Journal of Human Genetics - Table of Contents alert Volume 58 Issue 7

Special Section on Epigenomics: biological understanding and clinical application Featuring eight review articles and 2 original articles solicited from the leading researchers of the field, the second special section in the Journal of Human Genetics July issue focuses on Epigenomics. The journal would like to thank guest editors Professor Takeo Kubota and Professor Kenichiro Hata for their support with the planning and coordination of this section. TABLE OF CONTENTS Volume 58, Issue 7 (July 2013) In this issue Editorial Reviews Original Articles Corrigendum Also new AOP Sign up for e-alerts Recommend to your library Web feed Subscribe Advertisement Special section on epigenomics The special section on epigenomics in the July 2013 issue of Journal of Human Genetics features review and original articles by top-level epigenetic researchers, and covers various topics of epigenetic research, both basic and clinical.  Take advantage of FREE access to select articles today!    Editorial Top Epigenomics comes of age with expanding roles in biological understanding and clinical application Takeo Kubota and Kenichiro Hata J Hum Genet 2013 58: 395; 10.1038/jhg.2013.70 Full Text | PDF Reviews Top Epigenomic strategies at the interface of genetic and environmental risk factors for autism Janine M LaSalle J Hum Genet 2013 58: 396-401; advance online publication, May 16, 2013; 10.1038/jhg.2013.49 Abstract | Full Text Epigenetic and genetic alterations of the imprinting disorder Beckwith–Wiedemann syndrome and related disorders Hidenobu Soejima and Ken Higashimoto J Hum Genet 2013 58: 402-409; advance online publication, May 30, 2013; 10.1038/jhg.2013.51 Abstract | Full Text Metabolism–epigenome crosstalk in physiology and diseases Shinjiro Hino, Katsuya Nagaoka and Mitsuyoshi Nakao J Hum Genet 2013 58: 410-415; advance online publication, May 30, 2013; 10.1038/jhg.2013.57 Abstract | Full Text Effects of embryonic manipulation and epigenetics Takashi Kohda J Hum Genet 2013 58: 416-420; advance online publication, June 6, 2013; 10.1038/jhg.2013.61 Abstract | Full Text Tet family of 5-methylcytosine dioxygenases in mammalian development Hongbo Zhao and Taiping Chen J Hum Genet 2013 58: 421-427; advance online publication, May 30, 2013; 10.1038/jhg.2013.63 Abstract | Full Text Clinical application of the CpG island methylator phenotype to prognostic diagnosis in neuroblastomas Kiyoshi Asada, Masanobu Abe and Toshikazu Ushijima J Hum Genet 2013 58: 428-433; advance online publication, June 6, 2013; 10.1038/jhg.2013.64 Abstract | Full Text DNA methylation of the BDNF gene and its relevance to psychiatric disorders Tempei Ikegame, Miki Bundo, Yui Murata, Kiyoto Kasai, Tadafumi Kato and Kazuya Iwamoto J Hum Genet 2013 58: 434-438; advance online publication, June 6, 2013; 10.1038/jhg.2013.65 Abstract | Full Text Histone modifications for human epigenome analysis Hiroshi Kimura J Hum Genet 2013 58: 439-445; advance online publication, June 6, 2013; 10.1038/jhg.2013.66 Abstract | Full Text Original Articles Top Regional DNA methylation differences between humans and chimpanzees are associated with genetic changes, transcriptional divergence and disease genes Open Kei Fukuda, Kenji Ichiyanagi, Yoichi Yamada, Yasuhiro Go, Toshifumi Udono, Seitaro Wada, Toshiyuki Maeda, Hidenobu Soejima, Naruya Saitou, Takashi Ito and Hiroyuki Sasaki J Hum Genet 2013 58: 446-454; advance online publication, June 6, 2013; 10.1038/jhg.2013.55 Abstract | Full Text Three novel ZBTB24 mutations identified in Japanese and Cape Verdean type 2 ICF syndrome patients Hirohisa Nitta, Motoko Unoki, Kenji Ichiyanagi, Tomoki Kosho, Tomonari Shigemura, Hiroshi Takahashi, Guillaume Velasco, Claire Francastel, Capucine Picard, Takeo Kubota and Hiroyuki Sasaki J Hum Genet 2013 58: 455-460; advance online publication, June 6, 2013; 10.1038/jhg.2013.56 Abstract | Full Text Using multiple measures for quantitative trait association analyses: application to estimated glomerular filtration rate Adrienne Tin, Elizabeth Colantuoni, Eric Boerwinkle, Anna Kottgen, Nora Franceschini, Brad C Astor, Josef Coresh and Wen Hong Linda Kao J Hum Genet 2013 58: 461-466; advance online publication, March 28, 2013; 10.1038/jhg.2013.23 Abstract | Full Text Extracellular matrix remodeling genes polymorphisms and risk of chronic bronchitis and recurrent pneumonia in children Gulnaz Faritovna Korytina, Leysan Zinurovna Akhmadishina, Elena Vitalievna Viktorova, Olga Sergeevna Tselousova, Ksenia Vladimirovna Danilko, Olga Vladimirovna Kochetova and Tatyana Victorovna Viktorova J Hum Genet 2013 58: 467-474; advance online publication, April 11, 2013; 10.1038/jhg.2013.24 Abstract | Full Text Association studies of TNFSF4, TNFAIP3 and FAM167A-BLK polymorphisms with primary Sjogren’s syndrome in Han Chinese Fei Sun, Ping Li, Hua Chen, Ziyan Wu, Juanjuan Xu, Min Shen, Xiaomei Leng, Qun Shi, Wen Zhang, Xinping Tian, Yongzhe Li and Fengchun Zhang J Hum Genet 2013 58: 475-479; advance online publication, May 2, 2013; 10.1038/jhg.2013.26 Abstract | Full Text A molecular genetic analysis of childhood nephrotic syndrome in a cohort of Saudi Arabian families Mohamed H Al-Hamed, Essam Al-Sabban, Hamad Al-Mojalli, Naffaa Al-Harbi, Eissa Faqeih, Hammad Al Shaya, Khalid Alhasan, Safaa Al-Hissi, Mohamed Rajab, Noel Edwards, Abbas Al-Abbad, Ibrahim Al-Hassoun, John A Sayer and Brian F Meyer J Hum Genet 2013 58: 480-489; advance online publication, April 18, 2013; 10.1038/jhg.2013.27 Abstract | Full Text Replication study for the association of a single-nucleotide polymorphism, rs3746876, within KCNJ15, with susceptibility to type 2 diabetes in a Japanese population Hisashi Fukuda, Minako Imamura, Yasushi Tanaka, Minoru Iwata, Hiroshi Hirose, Kohei Kaku, Hiroshi Maegawa, Hirotaka Watada, Kazuyuki Tobe, Atsunori Kashiwagi, Ryuzo Kawamori and Shiro Maeda J Hum Genet 2013 58: 490-493; advance online publication, April 18, 2013; 10.1038/jhg.2013.28 Abstract | Full Text Corrigendum Top Genetic variation in phosphodiesterase (PDE) 7B in chronic lymphocytic leukemia: overview of genetic variants of cyclic nucleotide PDEs in human disease Ana M Peiró, Chih-Min Tang, Fiona Murray, Lingzhi Zhang, Loren M Brown, Daisy Chou, Laura Rassenti, Thomas J Kipps and Paul A Insel J Hum Genet 2013 58: 494; 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