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Journal of Human Genetics|May 9, 2022
Identification of non-synonymous variations in ROBO1 and GATA5 genes in a family with bicuspid aortic valve diseaseHager Jaouadi, Hilla Gérard, Alexis Théron, et al.Journal of Human Genetics|May 9, 2022
Inferring intelligence of ancient people based on modern genomic studiesKaisar Dauyey, Naruya SaitouJournal of Human Genetics|January 7, 2018
An epigenome-wide methylation study of healthy individuals with or without depressive symptomsMihoko Shimada, Takeshi Otowa, Taku Miyagawa, et al.Journal of Human Genetics|March 21, 2018
A case of new PCDH12 gene variants presented as dyskinetic cerebral palsy with epilepsySato Suzuki-Muromoto, Keisuke Wakusawa, Takuya Miyabayashi, et al.Journal of Human Genetics|March 21, 2018
Clinical and molecular consequences of exon 78 deletion in DMD geneMonica Traverso, Stefania Assereto, Serena Baratto, et al.Journal of Human Genetics|March 21, 2018
Functional splicing analysis in an infantile case of atypical hemolytic uremic syndrome caused by digenic mutations in C3 and MCP genesTomohiko Yamamura, Kandai Nozu, Hiroaki Ueda, et al.Journal of Human Genetics|March 22, 2018
A genome-wide association study on photic sneeze syndrome in a Japanese populationDaimei Sasayama, Shinya Asano, Shun Nogawa, et al.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 MutoPageof 351