Jack M. Fu

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Elise RobinsonAssistant Professor of Psychiatry, Massachusetts General Hospital and Harvard Medical SchoolBestätigte E-Mail-Adresse bei broadinstitute.org
Ryan L Collins, Ph.D.Instructor, Dana-Farber Cancer InstituteBestätigte E-Mail-Adresse bei dfci.harvard.edu
Harrison BrandAssistant Professor at Harvard Medical School, Massachusetts General Hospital, & Broad InstituteBestätigte E-Mail-Adresse bei mgh.harvard.edu
Xuefang ZhaoPostdoc Fellow, Center for Genomic Medicine Massachusetts General Hospital, Department ofBestätigte E-Mail-Adresse bei umich.edu
Daniel Weiner, MD PhDResident Physician (Internal Medicine), MGHBestätigte E-Mail-Adresse bei hms.harvard.edu
Mark DalyDirector, Institute for Molecular Medicine Finland (FIMM) & Chief, ATGU, MGH & Broad InstituteBestätigte E-Mail-Adresse bei atgu.mgh.harvard.edu
Alba Sanchis-JuanPostdoctoral Fellow at Broad Institute of MIT and HarvardBestätigte E-Mail-Adresse bei mgh.harvard.edu
Robert B. ScharpfJohns Hopkins UniversityBestätigte E-Mail-Adresse bei jhu.edu
Seth S. MargolisDepartment of Biological Chemistry, The Johns Hopkins University School of MedicineBestätigte E-Mail-Adresse bei jhmi.edu
Chan Hyun NaAssociate Professor of Neurology, Institute for Cell Engineering, Johns Hopkins UniversityBestätigte E-Mail-Adresse bei jhmi.edu
Alan F. ScottAssoc Professor of Medicine, Institute of Genetic Medicine, Johns Hopkins UniversityBestätigte E-Mail-Adresse bei jhmi.edu
Mary L. MarazitaProfessor, University of PIttsburghBestätigte E-Mail-Adresse bei pitt.edu
Alexandre BureauProfessor of biostatistics, Médecine sociale et préventive, Université LavalBestätigte E-Mail-Adresse bei fmed.ulaval.ca
Jeff LeekChief Data Officer, VP, and J Orin Edson Foundation Professor, Fred Hutchinson Cancer CenterBestätigte E-Mail-Adresse bei fredhutch.org
Margaret M. Parker, PhDBeam TherapeuticsBestätigte E-Mail-Adresse bei beamtx.com
Elizabeth J. LeslieEmory UniversityBestätigte E-Mail-Adresse bei emory.edu
Leonardo Collado-TorresInvestigator at LIBD + Asst. Prof., Department of Biostatistics, JHBSPHBestätigte E-Mail-Adresse bei libd.org
Kai KammersJohns Hopkins University School of MedicineBestätigte E-Mail-Adresse bei jhu.edu
Margaret TaubAssociate Scientist, Department of Biostatistics, Johns Hopkins UniversityBestätigte E-Mail-Adresse bei jhsph.edu
Abhinav Nellore

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Jack M. Fu

Instructor in Neurology at Harvard Medical School/Broad Institute/Massachusetts General Hospital

Bestätigte E-Mail-Adresse bei mgh.harvard.edu - Startseite

Computational Genomics Statistical Genetics Computational Biology


Titel Nach Zitationen sortieren Nach Jahr sortieren Nach Titel sortieren	Zitiert von Zitiert von	Jahr
A structural variation reference for medical and population genetics RL Collins, H Brand, KJ Karczewski, X Zhao, J Alföldi, LC Francioli, ... Nature 581 (7809), 444-451, 2020	940*	2020
Rare coding variation provides insight into the genetic architecture and phenotypic context of autism JM Fu, FK Satterstrom, M Peng, H Brand, RL Collins, S Dong, B Wamsley, ... Nature genetics 54 (9), 1320-1331, 2022	371	2022
A cross-disorder dosage sensitivity map of the human genome RL Collins, JT Glessner, E Porcu, M Lepamets, R Brandon, C Lauricella, ... Cell 185 (16), 3041-3055. e25, 2022	239	2022
Expectations and blind spots for structural variation detection from long-read assemblies and short-read genome sequencing technologies X Zhao, RL Collins, WP Lee, AM Weber, Y Jun, Q Zhu, B Weisburd, ... The American Journal of Human Genetics 108 (5), 919-928, 2021	115	2021
Activity-dependent degradation of the nascentome by the neuronal membrane proteasome KV Ramachandran, JM Fu, TB Schaffer, CH Na, M Delannoy, SS Margolis Molecular cell 71 (1), 169-177. e6, 2018	82	2018
The female protective effect against autism spectrum disorder EM Wigdor, DJ Weiner, J Grove, JM Fu, WK Thompson, CE Carey, ... Cell Genomics 2 (6), 2022	79	2022
Centers for Mendelian Genomics: A decade of facilitating gene discovery SM Baxter, JE Posey, NJ Lake, N Sobreira, JX Chong, S Buyske, EE Blue, ... Genetics in Medicine 24 (4), 784-797, 2022	59	2022
GATK-gCNV enables the discovery of rare copy number variants from exome sequencing data M Babadi, JM Fu, SK Lee, AN Smirnov, LD Gauthier, M Walker, ... Nature genetics 55 (9), 1589-1597, 2023	57*	2023
Whole exome sequencing analyses reveal gene–microbiota interactions in the context of IBD S Hu, AV Vila, R Gacesa, V Collij, C Stevens, JM Fu, I Wong, ... Gut 70 (2), 285-296, 2021	53	2021
Ballgown: flexible, isoform-level differential expression analysis J Fu, AC Frazee, L Collado-Torres, AE Jaffe, JT Leek R package version 2 (0), 2018	42*	2018
Landscape of mSWI/SNF chromatin remodeling complex perturbations in neurodevelopmental disorders AM Valencia, A Sankar, PJ van der Sluijs, FK Satterstrom, J Fu, ... Nature Genetics 55 (8), 1400-1412, 2023	39	2023
Genome Sequencing for Diagnosing Rare Diseases MH Wojcik, G Lemire, E Berger, MS Zaki, M Wissmann, W Win, SM White, ... New England Journal of Medicine 390 (21), 1985-1997, 2024	37*	2024
Prevalence and phenotypic impact of rare potentially damaging variants in autism spectrum disorder B Mahjani, S De Rubeis, C Gustavsson Mahjani, M Mulhern, X Xu, L Klei, ... Molecular autism 12, 1-12, 2021	32	2021
Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p DJ Weiner, E Ling, S Erdin, DJC Tai, R Yadav, J Grove, JM Fu, A Nadig, ... Nature genetics 54 (11), 1630-1639, 2022	30	2022
Systematic evaluation of genome sequencing for the diagnostic assessment of autism spectrum disorder and fetal structural anomalies C Lowther, E Valkanas, JL Giordano, HZ Wang, BB Currall, K O’Keefe, ... The American Journal of Human Genetics 110 (9), 1454-1469, 2023	25*	2023
Developmental variability in autism across 17 000 autistic individuals and 4000 siblings without an autism diagnosis: comparisons by cohort, intellectual disability, genetic … SS Kuo, C van der Merwe, JM Fu, CE Carey, ME Talkowski, SL Bishop, ... JAMA pediatrics 176 (9), 915-923, 2022	23	2022
Whole exome association of rare deletions in multiplex oral cleft families J Fu, TH Beaty, AF Scott, J Hetmanski, MM Parker, JEB Wilson, ... Genetic epidemiology 41 (1), 61-69, 2017	15	2017
Shared and distinct ultra-rare genetic risk for diverse epilepsies: A whole-exome sequencing study of 54,423 individuals across multiple genetic ancestries E Collaborative, S Chen, BM Neale, SF Berkovic medRxiv, 2023	13	2023
Exome copy number variant (CNV) detection, analysis, and curation from 6,678 families with undiagnosed rare genetic disease G Lemire, K Russell, S Baxter, K Chao, E Evangelista, M Singer-Berk, ... EUROPEAN JOURNAL OF HUMAN GENETICS 32, 45-45, 2024	7*	2024
Convergent coexpression of autism-associated genes suggests some novel risk genes may not be detectable in large-scale genetic studies C Liao, M Moyses-Oliveira, CEF De Esch, R Bhavsar, X Nuttle, A Li, A Yu, ... Cell Genomics 3 (4), 2023	7*	2023

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