Human Genetics

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Volume 127, Issue 6

June 2010

15 articles in this issue

Molecular pathogenesis of a novel mutation, G108D, in short-chain acyl-CoA dehydrogenase identified in subjects with short-chain acyl-CoA dehydrogenase deficiency
Kenichiro Shirao
Satoshi Okada
Masao Kobayashi
Review Article 08 April 2010 Pages: 619 - 628
West African and Amerindian ancestry and risk of myocardial infarction and metabolic syndrome in the Central Valley population of Costa Rica
Edward A. Ruiz-Narváez
Lance Bare
Hannia Campos
Original Investigation 06 March 2010 Pages: 629 - 638
Ethnic diversity of DNA methylation in the OPRM1 promoter region in lymphocytes of heroin addicts
David A. Nielsen
Sara Hamon
Mary Jeanne Kreek
Original Investigation 18 March 2010 Pages: 639 - 649
Comparison of the DNA methylation profiles of human peripheral blood cells and transformed B-lymphocytes
Yan V. Sun
Stephen T. Turner
Sharon L. R. Kardia
Original Investigation 18 March 2010 Pages: 651 - 658
Two-stage case–control designs for rare genetic variants
Daniel J. Schaid
Jason P. Sinnwell
Original Investigation 30 March 2010 Pages: 659 - 668
Heritability of chronic venous disease
Andreas Fiebig
Petra Krusche
Stefan Schreiber
Original Investigation Open access 31 March 2010 Pages: 669 - 674
Fine mapping of the 9q31 Hirschsprung’s disease locus
C. S. Tang
Y. Sribudiani
M. M. Garcia-Barceló
Original Investigation Open access 02 April 2010 Pages: 675 - 683
A single nucleotide polymorphism in the FADS1/FADS2 gene is associated with plasma lipid profiles in two genetically similar Asian ethnic groups with distinctive differences in lifestyle
Kazuhiro Nakayama
Tumenbayer Bayasgalan
Jichi Medical University Promotion Team of a Large-scale Human Genome Bank for All over Japan
Original Investigation 03 April 2010 Pages: 685 - 690
Replication and extension of association of choline acetyltransferase with nicotine dependence in European and African American smokers
Jinxue Wei
Jennie Z. Ma
Ming D. Li
Original Investigation 10 April 2010 Pages: 691 - 698
Power analysis for case–control association studies of samples with known family histories
Bo Peng
Biao Li
Christopher I. Amos
Original Investigation 11 April 2010 Pages: 699 - 704
Linkage and association analyses identify a candidate region for apoB level on chromosome 4q32.3 in FCHL families
Ellen M. Wijsman
Joseph H. Rothstein
Gail P. Jarvik
Original Investigation 11 April 2010 Pages: 705 - 719
A novel loss-of-function mutation in OTX2 in a patient with anophthalmia and isolated growth hormone deficiency
Liat Ashkenazi-Hoffnung
Yael Lebenthal
Galia Gat-Yablonski
Original Investigation 16 April 2010 Pages: 721 - 729
Evidence for inheritance in patients with VACTERL association
Benjamin D. Solomon
Daniel E. Pineda-Alvarez
Derek A. T. Cummings
Short Report 06 April 2010 Pages: 731 - 733
Philippe Collas (ed): Chromatin immunoprecipitation assays: methods and protocols
Ray Waters
Book Review 09 March 2010 Pages: 735 - 735
Malcolm Collins: Medicine and Sports Science, Vol. 54: Genetics and Sports
Jaikirty Singh Rawal
Book Review 04 April 2010 Pages: 737 - 737

Volume 127, Issue 6

Molecular pathogenesis of a novel mutation, G108D, in short-chain acyl-CoA dehydrogenase identified in subjects with short-chain acyl-CoA dehydrogenase deficiency

West African and Amerindian ancestry and risk of myocardial infarction and metabolic syndrome in the Central Valley population of Costa Rica

Ethnic diversity of DNA methylation in the OPRM1 promoter region in lymphocytes of heroin addicts

Comparison of the DNA methylation profiles of human peripheral blood cells and transformed B-lymphocytes

Two-stage case–control designs for rare genetic variants

Heritability of chronic venous disease

Fine mapping of the 9q31 Hirschsprung’s disease locus

A single nucleotide polymorphism in the FADS1/FADS2 gene is associated with plasma lipid profiles in two genetically similar Asian ethnic groups with distinctive differences in lifestyle

Replication and extension of association of choline acetyltransferase with nicotine dependence in European and African American smokers

Power analysis for case–control association studies of samples with known family histories

Linkage and association analyses identify a candidate region for apoB level on chromosome 4q32.3 in FCHL families

A novel loss-of-function mutation in OTX2 in a patient with anophthalmia and isolated growth hormone deficiency

Evidence for inheritance in patients with VACTERL association

Philippe Collas (ed): Chromatin immunoprecipitation assays: methods and protocols

Malcolm Collins: Medicine and Sports Science, Vol. 54: Genetics and Sports

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