Statistical power and significance testing in large-scale genetic studies

Cited by (565)

Items 101–200 of 565

1. Integrative analysis reveals disrupted pathways regulated by microRNAs in cancer
   Gary Wilk, Rosemary Braun · 2017 · Nucleic Acids Research
2. GWAS significance thresholds for deep phenotyping studies can depend upon minor allele frequencies and sample size
   Huma Asif, Ney Alliey‐Rodriguez, Sarah Keedy, Carol A. Tamminga, John A. Sweeney, Godfrey D. Pearlson, Brett A. Clementz, Matcheri S. Keshavan, P.F. Buckley, Chunyu Liu et al. · 2020 · Molecular Psychiatry
3. A Review of Whole-Exome Sequencing Efforts Toward Hereditary Breast Cancer Susceptibility Gene Discovery
   Madison R. Chandler, Erin P. Bilgili, Nancy D. Merner · 2016 · Human Mutation
4. Detection of M 6 A-associated SNPs as Potential Functional Variants for Coronary Artery Disease
   Xingbo Mo, Shu‐Feng Lei, Yonghong Zhang, Huan Zhang · 2018 · Epigenomics
5. Exploiting genetic variation to uncover rules of transcription factor binding and chromatin accessibility
   Vivek Behera, Perry Evans, Carolyne J. Face, Nicole Hamagami, Laavanya Sankaranarayanan, Cheryl A. Keller, Belinda M. Giardine, Kai Tan, Ross C. Hardison, Junwei Shi et al. · 2018 · Nature Communications
6. Meta-analysis of genome-wide association studies for litter size in sheep
   Mohsen Gholizadeh, Seyed Mehdi Esmaeili-Fard · 2021 · Theriogenology
7. Principal Component Analysis of the Effects of Environmental Enrichment and (-)-epigallocatechin-3-gallate on Age-Associated Learning Deficits in a Mouse Model of Down Syndrome
   Silvina Catuara‐Solarz, Jose Espinosa‐Carrasco, Ionas Erb, Klaus Langohr, Cédric Notredame, Juan R. González, Mara Dierssen · 2015 · Frontiers in Behavioral Neuroscience
8. Genomics of human aggression
   Veronika V. Odintsova, Peter J. Roetman, Hill Fung Ip, René Pool, Camiel M. van der Laan, Klodiana‐Daphne Tona, Robert R. J. M. Vermeiren, Dorret Irene Boomsma · 2019 · Psychiatric Genetics
9. ADuLT: An efficient and robust time-to-event GWAS
   Emil M. Pedersen, Esben Agerbo, Oleguer Plana‐Ripoll, Jette Steinbach, Morten Dybdahl Krebs, DAVID MICHAEL HOUGAARD, Thomas Mears Werge, Merete Nordentoft, Anders Dupont Børglum, Katherine Louise Musliner et al. · 2023 · Nature Communications
10. Imputation of the Rare HOXB13 G84E Mutation and Cancer Risk in a Large Population-Based Cohort
    Thomas J. Hoffmann, Lori C. Sakoda, Ling Shen, Eric Jorgenson, Laurel A. Habel, Jinghua Liu, Mark N. Kvale, Maryam M. Asgari, Yambazi Banda, Douglas A. Corley et al. · 2015 · PLoS Genetics
11. Genetic architecture differences between pediatric and adult-onset inflammatory bowel diseases in the Polish population
    Jerzy Ostrowski, Agnieszka Paziewska, Izabella Łazowska‐Przeorek, Filip Ambrożkiewicz, Krzysztof Goryca, Maria Kulecka, Tomasz Rawa, Jakub Karczmarski, Michalina Dąbrowska, Natalia Żeber‐Lubecka et al. · 2016 · Scientific Reports
12. Host genetics and microbiome associations through the lens of genome wide association studies
    Omer Weissbrod, Daphna Rothschild, Elad Barkan, Eran Segal · 2018 · Current Opinion in Microbiology
13. Rare germline variants in DNA repair genes and the angiogenesis pathway predispose prostate cancer patients to develop metastatic disease
    Martina Mijušković, Edward J. Saunders, Daniel A. Leongamornlert, Sarah Wakerell, Ian Whitmore, Tokhir Dadaev, Clara Cieza-Borrella, Koveela Govindasami, Mark N. Brook, Christopher A. Haiman et al. · 2018 · British Journal of Cancer
14. High‐Throughput Assays to Assess the Functional Impact of Genetic Variants: A Road Towards Genomic‐Driven Medicine
    Joseph Ipe, Marelize Swart, Kimberly Burgess, Todd C. Skaar · 2017 · Clinical and Translational Science
15. A Meta-Analysis Including Pre-selected Sequence Variants Associated With Seven Traits in Three French Dairy Cattle Populations
    Andrew Marete, Bernt Guldbrandtsen, Mogens Sandø Lund, Sébastien Fritz, Goutam Sahana, Didier Boichard · 2018 · Frontiers in Genetics
16. Association Between Single-Nucleotide Polymorphisms in HLA Alleles and Human Immunodeficiency Virus Type 1 Viral Load in Demographically Diverse, Antiretroviral Therapy–Naive Participants From the Strategic Timing of AntiRetroviral Treatment Trial
    Christina Ekenberg, Man‐Hung Eric Tang, Adrian G. Zucco, Daniel D. Murray, Cameron Ross MacPherson, Xiaojun Hu, Brad T. Sherman, Marcelo Horacio Losso, Robin Wood, Roger Paredes et al. · 2019 · The Journal of Infectious Diseases
17. Concepts and Relevance of Genome-Wide Association Studies
    Andreas Scherer, G. Bryce Christensen · 2016 · Science Progress
18. Genome-wide identification of m6A-associated single-nucleotide polymorphisms in Parkinson’s disease
    Xiaohui Qiu, Honghu He, Yanning Huang, Jin Wang, Yousheng Xiao · 2020 · Neuroscience Letters
19. Genetics of movement disorders in the next‐generation sequencing era
    Simone Olgiati, Marialuisa Quadri, Vincenzo Bonifati · 2016 · Movement Disorders
20. Fifteen years of quantitative trait loci studies in fish: challenges and future directions
    David T. Ashton, Peter A. Ritchie, Maren Wellenreuther · 2016 · Molecular Ecology
21. The association between cortisol, oxytocin, and immune cell mitochondrial oxygen consumption in postpartum women with childhood maltreatment
    Christina Boeck, Anja Maria Gumpp, Enrico Calzia, Peter Radermacher, Christiane Waller, Alexander Karabatsiakis, Iris‐Tatjana Kolassa · 2018 · Psychoneuroendocrinology
22. SECAT: Quantifying Protein Complex Dynamics across Cell States by Network-Centric Analysis of SEC-SWATH-MS Profiles
    George Rosenberger, Moritz Heusel, Isabell Bludau, Ben C. Collins, Claudia Martelli, Evan G. Williams, Peng Xue, Yansheng Liu, Ruedi H. Aebersold, Andrea Califano · 2020 · Cell Systems
23. Overlapping Dopaminergic Pathway Genetic Susceptibility to Heroin and Cocaine Addictions in African Americans
    Orna Levran, Matthew Randesi, Joel Corrêa da Rosa, Jürg Ott, John Rotrosen, Miriam Adelson, Mary Jeanne Kreek · 2015 · Annals of Human Genetics
24. A comparison of methods for whole-genome QTL mapping using dense markers in four livestock species
    Andrés Legarra, Pascal Croiseau, Marie Sanchez, Simon Teyssèdre, Guillaume Sallé, Sophie Allais, Sébastien Fritz, Carole Moreno, Anne Ricard, Jean-Michel Elsen · 2015 · Genetics Selection Evolution
25. A novel bivalent chromatin associates with rapid induction of camalexin biosynthesis genes in response to a pathogen signal in Arabidopsis
    Kangmei Zhao, Deze Kong, Benjamin Jin, Christina D. Smolke, Seung Y. Rhee · 2021 · eLife
26. Association of rare missense variants in the second intracellular loop of NaV1.7 sodium channels with familial autism
    Moran Rubinstein, Ashok Patowary, Ian B. Stanaway, Eedann McCord, Ryan Nesbitt, Marilyn Archer, Todd Scheuer, Deborah A. Nickerson, Wendy H. Raskind, Ellen M. Wijsman et al. · 2016 · Molecular Psychiatry
27. Ethical concerns relating to genetic risk scores for suicide
    Anna R. Docherty, Brent Michael Kious, Teneille R. Brown, Leslie P. Francis, Louisa A. Stark, Brooks R Keeshin, Jeffrey R. Botkin, Emily DiBlasi, Doug Gray, Hilary H Coon · 2021 · American Journal of Medical Genetics Part B Neuropsychiatric Genetics
28. Sample Size Calculation in Genetic Association Studies: A Practical Approach
    Cristina Politi, Stefanos K. Roumeliotis, Giovanni Tripepi, Belinda Spoto · 2023 · Life
29. Understanding Neurodevelopmental Disorders: The Promise of Regulatory Variation in the 3′UTRome
    Kai A. Wanke, Paolo Devanna, Sonja C. Vernes · 2017 · Biological Psychiatry
30. Identification of Germline Genetic Variants that Increase Prostate Cancer Risk and Influence Development of Aggressive Disease
    Edward J. Saunders, Zsofia Kote‐Jarai, Rosalind A. Eeles · 2021 · Cancers
31. Converging findings from linkage and association analyses on susceptibility genes for smoking and other addictions
    Jiekun Yang, M D Li · 2016 · Molecular Psychiatry
32. Antibiotic Bone Cement Cannot Reduce Deep Infection After Primary Total Knee Arthroplasty
    Hai Wang, Gui-xing Qiu, Jin Lin, Jin Jin, Wen-Wei Qian, Xisheng Weng · 2015 · Orthopedics
33. Genetic Variants Associated with Angiotensin-Converting Enzyme Inhibitor-Induced Cough: A Genome-Wide Association Study in a Swedish Population
    Pär Hallberg, Matilda Persson, Tomas Axelsson, Marco Cavalli, Pia Norling, Hans-Erik Johansson, Qun‐Ying Yue, Patrik K. E. Magnusson, Claes Wadelius, Niclas Eriksson et al. · 2017 · Pharmacogenomics
34. In silico genome‐wide identification of m6A‐associated SNPs as potential functional variants for periodontitis
    Weimin Lin, Hao Ying Xu, Yunshu Wu, Jun Wang, Quan Yuan · 2019 · Journal of Cellular Physiology
35. Pharmacogenetic Predictors of Cannabidiol Response and Tolerability in Treatment‐Resistant Epilepsy
    Brittney H. Davis, Timothy Mark Beasley, Michelle D. Amaral, Jerzy P. Szaflarski, Tyler E. Gaston, Leslie E. Grayson, David G. Standaert, Elizabeth Martina Bebin, Nita A. Limdi, the UAB CBD Study Group (includes all the investigators involved in the UAB EAP CBD program) · 2021 · Clinical Pharmacology & Therapeutics
36. Guidelines on statistics for researchers using laboratory animals: the essentials
    Romain‐Daniel Gosselin · 2018 · Laboratory Animals
37. Using machine learning and big data to explore the drug resistance landscape in HIV
    Luc Blassel, Anna Tostevin, Christian Julián Villabona‐Arenas, Martine Peeters, Stéphane Hué, Olivier Gascuel, On behalf of the UK HIV Drug Resistance Database · 2021 · PLoS Computational Biology
38. Performance of a blockwise approach in variable selection using linkage disequilibrium information
    Alia Dehman, Christophe Ambroise, Pierre Neuvial · 2015 · BMC Bioinformatics
39. A Replication Study for Association of 53 Single Nucleotide Polymorphisms in ScoliScore Test With Adolescent Idiopathic Scoliosis in French-Canadian Population
    Qi Tang, Cédric Julien, Robert J. M. Eveleigh, Guillaume Bourque, Anita Franco, Hubert Labelle, Guy Grimard, Stefan Parent, Jean Albert Ouellet, Jean‐Marc Mac‐Thiong et al. · 2015 · Spine
40. Genomic Prediction and Association Mapping of Curd-Related Traits in Gene Bank Accessions of Cauliflower
    Patrick Thorwarth, Eltohamy A. A. Yousef, Karl J Schmid · 2017 · G3 Genes Genomes Genetics
41. DeepNull models non-linear covariate effects to improve phenotypic prediction and association power
    Zachary Ryan McCaw, Thomas Colthurst, Taedong Yun, Nicholas A. Furlotte, Andrew W. Carroll, Babak Alipanahi, Cory Y. McLean, Farhad Hormozdiari · 2022 · Nature Communications
42. Rare and low-frequency variants in human common diseases and other complex traits
    Guillaume Lettre · 2014 · Journal of Medical Genetics
43. Novel quantitative pigmentation phenotyping enhances genetic association, epistasis, and prediction of human eye colour
    Andreas Wollstein, Susan Walsh, Fan Liu, Usha Chakravarthy, Mati Rahu, Johan H. Seland, Gisèle Soubrane, Laura Tomazzoli, Fotis Topouzis, Johannes R. Vingerling et al. · 2017 · Scientific Reports
44. Genomewide association of piglet responses to infection with one of two porcine reproductive and respiratory syndrome virus isolates
    Emily H. Waide, Christopher Keith Tuggle, Nick V. L. Serão, Martine Schroyen, Andrew S. Hess, Robert R. R. Rowland, Joan K. Lunney, Graham Stuart Plastow, Jack C. M. Dekkers · 2017 · Journal of Animal Science
45. Epistasis: Searching for Interacting Genetic Variants Using Crosses
    Ian M. Ehrenreich · 2017 · Genetics
46. Genome-wide Association Study of Axial Length in Population-based Cohorts in Japan
    Nobuo Fuse, Miyuki Sakurai, Ikuko N. Motoike, Kaname Kojima, Takako Takai‐Igarashi, Naoki Nakaya, Naho Tsuchiya, Tomohiro Nakamura, Mami Ishikuro, Taku Obara et al. · 2022 · Ophthalmology Science
47. OmniCrawl: Comprehensive Measurement of Web Tracking With Real Desktop and Mobile Browsers
    Darion Cassel, Su-Chin Lin, Alessio Buraggina, William Yang Wang, J. Andrew Zhang, Lujo Bauer, Hsu‐Chun Hsiao, Limin Jia, Timothy Libert · 2021 · Proceedings on Privacy Enhancing Technologies
48. Derandomizing Knockoffs
    Zhimei Ren, Yuting Wei, Emmanuel J. Candès · 2021 · Journal of the American Statistical Association
49. Sports genetics moving forward: lessons learned from medical research
    C. Mikael Mattsson, Matthew Thomas Wheeler, Daryl M. Waggott, Colleen A. Caleshu, Euan Angus Ashley · 2016 · Physiological Genomics
50. Ulk4 Regulates Neural Stem Cell Pool
    Min Liu, Zhenlong Guan, Qin Shen, Frances A. Flinter, Laura Domínguez, Joo Wook Ahn, David Andrew Collier, Timothy O’Brien, Sanbing Shen · 2016 · Stem Cells
51. Increasing proteomics throughput
    Nikolai Slavov · 2021 · Nature Biotechnology
52. Genome-wide haplotype-based association analysis of major depressive disorder in Generation Scotland and UK Biobank
    David M. Howard, Lynsey S. Hall, Jonathan D. Hafferty, Yanni Zeng, Mark J. Adams, Toni‐Kim Clarke, David John Porteous, Réka Nagy, Caroline Hayward, Blair H. Smith et al. · 2017 · Translational Psychiatry
53. Fronto‐Parietal Subnetworks Flexibility Compensates For Cognitive Decline Due To Mental Fatigue
    Fumihiko Taya, Stavros I. Dimitriadis, Andrei Dragomir, Julian Lim, Yu Sun, Kian Foong Wong, Nitish V. Thakor, Anastasios Bezerianos · 2018 · Human Brain Mapping
54. Genome-wide identification of m6A-associated SNPs as potential functional variants for bone mineral density
    Xingbo Mo, Y. H. Zhang, Shu‐Feng Lei · 2018 · Osteoporosis International
55. Genome-wide enrichment of m6A-associated single-nucleotide polymorphisms in the lipid loci
    Xingbo Mo, Shu‐Feng Lei, Yonghong Zhang, Huan Zhang · 2018 · The Pharmacogenomics Journal
56. Identification of genetic loci associated with higher resistance to pancreas disease (PD) in Atlantic salmon (Salmo salar L.)
    Borghild Hillestad, Shokouh Makvandi‐Nejad, Aleksei Krasnov, Hooman K. Moghadam · 2020 · BMC Genomics
57. A Novel Gene Underlies Bleomycin-Response Variation inCaenorhabditis elegans
    Shannon C. Brady, Stefan Zdraljevic, Karol W. Bisaga, Robyn E. Tanny, Daniel E. Cook, Daehan Lee, Ye Wang, Erik C. Andersen · 2019 · Genetics
58. Genetic markers are associated with the ruminal microbiome and metabolome in grain and sugar challenged dairy heifers
    Golder, Helen M., Thomson, Jennifer M., Denman, Stuart E., McSweeney, Chris S., Lean, Ian J. · 2018 · Frontiers in Genetics
59. Multimodal imaging of language reorganization in patients with left temporal lobe epilepsy
    Yu‐Hsuan A. Chang, Nobuko Kemmotsu, Kelly M. Leyden, Nuri Erkut Kucukboyaci, Vicente J. Iragui, Evelyn S. Tecoma, Leena Kansal, Marc A. Norman, Rachelle Compton, Tobin J. Ehrlich et al. · 2017 · Brain and Language
60. Genome-wide association study of angioedema induced by angiotensin-converting enzyme inhibitor and angiotensin receptor blocker treatment
    Eva Rye Rasmussen, Pär Hallberg, E.V. Baranova, Niclas Eriksson, Malgorzata Karawajczyk, Caroline Ulvin Johansson, Marco Cavalli, Cyrielle Maroteau, Abirami Veluchamy, Gunilla Islander et al. · 2020 · The Pharmacogenomics Journal
61. Pharmacogenomics in acute lymphoblastic leukemia
    Shawn H.R. Lee, Jun J.J. Yang · 2017 · Best Practice & Research Clinical Haematology
62. Quantile regression for genome-wide association study of flowering time-related traits in common bean
    Moysés Nascimento, Ana Carolina Campana Nascimento, Fabyano Fonseca e Silva, Leiri Daiane Barili, Naine Martins do Vale, José Eustáquio de Souza Carneiro, Cosme Damião Cruz, Pedro Crescêncio Souza Carneiro, Nick V. L. Serão · 2018 · PLoS ONE
63. A Model of Compound Heterozygous, Loss-of-Function Alleles Is Broadly Consistent with Observations from Complex-Disease GWAS Datasets
    Jaleal S. Sanjak, Anthony D. Long, Kevin Thornton · 2017 · PLoS Genetics
64. Evaluating genetic variants associated with breast cancer risk in high and moderate-penetrance genes in Asians
    Mi-Ryung Han, Wei Zheng, Qiuyin Cai, Yu-Tang Gao, Ying Zheng, Manjeet K. Bolla, Kyriaki Michailidou, Joe Dennis, Qin Wang, Alison M. Dunning et al. · 2017 · Carcinogenesis
65. Opportunities and challenges for the use of common controls in sequencing studies
    Genevieve L. Wojcik, Jessica I. Murphy, Jacob L Edelson, Christopher R. Gignoux, Alexander G. Ioannidis, Alisa Knodle Manning, Manuel A. Rivas, Steven G. Buyske, Audrey E. Hendricks · 2022 · Nature Reviews Genetics
66. Increase in power by obtaining 10 or more controls per case when type-1 error is small in large-scale association studies
    Hormuzd A. Katki, Sonja I. Berndt, Mitchell J. Machiela, Douglas R. Stewart, Montserrat García‐Closas, Jung Kim, Jianxin Shi, Kai Fun Yu, Nathaniel Rothman · 2023 · BMC Medical Research Methodology
67. Identification of genetic susceptibility loci for intestinal Behçet’s disease
    Seung Won Kim, Yoon Suk Jung, Jae Bum Ahn, Eun‐Soon Shin, Hui Won Jang, Hyun Jung Lee, Tae Il Kim, Do Young ‍Kim, Dongsik Bang, Won Ho Kim et al. · 2017 · Scientific Reports
68. A powerful conditional gene-based association approach implicated functionally important genes for schizophrenia
    Miaoxin Li, Lin Jiang, Timothy Shin Heng Mak, Johnny S. H. Kwan, Chao Xue, Peikai Chen, Henry C. M. Leung, Liqian Cui, Tao Li, Pak Chung Sham · 2018 · Bioinformatics
69. Association of Gout Polygenic Risk Score With Age at Disease Onset and Tophaceous Disease in European and Polynesian Men With Gout
    Nicholas A. Sumpter, Riku Takei, Murray J. Cadzow, Ruth Topless, Amanda J. Phipps‐Green, Rinki Murphy, Janak de Zoysa, Huti Watson, Muhammad Qasim, Alexa S. Lupi et al. · 2022 · Arthritis & Rheumatology
70. Advancing sports and exercise genomics: moving from hypothesis-driven single study approaches to large multi-omics collaborative science
    Masashi Tanaka, Guan Wang, Yannis Paul Pitsiladis · 2016 · Physiological Genomics
71. Machine learning approaches to study glioblastoma: A review of the last decade of applications
    Jessica Valdebenito, Felipe Medina · 2019 · Cancer Reports
72. Pyrolysis of Mixed Plastic Waste: II. Artificial Neural Networks Prediction and Sensitivity Analysis
    Ibrahim Dubdub, Mohammed Al‐Yaari · 2021 · Applied Sciences
73. Pathways to smoking behaviours: biological insights from the Tobacco and Genetics Consortium meta-analysis
    Camelia C. Minică, Hamdi Mbarek, René Pool, Conor V. Dolan, Dorret Irene Boomsma, Jacqueline M. Vink · 2016 · Molecular Psychiatry
74. TGMI: an efficient algorithm for identifying pathway regulators through evaluation of triple-gene mutual interaction
    Chathura Gunasekara, Kui Zhang, Wenping Deng, Laura Brown, Hairong Wei · 2018 · Nucleic Acids Research
75. Genome-Wide Association Study of Piscine Myocarditis Virus (PMCV) Resistance in Atlantic Salmon (Salmo salar)
    Borghild Hillestad, Hooman K. Moghadam · 2019 · Journal of Heredity
76. Targeted Sequencing Reveals Large-Scale Sequence Polymorphism in Maize Candidate Genes for Biomass Production and Composition
    Moses M. Muraya, Thomas Schmutzer, Chris Ulpinnis, Uwe Scholz, Thomas Altmann · 2015 · PLoS ONE
77. Family-based exome sequencing and case-control analysis implicate CEP41 as an ASD gene
    Ashok Patowary, So Yeon Won, Shin Ji Oh, Ryan Nesbitt, Marilyn Archer, Debbie A. Nickerson, Wendy H. Raskind, Raphael Bernier, Ji Eun Lee, Zoran Brkanac · 2019 · Translational Psychiatry
78. Atrial Fibrillation Genetics Update: Toward Clinical Implementation
    Silje Madeleine Kalstø, Joylene E. Siland, Michiel Rienstra, Ingrid Elisabeth Christophersen · 2019 · Frontiers in Cardiovascular Medicine
79. Lipoprotein(a) plasma levels are not associated with incident microvascular complications in type 2 diabetes mellitus
    Sunny S Singh, Mardin Rashid, Aloysius G. Lieverse, Florian Kronenberg, Claudia Lamina, Monique T Mulder, Yolanda B. de Rijke, Eric J.G. Sijbrands, Mandy van Hoek · 2020 · Diabetologia
80. The Musculoskeletal Knowledge Portal: Making Omics Data Useful to the Broader Scientific Community
    Douglas P. Kiel, John P. Kemp, Fernando Rivadeneira, Jennifer J. Westendorf, David Karasik, Emma L. Duncan, Yuuki Imai, Ralph Müller, Jason A. Flannick, Lynda Faye Bonewald et al. · 2020 · Journal of Bone and Mineral Research
81. Sulfasalazine‐Induced Agranulocytosis Is Associated With the Human Leukocyte Antigen Locus
    Mia Wadelius, Niclas Eriksson, Reinhold Hugo Kreutz, Emmanuelle Bondon‐Guitton, Luisa Ibáñez, Alfonso Carvajal, M. Isabel Lucena, Esther Sancho Ponce, Mariam Molokhia, Javier J. Martin et al. · 2017 · Clinical Pharmacology & Therapeutics
82. The UKB envirome of depression: from interactions to synergistic effects
    Gábor Hullám, Péter Antal, Péter Petschner, Xénia Gonda, György Bagdy, J.F.W. Deakin, Gabriella Juhász · 2019 · Scientific Reports
83. Meta-analysis and field synopsis of genetic variants associated with the risk and severity of acute pancreatitis
    Fons F. van den Berg, Marinus Abraham Kempeneers, Hjalmar C. van Santvoort, Aeilko H. Zwinderman, Yama Issa, Marja A. Boermeester · 2019 · BJS Open
84. Exploratory analyses in aetiologic research and considerations for assessment of credibility: mini-review of literature
    Kim Luijken, Olaf M. Dekkers, Frits Richard Rosendaal, Rolf H. H. Groenwold · 2022 · BMJ
85. Causal relationship between gut microbiota and polycystic ovary syndrome: a literature review and Mendelian randomization study
    Junwei Sun, Mingyu Wang, Zhisheng Kan · 2024 · Frontiers in Endocrinology
86. A simple and accurate method to determine genomewide significance for association tests in sequencing studies
    Danyu Y. Lin · 2019 · Genetic Epidemiology
87. Accumulated promoter methylation as a potential biomarker for esophageal cancer
    Xianzhen Peng, Hengchuan Xue, Lingshuang Lü, Peiyi Shi, Jianping Wang, Jianming Wang · 2016 · Oncotarget
88. Elevated expression of a minor isoform of ANK3 is a risk factor for bipolar disorder
    Timothy Hughes, Ida Elken Sønderby, Tatiana V. Polushina, Lars Hansson, Asbjørn Holmgren, Lavinia Athanasiu, Christian Melbø‐Jørgensen, Sahar Hassani, Louise K. Hoeffding, Stefan Herms et al. · 2018 · Translational Psychiatry
89. Behçet’s disease and genetic interactions between HLA-B*51 and variants in genes of autoinflammatory syndromes
    Sergio Burillo‐Sanz, Marco-Antonio Montes-Cano, José-Raúl Garcı́a-Lozano, Israel Olivas‐Martínez, Norberto Ortego‐Centeno, Francisco José García Hernández, Gerard Espinosa, Jenaro Graña Gil, Juan Sánchez‐Bursón, María Rosa Juliá et al. · 2019 · Scientific Reports
90. Genome-Wide Detection of m6A-Associated Genetic Polymorphisms Associated with Ischemic Stroke
    Ruixia Zhu, Dandan Tian, Yating Zhao, Chenguang Zhang, Xu Liu · 2021 · Journal of Molecular Neuroscience
91. Coexpression network revealing the plasticity and robustness of population transcriptome during the initial stage of domesticating energy crop Miscanthus lutarioriparius
    Shilai Xing, Chengcheng Tao, Zhihong Song, Wei Liu, Juan Yan, Lifang Kang, Cong Lin, Tao Sang · 2018 · Plant Molecular Biology
92. Exome Chip Analyses and Genetic Risk for IgA Nephropathy among Han Chinese
    Shu‐Feng Zhou, Lam C. Tsoi, Yong Hu, Matthew T. Patrick, Kevin He, Céline C. Berthier, Yanming Li, Yan‐na Wang, Yuanyuan Qi, Yuemiao Zhang et al. · 2021 · Clinical Journal of the American Society of Nephrology
93. Differential Transcript Profiles in Cumulus-Oocyte Complexes Originating from Pre-Ovulatory Follicles of Varied Physiological Maturity in Beef Cows
    Sarah E. Moorey, Jenna Marie Monnig, Michael F. Smith, Martha Sofia Ortega, Jonathan A. Green, Ky Garrett Pohler, G. Alan Bridges, Susanta K. Behura, Thomas W. Geary · 2021 · Genes
94. A genome-wide association study suggests correlations of common genetic variants with peritoneal solute transfer rates in patients with kidney failure receiving peritoneal dialysis
    Rajnish Mehrotra, Ian B. Stanaway, Gail Pairitz Jarvik, Mark Lambie, Johann Morelle, Jeffrey M. Perl, Jonathan Himmelfarb, Olof Heimbürger, David Wayne Johnson, Talha H. Imam et al. · 2021 · Kidney International
95. Single-Nucleotide Polymorphisms in the Beta-Tubulin Gene and Its Relationship with Treatment Response to Albendazole in Human Soil-Transmitted Helminths in Southern Mozambique
    Berta Grau-Pujol, Javier Gandasegui, Valdemiro Escola, Helena Martí-Soler, María Cambra-Pellejà, Maria Antonietta Demontis, Eric A. T. Brienen, José Carlos Jamine, Osvaldo Muchisse, Anélsio Cossa et al. · 2022 · American Journal of Tropical Medicine and Hygiene
96. Covariate selection for association screening in multiphenotype genetic studies
    Hugues Aschard, Vincent Guillemot, Bjarni Jóhann Vilhjálmsson, Chirag J. Patel, David Skurnik, Chun Ye, Brian Matthew Wolpin, Peter L. Kraft, Noah Zaitlen · 2017 · Nature Genetics
97. A nonsense mutation in the COL7A1 gene causes epidermolysis bullosa in Vorderwald cattle
    Hubert Pausch, Simon Ammermüller, Christine Wurmser, H. Hamann, Jens Tetens, Cord Drögemüller, Ruedi Fries · 2016 · BMC Genetics
98. Rewiring of gene expression in circulating white blood cells is associated with pregnancy outcome in heifers (Bos taurus)
    Sarah E. Moorey, Bailey N. Walker, Michelle F. Elmore, Joshua B. Elmore, Soren P P Rodning, Fernando H. Biase · 2020 · Scientific Reports
99. Novel Genes Affecting Blood Pressure Detected Via Gene-Based Association Analysis
    Huan Zhang, Xingbo Mo, Tan Xu, Xiaoqing Bu, Shu‐Feng Lei, Yong-Hong Zhang · 2015 · G3 Genes Genomes Genetics
100. Genomics of host–microbiome interactions in humans
     Pamela Ferretti, Kelsey E. Johnson, Sambhawa Priya, Ran Blekhman · 2025 · Nature Reviews Genetics