Journal of Human Genetics - Table of Contents alert Volume 63 Issue 12

TABLE OF CONTENTS Volume 63, Issue 12 In this issue Article Brief Communication Correction Also new AOP Article Molecular pathogenesis of triple-negative breast cancer based on microRNA expression signatures: antitumor miR-204-5p targets AP1S3 Hiroko Toda, Sasagu Kurozumi, Yuko Kijima, Tetsuya Idichi, Yoshiaki Shinden et al. Journal of Human Genetics 2018 63 :1197 - 1210; September 18, 2018; 10.1038/s10038-018-0510-3 Abstract | Full Text Biallelic mutations in FDXR cause neurodegeneration associated with inflammation Jesse Slone, Yanyan Peng, Adam Chamberlin, Belinda Harris, Julie Kaylor et al. Journal of Human Genetics 2018 63 :1211 - 1222; September 25, 2018; 10.1038/s10038-018-0515-y Abstract | Full Text Expanding the phenotype of IBA57 mutations: related leukodystrophy can remain asymptomatic Kohei Hamanaka, Satoko Miyatake, Ayelet Zerem, Dorit Lev, Luba Blumkin et al. Journal of Human Genetics 2018 63 :1223 - 1229; September 27, 2018; 10.1038/s10038-018-0516-x Abstract | Full Text Maternally inherited 133kb deletion of 14q32 causing Kagami–Ogata syndrome Hou-Sung Jung, Stephanie E. Vallee, Mary Beth Dinulos, Gregory J. Tsongalis & Joel A. Lefferts Journal of Human Genetics 2018 63 :1231 - 1239; September 19, 2018; 10.1038/s10038-018-0506-z Abstract | Full Text Genome-wide DNA methylation analysis of human peripheral blood reveals susceptibility loci of diabetes-related hearing loss Jin Hao, Lin Hua, Xinxing Fu, Xuelian Zhang, Qijuan Zou et al. Journal of Human Genetics 2018 63 :1241 - 1250; September 12, 2018; 10.1038/s10038-018-0507-y Abstract | Full Text Catechol-O-methyltransferase (COMT) genotypes are associated with varying soluble, but not membrane-bound COMT protein in the human prefrontal cortex Georgia M Parkin, Madhara Udawela, Andrew Gibbons, Elizabeth Scarr & Brian Dean Journal of Human Genetics 2018 63 :1251 - 1258; September 14, 2018; 10.1038/s10038-018-0511-2 Abstract | Full Text A variant at 9q34.11 is associated with HLA-DQB1*06:02 negative essential hypersomnia Taku Miyagawa, Seik-Soon Khor, Hiromi Toyoda, Takashi Kanbayashi, Aya Imanishi et al. Journal of Human Genetics 2018 63 :1259 - 1267; September 28, 2018; 10.1038/s10038-018-0518-8 Abstract | Full Text Brief Communication A Novel NDUFS3 mutation in a Chinese patient with severe Leigh syndrome Xiaoting Lou, Hao Shi, Shumeng Wen, Yuanyuan Li, Xiujuan Wei et al. Journal of Human Genetics 2018 63 :1269 - 1272; August 23, 2018; 10.1038/s10038-018-0505-0 Abstract | Full Text Clinical and genetic backgrounds of hypertrophic cardiomyopathy with mid-ventricular obstruction Natsuko Inagaki, Takeharu Hayashi, Yasuyoshi Takei, Kousuke Tanimoto, Taishiro Chikamori et al. Journal of Human Genetics 2018 63 :1273 - 1276; September 11, 2018; 10.1038/s10038-018-0509-9 Abstract | Full Text A novel truncating mutation in MYH3 causes spondylocarpotarsal synostosis syndrome with basilar invagination Masaki Takagi, Satoshi Shimomura, Ryuji Fukuzawa, Satoshi Narumi, Gen Nishimura et al. Journal of Human Genetics 2018 63 :1277 - 1281; September 18, 2018; 10.1038/s10038-018-0513-0 Abstract | Full Text Correction Correction: A novel NDUFS3 mutation in a Chinese patient with severe Leigh syndrome Xiaoting Lou, Hao Shi, Shumeng Wen, Yuanyuan Li, Xiujuan Wei et al. Journal of Human Genetics 2018 63 :1283 - 1284; September 28, 2018; 10.1038/s10038-018-0517-9 Abstract | Full Text Advertisement Nature Briefing is an essential round-up of science news, opinion and analysis, free in your inbox every weekday. With Nature Briefing, we'll keep you updated on the latest research, so you can focus on yours. Click here to sign up. Natureevents is a fully searchable, multi-disciplinary database designed to maximise exposure for events organisers. The contents of the Natureevents Directory are now live. The digital version is available here. Find the latest scientific conferences, courses, meetings and symposia on natureevents.com. For event advertising opportunities across the Nature Publishing Group portfolio please contact natureevents@nature.com More Nature Events Please note that you need to be a subscriber or site-licence holder to enjoy full-text access to Journal of Human Genetics. In order to do so, please purchase a subscription. 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