Five Years of GWAS Discovery

Visscher, Peter M., Brown, Matthew A., McCarthy, Mark I., Yang, Jian·2012·The American Journal of Human Genetics

Cited by (1,006)

Items 401–500 of 1,006

  1. Multidimensional heritability analysis of neuroanatomical shape
    Tian Ge, Martin Reuter, Anderson M. Winkler, Avram J. Holmes, Phil Hyoun Lee, Lee Sean Tirrell, Joshua L. Roffman, Randy L. Buckner, Jordan W. Smoller, Mert Rory Sabuncu · 2016 · Nature Communications
  2. ASEP: Gene-based detection of allele-specific expression across individuals in a population by RNA sequencing
    Jiaxin Fan, Jian Hu, Chenyi Xue, Hanrui Zhang, Katalin Suszták, Muredach P. Reilly, Rui Xiao, Mingyao Li · 2020 · PLoS Genetics
  3. Additive Genetic Variation in Schizophrenia Risk Is Shared by Populations of African and European Descent
    Teresa R de Candia, Sang Lee, Jian Yang, Brian L. Browning, Pablo V. Gejman, Douglas F. Levinson, Bryan J. Mowry, John K. Hewitt, Michael Edward Goddard, Michael C. O’Donovan et al. · 2013 · The American Journal of Human Genetics
  4. Genomic variations in non-coding RNAs: Structure, function and regulation
    Deeksha Bhartiya, Vinod Scaria · 2016 · Genomics
  5. JAM: A Scalable Bayesian Framework for Joint Analysis of Marginal SNP Effects
    Paul J. Newcombe, David V. Conti, Sylvia T. Richardson · 2016 · Genetic Epidemiology
  6. Insights into assessing the genetics of endometriosis
    Rahmioglu, Nilufer, Missmer, Stacey A., Montgomery, Grant W., Zondervan, Krina T. · 2012 · Current Obstetrics and Gynecology Reports
  7. Whole-exome sequencing in obsessive-compulsive disorder identifies rare mutations in immunological and neurodevelopmental pathways
    Cappi, C, Brentani, H, Lima, L, Sanders, S J, Zai, G, Diniz, B J, Reis, V N S, Hounie, A G, Conceição do Rosário, M, Mariani, D et al. · 2016 · Translational Psychiatry
  8. A genome-wide association study for extremely high intelligence
    Zabaneh, D, Krapohl, E, Gaspar, H A, Curtis, C, Lee, S H, Patel, H, Newhouse, S, Wu, H M, Simpson, M A, Putallaz, M et al. · 2018 · Molecular Psychiatry
  9. In Defense of Genopolitics
    James H. Fowler, Christopher T. Dawes · 2013 · American Political Science Review
  10. Genetics of irritable bowel syndrome
    Maria Henström, Mauro D’Amato · 2016 · Molecular and Cellular Pediatrics
  11. QTL Mapping of Leafy Heads by Genome Resequencing in the RIL Population of Brassica rapa
    Xiang Yu, Han Wang, Weili Zhong, Jinjuan Bai, Pinglin Liu, Yuke He · 2013 · PLoS ONE
  12. Genetic variants associated with disordered eating
    Tracey D. Wade, Scott D. Gordon, Sarah Elizabeth Medland, Cynthia Marie Bulik, Andrew C. Heath, Grant W. Montgomery, Nicholas G. Martin · 2013 · International Journal of Eating Disorders
  13. Omics-based biomarkers: current status and potential use in the clinic
    Héctor Quezada, Ana Laura Guzmán-Ortiz, Hugo Díaz-Sánchez, Ricardo Valle‐Rios, Jesús Aguirre‐Hernández · 2017 · Boletín Médico del Hospital Infantil de México
  14. Exploring the genetic architecture and improving genomic prediction accuracy for mastitis and milk production traits in dairy cattle by mapping variants to hepatic transcriptomic regions responsive to intra-mammary infection
    Lingzhao Fang, Goutam Sahana, Peipei Ma, Guosheng Su, Ying Yu, Shengli Zhang, Mogens Sandø Lund, Peter Borgen Sørensen · 2017 · Genetics Selection Evolution
  15. De novo mutations from whole exome sequencing in neurodevelopmental and psychiatric disorders: From discovery to application
    Wang, Weidi, Corominas, Roser, Lin, Guan Ning · 2019 · Frontiers in Genetics
  16. Chemical Synthesis of Human Proteoforms and Application in Biomedicine
    Hua-Song Ai, Man Pan, Lei Liu · 2024 · ACS Central Science
  17. Functional interpretation of non‐coding sequence variation: Concepts and challenges
    Dirk S. Paul, Nicole Soranzo, Stephan Beck · 2013 · BioEssays
  18. Confirmation of TNIP1 but not RHOB and PSORS1C1 as systemic sclerosis risk factors in a large independent replication study
    Lara Bossini‐Castillo, Jose‐Ezequiel Martín, Jasper C. A. Broen, Carmen Pilar Simeón‐Aznar, Lorenzo Beretta, Olga Y. Gorlova, Madelon C Vonk, Norberto Ortego‐Centeno, Gerard Espinosa, Patricia Esmeralda Carreira et al. · 2012 · Annals of the Rheumatic Diseases
  19. Pharmacogenomics in diabetes mellitus: insights into drug action and drug discovery
    Kaixin Zhou, Helle Pedersen, Adem Y. Dawed, Ewan R. Pearson · 2016 · Nature Reviews Endocrinology
  20. Association between COMT Val158Met and psychiatric disorders: A comprehensive meta‐analysis
    Steven J. Taylor · 2017 · American Journal of Medical Genetics Part B Neuropsychiatric Genetics
  21. Machine learning approaches for the prediction of obesity using publicly available genetic profiles
    Casimiro Aday Curbelo Montañez, Paul Fergus, Abir Jaafar Hussain, Dhiya Al‐Jumeily, Basma Abdulaimma, Jade Hind, Naeem Radi · 2017 · International Joint Conference on Neural Networks (IJCNN)
  22. Genetics of Clozapine-Associated Neutropenia: Recent Advances, Challenges and Future Perspective
    Sophie E. Legge, James Walters · 2019 · Pharmacogenomics
  23. SAFETY: Secure gwAs in Federated Environment through a hYbrid Solution
    Md Nazmus Sadat, Md Momin Al Aziz, Noman Mohammed, Feng Chen, Xiaoqian Jiang, Shuang Wang · 2018 · IEEE Transactions on Computational Biology and Bioinformatics
  24. Immunology Taught by Human Genetics
    Jean‐Laurent Casanova, Laurent Abel, Lluís Quintana‐Murci · 2013 · Cold Spring Harbor Symposia on Quantitative Biology
  25. Heterogeneity of genetic architecture of body size traits in a free‐living population
    Camillo Bérénos, Philip A. Ellis, Jill G. Pilkington, Sang Lee, Jacob Gratten, Josephine M. Pemberton · 2015 · Molecular Ecology
  26. Sociogenomics in the 21st Century: An Introduction to the History and Potential of Genetically-informed Social Science
    David B. Braudt · 2018 · Sociology Compass
  27. Genomic architecture of complex traits in loblolly pine
    Amanda R. De La Torre, Daniela Puiu, Marc Crepeau, Kristian Stevens, Steven L. Salzberg, Charles H. Langley, David B. Neale · 2018 · New Phytologist
  28. DeepWAS: Multivariate genotype-phenotype associations by directly integrating regulatory information using deep learning
    Janine Arloth, Gökçen Eraslan, Till F. M. Andlauer, Jade Martins, Stella Iurato, Brigitte Kühnel, Mélanie Waldenberger, Josef Frank, Ralf Gold, Bernhard Hemmer et al. · 2020 · PLoS Computational Biology
  29. Genetic heterogeneity: Challenges, impacts, and methods through an associative lens
    Alexa Woodward, Ryan J. Urbanowicz, Adam Christian Naj, Jason H. Moore · 2022 · Genetic Epidemiology
  30. Bayesian Genetic Colocalization Test of Two Traits Using coloc
    Danielle Rasooly, Gina Marie Peloso, Claudia Giambartolomei · 2022 · Current Protocols
  31. The impact of entrepreneurship research on other academic fields
    Roy Thurik, David Bruce Audretsch, Joern Block, Andrew Burke, Martin Carree, Marcus Dejardin, Cornelius A. Rietveld, Mark W. J. L. Sanders, Ute Stephan, Johan Wiklund · 2023 · Small Business Economics
  32. Identifying the Biological Basis of GWAS Hits for Endometriosis1
    Jenny N. Fung, Peter A. W. Rogers, Grant W. Montgomery · 2015 · Biology of Reproduction
  33. Multiple alleles at a single locus control seed dormancy in Swedish Arabidopsis
    Envel Kerdaffrec, Danièle L. Filiault, Arthur Korte, Eriko Sasaki, Viktoria Nizhynska, Ümit Seren, Magnus Nordborg · 2016 · eLife
  34. Powerful gene set analysis in GWAS with the Generalized Berk-Jones statistic
    Ryan Sun, Shirley Hui, Gary D. Bader, Xihong Lin, Peter Kraft · 2019 · PLoS Genetics
  35. Pedigree- and SNP-Associated Genetics and Recent Environment are the Major Contributors to Anthropometric and Cardiometabolic Trait Variation
    Charley Xia, Carmen Amador, Jennifer E. Huffman, Holly Trochet, Archie Campbell, David John Porteous, Generation Scotland, Nicholas D. Hastie, Caroline Hayward, Véronique Vitart et al. · 2016 · PLoS Genetics
  36. Endophenotype best practices
    William G. Iacono, Stephen M. Malone, Scott I. Vrieze · 2016 · International Journal of Psychophysiology
  37. Genetic Basis of Complex Genetic Disease: The Contribution of Disease Heterogeneity to Missing Heritability
    Wray, Naomi R., Maier, Robert · 2014 · Current Epidemiology Reports
  38. Drug enrichment and discovery from schizophrenia genome-wide association results: an analysis and visualisation approach
    Gaspar, H. A., Breen, G. · 2017 · Scientific Reports
  39. COVID-19 outcomes and the human genome
    Michael F. Murray, Eimear E. Kenny, Marylyn DeRiggi Ritchie, Daniel James Rader, Allen E. Bale, Monica A. Giovanni, Noura S. Abul‐Husn · 2020 · Genetics in Medicine
  40. UNC13A in amyotrophic lateral sclerosis: from genetic association to therapeutic target
    Sean W. Willemse, Peter Harley, Ruben P. A. van Eijk, Koen C. Demaegd, Pavol Zelina, R. Jeroen Pasterkamp, Philip Van Damme, Caroline Ingre, Wouter van Rheenen, Jan Herman Veldink et al. · 2023 · Journal of Neurology Neurosurgery & Psychiatry
  41. Systems Biology Approach Reveals Genome to Phenome Correlation in Type 2 Diabetes
    Priyanka Jain, Saurabh Vig, Malabika Datta, Dinesh Jindel, Ashok Kumar Mathur, Sandeep Kumar Mathur, Abhay Sharma · 2013 · PLoS ONE
  42. Identifying the genes underlying quantitative traits: a rationale for the QTN programme
    Young Wha Lee, Billie A. Gould, John R. Stinchcombe · 2014 · AoB Plants
  43. Hunting the genes in male‐pattern alopecia: how important are they, how close are we and what will they tell us?
    Stefanie Heilmann‐Heimbach, Lara M. Hochfeld, Ralf Paus, Markus Maria Nöthen · 2016 · Experimental Dermatology
  44. Joint Bayesian inference of risk variants and tissue-specific epigenomic enrichments across multiple complex human diseases
    Yue Li, M Kellis · 2016 · Nucleic Acids Research
  45. GCAT|Genomes for life: a prospective cohort study of the genomes of Catalonia
    Mireia Obón‐Santacana, Mireia Vilardell, Anna Carreras, Xavier Duran, Juan Velasco, Iván Galván‐Femenía, Teresa Alonso, Lluís Puig, Lauro Sumoy, Eric J. Duell et al. · 2018 · BMJ Open
  46. The Cambridge Handbook of Psychology and Human Rights
    Pat Dudgeon, Timothy A. Carey, Sabine Hammond, Tanja Hirvonen, Michael Kyrios, Louise Roufeil, Peter Smith · 2020 · Cambridge University Press eBooks
  47. Lessons from Functional Analysis of Genome-Wide Association Studies
    Inderpreet Sur, Sari Tuupanen, Thomas Whitington, Lauri A. Aaltonen, Jussi Taipale · 2013 · Cancer Research
  48. Genome-wide association study on detailed profiles of smoking behavior and nicotine dependence in a twin sample
    Anu Loukola, Juho Wedenoja, Kaisu Keskitalo‐Vuokko, Ulla Broms, Tellervo Korhonen, Samuli Ripatti, A-P Sarin, Janne M. Pitkäniemi, Liang He, Anja Häppölä et al. · 2013 · Molecular Psychiatry
  49. A genome-wide association study using international breeding-evaluation data identifies major loci affecting production traits and stature in the Brown Swiss cattle breed
    Jiazhong Guo, H. Jorjani, Örjan Carlborg · 2012 · BMC Genetics
  50. Genetics of coronary artery disease: Genome-wide association studies and beyond
    Bram Peter Prins, Vasiliki Lagou, Folkert Wouter Asselbergs, Harold Snieder, Jingyuan Fu · 2012 · Atherosclerosis
  51. Somatic Cell Genomics of Brain Disorders: A New Opportunity to Clarify Genetic-Environmental Interactions
    Ivan Yu. Iourov, Svetlana G. Vorsanova, Yuri B. Yurov · 2013 · Cytogenetic and Genome Research
  52. Agreement between TOAST and CCS ischemic stroke classification
    Patrick F. McArdle, Steven J. Kittner, Hakan Ay, Robert D. Brown, James Frederick Meschia, Tatjana Rundek, Sylvia W Wassertheil-Smoller, Daniel Woo, Gunnar Andsberg, Alessandro Biffi et al. · 2014 · Neurology
  53. Sarcococca Blight: Use of Whole-Genome Sequencing for Fungal Plant Disease Diagnosis
    Martha Malapi‐Wight, Catalina Salgado‐Salazar, Jill E. Demers, David L. Clement, Karen K. Rane, Jo Anne Crouch · 2016 · Plant Disease
  54. A continuum of genetic liability for minor and major depression
    Elizabeth C. Corfield, Yuanhao Yang, Nicholas G. Martin, Dale R. Nyholt · 2017 · Translational Psychiatry
  55. Genetic modifiers of Mendelian disease: Huntington’s disease and the trinucleotide repeat disorders
    Peter Holmans, Thomas H. Massey, Lesley Jones · 2017 · Human Molecular Genetics
  56. Behaviour Genetic Frameworks of Causal Reasoning for Personality Psychology
    Daniel A. Briley, Jonathan Livengood, Jaime L. Derringer · 2018 · European Journal of Personality
  57. Genetic Variant Set-Based Tests Using the Generalized Berk–Jones Statistic With Application to a Genome-Wide Association Study of Breast Cancer
    Ryan Sun, Xihong Lin · 2019 · Journal of the American Statistical Association
  58. Goat DNMT3B: An indel mutation detection, association analysis with litter size and mRNA expression in gonads
    Yiqing Hui, Yanghai Zhang, Ke Wang, Chuanying Pan, Hong Chen, Lei Qu, Xiaoyue Song, Xianyong Lan · 2020 · Theriogenology
  59. The future of genomics for developmentalists
    Robert J. Plomin, Michael A. Simpson · 2013 · Development and Psychopathology
  60. DeepCOMBI: explainable artificial intelligence for the analysis and discovery in genome-wide association studies
    Bettina Mieth, Alexandre Rozier, Juan Antonio Rodríguez, Marina Höhne, Nico Görnitz, Klaus‐Robert Müller · 2021 · NAR Genomics and Bioinformatics
  61. Implications of Large-Effect Loci for Conservation: A Review and Case Study with Pacific Salmon
    Robin S. Waples, Michael J. Ford, Krista M. Nichols, Marty D. Kardos, Jim Myers, Tasha Q. Thompson, Eric C. Anderson, Ilana Janowitz Koch, Garrett J. McKinney, Michael Ryan Miller et al. · 2021 · Journal of Heredity
  62. Transcriptomic-anatomic analysis of the mouse habenula uncovers a high molecular heterogeneity among neurons in the lateral complex, while gene expression in the medial complex largely obeys subnuclear boundaries
    Franziska Wagner, Leon French, Rüdiger W. Veh · 2014 · Brain Structure and Function
  63. Review: High-performance computing to detect epistasis in genome scale data sets
    Alex Upton, Oswaldo Trelles, José Antonio Cornejo-García, James Richard Perkins · 2015 · Briefings in Bioinformatics
  64. Robust Findings From 25 Years of PTSD Genetics Research
    Laramie E. Duncan, Bryna N. Cooper, Hanyang Shen · 2018 · Current Psychiatry Reports
  65. Genetics and Education: Recent Developments in the Context of an Ugly History and an Uncertain Future
    Daphne Oluwaseun Martschenko, Sam Trejo, Benjamin W. Domingue · 2019 · AERA Open
  66. Assessing the performance of genome-wide association studies for predicting disease risk
    Jonas Patron, Arnau Serra-Cayuela, Beomsoo Han, Carin Li, David Scott Wishart · 2019 · PLoS ONE
  67. Neuroscience and the future for mental health?
    Nikolas Rose · 2015 · Epidemiology and Psychiatric Sciences
  68. Confidentiality in Biobanking Research: A Comparison of Donor and Nondonor Families' Understanding of Risks
    Laura A. Siminoff, Maureen Wilson-Genderson, Maghboeba Mosavel, Laura K. Barker, Jennifer Trgina, Heather M. Traino · 2017 · Genetic Testing and Molecular Biomarkers
  69. Contrasting results from GWAS and QTL mapping on wing length in great reed warblers
    Bengt Hansson, Hanna Sigeman, Martin Stervander, Maja Tarka, Suvi Ponnikas, Maria Strandh, Helena Westerdahl, Dennis Hasselquist · 2018 · Molecular Ecology Resources
  70. Polygenic Risk Scores for Kidney Function and Their Associations with Circulating Proteome, and Incident Kidney Diseases
    Zhi Yu, Jin Jin, Adrienne Tin, Anna Köttgen, Bing Yu, Jingsha Chen, Aditya Surapaneni, Linda Zhou, Christie Mitchell Ballantyne, Ron Cornelis Hoogeveen et al. · 2021 · Journal of the American Society of Nephrology
  71. A cause–effect relationship between Graves’ disease and the gut microbiome contributes to the thyroid–gut axis: A bidirectional two-sample Mendelian randomization study
    Jiamin Cao, Nuo Wang, Yong Kun Luo, Chen Ma, Zhuo-Kun Chen, Changci Chenzhao, Feng Zhang, Xin Qi, Wei Xiong · 2023 · Frontiers in Immunology
  72. Mesenchymal Stromal Cells Derived From Crohn's Patients Deploy Indoleamine 2,3-dioxygenase-mediated Immune Suppression, Independent of Autophagy
    Raghavan Chinnadurai, Ian B. Copland, Spencer Ng, Marco A. Garcia, Mahadev Prasad, Dalia Arafat, Greg C. Gibson, Subra Kugathasan, Jacques Galipeau · 2015 · Molecular Therapy
  73. Multi-strategy genome-wide association studies identify the DCAF16-NCAPG region as a susceptibility locus for average daily gain in cattle
    Wengang Zhang, Junya Li, Yong Guo, Lupei Zhang, Lingyang Xu, Xue Gao, Bo Zhu, Huijiang Gao, Hemin Ni, Yan Chen · 2016 · Scientific Reports
  74. Leveraging population admixture to characterize the heritability of complex traits
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  75. FKBP51 inhibits GSK3β and augments the effects of distinct psychotropic medications
    Gassen, N C, Hartmann, J, Zannas, A S, Kretzschmar, A, Zschocke, J, Maccarrone, G, Hafner, K, Zellner, A, Kollmannsberger, L K, Wagner, K V et al. · 2016 · Molecular Psychiatry
  76. Global health metrics needs collaboration and competition
    Igor Rudan, Kit Yee Chan · 2014 · The Lancet
  77. A Genome-wide Association Meta-analysis of Preschool Internalizing Problems
    Kelly Suzanne Benke, Michel Guillaume Nivard, Fleur P. Velders, Raymond Kenney Walters, Irene Pappa, Paul A. Scheet, Xiangjun Xiao, Erik A. Ehli, Lyle John Palmer, Andrew Whitehouse et al. · 2014 · Journal of the American Academy of Child & Adolescent Psychiatry
  78. On high-dimensional misspecified mixed model analysis in genome-wide association study
    Jiming Jiang, Cong Li, Debashis Paul, Can Yang, Hongyu Zhao · 2016 · The Annals of Statistics
  79. Speech and Language: Translating the Genome
    Pelagia Deriziotis, Simon E. Fisher · 2017 · Trends in Genetics
  80. The Impact of CRISPR/Cas9 Technology on Cardiac Research: From Disease Modelling to Therapeutic Approaches
    B. Motta, P. Pramstaller, A. Hicks, A. Rossini · 2017 · Stem Cells International
  81. Variations in predicted risks in personal genome testing for common complex diseases
    Rachel R. J. Kalf, Raluca Mihăescu, Suman Kundu, Peter de Knijff, Robert C. Green, A. Cecile J.W. Janssens · 2013 · Genetics in Medicine
  82. Evidence of the phenotypic expression of a lethal recessive allele under inbreeding in a wild population of conservation concern
    Amanda E. Trask, Eric M. Bignal, D. I. McCracken, Pat Monaghan, Stuart B. Piertney, Jane M. Reid · 2016 · Journal of Animal Ecology
  83. The ENCODE Project and Perspectives on Pathways
    Vinicius Tragante, Jason H. Moore, Folkert Wouter Asselbergs · 2014 · Genetic Epidemiology
  84. What Drives the Development of Social Inequality Over the Life Course? The German TwinLife Study
    Elisabeth Hahn, Juliana Gottschling, Wiebke Bleidorn, Christian Kandler, Marion Spengler, Anna Elena Kornadt, Wiebke Schulz, Reinhard Schunck, Tina Baier, Kristina Krell et al. · 2016 · Twin Research and Human Genetics
  85. Multiancestry Study of Gene–Lifestyle Interactions for Cardiovascular Traits in 610 475 Individuals From 124 Cohorts
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  86. Genetic and environmental risk factors for developmental dyslexia in children: systematic review of the last decade
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  87. Mitochondrial – nuclear genetic interaction modulates whole body metabolism, adiposity and gene expression in vivo
    Kimberly J. Dunham‐Snary, Michael J. Sandel, Melissa J. Sammy, David G. Westbrook, Rui Xiao, Ryan J. McMonigle, William F. Ratcliffe, Arthur L. Penn, Martin Elliot Young, Scott W. Ballinger · 2018 · EBioMedicine
  88. Epigenomics and genotype-phenotype association analyses reveal conserved genetic architecture of complex traits in cattle and human
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  89. An Empirical Comparison of Meta‐analysis and Mega‐analysis of Individual Participant Data for Identifying Gene‐Environment Interactions
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  90. Attentional switching forms a genetic link between attention problems and autistic traits in adults
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  91. Predictive factors of diabetic complications: a possible link between family history of diabetes and diabetic retinopathy
    Zhila Maghbooli, Parvin Pasalar, Abbasali Keshtkar, Farshad Farzadfar, Bagher A. Larijani · 2014 · Journal of Diabetes & Metabolic Disorders
  92. Natural variation in a single amino acid substitution underlies physiological responses to topoisomerase II poisons
    Stefan Zdraljevic, Christine Strand, Hannah S. Seidel, Daniel E. Cook, John G. Doench, Erik C. Andersen · 2017 · PLoS Genetics
  93. Migrainomics — identifying brain and genetic markers of migraine
    Dale R. Nyholt, David Borsook, Lyn Robyn Griffiths · 2017 · Nature Reviews Neurology
  94. Exploiting next-generation sequencing to solve the haplotyping puzzle in polyploids: a simulation study
    Ehsan Motazedi, Richard Finkers, Chris A. Maliepaard, Dick de Ridder · 2016 · Briefings in Bioinformatics
  95. Biomarker development for axial spondyloarthritis
    Matthew Arthur Brown, Zhixiu Li, Kim‐Anh Lê Cao · 2020 · Nature Reviews Rheumatology
  96. Contrasting genetic architectures in different mouse reference populations used for studying complex traits
    David A. Buchner, Joseph H. Nadeau · 2015 · Genome Research
  97. GWA meta-analysis of personality in Korean cohorts
    Bohye Kim, Han‐Na Kim, Seung-Ju Roh, Mi Kyeong Lee, Sarah S. Yang, Seung Ku Lee, Yeon‐Ah Sung, Hye Won Chung, Nam H. Cho, Chol Shin et al. · 2015 · Journal of Human Genetics
  98. Dynamic Scan Procedure for Detecting Rare-Variant Association Regions in Whole-Genome Sequencing Studies
    Zilin Li, Xihao Li, Yaowu Liu, Jincheng Shen, Han Chen, Hufeng Zhou, Alanna C. Morrison, Eric Boerwinkle, Xihong Lin · 2019 · The American Journal of Human Genetics
  99. Accounting for Genetic Architecture Improves Sequence Based Genomic Prediction for a Drosophila Fitness Trait
    Ulrike Ober, Wen Huang, Michael M. Magwire, Martin Schlather, Henner Simianer, Trudy F. C. Mackay · 2015 · PLoS ONE
  100. Use of a targeted, combinatorial next-generation sequencing approach for the study of bicuspid aortic valve
    Elizabeth M. Bonachea, Gloria A. Zender, Peter White, Don Corsmeier, David L. Newsom, Sara M. Fitzgerald‐Butt, Vidu Garg, Kim L. McBride · 2014 · BMC Medical Genomics