Hong-Hee Won

Hong-Hee Won

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Hong-Hee Won

Hong-Hee Won

Publications by authors named "Hong-Hee Won"

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Heritability estimates of individual psychological distress symptoms from genetic variation.

J Affect Disord 2019 Jun 8;252:413-420. Epub 2019 Apr 8.

Samsung Advanced Institute for Health Sciences and Technology (SAIHST), Sungkyunkwan University, Samsung Medical Center, Seoul, South Korea. Electronic address:

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http://dx.doi.org/10.1016/j.jad.2019.04.011DOI Listing
June 2019

Analysis of dementia-related gene variants in APOE ε4 noncarrying Korean patients with early-onset Alzheimer's disease.

Neurobiol Aging 2019 May 22. Epub 2019 May 22.

Department of Neurology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea; Neuroscience Center, Samsung Medical Center, Seoul, Republic of Korea; Samsung Alzheimer Research Center, Samsung Medical Center, Seoul, Korea; Department of Clinical Research Design and Evaluation, SAIHST, Sungkyunkwan University, Seoul, Republic of Korea. Electronic address:

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http://dx.doi.org/10.1016/j.neurobiolaging.2019.05.009DOI Listing
May 2019

No causal effects of serum urate levels on the risk of chronic kidney disease: A Mendelian randomization study.

PLoS Med 2019 01 15;16(1):e1002725. Epub 2019 Jan 15.

Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, New York, United States of America.

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http://dx.plos.org/10.1371/journal.pmed.1002725
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http://dx.doi.org/10.1371/journal.pmed.1002725DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6333326PMC
January 2019

The Association of Single-Nucleotide Polymorphisms in the MMP-9 Gene with Normal Tension Glaucoma and Primary Open-Angle Glaucoma.

Curr Eye Res 2018 04 4;43(4):534-538. Epub 2017 Dec 4.

c Department of Ophthalmology , Samsung Medical Center, Sungkyunkwan University School of Medicine , Seoul , Korea.

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https://www.tandfonline.com/doi/full/10.1080/02713683.2017.1
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http://dx.doi.org/10.1080/02713683.2017.1410177DOI Listing
April 2018

Burden of Intracranial Atherosclerosis Is Associated With Long-Term Vascular Outcome in Patients With Ischemic Stroke.

Stroke 2017 10 10;48(10):2819-2826. Epub 2017 Aug 10.

From the Department of Neurology, Bundang Jesaeng General Hospital, Seongnam, Korea (B.-S.K.); Department of Neurology, Samsung Medical Center (B.-S.K., O.Y.B., C.-S.C., K.H.L., G.-M.K) and Department of Neurology, Kangbuk Samsung Hospital (P.-W.C.), Sungkyunkwan University School of Medicine, Seoul, Korea; Department of Neurology, Chung-Ang University Hospital, Chung-Ang University College of Medicine, Seoul, Korea (K.-Y.P.); and Samsung Advanced Institute for Health Sciences and Technology, Sungkyunkwan University, Samsung Medical Center, Seoul, Korea (H.-H.W.).

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http://dx.doi.org/10.1161/STROKEAHA.117.017806DOI Listing
October 2017

NUDT15 genotype distributions in the Korean population.

Pharmacogenet Genomics 2017 05;27(5):197-200

Departments of aLaboratory Medicine and Genetics bPediatrics cInternal Medicine dClinical Pharmacology and Therapeutics eSamsung Advanced Institute for Health Sciences and Technology (SAIHST), Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea.

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http://dx.doi.org/10.1097/FPC.0000000000000274DOI Listing
May 2017

Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease.

Authors:
Thomas R Webb Jeanette Erdmann Kathleen E Stirrups Nathan O Stitziel Nicholas G D Masca Henning Jansen Stavroula Kanoni Christopher P Nelson Paola G Ferrario Inke R König John D Eicher Andrew D Johnson Stephen E Hamby Christer Betsholtz Arno Ruusalepp Oscar Franzén Eric E Schadt Johan L M Björkegren Peter E Weeke Paul L Auer Ursula M Schick Yingchang Lu He Zhang Marie-Pierre Dube Anuj Goel Martin Farrall Gina M Peloso Hong-Hee Won Ron Do Erik van Iperen Jochen Kruppa Anubha Mahajan Robert A Scott Christina Willenborg Peter S Braund Julian C van Capelleveen Alex S F Doney Louise A Donnelly Rosanna Asselta Pier A Merlini Stefano Duga Nicola Marziliano Josh C Denny Christian Shaffer Nour Eddine El-Mokhtari Andre Franke Stefanie Heilmann Christian Hengstenberg Per Hoffmann Oddgeir L Holmen Kristian Hveem Jan-Håkan Jansson Karl-Heinz Jöckel Thorsten Kessler Jennifer Kriebel Karl L Laugwitz Eirini Marouli Nicola Martinelli Mark I McCarthy Natalie R Van Zuydam Christa Meisinger Tõnu Esko Evelin Mihailov Stefan A Escher Maris Alver Susanne Moebus Andrew D Morris Jarma Virtamo Majid Nikpay Oliviero Olivieri Sylvie Provost Alaa AlQarawi Neil R Robertson Karen O Akinsansya Dermot F Reilly Thomas F Vogt Wu Yin Folkert W Asselbergs Charles Kooperberg Rebecca D Jackson Eli Stahl Martina Müller-Nurasyid Konstantin Strauch Tibor V Varga Melanie Waldenberger Lingyao Zeng Rajiv Chowdhury Veikko Salomaa Ian Ford J Wouter Jukema Philippe Amouyel Jukka Kontto Børge G Nordestgaard Jean Ferrières Danish Saleheen Naveed Sattar Praveen Surendran Aline Wagner Robin Young Joanna M M Howson Adam S Butterworth John Danesh Diego Ardissino Erwin P Bottinger Raimund Erbel Paul W Franks Domenico Girelli Alistair S Hall G Kees Hovingh Adnan Kastrati Wolfgang Lieb Thomas Meitinger William E Kraus Svati H Shah Ruth McPherson Marju Orho-Melander Olle Melander Andres Metspalu Colin N A Palmer Annette Peters Daniel J Rader Muredach P Reilly Ruth J F Loos Alex P Reiner Dan M Roden Jean-Claude Tardif John R Thompson Nicholas J Wareham Hugh Watkins Cristen J Willer Nilesh J Samani Heribert Schunkert Panos Deloukas Sekar Kathiresan

J Am Coll Cardiol 2017 Feb;69(7):823-836

Center for Human Genetic Research, Massachusetts General Hospital, Boston, Massachusetts; Cardiovascular Research Center, Massachusetts General Hospital, Boston, Massachusetts; Department of Medicine, Harvard Medical School, Boston, Massachusetts; Program in Medical and Population Genetics, Broad Institute, Cambridge, Massachusetts; Cardiology Division, Massachusetts General Hospital, Boston, Massachusetts.

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http://dx.doi.org/10.1016/j.jacc.2016.11.056DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5314135PMC
February 2017

No Association of Coronary Artery Disease with X-Chromosomal Variants in Comprehensive International Meta-Analysis.

Sci Rep 2016 10 12;6:35278. Epub 2016 Oct 12.

Institut für Medizinische Biometrie und Statistik, Universität zu Lübeck, Universitätsklinikum Schleswig-Holstein, Campus Lübeck, Lübeck, Germany.

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http://dx.doi.org/10.1038/srep35278DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5059659PMC
October 2016

Analysis of protein-coding genetic variation in 60,706 humans.

Nature 2016 08;536(7616):285-91

Analytic and Translational Genetics Unit, Massachusetts General Hospital, Boston, Massachusetts 02114, USA.

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http://www.nature.com/articles/nature19057
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http://dx.doi.org/10.1038/nature19057DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5018207PMC
August 2016

Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease.

Authors:
Nathan O Stitziel Kathleen E Stirrups Nicholas G D Masca Jeanette Erdmann Paola G Ferrario Inke R König Peter E Weeke Thomas R Webb Paul L Auer Ursula M Schick Yingchang Lu He Zhang Marie-Pierre Dube Anuj Goel Martin Farrall Gina M Peloso Hong-Hee Won Ron Do Erik van Iperen Stavroula Kanoni Jochen Kruppa Anubha Mahajan Robert A Scott Christina Willenberg Peter S Braund Julian C van Capelleveen Alex S F Doney Louise A Donnelly Rosanna Asselta Piera A Merlini Stefano Duga Nicola Marziliano Josh C Denny Christian M Shaffer Nour Eddine El-Mokhtari Andre Franke Omri Gottesman Stefanie Heilmann Christian Hengstenberg Per Hoffman Oddgeir L Holmen Kristian Hveem Jan-Håkan Jansson Karl-Heinz Jöckel Thorsten Kessler Jennifer Kriebel Karl L Laugwitz Eirini Marouli Nicola Martinelli Mark I McCarthy Natalie R Van Zuydam Christa Meisinger Tõnu Esko Evelin Mihailov Stefan A Escher Maris Alver Susanne Moebus Andrew D Morris Martina Müller-Nurasyid Majid Nikpay Oliviero Olivieri Louis-Philippe Lemieux Perreault Alaa AlQarawi Neil R Robertson Karen O Akinsanya Dermot F Reilly Thomas F Vogt Wu Yin Folkert W Asselbergs Charles Kooperberg Rebecca D Jackson Eli Stahl Konstantin Strauch Tibor V Varga Melanie Waldenberger Lingyao Zeng Aldi T Kraja Chunyu Liu George B Ehret Christopher Newton-Cheh Daniel I Chasman Rajiv Chowdhury Marco Ferrario Ian Ford J Wouter Jukema Frank Kee Kari Kuulasmaa Børge G Nordestgaard Markus Perola Danish Saleheen Naveed Sattar Praveen Surendran David Tregouet Robin Young Joanna M M Howson Adam S Butterworth John Danesh Diego Ardissino Erwin P Bottinger Raimund Erbel Paul W Franks Domenico Girelli Alistair S Hall G Kees Hovingh Adnan Kastrati Wolfgang Lieb Thomas Meitinger William E Kraus Svati H Shah Ruth McPherson Marju Orho-Melander Olle Melander Andres Metspalu Colin N A Palmer Annette Peters Daniel Rader Muredach P Reilly Ruth J F Loos Alex P Reiner Dan M Roden Jean-Claude Tardif John R Thompson Nicholas J Wareham Hugh Watkins Cristen J Willer Sekkar Kathiresan Panos Deloukas Nilesh J Samani Heribert Schunkert

N Engl J Med 2016 03 2;374(12):1134-44. Epub 2016 Mar 2.

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http://dx.doi.org/10.1056/NEJMoa1507652DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4850838PMC
March 2016

The association of single nucleotide polymorphisms in the connective tissue growth factor gene with pseudoexfoliation syndrome/glaucoma.

Acta Ophthalmol 2015 Dec 3;93(8):e682-3. Epub 2015 Apr 3.

Department of Ophthalmology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.

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http://dx.doi.org/10.1111/aos.12719DOI Listing
December 2015

A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease.

Authors:
Majid Nikpay Anuj Goel Hong-Hee Won Leanne M Hall Christina Willenborg Stavroula Kanoni Danish Saleheen Theodosios Kyriakou Christopher P Nelson Jemma C Hopewell Thomas R Webb Lingyao Zeng Abbas Dehghan Maris Alver Sebastian M Armasu Kirsi Auro Andrew Bjonnes Daniel I Chasman Shufeng Chen Ian Ford Nora Franceschini Christian Gieger Christopher Grace Stefan Gustafsson Jie Huang Shih-Jen Hwang Yun Kyoung Kim Marcus E Kleber King Wai Lau Xiangfeng Lu Yingchang Lu Leo-Pekka Lyytikäinen Evelin Mihailov Alanna C Morrison Natalia Pervjakova Liming Qu Lynda M Rose Elias Salfati Richa Saxena Markus Scholz Albert V Smith Emmi Tikkanen Andre Uitterlinden Xueli Yang Weihua Zhang Wei Zhao Mariza de Andrade Paul S de Vries Natalie R van Zuydam Sonia S Anand Lars Bertram Frank Beutner George Dedoussis Philippe Frossard Dominique Gauguier Alison H Goodall Omri Gottesman Marc Haber Bok-Ghee Han Jianfeng Huang Shapour Jalilzadeh Thorsten Kessler Inke R König Lars Lannfelt Wolfgang Lieb Lars Lind Cecilia M Lindgren Marja-Liisa Lokki Patrik K Magnusson Nadeem H Mallick Narinder Mehra Thomas Meitinger Fazal-Ur-Rehman Memon Andrew P Morris Markku S Nieminen Nancy L Pedersen Annette Peters Loukianos S Rallidis Asif Rasheed Maria Samuel Svati H Shah Juha Sinisalo Kathleen E Stirrups Stella Trompet Laiyuan Wang Khan S Zaman Diego Ardissino Eric Boerwinkle Ingrid B Borecki Erwin P Bottinger Julie E Buring John C Chambers Rory Collins L Adrienne Cupples John Danesh Ilja Demuth Roberto Elosua Stephen E Epstein Tõnu Esko Mary F Feitosa Oscar H Franco Maria Grazia Franzosi Christopher B Granger Dongfeng Gu Vilmundur Gudnason Alistair S Hall Anders Hamsten Tamara B Harris Stanley L Hazen Christian Hengstenberg Albert Hofman Erik Ingelsson Carlos Iribarren J Wouter Jukema Pekka J Karhunen Bong-Jo Kim Jaspal S Kooner Iftikhar J Kullo Terho Lehtimäki Ruth J F Loos Olle Melander Andres Metspalu Winfried März Colin N Palmer Markus Perola Thomas Quertermous Daniel J Rader Paul M Ridker Samuli Ripatti Robert Roberts Veikko Salomaa Dharambir K Sanghera Stephen M Schwartz Udo Seedorf Alexandre F Stewart David J Stott Joachim Thiery Pierre A Zalloua Christopher J O'Donnell Muredach P Reilly Themistocles L Assimes John R Thompson Jeanette Erdmann Robert Clarke Hugh Watkins Sekar Kathiresan Ruth McPherson Panos Deloukas Heribert Schunkert Nilesh J Samani Martin Farrall

Nat Genet 2015 Oct 7;47(10):1121-1130. Epub 2015 Sep 7.

Division of Cardiovascular Medicine, Radcliffe Department of Medicine, University of Oxford, Oxford, UK.

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http://dx.doi.org/10.1038/ng.3396DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4589895PMC
October 2015

Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores.

Am J Hum Genet 2015 Oct;97(4):576-92

Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, MA 02115, USA; Program in Genetic Epidemiology and Statistical Genetics, Harvard T.H. Chan School of Public Health, Boston, MA 02115, USA; Program in Medical and Population Genetics, Broad Institute of Harvard and MIT, Cambridge, MA 02142, USA; Department of Biostatistics, Harvard T.H. Chan School of Public Health, Boston, MA 02115, USA. Electronic address:

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http://biorxiv.org/content/biorxiv/early/2015/03/01/015859.f
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http://linkinghub.elsevier.com/retrieve/pii/S000292971500365
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http://dx.doi.org/10.1016/j.ajhg.2015.09.001DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4596916PMC
October 2015

Disproportionate Contributions of Select Genomic Compartments and Cell Types to Genetic Risk for Coronary Artery Disease.

PLoS Genet 2015 Oct 28;11(10):e1005622. Epub 2015 Oct 28.

Program in Medical and Population Genetics, Broad Institute, Cambridge, Massachusetts, United States of America; Icahn Institute for Genomics and Multiscale Biology, Department of Genetics and Genomics, Icahn School of Medicine at Mount Sinai, New York, New York, United States of America; Charles Bronfman Institute for Personalized Medicine, Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, New York, United States of America; Center for Statistical Genetics, Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, New York, United States of America; Zena and Michael A. Weiner Cardiovascular Institute, Icahn School of Medicine at Mount Sinai, New York, New York, United States of America.

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http://dx.doi.org/10.1371/journal.pgen.1005622DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4625039PMC
October 2015

Genetic prediction of antidepressant drug response and nonresponse in Korean patients.

PLoS One 2014 16;9(9):e107098. Epub 2014 Sep 16.

Department of Psychiatry, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0107098PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4166419PMC
May 2015

Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction.

Nature 2015 Feb 10;518(7537):102-6. Epub 2014 Dec 10.

1] Center for Human Genetic Research, Massachusetts General Hospital, Boston, Massachusetts 02114, USA. [2] Cardiovascular Research Center, Massachusetts General Hospital, Boston, Massachusetts 02114, USA. [3] Department of Medicine, Harvard Medical School, Boston, Massachusetts 02114, USA. [4] Program in Medical and Population Genetics, Broad Institute, 7 Cambridge Center, Cambridge, Massachusetts 02142, USA.

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http://kooperberg.fhcrc.org/papers/2015do.pdf
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http://www.nature.com/doifinder/10.1038/nature13917
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http://dx.doi.org/10.1038/nature13917DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4319990PMC
February 2015

Systematic cell-based phenotyping of missense alleles empowers rare variant association studies: a case for LDLR and myocardial infarction.

PLoS Genet 2015 Feb 3;11(2):e1004855. Epub 2015 Feb 3.

Institute of Human Genetics, University of Heidelberg, Heidelberg, Germany; Molecular Medicine Partnership Unit (MMPU), University of Heidelberg/ EMBL, Heidelberg, Germany; Center of Human Genetic Research (CHGR), Massachusetts General Hospital, Boston, Massachusetts, United States of America; Broad Institute of MIT and Harvard, Cambridge, Massachusetts, United States of America.

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http://dx.doi.org/10.1371/journal.pgen.1004855DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4409815PMC
February 2015

Inactivating mutations in NPC1L1 and protection from coronary heart disease.

N Engl J Med 2014 Nov 12;371(22):2072-82. Epub 2014 Nov 12.

Cardiovascular Division, Department of Medicine, Division of Statistical Genomics, Washington University School of Medicine, St. Louis, MO, USA.

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http://dx.doi.org/10.1056/NEJMoa1405386DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4335708PMC
November 2014

Multiple associated variants increase the heritability explained for plasma lipids and coronary artery disease.

Circ Cardiovasc Genet 2014 Oct 28;7(5):583-7. Epub 2014 Aug 28.

From the Center for Human Genetic Research, Massachusetts General Hospital, Boston (H.T., H.-H.W., G.M.P., S.K.); Broad Institute, Program in Medical and Population Genetics, Cambridge, MA (H.T., H.-H.W., G.M.P., S.K.); Department of Clinical Sciences, Lund University, Lund, Sweden (O.M.); Department of Internal Medicine, Skåne University Hospital, Malmö, Sweden (O.M.); and Queensland Institute of Medical Research, Brisbane, Queensland, Australia (J.Y.).

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http://dx.doi.org/10.1161/CIRCGENETICS.113.000420DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4341828PMC
October 2014

Genome-wide linkage scan of quantitative traits representing symptom dimensions in multiplex schizophrenia families.

Psychiatry Res 2013 Dec 12;210(3):756-60. Epub 2013 Sep 12.

Department of Psychiatry, Sungkyunkwan University School of Medicine, Samsung Medical Center, Seoul, Republic of Korea.

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http://dx.doi.org/10.1016/j.psychres.2013.08.015DOI Listing
December 2013

Genome-wide linkage scan of quantitative traits representing symptom dimensions in multiplex schizophrenia families.

Psychiatry Res 2013 Dec 12;210(3):756-60. Epub 2013 Sep 12.

Department of Psychiatry, Sungkyunkwan University School of Medicine, Samsung Medical Center, Seoul, Republic of Korea.

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http://dx.doi.org/10.1016/j.psychres.2013.08.015DOI Listing
December 2013

Evaluation of lysyl oxidase-like 1 gene polymorphisms in pseudoexfoliation syndrome in a Korean population.

Mol Vis 2013 22;19:448-53. Epub 2013 Feb 22.

Department of Ophthalmology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3580964PMC
September 2013

A Bayesian ensemble approach with a disease gene network predicts damaging effects of missense variants of human cancers.

Hum Genet 2013 Jan 21;132(1):15-27. Epub 2012 Aug 21.

Department of Bio and Brain Engineering, Korea Advanced Institute of Science and Technology, 373-1 Guseong-dong, Yuseong-gu, Daejeon 305-710, South Korea.

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http://dx.doi.org/10.1007/s00439-012-1218-7DOI Listing
January 2013

Multiple single-nucleotide polymorphism-based risk model for clinical outcomes after allogeneic stem-cell transplantation, especially for acute graft-versus-host disease.

Transplantation 2012 Dec;94(12):1250-7

Allogeneic Blood and Marrow Transplantation Program, Department of Medical Oncology and Hematology, Princess Margaret Hospital, Toronto, ON, Canada.

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http://dx.doi.org/10.1097/TP.0b013e3182708e7cDOI Listing
December 2012

Genetic association study of individual symptoms in depression.

Psychiatry Res 2012 Aug 17;198(3):400-6. Epub 2012 Mar 17.

Department of Psychiatry, Samsung Medical Center, Sungkyunkwan University School of Medicine, 50 Irwon-dong, Kangnam-gu, Seoul 135-710, Republic of Korea.

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http://dx.doi.org/10.1016/j.psychres.2011.12.037DOI Listing
August 2012

Polymorphic markers associated with severe oxaliplatin-induced, chronic peripheral neuropathy in colon cancer patients.

Cancer 2012 Jun 21;118(11):2828-36. Epub 2011 Oct 21.

Samsung Biomedical Research Institute, Samsung Medical Center, Seoul, South Korea.

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http://dx.doi.org/10.1002/cncr.26614DOI Listing
June 2012

The 18p11.22 locus is associated with never smoker non-small cell lung cancer susceptibility in Korean populations.

Hum Genet 2012 Mar 25;131(3):365-72. Epub 2011 Aug 25.

Division of Hematology-Oncology, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, 50 Irwon-dong Gangnam-gu, Seoul 135-710, Korea.

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http://dx.doi.org/10.1007/s00439-011-1080-zDOI Listing
March 2012

Differentially expressed genes in human peripheral blood as potential markers for statin response.

J Mol Med (Berl) 2012 Feb 24;90(2):201-11. Epub 2011 Sep 24.

Samsung Biomedical Research Institute, Samsung Medical Center, Seoul 135-710, South Korea.

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http://dx.doi.org/10.1007/s00109-011-0818-3DOI Listing
February 2012

Evaluation of the effects of VKORC1 polymorphisms and haplotypes, CYP2C9 genotypes, and clinical factors on warfarin response in Sudanese patients.

Eur J Clin Pharmacol 2011 Nov 18;67(11):1119-30. Epub 2011 May 18.

Department of Laboratory Medicine and Genetics, Samsung Medical Center, Sungkyunkwan University School of Medicine, #50 Ilwon-dong, Gangnam-gu, Seoul 135-710, South Korea.

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http://dx.doi.org/10.1007/s00228-011-1060-1DOI Listing
November 2011

A genome-wide association study identifies novel loci associated with susceptibility to chronic myeloid leukemia.

Blood 2011 Jun 3;117(25):6906-11. Epub 2011 May 3.

Department of Hematology/Oncology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.

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http://dx.doi.org/10.1182/blood-2011-01-329797DOI Listing
June 2011

Interleukin 10 polymorphisms differentially influence the risk of gastric cancer in East Asians and Caucasians.

Cytokine 2010 Jul 2;51(1):73-7. Epub 2010 Apr 2.

Samsung Biomedical Research Institute, Samsung Medical Center, 50 Ilwon-Dong, Gangnam-Gu, Seoul 135-710, Republic of Korea.

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http://dx.doi.org/10.1016/j.cyto.2010.03.007DOI Listing
July 2010

Sequence Variations and Haplotypes of the GJB2 Gene Revealed by Resequencing of 192 Chromosomes from the General Population in Korea.

Clin Exp Otorhinolaryngol 2010 Jun 30;3(2):65-9. Epub 2010 Jun 30.

Department of Laboratory Medicine & Genetics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.

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http://dx.doi.org/10.3342/ceo.2010.3.2.65DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2896735PMC
June 2010

Comparison of identical single nucleotide polymorphisms genotyped by the GeneChip Targeted Genotyping 25K, Affymetrix 500K and Illumina 550K platforms.

Genomics 2009 Aug 24;94(2):89-93. Epub 2009 Apr 24.

Samsung Biomedical Research Institute, Samsung Medical Center, Seoul, South Korea.

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http://dx.doi.org/10.1016/j.ygeno.2009.04.005DOI Listing
August 2009

Genome-widely significant evidence of linkage of schizophrenia to chromosomes 2p24.3 and 6q27 in an SNP-Based analysis of Korean families.

Am J Med Genet B Neuropsychiatr Genet 2009 Jul;150B(5):647-52

Department of Psychiatry, Sungkyunkwan University School of Medicine, Samsung Medical Center, Kangnam-Gu, Seoul, South Korea.

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http://dx.doi.org/10.1002/ajmg.b.30884DOI Listing
July 2009

Cataloging coding sequence variations in human genome databases.

PLoS One 2008 30;3(10):e3575. Epub 2008 Oct 30.

Samsung Biomedical Research Institute, Samsung Medical Center, Gangnam-Gu, Seoul, South Korea.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0003575PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2570488PMC
February 2009

Comparative analysis of the JAK/STAT signaling through erythropoietin receptor and thrombopoietin receptor using a systems approach.

BMC Bioinformatics 2009 Jan 30;10 Suppl 1:S53. Epub 2009 Jan 30.

Department of Bio and Brain Engineering, Korea Advanced Institute of Science and Technology, 373-1 Guseong-dong, Yuseong-gu, Daejeon 305-710, South Korea.

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http://dx.doi.org/10.1186/1471-2105-10-S1-S53DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2648785PMC
January 2009

EnsemPro: an ensemble approach to predicting transcription start sites in human genomic DNA sequences.

Genomics 2008 Mar;91(3):259-66

Samsung Biomedical Research Institute, Sungkyunkwan University School of Medicine, Samsung Medical Center, 50 Ilwon-dong, Kangnam-gu, Seoul 135-710, South Korea.

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http://linkinghub.elsevier.com/retrieve/pii/S088875430700278
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http://dx.doi.org/10.1016/j.ygeno.2007.11.001DOI Listing
March 2008

Effectiveness of in silico tagSNP selection methods: virtual analysis of the genotypes of pharmacogenetic genes.

Pharmacogenomics 2007 Oct;8(10):1347-57

College of Medicine, Korea University, Department of Laboratory Medicine, Seoul 136-705, South Korea.

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https://www.futuremedicine.com/doi/10.2217/14622416.8.10.134
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http://dx.doi.org/10.2217/14622416.8.10.1347DOI Listing
October 2007

Association between a polymorphism in the lymphotoxin-a promoter region and migraine.

Headache 2007 Jul-Aug;47(7):1056-62

Department of Laboratory Medicine, Yonsei University College of Medicine, Seoul, South Korea.

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http://doi.wiley.com/10.1111/j.1526-4610.2007.00847.x
Publisher Site
http://dx.doi.org/10.1111/j.1526-4610.2007.00847.xDOI Listing
September 2007