TABLE OF CONTENTS
| | | | Volume 63, Issue 3 (March 2018) | | In this issue Article Brief Communication Correction Also new AOP | | | | | Article | | | Focal facial dermal dysplasia type 4: identification of novel CYP26C1 mutations in unrelated patients Journal of Human Genetics 2017 63 :257 - 261; December 20, 2017; 10.1038/s10038-017-0375-x Abstract | Full Text | | | | | Novel recessive mutations in MSTO1 cause cerebellar atrophy with pigmentary retinopathy Kazuhiro Iwama, Toru Takaori, Ai Fukushima, Jun Tohyama, Akihiko Ishiyama et al. Journal of Human Genetics 2018 63 :263 - 270; January 16, 2018; 10.1038/s10038-017-0405-8 Abstract | Full Text | | | | | Nationwide survey on cerebrotendinous xanthomatosis in Japan Journal of Human Genetics 2018 63 :271 - 280; January 10, 2018; 10.1038/s10038-017-0389-4 Abstract | Full Text | | | | | Clinical and mutational spectrum of Japanese patients with recessive variants in SH3TC2 Jun-Hui Yuan, Akihiro Hashiguchi, Yuji Okamoto, Akiko Yoshimura, Masahiro Ando et al. Journal of Human Genetics 2018 63 :281 - 287; January 10, 2018; 10.1038/s10038-017-0388-5 Abstract | Full Text | | | | | Genotypic variability-based genome-wide association study identifies non-additive loci HLA-C and IL12B for psoriasis Journal of Human Genetics 2017 63 :289 - 296; December 19, 2017; 10.1038/s10038-017-0350-6 Abstract | Full Text | | | | | GAREM1 regulates the PR interval on electrocardiograms Hye Ok Kim, Ji Eun Lim, Myung Jun Kim, Ji-One Kang, Sung-Moon Kim et al. Journal of Human Genetics 2017 63 :297 - 307; December 22, 2017; 10.1038/s10038-017-0367-x Abstract | Full Text | | | | | Decisional conflict and regret: shared decision-making about pregnancy affected by β-thalassemia major in Southeast of Iran Zahra Moudi, Zenab Phanodi, Hossein Ansari & Mostafa Montazer Zohour Journal of Human Genetics 2017 63 :309 - 317; December 22, 2017; 10.1038/s10038-017-0379-6 Abstract | Full Text | | | | | An epigenome-wide methylation study of healthy individuals with or without depressive symptoms Mihoko Shimada, Takeshi Otowa, Taku Miyagawa, Tadashi Umekage, Yoshiya Kawamura et al. Journal of Human Genetics 2018 63 :319 - 326; January 05, 2018; 10.1038/s10038-017-0382-y Abstract | Full Text | | | | | Genome-wide association study of homocysteine in African Americans from the Jackson Heart Study, the Multi-Ethnic Study of Atherosclerosis, and the Coronary Artery Risk in Young Adults study Laura M. Raffield, Jaclyn Ellis, Nels C. Olson, Qing Duan, Jin Li et al. Journal of Human Genetics 2018 63 :327 - 337; January 10, 2018; 10.1038/s10038-017-0384-9 Abstract | Full Text | | | | | Mediation analysis of alcohol consumption, DNA methylation, and epithelial ovarian cancer Dongyan Wu, Haitao Yang, Stacey J. Winham, Yanina Natanzon, Devin C. Koestler et al. Journal of Human Genetics 2018 63 :339 - 348; January 10, 2018; 10.1038/s10038-017-0385-8 Abstract | Full Text | | | | | Molecular characterization of HDAC8 deletions in individuals with atypical Cornelia de Lange syndrome Maria Helgeson, Jennifer Keller-Ramey, Amy Knight Johnson, Jennifer A. Lee, Daniel B. Magner et al. Journal of Human Genetics 2017 63 :349 - 356; December 26, 2017; 10.1038/s10038-017-0387-6 Abstract | Full Text | | | | | Detection of de novo single nucleotide variants in offspring of atomic-bomb survivors close to the hypocenter by whole-genome sequencing Makiko Horai, Hiroyuki Mishima, Chisa Hayashida, Akira Kinoshita, Yoshibumi Nakane et al. Journal of Human Genetics 2017 63 :357 - 363; December 26, 2017; 10.1038/s10038-017-0392-9 Abstract | Full Text | | | | | A novel human muscle cell model of Duchenne muscular dystrophy created by CRISPR/Cas9 and evaluation of antisense-mediated exon skipping Journal of Human Genetics 2018 63 :365 - 375; January 16, 2018; 10.1038/s10038-017-0400-0 Abstract | Full Text | | Brief Communication | | | A severely short-statured girl with 47,XX,â+â14/46,XX,upd(14)mat, mosaicism Kikumi Ushijima, Syuichi Yatsuga, Takako Matsumoto, Akie Nakamura, Maki Fukami et al. Journal of Human Genetics 2018 63 :377 - 381; January 09, 2018; 10.1038/s10038-017-0381-z Abstract | Full Text | | | | | Characteristic dysmorphic features in congenital disorders of glycosylation type IIb Yoon-Myung Kim, Go Hun Seo, Euiseok Jung, Ja-Hyun Jang, Sook Za Kim et al. Journal of Human Genetics 2017 63 :383 - 386; December 13, 2017; 10.1038/s10038-017-0386-7 Abstract | Full Text | | | | | A hot-spot mutation in CDC42 (p.Tyr64Cys) and novel phenotypes in the third patient with Takenouchi-Kosaki syndrome Midori Motokawa, Satoshi Watanabe, Akiko Nakatomi, Tatsuro Kondoh, Tadashi Matsumoto et al. Journal of Human Genetics 2018 63 :387 - 390; January 15, 2018; 10.1038/s10038-017-0396-5 Abstract | Full Text | | Correction | | | Correction: The absence that makes the difference: choroidal abnormalities in Legius syndrome Arianna Tucci, Veronica Saletti, Francesca Menni, Claudia Cesaretti, Giulietta Scuvera et al. Journal of Human Genetics 2018 63 :391 - 391; February 07, 2018; 10.1038/s10038-017-0369-8 Abstract | Full Text | | | | | | | | 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 | | | | | | | | 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. You have been sent this Table of Contents Alert because you have opted in to receive it. You can change or discontinue your e-mail alerts at any time, by modifying your preferences on your nature.com account at: www.nature.com/nams/svc/myaccount (You will need to log in to be recognised as a nature.com registrant). For further technical assistance, please contact our registration department. For print subscription enquiries, please contact our subscription department. For other enquiries, please contact our customer feedback department. 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