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Diabetes|September 11, 2009
SIRT1 genetic variation is related to BMI and risk of obesityM Carola Zillikens, Joyce B J van Meurs, Fernando Rivadeneira, et al.
Blood Cells, Molecules & Diseases|January 28, 2003
Dominant hemochromatosis due to N144H mutation of SLC11A3: clinical and biological characteristicsOmer T Njajou, Gerard de Jong, Bianca Berghuis, et al.
Neurology|September 16, 2005
Familial aggregation, the PDE4D gene, and ischemic stroke in a genetically isolated populationM J E van Rijn, A J C Slooter, A F C Schut, et al.
Stroke|October 22, 2005
Heritability of the function and structure of the arterial wall: findings of the Erasmus Rucphen Family (ERF) studyF A Sayed-Tabatabaei, M J E van Rijn, A F C Schut, et al.
Human Molecular Genetics|April 18, 2003
The FMR1 CGG repeat mouse displays ubiquitin-positive intranuclear neuronal inclusions; implications for the cerebellar tremor/ataxia syndromeRob Willemsen, Marianne Hoogeveen-Westerveld, Surya Reis, et al.
Genomics|May 18, 1999
A physical and transcriptional map of the preaxial polydactyly locus on chromosome 7q36H C Heus, A Hing, M J van Baren, et al.
European Journal of Human Genetics : EJHG|February 19, 2009
Predicting human height by Victorian and genomic methodsYurii S Aulchenko, Maksim V Struchalin, Nadezhda M Belonogova, et al.
Lancet (London, England)|February 1, 2005
A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's diseaseAlessio Di Fonzo, Christan F Rohé, Joaquim Ferreira, et al.
Neurogenetics|April 25, 2006
A common missense variant in the LRRK2 gene, Gly2385Arg, associated with Parkinson's disease risk in TaiwanAlessio Di Fonzo, Yah-Huei Wu-Chou, Chin-Song Lu, et al.
American Journal of Human Genetics|July 20, 2001
Park7, a novel locus for autosomal recessive early-onset parkinsonism, on chromosome 1p36C M van Duijn, M C Dekker, V Bonifati, et al.
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