Sung Chun
Sung Chun
Division of Pulmonary Medicine, Boston Children's Hospital
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Cited by
Cited by
Identification of deleterious mutations within three human genomes
S Chun, JC Fay
Genome research 19 (9), 1553-1561, 2009
Genome-wide patterns and properties of de novo mutations in humans
LC Francioli, PP Polak, A Koren, A Menelaou, S Chun, I Renkens, ...
Nature genetics 47 (7), 822-826, 2015
Minke whale genome and aquatic adaptation in cetaceans
HS Yim, YS Cho, X Guang, SG Kang, JY Jeong, SS Cha, HM Oh, JH Lee, ...
Nature genetics 46 (1), 88-92, 2014
Limited statistical evidence for shared genetic effects of eQTLs and autoimmune-disease-associated loci in three major immune-cell types
S Chun, A Casparino, NA Patsopoulos, DC Croteau-Chonka, BA Raby, ...
Nature Genetics 49 (4), 600-605, 2017
Genetic associations with obstructive sleep apnea traits in Hispanic/Latino Americans
BE Cade, H Chen, AM Stilp, KJ Gleason, T Sofer, S Ancoli-Israel, R Arens, ...
American journal of respiratory and critical care medicine 194 (7), 886-897, 2016
Evidence for hitchhiking of deleterious mutations within the human genome
S Chun, JC Fay
PLoS genetics 7 (8), e1002240, 2011
Genes with monoallelic expression contribute disproportionately to genetic diversity in humans
V Savova, S Chun, M Sohail, RB McCole, R Witwicki, L Gai, TL Lenz, ...
Nature genetics 48 (3), 231-237, 2016
Multiethnic Meta-Analysis Identifies RAI1 as a Possible Obstructive Sleep Apnea–related Quantitative Trait Locus in Men
H Chen, BE Cade, KJ Gleason, AC Bjonnes, AM Stilp, T Sofer, ...
American journal of respiratory cell and molecular biology 58 (3), 391-401, 2018
Using whole-genome sequences of the LG/J and SM/J inbred mouse strains to prioritize quantitative trait genes and nucleotides
I Nikolskiy, DF Conrad, S Chun, JC Fay, JM Cheverud, HA Lawson
BMC genomics 16 (1), 415, 2015
Mitigating False‐Positive Associations in Rare Disease Gene Discovery
S Akle, S Chun, DM Jordan, CA Cassa
Human mutation 36 (10), 998-1003, 2015
Fine-Mapping an Association of FSHR with Preterm Birth in a Finnish Population
S Chun, J Plunkett, K Teramo, LJ Muglia, JC Fay
PLOS ONE 8 (10), e78032, 2013
Non-parametric polygenic risk prediction via partitioned gwas summary statistics
S Chun, M Imakaev, D Hui, NA Patsopoulos, BM Neale, S Kathiresan, ...
The American Journal of Human Genetics 107 (1), 46-59, 2020
Non-parametric polygenic risk prediction using partitioned GWAS summary statistics
S Chun, M Imakaev, D Hui, NA Patsopoulos, BM Neale, S Kathiresan, ...
BioRxiv, 370064, 2020
An argument for early genomic sequencing in atypical cases: a WISP3 variant leads to diagnosis of progressive pseudorheumatoid arthropathy of childhood
CA Cassa, SE Smith, W Docken, E Hoffman, H McLaughlin, S Chun, ...
Rheumatology 55 (3), 586-589, 2016
Polygenic risk score validation using Korean genomes of 265 early-onset acute myocardial infarction patients and 636 healthy controls
Y Bhak, Y Jeon, S Jeon, C Yoon, M Kim, A Blazyte, Y Kim, Y Kang, C Kim, ...
PloS one 16 (2), e0246538, 2021
Leveraging pleiotropy to discover and interpret GWAS results for sleep-associated traits
S Akle, S Chun, A Teodosiadis, BE Cade, H Wang, T Sofer, DS Evans, ...
BioRxiv, 832162, 2019
Shared associations identify causal relationships between gene expression and immune cell phenotypes
C Gasperi, S Chun, SR Sunyaev, C Cotsapas
Communications Biology 4 (1), 1-11, 2021
Identification of Deleterious and Disease Alleles in a General Population and Preterm Labor Patients
SG Chun
Washington University in St. Louis, 2012
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