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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 NakamuraJournal of Human Genetics|April 29, 2018
Genetic variants in chemokine CC subfamily genes influence hepatitis C virus viral clearanceYinan Yao, Ming Yue, Feng Zang, et al.Journal of Human Genetics|May 3, 2018
Author Correction: Two large deletions extending beyond either end of the RHD gene and their red cell phenotypesKshitij Srivastava, David Alan Stiles, Franz Friedrich Wagner, et al.Journal of Human Genetics|July 24, 2018
Whole exome sequencing identifies a novel dominant missense mutation underlying leukonychia in a Pakistani familyTeka Khan, Manan Khan, Ayesha Yousaf, et al.Pageof 351