S
Stacey Gabriel
Researcher at Broad Institute
Publications - 411
Citations - 348501
Stacey Gabriel is an academic researcher from Broad Institute. The author has contributed to research in topics: Exome sequencing & Exome. The author has an hindex of 187, co-authored 383 publications receiving 294284 citations. Previous affiliations of Stacey Gabriel include National Institutes of Health & Massachusetts Institute of Technology.
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Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed Whole Genome Sequencing Study
Yuxuan Wang,M. Selvaraj,Xihao Li,Zilin Li,Donna K. Arnett,Joshua C. Bis,John Blangero,Eric Boerwinkle,Donald W. Bowden,Brian E. Cade,Jenna C. Carlson,April P Carson,Yii-Der Ida Chen,Joanne E. Curran,Paul S. de Vries,Susan K. Dutcher,Patrick T. Ellinor,James S. Floyd,Myriam Fornage,Barry I. Freedman,Stacey Gabriel,Soren Germer,Richard A. Gibbs,Xiuqing Guo,Jiang He,Nancy L. Heard-Costa,Bertha A. Hildalgo,Lifang Hou,Marguerite R. Irvin,Roby Joehanes,Robert C. Kaplan,Sharon L.R. Kardia,Tanika N. Kelly,Ryan W. Kim,Charles Kooperberg,Brian G. Kral,Daniel Levy,Changwei Li,Chunyu Liu,Ruth J. F. Loos,Michael C. Mahaney,Lisa W. Martin,Rasika A. Mathias,Ryan L. Minster,Braxton D. Mitchell,May E. Montasser,Alanna C. Morrison,Joanne M. Murabito,Take Naseri,Jeffrey R. O'Connell,Nicholette D. Palmer,Michael Preuss,Bruce M. Psaty,Laura M. Raffield,Dabeeru C. Rao,Susan Redline,Alexander P. Reiner,Stephen S. Rich,Wayne H-H Sheu,Jennifer A. Smith,Hemant K. Tiwari,Michael Y. Tsai,Karine A. Viaud-Martinez,Zhe Wang,Lisa R. Yanek,Wei Zhao,Jerome I. Rotter,Xihong Lin,Pradeep Natarajan,Gina M. Peloso +69 more
TL;DR: In this paper , the role of long non-coding RNAs (lncRNAs) in lipid variability was investigated using large-scale whole genome sequencing (WGS) studies and new statistical methods for variant set tests.
Journal ArticleDOI
Abstract 6084: The Osteosarcoma and Leiomyosarcoma Count Me In Projects of the Cancer Moonshot funded PE-CGS Network directly engage patient participants in genomics research
Katherine A. Janeway,Suzanne George,Corrie A. Painter,Carrie Cibulskis,T Cusher,Elana M. Anastasio,Benjamin Zola,Ashley E Mathews,Evelina Ceca,Beena Thomas,Jason L. Hornick,Alanna J. Church,Lorena Lazo de la Vega,Jill Stopfer,Ellen Sukharevsky,Sarah M. Winnicki,Brendan Reardon,Brian D. Crompton,Priscilla Merriam,Adrián Mariño-Enríquez,Diane S. Diehl,Eliezer VanAllen,Judy Garber,Gad Getz,Stacey Gabriel,Timothy R. Rebbeck,Jennifer S. Mack,Nikhil Wagle +27 more
TL;DR: The Count Me In (CMI) project as mentioned in this paper is a research initiative with prior success in angiosarcoma, working with patients and advocates created websites (OSProject.org and LMSproject.org) where patients register and consent to participation.
Posted ContentDOI
At-home Testing and Risk Factors for Acquisition of SARS-CoV-2 Infection in a Major US Metropolitan Area
Ann E. Woolley,Scott Dryden-Peterson,Andy Kim,Sarah Naz-McLean,Christine E. Kelly,Hannah H Laibinis,Joseph A. Bagnall,Jonathan Livny,Peijun Ma,Marek Orzechowski,James T. Gomez,Noam Shoresh,Stacey Gabriel,Deborah T. Hung,Lisa A. Cosimi +14 more
TL;DR: In this paper , the authors designed a fully remote longitudinal cohort study involving monthly at-home SARS-CoV-2 polymerase chain reaction (PCR) and serology self-testing and monthly surveys.
Pull for Knowledge Work
Sheila Dogde,Timothy De Smet,James Meldrim,Niall Lennon,Danielle Perrin,Steve Ferriera,Zachary Leber,Dennis C. Friedrich,Stacey Gabriel,Eric S. Lander,Don Kieffer,Nelson P. Repenning +11 more
Posted ContentDOI
Structural variation across 138,134 samples in the TOPMed consortium
Goo Jun,Adam B. English,Ginger A. Metcalf,Jianzhi Yang,Mark Chaisson,Nathan Pankratz,Vipin Menon,William J Salerno,Olga A. Krasheninina,John Lane,Thomas W. Blackwell,Hyun Min Kang,Sejal Salvi,Qingchang Meng,Hua Shen,Divya Pasham,Sravya Bhamidipati,Kavya Kottapalli,Donna K. Arnett,Allison E. Ashley-Koch,Paul L. Auer,Kathleen M. Beutel,Joshua A Bis,John Blangero,Donald W. Bowden,Jennifer A. Brody,Brian E. Cade,Yii-Der Ida Chen,Mi Ae Cho,Joanne E. Curran,Myriam Fornage,Barry Frredman,Tasha E. Fingerlin,Bruce Gelb,Lifang Hou,Yi Jen Hung,John P. Kane,Robert Kaplan,Wonji Kim,Ruth J. F. Loos,Gregory Marcus,Rasika A. Mathias,Stephen T. McGarvey,Courtney G. Montgomery,Take Naseri,Seyed Mehdi Nouraie,Michael Preuss,Nicholette D. Palmer,Patricia A. Peyser,Laura M. Raffield,Aakrosh Ratan,Susan Redline,Muagututi‘a Sefuiva Reupena,Jerome I. Rotter,Stephen S. Rich,Michiel Rienstra,Ingo Ruczinski,Vijay Austin Sankaran,David A. Schwartz,Christine E. Seidman,Jonathan Seidman,Edwin K. Silverman,Jennifer A. Smith,Adrienne M. Stilp,Kent D. Taylor,Marilyn I. Telen,Scott T. Weiss,L. Keoki Williams,Bao-Kuan Wu,Lisa R. Yanek,Yingze Zhang,Jessica Lasky-Su,Marie-Claude Gingras,Susan K. Dutcher,Evan E. Eichler,Stacey Gabriel,Soren Germer,Ryan W. Kim,Karine Martinez,Deborah A. Nickerson,James Luo,Alexander P. Reiner,Richard Gibbs,Eric Boerwinkle,Goncaol Abecasis,Fritz J. Sedlazeck +85 more
TL;DR: This article presented a catalog of 355,667 Structural Variants (SV) across autosomes and the X chromosome from 138,134 individuals in the diverse TOPMed consortium, with high variant quality and >90% allele concordance compared to long-read de-novo assemblies of well-characterized control samples.