Journal of Human Genetics - Table of Contents alert Volume 63 Issue 11

TABLE OF CONTENTS Volume 63, Issue 11 In this issue Article Brief Communication Correction Also new AOP Article Novel missense and 3′-UTR splice site variants in LHFPL5 cause autosomal recessive nonsyndromic hearing impairment Khurram Liaqat, Ilene Chiu, Kwanghyuk Lee, Imen Chakchouk, Paula B. Andrade-Elizondo et al. Journal of Human Genetics 2018 63 :1099 - 1107; September 03, 2018; 10.1038/s10038-018-0502-3 Abstract | Full Text Admixture mapping and fine-mapping of type 2 diabetes susceptibility loci in African American women José M. Uribe-Salazar, Julie R. Palmer, Stephen A. Haddad, Lynn Rosenberg & Edward A. Ruiz-Narváez Journal of Human Genetics 2018 63 :1109 - 1117; August 22, 2018; 10.1038/s10038-018-0503-2 Abstract | Full Text Whole-exome sequencing reveals known and novel variants in a cohort of intracranial vertebral–basilar artery dissection (IVAD) Kun Wang, Sen Zhao, Qianqian Zhang, Jian Yuan, Jiaqi Liu et al. Journal of Human Genetics 2018 63 :1119 - 1128; August 16, 2018; 10.1038/s10038-018-0496-x Abstract | Full Text Identification of a de novo fetal variant in osteogenesis imperfecta by targeted sequencing-based noninvasive prenatal testing Xiuju Yin, Yang Du, Han Zhang, Zhandong Wang, Juan Wang et al. Journal of Human Genetics 2018 63 :1129 - 1137; August 21, 2018; 10.1038/s10038-018-0489-9 Abstract | Full Text A comparison of genome cohort participants' genetic knowledge and preferences to receive genetic results before and after a genetics workshop Kayono Yamamoto, Atsushi Shimizu, Fumie Aizawa, Hiroshi Kawame, Tomoharu Tokutomi et al. Journal of Human Genetics 2018 63 :1139 - 1147; September 05, 2018; 10.1038/s10038-018-0494-z Abstract | Full Text Contribution of RAD51D germline mutations in breast and ovarian cancer in Greece Irene Konstanta, Florentia Fostira, Paraskevi Apostolou, Efstratios Stratikos, Despoina Kalfakakou et al. Journal of Human Genetics 2018 63 :1149 - 1158; August 15, 2018; 10.1038/s10038-018-0498-8 Abstract | Full Text Gastric cancer may share genetic predisposition with esophageal squamous cell carcinoma in Chinese populations Linhua Yao, Fei Yu, Yingying Mao, Tianpei Wang, Qi Qi et al. Journal of Human Genetics 2018 63 :1159 - 1168; September 10, 2018; 10.1038/s10038-018-0501-4 Abstract | Full Text Identification of novel pathogenic variants and novel gene-phenotype correlations in Mexican subjects with microphthalmia and/or anophthalmia by next-generation sequencing Diana Matías-Pérez, Leopoldo A. García-Montaño, Marisa Cruz-Aguilar, Iván A. García-Montalvo, Jessica Nava-Valdéz et al. Journal of Human Genetics 2018 63 :1169 - 1180; September 04, 2018; 10.1038/s10038-018-0504-1 Abstract | Full Text Brief Communication Increased risk of skin cancer in Japanese heterozygotes of xeroderma pigmentosum group A Yuko Hirai, Asao Noda, Yoshiaki Kodama, Kismet A. Cordova, Harry M. Cullings et al. Journal of Human Genetics 2018 63 :1181 - 1184; August 08, 2018; 10.1038/s10038-018-0495-y Abstract | Full Text Familial total anomalous pulmonary venous return with 15q11.2 (BP1-BP2) microdeletion Yukiko Kuroda, Ikuko Ohashi, Takuya Naruto, Kazumi Ida, Yumi Enomoto et al. Journal of Human Genetics 2018 63 :1185 - 1188; August 14, 2018; 10.1038/s10038-018-0499-7 Abstract | Full Text Co-occurrence of mutations in FOXP1 and PTCH1 in a girl with extreme megalencephaly, callosal dysgenesis and profound intellectual disability Melinda Zombor, Tibor Kalmár, Zoltán Maróti, Alíz Zimmermann, Adrienn Máté et al. Journal of Human Genetics 2018 63 :1189 - 1193; September 04, 2018; 10.1038/s10038-018-0508-x Abstract | Full Text Correction Correction: Nationwide survey for current clinical status of amniocentesis and maternal serum marker test in Japan Hidehiko Miyake, Shigehito Yamada, Yosuke Fujii, Hideaki Sawai, Naoko Arimori et al. Journal of Human Genetics 2018 63 :1195 - 1195; August 23, 2018; 10.1038/s10038-018-0500-5 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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