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RET is a potential tumor suppressor gene in colorectal cancer

Oncogene, 2013-04, Vol.32 (16), p.2037-2047

2013

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Epigenetic silencing of the intronic microRNA hsa-miR-342 and its host gene EVL in colorectal cancer

Oncogene, 2008-06, Vol.27 (27), p.3880-3888

2008

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Boundaries between Chromosomal Domains of X Inactivation and Escape Bind CTCF and Lack CpG Methylation during Early Development

Developmental cell, 2005, Vol.8 (1), p.31-42

2005

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A mouse model for cyclin E-dependent genetic instability and tumorigenesis

Cancer cell, 2005-07, Vol.8 (1), p.35-47

2005

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Section E9 of the American College of Medical Genetics technical standards and guidelines: Fluorescence in situ hybridization

Genetics in medicine, 2011-07, Vol.13 (7), p.667-675

2011

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Comparative Analysis of PCR-Based Biomarker Assay Methods for Colorectal Polyp Detection from Fecal DNA

Clinical chemistry (Baltimore, Md.), 2009-08, Vol.55 (8), p.1559-1563

2009

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Diverse mutational mechanisms cause pathogenic subtelomeric rearrangements

Human molecular genetics, 2011-10, Vol.20 (19), p.3769-3778

2011

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Fluorescence In Situ Hybridization

Clinics in laboratory medicine, 2011-12, Vol.31 (4), p.525-542

Tsuchiya, Karen D., MD

2011

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Activation of the Chromosome 19q MicroRNA Cluster in Sporadic and Androgenetic-Biparental Mosaicism–Associated Hepatic Mesenchymal Hamartoma

Pediatric and developmental pathology, 2014-03, Vol.17 (2), p.75-84

2014

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Supernumerary Chromosome of Nectria haematococca That Carries Pea-Pathogenicity-Related Genes Also Carries a Trait for Pea Rhizosphere Competitiveness

Applied and Environmental Microbiology, 2008-06, Vol.74 (12), p.3849-3856

2008

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Variability in interpreting and reporting copy number changes detected by array-based technology in clinical laboratories

Genetics in medicine, 2009-12, Vol.11 (12), p.866-873

2009

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A Malignant Mimicker: Features of Kikuchi-Fujimoto Disease in the Pediatric Population

Pediatric and developmental pathology, 2022-09, Vol.25 (5), p.538-547

2022

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How Many Tests Does It Take to Diagnose a Triple-Hit B-Lymphoblastic Lymphoma? (Hint, It’s A Lot)

Pediatric and developmental pathology, 2024-03, Vol.27 (2), p.193-197

2024

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Implementation, Evolution, and Laboratory Performance of Methods-Based Proficiency Testing for Next-Generation Sequencing Detection of Germline Sequence Variants

Archives of pathology & laboratory medicine (1976), 2024-07, Vol.148 (7), p.775-783

2024

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Characterization of unusual iAMP21 B‐lymphoblastic leukemia (iAMP21‐ALL) from the Mayo Clinic and Children's Oncology Group

Genes chromosomes & cancer, 2022-12, Vol.61 (12), p.710-719

2022

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Next-Generation Sequencing Somatic and Germline Assay Troubleshooting Guide Derived From Proficiency Testing Data

Archives of pathology & laboratory medicine (1976), 2022-04, Vol.146 (4), p.451-461

2022

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New cases and refinement of the critical region in the 1q41q42 microdeletion syndrome

European journal of medical genetics, 2011-01, Vol.54 (1), p.42-49

2011

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Recurrent 200-kb deletions of 16p11.2 that include the SH2B1 gene are associated with developmental delay and obesity

Genetics in medicine, 2010-10, Vol.12 (10), p.641-647

2010

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College of American Pathologists/American College of Medical Genetics proficiency testing for constitutional cytogenomic microarray analysis

Genetics in medicine, 2011-09, Vol.13 (9), p.765-769

2011

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The Smo/Smo Model : Hedgehog-Induced Medulloblastoma with 90% Incidence and Leptomeningeal Spread

Cancer research (Chicago, Ill.), 2008-03, Vol.68 (6), p.1768-1776

2008

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Is intrachromosomal amplification of chromosome 21 (iAMP21) always intrachromosomal?

Cancer genetics, 2017-12, Vol.218-219, p.10-14

2017

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Evaluation of the Utility of Bone Marrow Morphology and Ancillary Studies in Pediatric Patients Under Surveillance for Myelodysplastic Syndrome

American journal of clinical pathology, 2018-04, Vol.149 (6), p.499-513

2018

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Comparative sequence and x-inactivation analyses of a domain of escape in human xp11.2 and the conserved segment in mouse

Genome research, 2004-07, Vol.14 (7), p.1275-1284

2004

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The Ecoresponsive Genome of "Daphnia pulex"

Science (American Association for the Advancement of Science), 2011-02, Vol.331 (6017), p.555-561

2011

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TGF-β Receptor Inactivation and Mutant Kras Induce Intestinal Neoplasms in Mice via a β-Catenin-Independent Pathway

Gastroenterology (New York, N.Y. 1943), 2009-05, Vol.136 (5), p.1680-1688.e7

2009

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RET is a potential tumor suppressor gene in colorectal cancer

Epigenetic silencing of the intronic microRNA hsa-miR-342 and its host gene EVL in colorectal cancer

Boundaries between Chromosomal Domains of X Inactivation and Escape Bind CTCF and Lack CpG Methylation during Early Development

A mouse model for cyclin E-dependent genetic instability and tumorigenesis

Section E9 of the American College of Medical Genetics technical standards and guidelines: Fluorescence in situ hybridization

Comparative Analysis of PCR-Based Biomarker Assay Methods for Colorectal Polyp Detection from Fecal DNA

Diverse mutational mechanisms cause pathogenic subtelomeric rearrangements

Fluorescence In Situ Hybridization

Activation of the Chromosome 19q MicroRNA Cluster in Sporadic and Androgenetic-Biparental Mosaicism–Associated Hepatic Mesenchymal Hamartoma

Supernumerary Chromosome of Nectria haematococca That Carries Pea-Pathogenicity-Related Genes Also Carries a Trait for Pea Rhizosphere Competitiveness

Variability in interpreting and reporting copy number changes detected by array-based technology in clinical laboratories

A Malignant Mimicker: Features of Kikuchi-Fujimoto Disease in the Pediatric Population

How Many Tests Does It Take to Diagnose a Triple-Hit B-Lymphoblastic Lymphoma? (Hint, It’s A Lot)

Implementation, Evolution, and Laboratory Performance of Methods-Based Proficiency Testing for Next-Generation Sequencing Detection of Germline Sequence Variants

Characterization of unusual iAMP21 B‐lymphoblastic leukemia (iAMP21‐ALL) from the Mayo Clinic and Children's Oncology Group

Next-Generation Sequencing Somatic and Germline Assay Troubleshooting Guide Derived From Proficiency Testing Data

New cases and refinement of the critical region in the 1q41q42 microdeletion syndrome

Recurrent 200-kb deletions of 16p11.2 that include the SH2B1 gene are associated with developmental delay and obesity

College of American Pathologists/American College of Medical Genetics proficiency testing for constitutional cytogenomic microarray analysis

The Smo/Smo Model : Hedgehog-Induced Medulloblastoma with 90% Incidence and Leptomeningeal Spread

Is intrachromosomal amplification of chromosome 21 (iAMP21) always intrachromosomal?

Evaluation of the Utility of Bone Marrow Morphology and Ancillary Studies in Pediatric Patients Under Surveillance for Myelodysplastic Syndrome

Comparative sequence and x-inactivation analyses of a domain of escape in human xp11.2 and the conserved segment in mouse

The Ecoresponsive Genome of "Daphnia pulex"

TGF-β Receptor Inactivation and Mutant Kras Induce Intestinal Neoplasms in Mice via a β-Catenin-Independent Pathway

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