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Journal of Neurology|September 25, 2003
A clinical-genetic study of Parkinson's disease in a genetically isolated communityM C J Dekker, J C van Swieten, J J Houwing-Duistermaat, et al.Nature Medicine|April 26, 2011
Ablation of Fmrp in adult neural stem cells disrupts hippocampus-dependent learningWeixiang Guo, Andrea M Allan, Ruiting Zong, et al.Human Genetics|November 21, 2013
Common DNA variants predict tall stature in EuropeansFan Liu, A Emile J Hendriks, Arwin Ralf, et al.Molecular Psychiatry|August 28, 2013
Genome-wide analyses of borderline personality featuresG H Lubke, C Laurin, N Amin, et al.American Journal of Human Genetics|October 27, 1997
Screening and diagnosis for the fragile X syndrome among the mentally retarded: an epidemiological and psychological survey. Collaborative Fragile X Study GroupB B de Vries, A M van den Ouweland, S Mohkamsing, et al.American Journal of Human Genetics|May 1, 1996
Mental status of females with an FMR1 gene full mutationB B de Vries, A M Wiegers, A P Smits, et al.Neurogenetics|August 22, 2008
The LRRK2 Arg1628Pro variant is a risk factor for Parkinson's disease in the Chinese populationChin-Song Lu, Yah-Huei Wu-Chou, Marina van Doeselaar, et al.Journal of the American College of Cardiology|April 25, 2006
A common polymorphism in the complement factor H gene is associated with increased risk of myocardial infarction: the Rotterdam StudyIsabella Kardys, Caroline C W Klaver, Dominiek D G Despriet, et al.Human Molecular Genetics|February 28, 1998
Generalized glycogen storage and cardiomegaly in a knockout mouse model of Pompe diseaseA G Bijvoet, E H van de Kamp, M A Kroos, et al.Stroke|June 7, 2003
Polymorphism in the promoter region of the insulin-like growth factor I gene is related to carotid intima-media thickness and aortic pulse wave velocity in subjects with hypertensionA F C Schut, J A M J L Janssen, J Deinum, et al.Pageof 51