| Year |
Citation |
Score |
| 2024 |
Lincoln MR, Connally N, Axisa PP, Gasperi C, Mitrovic M, van Heel D, Wijmenga C, Withoff S, Jonkers IH, Padyukov L, Rich SS, Graham RR, Gaffney PM, Langefeld CD, Vyse TJ, ... ... Chun S, et al. Genetic mapping across autoimmune diseases reveals shared associations and mechanisms. Nature Genetics. 56: 838-845. PMID 38741015 DOI: 10.1038/s41588-024-01732-8 |
0.322 |
|
| 2022 |
Chun S, Akle S, Teodosiadis A, Cade BE, Wang H, Sofer T, Evans DS, Stone KL, Gharib SA, Mukherjee S, Palmer LJ, Hillman D, Rotter JI, Hanis CL, Stamatoyannopoulos JA, et al. Leveraging pleiotropy to discover and interpret GWAS results for sleep-associated traits. Plos Genetics. 18: e1010557. PMID 36574455 DOI: 10.1371/journal.pgen.1010557 |
0.351 |
|
| 2022 |
Connally NJ, Nazeen S, Lee D, Shi H, Stamatoyannopoulos J, Chun S, Cotsapas C, Cassa CA, Sunyaev SR. The missing link between genetic association and regulatory function. Elife. 11. PMID 36515579 DOI: 10.7554/eLife.74970 |
0.341 |
|
| 2022 |
Hecker J, Chun S, Samiei A, Liu C, Laurie C, Kachroo P, Lutz SM, Lee S, Smith AV, Lasky-Su J, Cho MH, Sharma S, Quirós MES, Avila L, Celedón JC, et al. FGF20 and PGM2 variants are associated with childhood asthma in family-based whole-genome sequencing studies. Human Molecular Genetics. PMID 36255742 DOI: 10.1093/hmg/ddac258 |
0.339 |
|
| 2021 |
Gasperi C, Chun S, Sunyaev SR, Cotsapas C. Shared associations identify causal relationships between gene expression and immune cell phenotypes. Communications Biology. 4: 279. PMID 33664438 DOI: 10.1038/s42003-021-01823-w |
0.338 |
|
| 2020 |
Chun S, Imakaev M, Hui D, Patsopoulos NA, Neale BM, Kathiresan S, Stitziel NO, Sunyaev SR. Non-parametric Polygenic Risk Prediction via Partitioned GWAS Summary Statistics. American Journal of Human Genetics. PMID 32470373 DOI: 10.1016/J.Ajhg.2020.05.004 |
0.393 |
|
| 2017 |
Chen H, Cade BE, Gleason KJ, Bjonnes AC, Stilp AM, Sofer T, Conomos MP, Ancoli-Israel S, Arens R, Azarbarzin A, Bell GI, Below JE, Chun S, Evans DS, Ewert R, et al. Multi-ethnic Meta-analysis Identifies RAI1 as a Possible Obstructive Sleep Apnea Related Quantitative Trait Locus in Men. American Journal of Respiratory Cell and Molecular Biology. PMID 29077507 DOI: 10.1165/Rcmb.2017-0237Oc |
0.378 |
|
| 2017 |
Chun S, Casparino A, Patsopoulos NA, Croteau-Chonka DC, Raby BA, De Jager PL, Sunyaev SR, Cotsapas C. Limited statistical evidence for shared genetic effects of eQTLs and autoimmune-disease-associated loci in three major immune-cell types. Nature Genetics. PMID 28218759 DOI: 10.1038/Ng.3795 |
0.429 |
|
| 2016 |
Cade BE, Chen H, Stilp AM, Gleason KJ, Sofer T, Ancoli-Israel S, Arens R, Bell GI, Below JE, Bjonnes AC, Chun S, Conomos MP, Evans DS, Johnson WC, Frazier-Wood AC, et al. Genetic Associations with Obstructive Sleep Apnea Traits in Hispanic/Latino Americans. American Journal of Respiratory and Critical Care Medicine. PMID 26977737 DOI: 10.1164/Rccm.201512-2431Oc |
0.315 |
|
| 2016 |
Savova V, Chun S, Sohail M, McCole RB, Witwicki R, Gai L, Lenz TL, Wu CT, Sunyaev SR, Gimelbrant AA. Genes with monoallelic expression contribute disproportionately to genetic diversity in humans. Nature Genetics. PMID 26808112 DOI: 10.1038/Ng.3493 |
0.436 |
|
| 2015 |
Cassa CA, Smith SE, Docken W, Hoffman E, McLaughlin H, Chun S, Leshchiner I, Miraoui H, Raychaudhuri S, Frank NY, Wilson BJ, Sunyaev SR, Maas RL, Vuzman D. An argument for early genomic sequencing in atypical cases: a WISP3 variant leads to diagnosis of progressive pseudorheumatoid arthropathy of childhood. Rheumatology (Oxford, England). PMID 26493744 DOI: 10.1093/Rheumatology/Kev367 |
0.38 |
|
| 2015 |
Akle S, Chun S, Jordan DM, Cassa CA. Mitigating False-Positive Associations in Rare Disease Gene Discovery. Human Mutation. 36: 998-1003. PMID 26378430 DOI: 10.1002/Humu.22847 |
0.414 |
|
| 2015 |
Nikolskiy I, Conrad DF, Chun S, Fay JC, Cheverud JM, Lawson HA. Using whole-genome sequences of the LG/J and SM/J inbred mouse strains to prioritize quantitative trait genes and nucleotides. Bmc Genomics. 16: 415. PMID 26016481 DOI: 10.1186/S12864-015-1592-3 |
0.579 |
|
| 2015 |
Francioli LC, Polak PP, Koren A, Menelaou A, Chun S, Renkens I, van Duijn CM, Swertz M, Wijmenga C, van Ommen G, Slagboom PE, Boomsma DI, Ye K, Guryev V, et al. Genome-wide patterns and properties of de novo mutations in humans. Nature Genetics. PMID 25985141 DOI: 10.1038/Ng.3292 |
0.442 |
|
| 2014 |
Yim HS, Cho YS, Guang X, Kang SG, Jeong JY, Cha SS, Oh HM, Lee JH, Yang EC, Kwon KK, Kim YJ, Kim TW, Kim W, Jeon JH, Kim SJ, ... ... Chun S, et al. Minke whale genome and aquatic adaptation in cetaceans. Nature Genetics. 46: 88-92. PMID 24270359 DOI: 10.1038/Ng.2835 |
0.434 |
|
| 2013 |
Chun S, Plunkett J, Teramo K, Muglia LJ, Fay JC. Fine-mapping an association of FSHR with preterm birth in a Finnish population. Plos One. 8: e78032. PMID 24205076 DOI: 10.1371/Journal.Pone.0078032 |
0.538 |
|
| 2011 |
Chun S, Fay JC. Evidence for hitchhiking of deleterious mutations within the human genome. Plos Genetics. 7: e1002240. PMID 21901107 DOI: 10.1371/Journal.Pgen.1002240 |
0.579 |
|
| 2009 |
Chun S, Fay JC. Identification of deleterious mutations within three human genomes. Genome Research. 19: 1553-61. PMID 19602639 DOI: 10.1101/Gr.092619.109 |
0.571 |
|
| 2009 |
Matkovich SJ, Druley TE, Van Booven DJ, Chun S, Vallania FM, Hindes A, Fay JC, Mitra RD, Dorn II GW. Genetic Diversity and Novel SNP Discovery in Signaling Genes Revealed by Pooled Sequencing of Cardiomyopathy DNAs Journal of Cardiac Failure. 15: S40. DOI: 10.1016/J.Cardfail.2009.06.297 |
0.548 |
|
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