M. Brownstein

发表

Germline mutations in the ribonuclease L gene in families showing linkage with HPC1

K. Klinger, P. Meltzer, J. Carpten, 2002, Nature Genetics.

Genome-wide scan in a large complex pedigree with predominantly male schizophrenics from the island of Kosrae: evidence for linkage to chromosome 2q

E. Wijsman, S. Heath, M. Karayiorgou, 2003, Molecular Psychiatry.

Cloning, genomic organization and expression of a putative human transmembrane protein related to the Caenorhabditis elegans M01F1.4 gene.

C. Robbins, I. Makałowska, M. Leyne, 1999, Gene.

Cloning, mapping, and expression of a novel brain-specific transcript in the Familial Dysautonomia candidate region on Chromosome 9q31

J. Gusella, C. Robbins, I. Makałowska, 2000, Mammalian Genome.

Tissue-specific expression of a splicing mutation in the IKBKAP gene causes familial dysautonomia.

C Maayan, J. Gusella, C. Robbins, 2001, American journal of human genetics.

Major Susceptibility Locus for Prostate Cancer on Chromosome 1 Suggested by a Genome-Wide Search

D A Meyers, T H Beaty, J M Trent, 1996, Science.

Evidence for a prostate cancer susceptibility locus on the X chromosome.

F. Collins, D. Schaid, J. Carpten, 1998, Nature Genetics.

Cloning, mapping, and expression of two novel actin genes, actin-like-7A (ACTL7A) and actin-like-7B (ACTL7B), from the familial dysautonomia candidate region on 9q31.

J. Gusella, C. Robbins, I. Makałowska, 1999, Genomics.

Progressive juvenile-onset punctate cataracts caused by mutation of the gammaD-crystallin gene.

E. Gillanders, D. Stephan, J. Trent, 1999, Proceedings of the National Academy of Sciences of the United States of America.

Localization of a gene for Duane retraction syndrome to chromosome 2q31.

E. Gillanders, J. Trent, S. Juo, 1999, American journal of human genetics.

Analysis of aldehyde oxidase and xanthine dehydrogenase/oxidase as possible candidate genes for autosomal recessive familial amyotrophic lateral sclerosis

M. Brownstein, J. Repine, É. Mezey, 1995, Somatic cell and molecular genetics.

Evidence for a Prostate Cancer Susceptibility Locus on the X Chromosome

F. Collins, D. Schaid, J. Carpten, 1999 .

A genetic epidemiological study of hereditary prostate cancer (HPC) in Finland: frequent HPCX linkage in families with late-onset disease.

J. Carpten, E. Gillanders, D. Stephan, 2000, Clinical cancer research : an official journal of the American Association for Cancer Research.

Genome-wide scan in a large complex pedigree with predominantly male schizophrenics from the island of Kosrae: evidence for linkage to chromosome 2q

E. Wijsman, S. Heath, M. Karayiorgou, 2003, Molecular Psychiatry.

BENIGN AND MALIGNANT NEOPLASMS OF PROSTATE Evidence for a Prostate Cancer Susceptibility Locus on the X Chromosome

F. Collins, D. Schaid, J. Carpten, 1999 .

Mapping a gene involved in regulating dietary cholesterol absorption. The sitosterolemia locus is found at chromosome 2p21.

M. Polymeropoulos, S. Grundy, M. Brownstein, 1998, The Journal of clinical investigation.

Modulation of non-templated nucleotide addition by Taq DNA polymerase: primer modifications that facilitate genotyping.

J. Carpten, M. Brownstein, J. Smith, 1996, BioTechniques.

Molecular cloning and expression of the cDNA for the alpha 1A-adrenergic receptor. The gene for which is located on human chromosome 5.

M. Caron, M. Brownstein, R. Lefkowitz, 1991, The Journal of biological chemistry.

Approach to genotyping errors caused by nontemplated nucleotide addition by Taq DNA polymerase.

F. Collins, J. Carpten, J. Trent, 1995, Genome research.

Methods for precise sizing, automated binning of alleles, and reduction of error rates in large-scale genotyping using fluorescently labeled dinucleotide markers. FUSION (Finland-U.S. Investigation of NIDDM Genetics) Study Group.

Joseph B. Rayman, J. Powell, F. Collins, 1997, Genome research.