PubRank

G E Houck

Author PubWeight™ 20.60‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Rapid fragile X carrier screening and prenatal diagnosis using a nonradioactive PCR test. JAMA 1993 2.59
2 Chromosome 21q21 sublocalisation of gene encoding beta-amyloid peptide in cerebral vessels and neuritic (senile) plaques of people with Alzheimer disease and Down syndrome. Lancet 1987 2.44
3 Familial transmission of the FMR1 CGG repeat. Am J Hum Genet 1996 1.53
4 Mosaicism in fragile X affected males. Am J Med Genet 1994 1.23
5 Chromosomal localization of several families of repetitive sequences by in situ hybridization. Am J Hum Genet 1985 1.14
6 Cytogenetic and molecular identification of a de novo direct duplication of the long arm of chromosome 4(q21.3-->q31.3). Am J Med Genet 1993 1.10
7 Distribution of FMR-1 and associated microsatellite alleles in a normal Chinese population. Am J Med Genet 1994 0.98
8 Reverse mutations in the fragile X syndrome. Am J Med Genet 1996 0.97
9 FMR1 CGG-repeat instability in single sperm and lymphocytes of fragile-X premutation males. Am J Hum Genet 1999 0.91
10 A comparison of adult and childhood progerias: Werner syndrome and Hutchinson-Gilford progeria syndrome. Adv Exp Med Biol 1985 0.88
11 Sanfilippo disease, type A with some features of ceroid lipofuscinosis. Neuropediatrics 1985 0.81
12 Ultrastructural, neurological, and glycosaminoglycan abnormalities in lowe's syndrome. Ann Neurol 1984 0.79
13 Elevation of urinary hyaluronic acid in Werner's syndrome and progeria. Biochem Med Metab Biol 1986 0.79
14 Localization of chromosome 21 probes by in situ hybridization. Ann N Y Acad Sci 1985 0.78
15 Isolation and regional localization by in situ hybridization of a unique gene segment to chromosome 21. Biochem Biophys Res Commun 1984 0.78
16 Fine mapping of an Alzheimer disease-associated gene encoding beta-amyloid protein. Biochem Biophys Res Commun 1988 0.77
17 Prenatal fragile X detection using cytoplasmic and nuclear-specific monoclonal antibodies. Am J Med Genet 1999 0.77
18 In-situ hybridisation of the beta-amyloid protein probe to chromosome 9 in patients with familial Alzheimer's disease. Lancet 1987 0.76
19 An anonymous single copy chromosome 21 probe, DS21D2, associated with a frequent RFLP. Nucleic Acids Res 1985 0.75
20 Fragile X induction systems in CVS cultures: effect on cytogenetic, PCR, and genomic Southern Blot DNA analyses of the FMR-1 gene. Am J Med Genet 1994 0.75
21 Molecular carrier testing for the fragile X syndrome: Issues for genetic counselors. J Genet Couns 1994 0.75
22 Beta-amyloid protein probe hybridized to chromosome 9 in 3 Alzheimer disease individuals. Prog Clin Biol Res 1989 0.75
23 Reassessment of a chromosome 12q+ marker by fluorescent in situ hybridization (FISH). Clin Genet 1992 0.75
24 Molecular quantitation of aneuploid conditions using chromosome 21 as a model. Ann N Y Acad Sci 1985 0.75
25 Low sulfated glycosaminoglycans are excreted in patients with the Lowe syndrome. Biochem Med 1984 0.75