Literature DB >> 19189911

STrengthening the REporting of Genetic Association studies (STREGA): an extension of the STROBE Statement.

Julian Little1, Julian P T Higgins, John P A Ioannidis, David Moher, France Gagnon, Erik von Elm, Muin J Khoury, Barbara Cohen, George Davey-Smith, Jeremy Grimshaw, Paul Scheet, Marta Gwinn, Robin E Williamson, Guang Yong Zou, Kim Hutchings, Candice Y Johnson, Valerie Tait, Miriam Wiens, Jean Golding, Cornelia van Duijn, John McLaughlin, Andrew Paterson, George Wells, Isabel Fortier, Matthew Freedman, Maja Zecevic, Richard King, Claire Infante-Rivard, Alex Stewart, Nick Birkett.   

Abstract

Making sense of rapidly evolving evidence on genetic associations is crucial to making genuine advances in human genomics and the eventual integration of this information into the practice of medicine and public health. Assessment of the strengths and weaknesses of this evidence, and hence the ability to synthesize it, has been limited by inadequate reporting of results. The STrengthening the REporting of Genetic Association studies (STREGA) initiative builds on the STrengthening the Reporting of Observational Studies in Epidemiology (STROBE) Statement and provides additions to 12 of the 22 items on the STROBE checklist. The additions concern population stratification, genotyping errors, modeling haplotype variation, Hardy-Weinberg equilibrium, replication, selection of participants, rationale for choice of genes and variants, treatment effects in studying quantitative traits, statistical methods, relatedness, reporting of descriptive and outcome data, and issues of data volume that are important to consider in genetic association studies. The STREGA recommendations do not prescribe or dictate how a genetic association study should be designed but seek to enhance the transparency of its reporting, regardless of choices made during design, conduct, or analysis.

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Year:  2009        PMID: 19189911     DOI: 10.7326/0003-4819-150-3-200902030-00011

Source DB:  PubMed          Journal:  Ann Intern Med        ISSN: 0003-4819            Impact factor:   25.391


  37 in total

Review 1.  A systematic review evaluating the methodological aspects of meta-analyses of genetic association studies in cancer research.

Authors:  Stefania Boccia; Emma De Feo; Paola Gallì; Francesco Gianfagna; Rosarita Amore; Gualtiero Ricciardi
Journal:  Eur J Epidemiol       Date:  2010-09-10       Impact factor: 8.082

Review 2.  Genetic susceptibility to renal scar formation after urinary tract infection: a systematic review and meta-analysis of candidate gene polymorphisms.

Authors:  Marco Zaffanello; Stefano Tardivo; Luigi Cataldi; Vassilios Fanos; Paolo Biban; Giovanni Malerba
Journal:  Pediatr Nephrol       Date:  2010-11-30       Impact factor: 3.714

3.  Genetic polymorphisms in pre-microRNAs and risk of ischemic stroke in a Chinese population.

Authors:  Yun Liu; Ying Ma; Bo Zhang; Shun-Xian Wang; Xiao-Ming Wang; Ju-Ming Yu
Journal:  J Mol Neurosci       Date:  2013-11-01       Impact factor: 3.444

4.  HFE genetic variability and risk of alcoholic liver disease: A meta-analysis.

Authors:  Yan-Yan Xu; Yu-Han Tang; Xiao-Ping Guo; Jing Wang; Ping Yao
Journal:  J Huazhong Univ Sci Technolog Med Sci       Date:  2016-10-18

Review 5.  Predicting outcomes in radiation oncology--multifactorial decision support systems.

Authors:  Philippe Lambin; Ruud G P M van Stiphout; Maud H W Starmans; Emmanuel Rios-Velazquez; Georgi Nalbantov; Hugo J W L Aerts; Erik Roelofs; Wouter van Elmpt; Paul C Boutros; Pierluigi Granone; Vincenzo Valentini; Adrian C Begg; Dirk De Ruysscher; Andre Dekker
Journal:  Nat Rev Clin Oncol       Date:  2012-11-20       Impact factor: 66.675

6.  Common genetic determinants of breast-cancer risk in East Asian women: a collaborative study of 23 637 breast cancer cases and 25 579 controls.

Authors:  Wei Zheng; Ben Zhang; Qiuyin Cai; Hyuna Sung; Kyriaki Michailidou; Jiajun Shi; Ji-Yeob Choi; Jirong Long; Joe Dennis; Manjeet K Humphreys; Qin Wang; Wei Lu; Yu-Tang Gao; Chun Li; Hui Cai; Sue K Park; Keun-Young Yoo; Dong-Young Noh; Wonshik Han; Alison M Dunning; Javier Benitez; Daniel Vincent; Francois Bacot; Daniel Tessier; Sung-Won Kim; Min Hyuk Lee; Jong Won Lee; Jong-Young Lee; Yong-Bing Xiang; Ying Zheng; Wenjin Wang; Bu-Tian Ji; Keitaro Matsuo; Hidemi Ito; Hiroji Iwata; Hideo Tanaka; Anna H Wu; Chiu-chen Tseng; David Van Den Berg; Daniel O Stram; Soo Hwang Teo; Cheng Har Yip; In Nee Kang; Tien Y Wong; Chen-Yang Shen; Jyh-Cherng Yu; Chiun-Sheng Huang; Ming-Feng Hou; Mikael Hartman; Hui Miao; Soo Chin Lee; Thomas Choudary Putti; Kenneth Muir; Artitaya Lophatananon; Sarah Stewart-Brown; Pornthep Siriwanarangsan; Suleeporn Sangrajrang; Hongbing Shen; Kexin Chen; Pei-Ei Wu; Zefang Ren; Christopher A Haiman; Aiko Sueta; Mi Kyung Kim; Ui Soon Khoo; Motoki Iwasaki; Paul D P Pharoah; Wanqing Wen; Per Hall; Xiao-Ou Shu; Douglas F Easton; Daehee Kang
Journal:  Hum Mol Genet       Date:  2013-03-27       Impact factor: 6.150

7.  Genetic variation in the prostaglandin E2 pathway is associated with primary graft dysfunction.

Authors:  Joshua M Diamond; Tatiana Akimova; Altaf Kazi; Rupal J Shah; Edward Cantu; Rui Feng; Matthew H Levine; Steven M Kawut; Nuala J Meyer; James C Lee; Wayne W Hancock; Richard Aplenc; Lorraine B Ware; Scott M Palmer; Sangeeta Bhorade; Vibha N Lama; Ann Weinacker; Jonathan Orens; Keith Wille; Maria Crespo; David J Lederer; Selim Arcasoy; Ejigayehu Demissie; Jason D Christie
Journal:  Am J Respir Crit Care Med       Date:  2014-03-01       Impact factor: 21.405

8.  Genome-wide association studies, field synopses, and the development of the knowledge base on genetic variation and human diseases.

Authors:  Muin J Khoury; Lars Bertram; Paolo Boffetta; Adam S Butterworth; Stephen J Chanock; Siobhan M Dolan; Isabel Fortier; Montserrat Garcia-Closas; Marta Gwinn; Julian P T Higgins; A Cecile J W Janssens; James Ostell; Ryan P Owen; Roberta A Pagon; Timothy R Rebbeck; Nathaniel Rothman; Jonine L Bernstein; Paul R Burton; Harry Campbell; Anand Chockalingam; Helena Furberg; Julian Little; Thomas R O'Brien; Daniela Seminara; Paolo Vineis; Deborah M Winn; Wei Yu; John P A Ioannidis
Journal:  Am J Epidemiol       Date:  2009-06-04       Impact factor: 4.897

Review 9.  Comparative effectiveness research, genomics-enabled personalized medicine, and rapid learning health care: a common bond.

Authors:  Geoffrey S Ginsburg; Nicole M Kuderer
Journal:  J Clin Oncol       Date:  2012-10-15       Impact factor: 44.544

Review 10.  Glutathione-S-transferase genes and asthma phenotypes: a Human Genome Epidemiology (HuGE) systematic review and meta-analysis including unpublished data.

Authors:  Cosetta Minelli; Raquel Granell; Roger Newson; Matthew J Rose-Zerilli; Maties Torrent; Sue M Ring; John W Holloway; Seif O Shaheen; John A Henderson
Journal:  Int J Epidemiol       Date:  2009-12-23       Impact factor: 7.196

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