S
Samuela Pollack
Researcher at Broad Institute
Publications - 3
Citations - 2867
Samuela Pollack is an academic researcher from Broad Institute. The author has contributed to research in topics: Genome-wide association study & Gene. The author has an hindex of 2, co-authored 2 publications receiving 2634 citations.
Papers
More filters
Journal ArticleDOI
Integrating common and rare genetic variation in diverse human populations
David Altshuler,Richard A. Gibbs,Leena Peltonen,Emmanouil T. Dermitzakis,Stephen F. Schaffner,Fuli Yu,Penelope E. Bonnen,de Bakker Piw.,Panagiotis Deloukas,Stacey Gabriel,R. Gwilliam,Sarah E. Hunt,Michael Inouye,Xiaoming Jia,Aarno Palotie,Melissa Parkin,Pamela Whittaker,Kyle Chang,Alicia Hawes,Lora Lewis,Yanru Ren,D Wheeler,Donna M. Muzny,Chris P. Barnes,Katayoon Darvishi,Matthew E. Hurles,Joshua M. Korn,K. Kristiansson,Charles Lee,S A McCarrol,James Nemesh,Alon Keinan,Stephen B. Montgomery,Samuela Pollack,Alkes L. Price,Nicole Soranzo,Claudia Gonzaga-Jauregui,Verneri Anttila,Wendy Brodeur,Mark J. Daly,Stephen Leslie,Gil McVean,Loukas Moutsianas,Huy Nguyen,Qingrun Zhang,Ghori Mjr.,Ralph McGinnis,William M. McLaren,Fumihiko Takeuchi,Sharon R. Grossman,Ilya Shlyakhter,Elizabeth Hostetter,Pardis C. Sabeti,Clement Adebamowo,Morris W. Foster,Deborah R. Gordon,Julio Licinio,M C Manca,Patricia A. Marshall,Ichiro Matsuda,D Ngare,Vivian Ota Wang,D Reddy,Charles N. Rotimi,Charmaine D.M. Royal,Richard R. Sharp,Changqing Zeng,Lisa D. Brooks,Jean E. McEwen +68 more
TL;DR: An expanded public resource of genome variants in global populations supports deeper interrogation of genomic variation and its role in human disease, and serves as a step towards a high-resolution map of the landscape of human genetic variation.
Posted ContentDOI
Mixed Model Association with Family-Biased Case-Control Ascertainment
Tristan J. Hayeck,Noah Zaitlen,Po-Ru Loh,Samuela Pollack,Alexander Gusev,Nick Patterson,Alkes L. Price +6 more
TL;DR: LT-Fam is introduced, a family-based association statistic that is robust to family-biased case-control ascertainment and uses published narrow-sense heritability estimates to avoid the problem of biased heritability estimation, enabling correct calibration.
Journal ArticleDOI
Erratum to Gene Set Enrichment Analyses Identify Pathways Involved in Genetic Risk for Diabetic Retinopathy. Am J Ophthalmol 2022;233:111-123.
Lucia Sobrin,Gayatri Susarla,Lynn K. Stanwyck,John M. Rouhana,A. Li,Samuela Pollack,Robert P. Igo,Richard A. Jensen,Xiaohui Li,Maggie C.Y. Ng,Jane Z. Kuo,Kent D. Taylor,Barry I. Freedman,Donald W. Bowden,Alan D. Penman,Cheng Chen,Jamie E Craig,Sharon G. Adler,Emily Y. Chew,Mary Frances Cotch,Brian L. Yaspan,Paul Mitchell,Jie Jin Wang,Barbara E.K. Klein,Tien Yin Wong,Jerome I. Rotter,Kathyrn P. Burdon,Sudha K. Iyengar,Ayellet V. Segrè +28 more
TL;DR: In this article , the authors identify functionally related genes associated with diabetic retinopathy (DR) risk using gene set enrichment analyses applied to genome-wide association study meta-analyses.