Works by Hyun Min Kang

Results: 61
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    A sequence-based variation map of 8.27 million SNPs in inbred mouse strains.

    Published in:
    Nature, 2007, v. 448, n. 7157, p. 1050, doi. 10.1038/nature06067
    By:
    • Frazer, Kelly A.;
    • Eskin, Eleazar;
    • Hyun Min Kang;
    • Bogue, Molly A.;
    • Hinds, David A.;
    • Beilharz, Erica J.;
    • Gupta, Robert V.;
    • Montgomery, Julie;
    • Morenzoni, Matt M.;
    • Nilsen, Geoffrey B.;
    • Pethiyagoda, Charit L.;
    • Stuve, Laura L.;
    • Johnson, Frank M.;
    • Daly, Mark J.;
    • Wade, Claire M.;
    • Cox, David R.
    Publication type:
    Article
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    muCNV: genotyping structural variants for population-level sequencing.

    Published in:
    Bioinformatics, 2021, v. 37, n. 14/15, p. 2055, doi. 10.1093/bioinformatics/btab199
    By:
    • Jun, Goo;
    • Sedlazeck, Fritz;
    • Zhu, Qihui;
    • English, Adam;
    • Metcalf, Ginger;
    • Kang, Hyun Min;
    • (HGSVC), Human Genome Structural Variation Consortium;
    • Lee, Charles;
    • Gibbs, Richard;
    • Boerwinkle, Eric
    Publication type:
    Article
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    Nasal airway transcriptome-wide association study of asthma reveals genetically driven mucus pathobiology.

    Published in:
    Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-28973-7
    By:
    • Sajuthi, Satria P.;
    • Everman, Jamie L.;
    • Jackson, Nathan D.;
    • Saef, Benjamin;
    • Rios, Cydney L.;
    • Moore, Camille M.;
    • Mak, Angel C. Y.;
    • Eng, Celeste;
    • Fairbanks-Mahnke, Ana;
    • Salazar, Sandra;
    • Elhawary, Jennifer;
    • Huntsman, Scott;
    • Medina, Vivian;
    • Nickerson, Deborah A.;
    • Germer, Soren;
    • Zody, Michael C.;
    • Abecasis, Gonçalo;
    • Kang, Hyun Min;
    • Rice, Kenneth M.;
    • Kumar, Rajesh
    Publication type:
    Article
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    Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes.

    Published in:
    Nature Genetics, 2012, v. 44, n. 9, p. 981, doi. 10.1038/ng.2383
    By:
    • Morris, Andrew P;
    • Voight, Benjamin F;
    • Teslovich, Tanya M;
    • Ferreira, Teresa;
    • Segrè, Ayellet V;
    • Steinthorsdottir, Valgerdur;
    • Strawbridge, Rona J;
    • Khan, Hassan;
    • Grallert, Harald;
    • Mahajan, Anubha;
    • Prokopenko, Inga;
    • Kang, Hyun Min;
    • Dina, Christian;
    • Esko, Tonu;
    • Fraser, Ross M;
    • Kanoni, Stavroula;
    • Kumar, Ashish;
    • Lagou, Vasiliki;
    • Langenberg, Claudia;
    • Luan, Jian'an
    Publication type:
    Article
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    The Metabochip, a Custom Genotyping Array for Genetic Studies of Metabolic, Cardiovascular, and Anthropometric Traits.

    Published in:
    PLoS Genetics, 2012, v. 8, n. 8, p. 1, doi. 10.1371/journal.pgen.1002793
    By:
    • Voight, Benjamin F.;
    • Hyun Min Kang;
    • Ding, Jun;
    • Palmer, Cameron D.;
    • Sidore, Carlo;
    • Chines, Peter S.;
    • Burtt, Noël P.;
    • Fuchsberger, Christian;
    • Yanming Li;
    • Erdmann, Jeanette;
    • Frayling, Timothy M.;
    • Heid, Iris M.;
    • Jackson, Anne U.;
    • Johnson, Toby;
    • Kilpeläinen, Tuomas O.;
    • Lindgren, Ceciliam.;
    • Morris, Andrew P.;
    • Prokopenko, Inga;
    • Randall, Joshua C.;
    • Saxena, Richa
    Publication type:
    Article
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    Identification of CFTR variants in Latino patients with cystic fibrosis from the Dominican Republic and Puerto Rico.

    Published in:
    Pediatric Pulmonology, 2020, v. 55, n. 2, p. 533, doi. 10.1002/ppul.24549
    By:
    • Zeiger, Andrew M.;
    • McGarry, Meghan E.;
    • Mak, Angel C. Y.;
    • Medina, Vivian;
    • Salazar, Sandra;
    • Eng, Celeste;
    • Liu, Amy K.;
    • Oh, Sam S.;
    • Nuckton, Thomas J.;
    • Jain, Deepti;
    • Blackwell, Thomas W.;
    • Kang, Hyun Min;
    • Abecasis, Goncalo;
    • Oñate, Leandra Cordero;
    • Seibold, Max A.;
    • Burchard, Esteban G.;
    • Rodriguez‐Santana, Jose
    Publication type:
    Article
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    In search of rare variants: Preliminary results from whole genome sequencing of 1,325 individuals with psychophysiological endophenotypes.

    Published in:
    Psychophysiology, 2014, v. 51, n. 12, p. 1309, doi. 10.1111/psyp.12350
    By:
    • Vrieze, Scott I.;
    • Malone, Stephen M.;
    • Vaidyanathan, Uma;
    • Kwong, Alan;
    • Kang, Hyun Min;
    • Zhan, Xiaowei;
    • Flickinger, Matthew;
    • Irons, Daniel;
    • Jun, Goo;
    • Locke, Adam E.;
    • Pistis, Giorgio;
    • Porcu, Eleonora;
    • Levy, Shawn;
    • Myers, Richard M.;
    • Oetting, William;
    • McGue, Matt;
    • Abecasis, Goncalo;
    • Iacono, William G.
    Publication type:
    Article
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    Identification of a rare coding variant in complement 3 associated with age-related macular degeneration.

    Published in:
    Nature Genetics, 2013, v. 45, n. 11, p. 1375, doi. 10.1038/ng.2758
    By:
    • Zhan, Xiaowei;
    • Larson, David E;
    • Wang, Chaolong;
    • Koboldt, Daniel C;
    • Sergeev, Yuri V;
    • Fulton, Robert S;
    • Fulton, Lucinda L;
    • Fronick, Catrina C;
    • Branham, Kari E;
    • Bragg-Gresham, Jennifer;
    • Jun, Goo;
    • Hu, Youna;
    • Kang, Hyun Min;
    • Liu, Dajiang;
    • Othman, Mohammad;
    • Brooks, Matthew;
    • Ratnapriya, Rinki;
    • Boleda, Alexis;
    • Grassmann, Felix;
    • von Strachwitz, Claudia
    Publication type:
    Article
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    Nasal airway transcriptome-wide association study of asthma reveals genetically driven mucus pathobiology.

    Published in:
    Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-28973-7
    By:
    • Sajuthi, Satria P.;
    • Everman, Jamie L.;
    • Jackson, Nathan D.;
    • Saef, Benjamin;
    • Rios, Cydney L.;
    • Moore, Camille M.;
    • Mak, Angel C. Y.;
    • Eng, Celeste;
    • Fairbanks-Mahnke, Ana;
    • Salazar, Sandra;
    • Elhawary, Jennifer;
    • Huntsman, Scott;
    • Medina, Vivian;
    • Nickerson, Deborah A.;
    • Germer, Soren;
    • Zody, Michael C.;
    • Abecasis, Gonçalo;
    • Kang, Hyun Min;
    • Rice, Kenneth M.;
    • Kumar, Rajesh
    Publication type:
    Article
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    Author Correction: Nasal airway transcriptome-wide association study of asthma reveals genetically driven mucus pathobiology.

    Published in:
    Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-33097-z
    By:
    • Sajuthi, Satria P.;
    • Everman, Jamie L.;
    • Jackson, Nathan D.;
    • Saef, Benjamin;
    • Rios, Cydney L.;
    • Moore, Camille M.;
    • Mak, Angel C. Y.;
    • Eng, Celeste;
    • Fairbanks–Mahnke, Ana;
    • Salazar, Sandra;
    • Elhawary, Jennifer;
    • Huntsman, Scott;
    • Medina, Vivian;
    • Nickerson, Deborah A.;
    • Germer, Soren;
    • Zody, Michael C.;
    • Abecasis, Gonçalo;
    • Kang, Hyun Min;
    • Rice, Kenneth M.;
    • Kumar, Rajesh
    Publication type:
    Article
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    Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projects.

    Published in:
    Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-06159-4
    By:
    • Regier, Allison A.;
    • Farjoun, Yossi;
    • Larson, David E.;
    • Krasheninina, Olga;
    • Kang, Hyun Min;
    • Howrigan, Daniel P.;
    • Chen, Bo-Juen;
    • Kher, Manisha;
    • Banks, Eric;
    • Ames, Darren C.;
    • English, Adam C.;
    • Li, Heng;
    • Xing, Jinchuan;
    • Zhang, Yeting;
    • Matise, Tara;
    • Abecasis, Goncalo R.;
    • Salerno, Will;
    • Zody, Michael C.;
    • Neale, Benjamin M.;
    • Hall, Ira M.
    Publication type:
    Article
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    MEPE loss-of-function variant associates with decreased bone mineral density and increased fracture risk.

    Published in:
    Nature Communications, 2020, v. 11, n. 1, p. N.PAG, doi. 10.1038/s41467-020-17315-0
    By:
    • Surakka, Ida;
    • Fritsche, Lars G.;
    • Zhou, Wei;
    • Backman, Joshua;
    • Kosmicki, Jack A.;
    • Lu, Haocheng;
    • Brumpton, Ben;
    • Nielsen, Jonas B.;
    • Gabrielsen, Maiken E.;
    • Skogholt, Anne Heidi;
    • Wolford, Brooke;
    • Graham, Sarah E.;
    • Chen, Y. Eugene;
    • Lee, Seunggeun;
    • Kang, Hyun Min;
    • Langhammer, Arnulf;
    • Forsmo, Siri;
    • Åsvold, Bjørn O.;
    • Styrkarsdottir, Unnur;
    • Holm, Hilma
    Publication type:
    Article
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    Evaluation of the Metabochip Genotyping Array in African Americans and Implications for Fine Mapping of GWAS-Identified Loci: The PAGE Study.

    Published in:
    PLoS ONE, 2012, v. 7, n. 4, p. 1, doi. 10.1371/journal.pone.0035651
    By:
    • Buyske, Steven;
    • Ying Wu;
    • Carty, Cara L.;
    • Iona Cheng;
    • Assimes, Themistocles L.;
    • Dumitrescu, Logan;
    • Hindorff, Lucia A.;
    • Mitchell, Sabrina;
    • Ambite, Jose Luis;
    • Boerwinkle, Eric;
    • Buzkova, Petra;
    • Carlson, Chris S.;
    • Cochran, Barbara;
    • Duggan, David;
    • Eaton, Charles B.;
    • Fesinmeyer, Megan D.;
    • Franceschini, Nora;
    • Haessler, Jeffrey;
    • Jenny, Nancy;
    • Kang, Hyun Min
    Publication type:
    Article
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    Lung Function in African American Children with Asthma Is Associated with Novel Regulatory Variants of the KIT Ligand KITLG/SCF and Gene-By-Air-Pollution Interaction.

    Published in:
    Genetics, 2020, v. 215, n. 3, p. 869, doi. 10.1534/genetics.120.303231
    By:
    • Mak, Angel C. Y.;
    • Sajuthi, Satria;
    • Jaehyun Joo;
    • Shujie Xiao;
    • Sleiman, Patrick M.;
    • White, Marquitta J.;
    • Lee, Eunice Y.;
    • Saef, Benjamin;
    • Donglei Hu;
    • Hongsheng Gui;
    • Keys, Kevin L.;
    • Lurmann, Fred;
    • Jain, Deepti;
    • Abecasis, Gonçalo;
    • Hyun Min Kang;
    • Nickerson, Deborah A.;
    • Germer, Soren;
    • Zody, Michael C.;
    • Winterkorn, Lara;
    • Reeves, Catherine
    Publication type:
    Article