Goo Jun

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Hyun Min KangProfessor of Biostatistics, University of Michigan, Ann ArborVerifisert e-postadresse på umich.edu
Goncalo AbecasisUniversity of Michigan School of Public HealthVerifisert e-postadresse på umich.edu
Joydeep Ghosh(Chaired) Professor, ECE Dept., Univ. Texas at Austin; Faculty Dell Med, UT-Comp. Sc., McCombsVerifisert e-postadresse på utexas.edu
Michael BoehnkeProfessor of Biostatistics, University of MichiganVerifisert e-postadresse på umich.edu
John BlangeroProfessor of Human Genetics, School of Medicine, University of Texas Rio Grande ValleyVerifisert e-postadresse på utrgv.edu
Joshua AkeyProfessor of Ecology and Evolutionary Biology and Lewis Sigler Institute, Princeton UniversityVerifisert e-postadresse på princeton.edu
Jay ShendureProfessor of Genome Sciences, University of WashingtonVerifisert e-postadresse på uw.edu
Deborah A. NickersonUniversity of WashingtonVerifisert e-postadresse på uw.edu
Ranga Raju VatsavaiCFEP Professor, Computer Science Dept., NCSUVerifisert e-postadresse på ncsu.edu
Amy L. WilliamsCornell UniversityVerifisert e-postadresse på cornell.edu
Muhittin GökmenProfessor of Computer Engineering, MEF UniversityVerifisert e-postadresse på mef.edu.tr
J K AggarwalProfessor of Electrical and Computer Engineering, The University of Texas at Austin, Austin, TXVerifisert e-postadresse på utexas.edu
Eimear KennyIcahn School of Medicine at Mount SinaiVerifisert e-postadresse på mssm.edu
Adam E. LockeSenior Director, Statistical Genetics, Regeneron Genetics CenterVerifisert e-postadresse på regeneron.com
Scott VriezeUniversity of MinnesotaVerifisert e-postadresse på umn.edu
Varun ChandolaAssociate Professor, Computer Science Department, University at BuffaloVerifisert e-postadresse på buffalo.edu
Zoran ObradovicData Analytics and Biomedical Informatics Center, Temple UniversityVerifisert e-postadresse på temple.edu
Simon GravelAssociate Professor, McGill UniversityVerifisert e-postadresse på mcGill.ca
Jacob A TennessenHarvard T. H. Chan School of Public HealthVerifisert e-postadresse på hsph.harvard.edu
Xiaoming LiuAssociate Professor, College of Public Health, University of South FloridaVerifisert e-postadresse på usf.edu

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Goo Jun

Human Genetics Center, School of Public Health, University of Texas Health Science Center Houston

Verifisert e-postadresse på uth.tmc.edu

Statistical Genetics Human Genetics Bioinformatics Computational Biology Machine Learning


Tittel Sorter etter sitater Sorter etter år Sorter etter tittel	Sitert av Sitert av	År
A global reference for human genetic variation 1000 Genomes Project Consortium Nature 526 (7571), 68, 2015	16534	2015
An integrated map of genetic variation from 1,092 human genomes 1000 Genomes Project Consortium Nature 491 (7422), 56, 2012	8491	2012
An integrated map of structural variation in 2,504 human genomes PH Sudmant, T Rausch, EJ Gardner, RE Handsaker, A Abyzov, ... Nature 526 (7571), 75-81, 2015	2564	2015
Evolution and functional impact of rare coding variation from deep sequencing of human exomes JA Tennessen, AW Bigham, TD O’connor, W Fu, EE Kenny, S Gravel, ... science 337 (6090), 64-69, 2012	1918	2012
The genetic architecture of type 2 diabetes C Fuchsberger, J Flannick, TM Teslovich, A Mahajan, V Agarwala, ... Nature 536 (7614), 41-47, 2016	1299	2016
Analysis of 6,515 exomes reveals the recent origin of most human protein-coding variants W Fu, TD O’connor, G Jun, HM Kang, G Abecasis, SM Leal, S Gabriel, ... Nature 493 (7431), 216-220, 2013	1223	2013
Loss-of-function mutations in APOC3, triglycerides, and coronary disease NHLBI ESP New England Journal of Medicine 371, 22-31, 2014	909*	2014
Multi-platform discovery of haplotype-resolved structural variation in human genomes MJP Chaisson, AD Sanders, X Zhao, A Malhotra, D Porubsky, T Rausch, ... Nature communications 10 (1), 1784, 2019	848	2019
Detecting and estimating contamination of human DNA samples in sequencing and array-based genotype data G Jun, M Flickinger, KN Hetrick, JM Romm, KF Doheny, GR Abecasis, ... The American Journal of Human Genetics 91 (5), 839-848, 2012	566	2012
An efficient and scalable analysis framework for variant extraction and refinement from population-scale DNA sequence data G Jun, MK Wing, GR Abecasis, HM Kang Genome research 25 (6), 918-925, 2015	408	2015
Microscopic examination of spatial transcriptome using Seq-Scope CS Cho, J Xi, Y Si, SR Park, JE Hsu, M Kim, G Jun, HM Kang, JH Lee Cell 184 (13), 3559-3572. e22, 2021	376	2021
Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol LA Lange, Y Hu, H Zhang, C Xue, EM Schmidt, ZZ Tang, C Bizon, ... The American Journal of Human Genetics 94 (2), 233-245, 2014	251*	2014
Randomised clinical trial: faecal microbiota transplantation for recurrent Clostridum difficile infection – fresh, or frozen, or lyophilised microbiota from a small pool of … ZD Jiang, NJ Ajami, JF Petrosino, G Jun, CL Hanis, M Shah, L Hochman, ... Alimentary Pharmacology & Therapeutics 45 (7), 899-908, 2017	228	2017
Identification of a rare coding variant in complement 3 associated with age-related macular degeneration X Zhan, DE Larson, C Wang, DC Koboldt, YV Sergeev, RS Fulton, ... Nature genetics 45 (11), 1375-1379, 2013	194	2013
Non-crossover gene conversions show strong GC bias and unexpected clustering in humans AL Williams, G Genovese, T Dyer, N Altemose, K Truax, G Jun, ... Elife 4, e04637, 2015	126	2015
Identification and Functional Characterization of G6PC2 Coding Variants Influencing Glycemic Traits Define an Effector Transcript at the G6PC2-ABCB11 Locus A Mahajan, X Sim, HJ Ng, A Manning, MA Rivas, HM Highland, AE Locke, ... PLoS genetics 11 (1), e1004876, 2015	121	2015
Human-specific tandem repeat expansion and differential gene expression during primate evolution A Sulovari, R Li, PA Audano, D Porubsky, MR Vollger, GA Logsdon, ... Proceedings of the national academy of sciences 116 (46), 23243-23253, 2019	113	2019
Prosaposin is a regulator of progranulin levels and oligomerization AM Nicholson, NCA Finch, M Almeida, RB Perkerson, M Van Blitterswijk, ... Nature communications 7 (1), 11992, 2016	85	2016
Data for Genetic Analysis Workshop 18: human whole genome sequence, blood pressure, and simulated phenotypes in extended pedigrees L Almasy, TD Dyer, JM Peralta, G Jun, AR Wood, C Fuchsberger, ... BMC proceedings 8, 1-9, 2014	83*	2014
Parliament2: Accurate structural variant calling at scale S Zarate, A Carroll, M Mahmoud, O Krasheninina, G Jun, WJ Salerno, ... GigaScience 9 (12), giaa145, 2020	72	2020

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