Goo Jun
Cited by
Cited by
A global reference for human genetic variation
1000 Genomes Project Consortium
Nature 526 (7571), 68, 2015
An integrated map of genetic variation from 1,092 human genomes
1000 Genomes Project Consortium
Nature 491 (7422), 56, 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
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
The genetic architecture of type 2 diabetes
C Fuchsberger, J Flannick, TM Teslovich, A Mahajan, V Agarwala, ...
Nature 536 (7614), 41-47, 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
Loss-of-function mutations in APOC3, triglycerides, and coronary disease
New England Journal of Medicine 371, 22-31, 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
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
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
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
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
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
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
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
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
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
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
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
Tracking and segmentation of highway vehicles in cluttered and crowded scenes
G Jun, JK Aggarwal, M Gokmen
2008 IEEE Workshop on Applications of Computer Vision, 1-6, 2008
The system can't perform the operation now. Try again later.
Articles 1–20