Volume 130, Issue 4

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October 2011

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11 articles in this issue

Integrative computational biology for cancer research
Kristen Fortney
Igor Jurisica
Review Paper Open access 22 April 2011 Pages: 465 - 481
The −14010*C variant associated with lactase persistence is located between an Oct-1 and HNF1α binding site and increases lactase promoter activity
Tine G. K. Jensen
Anke Liebert
Jesper T. Troelsen
Original Investigation 15 February 2011 Pages: 483 - 493
BMP4 loss-of-function mutations in developmental eye disorders including SHORT syndrome
Linda M. Reis
Rebecca C. Tyler
Elena V. Semina
Original Investigation Open access 22 February 2011 Pages: 495 - 504
Technology-specific error signatures in the 1000 Genomes Project data
Michael Nothnagel
Alexander Herrmann
Jochen Hampe
Original Investigation 23 February 2011 Pages: 505 - 516
Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: a susceptibility region for neurological dysfunction including developmental and language delay
Rachel D. Burnside
Romela Pasion
Merlin G. Butler
Original Investigation 27 February 2011 Pages: 517 - 528
Potential novel candidate polymorphisms identified in genome-wide association study for breast cancer susceptibility
Badan Sehrawat
Malinee Sridharan
Sambasivarao Damaraju
Original Investigation Open access 19 March 2011 Pages: 529 - 537
Identification of QTL genes for BMD variation using both linkage and gene-based association approaches
Gloria Hoi-Yee Li
Ching-Lung Cheung
Annie Wai-Chee Kung
Original Investigation Open access 19 March 2011 Pages: 539 - 546
The role of polymorphisms in Toll-like receptors and their associated intracellular signaling genes in measles vaccine immunity
Inna G. Ovsyannikova
Iana H. Haralambieva
Gregory A. Poland
Original Investigation 19 March 2011 Pages: 547 - 561
Truncating mutations in NRXN2 and NRXN1 in autism spectrum disorders and schizophrenia
Julie Gauthier
Tabrez J. Siddiqui
Guy A. Rouleau
Original Investigation 22 March 2011 Pages: 563 - 573
ATXN-2 CAG repeat expansions are interrupted in ALS patients
Lucia Corrado
Letizia Mazzini
Sandra D’Alfonso
Original Investigation 03 May 2011 Pages: 575 - 580
Cassidy and Allanson: Management of Genetic Syndromes, 3rd edition
Peter D. Turnpenny
Book Review 22 March 2011 Pages: 581 - 582

Volume 130, Issue 4

Integrative computational biology for cancer research

The −14010*C variant associated with lactase persistence is located between an Oct-1 and HNF1α binding site and increases lactase promoter activity

BMP4 loss-of-function mutations in developmental eye disorders including SHORT syndrome

Technology-specific error signatures in the 1000 Genomes Project data

Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: a susceptibility region for neurological dysfunction including developmental and language delay

Potential novel candidate polymorphisms identified in genome-wide association study for breast cancer susceptibility

Identification of QTL genes for BMD variation using both linkage and gene-based association approaches

The role of polymorphisms in Toll-like receptors and their associated intracellular signaling genes in measles vaccine immunity

Truncating mutations in NRXN2 and NRXN1 in autism spectrum disorders and schizophrenia

ATXN-2 CAG repeat expansions are interrupted in ALS patients

Cassidy and Allanson: Management of Genetic Syndromes, 3rd edition

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