G
Gonçalo R. Abecasis
Researcher at University of Michigan
Publications - 629
Citations - 271012
Gonçalo R. Abecasis is an academic researcher from University of Michigan. The author has contributed to research in topics: Genome-wide association study & Population. The author has an hindex of 179, co-authored 595 publications receiving 230323 citations. Previous affiliations of Gonçalo R. Abecasis include Johns Hopkins University School of Medicine & Wellcome Trust Centre for Human Genetics.
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Journal ArticleDOI
Rare variant associations with waist-to-hip ratio in European-American and African-American women from the NHLBI-Exome Sequencing Project
Mengyuan Kan,Paul L. Auer,Paul L. Auer,Gao Wang,Kristine L. Bucasas,Stanley Hooker,Alejandra Rodriguez,Alejandra Rodriguez,Biao Li,Jaclyn Ellis,L. Adrienne Cupples,L. Adrienne Cupples,Yii-Der Ida Chen,Josée Dupuis,Josée Dupuis,Caroline S. Fox,Myron D. Gross,Joshua D. Smith,Nancy L. Heard-Costa,Nancy L. Heard-Costa,James B. Meigs,James S. Pankow,Jerome I. Rotter,David S. Siscovick,James G. Wilson,Jay Shendure,Rebecca D. Jackson,Ulrike Peters,Hua Zhong,Danyu Lin,Li Hsu,Nora Franceschini,Christopher S. Carlson,Gonçalo R. Abecasis,Stacey Gabriel,Michael J. Bamshad,David Altshuler,Deborah A. Nickerson,Kari E. North,Leslie A. Lange,Alexander P. Reiner,Alexander P. Reiner,Suzanne M. Leal +42 more
TL;DR: This study indicates that the combined effect of rare variants contribute to the inter-individual variation in fat distribution through the regulation of insulin response.
Journal ArticleDOI
No bias in linkage analysis.
Gonçalo R. Abecasis,Nancy J. Cox,Mark J. Daly,Leonid Kruglyak,Leonid Kruglyak,Nan M. Laird,Kyriacos Markianos,Nick Patterson +7 more
TL;DR: The alarming claim that nonparametric linkage analysis methods have a previously unrecognized inherent bias against detection of linkage and proposed that linkage studies that have used these methods should be reexamined is not well founded.
Journal ArticleDOI
Correction to: Assessing Mitochondrial DNA Variation and Copy Number in Lymphocytes of ~2,000 Sardinians Using Tailored Sequencing Analysis Tools (PLoS Genet, (2015), 11(9))
Jun Ding,Carlo Sidore,Thomas J. Butler,Mary Kate Wing,Yong Qian,Osorio Meirelles,Fabio Busonero,Lam C. Tsoi,Andrea Maschio,Andrea Angius,Hyun Min Kang,Ramaiah Nagaraja,Francesco Cucca,Gonçalo R. Abecasis,David Schlessinger +14 more
TL;DR: This is the largest population analysis to date of mtDNA dynamics, revealing the age-imposed increase in heteroplasmy, the relatively high heritability of copy number, and the association ofcopy number with metabolic traits.
Posted ContentDOI
Tissue-Specific Alteration of Metabolic Pathways Influences Glycemic Regulation
Natasha H. J. Ng,Natasha H. J. Ng,Sara M. Willems,Juan P. Fernandez,Rebecca S. Fine,Rebecca S. Fine,Rebecca S. Fine,Eleanor Wheeler,Eleanor Wheeler,Jennifer Wessel,Hidetoshi Kitajima,Gaëlle Marenne,Jana K. Rundle,Xueling Sim,Xueling Sim,Hanieh Yeghootkar,Nicola L. Beer,Anne Raimondo,A. I. Tarasov,Soren K. Thomsen,Soren K. Thomsen,Martijn van de Bunt,Shuai Wang,Sai Chen,Yuning Chen,Yii-Der Ida Chen,Hugoline G. de Haan,Niels Grarup,Ruifang Li-Gao,Tibor V. Varga,Jennifer L. Asimit,Jennifer L. Asimit,Shuang Feng,Rona J. Strawbridge,Rona J. Strawbridge,Erica L. Kleinbrink,Tarunveer S. Ahluwalia,Tarunveer S. Ahluwalia,Ping An,Emil V. R. Appel,Dan E. Arking,Juha Auvinen,Juha Auvinen,Lawrence F. Bielak,Nathan A. Bihlmeyer,Jette Bork-Jensen,Jennifer A. Brody,Archie Campbell,Audrey Y. Chu,Gail Davies,Ayse Demirkan,James S. Floyd,Franco Giulianini,Xiuqing Guo,Stefan Gustafsson,Benoit Hastoy,Anne U. Jackson,Johanna Jakobsdottir,Marjo-Riitta Järvelin,Marjo-Riitta Järvelin,Richard A. Jensen,Stavroula Kanoni,Sirkka Keinänen-Kiukaanniemi,Sirkka Keinänen-Kiukaanniemi,Jin Li,Man Li,Man Li,Kurt Lohman,Yingchang Lu,Yingchang Lu,Jian'an Luan,Alisa K. Manning,Jonathan Marten,Carola Marzi,Karina Meidtner,Dennis O. Mook-Kanamori,Taulant Muka,Taulant Muka,Giorgio Pistis,Giorgio Pistis,Bram P. Prins,Kenneth Rice,Neil Robertson,Serena Sanna,Serena Sanna,Yuan Shi,Albert V. Smith,Jennifer A. Smith,Lorraine Southam,Lorraine Southam,Heather M. Stringham,Salman M. Tajuddin,Vinicius Tragante,Sander W. van der Laan,Helen R. Warren,Jie Yao,Andrianos M. Yiorkas,Andrianos M. Yiorkas,Weihua Zhang,Weihua Zhang,Wei Zhao,Emma Ahlqvist,Mariaelisa Graff,Heather M. Highland,Heather M. Highland,Anne E. Justice,Ken Sin Lo,Eirini Marouli,Carolina Medina-Gomez,Saima Afaq,Wesam A Alhejily,Wesam A Alhejily,Najaf Amin,Folkert W. Asselbergs,Folkert W. Asselbergs,Lori L. Bonnycastle,Michiel L. Bots,Ivan Brandslund,Ji Chen,Cramer Christensen,John Danesh,Renée de Mutsert,Abbas Dehghan,Abbas Dehghan,Tapani Ebeling,Paul Elliott,Aliki-Eleni Farmaki,Aliki-Eleni Farmaki,Jessica D. Faul,Paul W. Franks,Paul W. Franks,Paul W. Franks,Steve Franks,Andreas Fritsche,Anette P. Gjesing,Mark O. Goodarzi,Vilmundur Gudnason,Göran Hallmans,Tamara B. Harris,Karl-Heinz Herzig,Karl-Heinz Herzig,Marie-France Hivert,Jan-Håkan Jansson,Min A. Jhun,Min A. Jhun,Torben Jørgensen,Torben Jørgensen,Torben Jørgensen,Marit E. Jørgensen,Marit E. Jørgensen,Pekka Jousilahti,Eero Kajantie,Maria Karaleftheri,Sharon L.R. Kardia,Leena Kinnunen,Heikki A. Koistinen,Heikki A. Koistinen,Heikki A. Koistinen,Pirjo Komulainen,Peter Kovacs,Johanna Kuusisto,Markku Laakso,Leslie A. Lange,Lenore J. Launer,Jung-Jin Lee,Aaron Leong,Jaana Lindström,Jocelyn E. Manning Fox,Satu Männistö,Nisa M. Maruthur,Nisa M. Maruthur,Leena Moilanen,Antonella Mulas,Antonella Mulas,Mike A. Nalls,Matt J. Neville,James S. Pankow,Alison Pattie,Eva Rabing Brix Petersen,Hannu Puolijoki,Asif Rasheed,Paul Redmond,Frida Renström,Frida Renström,Michael Roden,Danish Saleheen,Juha Saltevo,Kai Savonen,Sylvain Sebert,Tea Skaaby,Kerrin S. Small,Alena Stančáková,Jakob Stokholm,Konstantin Strauch,E-Shyong Tai,Kent D. Taylor,Betina H. Thuesen,Anke Tönjes,Emmanouil Tsafantakis,Tiinamaija Tuomi,Tiinamaija Tuomi,Jaakko Tuomilehto,Matti Uusitupa,Marja Vääräsmäki,Marja Vääräsmäki,Ilonca Vaartjes,Magdalena Zoledziewska,Gonçalo R. Abecasis,Beverley Balkau,Hans Bisgaard,Alexandra I. F. Blakemore,Alexandra I. F. Blakemore,Matthias Blüher,Heiner Boeing,Eric Boerwinkle,Klaus Bønnelykke,Erwin P. Bottinger,Mark J. Caulfield,John C. Chambers,John C. Chambers,John C. Chambers,Daniel I. Chasman,Daniel I. Chasman,Ching-Yu Cheng,Anne Clark,Francis S. Collins,Josef Coresh,Francesco Cucca,Francesco Cucca,Gert J. de Borst,Ian J. Deary,George Dedoussis,Panos Deloukas,Panos Deloukas,Hester M. den Ruijter,Josée Dupuis,Josée Dupuis,Michele K. Evans,Ele Ferrannini,Oscar H. Franco,Oscar H. Franco,Harald Grallert,Leif Groop,Leif Groop,Torben Hansen,Torben Hansen,Andrew T. Hattersley,Caroline Hayward,Joel N. Hirschhorn,Joel N. Hirschhorn,Joel N. Hirschhorn,Arfan Ikram,Erik Ingelsson,Fredrik Karpe,Fredrik Karpe,Kay-Tee Kaw,Wieland Kiess,Jaspal S. Kooner,Jaspal S. Kooner,Jaspal S. Kooner,Antje Körner,Timo A. Lakka,Claudia Langenberg,Lars Lind,Cecilia M. Lindgren,Allan Linneberg,Allan Linneberg,Leonard Lipovich,Ching-Ti Liu,Jun Liu,Yongmei Liu,Ruth J. F. Loos,Patrick E. MacDonald,Karen L. Mohlke,Andrew D. Morris,Patricia B. Munroe,Alison D. Murray,Sandosh Padmanabhan,Colin N. A. Palmer,Gerard Pasterkamp,Oluf Pedersen,Patricia A. Peyser,Ozren Polasek,David J. Porteous,Michael A. Province,Bruce M. Psaty,Rainer Rauramaa,Paul M. Ridker,Paul M. Ridker,Olov Rolandsson,Patrik Rorsman,Patrik Rorsman,Frits R. Rosendaal,Igor Rudan,Veikko Salomaa,Matthias B. Schulze,Robert Sladek,Blair H. Smith,Tim D. Spector,John M. Starr,Michael Stumvoll,Cornelia M. van Duijn,Mark Walker,Nicholas J. Wareham,David R. Weir,James G. Wilson,Tien Yin Wong,Eleftheria Zeggini,Alan B. Zonderman,Jerome I. Rotter,Andrew P. Morris,Andrew P. Morris,Michael Boehnke,Jose C. Florez,Mark I. McCarthy,Mark I. McCarthy,James B. Meigs,James B. Meigs,Anubha Mahajan,Robert A. Scott,Anna L. Gloyn,Anna L. Gloyn,Inês Barroso,Inês Barroso +323 more
TL;DR: In this paper, the authors investigated associations of exome-array variants in up to 144,060 individuals without diabetes of multiple ancestries, and found that a novel FG/FI association at the liver-enriched G6PC transcript was driven by multiple rare loss-of-function variants.
Journal ArticleDOI
Identification of CFTR variants in Latino patients with cystic fibrosis from the Dominican Republic and Puerto Rico.
Andrew M. Zeiger,Meghan E. McGarry,Angel C.Y. Mak,Vivian Medina,Sandra Salazar,Celeste Eng,Amy K. Liu,Sam S. Oh,Thomas J. Nuckton,Deepti Jain,Thomas W. Blackwell,Hyun Min Kang,Gonçalo R. Abecasis,Leandra Cordero Oñate,Max A. Seibold,Esteban G. Burchard,Jose R. Rodriguez-Santana +16 more
TL;DR: In cystic fibrosis (CF), the spectrum and frequency ofCFTR variants differ by geography and race/ethnicity, and CFTR variants in White patients are well‐described compared with Latino patients.