Literature DB >> 26733287

The effect of phenotypic outliers and non-normality on rare-variant association testing.

Paul L Auer1, Alex P Reiner2, Suzanne M Leal3.   

Abstract

Rare-variant association studies (RVAS) have made important contributions to human complex trait genetics. These studies rely on specialized statistical methods for analyzing rare-variant associations, both individually and in aggregate. We investigated the impact that phenotypic outliers and non-normality have on the performance of rare-variant association testing procedures. Ignoring outliers or non-normality can significantly inflate Type I error rates. We found that rank-based inverse normal transformation (INT) and trait winsorisation were both effective at maintaining Type I error control without sacrificing power in the presence of outliers. INT was the optimal method for non-normally distributed traits. For RVAS of quantitative traits with outliers or non-normality, we recommend using INT to transform phenotypic values before association testing.

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Mesh:

Year:  2016        PMID: 26733287      PMCID: PMC4970685          DOI: 10.1038/ejhg.2015.270

Source DB:  PubMed          Journal:  Eur J Hum Genet        ISSN: 1018-4813            Impact factor:   4.246


  27 in total

1.  Pooled association tests for rare variants in exon-resequencing studies.

Authors:  Alkes L Price; Gregory V Kryukov; Paul I W de Bakker; Shaun M Purcell; Jeff Staples; Lee-Jen Wei; Shamil R Sunyaev
Journal:  Am J Hum Genet       Date:  2010-05-13       Impact factor: 11.025

2.  A general framework for detecting disease associations with rare variants in sequencing studies.

Authors:  Dan-Yu Lin; Zheng-Zheng Tang
Journal:  Am J Hum Genet       Date:  2011-09-01       Impact factor: 11.025

3.  Association of exome sequences with plasma C-reactive protein levels in >9000 participants.

Authors:  Ursula M Schick; Paul L Auer; Joshua C Bis; Honghuang Lin; Peng Wei; Nathan Pankratz; Leslie A Lange; Jennifer Brody; Nathan O Stitziel; Daniel S Kim; Christopher S Carlson; Myriam Fornage; Jeffery Haessler; Li Hsu; Rebecca D Jackson; Charles Kooperberg; Suzanne M Leal; Bruce M Psaty; Eric Boerwinkle; Russell Tracy; Diego Ardissino; Svati Shah; Cristen Willer; Ruth Loos; Olle Melander; Ruth Mcpherson; Kees Hovingh; Muredach Reilly; Hugh Watkins; Domenico Girelli; Pierre Fontanillas; Daniel I Chasman; Stacey B Gabriel; Richard Gibbs; Deborah A Nickerson; Sekar Kathiresan; Ulrike Peters; Josée Dupuis; James G Wilson; Stephen S Rich; Alanna C Morrison; Emelia J Benjamin; Myron D Gross; Alex P Reiner
Journal:  Hum Mol Genet       Date:  2014-09-03       Impact factor: 6.150

4.  A variational Bayes discrete mixture test for rare variant association.

Authors:  Benjamin A Logsdon; James Y Dai; Paul L Auer; Jill M Johnsen; Santhi K Ganesh; Nicholas L Smith; James G Wilson; Russell P Tracy; Leslie A Lange; Shuo Jiao; Stephen S Rich; Guillaume Lettre; Christopher S Carlson; Rebecca D Jackson; Christopher J O'Donnell; Mark M Wurfel; Deborah A Nickerson; Hua Tang; Alexander P Reiner; Charles Kooperberg
Journal:  Genet Epidemiol       Date:  2014-01       Impact factor: 2.135

5.  Design of the Women's Health Initiative clinical trial and observational study. The Women's Health Initiative Study Group.

Authors: 
Journal:  Control Clin Trials       Date:  1998-02

6.  Loss-of-function mutations in APOC3, triglycerides, and coronary disease.

Authors:  Jacy Crosby; Gina M Peloso; Paul L Auer; David R Crosslin; Nathan O Stitziel; Leslie A Lange; Yingchang Lu; Zheng-zheng Tang; He Zhang; George Hindy; Nicholas Masca; Kathleen Stirrups; Stavroula Kanoni; Ron Do; Goo Jun; Youna Hu; Hyun Min Kang; Chenyi Xue; Anuj Goel; Martin Farrall; Stefano Duga; Pier Angelica Merlini; Rosanna Asselta; Domenico Girelli; Oliviero Olivieri; Nicola Martinelli; Wu Yin; Dermot Reilly; Elizabeth Speliotes; Caroline S Fox; Kristian Hveem; Oddgeir L Holmen; Majid Nikpay; Deborah N Farlow; Themistocles L Assimes; Nora Franceschini; Jennifer Robinson; Kari E North; Lisa W Martin; Mark DePristo; Namrata Gupta; Stefan A Escher; Jan-Håkan Jansson; Natalie Van Zuydam; Colin N A Palmer; Nicholas Wareham; Werner Koch; Thomas Meitinger; Annette Peters; Wolfgang Lieb; Raimund Erbel; Inke R Konig; Jochen Kruppa; Franziska Degenhardt; Omri Gottesman; Erwin P Bottinger; Christopher J O'Donnell; Bruce M Psaty; Christie M Ballantyne; Goncalo Abecasis; Jose M Ordovas; Olle Melander; Hugh Watkins; Marju Orho-Melander; Diego Ardissino; Ruth J F Loos; Ruth McPherson; Cristen J Willer; Jeanette Erdmann; Alistair S Hall; Nilesh J Samani; Panos Deloukas; Heribert Schunkert; James G Wilson; Charles Kooperberg; Stephen S Rich; Russell P Tracy; Dan-Yu Lin; David Altshuler; Stacey Gabriel; Deborah A Nickerson; Gail P Jarvik; L Adrienne Cupples; Alex P Reiner; Eric Boerwinkle; Sekar Kathiresan
Journal:  N Engl J Med       Date:  2014-06-18       Impact factor: 91.245

7.  Rank-based inverse normal transformations are increasingly used, but are they merited?

Authors:  T Mark Beasley; Stephen Erickson; David B Allison
Journal:  Behav Genet       Date:  2009-06-14       Impact factor: 2.805

8.  Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks.

Authors:  Gina M Peloso; Paul L Auer; Joshua C Bis; Arend Voorman; Alanna C Morrison; Nathan O Stitziel; Jennifer A Brody; Sumeet A Khetarpal; Jacy R Crosby; Myriam Fornage; Aaron Isaacs; Johanna Jakobsdottir; Mary F Feitosa; Gail Davies; Jennifer E Huffman; Ani Manichaikul; Brian Davis; Kurt Lohman; Aron Y Joon; Albert V Smith; Megan L Grove; Paolo Zanoni; Valeska Redon; Serkalem Demissie; Kim Lawson; Ulrike Peters; Christopher Carlson; Rebecca D Jackson; Kelli K Ryckman; Rachel H Mackey; Jennifer G Robinson; David S Siscovick; Pamela J Schreiner; Josyf C Mychaleckyj; James S Pankow; Albert Hofman; Andre G Uitterlinden; Tamara B Harris; Kent D Taylor; Jeanette M Stafford; Lindsay M Reynolds; Riccardo E Marioni; Abbas Dehghan; Oscar H Franco; Aniruddh P Patel; Yingchang Lu; George Hindy; Omri Gottesman; Erwin P Bottinger; Olle Melander; Marju Orho-Melander; Ruth J F Loos; Stefano Duga; Piera Angelica Merlini; Martin Farrall; Anuj Goel; Rosanna Asselta; Domenico Girelli; Nicola Martinelli; Svati H Shah; William E Kraus; Mingyao Li; Daniel J Rader; Muredach P Reilly; Ruth McPherson; Hugh Watkins; Diego Ardissino; Qunyuan Zhang; Judy Wang; Michael Y Tsai; Herman A Taylor; Adolfo Correa; Michael E Griswold; Leslie A Lange; John M Starr; Igor Rudan; Gudny Eiriksdottir; Lenore J Launer; Jose M Ordovas; Daniel Levy; Y-D Ida Chen; Alexander P Reiner; Caroline Hayward; Ozren Polasek; Ian J Deary; Ingrid B Borecki; Yongmei Liu; Vilmundur Gudnason; James G Wilson; Cornelia M van Duijn; Charles Kooperberg; Stephen S Rich; Bruce M Psaty; Jerome I Rotter; Christopher J O'Donnell; Kenneth Rice; Eric Boerwinkle; Sekar Kathiresan; L Adrienne Cupples
Journal:  Am J Hum Genet       Date:  2014-02-06       Impact factor: 11.025

9.  An evaluation of statistical approaches to rare variant analysis in genetic association studies.

Authors:  Andrew P Morris; Eleftheria Zeggini
Journal:  Genet Epidemiol       Date:  2010-02       Impact factor: 2.135

10.  Rare and low-frequency coding variants in CXCR2 and other genes are associated with hematological traits.

Authors:  Paul L Auer; Alexander Teumer; Ursula Schick; Andrew O'Shaughnessy; Ken Sin Lo; Nathalie Chami; Chris Carlson; Simon de Denus; Marie-Pierre Dubé; Jeff Haessler; Rebecca D Jackson; Charles Kooperberg; Louis-Philippe Lemieux Perreault; Matthias Nauck; Ulrike Peters; John D Rioux; Frank Schmidt; Valérie Turcot; Uwe Völker; Henry Völzke; Andreas Greinacher; Li Hsu; Jean-Claude Tardif; George A Diaz; Alexander P Reiner; Guillaume Lettre
Journal:  Nat Genet       Date:  2014-04-28       Impact factor: 38.330

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  14 in total

1.  Effect of non-normality and low count variants on cross-phenotype association tests in GWAS.

Authors:  Debashree Ray; Nilanjan Chatterjee
Journal:  Eur J Hum Genet       Date:  2019-10-03       Impact factor: 4.246

2.  Family-based quantitative trait meta-analysis implicates rare noncoding variants in DENND1A in polycystic ovary syndrome.

Authors:  Matthew Dapas; Ryan Sisk; Richard S Legro; Margrit Urbanek; Andrea Dunaif; M Geoffrey Hayes
Journal:  J Clin Endocrinol Metab       Date:  2019-04-30       Impact factor: 5.958

Review 3.  Transcriptome analysis provides critical answers to the "variants of uncertain significance" conundrum.

Authors:  Mackenzie D Postel; Julie O Culver; Charité Ricker; David W Craig
Journal:  Hum Mutat       Date:  2022-05-18       Impact factor: 4.700

4.  A fully adjusted two-stage procedure for rank-normalization in genetic association studies.

Authors:  Tamar Sofer; Xiuwen Zheng; Stephanie M Gogarten; Cecelia A Laurie; Kelsey Grinde; John R Shaffer; Dmitry Shungin; Jeffrey R O'Connell; Ramon A Durazo-Arvizo; Laura Raffield; Leslie Lange; Solomon Musani; Ramachandran S Vasan; L Adrienne Cupples; Alexander P Reiner; Cathy C Laurie; Kenneth M Rice
Journal:  Genet Epidemiol       Date:  2019-01-17       Impact factor: 2.344

5.  Activation of cryptic splicing in bovine WDR19 is associated with reduced semen quality and male fertility.

Authors:  Maya Hiltpold; Guanglin Niu; Naveen Kumar Kadri; Danang Crysnanto; Zih-Hua Fang; Mirjam Spengeler; Fritz Schmitz-Hsu; Christian Fuerst; Hermann Schwarzenbacher; Franz R Seefried; Frauke Seehusen; Ulrich Witschi; Angelika Schnieke; Ruedi Fries; Heinrich Bollwein; Krzysztof Flisikowski; Hubert Pausch
Journal:  PLoS Genet       Date:  2020-05-14       Impact factor: 5.917

6.  Genetic effects on the commensal microbiota in inflammatory bowel disease patients.

Authors:  Hugues Aschard; Vincent Laville; Eric Tchetgen Tchetgen; Dan Knights; Floris Imhann; Philippe Seksik; Noah Zaitlen; Mark S Silverberg; Jacques Cosnes; Rinse K Weersma; Ramnik Xavier; Laurent Beaugerie; David Skurnik; Harry Sokol
Journal:  PLoS Genet       Date:  2019-03-08       Impact factor: 5.917

7.  Computational modeling of tau pathology spread reveals patterns of regional vulnerability and the impact of a genetic risk factor.

Authors:  Eli J Cornblath; Howard L Li; Lakshmi Changolkar; Bin Zhang; Hannah J Brown; Ronald J Gathagan; Modupe F Olufemi; John Q Trojanowski; Danielle S Bassett; Virginia M Y Lee; Michael X Henderson
Journal:  Sci Adv       Date:  2021-06-09       Impact factor: 14.136

8.  On Robust Association Testing for Quantitative Traits and Rare Variants.

Authors:  Peng Wei; Ying Cao; Yiwei Zhang; Zhiyuan Xu; Il-Youp Kwak; Eric Boerwinkle; Wei Pan
Journal:  G3 (Bethesda)       Date:  2016-12-07       Impact factor: 3.154

9.  Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.

Authors:  Valérie Turcot; Yingchang Lu; Heather M Highland; Claudia Schurmann; Anne E Justice; Rebecca S Fine; Jonathan P Bradfield; Tõnu Esko; Ayush Giri; Mariaelisa Graff; Xiuqing Guo; Audrey E Hendricks; Tugce Karaderi; Adelheid Lempradl; Adam E Locke; Anubha Mahajan; Eirini Marouli; Suthesh Sivapalaratnam; Kristin L Young; Tamuno Alfred; Mary F Feitosa; Nicholas G D Masca; Alisa K Manning; Carolina Medina-Gomez; Poorva Mudgal; Maggie C Y Ng; Alex P Reiner; Sailaja Vedantam; Sara M Willems; Thomas W Winkler; Gonçalo Abecasis; Katja K Aben; Dewan S Alam; Sameer E Alharthi; Matthew Allison; Philippe Amouyel; Folkert W Asselbergs; Paul L Auer; Beverley Balkau; Lia E Bang; Inês Barroso; Lisa Bastarache; Marianne Benn; Sven Bergmann; Lawrence F Bielak; Matthias Blüher; Michael Boehnke; Heiner Boeing; Eric Boerwinkle; Carsten A Böger; Jette Bork-Jensen; Michiel L Bots; Erwin P Bottinger; Donald W Bowden; Ivan Brandslund; Gerome Breen; Murray H Brilliant; Linda Broer; Marco Brumat; Amber A Burt; Adam S Butterworth; Peter T Campbell; Stefania Cappellani; David J Carey; Eulalia Catamo; Mark J Caulfield; John C Chambers; Daniel I Chasman; Yii-Der I Chen; Rajiv Chowdhury; Cramer Christensen; Audrey Y Chu; Massimiliano Cocca; Francis S Collins; James P Cook; Janie Corley; Jordi Corominas Galbany; Amanda J Cox; David S Crosslin; Gabriel Cuellar-Partida; Angela D'Eustacchio; John Danesh; Gail Davies; Paul I W Bakker; Mark C H Groot; Renée Mutsert; Ian J Deary; George Dedoussis; Ellen W Demerath; Martin Heijer; Anneke I Hollander; Hester M Ruijter; Joe G Dennis; Josh C Denny; Emanuele Di Angelantonio; Fotios Drenos; Mengmeng Du; Marie-Pierre Dubé; Alison M Dunning; Douglas F Easton; Todd L Edwards; David Ellinghaus; Patrick T Ellinor; Paul Elliott; Evangelos Evangelou; Aliki-Eleni Farmaki; I Sadaf Farooqi; Jessica D Faul; Sascha Fauser; Shuang Feng; Ele Ferrannini; Jean Ferrieres; Jose C Florez; Ian Ford; Myriam Fornage; Oscar H Franco; Andre Franke; Paul W Franks; Nele Friedrich; Ruth Frikke-Schmidt; Tessel E Galesloot; Wei Gan; Ilaria Gandin; Paolo Gasparini; Jane Gibson; Vilmantas Giedraitis; Anette P Gjesing; Penny Gordon-Larsen; Mathias Gorski; Hans-Jörgen Grabe; Struan F A Grant; Niels Grarup; Helen L Griffiths; Megan L Grove; Vilmundur Gudnason; Stefan Gustafsson; Jeff Haessler; Hakon Hakonarson; Anke R Hammerschlag; Torben Hansen; Kathleen Mullan Harris; Tamara B Harris; Andrew T Hattersley; Christian T Have; Caroline Hayward; Liang He; Nancy L Heard-Costa; Andrew C Heath; Iris M Heid; Øyvind Helgeland; Jussi Hernesniemi; Alex W Hewitt; Oddgeir L Holmen; G Kees Hovingh; Joanna M M Howson; Yao Hu; Paul L Huang; Jennifer E Huffman; M Arfan Ikram; Erik Ingelsson; Anne U Jackson; Jan-Håkan Jansson; Gail P Jarvik; Gorm B Jensen; Yucheng Jia; Stefan Johansson; Marit E Jørgensen; Torben Jørgensen; J Wouter Jukema; Bratati Kahali; René S Kahn; Mika Kähönen; Pia R Kamstrup; Stavroula Kanoni; Jaakko Kaprio; Maria Karaleftheri; Sharon L R Kardia; Fredrik Karpe; Sekar Kathiresan; Frank Kee; Lambertus A Kiemeney; Eric Kim; Hidetoshi Kitajima; Pirjo Komulainen; Jaspal S Kooner; Charles Kooperberg; Tellervo Korhonen; Peter Kovacs; Helena Kuivaniemi; Zoltán Kutalik; Kari Kuulasmaa; Johanna Kuusisto; Markku Laakso; Timo A Lakka; David Lamparter; Ethan M Lange; Leslie A Lange; Claudia Langenberg; Eric B Larson; Nanette R Lee; Terho Lehtimäki; Cora E Lewis; Huaixing Li; Jin Li; Ruifang Li-Gao; Honghuang Lin; Keng-Hung Lin; Li-An Lin; Xu Lin; Lars Lind; Jaana Lindström; Allan Linneberg; Ching-Ti Liu; Dajiang J Liu; Yongmei Liu; Ken S Lo; Artitaya Lophatananon; Andrew J Lotery; Anu Loukola; Jian'an Luan; Steven A Lubitz; Leo-Pekka Lyytikäinen; Satu Männistö; Gaëlle Marenne; Angela L Mazul; Mark I McCarthy; Roberta McKean-Cowdin; Sarah E Medland; Karina Meidtner; Lili Milani; Vanisha Mistry; Paul Mitchell; Karen L Mohlke; Leena Moilanen; Marie Moitry; Grant W Montgomery; Dennis O Mook-Kanamori; Carmel Moore; Trevor A Mori; Andrew D Morris; Andrew P Morris; Martina Müller-Nurasyid; Patricia B Munroe; Mike A Nalls; Narisu Narisu; Christopher P Nelson; Matt Neville; Sune F Nielsen; Kjell Nikus; Pål R Njølstad; Børge G Nordestgaard; Dale R Nyholt; Jeffrey R O'Connel; Michelle L O'Donoghue; Loes M Olde Loohuis; Roel A Ophoff; Katharine R Owen; Chris J Packard; Sandosh Padmanabhan; Colin N A Palmer; Nicholette D Palmer; Gerard Pasterkamp; Aniruddh P Patel; Alison Pattie; Oluf Pedersen; Peggy L Peissig; Gina M Peloso; Craig E Pennell; Markus Perola; James A Perry; John R B Perry; Tune H Pers; Thomas N Person; Annette Peters; Eva R B Petersen; Patricia A Peyser; Ailith Pirie; Ozren Polasek; Tinca J Polderman; Hannu Puolijoki; Olli T Raitakari; Asif Rasheed; Rainer Rauramaa; Dermot F Reilly; Frida Renström; Myriam Rheinberger; Paul M Ridker; John D Rioux; Manuel A Rivas; David J Roberts; Neil R Robertson; Antonietta Robino; Olov Rolandsson; Igor Rudan; Katherine S Ruth; Danish Saleheen; Veikko Salomaa; Nilesh J Samani; Yadav Sapkota; Naveed Sattar; Robert E Schoen; Pamela J Schreiner; Matthias B Schulze; Robert A Scott; Marcelo P Segura-Lepe; Svati H Shah; Wayne H-H Sheu; Xueling Sim; Andrew J Slater; Kerrin S Small; Albert V Smith; Lorraine Southam; Timothy D Spector; Elizabeth K Speliotes; John M Starr; Kari Stefansson; Valgerdur Steinthorsdottir; Kathleen E Stirrups; Konstantin Strauch; Heather M Stringham; Michael Stumvoll; Liang Sun; Praveen Surendran; Amy J Swift; Hayato Tada; Katherine E Tansey; Jean-Claude Tardif; Kent D Taylor; Alexander Teumer; Deborah J Thompson; Gudmar Thorleifsson; Unnur Thorsteinsdottir; Betina H Thuesen; Anke Tönjes; Gerard Tromp; Stella Trompet; Emmanouil Tsafantakis; Jaakko Tuomilehto; Anne Tybjaerg-Hansen; Jonathan P Tyrer; Rudolf Uher; André G Uitterlinden; Matti Uusitupa; Sander W Laan; Cornelia M Duijn; Nienke Leeuwen; Jessica van Setten; Mauno Vanhala; Anette Varbo; Tibor V Varga; Rohit Varma; Digna R Velez Edwards; Sita H Vermeulen; Giovanni Veronesi; Henrik Vestergaard; Veronique Vitart; Thomas F Vogt; Uwe Völker; Dragana Vuckovic; Lynne E Wagenknecht; Mark Walker; Lars Wallentin; Feijie Wang; Carol A Wang; Shuai Wang; Yiqin Wang; Erin B Ware; Nicholas J Wareham; Helen R Warren; Dawn M Waterworth; Jennifer Wessel; Harvey D White; Cristen J Willer; James G Wilson; Daniel R Witte; Andrew R Wood; Ying Wu; Hanieh Yaghootkar; Jie Yao; Pang Yao; Laura M Yerges-Armstrong; Robin Young; Eleftheria Zeggini; Xiaowei Zhan; Weihua Zhang; Jing Hua Zhao; Wei Zhao; Wei Zhao; Wei Zhou; Krina T Zondervan; Jerome I Rotter; John A Pospisilik; Fernando Rivadeneira; Ingrid B Borecki; Panos Deloukas; Timothy M Frayling; Guillaume Lettre; Kari E North; Cecilia M Lindgren; Joel N Hirschhorn; Ruth J F Loos
Journal:  Nat Genet       Date:  2017-12-22       Impact factor: 38.330

10.  Large-Scale Exome-wide Association Analysis Identifies Loci for White Blood Cell Traits and Pleiotropy with Immune-Mediated Diseases.

Authors:  Salman M Tajuddin; Ursula M Schick; John D Eicher; Nathalie Chami; Ayush Giri; Jennifer A Brody; W David Hill; Tim Kacprowski; Jin Li; Leo-Pekka Lyytikäinen; Ani Manichaikul; Evelin Mihailov; Michelle L O'Donoghue; Nathan Pankratz; Raha Pazoki; Linda M Polfus; Albert Vernon Smith; Claudia Schurmann; Caterina Vacchi-Suzzi; Dawn M Waterworth; Evangelos Evangelou; Lisa R Yanek; Amber Burt; Ming-Huei Chen; Frank J A van Rooij; James S Floyd; Andreas Greinacher; Tamara B Harris; Heather M Highland; Leslie A Lange; Yongmei Liu; Reedik Mägi; Mike A Nalls; Rasika A Mathias; Deborah A Nickerson; Kjell Nikus; John M Starr; Jean-Claude Tardif; Ioanna Tzoulaki; Digna R Velez Edwards; Lars Wallentin; Traci M Bartz; Lewis C Becker; Joshua C Denny; Laura M Raffield; John D Rioux; Nele Friedrich; Myriam Fornage; He Gao; Joel N Hirschhorn; David C M Liewald; Stephen S Rich; Andre Uitterlinden; Lisa Bastarache; Diane M Becker; Eric Boerwinkle; Simon de Denus; Erwin P Bottinger; Caroline Hayward; Albert Hofman; Georg Homuth; Ethan Lange; Lenore J Launer; Terho Lehtimäki; Yingchang Lu; Andres Metspalu; Chris J O'Donnell; Rakale C Quarells; Melissa Richard; Eric S Torstenson; Kent D Taylor; Anne-Claire Vergnaud; Alan B Zonderman; David R Crosslin; Ian J Deary; Marcus Dörr; Paul Elliott; Michele K Evans; Vilmundur Gudnason; Mika Kähönen; Bruce M Psaty; Jerome I Rotter; Andrew J Slater; Abbas Dehghan; Harvey D White; Santhi K Ganesh; Ruth J F Loos; Tõnu Esko; Nauder Faraday; James G Wilson; Mary Cushman; Andrew D Johnson; Todd L Edwards; Neil A Zakai; Guillaume Lettre; Alex P Reiner; Paul L Auer
Journal:  Am J Hum Genet       Date:  2016-06-23       Impact factor: 11.025

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