| Exome sequencing of Finnish isolates enhances rare-variant association power AE Locke, KM Steinberg, CWK Chiang, SK Service, AS Havulinna, L Stell, ... Nature 572 (7769), 323-328, 2019 | 161 | 2019 |
| IRF6 mutation screening in non‐syndromic orofacial clefting: analysis of 1521 families EJ Leslie, DC Koboldt, CJ Kang, L Ma, JT Hecht, GL Wehby, ... Clinical genetics 90 (1), 28-34, 2016 | 62 | 2016 |
| SVEP1 is a human coronary artery disease locus that promotes atherosclerosis IH Jung, JS Elenbaas, A Alisio, K Santana, EP Young, CJ Kang, ... Science translational medicine 13 (586), eabe0357, 2021 | 33 | 2021 |
| Association of structural variation with cardiometabolic traits in Finns L Chen, HJ Abel, I Das, DE Larson, L Ganel, KL Kanchi, AA Regier, ... The American Journal of Human Genetics 108 (4), 583-596, 2021 | 26 | 2021 |
| Mitochondrial genome copy number measured by DNA sequencing in human blood is strongly associated with metabolic traits via cell-type composition differences L Ganel, L Chen, R Christ, J Vangipurapu, E Young, I Das, K Kanchi, ... Human genomics 15 (1), 34, 2021 | 13 | 2021 |
| Inference of population mutation rate and detection of segregating sites from next-generation sequence data CJ Kang, P Marjoram Genetics 189 (2), 595-605, 2011 | 9 | 2011 |
| SVEP1 is an endogenous ligand for the orphan receptor PEAR1 JS Elenbaas, U Pudupakkam, KJ Ashworth, CJ Kang, V Patel, K Santana, ... Nature communications 14 (1), 850, 2023 | 8 | 2023 |
| A sample selection strategy for next‐generation sequencing CJ Kang, P Marjoram Genetic epidemiology 36 (7), 696-709, 2012 | 8 | 2012 |
| ANGPTL3 deficiency and risk of hepatic steatosis L D’Erasmo, M Di Martino, T Neufeld, TJ Fraum, CJ Kang, KH Burks, ... Circulation 148 (19), 1479-1489, 2023 | 5 | 2023 |
| The full likelihood approach for inferring variation of recombination rate using a Markov chain Monte Carlo method with a hidden Markov model CJ Kang University of Washington, 2008 | 3 | 2008 |
| Mitochondrial genome copy number in human blood-derived DNA is strongly associated with insulin levels and related metabolic traits and primarily reflects cell-type composition … L Ganel, L Chen, R Christ, J Vangipurapu, E Young, I Das, K Kanchi, ... MedRxiv, 2020.10. 23.20218586, 2020 | 1 | 2020 |
| Exome sequencing identifies high-impact trait-associated alleles enriched in Finns AE Locke, K Meltz Steinberg, CWK Chiang, SK Service, AS Havulinna, ... bioRxiv, 464255, 2018 | 1 | 2018 |
| Exact coalescent simulation of new haplotype data from existing reference haplotypes CJ Kang, P Marjoram Bioinformatics 28 (6), 838-844, 2012 | 1 | 2012 |
| Methods for detecting associations between phenotype and aggregations of rare variants F Yang, CJ Kang, P Marjoram BMC proceedings 5, 1-12, 2011 | 1 | 2011 |
| The Cardiometabolic Disease Risk Protein SVEP1 Activates AKT/mTOR By Signaling Through The Orphan Receptor PEAR1 JS Elenbaas, U Pudupakkam, V Patel, K Ashworth, CJ Kang, IH Jung, ... Arteriosclerosis, Thrombosis, and Vascular Biology 42 (Suppl_1), A496-A496, 2022 | | 2022 |
| SVEP1, a novel human coronary artery disease locus, promotes atherosclerosis IH Jung, JS Elenbaas, A Alisio, K Santana, EP Young, CJ Kang, ... bioRxiv, 2020.06. 15.151027, 2020 | | 2020 |
