Once and Again—Issues Surrounding Replication in Genetic Association Studies

Cited by (180)

Items 101–180 of 180

1. HindIII(+/−) Polymorphism of the Y Chromosome, Blood Pressure, and Serum Lipids: No Evidence of Association in Three White Populations
   Paola Russo, Antonella Venezia, Fabio Lauria, Pasquale Strazzullo, Francesco Paolo Cappuccio, Licia Iacoviello, Gianvincenzo Barba, Alfonso Siani · 2006 · American Journal of Hypertension
2. Xenobiotic metabolizing enzyme gene polymorphisms predict response to lung volume reduction surgery
   Craig P. Hersh, Dawn Lisa DeMeo, John J. Reilly, Edwin K. Silverman · 2007 · Respiratory Research
3. Genetic variants of FOXP3 influence graft survival in kidney transplant patients
   Anja U. Engela, Karin Boer, Joke I. Roodnat, Annemiek M. A. Peeters, Paul H.C. Eilers, Judith A. Kal-van Gestel, Fernando Rivadeneira, Willem Weimar, Carla C. Baan · 2013 · Human Immunology
4. Partners in crime
   Mark J. Daly, David Altshuler · 2005 · Nature Genetics
5. Association of an IL-4 gene haplotype with Graves disease in children: experimental study and meta-analysis
   Yann‐Jinn Lee, Chi‐Yu Huang, Wei‐Hsin Ting, Hung‐Chang Lee, Wenling Guo, Wei-Fang Chen, Chiung‐Ling Lin, Hsin‐Fu Liu, Marie Lin, Fu‐Sung Lo · 2011 · Human Immunology
6. American Gastroenterological Association Future Trends Committee Report: The Application of Genomic and Proteomic Technologies to Digestive Disease Diagnosis and Treatment and Their Likely Impact on Gastroenterology Clinical Practice
   Konstantinos N. Lazaridis, Brian D. Juran · 2005 · Gastroenterology
7. Putative association of peroxisome proliferator‐activated receptor γ co‐activator 1β (PPARGC1B) polymorphism with Type 2 diabetes mellitus
   Kyong Soo Park, Hyoung Doo Shin, B. L. Park, Hyun Sub Cheong, Young‐Man Cho, H. K. Lee, Jee‐Young Lee, Jong‐Koo Lee, Hong-Kook Kim, C.‐S. Park et al. · 2006 · Diabetic Medicine
8. Chronic Beryllium Disease and Glutathione Biosynthesis Genes
   Lynn M. Bekris, Hannah-Malia A. Viernes, Federico M. Farin, Lisa A. Maier, Terrance J. Kavanagh, Tim K. Takaro · 2006 · Journal of Occupational and Environmental Medicine
9. Association of the promoter polymorphism −232C/G of the phosphoenolpyruvate carboxykinase gene (PCK1) with Type 2 diabetes mellitus
   Ioanna Gouni‐Berthold, Eleni Giannakidou, Michael Faust, Heiner K. Berthold, Wilhelm Krone · 2006 · Diabetic Medicine
10. Do allelic variants of SLC6A14 predispose to obesity?
    Hemant K. Tiwari, David B. Allison · 2003 · Journal of Clinical Investigation
11. Association of the ENPP1 K121Q polymorphism with susceptibility to type 2 diabetes in different populations: evidence based on 40 studies
    Songtao Tang, Xinru Shen, Hai‐qin Tang, Changjiang Wang, Wei Wei, Qiu Zhang, Yuan Wang · 2014 · Endocrine Journal
12. Genetic Susceptibility to RSV Disease
    Jeremy Hull · 2006 · Perspectives in medical virology
13. Polymorphism E23K (rs5219) in the KCNJ11 gene in Euro-Brazilian subjects with type 1 and 2 diabetes
    Susan Webber de Souza, Larissa Pontes Alcazar, Pricila A. Arakaki, Izabella Castilhos Ribeiro dos Santos-Weiss, Dayane Alberton, Geraldo Picheth, Fabiane Gomes de Moraes Rego · 2017 · Genetics and Molecular Research
14. Confidence Intervals for Genotype Relative Risks and Allele Frequencies from the Case Parent Trio Design for Candidate-Gene Studies
    André Scherag, Astrid Dempfle, Anke Hinney, Johannes Hebebrand, Helmut Schäfer · 2002 · Human Heredity
15. The influence of ethnicity in the association of WC, WHR, hypertension and PGC-1α (Gly482Ser), UCP2 − 866 G/A and SIRT1 − 1400 T/C polymorphisms with T2D in the population of Punjab
    Nabodita Kaul, Yoginder Pal Singh, A.J.S. Bhanwer · 2015 · Gene
16. Genetics of Human Obesity
    Richard Baumgartner, Chenxi Wang, David B. Allison · 2007 · CRC Press eBooks
17. Association Claims in the Sequencing Era
    Sara L. Pulit, Maarten Leusink, Androniki Menelaou, Paul I. W. de Bakker · 2014 · Genes
18. Tackling the genetic bases of metabolic syndrome: A realistic objective?
    Alfonso Siani, Pasquale Strazzullo · 2006 · Nutrition Metabolism and Cardiovascular Diseases
19. The continuing search for predisposing colorectal cancer variants.
    Simone Picelli, Susanna von Holst, Petra Wessendorf · 2009 · PubMed
20. A systematic evaluation of the ataxia telangiectasia mutated gene does not show an association with non‐Hodgkin lymphoma
    Payal Sipahimalani, John Joseph Spinelli, Amy C. MacArthur, Agnes S. Lai, Stephen R. Leach, Rozmin Janoo-Gilani, Diana L. Palmquist, Joseph Michael Connors, Randy D. Gascoyne, Richard P. Gallagher et al. · 2007 · International Journal of Cancer
21. New Jersey Center for Tourette Syndrome Sharing Repository: methods and sample description
    Gary A. Heiman, Robert A. King, Jay A. Tischfield · 2008 · BMC Medical Genomics
22. Can We Increase the Likelihood of Success for Future Association Studies in Epilepsy?
    Martina Durner, Prakash Gorroochurn, Carla Marini, Renzo Guerrini · 2006 · Epilepsia
23. Genomic Approaches to Identifying Breast Cancer Susceptibility Factors
    Jeffery P. Struewing · 2004 · Breast Disease
24. Practicing Medicine at the Front Lines of the Genomic Revolution
    Wendy S. Rubinstein, Hemant K. Roy · 2005 · Archives of Internal Medicine
25. Genome-wide association identifies novel ROP risk loci in a multiethnic cohort
    Xiaohui Li, Leah A. Owen, Kent D. Taylor, Susan R. Ostmo, Yii-Der Ida Chen, Aaron S. Coyner, Kemal Sönmez, M. Elizabeth Hartnett, Xiuqing Guo, Eli Ipp et al. · 2024 · Communications Biology
26. Replication of genetic associations as pseudoreplication due to shared genealogy
    Noah A. Rosenberg, Jenna VanLiere Canzoniero · 2009 · Genetic Epidemiology
27. Genetic mapping approaches in neuropsychiatry
    Nadine Norton, Sarah Dwyer, Michael C. O’Donovan, Nigel M. Williams · 2005 · Psychiatry
28. Whole genome sequence analysis of apparent treatment resistant hypertension status in participants from the Trans-Omics for Precision Medicine program
    Nicole D. Armstrong, Vinodh Srinivasasainagendra, Farah Ammous, Themistocles L. Assimes, Amber L. Beitelshees, Jennifer A. Brody, Brian E. Cade, Yii-Der Ida Chen, Han Chen, Paul S. de Vries et al. · 2023 · Frontiers in Genetics
29. MLH1 Ile219Val Polymorphism in Argentinean Families with Suspected Lynch Syndrome
    Mev Dominguez–Valentin, Patrik Wernhoff, Andrea Romina Cajal, Pablo German Kalfayan, Tamara Alejandra Piñero, María Laura González, Alejandra Ferro, Inés Sammartino, Natalia S. Causada Calo, Carlos Alberto Vaccaro · 2016 · Frontiers in Oncology
30. Genome-Wide Association Studies in Pediatric Endocrinology
    Andrew Nahum Dauber, Joel N. Hirschhorn · 2011 · Hormone Research in Paediatrics
31. Perspective on the genetics of attention deficit/hyperactivity disorder
    Benjamin M. Neale, Stephen V. Faraone · 2008 · American Journal of Medical Genetics Part B Neuropsychiatric Genetics
32. Pharmacogenetics in Cancer Chemotherapy
    Xifeng Wu, Jian Hong Gu · 2008 · CRC Press eBooks
33. Experimental Approaches for Identifying Schizophrenia Risk Genes
    Kiran K. Mantripragada, Liam Stuart Carroll, Nigel M. Williams · 2010 · Current topics in behavioral neurosciences
34. The lack of association between catechol-O-methyltransferase (COMT) Val108/158Met and brain-derived neurotrophic factor (BDNF) Val66Met polymorphisms and schizophrenia in a group of Turkish population
    Bülent Kayahan, Burçin Tezcanlı Kaymaz, Ayşe Ender Altıntoprak, Çağdaş Aktan, Baybars Veznedaroğlu, Buket Kosova · 2013 · Neurology Psychiatry and Brain Research
35. The Significance of Non‐Replication of Gene‐Phenotype Associations
    Carolyn Tucker Halpern · 2010 · Wiley eBooks
36. K121Q variant in ENPP1 gene is associated with T2DM in the Egyptian population
    Magda I. Mohamad, Neveen Salah El Din Hemimi, Mona Mohamed Abd El Salam, Mahmoud Abd Elwahab · 2018 · International Journal of Diabetes in Developing Countries
37. Genetic Determinants in Airways Obstructive Diseases: The Case of Asthma Chronic Obstructive Pulmonary Disease Overlap
    Aabida Saferali, Craig P. Hersh · 2022 · Immunology and Allergy Clinics of North America
38. Epidemiology and risk factors
    Veronica Wendy Setiawan, Heather Spencer Feigelson, Brian E. Henderson · 2006 · CRC Press eBooks
39. About the genetics of pulmonary emphysema
    Ivchik Tv · 2011 · PULMONOLOGIYA
40. Examining Gene–Environment Interplay in Psychiatric Disorders
    Judith Allardyce, Jim van Os · 2011 · Wiley eBooks
41. The future of pediatric cancer and complex diseases: Aren't they all?
    Stephen Jacob Chanock, Meredith Yeager · 2007 · Pediatric Blood & Cancer
42. GENETIC SUSCEPTIBILITY TO THE METABOLIC SYNDROME
    Yohan Bossé · 2004 · Corpus Université Laval (Université Laval)
43. National Emphysema Treatment Trial State of the Art
    Craig P. Hersh, Dawn Lisa DeMeo, Edwin K. Silverman · 2012 · Proceedings of the American Thoracic Society
44. The role of gene polymorphisms in the pathogenesis of chronic obstructive pulmonary disease
    Eva Slabá, Pavol Joppa, Jan Salagovic, Ružena Tkáčová · 2008 · Biologia
45. GWAS: a milestone in the road from genotypes to phenotypes
    Urko M. Marigorta, Juan Antonio Rodríguez, Arcadi Navarro · 2015 · Cambridge University Press eBooks
46. Pharmacogenomics in rheumatology
    Jeffrey D. Greenberg, Bruce Neil Cronstein · 2015 · Elsevier eBooks
47. Molecular Genetics of Obesity Syndrome
    Atul Sahai, Rama S. Dwivedi, Bernard L. Mirkin · 2007 · CRC Press eBooks
48. Reciprocity and the tragedies of maintaining and providing the commons: A replication and an extension to income inequality
    Michalis Drouvelis, Zeyu Qiu · 2025 · Economic Inquiry
49. Powerful Partial Conjunction Hypothesis Testing via Conditioning
    Biyonka Liang, Lu Zhang, Lucas Janson · 2022 · Biometrika
50. Methods for Association Studies
    Rebecca E. Graff, Caroline Gar-Ling Tai, Linda Kachuri, John S. Witte · 2021 · Springer eBooks
51. Principles of High-Quality Genotyping
    Stephen Jacob Chanock · 2008 · CRC Press eBooks
52. Genetic Association Studies: Concepts and Applications
    Jun Z. Li · 2007 · WORLD SCIENTIFIC eBooks
53. Genetics of Human Obesity
    Richard Baumgartner, Chenxi Wang, David B. Allison · 2007 · CRC Press eBooks
54. Human Genome Project, Genomics, and Clinical Research
    Bruce R. Korf, Nianjun Liu · 2012 · Elsevier eBooks
55. Most of rare missense alleles in humans are deleterious: implications for evolution of complex disease and association studies
    Gregory V. Kryukov, Len A. Pennacchio, Shamil R. Sunyaev · 2006 · University of North Texas Digital Library (University of North Texas)
56. Bioinformatics Approaches for Identifying Allelic Variants in Candidate Pathways underlying Major Depression and Antidepressant Treatment Response
    Kristopher J. L. Irizarry · 2005
57. Importance of Statistics in the Qualification and Application of Biomarkers
    Mary E. Zacour · 2010 · Wiley eBooks
58. IDENTIFICATION OF GENES THAT REGULATE ARTHRITIS AND IgE PRODUCTION IN RAT AND HUMAN
    Ulrica Ribbhammar · 2005 · Figshare
59. Estudo de associação entre genes do sistema dopaminérgico e esquizofrenia
    Quirino Cordeiro · 2007 · Digital Library of Theses and Dissertations (Universidade de São Paulo)
60. Post-GWAS Analyses
    Daniel O. Stram · 2013 · Statistics for biology and health
61. MELANOCORTIN-4 RECEPTOR (MC4R) VARIANTS AND MEASURES OF ADIPOSITY IN THE GENERAL POPULATION
    Mechele Rennay Lee · 2006 · D-Scholarship@Pitt (University of Pittsburgh)
62. EDITORIALS Betting Odds and Genetic Associations
    Duncan C. Thomas, David G Clayton · 2013
63. Genetic Analyses of Polycystic Ovary Syndrome
    Margrit Urbanek · 2008 · Humana Press eBooks
64. The Use of Genotypic Information for the Genetic Improvement of 'Pinus radiata'
    Adrian Hathorn, Bruce Tier, Harry X. Wu · 2012 · RUNE (Research UNE)
65. Genetic architecture of complex disease in humans: a cross-population exploration
    Martínez Marigorta, Urko · 2012 · Repositori digital de la UPF (Universitat Pompeu Fabra)
66. A large-scale candidate gene association study of age at menarche and age at natural menopause Chunyan HePeter KraftDaniel I. ChasmanJulie E. BuringConstance Chen • Susan E. HankinsonGuillaume Pare ´ • Stephen ChanockPaul M. RidkerDavid J. Hunter
    Chunyan He, E. Hankinson, Jessica Ezzell Hunter, Paul M. Ridker, Donald W. Reynolds, Stephen Jacob Chanock, David J. Hunter · 2010
67. The pharmacogenomics of cisplatin-induced hearing loss
    Kusala Pussegoda · 2012 · cIRcle (University of British Columbia)
68. Improving Discovery of Causal Variants in Genetic Association Studies
    Samuel P. Dickson · 2009 · NCSU Libraries Repository (North Carolina State University Libraries)
69. Methoden zur Designveränderungen in genetischen Assoziationsstudien
    André Scherag · 2008 · Publikationsserver (Universitat Marburg)
70. Human Genome Project, Genomics, and Clinical Research
    Helen N. Lyon, Bruce R. Korf · 2007 · Elsevier eBooks
71. Applying Statistics Appropriately for Your Biomarker Application
    Mary E. Zacour · 2020 · Wiley eBooks
72. Genetic epidemiological approaches in complex neurological disorders
    Jouke‐Jan Hottenga · 2005 · Leiden Repository (Leiden University)
73. Faculty Opinions recommendation of Most rare missense alleles are deleterious in humans: implications for complex disease and association studies.
    Joshua M. Akey · 2007 · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature
74. Grand Celebration: 10th Anniversary of the Human Genome Project
    Pabulo Henrique Rampelotto, John Burn, Lupski, James, Nelson, Karen · 2016 · MDPI eBooks
75. Genetic Factors
    Paola Russo, Fabio Lauria, Alfonso Siani · 2010 · Springer eBooks
76. Faculty Opinions recommendation of Most rare missense alleles are deleterious in humans: implications for complex disease and association studies.
    Andrew O.M. Wilkie · 2007 · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature
77. Pharmacogenomics in rheumatology
    Jeffrey D. Greenberg, Bruce Neil Cronstein · 2011 · Elsevier eBooks
78. Association between rs735482 polymorphism and risk of cancer: A meta-analysis of 10 case–control studies
    Shilin Xue, Wenya Shen, Jianning Cai, Jinhai Jia, Dan Zhao, Shan Zhang, Xiujun Zhao, Ning Ma, Wenjuan Wang, Bingshuang Wang et al. · 2022 · Medicine
79. Gene–environment interactions: The exposome and cancer susceptibility
    Meshack Bida, Catherine Cawekazi Cingo, Nisange Janda, Benny Mosoane, Maria Garcia Requesens, Krane Huang, Michelle F. Green, Kamal S. Saini, Zodwa Dlamini · 2026 · Elsevier eBooks
80. The Association Between APOE Genotype, Race, and Dementia
    Natalia Lakomski, Katherine Giorgio, John J. Stephen, Maxwell Armand Mansolf, Aïcha Soumaré, Alden L. Gross, Allison E. Aiello, Archana Singh‐Manoux, M. Arfan Ikram, Catherine Helmer et al. · 2026 · Neurology Genetics