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Journal of Human Genetics|January 12, 2018
Mediation analysis of alcohol consumption, DNA methylation, and epithelial ovarian cancerDongyan Wu, Haitao Yang, Stacey J Winham, et al.Journal of Human Genetics|November 29, 2017
Genome editing for the reproduction and remedy of human diseases in miceSatoshi Hara, Shuji TakadaJournal of Human Genetics|December 3, 2017
Regulation of HMGB3 by antitumor miR-205-5p inhibits cancer cell aggressiveness and is involved in prostate cancer pathogenesisYasutaka Yamada, Rika Nishikawa, Mayuko Kato, et al.Journal of Human Genetics|March 7, 2018
Clinical phenotype and molecular analysis of a homozygous ABCB11 mutation responsible for progressive infantile cholestasisKazuo Imagawa, Hisamitsu Hayashi, Yusuke Sabu, et al.Journal of Human Genetics|February 15, 2018
Systematic assessment of the performance of whole-genome amplification for SNP/CNV detection and β-thalassemia genotypingFei He, Wanjun Zhou, Ren Cai, et al.Journal of Human Genetics|March 2, 2018
A novel missense SNAP25b mutation in two affected siblings from an Israeli family showing seizures and cerebellar ataxiaHiroyuki Fukuda, Eri Imagawa, Kohei Hamanaka, et al.Journal of Human Genetics|May 26, 2017
Replication and fine-mapping of genetic predictors of lipid traits in African-AmericansQiPing Feng, Wei-Qi Wei, Rebecca T Levinson, et al.Journal of Human Genetics|May 23, 2018
The era of immunogenomics/immunopharmacogenomicsMakda Zewde, Kazuma Kiyotani, Jae-Hyun Park, et al.Journal of Human Genetics|June 16, 2017
Meta-analysis of genome-wide SNP- and pathway-based associations for facets of neuroticismSong E Kim, Han-Na Kim, Yeo-Jun Yun, et al.Journal of Human Genetics|June 23, 2017
Inter-generational instability of inserted repeats during transmission in spinocerebellar ataxia type 31Kunihiro Yoshida, Akira Matsushima, Katsuya NakamuraPageof 353