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Annals of Neurology|February 9, 2002
Localization of autosomal recessive early-onset parkinsonism to chromosome 1p36 (PARK7) in an independent datasetVincenzo Bonifati, Guido J Breedveld, Ferdinando Squitieri, et al.Molecular Psychiatry|August 10, 2011
A genome-wide linkage study of individuals with high scores on NEO personality traitsN Amin, M Schuur, E S Gusareva, et al.Brain : a Journal of Neurology|May 8, 2004
Familial clustering and genetic risk for dementia in a genetically isolated Dutch populationK Sleegers, G Roks, J Theuns, et al.Investigative Ophthalmology & Visual Science|July 27, 2007
Genetic contributions to glaucoma: heritability of intraocular pressure, retinal nerve fiber layer thickness, and optic disc morphologyLeonieke M E van Koolwijk, Dominiek D G Despriet, Cornelia M van Duijn, et al.Diabetes|November 25, 2003
A genome-wide search for genes involved in type 2 diabetes in a recently genetically isolated population from the NetherlandsYurii S Aulchenko, Norbert Vaessen, Peter Heutink, et al.Calcified Tissue International|December 4, 2009
The role of body mass index, insulin, and adiponectin in the relation between fat distribution and bone mineral densityM Carola Zillikens, André G Uitterlinden, Johannes P T M van Leeuwen, et al.Nature Genetics|June 30, 2001
A mutation in SLC11A3 is associated with autosomal dominant hemochromatosisO T Njajou, N Vaessen, M Joosse, et al.Journal of Medical Genetics|February 1, 1993
The fragile X syndrome: no evidence for any recent mutationsA P Smits, J C Dreesen, J G Post, et al.The American Journal of Clinical Nutrition|March 26, 2010
Interactions between dietary vitamin E intake and SIRT1 genetic variation influence body mass indexM Carola Zillikens, Joyce B J van Meurs, Fernando Rivadeneira, et al.Cephalalgia : an International Journal of Headache|November 14, 2012
Migraine is not associated with enhanced atherosclerosisAnine H Stam, Claudia M Weller, A Cecile Jw Janssens, et al.Pageof 51