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Journal of Human Genetics|December 21, 2019
Identification of susceptibility locus shared by IgA nephropathy and inflammatory bowel disease in a Chinese Han populationDianchun Shi, Zhong Zhong, Meng Wang, et al.Journal of Human Genetics|May 17, 2022
Genome-wide DNA methylation profiling and exome sequencing resolved a long-time misdiagnosed caseAnnalisa Paparella, Gabriella Maria Squeo, Eleonora Di Venere, et al.Journal of Human Genetics|May 9, 2022
Avoidance of cutaneous adverse drug reactions induced by antiepileptic drugs based on pharmacogenomicsTaisei MushirodaJournal 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.Pageof 353