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JAMA|July 20, 2006
Complement factor H polymorphism, complement activators, and risk of age-related macular degenerationDominiek D G Despriet, Caroline C W Klaver, Jacqueline C M Witteman, et al.
Science (New York, N.Y.)|November 26, 2002
Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonismVincenzo Bonifati, Patrizia Rizzu, Marijke J van Baren, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 28, 2003
PARK6 is a common cause of familial parkinsonismE M Valente, F Brancati, V Caputo, et al.
Diabetes|April 21, 2007
Effects of the renin-angiotensin system genes and salt sensitivity genes on blood pressure and atherosclerosis in the total population and patients with type 2 diabetesMojgan Yazdanpanah, Yuri S Aulchenko, Albert Hofman, et al.
Frontiers in Genetics|November 24, 2016
A Combined Linkage and Exome Sequencing Analysis for Electrocardiogram Parameters in the Erasmus Rucphen Family StudyClaudia T Silva, Irina V Zorkoltseva, Najaf Amin, et al.
European Journal of Human Genetics : EJHG|January 28, 2018
CXorf56, a dendritic neuronal protein, identified as a new candidate gene for X-linked intellectual disabilityAnnemieke J M H Verkerk, Shimriet Zeidler, Guido Breedveld, et al.
Diabetes|September 7, 2007
LPIN2 is associated with type 2 diabetes, glucose metabolism, and body compositionYurii S Aulchenko, Jan Pullen, Wigard P Kloosterman, et al.
Neurology|November 29, 2008
FBXO7 mutations cause autosomal recessive, early-onset parkinsonian-pyramidal syndromeA Di Fonzo, M C J Dekker, P Montagna, et al.
Human Molecular Genetics|April 25, 2002
Mutations in TITF-1 are associated with benign hereditary choreaGuido J Breedveld, Jeroen W F van Dongen, Cesare Danesino, et al.
Parkinsonism & Related Disorders|June 6, 2006
LRRK2 G2019S mutation and Parkinson's disease: a clinical, neuropsychological and neuropsychiatric study in a large Italian sampleStefano Goldwurm, Michela Zini, Alessio Di Fonzo, et al.
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