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High-Throughput Development and Characterization of a Genomewide Collection of Gene-Based Single Nucleotide Polymorphism Markers by Chip-Based Matrix-Assisted Laser Desorption/Ionization Time-of-Flight Mass Spectrometry

Proceedings of the National Academy of Sciences - PNAS, 2001-01, Vol.98 (2), p.581-584

2001

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Reliable identification of large numbers of candidate SNPs from public EST data

Nature genetics, 1999-03, Vol.21 (3), p.323-325

1999

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Identification of inbred mouse strains harboring genetic modifiers of mammary tumor age of onset and metastatic progression

International journal of cancer, 1998-08, Vol.77 (4), p.640-644

1998

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Constitutional genetic variation at the human aromatase gene ( ) and breast cancer risk

British journal of cancer, 1999-02, Vol.79 (3-4), p.456-463

1999

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The Cancer Genome Anatomy Project: building an annotated gene index

Trends in genetics, 2000-03, Vol.16 (3), p.103-106

2000

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Integrated human genome-wide maps constructed using the CEPH reference panel

Nature genetics, 1994-04, Vol.6 (4), p.391-393

1994

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Influence of aberrant observations on high-resolution linkage analysis outcomes

American journal of human genetics, 1991-11, Vol.49 (5), p.985-994

BUETOW, K. H

1991

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Association of genetic variation of the transforming growth factor-alpha gene with cleft lip and palate

American journal of human genetics, 1989-09, Vol.45 (3), p.348-353

1989

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

Human molecular genetics, 1995-10, Vol.4 (10), p.1837-1844

1995

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Loss of Heterozygosity Suggests Tumor Suppressor Gene Responsible for Primary Hepatocellular Carcinoma

Proceedings of the National Academy of Sciences - PNAS, 1989-11, Vol.86 (22), p.8852-8856

1989

Volltextzugriff (PDF)

Clinical and epidemiologic studies of cleft lip and palate in the Philippines

The Cleft palate-craniofacial journal, 1997-01, Vol.34 (1), p.7

1997

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Expression-based genetic/physical maps of single-nucleotide polymorphisms identified by the cancer genome anatomy project

Genome research, 2000-08, Vol.10 (8), p.1259

2000

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An international database and integrated analysis tools for the study of cancer gene expression

The pharmacogenomics journal, 2002, Vol.2 (3), p.156-164

2002

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Studies of the candidate genes TGFB2, MSX1, TGFA, and TGFB3 in the etiology of cleft lip and palate in the Philippines

The Cleft palate-craniofacial journal, 1997-01, Vol.34 (1), p.1

1997

Volltextzugriff (PDF)

A single-gene explanation for the probability of having idiopathic talipes equinovarus

American journal of human genetics, 1993-11, Vol.53 (5), p.1051-1063

1993

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Susceptibility to Renal Carcinoma in the Eker Rat Involves a Tumor Suppressor Gene on Chromosome 10

Proceedings of the National Academy of Sciences - PNAS, 1993-09, Vol.90 (17), p.8038-8042

1993

Volltextzugriff (PDF)

Survey of trinucleotide repeats in the human genome: assessment of their utility as genetic markers

Human molecular genetics, 1995-10, Vol.4 (10), p.1829-1836

1995

Volltextzugriff (PDF)

Error Filtration, Interference, and the Human Linkage Map

Proceedings of the National Academy of Sciences - PNAS, 1991-08, Vol.88 (15), p.6501-6505

1991

Volltextzugriff (PDF)

Universal Mapping Probes and the Origin of Human Chromosome 3

Proceedings of the National Academy of Sciences - PNAS, 1993-01, Vol.90 (2), p.730-734

1993

Volltextzugriff (PDF)

Asthma and Bronchial Hyperresponsiveness Linked to the XY Long Arm Pseudoautosomal Region

Genomics (San Diego, Calif.), 1998-09, Vol.52 (2), p.233-235

1998

Volltextzugriff (PDF)

Interleukin 9: A Candidate Gene for Asthma

Proceedings of the National Academy of Sciences - PNAS, 1997-11, Vol.94 (24), p.13175-13180

1997

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Low Frequency of p53 Mutations Observed in a Diverse Collection of Primary Hepatocellular Carcinomas

Proceedings of the National Academy of Sciences - PNAS, 1992-10, Vol.89 (20), p.9622-9626

1992

Volltextzugriff (PDF)

Characterization of the human HOX 7 cDNA and identification of polymorphic markers

Human molecular genetics, 1992-09, Vol.1 (6), p.407-410

1992

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Direct detection of novel expanded trinucleotide repeats in the human genome

Nature genetics, 1993-06, Vol.4 (2), p.135-139

1993

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Multipoint gene mapping using seriation. I: General methods

American journal of human genetics, 1987-08, Vol.41 (2), p.180-188

1987

Volltextzugriff (PDF)

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High-Throughput Development and Characterization of a Genomewide Collection of Gene-Based Single Nucleotide Polymorphism Markers by Chip-Based Matrix-Assisted Laser Desorption/Ionization Time-of-Flight Mass Spectrometry

Reliable identification of large numbers of candidate SNPs from public EST data

Identification of inbred mouse strains harboring genetic modifiers of mammary tumor age of onset and metastatic progression

Constitutional genetic variation at the human aromatase gene ( ) and breast cancer risk

The Cancer Genome Anatomy Project: building an annotated gene index

Integrated human genome-wide maps constructed using the CEPH reference panel

Influence of aberrant observations on high-resolution linkage analysis outcomes

Association of genetic variation of the transforming growth factor-alpha gene with cleft lip and palate

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

Loss of Heterozygosity Suggests Tumor Suppressor Gene Responsible for Primary Hepatocellular Carcinoma

Clinical and epidemiologic studies of cleft lip and palate in the Philippines

Expression-based genetic/physical maps of single-nucleotide polymorphisms identified by the cancer genome anatomy project

An international database and integrated analysis tools for the study of cancer gene expression

Studies of the candidate genes TGFB2, MSX1, TGFA, and TGFB3 in the etiology of cleft lip and palate in the Philippines

A single-gene explanation for the probability of having idiopathic talipes equinovarus

Susceptibility to Renal Carcinoma in the Eker Rat Involves a Tumor Suppressor Gene on Chromosome 10

Survey of trinucleotide repeats in the human genome: assessment of their utility as genetic markers

Error Filtration, Interference, and the Human Linkage Map

Universal Mapping Probes and the Origin of Human Chromosome 3

Asthma and Bronchial Hyperresponsiveness Linked to the XY Long Arm Pseudoautosomal Region

Interleukin 9: A Candidate Gene for Asthma

Low Frequency of p53 Mutations Observed in a Diverse Collection of Primary Hepatocellular Carcinomas

Characterization of the human HOX 7 cDNA and identification of polymorphic markers

Direct detection of novel expanded trinucleotide repeats in the human genome

Multipoint gene mapping using seriation. I: General methods

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