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Inflammatory bowel disease is associated with a TNF polymorphism that affects an interaction between the OCT1 and NF-κB transcription factors

Human molecular genetics, 2002-05, Vol.11 (11), p.1281-1289

2002

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Congenital non-syndromal sensorineural hearing impairment due to connexin 26 gene mutations — molecular and audiological findings

International journal of pediatric otorhinolaryngology, 1999-10, Vol.50 (1), p.3-13

1999

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The IBD6 Crohn's disease locus demonstrates complex interactions with CARD15 and IBD5 disease-associated variants

Human molecular genetics, 2003-10, Vol.12 (20), p.2569-2575

2003

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A candidate for the cystic fibrosis locus isolated by selection for methylation-free islands

Nature (London), 1987-04, Vol.326 (6116), p.840-845

1987

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The human gene encoding FKBP-rapamycin associated protein (FRAP) maps to chromosomal band 1p36.2

Human genetics, 1997-04, Vol.99 (4), p.547-549

1997

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A region of homozygosity within 22q11.2 associated with congenital heart disease: recessive DiGeorge/velocardiofacial syndrome?

Journal of medical genetics, 2001-08, Vol.38 (8), p.533-536

2001

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Vectorette PCR isolation of microsatellite repeat sequences using anchored dinucleotide repeat primers

Nucleic acids research, 1996-06, Vol.24 (11), p.2190-2191

1996

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Cloning the mouse homolog of the human cystic fibrosis transmembrane conductance regulator gene

Genomics (San Diego, Calif.), 1991-06, Vol.10 (2), p.301-307

1991

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Assignment of the STAT6 gene (STAT6) to human chromosome band 12q13 by in situ hybridization

Cytogenetic and genome research, 1997-01, Vol.79 (3-4), p.208-209

1997

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An EST and STS-Based YAC Contig Map of Human Chromosome 9q22.3

Genomics (San Diego, Calif.), 1996-12, Vol.38 (2), p.199-205

1996

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Assignment of the DNA fragmentation factor gene (DFFA) to human chromosome bands 1p36.3-->p36.2 by in situ hybridization

Cytogenetic and genome research, 1997-01, Vol.79 (3-4), p.212-213

1997

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Detailed genetic mapping around a putative prostate-specific membrane antigen locus on human chromosome 11p11.2

Cytogenetic and genome research, 1998, Vol.81 (1), p.3-9

1998

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Population genomics and dental public health

Community dental health, 2006-09, Vol.23 (3), p.130

2006

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Assignment of Indian hedgehog (IHH) to human chromosome bands 2q33-->q35 by in situ hybridization

Cytogenetic and genome research, 1997-01, Vol.76 (3-4), p.187-188

1997

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Assignment of the Rab13 gene (RAB13) to human chromosome band 12q13 by in situ hybridization

Cytogenetic and genome research, 1997-01, Vol.79 (3-4), p.210-211

1997

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Inflammatory bowel disease susceptibility loci defined by genome scan meta-analysis of 1952 affected relative pairs

Human molecular genetics, 2004-04, Vol.13 (7), p.763-770

2004

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Human sequences homologous to the gene for the cochlear protein Ocp‐II do not map to currently known non‐syndromic hearing loss loci

Annals of human genetics, 1996-09, Vol.60 (5), p.385-389

1996

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Genetics – getting personal

Drug discovery today, 2008-03, Vol.13 (5), p.189-191

Lench, Nicholas J.

2008

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A human ubiquitin conjugating enzyme, L-UBC, maps in the Alzheimer's disease locus on chromosome 14q24.3

Mammalian genome, 1995-10, Vol.6 (10), p.725-731

1995

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(CGG) trinucleotide repeat polymorphism in the 5' region of the HHR6B gene : the human homolog of the yeast DNA repair gene RAD6

Human genetics, 1995-09, Vol.96 (3), p.369-370

1995

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YAC clones that extend the human chromosome 12cen-12q15 region contig map

Mammalian genome, 1996-10, Vol.7 (10), p.780-783

1996

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Yeast artificial chromosome cloning and chromosomal localization of the abundant odontogenic keratocyst protein elafin

Archives of oral biology, 1996-05, Vol.41 (5), p.445-452

1996

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DNA Marker D11S384 Shows Zero Recombination with the Ataxia-telangiectasia Locus in North American Families

International journal of radiation biology, 1994, Vol.66 (6), p.S67-S69

1994

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Genetic aspects of ataxia telangiectasia

Advances in neurology, 1993, Vol.61, p.115

1993

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Inflammatory bowel disease is associated with a TNF polymorphism that affects an interaction between the OCT1 and NF-κB transcription factors

Congenital non-syndromal sensorineural hearing impairment due to connexin 26 gene mutations — molecular and audiological findings

Prelingual Deafness: High Prevalence of a 30delG Mutation in the Connexin 26 Gene

The IBD6 Crohn's disease locus demonstrates complex interactions with CARD15 and IBD5 disease-associated variants

A candidate for the cystic fibrosis locus isolated by selection for methylation-free islands

The human gene encoding FKBP-rapamycin associated protein (FRAP) maps to chromosomal band 1p36.2

A region of homozygosity within 22q11.2 associated with congenital heart disease: recessive DiGeorge/velocardiofacial syndrome?

Vectorette PCR isolation of microsatellite repeat sequences using anchored dinucleotide repeat primers

Cloning the mouse homolog of the human cystic fibrosis transmembrane conductance regulator gene

Assignment of the STAT6 gene (STAT6) to human chromosome band 12q13 by in situ hybridization

An EST and STS-Based YAC Contig Map of Human Chromosome 9q22.3

Assignment of the DNA fragmentation factor gene (DFFA) to human chromosome bands 1p36.3-->p36.2 by in situ hybridization

Detailed genetic mapping around a putative prostate-specific membrane antigen locus on human chromosome 11p11.2

Population genomics and dental public health

Assignment of Indian hedgehog (IHH) to human chromosome bands 2q33-->q35 by in situ hybridization

Assignment of the Rab13 gene (RAB13) to human chromosome band 12q13 by in situ hybridization

Inflammatory bowel disease susceptibility loci defined by genome scan meta-analysis of 1952 affected relative pairs

Human sequences homologous to the gene for the cochlear protein Ocp‐II do not map to currently known non‐syndromic hearing loss loci

Genetics – getting personal

A human ubiquitin conjugating enzyme, L-UBC, maps in the Alzheimer's disease locus on chromosome 14q24.3

(CGG) trinucleotide repeat polymorphism in the 5' region of the HHR6B gene : the human homolog of the yeast DNA repair gene RAD6

YAC clones that extend the human chromosome 12cen-12q15 region contig map

Yeast artificial chromosome cloning and chromosomal localization of the abundant odontogenic keratocyst protein elafin

DNA Marker D11S384 Shows Zero Recombination with the Ataxia-telangiectasia Locus in North American Families

Genetic aspects of ataxia telangiectasia

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