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Journal of Human Genetics|August 11, 2020
Personalized medicine for cardiovascular diseasesHayato Tada, Noboru Fujino, Akihiro Nomura, et al.Journal of Human Genetics|April 3, 2015
Genetic and linguistic correlation of the Kra-Dai-speaking groups in ThailandSuparat Srithawong, Metawee Srikummool, Pittayawat Pittayaporn, et al.Journal of Human Genetics|April 3, 2023
Hematologic traits and primary biliary cholangitis: a Mendelian randomization studyBin Ke, Chunyu Li, Huifang ShangJournal of Human Genetics|April 27, 2023
Illuminating the potential causality of serum level of matrix metalloproteinases and the occurrence of cardiovascular and cerebrovascular diseases: a Mendelian randomization studyXuelun Zou, Leiyun Wang, Yi Zeng, et al.Journal of Human Genetics|June 21, 2008
SCN1A, SCN1B, and GABRG2 gene mutation analysis in Chinese families with generalized epilepsy with febrile seizures plusHuihui Sun, Yuehua Zhang, Jianmin Liang, et al.Journal of Human Genetics|July 16, 2008
VSX1 gene variants are associated with keratoconus in unrelated Korean patientsJee-Won Mok, Sun-Jin Baek, Choun-Ki JooJournal of Human Genetics|May 25, 2006
A novel 111/121 diplotype in the Calpain-10 gene is associated with type 2 diabetesEun Seok Kang, Hye Joo Kim, Moonsuk Nam, et al.Journal of Human Genetics|May 25, 2006
A common functional exon polymorphism in the microsomal triglyceride transfer protein gene is associated with type 2 diabetes, impaired glucose metabolism and insulin levelsDiana Rubin, Ulf Helwig, Maria Pfeuffer, et al.Journal of Human Genetics|April 12, 2007
Mutation analysis and genotype/phenotype relationships of Gaucher disease patients in SpainPilar Alfonso, Sofía Aznarez, Manuel Giralt, et al.Journal of Human Genetics|October 17, 2008
LRRK2 P755L variant in sporadic Parkinson's diseaseHiroyuki Tomiyama, Ikuko Mizuta, Yuanzhe Li, et al.Pageof 353