Journal of Human Genetics - Table of Contents alert Volume 61 Issue 3

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TABLE OF CONTENTS Volume 61, Issue 3 (March 2016) In this issue Original Articles Short Communications Correspondence Also new AOP Sign up for e-alerts Recommend to your library Web feed Subscribe Advertisement Human Genome Variation (HGV) is an online, open access journal dedicated to sharing output of the studies to explore variation and mutation in the human genome in different format. Read the latest featured article on genomic architecture of inflammatory bowel disease.  Original Articles Top Coevolution of genes and languages and high levels of population structure among the highland populations of Daghestan Tatiana M Karafet, Kazima B Bulayeva, Johanna Nichols, Oleg A Bulayev, Farida Gurgenova, Jamilia Omarova, Levon Yepiskoposyan, Olga V Savina, Barry H Rodrigue and Michael F Hammer J Hum Genet 2016 61: 181-191; advance online publication, November 26, 2015; 10.1038/jhg.2015.132 Abstract | Full Text Birth weight modifies the association between central nervous system gene variation and adult body mass index Edward A Ruiz-Narváez, Stephen A Haddad, Lynn Rosenberg and Julie R Palmer J Hum Genet 2016 61: 193-198; advance online publication, November 19, 2015; 10.1038/jhg.2015.139 Abstract | Full Text Whole-exome sequencing and neurite outgrowth analysis in autism spectrum disorder OPEN Ryota Hashimoto, Takanobu Nakazawa, Yoshinori Tsurusaki, Yuka Yasuda, Kazuki Nagayasu, Kensuke Matsumura, Hitoshi Kawashima, Hidenaga Yamamori, Michiko Fujimoto, Kazutaka Ohi, Satomi Umeda-Yano, Masaki Fukunaga, Haruo Fujino, Atsushi Kasai, Atsuko Hayata-Takano, Norihito Shintani, Masatoshi Takeda, Naomichi Matsumoto and Hitoshi Hashimoto J Hum Genet 2016 61: 199-206; advance online publication, November 19, 2015; 10.1038/jhg.2015.141 Abstract | Full Text Homozygous sequence variants in the FKBP10 gene underlie osteogenesis imperfecta in consanguineous families Muhammad Umair, Annum Hassan, Abid Jan, Farooq Ahmad, Muhammad Imran, Muhammad I Samman, Sulman Basit and Wasim Ahmad J Hum Genet 2016 61: 207-213; advance online publication, November 5, 2015; 10.1038/jhg.2015.129 Abstract | Full Text Spinocerebellar ataxias in Venezuela: genetic epidemiology and their most likely ethnic descent Irene Paradisi, Vassiliki Ikonomu and Sergio Arias J Hum Genet 2016 61: 215-222; advance online publication, November 5, 2015; 10.1038/jhg.2015.131 Abstract | Full Text A de novo mosaic mutation of PHEX in a boy with hypophosphatemic rickets Chen Weng, Jiao Chen, Li Sun, Zhong-Wei Zhou, Xue Feng, Jun-Hui Sun, Ling-Ping Lu, Ping Yu and Ming Qi J Hum Genet 2016 61: 223-227; advance online publication, November 12, 2015; 10.1038/jhg.2015.133 Abstract | Full Text Broadening the phenotypic spectrum of pathogenic LARP7 variants: two cases with intellectual disability, variable growth retardation and distinct facial features Iris HIM Hollink, Majid Alfadhel, Anwar S Al-Wakeel, Farough Ababneh, Rolph Pfundt, Stella A de Man, Rami Abou Jamra, Arndt Rolfs, Aida M Bertoli-Avella and Ingrid MBH van de Laar J Hum Genet 2016 61: 229-233; advance online publication, November 26, 2015; 10.1038/jhg.2015.134 Abstract | Full Text Cerebellar vermis hypoplasia in CHARGE syndrome: clinical and molecular characterization of 18 unrelated Korean patients Young Bae Sohn, Jung Min Ko, Choong Ho Shin, Sei Won Yang, Jong-Hee Chae and Kyung-A Lee J Hum Genet 2016 61: 235-239; advance online publication, November 5, 2015; 10.1038/jhg.2015.135 Abstract | Full Text An epigenomic signature of postprandial hyperglycemia in peripheral blood leukocytes Sung-Mi Shim, Yoon-Kyung Cho, Eun-Jung Hong, Bok-Ghee Han and Jae-Pil Jeon J Hum Genet 2016 61: 241-246; advance online publication, December 3, 2015; 10.1038/jhg.2015.140 Abstract | Full Text Noninvasive fetal trisomy detection by multiplexed semiconductor sequencing: a barcoding analysis strategy Jiawei Shen, Zujia Wen, Xiaolan Qin and Yongyong Shi J Hum Genet 2016 61: 247-252; advance online publication, December 10, 2015; 10.1038/jhg.2015.142 Abstract | Full Text An effective screening strategy for deafness in combination with a next-generation sequencing platform: a consecutive analysis OPEN Naoko Sakuma, Hideaki Moteki, Masahiro Takahashi, Shin-ya Nishio, Yasuhiro Arai, Yukiko Yamashita, Nobuhiko Oridate and Shin-ichi Usami J Hum Genet 2016 61: 253-261; advance online publication, January 14, 2016; 10.1038/jhg.2015.143 Abstract | Full Text Short Communications Top APOBEC3H polymorphisms and susceptibility to HIV-1 infection in an Indian population Taeko K Naruse, Daisuke Sakurai, Hitoshi Ohtani, Gaurav Sharma, Surendra K Sharma, Madhu Vajpayee, Narinder K Mehra, Gurvinder Kaur and Akinori Kimura J Hum Genet 2016 61: 263-265; advance online publication, November 12, 2015; 10.1038/jhg.2015.136 Abstract | Full Text Six-layer structure for genomics and its applications Naoyuki Kamatani J Hum Genet 2016 61: 267-270; advance online publication, November 12, 2015; 10.1038/jhg.2015.137 Abstract | Full Text Correspondence Top A novel splice site mutation in CEP135 is associated with primary microcephaly in a Pakistani family Muhammad Farooq, Ambrin Fatima, Yuan Mang, Lars Hansen, Klaus Wilbrandt Kjaer, Shahid Mahmood Baig, Lars Allan Larsen and Niels Tommerup J Hum Genet 2016 61: 271-273; advance online publication, December 10, 2015; 10.1038/jhg.2015.138 Full Text Natureevents is a fully searchable, multi-disciplinary database designed to maximise exposure for events organisers. 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