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High-depth, high-accuracy microsatellite genotyping enables precision lung cancer risk classification

Oncogene, 2017-11, Vol.36 (46), p.6383-6390

2017

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Evaluation of microsatellite variation in the 1000 Genomes Project pilot studies is indicative of the quality and utility of the raw data and alignments

Genomics (San Diego, Calif.), 2011-04, Vol.97 (4), p.193-199

2011

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Genome-wide responses to mitochondrial dysfunction

Molecular biology of the cell, 2001-02, Vol.12 (2), p.297-308

2001

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High resolution chromosome 3p allelotyping of human lung cancer and preneoplastic/preinvasive bronchial epithelium reveals multiple, discontinuous sites of 3p allele loss and three regions of frequent breakpoints

Cancer research (Chicago, Ill.), 2000-04, Vol.60 (7), p.1949-1960

2000

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A long AAAG repeat allele in the 5′ UTR of the ERR-γ gene is correlated with breast cancer predisposition and drives promoter activity in MCF-7 breast cancer cells

Breast cancer research and treatment, 2011-11, Vol.130 (1), p.41-48

2011

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Heuristics for identification of acronym-definition patterns within text: towards an automated construction of comprehensive acronym-definition dictionaries

Methods of information in medicine, 2002-01, Vol.41 (5), p.426-434

2002

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Shared relationship analysis: ranking set cohesion and commonalities within a literature-derived relationship network

Bioinformatics, 2004-01, Vol.20 (2), p.191-198

2004

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Global Microsatellite Content Distinguishes Humans, Primates, Animals, and Plants

Molecular biology and evolution, 2009-12, Vol.26 (12), p.2809-2819

2009

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Microsatellite genotyping reveals a signature in breast cancer exomes

Breast cancer research and treatment, 2014-06, Vol.145 (3), p.791-798

2014

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Repeat Polymorphisms within Gene Regions: Phenotypic and Evolutionary Implications

American journal of human genetics, 2000-08, Vol.67 (2), p.345-356

2000

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Combating unethical publications with plagiarism detection services

Urologic oncology, 2011, Vol.29 (1), p.95-99

Garner, H.R., Ph.D

2011

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Association of Extensive Polymorphisms in the SLAM/CD2 Gene Cluster with Murine Lupus

Immunity (Cambridge, Mass.), 2004-12, Vol.21 (6), p.769-780

2004

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Population-scale analysis of human microsatellites reveals novel sources of exonic variation

Gene, 2013-03, Vol.516 (2), p.328-334

2013

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Knowledge discovery by automated identification and ranking of implicit relationships

Bioinformatics, 2004-02, Vol.20 (3), p.389-398

2004

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Comparative analysis of the early transcriptome of Brucella abortus – Infected monocyte-derived macrophages from cattle naturally resistant or susceptible to brucellosis

Research in veterinary science, 2011-08, Vol.91 (1), p.40-51

2011

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Butorphanol-mediated antinociception in mice: partial agonist effects and mu receptor involvement

The Journal of pharmacology and experimental therapeutics, 1997-09, Vol.282 (3), p.1253

1997

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Data‐Mining Analysis Suggests an Epigenetic Pathogenesis for Type 2 Diabetes

BioMed research international, 2005-06, Vol.2005 (2), p.104-112

2005

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Instrumentation for the Genome Project

Annual review of biomedical engineering, 1999, Vol.1 (1), p.649-678

1999

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Evidence for the regulation of alternative splicing via complementary DNA sequence repeats

Bioinformatics, 2005-04, Vol.21 (8), p.1358-1364

2005

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MarC-V: A Spreadsheet-Based Tool for Analysis, Normalization, and Visualization of Single cDNA Microarray Experiments

BioTechniques, 2002-02, Vol.32 (2), p.338-344

2002

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Biomedical term mapping databases

Nucleic acids research, 2005-01, Vol.33 (Database issue), p.D289-D293

2005

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PRIMO: A Primer Design Program That Applies Base Quality Statistics for Automated Large-Scale DNA Sequencing

Genomics (San Diego, Calif.), 1997-03, Vol.40 (3), p.476-485

1997

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Towards the elimination of duplication in Anaesthesia and Intensive Care

Anaesthesia and intensive care, 2008-09, Vol.36 (5), p.643-645

2008

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Mix of Sequencing Technologies for Sequence Closure: An Example

BioTechniques, 2000-04, Vol.28 (4), p.630-634

2000

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Prioritized selection of oligodeoxyribonucleotide probes for efficient hybridization to RNA transcripts

Nucleic acids research, 2003-01, Vol.31 (2), p.750-758

2003

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High-depth, high-accuracy microsatellite genotyping enables precision lung cancer risk classification

Evaluation of microsatellite variation in the 1000 Genomes Project pilot studies is indicative of the quality and utility of the raw data and alignments

Genome-wide responses to mitochondrial dysfunction

High resolution chromosome 3p allelotyping of human lung cancer and preneoplastic/preinvasive bronchial epithelium reveals multiple, discontinuous sites of 3p allele loss and three regions of frequent breakpoints

A long AAAG repeat allele in the 5′ UTR of the ERR-γ gene is correlated with breast cancer predisposition and drives promoter activity in MCF-7 breast cancer cells

Heuristics for identification of acronym-definition patterns within text: towards an automated construction of comprehensive acronym-definition dictionaries

Shared relationship analysis: ranking set cohesion and commonalities within a literature-derived relationship network

Global Microsatellite Content Distinguishes Humans, Primates, Animals, and Plants

Microsatellite genotyping reveals a signature in breast cancer exomes

Repeat Polymorphisms within Gene Regions: Phenotypic and Evolutionary Implications

Combating unethical publications with plagiarism detection services

Association of Extensive Polymorphisms in the SLAM/CD2 Gene Cluster with Murine Lupus

Population-scale analysis of human microsatellites reveals novel sources of exonic variation

Knowledge discovery by automated identification and ranking of implicit relationships

Comparative analysis of the early transcriptome of Brucella abortus – Infected monocyte-derived macrophages from cattle naturally resistant or susceptible to brucellosis

Butorphanol-mediated antinociception in mice: partial agonist effects and mu receptor involvement

Data‐Mining Analysis Suggests an Epigenetic Pathogenesis for Type 2 Diabetes

Instrumentation for the Genome Project

Evidence for the regulation of alternative splicing via complementary DNA sequence repeats

MarC-V: A Spreadsheet-Based Tool for Analysis, Normalization, and Visualization of Single cDNA Microarray Experiments

Biomedical term mapping databases

PRIMO: A Primer Design Program That Applies Base Quality Statistics for Automated Large-Scale DNA Sequencing

Towards the elimination of duplication in Anaesthesia and Intensive Care

Mix of Sequencing Technologies for Sequence Closure: An Example

Prioritized selection of oligodeoxyribonucleotide probes for efficient hybridization to RNA transcripts

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