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Journal of Human Genetics|March 24, 2018
Dysosteosclerosis is also caused by TNFRSF11A mutationLong Guo, Nursel H Elcioglu, Ozge K Karalar, et al.Journal of Human Genetics|March 16, 2018
Dual strands of the miR-223 duplex (miR-223-5p and miR-223-3p) inhibit cancer cell aggressiveness: targeted genes are involved in bladder cancer pathogenesisSho Sugawara, Yasutaka Yamada, Takayuki Arai, et al.Journal of Human Genetics|March 17, 2018
Survey on the perception of germline genome editing among the general public in JapanMasato Uchiyama, Akiko Nagai, Kaori MutoJournal of Human Genetics|February 28, 2018
Nature vs. nurture in human sociality: multi-level genomic analyses of social conformityBiqing Chen, Zijian Zhu, Yingying Wang, et al.Journal of Human Genetics|February 28, 2018
The second point mutation in PREPL: a case report and literature reviewSebastian Silva, Noriko Miyake, Carolina Tapia, et al.Journal of Human Genetics|February 28, 2018
Could inherited predisposition drive non-obese fatty liver disease? Results from German tertiary referral centersMarcin Krawczyk, Heike Bantel, Monika Rau, et al.Journal of Human Genetics|June 10, 2022
CDiP technology for reverse engineering of sporadic Alzheimer's diseaseTakayuki Kondo, Yuichiro Yada, Takeshi Ikeuchi, et al.Journal of Human Genetics|June 27, 2022
Comparison of two families with and without ataxia harboring novel variants in PRKCGYui Tada, Kodai Kume, Soma Noguchi, et al.Journal of Human Genetics|June 7, 2021
Genomic alterations in gynecological malignancies: histotype-associated driver mutations, molecular subtyping schemes, and tumorigenic mechanismsSeiichi Mori, Osamu Gotoh, Kazuma Kiyotani, et al.Journal of Human Genetics|January 6, 2021
Positional cloning and comprehensive mutation analysis identified a novel KDM2B mutation in a Japanese family with minor malformations, intellectual disability, and schizophreniaSaeko Yokotsuka-Ishida, Masayuki Nakamura, Yoko Tomiyasu, et al.Pageof 353