Volume 21, Issue 7, 1 April 2012
Articles
HSC20 interacts with frataxin and is involved in iron–sulfur cluster biogenesis and iron homeostasis
Human Molecular Genetics, Volume 21, Issue 7, 1 April 2012, Pages 1457–1469, https://doi.org/10.1093/hmg/ddr582
An eQTL-based method identifies CTTN and ZMAT3 as pemetrexed susceptibility markers
Human Molecular Genetics, Volume 21, Issue 7, 1 April 2012, Pages 1470–1480, https://doi.org/10.1093/hmg/ddr583
GM130 gain-of-function induces cell pathology in a model of lysosomal storage disease
Human Molecular Genetics, Volume 21, Issue 7, 1 April 2012, Pages 1481–1495, https://doi.org/10.1093/hmg/ddr584
Mutations in genes encoding the glycine cleavage system predispose to neural tube defects in mice and humans
Human Molecular Genetics, Volume 21, Issue 7, 1 April 2012, Pages 1496–1503, https://doi.org/10.1093/hmg/ddr585
Polyunsaturated fatty acid levels in blood during pregnancy, at birth and at 7 years: their associations with two common FADS2 polymorphisms
Human Molecular Genetics, Volume 21, Issue 7, 1 April 2012, Pages 1504–1512, https://doi.org/10.1093/hmg/ddr588
Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controls
Human Molecular Genetics, Volume 21, Issue 7, 1 April 2012, Pages 1513–1520, https://doi.org/10.1093/hmg/ddr589
Lafora bodies and neurological defects in malin-deficient mice correlate with impaired autophagy
Human Molecular Genetics, Volume 21, Issue 7, 1 April 2012, Pages 1521–1533, https://doi.org/10.1093/hmg/ddr590
Mutations of ATIC and ADSL affect purinosome assembly in cultured skin fibroblasts from patients with AICA-ribosiduria and ADSL deficiency
Human Molecular Genetics, Volume 21, Issue 7, 1 April 2012, Pages 1534–1543, https://doi.org/10.1093/hmg/ddr591
LMNA variants cause cytoplasmic distribution of nuclear pore proteins in Drosophila and human muscle
Human Molecular Genetics, Volume 21, Issue 7, 1 April 2012, Pages 1544–1556, https://doi.org/10.1093/hmg/ddr592
Microbiomic subprofiles and MDR1 promoter methylation in head and neck squamous cell carcinoma
Human Molecular Genetics, Volume 21, Issue 7, 1 April 2012, Pages 1557–1565, https://doi.org/10.1093/hmg/ddr593
Cut-like homeobox 1 and nuclear factor I/B mediate ENGRAILED2 autism spectrum disorder-associated haplotype function
Human Molecular Genetics, Volume 21, Issue 7, 1 April 2012, Pages 1566–1580, https://doi.org/10.1093/hmg/ddr594
Distal enhancers upstream of the Charcot-Marie-Tooth type 1A disease gene PMP22
Human Molecular Genetics, Volume 21, Issue 7, 1 April 2012, Pages 1581–1591, https://doi.org/10.1093/hmg/ddr595
β1D chain increases α7β1 integrin and laminin and protects against sarcolemmal damage in mdx mice
Human Molecular Genetics, Volume 21, Issue 7, 1 April 2012, Pages 1592–1603, https://doi.org/10.1093/hmg/ddr596
Laforin and malin knockout mice have normal glucose disposal and insulin sensitivity
Human Molecular Genetics, Volume 21, Issue 7, 1 April 2012, Pages 1604–1610, https://doi.org/10.1093/hmg/ddr598
A systematic characterization of genes underlying both complex and Mendelian diseases
Human Molecular Genetics, Volume 21, Issue 7, 1 April 2012, Pages 1611–1624, https://doi.org/10.1093/hmg/ddr599
A single administration of morpholino antisense oligomer rescues spinal muscular atrophy in mouse
Human Molecular Genetics, Volume 21, Issue 7, 1 April 2012, Pages 1625–1638, https://doi.org/10.1093/hmg/ddr600
ARX homeodomain mutations abolish DNA binding and lead to a loss of transcriptional repression
Human Molecular Genetics, Volume 21, Issue 7, 1 April 2012, Pages 1639–1647, https://doi.org/10.1093/hmg/ddr601
ASSOCIATION STUDIES ARTICLES
Post-genome wide association studies and functional analyses identify association of MPP7 gene variants with site-specific bone mineral density
Human Molecular Genetics, Volume 21, Issue 7, 1 April 2012, Pages 1648–1657, https://doi.org/10.1093/hmg/ddr586
A genome-wide association and gene–environment interaction study for serum triglycerides levels in a healthy Chinese male population
Human Molecular Genetics, Volume 21, Issue 7, 1 April 2012, Pages 1658–1664, https://doi.org/10.1093/hmg/ddr587
A genome-wide association study identifies locus at 10q22 associated with clinical outcomes of adjuvant tamoxifen therapy for breast cancer patients in Japanese
Human Molecular Genetics, Volume 21, Issue 7, 1 April 2012, Pages 1665–1672, https://doi.org/10.1093/hmg/ddr597
FRONT-MATTER/BACK-MATTER
Contents Page
Human Molecular Genetics, Volume 21, Issue 7, 1 April 2012, Page NP, https://doi.org/10.1093/hmg/dds074
Cover Page
Human Molecular Genetics, Volume 21, Issue 7, 1 April 2012, Page NP, https://doi.org/10.1093/hmg/dds075
Editorial Board
Human Molecular Genetics, Volume 21, Issue 7, 1 April 2012, Page NP, https://doi.org/10.1093/hmg/dds076
Subscription Page
Human Molecular Genetics, Volume 21, Issue 7, 1 April 2012, Page NP, https://doi.org/10.1093/hmg/dds077
