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Annals of Human Genetics|May 4, 2011
Variation in the VWF gene in Swedish patients with type 1 von Willebrand DiseaseAnna M Johansson, Christer Halldén, Torbjörn Säll, et al.
Annals of Human Genetics|April 15, 2011
Glucuronic acid epimerase is associated with plasma triglyceride and high-density lipoprotein cholesterol levels in TurksUğur Hodoğlugil, David W Williamson, Yi Yu, et al.
Annals of Human Genetics|April 16, 2024
Attention-deficit/hyperactivity disorder and dopamine receptor D4 (DRD4) exon 3 variable number of tandem repeats (VNTR) 2-repeat alleleLarry Baum, Chi Chiu Lee, Rui Ye, et al.
Annals of Human Genetics|August 14, 2014
Novel ABCC8 (SUR1) gene mutations in Asian Indian children with congenital hyperinsulinemic hypoglycemiaSuresh Jahnavi, Varadarajan Poovazhagi, Sekar Kanthimathi, et al.
Annals of Human Genetics|August 14, 2014
Likelihood ratio tests in rare variant detection for continuous phenotypesPing Zeng, Yang Zhao, Jin Liu, et al.
Annals of Human Genetics|December 24, 2013
Genetic evaluation and application of posterior cranial fossa traits as endophenotypes for Chiari type I malformationChristina A Markunas, David S Enterline, Kaitlyn Dunlap, et al.
Annals of Human Genetics|December 24, 2013
The dopamine receptor D2 (DRD2) SNP rs1076560 is associated with opioid addictionToni-Kim Clarke, Amy R D Weiss, Thomas N Ferarro, et al.
Annals of Human Genetics|June 28, 2016
A Genetic Variant rs1020760at NFKB1 is Associated with Clinical Features of Psoriasis Vulgaris in a Han Chinese PopulationWenjun Wang, Zhengwei Zhu, Caihong Zhu, et al.
Annals of Human Genetics|May 22, 2012
Molecular and population analysis of natural selection on the human haptoglobin duplicationSantiago Rodriguez, Dylan M Williams, Philip A I Guthrie, et al.
Annals of Human Genetics|April 26, 2012
The joint association of REST and NFKB1 polymorphisms on the risk of colorectal cancerYunxian Yu, Hui Liu, Mingjuan Jin, et al.
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