V C Sheffield

发表

Nonsyndromic autosomal recessive deafness is linked to the DFNB1 locus in a large inbred Bedouin family from Israel.

V. Sheffield, E. Stone, K. Elbedour, 1995, American journal of human genetics.

Catechol-O-methyl transferase Val158Met gene polymorphism in schizophrenia: working memory, frontal lobe MRI morphology and frontal cerebral blood flow

N C Andreasen, D S O'Leary, V C Sheffield, 2005 .

Refining the DFNB7-DFNB11 deafness locus using intragenic polymorphisms in a novel gene, TMEM2.

B J Keats, V. Sheffield, R. Swiderski, 2000, Gene.

Use of isolated inbred human populations for identification of disease genes.

V. Sheffield, E. Stone, R. Carmi, 1998, Trends in genetics : TIG.

Identification of a Bardet-Biedl syndrome locus on chromosome 3 and evaluation of an efficient approach to homozygosity mapping.

V. Sheffield, E. Stone, K. Elbedour, 1994, Human molecular genetics.

Examination of AVPR1a as an autism susceptibility gene

V J Vieland, S. Folstein, J. Piven, 2004, Molecular Psychiatry.

Involvement of multiple chromosome 17p loci in medulloblastoma tumorigenesis.

V. Sheffield, G. Duyk, P. Cogen, 1992, American journal of human genetics.

Functional differences of the PDS gene product are associated with phenotypic variation in patients with Pendred syndrome and non-syndromic hearing loss (DFNB4).

V. Sheffield, J. Bishop, D. Scott, 2000, Human molecular genetics.

Catechol-O-methyl transferase Val158Met gene polymorphism in schizophrenia: working memory, frontal lobe MRI morphology and frontal cerebral blood flow

N C Andreasen, D S O'Leary, V. Sheffield, 2005, Molecular Psychiatry.

A comprehensive human linkage map with centimorgan density. Cooperative Human Linkage Center (CHLC).

K H Buetow, J C Murray, J. Weber, 1994, Science.

Use of a DNA pooling strategy to identify a human obesity syndrome locus on chromosome 15.

V. Sheffield, E. Stone, K. Elbedour, 1995, Human molecular genetics.

An autosomal recessive nonsyndromic-hearing-loss locus identified by DNA pooling using two inbred Bedouin kindreds.

V. Sheffield, E. Stone, K. Elbedour, 1996, American journal of human genetics.

A collection of tri- and tetranucleotide repeat markers used to generate high quality, high resolution human genome-wide linkage maps.

K H Buetow, J C Murray, J. Weber, 1995, Human molecular genetics.

Evaluation of the myocilin (MYOC) glaucoma gene in monkey and human steroid-induced ocular hypertension.

V. Sheffield, D. Mackey, E. Stone, 2001, Investigative ophthalmology & visual science.

Delayed secondary glucocorticoid responsiveness of MYOC in human trabecular meshwork cells.

V. Sheffield, E. Stone, J. Fingert, 2001, Investigative ophthalmology & visual science.

A spectrum of FOXC1 mutations suggests gene dosage as a mechanism for developmental defects of the anterior chamber of the eye.

D Y Nishimura, V. Sheffield, D. Mackey, 2001, American journal of human genetics.

J C Murray, J. Weber, V. Sheffield, 1998 .

A cerebellar ataxia locus identified by DNA pooling to search for linkage disequilibrium in an isolated population from the Cayman Islands.

V. Sheffield, E. Stone, A. Nystuen, 1996, Human molecular genetics.

Variation of codons 1961 and 2177 of the Stargardt disease gene is not associated with age-related macular degeneration.

D F Schorderet, V. Sheffield, E. Stone, 2001, Archives of ophthalmology.

Automated construction of high-density comparative maps between rat, human, and mouse.

V. Sheffield, M. Nóbrega, M. Soares, 2001, Genome research.

Attachment of a 40-base-pair G + C-rich sequence (GC-clamp) to genomic DNA fragments by the polymerase chain reaction results in improved detection of single-base changes.

V. Sheffield, R. Myers, D. Cox, 1989, Proceedings of the National Academy of Sciences of the United States of America.