Volume 127, Issue 2

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February 2010

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13 articles in this issue

Evaluation of genetic tests for susceptibility to common complex diseases: why, when and how?
Caroline Fiona Wright
Mark Kroese
Review Article 20 November 2009 Pages: 125 - 134
Transposable elements in disease-associated cryptic exons
Igor Vorechovsky
Original Investigation 10 October 2009 Pages: 135 - 154
Genetic variants in the RELN gene are associated with otosclerosis in multiple European populations
Isabelle Schrauwen
Megan Ealy
Guy Van Camp
Original Investigation 22 October 2009 Pages: 155 - 162
Malaria severity and human nitric oxide synthase type 2 (NOS2) promoter haplotypes
Marc C. Levesque
Maurine R. Hobbs
J. Brice Weinberg
Original Investigation 27 October 2009 Pages: 163 - 182
Genetic variation in PARL influences mitochondrial content
Joanne E. Curran
Jeremy B. M. Jowett
Ahmed H. Kissebah
Original Investigation 28 October 2009 Pages: 183 - 190
A novel mutation in the connexin 29 gene may contribute to nonsyndromic hearing loss
Hui-Mei Hong
Jiann-Jou Yang
Shuan-Yow Li
Original Investigation 30 October 2009 Pages: 191 - 199
Common CFTR gene variants influence body composition and survival in rural Ghana
Maris Kuningas
David van Bodegom
Rudi G. J. Westendorp
Original Investigation Open access 05 November 2009 Pages: 201 - 206
Rubella vaccine-induced cellular immunity: evidence of associations with polymorphisms in the Toll-like, vitamin A and D receptors, and innate immune response genes
Inna G. Ovsyannikova
Neelam Dhiman
Gregory A. Poland
Original Investigation 10 November 2009 Pages: 207 - 221
Monoamine oxidase A gene polymorphisms and enzyme activity associated with risk of gout in Taiwan aborigines
Hung-Pin Tu
Albert Min-Shan Ko
Ying-Chin Ko
Original Investigation 14 November 2009 Pages: 223 - 229
Linkage and sequence analysis indicate that CCBE1 is mutated in recessively inherited generalised lymphatic dysplasia
Fiona Connell
Kamini Kalidas
Lymphoedema Consortium
Original Investigation 13 November 2009 Pages: 231 - 241
Erratum to: Linkage and sequence analysis indicate that CCBE1 is mutated in recessively inherited generalised lymphatic dysplasia
Fiona Connell
Kamini Kalidas
Lymphoedema Consortium
Erratum 05 December 2009 Pages: 243 - 243
Genetic analysis of ABCG2 gene C421A polymorphism with gout disease in Chinese Han male population
Binbin Wang
Zhimin Miao
Xu Ma
Short Report 17 November 2009 Pages: 245 - 246
R. C. Elston and W. D. Johnson: Basic biostatistics for geneticists and epidemiologists
Peter Holmans
Lesley Jones
Book Review 26 November 2009 Pages: 247 - 248

Volume 127, Issue 2

Evaluation of genetic tests for susceptibility to common complex diseases: why, when and how?

Transposable elements in disease-associated cryptic exons

Genetic variants in the RELN gene are associated with otosclerosis in multiple European populations

Malaria severity and human nitric oxide synthase type 2 (NOS2) promoter haplotypes

Genetic variation in PARL influences mitochondrial content

A novel mutation in the connexin 29 gene may contribute to nonsyndromic hearing loss

Common CFTR gene variants influence body composition and survival in rural Ghana

Rubella vaccine-induced cellular immunity: evidence of associations with polymorphisms in the Toll-like, vitamin A and D receptors, and innate immune response genes

Monoamine oxidase A gene polymorphisms and enzyme activity associated with risk of gout in Taiwan aborigines

Linkage and sequence analysis indicate that CCBE1 is mutated in recessively inherited generalised lymphatic dysplasia

Erratum to: Linkage and sequence analysis indicate that CCBE1 is mutated in recessively inherited generalised lymphatic dysplasia

Genetic analysis of ABCG2 gene C421A polymorphism with gout disease in Chinese Han male population

R. C. Elston and W. D. Johnson: Basic biostatistics for geneticists and epidemiologists

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