Fast and accurate genotype imputation in genome-wide association studies through pre-phasing

Cited by (1,003)

Items 401–500 of 1,003

1. Endophenotype best practices
   William G. Iacono, Stephen M. Malone, Scott I. Vrieze · 2016 · International Journal of Psychophysiology
2. Clinical Utility of Multimarker Genetic Risk Scores for Prediction of Incident Coronary Heart Disease
   Carlos Iribarren, Meng Lü, Eric Jorgenson, Manuel Martínez, Carla Lluís-Ganella, Isaac Subirana, Eduardo Salas, Roberto Elosúa · 2016 · Circulation Cardiovascular Genetics
3. Genome-wide association study of familial lung cancer
   Jinyoung Byun, Ann G. Schwartz, Christine M. Lusk, Angela S. Wenzlaff, Mariza de Andrade, Diptasri M. Mandal, Colette Gaba, Ping Yang, Ming You, Elena Y. Kupert et al. · 2018 · Carcinogenesis
4. Meta-analysis of lipid-traits in Hispanics identifies novel loci, population-specific effects and tissue-specific enrichment of eQTLs
   Jennifer Elizabeth Below, Esteban Juan Parra, Eric R. Gamazon, Jason Torres, S. Krithika, Sophie I. Candille, Yingchang Lu, Ani Manichakul, Jesús Peralta‐Romero, Qing Duan et al. · 2016 · Scientific Reports
5. Genome-wide meta-analysis of macronutrient intake of 91,114 European ancestry participants from the cohorts for heart and aging research in genomic epidemiology consortium
   Merino, Jordi, Dashti, Hassan S., Li, Sherly X., Sarnowski, Chloé, Justice, Anne E., Graff, Misa, Papoutsakis, Constantina, Smith, Caren E., Dedoussis, George V., Lemaitre, Rozenn N. et al. · 2019 · Molecular Psychiatry
6. Genome-wide association study of hepatitis C virus- and cryoglobulin-related vasculitis
   Anna Linda Zignego, Genevieve L. Wojcik, P. Cacoub, Marcella Visentini, Milvia Casato, Alessandra Mangia, Rachel Latanich, Edgar D. Charles, Laura Gragnani, Benjamin Terrier et al. · 2014 · Genes and Immunity
7. A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation
   Betty Bonfante, Pierre Faux, Nicolas Navarro, Javier Mendoza‐Revilla, Morgane Dubied, Charlotte Montillot, Emma Wentworth Winchester, Lauriane Poloni, Ceferino Varón‐González, Philip Jones et al. · 2021 · Science Advances
8. Association Between Substance Use Disorder and Polygenic Liability to Schizophrenia
   Sarah M. Hartz, Amy C. Horton, Mary E. Oehlert, Caitlin E. Carey, Arpana Agrawal A, Ryan Bogdan, Li‐Shiun Chen, Dana B. Hancock, Eric Otto Johnson, Carlos N. Pato et al. · 2017 · Biological Psychiatry
9. Analysis of Heritability and Genetic Architecture of Pancreatic Cancer: A PanC4 Study
   Fei Chen, Erica J. Childs, Evelina Mocci, Paige M. Bracci, Steve Gallinger, Donghui Li, Rachel Ε. Neale, Sara H. Olson, Ghislaine Scélo, William R. Bamlet et al. · 2019 · Cancer Epidemiology Biomarkers & Prevention
10. Functional validity, role, and implications of heavy alcohol consumption genetic loci
    Andrew Thompson, James P. Cook, Hélène Choquet, Eric Jorgenson, Jie Yin, Tarja K Kinnunen, Jeff W. Barclay, Andrew P. Morris, Munir Pirmohamed · 2020 · Science Advances
11. A variant-centric perspective on geographic patterns of human allele frequency variation
    Arjun Biddanda, Daniel P. Rice, John Novembre · 2020 · eLife
12. An Immunochip-based interrogation of scleroderma susceptibility variants identifies a novel association at DNASE1L3
    Jane Zochling, Felicity Newell, Jac Charlesworth, Paul Leo, Jim M. Stankovich, Adrián Cortés, Yuan Zhou, Wendy Stevens, Joanne Sahhar, Janet Roddy et al. · 2014 · Arthritis Research & Therapy
13. Cis-eQTL analysis and functional validation of candidate susceptibility genes for high-grade serous ovarian cancer
    Kate Lawrenson, Qiyuan Li, Siddhartha Kar, Ji-Heui Seo, Jonathan P. Tyrer, Tassja J. Spindler, Janet S. Lee, Yibu Chen, Alison M. Karst, Ronny Drapkin et al. · 2015 · Nature Communications
14. Narcolepsy risk loci outline role of T cell autoimmunity and infectious triggers in narcolepsy
    Hanna Maria Ollila, Eilon Sharon, Ling Lin, Nasa Sinnott-Armstrong, Aditya Ambati, Selina Yogeshwar, Ryan P. Hillary, Otto Jolanki, Juliette H. Faraco, Mali A. Einen et al. · 2023 · Nature Communications
15. Genome-wide association study of prostate-specific antigen levels identifies novel loci independent of prostate cancer
    Thomas J. Hoffmann, Michael N. Passarelli, Rebecca E. Graff, Nima C. Emami, Lori C. Sakoda, Eric Jorgenson, Laurel A. Habel, Jun Shan, Dilrini K. Ranatunga, Charles P. Quesenberry et al. · 2017 · Nature Communications
16. ABCB1 (MDR1) polymorphisms and ovarian cancer progression and survival: A comprehensive analysis from the Ovarian Cancer Association Consortium and The Cancer Genome Atlas
    Sharon E. Johnatty, Jonathan Beesley, Bo Gao, Xiaoqing Chen, Yi Lu, Matthew H. Law, Michelle J. Henderson, Amanda J. Russell, Ellen L. Hedditch, Catherine Emmanuel et al. · 2013 · Gynecologic Oncology
17. Genome-Wide Association Shows that Pigmentation Genes Play a Role in Skin Aging
    Matthew H. Law, Sarah Elizabeth Medland, Gu Zhu, Seyhan Yazar, Ana Viñuela, Leanne M. Wallace, Sri Niranjan Shekar, David L. Duffy, Veronique A. Bataille, Dan Glass et al. · 2017 · Journal of Investigative Dermatology
18. 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
19. Genetic ancestry does not explain increased atopic dermatitis susceptibility or worse disease control among African Americans in two large US cohorts
    K. Abuabara, Y. You, D. Margolis, T. Hoffmann, N. Risch, E. Jorgenson · 2019 · Journal of Allergy and Clinical Immunology
20. Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid
    Jurjen Justin Luykx, S C Bakker, Eef G.W.M. Lentjes, M Neeleman, Eric Strengman, Lara J. Mentink, Joseph A. DeYoung, Simone de Jong, Jae Hoon Sul, Eleazar Eskin et al. · 2013 · Molecular Psychiatry
21. Local and Global Ancestry Inference and Applications to Genetic Association Analysis for Admixed Populations
    Timothy A. Thornton, Justo Lorenzo Bermejo · 2014 · Genetic Epidemiology
22. High Risk Population Isolate Reveals Low Frequency Variants Predisposing to Intracranial Aneurysms
    Mitja Kurki, Emília Ilona Gaál, Johannes Kettunen, Tuuli Lappalainen, Androniki Menelaou, Verneri Anttila, Femke N. G. van ’t Hof, Mikael von und zu Fraunberg, Seppo Helisalmi, Mikko O. Hiltunen et al. · 2014 · PLoS Genetics
23. Diabetes Pathology and Risk of Primary Open-Angle Glaucoma: Evaluating Causal Mechanisms by Using Genetic Information
    Ling Shen, Stefan Walter, Ronald B. Melles, M. Maria Glymour, Eric Jorgenson · 2015 · American Journal of Epidemiology
24. Effect of Human Genetic Variability on Gene Expression in Dorsal Root Ganglia and Association with Pain Phenotypes
    Marc Parisien, Samar Khoury, Anne‐Julie Chabot‐Doré, Susana G. Sotocinal, Gary D. Slade, Shad B. Smith, Roger Benton Fillingim, Richard K. Ohrbach, Joel D. Greenspan, William D. Maixner et al. · 2017 · Cell Reports
25. Childhood behaviour problems show the greatest gap between DNA-based and twin heritability
    Rosa Cheesman, Saskia Selzam, Angelica Ronald, Philip S. Dale, Tom A. McAdams, Thalia Catherine Eley, Robert J. Plomin · 2017 · Translational Psychiatry
26. 12 new susceptibility loci for prostate cancer identified by genome-wide association study in Japanese population
    Ryo Takata, Atsushi Takahashi, Masashi Fujita, Yukihide Momozawa, Edward J. Saunders, Hiroki Yamada, Kazuhiro Maejima, Kaoru Nakano, Yuichiro Nishida, Asahi Hishida et al. · 2019 · Nature Communications
27. Identification of genetic effects underlying type 2 diabetes in South Asian and European populations
    Marie Chiew Shia Loh, Weihua Zhang, Hong Kiat Ng, Katharina Schmid, Amel Lamri, Tong Lin, Meraj Ahmad, Jung‐Jin Lee, Maggie C.Y. Ng, Lauren E. Petty et al. · 2022 · Communications Biology
28. Heritability and molecular‐genetic basis of resting EEG activity: A genome‐wide association study
    Stephen M. Malone, Scott J. Burwell, Uma Vaidyanathan, Michael B. Miller, Matt K. McGue, William G. Iacono · 2014 · Psychophysiology
29. Genome-wide genetic homogeneity between sexes and populations for human height and body mass index
    Jian Yang, Andrew Bakshi, Zhihong Zhu, Gibran Hemani, Anna A. E. Vinkhuyzen, Ilja Maria Nolte, Jana V. van Vliet‐Ostaptchouk, Harold Snieder, The Lifelines Cohort Study, Tõnu Esko et al. · 2015 · Human Molecular Genetics
30. Genome-wide association study of breakfast skipping links clock regulation with food timing
    Hassan S. Dashti, Jordi Merino, Jacqueline M. Lane, Yanwei Song, Caren E. Smith, Toshiko Tanaka, Nicola Mary McKeown, Chandler Tucker, Dianjianyi Sun, Traci M. Bartz et al. · 2019 · American Journal of Clinical Nutrition
31. Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains
    Ditte Demontis, G. Bragi Walters, Georgios I. Athanasiadis, Raymond Kenney Walters, Karen Therrien, Leila Farajzadeh, Georgios Voloudakis, Jaroslav M. Bendl, Biao Zeng, Wen Zhang et al. · 2022 · medRxiv
32. Efficient cross-trait penalized regression increases prediction accuracy in large cohorts using secondary phenotypes
    Chung, Wonil, Chen, Jun, Turman, Constance, Lindstrom, Sara, Zhu, Zhaozhong, Loh, Po-Ru, Kraft, Peter, Liang, Liming · 2019 · Nature Communications
33. Imputation from SNP chip to sequence: a case study in a Chinese indigenous chicken population
    Shaopan Ye, Xiaolong Yuan, Xiran Lin, Ning Gao, Yuanyu Luo, Zanmou Chen, Jiaqi Li, Xiquan Zhang, Zhe Zhang · 2018 · Journal of Animal Science and Biotechnology/Journal of animal science and biotechnology
34. A Common Type 2 Diabetes Risk Variant Potentiates Activity of an Evolutionarily Conserved Islet Stretch Enhancer and Increases C2CD4A and C2CD4B Expression
    Ina Kycia, Brooke N. Wolford, Jeroen R. Huyghe, Christian Fuchsberger, Swarooparani Vadlamudi, Romy Kursawe, Ryan Welch, Ricardo D’Oliveira Albanus, Asli Uyar, Shubham Khetan et al. · 2018 · The American Journal of Human Genetics
35. Genetic and Epigenetic Fine Mapping of Complex Trait Associated Loci in the Human Liver
    Minal Çalışkan, Elisabetta Manduchi, H. Shanker Rao, Julian A. Segert, Márcia Holsbach Beltrame, Marco Trizzino, YoSon Park, Samuel W. Baker, Alessandra Chesi, Matthew E. Johnson et al. · 2019 · The American Journal of Human Genetics
36. Genetic regulation of serum IgA levels and susceptibility to common immune, infectious, kidney, and cardio-metabolic traits
    Lili Liu, Atlas Khan, Elena Sánchez, Francesca Zanoni, Yifu Li, Nicholas J. Steers, Olivia Balderes, Jun Y. Zhang, Priya Krithivasan, Robert A. LeDesma et al. · 2022 · Nature Communications
37. Genome of the Netherlands population-specific imputations identify an ABCA6 variant associated with cholesterol levels
    Elisabeth M. van Leeuwen, Lennart C. Karssen, Joris Deelen, Aaron J. Isaacs, Carolina Medina‐Gómez, Hamdi Mbarek, Alexandros Kanterakis, Stella Trompet, Iris Postmus, Niek Verweij et al. · 2015 · Nature Communications
38. Childhood asthma is associated with COPD and known asthma variants in COPDGene: a genome-wide association study
    on behalf of the COPDGene Investigators, Lystra P. Hayden, Michael H. Cho, Benjamin A. Raby, Terri H. Beaty, Edwin K. Silverman, Craig P. Hersh · 2018 · Respiratory Research
39. Activation of cryptic splicing in bovine WDR19 is associated with reduced semen quality and male fertility
    Maya Hiltpold, Guanglin Niu, Naveen Kumar Kadri, Danang Crysnanto, Zih‐Hua Fang, Mirjam Spengeler, Fritz Schmitz‐Hsu, C. Fuerst, Hermann Schwarzenbacher, Franz R. Seefried et al. · 2020 · PLoS Genetics
40. Large multi-ethnic genetic analyses of amyloid imaging identify new genes for Alzheimer disease
    Muhammad Ali, Derek B. Archer, Priyanka Gorijala, Daniel Western, Jigyasha Timsina, María Victoria Fernández, Ting‐Chen Wang, Claudia Liliana Satizábal, Qiong Yang, Alexa Beiser et al. · 2023 · Acta Neuropathologica Communications
41. A genome-wide gene-environment interaction analysis for tobacco smoke and lung cancer susceptibility
    Ruyang Zhang, Mingxing Chu, Yang Zhao, Chen Hsuan Wu, Hui Guo, Yongyong Shi, Juncheng Dai, Yongyue Wei, G. Jin, Huimin Ma et al. · 2014 · Carcinogenesis
42. Novel genetic predictors of venous thromboembolism risk in African Americans
    Wenndy Hernandez, Eric R. Gamazon, Erin Smithberger, Travis J. O’Brien, Arthur F. Harralson, Matthew Tuck, April Barbour, Rick A. Kittles, Larisa H. Cavallari, Minoli A. Perera · 2016 · Blood
43. Chronic Periodontitis Genome-wide Association Study in the Hispanic Community Health Study / Study of Latinos
    Anne E. Sanders, Tamar Sofer, Quenna Wong, Kathleen F. Kerr, Cary S. Agler, John R. Shaffer, James D. Beck, Steven Offenbacher, Christian R. Salazar, Kari E. North et al. · 2016 · Journal of Dental Research
44. Polygenic Contribution in Individuals With Early-Onset Coronary Artery Disease
    Sébastien Thériault, Ricky Lali, Michael Chong, James L. Velianou, Madhu K. Natarajan, Guillaume Paré · 2018 · Circulation Genomic and Precision Medicine
45. Genomewide Association Study of Statin‐Induced Myopathy in Patients Recruited Using the UK Clinical Practice Research Datalink
    Daniel F. Carr, Ben Francis, Andrea Jorgensen, Eunice Zhang, Hector Chinoy, Susan R. Heckbert, Joshua C. Bis, Jennifer A. Brody, James S. Floyd, Bruce M. Psaty et al. · 2019 · Clinical Pharmacology & Therapeutics
46. Mendelian randomization while jointly modeling cis genetics identifies causal relationships between gene expression and lipids
    Adriaan van der Graaf, Annique Claringbould, Antoine Rimbert, Bastiaan T. Heijmans, Peter A.C. ’t Hoen, Joyce B. J. van Meurs, Rick Jansen, Lude Franke, Harm-Jan Westra, Yang Li et al. · 2020 · Nature Communications
47. On the use of whole-genome sequence data for across-breed genomic prediction and fine-scale mapping of QTL
    T.H.E. Meuwissen, Irene van den Berg, Michael Edward Goddard · 2021 · Genetics Selection Evolution
48. A genome-wide association study of heparin-induced thrombocyto - penia using an electronic medical record
    Jason H. Karnes, Robert Michael Cronin, Jérôme Rollin, Alexander Teumer, Claire Pouplard, Christian M. Shaffer, Carmelo Blanquicett, Erica Bowton, James D. Cowan, Jonathan D. Mosley et al. · 2014 · Thrombosis and Haemostasis
49. Impact of Type 2 Diabetes and Postmenopausal Hormone Therapy on Incidence of Cognitive Impairment in Older Women
    Mark Andrew Espeland, Roberta Dı́az Brinton, Christina E. Hugenschmidt, JoAnn E. Manson, Suzanne Craft, Kristine S. Yaffe, Julie C. Weitlauf, Leslie Vaughan, Karen Johnson, Claudia B. Padula et al. · 2015 · Diabetes Care
50. Multiple Hepatic Regulatory Variants at the GALNT2 GWAS Locus Associated with High-Density Lipoprotein Cholesterol
    Tamara S. Roman, Amanda F. Marvelle, Marie P. Fogarty, Swarooparani Vadlamudi, Arlene J. Gonzalez, Martin L. Buchkovich, Jeroen R. Huyghe, Christian Fuchsberger, Anne Jackson, Ying Wu et al. · 2015 · The American Journal of Human Genetics
51. Exon-focused genome-wide association study of obsessive-compulsive disorder and shared polygenic risk with schizophrenia
    Javier Costas, Noa Carrera, Pino Alonso, Xaquín Gurriarán, Cinto Segalàs, Eva Real, Clara López‐Solà, Sergi Mas, Patricia Gassó, Laura Domènech et al. · 2016 · Translational Psychiatry
52. Characterization of cross-tissue genetic-epigenetic effects and their patterns in schizophrenia
    Dongdong Lin, Jiayu Chen, Nora I. Perrone‐Bizzozero, Juan Bustillo, Yuhui Du, Vince D. Calhoun, Jingyu Liu · 2018 · Genome Medicine
53. Genetic fine mapping of systemic lupus erythematosus MHC associations in Europeans and African Americans
    Ken Benjamin Hanscombe, David Lester Morris, Janelle Annette Noble, Alexander Dilthey, Philip Tombleson, Kenneth M. Kaufman, Mary E. Comeau, Carl D. Langefeld, Marta Eugenia Alarcón-Riquelme, Patrick M. Gaffney et al. · 2018 · Human Molecular Genetics
54. Gene expression and RNA splicing explain large proportions of the heritability for complex traits in cattle
    Ruidong Xiang, Lingzhao Fang, Shuli Liu, Iona M. MacLeod, Zhiqian Liu, Edmond J. Breen, Yahui Gao, George E. Liu, Albert Tenesa, Brett Mason et al. · 2023 · Cell Genomics
55. Simple, standardized incorporation of genetic risk into non-genetic risk prediction tools for complex traits: coronary heart disease as an example
    Benjamin Alan Goldstein, Joshua W. Knowles, Elias Salfati, John P. A. Ioannidis, Themistocles L. Assimes · 2014 · Frontiers in Genetics
56. Genetic susceptibility for chronic bronchitis in chronic obstructive pulmonary disease
    Jin Hwa Lee, Michael Cho, Craig P. Hersh, Merry‐Lynn McDonald, James D. Crapo, Per Sigvald Bakke, Amund Gulsvik, Alejandro P. Comellas, Chris H. Wendt, David A. Lomas et al. · 2014 · Respiratory Research
57. Genome-wide association study of recalcitrant atopic dermatitis in Korean children
    Kyung Won Kim, Rachel A. Myers, Ji Hyun Lee, Catherine Igartua, Kyung Eun Lee, Yoon Hee Kim, Eun‐jin Kim, Dankyu Yoon, Joo-Shil Lee, Tomomitsu Hirota et al. · 2015 · Journal of Allergy and Clinical Immunology
58. Nationwide Genomic Study in Denmark Reveals Remarkable Population Homogeneity
    Georgios I. Athanasiadis, Jade Yu Cheng, Bjarni Jóhann Vilhjálmsson, Frank Grønlund Jørgensen, Thomas D. Als, Stéphanie Le Hellard, Thomas Espeseth, Patrick F. Sullivan, Christina M. Hultman, Peter C. Kjærgaard et al. · 2016 · Genetics
59. Genome-wide variants of Eurasian facial shape differentiation and a prospective model of DNA based face prediction
    Lu Qiao, Yajun Yang, Pengcheng Fu, Sile Hu, Hang Zhou, Shouneng Peng, Jingze Tan, Yan Lü, Haiyi Lou, Dongsheng Lu et al. · 2018 · Journal of genetics and genomics/Journal of Genetics and Genomics
60. Genetically Elevated LDL Associates with Lower Risk of Intracerebral Hemorrhage
    Guido J. Falcone, Elayna P. Kirsch, Julián Acosta, Rommell B. Noche, Audrey C. Leasure, Sandro Marini, Jaeyoon Chung, Magdy H. Selim, James Frederick Meschia, Devin L. Brown et al. · 2020 · Annals of Neurology
61. Identification of 31 loci for mammographic density phenotypes and their associations with breast cancer risk
    Weiva Sieh, Joseph H. Rothstein, Robert J. Klein, Stacey Alexeeff, Lori C. Sakoda, Eric Jorgenson, Russell B. McBride, Rebecca E. Graff, Valerie M. McGuire, Ninah S. Achacoso et al. · 2020 · Nature Communications
62. Admixture mapping identifies novel loci for obstructive sleep apnea in Hispanic/Latino Americans
    Wang, Heming, Cade, Brian E, Sofer, Tamar, Sands, Scott A, Chen, Han, Browning, Sharon R, Stilp, Adrienne M, Louie, Tin L, Thornton, Timothy A, Johnson, W Craig et al. · 2019 · Human Molecular Genetics
63. Imaging-wide association study: integrating imaging endophenotypes in GWAS
    Xu, Zhiyuan, Wu, Chong, Pan, Wei · 2017 · NeuroImage
64. Surfactant protein D is a causal risk factor for COPD: results of Mendelian randomisation
    Ma’en Obeidat, Xuan Li, Stephen Burgess, Guohai Zhou, Nick Fishbane, Nadia N. Hansel, Yohan Bossé, Philippe Joubert, Ke Hao, David C. Nickle et al. · 2017 · European Respiratory Journal
65. The SWine IMputation (SWIM) haplotype reference panel enables nucleotide resolution genetic mapping in pigs
    Rongrong Ding, Rodrigo Pelicioni Savegnago, Jinding Liu, Nanye Long, Cheng Peow Bobby Tan, Gengyuan Cai, Zhanwei Zhuang, Jie Wu, Ming Jun Yang, Yibin Qiu et al. · 2023 · Communications Biology
66. Polygenic and developmental profiles of autism differ by age at diagnosis
    Xinhe Zhang, Jakob Grove, Yuanjun Gu, Cornelia K. Buus, Lea K. Nielsen, Sharon Neufeld, Mahmoud Koko, Daniel Shiloh Malawsky, Emma E. Wade, Ellen Verhoef et al. · 2025 · Nature
67. Genomewide association study in cervical dystonia demonstrates possible association with sodium leak channel
    Kin Ying Mok, Susanne A. Schneider, Daniah Trabzuni, María Stamelou, Mark John Edwards, Dalia Kasperavičiūtė, Stuart M. Pickering-Brown, Monty Silverdale, John Hardy, Kailash P. Bhatia · 2013 · Movement Disorders
68. Circulating Proneurotensin Concentrations and Cardiovascular Disease Events in the Community
    James L. Januzzi, Asya Lyass, Yuyin Liu, Hanna Kim Gaggin, April Trebnick, Alan S. Maisel, Ralph B. D’Agostino, Thomas J. Wang, Joseph M. Massaro, Ramachandran Srini Vasan · 2016 · Arteriosclerosis Thrombosis and Vascular Biology
69. Fine mapping of 2q35 high‐risk neuroblastoma locus reveals independent functional risk variants and suggests full‐length BARD1 as tumor‐suppressor
    Flora Cimmino, Marianna Avitabile, Sharon J. Diskin, Zalman Vaksman, Piero Pignataro, Daniela Formicola, Antonella Cardinale, Alessandro Testori, Jan Köster, Carmen de Torres et al. · 2018 · International Journal of Cancer
70. Identification of the ABCC4, IER3, and CBFA2T2 candidate genes for resistance to paratuberculosis from sequence-based GWAS in Holstein and Normande dairy cattle
    Marie-Pierre Sanchez, Raphaël R. Guatteo, Aurore Davergne, Judikael Saout, Cécile Grohs, Marie-Christine Deloche, Sébastien Taussat, Sébastien Fritz, Mekki Boussaha, Philippe Blanquefort et al. · 2020 · Genetics Selection Evolution
71. Evidence of a genetic link between endometriosis and ovarian cancer
    Alice W. Lee, Claire E. Templeman, Douglas A. Stram, Jonathan Beesley, Jonathan P. Tyrer, Andrew Berchuck, Paul D.P. Pharoah, Georgia Chenevix‐Trench, Celeste Leigh Pearce, Roberta B. Ness et al. · 2015 · Fertility and Sterility
72. Trans-ethnic Meta-analysis and Functional Annotation Illuminates the Genetic Architecture of Fasting Glucose and Insulin
    Ching-Ti Liu, Sridharan Raghavan, Nisa M. Maruthur, Edmond Kato Kabagambe, Jaeyoung Hong, Maggie C.Y. Ng, Marie‐France Hivert, Yingchang Lu, Ping An, Amy R. Bentley et al. · 2016 · The American Journal of Human Genetics
73. Excess Synaptojanin 1 Contributes to Place Cell Dysfunction and Memory Deficits in the Aging Hippocampus in Three Types of Alzheimer’s Disease
    André Miguel Miranda, Mathieu Herman, Rong Cheng, Eden Nahmani, Geoffrey Barrett, Elizabeta Micevska, Gaelle Fontaine, Marie‐Claude Potier, Elizabeth Head, Frederick A. Schmitt et al. · 2018 · Cell Reports
74. A genome-wide association study identifies new loci for factor VII and implicates factor VII in ischemic stroke etiology
    Paul S. de Vries, Maria Sabater‐Lleal, Jennifer E. Huffman, Jonathan Marten, Ci Song, Nathan Pankratz, Traci M. Bartz, Hugoline G. de Haan, Graciela E. Delgado, John D. Eicher et al. · 2019 · Blood
75. Genetic discovery and risk characterization in type 2 diabetes across diverse populations
    Linda M. Polfus, Burcu F. Darst, Heather M. Highland, Xin Sheng, Maggie C.Y. Ng, Jennifer Elizabeth Below, Lauren E. Petty, Stephanie A. Bien, Xueling Sim, Wei Wang et al. · 2021 · Human Genetics and Genomics Advances
76. Genome-wide association and genotype by environment interactions for growth traits in U.S. Red Angus cattle
    Johanna L. Smith, Miranda L. Wilson, Sara M. Nilson, Troy N. Rowan, Robert D. Schnabel, Jared E. Decker, Christopher M. Seabury · 2022 · BMC Genomics
77. Association of Chronic Kidney Disease With Risk of Intracerebral Hemorrhage
    Kevin N Vanent, Audrey C. Leasure, Julián Acosta, Lindsey R. Kuohn, Daniel Woo, Santosh B. Murthy, Hooman Kamel, Steven Russell Messe, Michael T. Mullen, Jordana B. Cohen et al. · 2022 · JAMA Neurology
78. Polymorphisms in HLA Class II Genes Are Associated With Susceptibility toStaphylococcus aureusInfection in a White Population
    Gerald N. DeLorenze, Charlotte L. Nelson, William K. Scott, Andrew S. Allen, G. Thomas Ray, Ai‐Lin Tsai, Charles P. Quesenberry, Vance G. Fowler · 2015 · The Journal of Infectious Diseases
79. African genetic diversity provides novel insights into evolutionary history and local adaptations
    Ananyo Choudhury, Shaun Aron, Dhriti Sengupta, Scott Hazelhurst, Michèle Ramsay · 2018 · Human Molecular Genetics
80. The germline genetic component of drug sensitivity in cancer cell lines
    Michael P. Menden, Francesco Paolo Casale, Johannes Stephan, Graham R. Bignell, Francesco Iorio, Ultan McDermott, Mathew J. Garnett, Julio Sáez-Rodríguez, Oliver Stegle · 2018 · Nature Communications
81. Genome‐wide association study identifies gastric cancer susceptibility loci at 12q24.11‐12 and 20q11.21
    Chizu Tanikawa, Yoichiro Kamatani, Osamu Toyoshima, Hiromi Sakamoto, Hidemi M. Ito, Atsushi Takahashi, Yukihide Momozawa, Makoto Hirata, Nobuo Fuse, Takako Takai‐Igarashi et al. · 2018 · Cancer Science
82. An Atlas of Genetic Variation Linking Pathogen-Induced Cellular Traits to Human Disease
    Liuyang Wang, Kelly J. Pittman, Jeffrey R. Barker, Raul Salinas, Ian B. Stanaway, Graham D. Williams, Robert J. Carroll, Tom Balmat, Andy Ingham, Anusha M. Gopalakrishnan et al. · 2018 · Cell Host & Microbe
83. Genome‐wide association study of rate of cognitive decline in Alzheimer's disease patients identifies novel genes and pathways
    Sherva, Richard, Gross, Alden, Mukherjee, Shubhabrata, Koesterer, Ryan, Amouyel, Philippe, Bellenguez, Celine, Dufouil, Carole, Bennett, David A., Chibnik, Lori, Cruchaga, Carlos et al. · 2020 · Alzheimer's & Dementia
84. Imputing Phenotypes for Genome-wide Association Studies
    Hormozdiari, Farhad, Kang, Eun Yong, Bilow, Michael, Ben-David, Eyal, Vulpe, Chris, McLachlan, Stela, Lusis, Aldons J., Han, Buhm, Eskin, Eleazar · 2016 · The American Journal of Human Genetics
85. Genome-wide association study of circulating interleukin 6 levels identifies novel loci
    Tarunveer S. Ahluwalia, Bram Peter Prins, Mohammadreza Abdollahi, Nicola J. Armstrong, Stella W. Aslibekyan, Lisa Bain, Barbara J.M.H. Jefferis, Jens J Baumert, Marian Beekman, Yoav Ben‐Shlomo et al. · 2021 · Human Molecular Genetics
86. Genetic analysis of dietary intake identifies new loci and functional links with metabolic traits
    Jordi Merino, Hassan S. Dashti, Chloé Sarnowski, Jacqueline M. Lane, Petar V. Todorov, Miriam S. Udler, Yanwei Song, Heming Wang, Jaegil Kim, Chandler Tucker et al. · 2021 · Nature Human Behaviour
87. Genotype Imputation in Genome‐Wide Association Studies
    Eleonora Porcu, Serena Sanna, Christian Fuchsberger, Lars G. Fritsche · 2013 · Current Protocols in Human Genetics
88. High-Throughput Characterization of Blood Serum Proteomics of IBD Patients with Respect to Aging and Genetic Factors
    Antonio Di Narzo, Shannon Telesco, Carrie M. Brodmerkel, Carmen Argmann, Lauren A. Peters, Katherine Li, Brian A. Kidd, Joel T. Dudley, Judy H. Cho, Eric E. Schadt et al. · 2017 · PLoS Genetics
89. Association of schizophrenia polygenic risk score with manic and depressive psychosis in bipolar disorder
    Matej Markota, Brandon J. Coombes, Beth R. Larrabee, Susan L. McElroy, David J. Bond, Marin Veldić, Colin L. Colby, Mohit Chauhan, Alfredo B. Cuellar Barboza, Manuel Enrique Fuentes et al. · 2018 · Translational Psychiatry
90. Probing the Virtual Proteome to Identify Novel Disease Biomarkers
    Jonathan D. Mosley, Mark D. Benson, J. Gustav Smith, Olle Melander, Debby Ngo, Christian M. Shaffer, Jane F. Ferguson, Matthew S. Herzig, Catherine Anne McCarty, Christopher G. Chute et al. · 2018 · Circulation
91. Genome-Wide Association Study of Meat Quality Traits in Hanwoo Beef Cattle Using Imputed Whole-Genome Sequence Data
    Mohammed Bedhane, Julius H. J. van der Werf, Cedric Gondro, Naomi Duijvesteijn, Dajeong Lim, Byoungho Park, Mi Na Park, Roh Seung Hee, Sam Clark · 2019 · Frontiers in Genetics
92. Pupillary dilation responses as a midlife indicator of risk for Alzheimer's disease: association with Alzheimer's disease polygenic risk
    William S. Kremen, Matthew S. Panizzon, Jeremy A. Elman, Eric L. Granholm, Ole A. Andreassen, Anders Martin Dale, Nathan A. Gillespie, Daniel E. Gustavson, Mark W. Logue, Michael J. Lyons et al. · 2019 · Neurobiology of Aging
93. Assumption-free estimation of the genetic contribution to refractive error across childhood.
    Jeremy A. Guggenheim, Beaté St Pourcain, George McMahon, Nicholas John Timpson, David M. Evans, Cathy Williams · 2015 · PubMed Central
94. The genetic association of RUNX3 with ankylosing spondylitis can be explained by allele-specific effects on IRF4 recruitment that alter gene expression
    Matteo L. Vecellio, Amity R. Roberts, C. Cohen, Adrián Cortés, Julian Charles Knight, Paul Bowness, B. P. Wordsworth · 2015 · Annals of the Rheumatic Diseases
95. Genome-wide association and Mendelian randomization study of NT-proBNP in patients with acute coronary syndrome
    Åsa Johansson, Niclas Eriksson, Daniel P. Lindholm, Christoph Varenhorst, Stefan Karl James, Ann‐Christine Syvänen, Tomas Axelsson, Agneta Siegbahn, Bryan J. Barratt, Richard Clinton Becker et al. · 2016 · Human Molecular Genetics
96. Characterization of ADME gene variation in 21 populations by exome sequencing
    Daniel H. Hovelson, Zhengyu Xue, Matthew Zawistowski, Margaret G. Ehm, Elizabeth C. Harris, SOPHIE LENA STOCKER, Annette S. Gross, In‐Jin Jang, Ichiro Ieiri, Jong-Eun Lee et al. · 2016 · Pharmacogenetics and Genomics
97. The feasibility of using low-density marker panels for genotype imputation and genomic prediction of crossbred dairy cattle of East Africa
    Hassan Aliloo, Raphael Mrode, A.M. Okeyo, Guiyan Ni, Michael Edward Goddard, John P. Gibson · 2018 · Journal of Dairy Science
98. Genome-wide association study of 23,500 individuals identifies 7 loci associated with brain ventricular volume
    Vojinovic, Dina, Adams, Hieab H., Jian, Xueqiu, Yang, Qiong, Smith, Albert Vernon, Bis, Joshua C., Teumer, Alexander, Scholz, Markus, Armstrong, Nicola J., Hofer, Edith et al. · 2018 · Nature Communications
99. Profiling allele-specific gene expression in brains from individuals with autism spectrum disorder reveals preferential minor allele usage
    Chang‐Hoon Lee, Eun Yong Kang, Michael J. Gandal, Eleazar Eskin, Daniel H. Geschwind · 2019 · Nature Neuroscience
100. Common variants at 10p12.31, 10q21.1 and 13q12.13 are associated with sporadic pituitary adenoma
     Zhao Ye, Zhiqiang Li, Yongfei Wang, Ying Qing Mao, Ming Shen, Qilin Zhang, Shiqi Li, Liangfu Zhou, Xuefei Shou, Jianhua Chen et al. · 2015 · Nature Genetics