Genomics

Transcriptome of the human retina, retinal pigmented epithelium and choroid.  105:253-264. 2015

Prioritizing drug targets in Clostridium botulinum with a computational systems biology approach.  104:24-35. 2014

Genome-wide analysis of genetic alterations in testicular primary seminoma using high resolution single nucleotide polymorphism arrays.  97:341-349. 2011

Redefining regulation of DNA methylation by RNA interference.  96:191-198. 2010

Single nucleotide polymorphisms affect both cis- and trans-eQTLs.  93:501-508. 2009

Comparative genomic and phylogenetic analysis of short-chain dehydrogenases/reductases with dual retinol/sterol substrate specificity.  88:820-830. 2006

Genome-wide detection of LOH in prostate cancer using human SNP microarray technology.  81:260-269. 2003

Identification of FOXC1 as a TGF-β1 responsive gene and its involvement in negative regulation of cell growth.  80:465-472. 2002

Structural conservation of the genes encoding CaT1, CaT2, and related cation channels.  76:99-109. 2001

Mutations in Cdh23 cause nonsyndromic hearing loss in waltzer mice.  74:228-233. 2001

Identification of BPESC1, a novel gene disrupted by a balanced chromosomal translocation, t(3;4)(q23;p15.2), in a patient with BPES.  68:296-304. 2000

Isolation and preliminary characterization of the human and mouse homologues of the bacterial cell cycle gene Era.  67:78-82. 2000

Erratum: The uroguanylin gene (Guca1b) is linked to guanylin (Guca2) on mouse chromosome 4 (Genomics (1997) 45:2 (348-354)).  66:122. 2000

Closing in on the BPES gene on 3q23: Mapping of a de Novo reciprocal translocation t(3;4)(q23;p15.2) Breakpoint within a 45-kb cosmid and mapping of three candidate genes, RBP1, RBP2, and β'-COP, distal to the breakpoint.  57:70-78. 1999

Assembly of a BAC contig of the complementation group B cell senescence gene candidate region at 4q33-q34.1 and identification of expressed sequences.  56:353-354. 1999

Genetic analysis of susceptibility to dextran sulfate sodium-induced colitis in mice.  55:147-156. 1999

Genomic cloning, molecular characterization, and functional analysis of human CLCA1, the first human member of the family of Ca²⁺-activated Cl^- channel proteins.  54:200-214. 1998

Chromosome localization and genomic structure of the KiSS-1 metastasis suppressor gene (KISS1).  54:145-148. 1998

Localization of HuC (ELAVL3) to chromosome 19p13.2 by fluorescence in situ hybridization utilizing a novel tyramide labeling technique.  53:296-299. 1998

Genomic structure and chromosomal mapping of the nuclear orphan receptor RORγ (RORC) gene.  46:93-102. 1997

The human angiotensinase C gene (HUMPCP) maps to 11q14 within 700 kb of D11S901: A candidate gene for essential hypertension.  44:365-367. 1997

Identification and characterization of the human homologue of SH3BP2, an SH3 binding domain protein within a common region of deletion at 4p16.3 Involved in bladder cancer.  44:163-170. 1997

cDNA cloning, genomic structure, and chromosome mapping of the human epithelial membrane protein CL-20 gene (EMP1), a member of the PMP22 family.  41:40-48. 1997

The uroguanylin gene (Guca1b) is linked to guanylin (Guca2) on mouse chromosome 4.  45:348-354. 1997

Localization of human elav-like neuronal protein 1 (Hel-N1) on chromosome 9p21 by chromosome microdissection polymerase chain reaction and fluorescence in situ hybridization.  36:189-191. 1996

Gene structure and chromosome localization to 7q21.3 of the human rod photoreceptor transducin γ-subunit gene (GNGT1).  35:241-243. 1996

The mouse BP-1 gene: Stucture, chromosomal localization, and regulation of expression by type I interferons and interleukin-7.  33:167-176. 1996

Identification and characterization of a new human gene (APOC4) in the apolipoprotein E, C-I, and C-II gene locus.  28:291-300. 1995

cDNA, gene structure, and chromosomal localization of human GAR1 (CNCG3L), a homolog of the third subunit of bovine photoreceptor cGMP-gated channel.  28:32-38. 1995

A novel creb family gene telomeric of HLA-DRA in the HLA complex.  30:149-156. 1995

Feature mapping of the HLA class I region: Localization of the POU5F1 and TCF19 genes.  30:53-58. 1995

Mapping of guanylin to murine chromosome 4 and human chromosome 1p34-p35.  26:427-429. 1995

Localization of the α2-Macroglobulin Receptor-Associated Protein 1 Gene (LRPAP1) and Other Gene Fragments to Human Chromosome 4p16.3 by Direct cDNA Selection.  24:410-413. 1994

A yac contig of approximately 3 mb from human chromosome 5q31 → q33.  19:470-477. 1994

Genomic sequence of the murine guanylin gene.  24:583-587. 1994

Human retinal guanylate cyclase (GUC2D) maps to chromosome 17p13.1.  22:478-481. 1994

Chromosomal Localization of Five Murine HSP70 Gene Family Members: Hsp70.1, Hsp70-2, Hsp70-3, Hsc70t, and Grp78.  16:193-198. 1993

Highly informative typing of the human TNF locus using six adjacent polymorphic markers.  16:180-186. 1993

Mitochondrial dna variants observed in alzheimer disease and parkinson disease patients.  17:171-184. 1993

Rapid identification of VNTR alleles of the human thyroid peroxidase gene by PCR: A study in a population sample from south Italy.  17:796-798. 1993

A radiation hybrid map of the region on human chromosome 22 containing the neurofibromatosis type 2 locus.  14:574-584. 1992

Chromosome mapping of the rod photoreceptor cGMP phosphodiesterase β-subunit gene in mouse and human: Tight linkage to the Huntington disease region (4p16.3).  12:750-754. 1992

Exclusion of linkage between hypokalemic periodic paralysis (HOKPP) and three candidate loci.  14:493-494. 1992

Mapping of the mouse Rxr loci encoding nuclear retinoid X receptors RXRα, RXRβ, and RXRγ.  14:611-617. 1992

Syntenic assignments of visual transduction genes in cattle.  14:699-706. 1992

A map of the distal region of the long arm of human chromosome 21 constructed by radiation hybrid mapping and pulsed-field gel electrophoresis.  9:19-30. 1991

Characterization of the 3′ half of the human type IV collagen α5 gene that is affected in the Alport syndrome.  9:1-9. 1991

Localization of the expressed human p58 protein kinase chromosomal gene to chromosome 1p36 and a highly related sequence to chromosome 15.  11:621-629. 1991

Molecular linkage of the HLA-DR, HLA-DQ, and HLA-DO genes in yeast artificial chromosomes.  11:577-586. 1991

Physical mapping of yeast artificial chromosomes containing sequences from the human β-globin gene region.  10:976-984. 1991

Genetic linkage of the human apolipoprotein AI-CIII-AIV gene cluster and the neural cell adhesion molecule (NCAM) gene.  7:633-637. 1990

Molecular characterization of human and bovine rod photoreceptor cGMP phosphodiesterase α-subunit and chromosomal localization of the human gene.  6:272-283. 1990

Huntington disease: No evidence for locus heterogeneity.  5:304-308. 1989

Isolation and field-inversion gel electrophoresis analysis of DNA markers located close to the Huntington disease gene.  4:408-418. 1989

Segregation of the Huntington disease region of human chromosome 4 in a somatic cell hybrid.  4:397-407. 1989

Nucleotide sequence and expression of the human skeletal α-actin gene: Evolution of functional regulatory domains.  3:323-336. 1988

Linkage analysis in von Recklinghausen neurofibromatosis (NF1) with DNA markers for chromosome 17.  1:346-348. 1987