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6 result(s) for 'author#Bok-Ghee Han' within BMC

1. A genome-wide association study identifies a breast cancer risk variant in ERBB4 at 2q34: results from the Seoul Breast Cancer Study

   Although approximately 25 common genetic susceptibility loci have been identified to be independently associated with breast cancer risk through genome-wide association studies (GWAS), the genetic risk variant...

   Authors: Hyung-cheol Kim, Ji-Young Lee, Hyuna Sung, Ji-Yeob Choi, Sue K Park, Kyoung-Mu Lee, Young Jin Kim, Min Jin Go, Lian Li, Yoon Shin Cho, Miey Park, Dong-Joon Kim, Ji Hee Oh, Jun-Woo Kim, Jae-Pil Jeon, Soon-Young Jeon…

   Citation: Breast Cancer Research 2012 14:R56

   Content type: Research article Published on: 27 March 2012

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2. Identification of a genetic variant at 2q12.1 associated with blood pressure in East-Asians by genome-wide scan including gene-environment interactions

   Genome-wide association studies have identified many genetic loci associated with blood pressure (BP). Genetic effects on BP can be altered by environmental exposures via multiple biological pathways. Especial...

   Authors: Yun Kyoung Kim, Youngdoe Kim, Mi Yeong Hwang, Kazuro Shimokawa, Sungho Won, Norihiro Kato, Yasuharu Tabara, Mitsuhiro Yokota, Bok-Ghee Han, Jong Ho Lee and Bong-Jo Kim

   Citation: BMC Medical Genetics 2014 15:65

   Content type: Research article Published on: 5 June 2014

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3. Targeted exon sequencing fails to identify rare coding variants with large effect in rheumatoid arthritis

   Although it has been suggested that rare coding variants could explain the substantial missing heritability, very few sequencing studies have been performed in rheumatoid arthritis (RA). We aimed to identify n...

   Authors: So-Young Bang, Young-Ji Na, Kwangwoo Kim, Young Bin Joo, Youngho Park, Jaemoon Lee, Sun-Young Lee, Adnan A Ansari, Junghee Jung, Hwanseok Rhee, Jong-Young Lee, Bok-Ghee Han, Sung-Min Ahn, Sungho Won, Hye-Soon Lee and Sang-Cheol Bae

   Citation: Arthritis Research & Therapy 2014 16:447

   Content type: Research article Published on: 30 September 2014

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4. Copy number variation at leptin receptor gene locus associated with metabolic traits and the risk of type 2 diabetes mellitus

   Recent efforts have been made to link complex human traits and disease susceptibility to DNA copy numbers. The leptin receptor (LEPR) has been implicated in obesity and diabetes. Mutations and genetic variatio...

   Authors: Jae-Pil Jeon, Sung-Mi Shim, Hye-Young Nam, Gil-Mi Ryu, Eun-Jung Hong, Hyung-Lae Kim and Bok-Ghee Han

   Citation: BMC Genomics 2010 11:426

   Content type: Research article Published on: 12 July 2010

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5. Expression of P2 receptors in human B cells and Epstein-Barr virus-transformed lymphoblastoid cell lines

   Epstein-Barr virus (EBV) infection immortalizes primary B cells in vitro and generates lymphoblastoid cell lines (LCLs), which are used for several purposes in immunological and genetic studies. Purinergic rec...

   Authors: Dong Hyeon Lee, Kyu Sang Park, In Deok Kong, Jun Woo Kim and Bok Ghee Han

   Citation: BMC Immunology 2006 7:22

   Content type: Research article Published on: 14 September 2006

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6. A genome-wide association study of copy-number variation identifies putative loci associated with osteoarthritis in Koreans

   OA is a complex disease caused by environmental and genetic risk factors. The purpose of this study is to identify candidate copy number variations (CNVs) associated with OA.

   Authors: Sanghoon Moon, Bhumsuk Keam, Mi Yeong Hwang, Young Lee, Suyeon Park, Ji Hee Oh, Yeon-Jung Kim, Heun-Sik Lee, Nam Hee Kim, Young Jin Kim, Dong-Hyun Kim, Bok-Ghee Han, Bong-Jo Kim and Juyoung Lee

   Citation: BMC Musculoskeletal Disorders 2015 16:76

   Content type: Research article Published on: 4 April 2015

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