B Anar

Author PubWeight™ 10.10^‹?›

Rank	Title	Journal	Year	PubWeight™‹?›
1	Distinct genetic forms of frontotemporal dementia.	Neurology	2008	2.15
2	Familial aggregation of parkinsonism in progressive supranuclear palsy.	Neurology	2009	1.68
3	Different targets for the fragile X-related proteins revealed by their distinct nuclear localizations.	Hum Mol Genet	1999	1.35
4	Noninvasive test for fragile X syndrome, using hair root analysis.	Am J Hum Genet	1999	0.95
5	Association of the 677C-->T mutation on the methylenetetrahydrofolate reductase gene in Turkish patients with neural tube defects.	J Child Neurol	1999	0.85
6	Clinical and genetic correlate in childhood onset Friedreich ataxia.	Neuropediatrics	1999	0.84
7	677-->CT mutation on the methylenetetrahydrofolate reductase gene is not a risk factor for neural tube defects in Turkey.	Arch Dis Child Fetal Neonatal Ed	1998	0.80
8	Frequency of fragile X syndrome among Turkish patients with mental retardation of unknown etiology.	Am J Med Genet	1999	0.79
9	Screening for the fragile X syndrome among mentally retarded males by hair root analysis.	Am J Med Genet	2000	0.78
10	Angiotensin converting enzyme gene polymorphism and the risk and extent of ischemic heart disease among Turkish patients.	Coron Artery Dis	1997	0.75