Friday, November 14, 2014

European Journal of Human Genetics - Table of Contents alert Volume 22 Issue 12

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European Journal of Human Genetics

TABLE OF CONTENTS

Volume 22, Issue 12 (December 2014)

In this issue
News And Commentary
Obituary
Articles
Short Report
Letter
Book Review

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News And Commentary

Top

Do early paternal exposures to lifestyle factors such as smoking increase the risk of chronic diseases in the offspring?

Adelheid Soubry, Geert Verbeke and Cathrine Hoyo

Eur J Hum Genet 2014 22: 1341-1342; advance online publication, October 8, 2014; 10.1038/ejhg.2014.206

Full Text

Obituary

Top

Charles Buys (1942–2014)

Rolf H Sijmons, Gerard J te Meerman and Robert MW Hofstra

Eur J Hum Genet 2014 22: 1343-1344; 10.1038/ejhg.2014.207

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Articles

Top

Attitudes of pregnant women and male partners towards non-invasive prenatal testing and widening the scope of prenatal screening

Rachèl V van Schendel, Johanna H Kleinveld, Wybo J Dondorp, Eva Pajkrt, Danielle R M Timmermans, Kim C A Holtkamp, Margreet Karsten, Anne L Vlietstra, Augusta M A Lachmeijer and Lidewij Henneman

Eur J Hum Genet 2014 22: 1345-1350; advance online publication, March 19, 2014; 10.1038/ejhg.2014.32

Abstract | Full Text

Predictive testing for inherited prion disease: report of 22 years experience

Jane Owen, Jon Beck, Tracy Campbell, Gary Adamson, Michele Gorham, Andrew Thompson, Sarah Smithson, Elizabeth Rosser, Peter Rudge, John Collinge and Simon Mead

Eur J Hum Genet 2014 22: 1351-1356; advance online publication, April 9, 2014; 10.1038/ejhg.2014.42

Abstract | Full Text

Brugada syndrome risk loci seem protective against atrial fibrillation

Laura Andreasen, Jonas B Nielsen, Stine Darkner, Ingrid E Christophersen, Javad Jabbari, Lena Refsgaard, Jens J Thiis, Ahmad Sajadieh, Arnljot Tveit, Stig Haunsø, Jesper H Svendsen, Nicole Schmitt and Morten S Olesen

Eur J Hum Genet 2014 22: 1357-1361; advance online publication, March 26, 2014; 10.1038/ejhg.2014.46

Abstract | Full Text

Functional characterization of BRCA1 gene variants by mini-gene splicing assayEJHGOPEN

Ane Y Steffensen, Mette Dandanell, Lars Jønson, Bent Ejlertsen, Anne-Marie Gerdes, Finn C Nielsen and Thomas vO Hansen

Eur J Hum Genet 2014 22: 1362-1368; advance online publication, March 26, 2014; 10.1038/ejhg.2014.40

Abstract | Full Text

Allele-specific silencing of mutant Ataxin-7 in SCA7 patient-derived fibroblasts

Janine Scholefield, Lauren Watson, Danielle Smith, Jacquie Greenberg and Matthew JA Wood

Eur J Hum Genet 2014 22: 1369-1375; advance online publication, March 26, 2014; 10.1038/ejhg.2014.39

Abstract | Full Text

Human active X-specific DNA methylation events showing stability across time and tissues

Jihoon Eric Joo, Boris Novakovic, Mark Cruickshank, Lex W Doyle, Jeffrey M Craig and Richard Saffery

Eur J Hum Genet 2014 22: 1376-1381; advance online publication, April 9, 2014; 10.1038/ejhg.2014.34

Abstract | Full Text

Prepubertal start of father’s smoking and increased body fat in his sons: further characterisation of paternal transgenerational responsesEJHGOPEN

Kate Northstone, Jean Golding, George Davey Smith, Laura L Miller and Marcus Pembrey

Eur J Hum Genet 2014 22: 1382-1386; advance online publication, April 2, 2014; 10.1038/ejhg.2014.31

Abstract | Full Text

Y-chromosome E haplogroups: their distribution and implication to the origin of Afro-Asiatic languages and pastoralismEJHGOPEN

Eyoab I Gebremeskel and Muntaser E Ibrahim

Eur J Hum Genet 2014 22: 1387-1392; advance online publication, March 26, 2014; 10.1038/ejhg.2014.41

Abstract | Full Text

Human genetics of the Kula Ring: Y-chromosome and mitochondrial DNA variation in the Massim of Papua New Guinea

Mannis van Oven, Silke Brauer, Ying Choi, Joe Ensing, Wulf Schiefenhövel, Mark Stoneking and Manfred Kayser

Eur J Hum Genet 2014 22: 1393-1403; advance online publication, March 12, 2014; 10.1038/ejhg.2014.38

Abstract | Full Text

Unravelling the distinct strains of Tharu ancestry

Gyaneshwer Chaubey, Manvendra Singh, Federica Crivellaro, Rakesh Tamang, Amrita Nandan, Kamayani Singh, Varun Kumar Sharma, Ajai Kumar Pathak, Anish M Shah, Vishwas Sharma, Vipin Kumar Singh, Deepa Selvi Rani, Niraj Rai, Alena Kushniarevich, Anne-Mai Ilumäe, Monika Karmin, Anand Phillip, Abhilasha Verma, Erik Prank, Vijay Kumar Singh, Blaise Li, Periyasamy Govindaraj, Akhilesh Kumar Chaubey, Pavan Kumar Dubey, Alla G Reddy, Kumpati Premkumar, Satti Vishnupriya, Veena Pande, Jüri Parik, Siiri Rootsi, Phillip Endicott, Mait Metspalu, Marta Mirazon Lahr, George van Driem, Richard Villems, Toomas Kivisild, Lalji Singh and Kumarasamy Thangaraj

Eur J Hum Genet 2014 22: 1404-1412; advance online publication, March 26, 2014; 10.1038/ejhg.2014.36

Abstract | Full Text

Short Report

Top

Clinical spectrum and outcomes in families with coronal synostosis and TCF12 mutations

Federico di Rocco, Geneviève Baujat, Eric Arnaud, Dominique Rénier, Jean-Louis Laplanche, Valérie Cormier Daire and Corinne Collet

Eur J Hum Genet 2014 22: 1413-1416; advance online publication, April 16, 2014; 10.1038/ejhg.2014.57

Abstract | Full Text

Letter

Top

Common variant rs10033900 near the complement factor I gene is associated with age-related macular degeneration risk in Han Chinese population

Dingguo Qian, Mengyuan Kan, Xiaoling Weng, Yugeng Huang, Changbo Zhou, Genlong Yu, Ting Wang, Daizhan Zhou, Zhou Zhang, Di Zhang, Wei Tang and Yun Liu

Eur J Hum Genet 2014 22: 1417-1419; advance online publication, March 19, 2014; 10.1038/ejhg.2014.37

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Book Review

Top

A vision of personalised medicine revealed through modern genomics and open science

Barbara Jennings

Eur J Hum Genet 2014 22: 1420; 10.1038/ejhg.2014.100

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