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Journal of Human Genetics|September 20, 2018
Molecular pathogenesis of triple-negative breast cancer based on microRNA expression signatures: antitumor miR-204-5p targets AP1S3Hiroko Toda, Sasagu Kurozumi, Yuko Kijima, et al.Journal of Human Genetics|August 25, 2018
Correction: Nationwide survey for current clinical status of amniocentesis and maternal serum marker test in JapanHidehiko Miyake, Shigehito Yamada, Yosuke Fujii, et al.Journal of Human Genetics|August 16, 2018
Familial total anomalous pulmonary venous return with 15q11.2 (BP1-BP2) microdeletionYukiko Kuroda, Ikuko Ohashi, Takuya Naruto, et al.Journal of Human Genetics|September 12, 2018
Gastric cancer may share genetic predisposition with esophageal squamous cell carcinoma in Chinese populationsLinhua Yao, Fei Yu, Yingying Mao, et al.Journal of Human Genetics|June 1, 2018
Maternal age-specific risk for trisomy 21 based on the clinical performance of NIPT and empirically derived NIPT age-specific positive and negative predictive values in JapanTakahiro Yamada, Akihiko Sekizawa, Yosuke Fujii, et al.Journal of Human Genetics|May 22, 2019
Urea cycle disorders-updateShirou Matsumoto, Johannes Häberle, Jun Kido, et al.Journal of Human Genetics|May 25, 2019
Author Correction: Genotypic variability-based genome-wide association study identifies non-additive loci HLA-C and IL12B for psoriasisWen-Hua Wei, Jonathan Massey, Jane Worthington, et al.Journal of Human Genetics|May 10, 2019
Exome sequencing identifies a novel missense variant in CTSC causing nonsyndromic aggressive periodontitisAnne Molitor, Tony Prud'homme, Zhichao Miao, et al.Journal of Human Genetics|January 22, 2020
Molecular mechanisms determining severity in patients with Pierson syndromeShogo Minamikawa, Saori Miwa, Tetsuji Inagaki, et al.Journal of Human Genetics|February 2, 2020
A novel PAK1 variant causative of neurodevelopmental disorder with postnatal macrocephalySachiko Ohori, Satomi Mitsuhashi, Revital Ben-Haim, et al.Pageof 353