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Journal of Human Genetics|February 1, 2005
Association between the GLUT1 gene polymorphism and the risk of diabetic nephropathy: a meta-analysisElias Zintzaras, Ioannis StefanidisJournal of Human Genetics|October 2, 2004
The important role for betaVLDLs binding at the fourth cysteine of first ligand-binding domain in the low-density lipoprotein receptorTadao Iwasaki, Sadao Takahashi, Mitsuaki Ishihara, et al.Journal of Human Genetics|August 13, 2008
Appropriate data cleaning methods for genome-wide association studyTaku Miyagawa, Nao Nishida, Jun Ohashi, et al.Journal of Human Genetics|August 6, 2008
Case report of de novo dup(18p)/del(18q) and r(18) mosaicismEnkhtuvshin Gereltzul, Yoshiyuki Baba, Naoto Suda, et al.Journal of Human Genetics|September 18, 2008
Genetic variants of FOXA2: risk of type 2 diabetes and effect on metabolic traits in North IndiansRubina Tabassum, Sreenivas Chavali, Om Prakash Dwivedi, et al.Journal of Human Genetics|June 23, 2017
al mena: a comprehensive resource of human genetic variants integrating genomes and exomes from Arab, Middle Eastern and North African populationsRemya Koshy, Anop Ranawat, Vinod ScariaJournal of Human Genetics|February 9, 2010
Prediction of the clinical phenotype of Fabry disease based on protein sequential and structural informationSeiji Saito, Kazuki Ohno, Jun Sese, et al.Journal of Human Genetics|February 27, 2010
Concordance of two multiple analytical approaches demonstrate that interaction between BMI and ADIPOQ haplotypes is a determinant of LDL cholesterol in a general French populationFrancis Vasseur, Thomas Caeyseele, Mouna Barat-Houari, et al.Journal of Human Genetics|July 29, 2018
Genome-wide association study suggests four variants influencing outcomes with ranibizumab therapy in exudative age-related macular degenerationMasato Akiyama, Atsushi Takahashi, Yukihide Momozawa, et al.Journal of Human Genetics|July 19, 2018
A novel SLC9A1 mutation causes cerebellar ataxiaKazuhiro Iwama, Hitoshi Osaka, Takahiro Ikeda, et al.Pageof 353