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Journal of Human Genetics|May 12, 2025
Reclassification of variants of uncertain significance in neonatal genetic diseases: implications from a clinician's perspectiveXiaojiao Wu, Jiancheng Jiao, Weicong Pu, et al.Journal of Human Genetics|August 21, 2025
Early lipid genetics: identification of common and rare genetic variants for lipid traits in Indian adolescentsJanaki M Nair, Analabha Basu, Nikhil Tandon, et al.Journal of Human Genetics|August 21, 2025
A Japanese familial spastic paraplegia associated with a missense UBQLN2 variantKazuki Watanabe, Tatsuya Ema, Kenji Shimizu, et al.Journal of Human Genetics|October 1, 2003
The apolipoprotein CIII T2854G variants are associated with postprandial triacylglycerol concentrations in normolipidemic Korean menSang-Koo Woo, Hyun-Sik KangJournal of Human Genetics|May 17, 2013
Impact of polymorphisms in drug pathway genes on disease-free survival in adults with acute myeloid leukemiaSook Wah Yee, Joel A Mefford, Natasha Singh, et al.Journal of Human Genetics|May 17, 2013
Newborn screening for Fabry disease in Japan: prevalence and genotypes of Fabry disease in a pilot studyTakahito Inoue, Kiyoko Hattori, Kenji Ihara, et al.Journal of Human Genetics|February 1, 2013
Follow-up study of 22 Chinese children with Alexander disease and analysis of parental origin of de novo GFAP mutationsLili Zang, Jingmin Wang, Yuwu Jiang, et al.Journal of Human Genetics|February 1, 2013
DRD2 haplotype associated with negative symptoms and sustained attention deficits in Han Chinese with schizophrenia in TaiwanYi-Ling Chien, Hai-Gwo Hwu, Cathy S-J Fann, et al.Journal of Human Genetics|February 1, 2013
Exome sequencing identifies novel rheumatoid arthritis-susceptible variants in the BTNL2Shigeki Mitsunaga, Kazuyoshi Hosomichi, Yuko Okudaira, et al.Journal of Human Genetics|February 1, 2013
A microRNA-520 mirSNP at the MMP2 gene influences susceptibility to endometriosis in Chinese womenEing-Mei Tsai, Yung-Song Wang, Chang-Shen Lin, et al.Pageof 353