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From: steven perkins <>
Subject: [DNA] Fwd: European Journal of Human Genetics - Table of Contentsalert Volume 18 Issue 3
Date: Thu, 18 Feb 2010 12:09:06 -0500
References: <24046373.189236671266496645238.JavaMail.app@rbg01.pdkp2>
In-Reply-To: <24046373.189236671266496645238.JavaMail.app@rbg01.pdkp2>


A Number of interesting articles in this issue:

---------- Forwarded message ----------
From: European Journal of Human Genetics Alert
<>
Date: Thu, Feb 18, 2010 at 7:37 AM
Subject: European Journal of Human Genetics - Table of Contents alert
Volume 18 Issue 3
To:

http://www.nature.com/ejhg/index.html

TABLE OF CONTENTS
________________________________

Volume 18, Issue 3 (March 2010)

In this issue
Practical Genetics
Policy
Articles
Book Reviews

Also new
AOP

Practical Genetics

Top

Triple X syndrome: a review of the literature

Maarten Otter, Constance TRM Schrander-Stumpel and Leopold MG Curfs

Eur J Hum Genet 2010 18: 265-271; advance online publication, July 1,
2009; 10.1038/ejhg.2009.109

Abstract | Full Text

Policy

Top

Non-invasive prenatal testing: ethical issues explored

Antina de Jong, Wybo J Dondorp, Christine E M de Die-Smulders, Suzanne
G M Frints and Guido M W R de Wert

Eur J Hum Genet 2010 18: 272-277; advance online publication, December
2, 2009; 10.1038/ejhg.2009.203

Abstract | Full Text

Articles

Top

Clinical spectrum associated with recurrent genomic rearrangements in
chromosome 17q12

Sandesh Chakravarthy Sreenath Nagamani, Ayelet Erez, Joseph Shen,
Chumei Li, Elizabeth Roeder, Sarah Cox, Lefkothea Karaviti, Margret
Pearson, Sung-Hae L Kang, Trilochan Sahoo, Seema R Lalani, Pawel
Stankiewicz, V Reid Sutton and Sau Wai Cheung

Eur J Hum Genet 2010 18: 278-284; advance online publication, October
21, 2009; 10.1038/ejhg.2009.174

Abstract | Full Text

Familial interstitial Xq27.3q28 duplication encompassing the FMR1 gene
but not the MECP2 gene causes a new syndromic mental retardation
condition

Marlène Rio, Valérie Malan, Sarah Boissel, Annick Toutain, Ghislaine
Royer, Stéphanie Gobin, Nicole Morichon-Delvallez, Catherine Turleau,
Jean-Paul Bonnefont, Arnold Munnich, Michel Vekemans and Laurence
Colleaux

Eur J Hum Genet 2010 18: 285-290; advance online publication, October
21, 2009; 10.1038/ejhg.2009.159

Abstract | Full Text

Chromosome aberrations involving 10q22: report of three overlapping
interstitial deletions and a balanced translocation disrupting
C10orf11

Andreas Tzschach, Anne-Marie Bisgaard, Maria Kirchhoff, Luitgard M
Graul-Neumann, Heidemarie Neitzel, Stephanie Page, Alischo Ahmed, Ines
Müller, Fikret Erdogan, Hans-Hilger Ropers, Vera M Kalscheuer and
Reinhard Ullmann

Eur J Hum Genet 2010 18: 291-295; advance online publication, October
21, 2009; 10.1038/ejhg.2009.163

Abstract | Full Text

Comparison of participant information and informed consent forms of
five European studies in genetic isolated populations

Deborah Mascalzoni, A Cecile JW Janssens, Alison Stewart, Peter
Pramstaller, Ulf Gyllensten, Igor Rudan, Cornelia M van Duijn, James F
Wilson, Harry Campbell and Ruth Mc Quillan on behalf of the EUROSPAN
consortium

Eur J Hum Genet 2010 18: 296-302; advance online publication, October
14, 2009; 10.1038/ejhg.2009.155

Abstract | Full Text

Understanding sickle cell carrier status identified through newborn
screening: a qualitative study

Fiona A Miller, Martha Paynter, Robin Z Hayeems, Julian Little, June C
Carroll, Brenda J Wilson, Judith Allanson, Jessica P Bytautas and
Pranesh Chakraborty

Eur J Hum Genet 2010 18: 303-308; advance online publication, October
7, 2009; 10.1038/ejhg.2009.173

Abstract | Full Text

European admixture on the Micronesian island of Kosrae: lessons from
complete genetic information

Penelope E Bonnen, Jennifer K Lowe, David M Altshuler, Jan L Breslow,
Markus Stoffel, Jeffrey M Friedman and Itsik Pe'er

Eur J Hum Genet 2010 18: 309-316; advance online publication, October
21, 2009; 10.1038/ejhg.2009.180

Abstract | Full Text

Identification and characterization of seven novel mutations of
elastin gene in a cohort of patients affected by supravalvular aortic
stenosis

Lucia Micale, Maria Giuseppina Turturo, Carmela Fusco, Bartolomeo
Augello, Luis A Pérez Jurado, Claudia Izzi, Maria Cristina Digilio,
Donatella Milani, Elisabetta Lapi, Leopoldo Zelante and Giuseppe Merla

Eur J Hum Genet 2010 18: 317-323; advance online publication, October
21, 2009; 10.1038/ejhg.2009.181

Abstract | Full Text

Functional consequences of mitochondrial tRNATrp and tRNAArg mutations
causing combined OXPHOS defects

Paulien Smits, Sandy Mattijssen, Eva Morava, Mariël van den Brand,
Frans van den Brandt, Frits Wijburg, Ger Pruijn, Jan Smeitink, Leo
Nijtmans, Richard Rodenburg and Lambert van den Heuvel

Eur J Hum Genet 2010 18: 324-329; advance online publication, October
7, 2009; 10.1038/ejhg.2009.169

Abstract | Full Text

Identification and characterization of two novel JARID1C mutations:
suggestion of an emerging genotype–phenotype correlation

Sinitdhorn Rujirabanjerd, John Nelson, Patrick S Tarpey, Anna Hackett,
Sarah Edkins, F Lucy Raymond, Charles E Schwartz, Gillian Turner,
Shigeki Iwase, Yang Shi, P Andrew Futreal, Michael R Stratton and
Jozef Gecz

Eur J Hum Genet 2010 18: 330-335; advance online publication, October
14, 2009; 10.1038/ejhg.2009.175

Abstract | Full Text

Gain-of-function variant in GLUD2 glutamate dehydrogenase modifies
Parkinson's disease onset

Andreas Plaitakis, Helen Latsoudis, Konstantinos Kanavouras, Beate
Ritz, Jeff M Bronstein, Irene Skoula, Vasileios Mastorodemos, Spyridon
Papapetropoulos, Nikolas Borompokas, Ioannis Zaganas, Georgia
Xiromerisiou, George M Hadjigeorgiou and Cleanthe Spanaki

Eur J Hum Genet 2010 18: 336-341; advance online publication, October
14, 2009; 10.1038/ejhg.2009.179

Abstract | Full Text

Fine mapping and association studies of a high-density lipoprotein
cholesterol linkage region on chromosome 16 in French-Canadian
subjects

Zari Dastani, Päivi Pajukanta, Michel Marcil, Nicholas Rudzicz,
Isabelle Ruel, Swneke D Bailey, Jenny C Lee, Mathieu Lemire, Janet
Faith, Jill Platko, John Rioux, Thomas J Hudson, Daniel Gaudet, James
C Engert and Jacques Genest

Eur J Hum Genet 2010 18: 342-347; advance online publication, October
21, 2009; 10.1038/ejhg.2009.157

Abstract | Full Text

The emergence of Y-chromosome haplogroup J1e among Arabic-speaking populations

Jacques Chiaroni, Roy J King, Natalie M Myres, Brenna M Henn, Axel
Ducourneau, Michael J Mitchell, Gilles Boetsch, Issa Sheikha, Alice A
Lin, Mahnoosh Nik-Ahd, Jabeen Ahmad, Francesca Lattanzi, Rene J
Herrera, Muntaser E Ibrahim, Aaron Brody, Ornella Semino, Toomas
Kivisild and Peter A Underhill

Eur J Hum Genet 2010 18: 348-353; advance online publication, October
14, 2009; 10.1038/ejhg.2009.166

Abstract | Full Text

Traces of sub-Saharan and Middle Eastern lineages in Indian Muslim populations

Muthukrishnan Eaaswarkhanth, Ikramul Haque, Zeinab Ravesh, Irene
Gallego Romero, Poorlin Ramakodi Meganathan, Bhawna Dubey, Faizan
Ahmed Khan, Gyaneshwer Chaubey, Toomas Kivisild, Chris Tyler-Smith,
Lalji Singh and Kumarasamy Thangaraj

Eur J Hum Genet 2010 18: 354-363; advance online publication, October
7, 2009; 10.1038/ejhg.2009.168

Abstract | Full Text

Genetic variants in human CLOCK associate with total energy intake and
cytokine sleep factors in overweight subjects (GOLDN population)

Marta Garaulet, Yu-Chi Lee, Jian Shen, Laurence D Parnell, Donna K
Arnett, Michael Y Tsai, Chao-Qiang Lai and Jose M Ordovas

Eur J Hum Genet 2010 18: 364-369; advance online publication, November
4, 2009; 10.1038/ejhg.2009.176

Abstract | Full Text

Methionine synthase A2756G polymorphism and cancer risk: a meta-analysis

Ke Yu, Jing Zhang, Jiyuan Zhang, Chao Dou, Shaohua Gu, Yi Xie, Yumin
Mao and Chaoneng Ji

Eur J Hum Genet 2010 18: 370-378; advance online publication, October
14, 2009; 10.1038/ejhg.2009.131

Abstract | Full Text

A powerful genome-wide feasible approach to detect parent-of-origin
effects in studies of quantitative traits

Nadezhda M Belonogova, Tatiana I Axenovich and Yurii S Aulchenko

Eur J Hum Genet 2010 18: 379-384; advance online publication, October
7, 2009; 10.1038/ejhg.2009.167

Abstract | Full Text

Large-scale parent–child comparison confirms a strong paternal
influence on telomere length

Katarina Nordfjäll, Ulrika Svenson, Karl-Fredrik Norrback, Rolf
Adolfsson and Göran Roos

Eur J Hum Genet 2010 18: 385-389; advance online publication, October
14, 2009; 10.1038/ejhg.2009.178

Abstract | Full Text

Book Review

Top

Research and applied medical genetics: filling the gap

Alessandra Ferlini

Eur J Hum Genet 2010 18: 390-391; 10.1038/ejhg.2009.132

Abstract | Full Text

‘Me, Myself, and Why. Understanding your own genome and evolutionary history’

Peter de Knijff

Eur J Hum Genet 2010 18: 391-392; 10.1038/ejhg.2009.146

Abstract | Full Text






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