Literature DB >> 32348452

KRGDB: the large-scale variant database of 1722 Koreans based on whole genome sequencing.

Kwang Su Jung1, Kyung-Won Hong1,2, Hyun Youn Jo1, Jongpill Choi1,3, Hyo-Jeong Ban1,4, Seong Beom Cho1, Myungguen Chung1.   

Abstract

Year:  2020        PMID： 32348452      PMCID： PMC7190023          DOI： 10.1093/database/baaa030

Source DB:  PubMed          Journal:  Database (Oxford)        ISSN： 1758-0463            Impact factor:   3.451


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The original version of this article did not include Kyung-Won Hong's affiliation with Theragen Etex Bio Institute or Jongpill Choi's affiliation with Thermo Fisher Scientific Solutions, and incorrectly stated that Hyo-Jeong Ban was affiliated with both Theragen Etex and Thermo Fisher. These errors have now been corrected.
  8 in total

1.  Machine learning-based quantitative prediction of drug exposure in drug-drug interactions using drug label information.

Authors:  Ha Young Jang; Jihyeon Song; Jae Hyun Kim; Howard Lee; In-Wha Kim; Bongki Moon; Jung Mi Oh
Journal:  NPJ Digit Med       Date:  2022-07-11

Review 2.  Genetic variation analyses indicate conserved SARS-CoV-2-host interaction and varied genetic adaptation in immune response factors in modern human evolution.

Authors:  Ji-Won Lee; In-Hee Lee; Takanori Sato; Sek Won Kong; Tadahiro Iimura
Journal:  Dev Growth Differ       Date:  2021-03-21       Impact factor: 3.063

3.  Major Contribution of GREB1L Alterations to Severe Inner Ear Malformation Largely in a Non-mendelian Fashion.

Authors:  Bong Jik Kim; Hyoungwon Jeon; Sang-Yeon Lee; Nayoung Yi; Jin Hee Han; Go Hun Seo; Seung-Ha Oh; Byung Yoon Choi
Journal:  Clin Exp Otorhinolaryngol       Date:  2022-01-12       Impact factor: 3.372

4.  The First Korean Siblings With Adult-Onset 4H Leukodystrophy Related to Nonsynonymous POLR3B Mutations.

Authors:  Hui-Jun Yang; Gyeongmin Park; Il Seong Nam-Goong; Jun-Woo Ahn; Young Cheol Weon
Journal:  Neurol Genet       Date:  2022-04-13

5.  Whole-genome sequencing reveals novel ethnicity-specific rare variants associated with Alzheimer's disease.

Authors:  Daichi Shigemizu; Yuya Asanomi; Shintaro Akiyama; Risa Mitsumori; Shumpei Niida; Kouichi Ozaki
Journal:  Mol Psychiatry       Date:  2022-03-10       Impact factor: 13.437

6.  Network-based meta-analysis and the candidate gene association studies reveal novel ethnicity-specific variants in MFSD3 and MRPL43 associated with dementia with Lewy bodies.

Authors:  Daichi Shigemizu; Yuya Asanomi; Shintaro Akiyama; Sayuri Higaki; Takashi Sakurai; Kengo Ito; Shumpei Niida; Kouichi Ozaki
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2022-06-28       Impact factor: 3.358

7.  Identification of potential causal variants for premature ovarian failure by whole exome sequencing.

Authors:  Haengun Jin; JuWon Ahn; YoungJoon Park; JeongMin Sim; Han Sung Park; Chang Soo Ryu; Nam Keun Kim; KyuBum Kwack
Journal:  BMC Med Genomics       Date:  2020-10-27       Impact factor: 3.063

8.  Exome Chip Analysis of 14,026 Koreans Reveals Known and Newly Discovered Genetic Loci Associated with Type 2 Diabetes Mellitus.

Authors:  Seong Beom Cho; Jin Hwa Jang; Myung Guen Chung; Sang Cheol Kim
Journal:  Diabetes Metab J       Date:  2020-07-28       Impact factor: 5.893
  8 in total

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