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Sek Won Kong

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Boston Children's Hospital

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Publications listed in Europe PMC (67)

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Altered microRNA expression in human heart disease.
Ikeda S, Kong SW, Lu J, Bisping E, Zhang H, Allen PD, Golub TR, Pieske B, Pu WT
Physiol Genomics, 31(3):367-373, 21 Aug 2007
Cited by: 402 articles | PMID: 17712037
Co-occupancy by multiple cardiac transcription factors identifies transcriptional enhancers active in heart.
He A, Kong SW, Ma Q, Pu WT
Proc Natl Acad Sci U S A, 108(14):5632-5637, 17 Mar 2011
Cited by: 254 articles | PMID: 21415370 | PMCID: PMC3078411
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The insulin-like growth factor 1 receptor induces physiological heart growth via the phosphoinositide 3-kinase(p110alpha) pathway.
McMullen JR, Shioi T, Huang WY, Zhang L, Tarnavski O, Bisping E, Schinke M, Kong S, Sherwood MC, Brown J, Riggi L, Kang PM, Izumo S
J Biol Chem, 279(6):4782-4793, 03 Nov 2003
Cited by: 254 articles | PMID: 14597618
MicroRNA-1 negatively regulates expression of the hypertrophy-associated calmodulin and Mef2a genes.
Ikeda S, He A, Kong SW, Lu J, Bejar R, Bodyak N, Lee KH, Ma Q, Kang PM, Golub TR, Pu WT
Mol Cell Biol, 29(8):2193-2204, 02 Feb 2009
Cited by: 250 articles | PMID: 19188439 | PMCID: PMC2663304
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Mouse cardiac surgery: comprehensive techniques for the generation of mouse models of human diseases and their application for genomic studies.
Tarnavski O, McMullen JR, Schinke M, Nie Q, Kong S, Izumo S
Physiol Genomics, 16(3):349-360, 13 Feb 2004
Cited by: 204 articles | PMID: 14679301
Type I interferon-inducible gene expression in blood is present and reflects disease activity in dermatomyositis and polymyositis.
Walsh RJ, Kong SW, Yao Y, Jallal B, Kiener PA, Pinkus JL, Beggs AH, Amato AA, Greenberg SA
Arthritis Rheum, 56(11):3784-3792, 01 Nov 2007
Cited by: 180 articles | PMID: 17968926 | PMCID: PMC2443782
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Polycomb repressive complex 2 regulates normal development of the mouse heart.
He A, Ma Q, Cao J, von Gise A, Zhou P, Xie H, Zhang B, Hsing M, Christodoulou DC, Cahan P, Daley GQ, Kong SW, Orkin SH, Seidman CE, Seidman JG, Pu WT
Circ Res, 110(3):406-415, 08 Dec 2011
Cited by: 131 articles | PMID: 22158708 | PMCID: PMC3282145
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Cytosolic 5'-nucleotidase 1A autoimmunity in sporadic inclusion body myositis.
Larman HB, Salajegheh M, Nazareno R, Lam T, Sauld J, Steen H, Kong SW, Pinkus JL, Amato AA, Elledge SJ, Greenberg SA
Ann Neurol, 73(3):408-418, 01 Mar 2013
Cited by: 128 articles | PMID: 23596012
Gata4 is required for maintenance of postnatal cardiac function and protection from pressure overload-induced heart failure.
Bisping E, Ikeda S, Kong SW, Tarnavski O, Bodyak N, McMullen JR, Rajagopal S, Son JK, Ma Q, Springer Z, Kang PM, Izumo S, Pu WT
Proc Natl Acad Sci U S A, 103(39):14471-14476, 18 Sep 2006
Cited by: 128 articles | PMID: 16983087 | PMCID: PMC1636702
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Development of heart valves requires Gata4 expression in endothelial-derived cells.
Rivera-Feliciano J, Lee KH, Kong SW, Rajagopal S, Ma Q, Springer Z, Izumo S, Tabin CJ, Pu WT
Development, 133(18):3607-3618, 16 Aug 2006
Cited by: 127 articles | PMID: 16914500 | PMCID: PMC2735081
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Network-based analysis of affected biological processes in type 2 diabetes models.
Liu M, Liberzon A, Kong SW, Lai WR, Park PJ, Kohane IS, Kasif S
PLoS Genet, 3(6):e96, 01 Jun 2007
Cited by: 110 articles | PMID: 17571924 | PMCID: PMC1904360
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Interferon-stimulated gene 15 (ISG15) conjugates proteins in dermatomyositis muscle with perifascicular atrophy.
Salajegheh M, Kong SW, Pinkus JL, Walsh RJ, Liao A, Nazareno R, Amato AA, Krastins B, Morehouse C, Higgs BW, Jallal B, Yao Y, Sarracino DA, Parker KC, Greenberg SA
Ann Neurol, 67(1):53-63, 01 Jan 2010
Cited by: 106 articles | PMID: 20186858 | PMCID: PMC2875060
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The MedSeq Project: a randomized trial of integrating whole genome sequencing into clinical medicine.
Vassy JL, Lautenbach DM, McLaughlin HM, Kong SW, Christensen KD, Krier J, Kohane IS, Feuerman LZ, Blumenthal-Barby J, Roberts JS, Lehmann LS, Ho CY, Ubel PA, MacRae CA, Seidman CE, Murray MF, McGuire AL, Rehm HL, Green RC, MedSeq Project
Trials, 15:85, 20 Mar 2014
Cited by: 96 articles | PMID: 24645908 | PMCID: PMC4113228
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Characteristics and predictive value of blood transcriptome signature in males with autism spectrum disorders.
Kong SW, Collins CD, Shimizu-Motohashi Y, Holm IA, Campbell MG, Lee IH, Brewster SJ, Hanson E, Harris HK, Lowe KR, Saada A, Mora A, Madison K, Hundley R, Egan J, McCarthy J, Eran A, Galdzicki M, Rappaport L, [...] Kohane IS
PLoS One, 7(12):e49475, 05 Dec 2012
Cited by: 96 articles | PMID: 23227143 | PMCID: PMC3515554
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Heart failure-associated changes in RNA splicing of sarcomere genes.
Kong SW, Hu YW, Ho JW, Ikeda S, Polster S, John R, Hall JL, Bisping E, Pieske B, dos Remedios CG, Pu WT
Circ Cardiovasc Genet, 3(2):138-146, 02 Feb 2010
Cited by: 96 articles | PMID: 20124440 | PMCID: PMC3073230
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Genetic expression profiles during physiological and pathological cardiac hypertrophy and heart failure in rats.
Kong SW, Bodyak N, Yue P, Liu Z, Brown J, Izumo S, Kang PM
Physiol Genomics, 21(1):34-42, 28 Dec 2004
Cited by: 81 articles | PMID: 15623566
A multivariate approach for integrating genome-wide expression data and biological knowledge.
Kong SW, Pu WT, Park PJ
Bioinformatics, 22(19):2373-2380, 28 Jul 2006
Cited by: 79 articles | PMID: 16877751 | PMCID: PMC2813864
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Taxonomizing, sizing, and overcoming the incidentalome.
Kohane IS, Hsing M, Kong SW
Genet Med, 14(4):399-404, 09 Feb 2012
Cited by: 78 articles | PMID: 22323072 | PMCID: PMC3821385
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Relationship between disease activity and type 1 interferon- and other cytokine-inducible gene expression in blood in dermatomyositis and polymyositis.
Greenberg SA, Higgs BW, Morehouse C, Walsh RJ, Kong SW, Brohawn P, Zhu W, Amato A, Salajegheh M, White B, Kiener PA, Jallal B, Yao Y
Genes Immun, 13(3):207-213, 01 Sep 2011
Cited by: 74 articles | PMID: 21881594
Pluripotent stem cell-based therapy for Parkinson's disease: Current status and future prospects.
Sonntag KC, Song B, Lee N, Jung JH, Cha Y, Leblanc P, Neff C, Kong SW, Carter BS, Schweitzer J, Kim KS
Prog Neurobiol, 168:1-20, 11 Apr 2018
Cited by: 59 articles | PMID: 29653250 | PMCID: PMC6077089
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Mitf is a master regulator of the v-ATPase, forming a control module for cellular homeostasis with v-ATPase and TORC1.
Zhang T, Zhou Q, Ogmundsdottir MH, Möller K, Siddaway R, Larue L, Hsing M, Kong SW, Goding CR, Palsson A, Steingrimsson E, Pignoni F
J Cell Sci, 128(15):2938-2950, 19 Jun 2015
Cited by: 53 articles | PMID: 26092939 | PMCID: PMC4540953
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Fog2 is critical for cardiac function and maintenance of coronary vasculature in the adult mouse heart.
Zhou B, Ma Q, Kong SW, Hu Y, Campbell PH, McGowan FX, Ackerman KG, Wu B, Zhou B, Tevosian SG, Pu WT
J Clin Invest, 119(6):1462-1476, 01 Jun 2009
Cited by: 53 articles | PMID: 19411759 | PMCID: PMC2689123
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Integrative analysis reveals the direct and indirect interactions between DNA copy number aberrations and gene expression changes.
Lee H, Kong SW, Park PJ
Bioinformatics, 24(7):889-896, 08 Feb 2008
Cited by: 49 articles | PMID: 18263644 | PMCID: PMC2600603
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Absence of evidence for increase in risk for autism or attention-deficit hyperactivity disorder following antidepressant exposure during pregnancy: a replication study.
Castro VM, Kong SW, Clements CC, Brady R, Kaimal AJ, Doyle AE, Robinson EB, Churchill SE, Kohane IS, Perlis RH
Transl Psychiatry, 6:e708, 05 Jan 2016
Cited by: 46 articles | PMID: 26731445 | PMCID: PMC5068870
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Comparative analysis of whole-genome sequencing pipelines to minimize false negative findings.
Hwang KB, Lee IH, Li H, Won DG, Hernandez-Ferrer C, Negron JA, Kong SW
Sci Rep, 9(1):3219, 01 Mar 2019
Cited by: 41 articles | PMID: 30824715 | PMCID: PMC6397176
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Blood transcriptomic comparison of individuals with and without autism spectrum disorder: A combined-samples mega-analysis.
Tylee DS, Hess JL, Quinn TP, Barve R, Huang H, Zhang-James Y, Chang J, Stamova BS, Sharp FR, Hertz-Picciotto I, Faraone SV, Kong SW, Glatt SJ
Am J Med Genet B Neuropsychiatr Genet, 174(3):181-201, 11 Nov 2016
Cited by: 37 articles | PMID: 27862943 | PMCID: PMC5499528
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Measuring coverage and accuracy of whole-exome sequencing in clinical context.
Kong SW, Lee IH, Liu X, Hirschhorn JN, Mandl KD
Genet Med, 20(12):1617-1626, 12 Apr 2018
Cited by: 32 articles | PMID: 29789557 | PMCID: PMC6185824
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CompleteMOTIFs: DNA motif discovery platform for transcription factor binding experiments.
Kuttippurathu L, Hsing M, Liu Y, Schmidt B, Maskell DL, Lee K, He A, Pu WT, Kong SW
Bioinformatics, 27(5):715-717, 23 Dec 2010
Cited by: 32 articles | PMID: 21183585 | PMCID: PMC3105477
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Fast-twitch sarcomeric and glycolytic enzyme protein loss in inclusion body myositis.
Parker KC, Kong SW, Walsh RJ, Bch, Salajegheh M, Moghadaszadeh B, Amato AA, Nazareno R, Lin YY, Krastins B, Sarracino DA, Beggs AH, Pinkus JL, Greenberg SA
Muscle Nerve, 39(6):739-753, 01 Jun 2009
Cited by: 31 articles | PMID: 19291799 | PMCID: PMC2753483
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Co-inhibitory T cell receptor KLRG1: human cancer expression and efficacy of neutralization in murine cancer models.
Greenberg SA, Kong SW, Thompson E, Gulla SV
Oncotarget, 10(14):1399-1406, 15 Feb 2019
Cited by: 28 articles | PMID: 30858925 | PMCID: PMC6402715
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Peripheral blood gene expression signature differentiates children with autism from unaffected siblings.
Kong SW, Shimizu-Motohashi Y, Campbell MG, Lee IH, Collins CD, Brewster SJ, Holm IA, Rappaport L, Kohane IS, Kunkel LM
Neurogenetics, 14(2):143-152, 28 Apr 2013
Cited by: 27 articles | PMID: 23625158 | PMCID: PMC3686296
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Analysis of the Otd-dependent transcriptome supports the evolutionary conservation of CRX/OTX/OTD functions in flies and vertebrates.
Ranade SS, Yang-Zhou D, Kong SW, McDonald EC, Cook TA, Pignoni F
Dev Biol, 315(2):521-534, 31 Jan 2008
Cited by: 26 articles | PMID: 18241855 | PMCID: PMC2329912
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Summarizing polygenic risks for complex diseases in a clinical whole-genome report.
Kong SW, Lee IH, Leshchiner I, Krier J, Kraft P, Rehm HL, Green RC, Kohane IS, MacRae CA, MedSeq Project
Genet Med, 17(7):536-544, 23 Oct 2014
Cited by: 24 articles | PMID: 25341114 | PMCID: PMC4547452
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The Genomics Research and Innovation Network: creating an interoperable, federated, genomics learning system.
Mandl KD, Glauser T, Krantz ID, Avillach P, Bartels A, Beggs AH, Biswas S, Bourgeois FT, Corsmo J, Dauber A, Devkota B, Fleisher GR, Heath AP, Helbig I, Hirschhorn JN, Kilbourn J, Kong SW, Kornetsky S, Majzoub JA, [...] Genomics Research and Innovation Network
Genet Med, 22(2):371-380, 04 Sep 2019
Cited by: 22 articles | PMID: 31481752 | PMCID: PMC7000325
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I148M variant in PNPLA3 reduces central adiposity and metabolic disease risks while increasing nonalcoholic fatty liver disease.
Park JH, Cho B, Kwon H, Prilutsky D, Yun JM, Choi HC, Hwang KB, Lee IH, Kim JI, Kong SW
Liver Int, 35(12):2537-2546, 23 Jul 2015
Cited by: 21 articles | PMID: 26148225
Two macrophages, osteoclasts and microglia: from development to pleiotropy.
Lee JW, Lee IH, Iimura T, Kong SW
Bone Res, 9(1):11, 10 Feb 2021
Cited by: 20 articles | PMID: 33568650 | PMCID: PMC7875961
Review
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ksRepo: a generalized platform for computational drug repositioning.
Brown AS, Kong SW, Kohane IS, Patel CJ
BMC Bioinformatics, 17:78, 09 Feb 2016
Cited by: 19 articles | PMID: 26860211 | PMCID: PMC4746802
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Prioritizing disease-linked variants, genes, and pathways with an interactive whole-genome analysis pipeline.
Lee IH, Lee K, Hsing M, Choe Y, Park JH, Kim SH, Bohn JM, Neu MB, Hwang KB, Green RC, Kohane IS, Kong SW
Hum Mutat, 35(5):537-547, 06 Mar 2014
Cited by: 18 articles | PMID: 24478219 | PMCID: PMC4130156
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Pathway-based outlier method reveals heterogeneous genomic structure of autism in blood transcriptome.
Campbell MG, Kohane IS, Kong SW
BMC Med Genomics, 6:34, 24 Sep 2013
Cited by: 18 articles | PMID: 24063311 | PMCID: PMC3849321
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Development of the Precision Link Biobank at Boston Children's Hospital: Challenges and Opportunities.
Bourgeois FT, Avillach P, Kong SW, Heinz MM, Tran TA, Chakrabarty R, Bickel J, Sliz P, Borglund EM, Kornetsky S, Mandl KD
J Pers Med, 7(4):E21, 15 Dec 2017
Cited by: 15 articles | PMID: 29244735 | PMCID: PMC5748633
Review
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Altered vulnerability to asthma at various levels of ambient Benzo[a]Pyrene by CTLA4, STAT4 and CYP2E1 polymorphisms.
Choi H, Tabashidze N, Rossner P, Dostal M, Pastorkova A, Kong SW, Gmuender H, Sram RJ
Environ Pollut, 231(pt 1):1134-1144, 12 Aug 2017
Cited by: 14 articles | PMID: 28807506
Divergent dysregulation of gene expression in murine models of fragile X syndrome and tuberous sclerosis.
Kong SW, Sahin M, Collins CD, Wertz MH, Campbell MG, Leech JD, Krueger D, Bear MF, Kunkel LM, Kohane IS
Mol Autism, 5(1):16, 24 Feb 2014
Cited by: 14 articles | PMID: 24564913 | PMCID: PMC3940253
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Integration of heterogeneous expression data sets extends the role of the retinol pathway in diabetes and insulin resistance.
Park PJ, Kong SW, Tebaldi T, Lai WR, Kasif S, Kohane IS
Bioinformatics, 25(23):3121-3127, 28 Sep 2009
Cited by: 14 articles | PMID: 19786482 | PMCID: PMC2778339
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Gene expression analysis in Fmr1KO mice identifies an immunological signature in brain tissue and mGluR5-related signaling in primary neuronal cultures.
Prilutsky D, Kho AT, Palmer NP, Bhakar AL, Smedemark-Margulies N, Kong SW, Margulies DM, Bear MF, Kohane IS
Mol Autism, 6:66, 21 Dec 2015
Cited by: 11 articles | PMID: 26697163 | PMCID: PMC4687343
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DEPTOR modulates activation responses in CD4⁺ T cells and enhances immunoregulation following transplantation.
Wedel J, Bruneau S, Liu K, Kong SW, Sage PT, Sabatini DM, Laplante M, Briscoe DM
Am J Transplant, 19(1):77-88, 17 Aug 2018
Cited by: 10 articles | PMID: 29969188 | PMCID: PMC6310634
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Comprehensive Analysis of Tissue-wide Gene Expression and Phenotype Data Reveals Tissues Affected in Rare Genetic Disorders.
Feiglin A, Allen BK, Kohane IS, Kong SW
Cell Syst, 5(2):140-148.e2, 16 Aug 2017
Cited by: 10 articles | PMID: 28822752 | PMCID: PMC5928498
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Learning a Comorbidity-Driven Taxonomy of Pediatric Pulmonary Hypertension.
Ong MS, Mullen MP, Austin ED, Szolovits P, Natter MD, Geva A, Cai T, Kong SW, Mandl KD
Circ Res, 121(4):341-353, 13 Jun 2017
Cited by: 9 articles | PMID: 28611076 | PMCID: PMC5559726
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A model-driven methodology for exploring complex disease comorbidities applied to autism spectrum disorder and inflammatory bowel disease.
Somekh J, Peleg M, Eran A, Koren I, Feiglin A, Demishtein A, Shiloh R, Heiner M, Kong SW, Elazar Z, Kohane I
J Biomed Inform, 63:366-378, 10 Aug 2016
Cited by: 8 articles | PMID: 27522000 | PMCID: PMC5155638
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Solving for X: Evidence for sex-specific autism biomarkers across multiple transcriptomic studies.
Lee SC, Quinn TP, Lai J, Kong SW, Hertz-Picciotto I, Glatt SJ, Crowley TM, Venkatesh S, Nguyen T
Am J Med Genet B Neuropsychiatr Genet, 180(6):377-389, 06 Dec 2018
Cited by: 7 articles | PMID: 30520558 | PMCID: PMC6551334
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WEScover: selection between clinical whole exome sequencing and gene panel testing.
Lee IH, Lin Y, Alvarez WJ, Hernandez-Ferrer C, Mandl KD, Kong SW
BMC Bioinformatics, 22(1):259, 20 May 2021
Cited by: 5 articles | PMID: 34016036 | PMCID: PMC8139020
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Reducing false-positive incidental findings with ensemble genotyping and logistic regression based variant filtering methods.
Hwang KB, Lee IH, Park JH, Hambuch T, Choe Y, Kim M, Lee K, Song T, Neu MB, Gupta N, Kohane IS, Green RC, Kong SW
Hum Mutat, 35(8):936-944, 24 Jun 2014
Cited by: 5 articles | PMID: 24829188 | PMCID: PMC4112476
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Quantitative trait locus analysis for endophenotypes reveals genetic substrates of core symptom domains and neurocognitive function in autism spectrum disorder.
Lee IH, Koelliker E, Kong SW
Transl Psychiatry, 12(1):407, 24 Sep 2022
Cited by: 4 articles | PMID: 36153334 | PMCID: PMC9509384
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Plasma metabolomics of autism spectrum disorder and influence of shared components in proband families.
Chung MK, Smith MR, Lin Y, Walker DI, Jones D, Patel CJ, Kong SW
Exposome, 1(1):osab004, 07 Oct 2021
Cited by: 4 articles | PMID: 35028569 | PMCID: PMC8739333
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Association between Neuroligin-1 polymorphism and plasma glutamine levels in individuals with autism spectrum disorder.
Lee IH, Walker DI, Lin Y, Smith MR, Mandl KD, Jones DP, Kong SW
EBioMedicine, 95:104746, 04 Aug 2023
Cited by: 2 articles | PMID: 37544204 | PMCID: PMC10427990
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Inhibition of mevalonate metabolism by statins augments the immunoregulatory phenotype of vascular endothelial cells and inhibits the costimulation of CD4⁺ T cells.
Agur T, Wedel J, Bose S, Sahankumari AGP, Goodman D, Kong SW, Ghosh CC, Briscoe DM
Am J Transplant, 22(3):947-954, 08 Nov 2021
Cited by: 2 articles | PMID: 34687147
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T Cell-Specific Adaptor Protein Regulates Mitochondrial Function and CD4⁺ T Regulatory Cell Activity In Vivo following Transplantation.
Wedel J, Stack MP, Seto T, Sheehan MM, Flynn EA, Stillman IE, Kong SW, Liu K, Briscoe DM
J Immunol, 203(8):2328-2338, 20 Sep 2019
Cited by: 2 articles | PMID: 31541025 | PMCID: PMC6783373
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BrainGENIE: The Brain Gene Expression and Network Imputation Engine.
Hess JL, Quinn TP, Zhang C, Hearn GC, Chen S, Neuropsychiatric Consortium for Analysis and Sharing of Transcriptomes, Kong SW, Cairns M, Tsuang MT, Faraone SV, Glatt SJ
Transl Psychiatry, 13(1):98, 22 Mar 2023
Cited by: 1 article | PMID: 36949060 | PMCID: PMC10033657
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Evolution of multiple omics approaches to define pathophysiology of pediatric acute respiratory distress syndrome.
Whitney JE, Lee IH, Lee JW, Kong SW
Elife, 11:e77405, 01 Aug 2022
Cited by: 1 article | PMID: 35913450 | PMCID: PMC9342956
Review
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Increased Prevalence of Familial Autoimmune Disease in Children With Opsoclonus-Myoclonus Syndrome.
Santoro JD, Kerr LM, Codden R, Casper TC, Greenberg BM, Waubant E, Kong SW, Mandl KD, Gorman MP
Neurol Neuroimmunol Neuroinflamm, 8(6):e1079, 02 Sep 2021
Cited by: 1 article | PMID: 34475249 | PMCID: PMC8422990
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Statistical methods in cardiac gene expression profiling: from image to function.
Kong SW
Methods Mol Biol, 366:75-105, 01 Jan 2007
Cited by: 1 article | PMID: 17568120
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GSDMB/ORMDL3 Rare/Common Variants Are Associated with Inhaled Corticosteroid Response among Children with Asthma.
Voorhies K, Mohammed A, Chinthala L, Kong SW, Lee IH, Kho AT, McGeachie M, Mandl KD, Raby B, Hayes M, Davis RL, Wu AC, Lutz SM
Genes (Basel), 15(4):420, 28 Mar 2024
Cited by: 0 articles | PMID: 38674355 | PMCID: PMC11049905
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Neutrophil extracellular traps formation is associated with postoperative complications in neonates and infants undergoing congenital cardiac surgery
Maisat W, Hou L, Sandhu S, Sin Y, Kim S, Pelt HV, Chen Y, Emani S, Kong SW, Emani S, Ibla J, Yuki K
bioRxiv, 23 Dec 2023
Cited by: 0 articles | PPR: PPR778136
Preprint
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ADGR: Admixture-Informed Differential Gene Regulation.
Lee IH, Kong SW
Genes (Basel), 14(1):147, 05 Jan 2023
Cited by: 0 articles | PMID: 36672888 | PMCID: PMC9859415
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Endophenotype-Wide Association Study Reveals Genetic Substrates of Core Symptom Domains and Neurocognitive Function in Autism.
Lee I, Koelliker E, Kong SW
Research Square, 12 Oct 2021
Cited by: 0 articles | PPR: PPR407099
Preprint v1
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BrainGENIE: The Brain Gene Expression and Network Imputation Engine
Hess JL, Quinn TP, Zhang C, Hearn GC, Chen S, Neuropsychiatric Consortium for Analysis and Sharing of Transcriptomes, Kong SW, Cairns MJ, Cairns MJ, Tsuang MT, Faraone SV, Glatt SJ
bioRxiv, 27 Oct 2020
Cited by: 0 articles | PPR: PPR231292
Preprint
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Correction: The Genomics Research and Innovation Network: creating an interoperable, federated, genomics learning system.
Mandl KD, Glauser T, Krantz ID, Avillach P, Bartels A, Beggs AH, Biswas S, Bourgeois FT, Corsmo J, Dauber A, Devkota B, Fleisher GR, Heath AP, Helbig I, Hirschhorn JN, Kilbourn J, Kong SW, Kornetsky S, Majzoub JA, [...] Genomics Research and Innovation Network
Genet Med, 22(2):449, 01 Feb 2020
Cited by: 0 articles | PMID: 31772351 | PMCID: PMC7000329
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The Clinical Genome and Ancestry Report: An interactive web application for prioritizing clinically implicated variants from genome sequencing data with ancestry composition.
Lee IH, Negron JA, Hernandez-Ferrer C, Alvarez WJ, Mandl KD, Kong SW
Hum Mutat, 41(2):387-396, 15 Nov 2019
Cited by: 0 articles | PMID: 31691385 | PMCID: PMC7180092
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Sek Won Kong

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