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Genome-wide analysis of the odorant-binding protein gene family in Drosophila melanogaster

Genome research, 2002-09, Vol.12 (9), p.1357-1369

2002

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Genomic binding sites of the yeast cell-cycle transcription factors SBF and MBF

Nature (London), 2001-01, Vol.409 (6819), p.533-538

2001

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Profiling molecular regulators of recurrence in chemorefractory triple-negative breast cancers

Breast cancer research : BCR, 2019-08, Vol.21 (1), p.87-87, Article 87

2019

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Next-generation sequencing of circulating tumor DNA to predict recurrence in triple-negative breast cancer patients with residual disease after neoadjuvant chemotherapy

NPJ breast cancer, 2017-07, Vol.3 (1), p.24-6, Article 24

2017

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BRCA1/2 somatic mutation detection in formalin-fixed paraffin embedded tissue by next-generation sequencing in Korean ovarian cancer patients

Pathology, research and practice, 2019-11, Vol.215 (11), p.152595-152595, Article 152595

2019

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Integrating functional genomic information into the Saccharomyces genome database

Nucleic acids research, 2000-01, Vol.28 (1), p.77-80

2000

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Abstract 5132: Assessing tumor mutational burden and profiling variants from FFPE samples using a PCR-based next-generation sequencing assay

Cancer research (Chicago, Ill.), 2019-07, Vol.79 (13_Supplement), p.5132-5132

2019

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Abstract 2505: The Oncomine BRCA expanded next-generation sequencing assay: Development and analytical validation of a new panel for detection of SNV, insertions, deletions and copy number variants in a panel of 15 genes involved in homologous recombination repair of double-strand break DNA damage

Cancer research (Chicago, Ill.), 2020-08, Vol.80 (16_Supplement), p.2505-2505

2020

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Abstract 170: Development and analytical validation of a novel next-generation DNA sequencing assay, the oncomine lymphoma panel, to detect SNV, insertion, deletion and copy number variants in 25 Lymphoma genes in FFPE samples

Cancer research (Chicago, Ill.), 2020-08, Vol.80 (16_Supplement), p.170-170

2020

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Abstract 1326: A novel system that produces pre-qualified cancer NGS panels with customizable content

Cancer research (Chicago, Ill.), 2020-08, Vol.80 (16_Supplement), p.1326-1326

2020

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Abstract 2402: A research approach for the detection of somatic mutations at 0.5% frequency from cfDNA and cTc DNA using a multiplex sequencing assay targeting 2000 tumor mutations

Cancer research (Chicago, Ill.), 2015-08, Vol.75 (15_Supplement), p.2402-2402

2015

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Abstract 4931: A circulating cell free DNA workflow for targeted sequencing - from isolation through validation

Cancer research (Chicago, Ill.), 2015-08, Vol.75 (15_Supplement), p.4931-4931

2015

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Abstract 4751: Simple modifications in Ion Torrent Variant Caller (TVC) parameters improve somatic variant detection from circulating tumor cells and cell free DNA to 1% allele frequency

Cancer research (Chicago, Ill.), 2015-08, Vol.75 (15_Supplement), p.4751-4751

2015

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A High-Density Admixture Map for Disease Gene Discovery in African Americans

American journal of human genetics, 2004-05, Vol.74 (5), p.1001-1013

2004

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Abstract 232: Fully automated comprehensive genomic profiling for detection of cancer variants, gene fusions, and complex oncology endpoints

Cancer research (Chicago, Ill.), 2023-04, Vol.83 (7_Supplement), p.232-232

2023

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Abstract 4215: Rapid, inexpensive and accurate detection of rare variants by targeted sequencing

Cancer research (Chicago, Ill.), 2013-04, Vol.73 (8_Supplement), p.4215-4215

2013

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Genetic association between the PRKCH gene encoding protein kinase Cη isozyme and rheumatoid arthritis in the Japanese population

Arthritis and rheumatism, 2007-01, Vol.56 (1), p.30-42

2007

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A tool for selecting SNPs for association studies based on observed linkage disequilibrium patterns

Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing, 2006, p.487

2006

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Association between single‐nucleotide polymorphisms in the SEC8L1 gene, which encodes a subunit of the exocyst complex, and rheumatoid arthritis in a Japanese population

Arthritis and rheumatism, 2005-05, Vol.52 (5), p.1371-1380

2005

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Using the Saccharomyces Genome Database (SGD) for analysis of protein similarities and structure

Nucleic acids research, 1999-01, Vol.27 (1), p.74-78

1999

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Power and Sample Size Calculations for Genetic Case/Control Studies Using Gene-Centric SNP Maps: Application to Human Chromosomes 6, 21, and 22 in Three Populations

Human heredity, 2005-01, Vol.60 (1), p.43-60

2005

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RNA polymerase II C-terminal repeat influences response to transcriptional enhancer signals

Nature (London), 1990-10, Vol.347 (6292), p.491-494

1990

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Genome-wide maps of DNA-protein interactions using a yeast ORF and intergenic microarray

Nature genetics, 1999-11, Vol.23 (S3), p.53-53

1999

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RNA polymerase II mutants defective in transcription of a subset of genes

Molecular and Cellular Biology, 1990-03, Vol.10 (3), p.1010-1016

1990

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Genome-wide analysis of the odorant-binding protein gene family in Drosophila melanogaster

Genomic binding sites of the yeast cell-cycle transcription factors SBF and MBF

Profiling molecular regulators of recurrence in chemorefractory triple-negative breast cancers

Next-generation sequencing of circulating tumor DNA to predict recurrence in triple-negative breast cancer patients with residual disease after neoadjuvant chemotherapy

BRCA1/2 somatic mutation detection in formalin-fixed paraffin embedded tissue by next-generation sequencing in Korean ovarian cancer patients

The linkage disequilibrium maps of three human chromosomes across four populations reflect their demographic history and a common underlying recombination pattern

Integrating functional genomic information into the Saccharomyces genome database

Abstract 5132: Assessing tumor mutational burden and profiling variants from FFPE samples using a PCR-based next-generation sequencing assay

Abstract 2505: The Oncomine BRCA expanded next-generation sequencing assay: Development and analytical validation of a new panel for detection of SNV, insertions, deletions and copy number variants in a panel of 15 genes involved in homologous recombination repair of double-strand break DNA damage

Abstract 170: Development and analytical validation of a novel next-generation DNA sequencing assay, the oncomine lymphoma panel, to detect SNV, insertion, deletion and copy number variants in 25 Lymphoma genes in FFPE samples

Abstract 1326: A novel system that produces pre-qualified cancer NGS panels with customizable content

Abstract 2402: A research approach for the detection of somatic mutations at 0.5% frequency from cfDNA and cTc DNA using a multiplex sequencing assay targeting 2000 tumor mutations

Abstract 4931: A circulating cell free DNA workflow for targeted sequencing - from isolation through validation

Abstract 4751: Simple modifications in Ion Torrent Variant Caller (TVC) parameters improve somatic variant detection from circulating tumor cells and cell free DNA to 1% allele frequency

A High-Density Admixture Map for Disease Gene Discovery in African Americans

Abstract 232: Fully automated comprehensive genomic profiling for detection of cancer variants, gene fusions, and complex oncology endpoints

Abstract 4215: Rapid, inexpensive and accurate detection of rare variants by targeted sequencing

Genetic association between the PRKCH gene encoding protein kinase Cη isozyme and rheumatoid arthritis in the Japanese population

A tool for selecting SNPs for association studies based on observed linkage disequilibrium patterns

Association between single‐nucleotide polymorphisms in the SEC8L1 gene, which encodes a subunit of the exocyst complex, and rheumatoid arthritis in a Japanese population

Using the Saccharomyces Genome Database (SGD) for analysis of protein similarities and structure

Power and Sample Size Calculations for Genetic Case/Control Studies Using Gene-Centric SNP Maps: Application to Human Chromosomes 6, 21, and 22 in Three Populations

RNA polymerase II C-terminal repeat influences response to transcriptional enhancer signals

Genome-wide maps of DNA-protein interactions using a yeast ORF and intergenic microarray

RNA polymerase II mutants defective in transcription of a subset of genes

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