research and Public Health
  63. Very Early-onset Inflammatory Bowel Disease
    Christopher J. Moran, Christoph Klein, Aleixo M. Muise, Scott B. Snapper · 2015 · Inflammatory Bowel Diseases
  64. Polycystic Ovary Syndrome: An Evolutionary Adaptation to Lifestyle and the Environment
    parker, jim, O'Brien, Claire, Hawrelak, Jason, Gersh, Felice · 2021
  65. Metabolomics platforms for genome wide association studies—linking the genome to the metabolome
    Jerzy Adamski, Karsten Suhre · 2012 · Current Opinion in Biotechnology
  66. 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function
    Mathias Gorski, Peter J. van der Most, Alexander Teumer, Audrey Y. Chu, Man Li, Vladan Mijatovic, Ilja Maria Nolte, Massimiliano Cocca, Daniel Taliun, Felicia Gomez et al. · 2017 · Scientific Reports
  67. Congenital heart disease risk loci identified by genome-wide association study in European patients
    Harald Lahm, Meiwen Jia, Martina Dreßen, Felix Wirth, Nazan Puluca, Ralf Gilsbach, Bernard D. Keavney, Julie Cleuziou, Nicole Beck, Olga Bondareva et al. · 2020 · Journal of Clinical Investigation
  68. Replicability and Robustness of Genome-Wide-Association Studies for Behavioral Traits
    Rietveld, Cornelius A., Conley, Dalton, Eriksson, Nicholas, Esko, Tõnu, Medland, Sarah E., Vinkhuyzen, Anna A. E., Yang, Jian, Boardman, Jason D., Chabris, Christopher F., Dawes, Christopher T. et al. · 2014 · Psychological Science
  69. A century after Fisher: time for a new paradigm in quantitative genetics
    Ronald M. Nelson, Mats E. Pettersson, Örjan Carlborg · 2013 · Trends in Genetics
  70. Editing the genome of hiPSC with CRISPR/Cas9: disease models
    Andrew Roger Bassett · 2017 · Mammalian Genome
  71. Dynamic Role of trans Regulation of Gene Expression in Relation to Complex Traits
    Yao, Chen, Joehanes, Roby, Johnson, Andrew D., Huan, Tianxiao, Liu, Chunyu, Freedman, Jane E., Munson, Peter J., Hill, David E., Vidal, Marc, Levy, Daniel · 2017 · The American Journal of Human Genetics
  72. Predicting gene targets from integrative analyses of summary data from GWAS and eQTL studies for 28 human complex traits
    Pavlides, Jennifer M. Whitehead, Zhu, Zhihong, Gratten, Jacob, McRae, Allan F., Wray, Naomi R., Yang, Jian · 2016 · Genome Medicine
  73. Systematic identification of interaction effects between genome- and environment-wide associations in type 2 diabetes mellitus
    Chirag J. Patel, Rong Chen, Keiichi Kodama, John P. A. Ioannidis, Atul Janardhan Butte · 2013 · Human Genetics
  74. Challenges in Elucidating the Genetics of Diabetic Retinopathy
    Jane Zea-Chin Kuo, Tien Yin Wong, Jerome I. Rotter · 2013 · JAMA Ophthalmology
  75. Understanding the development of psychopathy: progress and challenges
    Essi M. Viding, Eamon J. P. McCrory · 2017 · Psychological Medicine
  76. Using GWAS to identify genetic predisposition in hepatic autoimmunity
    Webb, G.J., Hirschfield, G.M. · 2016 · Journal of Autoimmunity
  77. HEALER: homomorphic computation of ExAct Logistic rEgRession for secure rare disease variants analysis in GWAS
    Shuang Wang, Yuchen Zhang, Wenrui Dai, Kristin Lauter, Miran Kim, Yuzhe Tang, Hongkai Xiong, Xiaoqian Jiang · 2015 · Bioinformatics
  78. Regulatory variants: from detection to predicting impact
    E. Rojano, P. Seoane, J. A. Ranea, J. Perkins · 2018 · Briefings Bioinform.
  79. What can genome‐wide association studies tell us about the evolutionary forces maintaining genetic variation for quantitative traits?
    Emily B. Josephs, John R. Stinchcombe, Stephen Wright · 2017 · New Phytologist
  80. Cross-ethnic meta-analysis identifies association of the GPX3-TNIP1 locus with amyotrophic lateral sclerosis
    Beben Benyamin, Ji He, Qiongyi Zhao, Jacob Gratten, Fleur C. Garton, Paul J. Leo, Zhijun Liu, Marie Mangelsdorf, Ammar Al‐Chalabi, Lisa K. Anderson et al. · 2017 · Nature Communications
  81. The genetics of drug efficacy: opportunities and challenges
    Matthew R. Nelson, Toby Johnson, Liling L. Warren, Arlene R. Hughes, Stephanie L. Chissoe, Chun‐Fang Xu, Dawn M. Waterworth · 2016 · Nature Reviews Genetics
  82. Detecting epistasis with the marginal epistasis test in genetic mapping studies of quantitative traits
    Lorin A. Crawford, Ping Zeng, Sayan Mukherjee, Xiang Zhou · 2017 · PLoS Genetics
  83. Heritability and genome-wide association of swine gut microbiome features with growth and fatness parameters
    Matteo Bergamaschi, Christian Maltecca, Constantino Schillebeeckx, Nathan P. McNulty, Clint Ray Schwab, Caleb M Shull, Justin Fix, Francesco Tiezzi · 2020 · Scientific Reports
  84. Molecular genetics and subjective well-being
    Rietveld, Cornelius A., Cesarini, David, Benjamin, Daniel J., Koellinger, Philipp D., De Neve, Jan-Emmanuel, Tiemeier, Henning, Johannesson, Magnus, Magnusson, Patrik K. E., Pedersen, Nancy L., Krueger, Robert F. et al. · 2013 · Proceedings of the National Academy of Sciences
  85. The Genetics of Loneliness: Linking Evolutionary Theory to Genome-Wide Genetics, Epigenetics, and Social Science
    Goossens, Luc, van Roekel, Eeske, Verhagen, Maaike, Cacioppo, John T., Cacioppo, Stephanie, Maes, Marlies, Boomsma, Dorret I. · 2015 · Perspectives on Psychological Science
  86. The Heritability of Breast Cancer among Women in the Nordic Twin Study of Cancer
    Sören Möller, Lorelei Ann Mucci, Jennifer Ruth Harris, Thomas Scheike, Klaus K. Holst, Ulrich Halekoh, Hans‐Olov Adami, Kamila Czene, Kaare Christensen, Niels Vilstrup Holm et al. · 2015 · Cancer Epidemiology Biomarkers & Prevention
  87. Exploring regulation in tissues with eQTL networks
    Maud Fagny, Joseph Nathaniel Paulson, Marieke L. Kuijjer, Abhijeet R. Sonawane, Cho-Yi Chen, Camila M. Lopes‐Ramos, Kimberly Glass, John F Quackenbush, John Platig · 2017 · Proceedings of the National Academy of Sciences
  88. The ubiquity of pleiotropy in human disease
    Kevin N. Chesmore, Jacquelaine Bartlett, Scott M. Williams · 2017 · Human Genetics
  89. Stability of Proteins in Dried Blood Spot Biobanks
    Johan Björkesten, Stefan Enroth, Qiujin Shen, Lotta Wik, DAVID MICHAEL HOUGAARD, Arieh Sierra Cohen, Lene Sörensen, Vilmantas Giedraitis, Martin Ingelsson, Anders Larsson et al. · 2017 · Molecular & Cellular Proteomics
  90. The genetic basis of ankylosing spondylitis: new insights into disease pathogenesis
    Florence W. L. Tsui, Hing Wo Tsui, Ali Akram, Nigil Haroon, Robert Davies Inman · 2014 · The Application of Clinical Genetics
  91. DNA evidence for strong genetic stability and increasing heritability of intelligence from age 7 to 12
    M. Trzaskowski, Jennifer Yang, P. Visscher, R. Plomin · 2013 · Molecular Psychiatry
  92. Genome-wide association study identifies loci on 12q24 and 13q32 associated with Tetralogy of Fallot
    Heather Jane Cordell, Ana Töpf, Chrysovalanto Mamasoula, Alex Vincent Postma, Jamie Bentham, Diana Zélénika, Simon Charles Heath, Gillian M. Blue, Catherine Cosgrove, Javier T Granados-Riveron et al. · 2013 · Human Molecular Genetics
  93. Large-scale genome-wide enrichment analyses identify new trait-associated genes and pathways across 31 human phenotypes
    Xiang Zhu, Matthew Stephens · 2018 · Nature Communications
  94. Preventive effects of low‐dose aspirin on colorectal adenoma growth in patients with familial adenomatous polyposis: double‐blind, randomized clinical trial
    Hideki Ishikawa, Keiji Wakabayashi, Sadao Suzuki, Michihiro Mutoh, Keiji Hirata, Tomiyo Nakamura, Ikuko Takeyama, Atsuko Kawano, Nobuhisa Gondo, Takashi Abe et al. · 2012 · Cancer Medicine
  95. Monozygotic twins affected with major depressive disorder have greater variance in methylation than their unaffected co-twin
    Enda M. Byrne, Tania Carrillo‐Roa, Anjali K. Henders, Lisa M. Bowdler, Allan F. McRae, Andrew C. Heath, Nicholas G. Martin, Grant W. Montgomery, Lutz Krause, Naomi R. Wray · 2013 · Translational Psychiatry
  96. The Generalized Higher Criticism for Testing SNP-Set Effects in Genetic Association Studies
    Ian Barnett, Rajarshi Mukherjee, Xihong Lin · 2016 · Journal of the American Statistical Association
  97. Integrating Sequence-based GWAS and RNA-Seq Provides Novel Insights into the Genetic Basis of Mastitis and Milk Production in Dairy Cattle
    Lingzhao Fang, Goutam Sahana, Guosheng Su, Ying Yu, Shengli Zhang, Mogens Sandø Lund, Peter Sørensen · 2017 · Scientific Reports
  98. Genetic and environmental risk factors for chronic kidney disease
    Gregorio T. Obrador, Ulla T. Schultheiß, Matthias Kretzler, Robyn G. Langham, Masaomi Nangaku, Roberto Pecoits‐Filho, Carol A. Pollock, Jérôme Rossert, Ricardo Correa‐Rotter, Peter Stenvinkel et al. · 2017 · Kidney International Supplements
  99. The genetic etiology of eosinophilic esophagitis
    Leah Claire Kottyan, Sreeja Parameswaran, Matthew T. Weirauch, Marc E. Rothenberg, Lisa Joy Martin · 2020 · Journal of Allergy and Clinical Immunology
  100. A Large Genome-Wide Association Study of Age-Related Hearing Impairment Using Electronic Health Records
    Thomas J. Hoffmann, Bronya J.B. Keats, Noriko Yoshikawa, Catherine A. Schaefer, NEIL J. RISCH, Lawrence R. Lustig · 2016 · PLoS Genetics