Published in Clin Genet on September 01, 1994
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An alpha-2-macroglobulin insertion-deletion polymorphism in Alzheimer disease. Nat Genet (1999) 2.01
Assignment of the gene for Wilson disease to chromosome 13: linkage to the esterase D locus. Proc Natl Acad Sci U S A (1985) 2.00
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Saccades in presymptomatic and early stages of Huntington disease. Neurology (2006) 1.92
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Transmission of a balanced homologous t(22q;22q) translocation from mother to normal daughter. Clin Genet (1980) 1.84
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Autosomal genomic scan for loci linked to obesity and energy metabolism in Pima Indians. Am J Hum Genet (1998) 1.78
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Differences in duration of Huntington's disease based on age at onset. J Neurol Neurosurg Psychiatry (1999) 1.63
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Genetic anticipation and abnormal gender ratio at birth in familial primary pulmonary hypertension. Am J Respir Crit Care Med (1995) 1.60
The genetic defect in familial Alzheimer's disease is not tightly linked to the amyloid beta-protein gene. Nature (1987) 1.57
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Linkage of structure at the proximal femur to chromosomes 3, 7, 8, and 19. J Bone Miner Res (2003) 1.55
The normal Huntington disease (HD) allele, or a closely linked gene, influences age at onset of HD. Am J Hum Genet (1993) 1.55
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Localization of the gene for familial primary pulmonary hypertension to chromosome 2q31-32. Nat Genet (1997) 1.52
Variation in GIGYF2 is not associated with Parkinson disease. Neurology (2009) 1.47
Evidence for a locus on chromosome 1 that influences vulnerability to alcoholism and affective disorder. Am J Psychiatry (2001) 1.46
No genetic effect of alpha1-antichymotrypsin in Alzheimer disease. Genomics (1996) 1.45
Sibling pair linkage and association studies between bone mineral density and the insulin-like growth factor I gene locus. J Clin Endocrinol Metab (1999) 1.45
A non-organic and non-enzymatic extraction method gives higher yields of genomic DNA from whole-blood samples than do nine other methods tested. J Biochem Biophys Methods (1992) 1.44
Genome screen for QTLs contributing to normal variation in bone mineral density and osteoporosis. J Clin Endocrinol Metab (2000) 1.43
Quantitative trait loci analysis of human event-related brain potentials: P3 voltage. Electroencephalogr Clin Neurophysiol (1998) 1.43
Familial occurrence of renal and Müllerian duct hypoplasia, craniofacial anomalies, severe growth and developmental delay. Am J Med Genet (1992) 1.43
A DNA polymorphism for Huntington's disease marks the future. Arch Neurol (1985) 1.43
Association of the kappa-opioid system with alcohol dependence. Mol Psychiatry (2006) 1.42
Longitudinal cognitive and motor changes among presymptomatic Huntington disease gene carriers. Arch Neurol (1999) 1.41
Mutant prion proteins in Gerstmann-Sträussler-Scheinker disease with neurofibrillary tangles. Nat Genet (1992) 1.41
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Holoprosencephaly: birth data, benetic and demographic analyses of 30 families. Birth Defects Orig Artic Ser (1975) 1.40
Analysis of association at single nucleotide polymorphisms in the APOE region. Genomics (2000) 1.40
Huntington disease: estimation of heterozygote status using linked genetic markers. Genet Epidemiol (1984) 1.39
Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson disease. Neurology (2008) 1.39
Biochemical and molecular genetic characterization of a new variant prealbumin associated with hereditary amyloidosis. J Clin Invest (1986) 1.38
Human amylase loci: genetic linkage with the Duffy blood group locus and assignment to linkage group I. Am J Hum Genet (1973) 1.38
A quantitative trait locus for alcohol consumption in selectively bred rat lines. Alcohol Clin Exp Res (1998) 1.37
Huntington's disease: two families with differing clinical features show linkage to the G8 probe. Science (1985) 1.37
Two models for a maternal factor in the inheritance of Huntington disease. Am J Hum Genet (1983) 1.37
A genetic linkage map of the long arm of human chromosome 22. Genomics (1989) 1.37
Genetic analysis in families with van der Woude syndrome. J Craniofac Genet Dev Biol (1985) 1.37