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Bases adjacent to mononucleotide repeats show an increased single nucleotide polymorphism frequency in the human genome

Bioinformatics, 2011-04, Vol.27 (7), p.895-898

2011

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Germ-line mutations of TP53 in Li-Fraumeni families : An extended study of 39 families

Cancer research (Chicago, Ill.), 1997-08, Vol.57 (15), p.3245-3252

1997

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An Expectation-Maximization Algorithm for the Analysis of Allelic Expression Imbalance

American journal of human genetics, 2006-09, Vol.79 (3), p.539-543

2006

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Conservation of polyglutamine tract size between mice and humans depends on codon interruption

Molecular biology and evolution, 1999-11, Vol.16 (11), p.1641-1644

1999

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The alleles of the DNA repair gene O6-alkylguanine-DNA alkyltransferase are expressed at different levels in normal human lung tissue

Carcinogenesis (New York), 2003-10, Vol.24 (10), p.1691-1694

2003

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A Molecular Genetic and Statistical Approach for the Diagnosis of Dual-Site Cancers

JNCI : Journal of the National Cancer Institute, 2004-10, Vol.96 (19), p.1441-1446

2004

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Overexpression of aurora B kinase (AURKB) in primary non-small cell lung carcinoma is frequent, generally driven from one allele, and correlates with the level of genetic instability

British journal of cancer, 2005-09, Vol.93 (6), p.719-729

2005

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An extended Li-Fraumeni kindred with gastric carcinoma and a codon 175 mutation in TP53

Journal of medical genetics, 1995-12, Vol.32 (12), p.942-945

1995

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The use of loss of constitutional heterozygosity data to ascertain the location of predisposing genes in cancer families

Journal of medical genetics, 1994-06, Vol.31 (6), p.448-452

1994

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O 6 ‐alkylguanine‐DNA alkyltransferase: Role in carcinogenesis and chemotherapy

BioEssays, 2002-03, Vol.24 (3), p.255-266

2002

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Polymorphism in exon 1 of the C-Ha-ras gene, (HRAS)

Nucleic acids research, 1991-12, Vol.19 (24), p.6976-6976

1991

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Unexpected effects on bacterial phenotype induced by expression of a tumour-amplified human sequence

Nucleic acids research, 1989-09, Vol.17 (17), p.6893-6901

1989

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The Comparative Genomics of Polyglutamine Repeats: Extreme Difference in the Codon Organization of Repeat-Encoding Regions Between Mammals and Drosophila

Journal of molecular evolution, 2001-03, Vol.52 (3), p.249-259

2001

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A strategy for the rapid isolation of new PCR based DNA polymorphisms

Journal of medical genetics, 1992-04, Vol.29 (4), p.249-250

1992

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A role for selection in regulating the evolutionary emergence of disease-causing and other coding CAG repeats in humans and mice

Molecular biology and evolution, 2001-06, Vol.18 (6), p.1014-1023

2001

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Linkage analysis and the study of Mendelian disease in the era of whole exome and genome sequencing

Briefings in functional genomics, 2014-09, Vol.13 (5), p.378-383

2014

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Alkyltransferase-like proteins

DNA repair, 2007-08, Vol.6 (8), p.1222-1228

2007

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Lung cancer risk and variation in MGMT activity and sequence

DNA repair, 2007-08, Vol.6 (8), p.1134-1144

2007

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Rare variant (Glu to Lys) in the leucine zipper region of CHOP (GADD153)

Oncogene, 1994-09, Vol.9 (9), p.2737-2738

1994

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Prevalence and diversity of constitutional mutations in the p53 gene among 21 Li-fraumeni families

Cancer research (Chicago, Ill.), 1994-03, Vol.54 (5), p.1298-1304

1994

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p53 germline mutations in Li-Fraumeni syndrome

The Lancet (British edition), 1991-12, Vol.338 (8781), p.1490-1491

1991

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Identification of microsatellite instability and mismatch repair gene mutations in breast cancer cell lines

Genes chromosomes & cancer, 2003-05, Vol.37 (1), p.29-35

2003

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A phylogenetic approach to assessing the significance of missense mutations in disease genes

Human mutation, 2003-07, Vol.22 (1), p.51-58

2003

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Amino acid reiterations in yeast are overrepresented in particular classes of proteins and show evidence of a slippage-like mutational process

Journal of molecular evolution, 1999-12, Vol.49 (6), p.789-797

1999

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A relationship between lengths of microsatellites and nearby substitution rates in mammalian genomes

Molecular biology and evolution, 2001-11, Vol.18 (11), p.2119-2123

2001

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Bases adjacent to mononucleotide repeats show an increased single nucleotide polymorphism frequency in the human genome

Germ-line mutations of TP53 in Li-Fraumeni families : An extended study of 39 families

An Expectation-Maximization Algorithm for the Analysis of Allelic Expression Imbalance

Conservation of polyglutamine tract size between mice and humans depends on codon interruption

The alleles of the DNA repair gene O6-alkylguanine-DNA alkyltransferase are expressed at different levels in normal human lung tissue

A Molecular Genetic and Statistical Approach for the Diagnosis of Dual-Site Cancers

Overexpression of aurora B kinase (AURKB) in primary non-small cell lung carcinoma is frequent, generally driven from one allele, and correlates with the level of genetic instability

An extended Li-Fraumeni kindred with gastric carcinoma and a codon 175 mutation in TP53

The use of loss of constitutional heterozygosity data to ascertain the location of predisposing genes in cancer families

O 6 ‐alkylguanine‐DNA alkyltransferase: Role in carcinogenesis and chemotherapy

Polymorphism in exon 1 of the C-Ha-ras gene, (HRAS)

Unexpected effects on bacterial phenotype induced by expression of a tumour-amplified human sequence

The Comparative Genomics of Polyglutamine Repeats: Extreme Difference in the Codon Organization of Repeat-Encoding Regions Between Mammals and Drosophila

A strategy for the rapid isolation of new PCR based DNA polymorphisms

A role for selection in regulating the evolutionary emergence of disease-causing and other coding CAG repeats in humans and mice

Linkage analysis and the study of Mendelian disease in the era of whole exome and genome sequencing

Alkyltransferase-like proteins

Lung cancer risk and variation in MGMT activity and sequence

Rare variant (Glu to Lys) in the leucine zipper region of CHOP (GADD153)

Prevalence and diversity of constitutional mutations in the p53 gene among 21 Li-fraumeni families

p53 germline mutations in Li-Fraumeni syndrome

Identification of microsatellite instability and mismatch repair gene mutations in breast cancer cell lines

A phylogenetic approach to assessing the significance of missense mutations in disease genes

Amino acid reiterations in yeast are overrepresented in particular classes of proteins and show evidence of a slippage-like mutational process

A relationship between lengths of microsatellites and nearby substitution rates in mammalian genomes

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