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Human Epidermal Growth Factor Receptor 2 Testing in Breast Cancer: American Society of Clinical Oncology/College of American Pathologists Clinical Practice Guideline Focused Update

Journal of clinical oncology, 2018-07, Vol.36 (20), p.2105-2122

2018

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Human Epidermal Growth Factor Receptor 2 Testing in Breast Cancer: American Society of Clinical Oncology/College of American Pathologists Clinical Practice Guideline Focused Update

Archives of pathology & laboratory medicine (1976), 2018-11, Vol.142 (11), p.1364-1382

2018

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Recommendations for Human Epidermal Growth Factor Receptor 2 Testing in Breast Cancer: American Society of Clinical Oncology/College of American Pathologists Clinical Practice Guideline Update

Journal of clinical oncology, 2013-11, Vol.31 (31), p.3997-4013

2013

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Recommendations for human epidermal growth factor receptor 2 testing in breast cancer: American Society of Clinical Oncology/College of American Pathologists clinical practice guideline update

Archives of pathology & laboratory medicine (1976), 2014-02, Vol.138 (2), p.241-256

2014

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Utility of Fluorescence In Situ Hybridization in Clinical and Research Applications

Clinics in laboratory medicine, 2022-12, Vol.42 (4), p.573-586

2022

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Preanalytics and Precision Pathology: Pathology Practices to Ensure Molecular Integrity of Cancer Patient Biospecimens for Precision Medicine

Archives of pathology & laboratory medicine (1976), 2019-11, Vol.143 (11), p.1346-1363

2019

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ZMIZ1::ABL1 Fusion: An Uncommon Molecular Event With Clinical Implications in Pediatric Cancer

Archives of pathology & laboratory medicine (1976), 2024-05

2024

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Complementation of hypersensitivity to DNA interstrand crosslinking agents demonstrates that XRCC2 is a Fanconi anaemia gene

Journal of medical genetics, 2016-10, Vol.53 (10), p.672-680

2016

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Fatal melanoma with a novel MYO5A‐BRAF fusion and small associated conventional nevus: A case report and review of literature

Journal of cutaneous pathology, 2022-09, Vol.49 (9), p.808-812

2022

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Rapid quantification of underivatized alloisoleucine and argininosuccinate using mixed-mode chromatography with tandem mass spectrometry

Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 2019-10, Vol.1128, p.121786-121786, Article 121786

2019

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Genetic counseling program remediation practices for students underperforming in clinical skills: An exploratory study

Journal of genetic counseling, 2024-02, Vol.33 (1), p.4-14

2024

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Genome-Wide Association Studies for Taxane-Induced Peripheral Neuropathy in ECOG-5103 and ECOG-1199

Clinical cancer research, 2015-11, Vol.21 (22), p.5082-5091

2015

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Genetic heterogeneity in HER2 testing in breast cancer: panel summary and guidelines

Archives of pathology & laboratory medicine (1976), 2009-04, Vol.133 (4), p.611-612

2009

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Two Patients with Complex Rearrangements Suggestive of Germline Chromoanagenesis

Cytogenetic and genome research, 2021-04, Vol.160 (11-12), p.671-679

2021

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Laboratory and Clinical Implications of Incidental and Secondary Germline Findings During Tumor Testing

Archives of pathology & laboratory medicine (1976), 2022-01, Vol.146 (1), p.70-77

2022

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College of american pathologists proposal for the oversight of laboratory-developed tests

Archives of pathology & laboratory medicine (1976), 2011-11, Vol.135 (11), p.1432-1435

Vance, Gail H

2011

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Positive and negative professionalism experiences of genetic counseling students in the United States and Canada

Journal of genetic counseling, 2021-04, Vol.30 (2), p.478-492

2021

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Malignant gastrointestinal neuroectodermal tumour arising in the extrahepatic bile ducts; a rare neoplasm in an unusual anatomic location

BMJ case reports, 2022-07, Vol.15 (7), p.e250094

2022

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Combined DOG1 and Mammaglobin Immunohistochemistry Is Comparable to ETV6-breakapart Analysis for Differentiating Between Papillary Cystic Variants of Acinic Cell Carcinoma and Mammary Analogue Secretory Carcinoma

International journal of surgical pathology, 2017-04, Vol.25 (2), p.127-140

2017

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Klinefelter's Syndrome with Maternal Uniparental Disomy X, Interstitial Xp22.31 Deletion, X-linked Ichthyosis, and Severe Central Nervous System Regression

Journal of pediatric genetics (Birmingham, Ala.), 2021-09, Vol.10 (3), p.222-229

2021

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Positive cell-free fetal DNA testing for trisomy 13 reveals confined placental mosaicism

Genetics in medicine, 2013-09, Vol.15 (9), p.729-732

2013

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Pretransplant HLA typing revealed loss of heterozygosity in the major histocompatibility complex in a patient with acute myeloid leukemia

Human immunology, 2019-04, Vol.80 (4), p.257-262

2019

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Human Epidermal Growth Factor Receptor 2 Testing in Breast Cancer: American Society of Clinical Oncology/College of American Pathologists Clinical Practice Guideline Focused Update

Human Epidermal Growth Factor Receptor 2 Testing in Breast Cancer: American Society of Clinical Oncology/College of American Pathologists Clinical Practice Guideline Focused Update

Recommendations for Human Epidermal Growth Factor Receptor 2 Testing in Breast Cancer: American Society of Clinical Oncology/College of American Pathologists Clinical Practice Guideline Update

Recommendations for human epidermal growth factor receptor 2 testing in breast cancer: American Society of Clinical Oncology/College of American Pathologists clinical practice guideline update

Utility of Fluorescence In Situ Hybridization in Clinical and Research Applications

Preanalytics and Precision Pathology: Pathology Practices to Ensure Molecular Integrity of Cancer Patient Biospecimens for Precision Medicine

Karyotype is an independent prognostic factor in adult acute lymphoblastic leukemia (ALL): analysis of cytogenetic data from patients treated on the Medical Research Council (MRC) UKALLXII/Eastern Cooperative Oncology Group (ECOG) 2993 trial

ZMIZ1::ABL1 Fusion: An Uncommon Molecular Event With Clinical Implications in Pediatric Cancer

Complementation of hypersensitivity to DNA interstrand crosslinking agents demonstrates that XRCC2 is a Fanconi anaemia gene

Fatal melanoma with a novel MYO5A‐BRAF fusion and small associated conventional nevus: A case report and review of literature

Rapid quantification of underivatized alloisoleucine and argininosuccinate using mixed-mode chromatography with tandem mass spectrometry

Genetic counseling program remediation practices for students underperforming in clinical skills: An exploratory study

Genome-Wide Association Studies for Taxane-Induced Peripheral Neuropathy in ECOG-5103 and ECOG-1199

Genetic heterogeneity in HER2 testing in breast cancer: panel summary and guidelines

Two Patients with Complex Rearrangements Suggestive of Germline Chromoanagenesis

Laboratory and Clinical Implications of Incidental and Secondary Germline Findings During Tumor Testing

College of american pathologists proposal for the oversight of laboratory-developed tests

Positive and negative professionalism experiences of genetic counseling students in the United States and Canada

Malignant gastrointestinal neuroectodermal tumour arising in the extrahepatic bile ducts; a rare neoplasm in an unusual anatomic location

Combined DOG1 and Mammaglobin Immunohistochemistry Is Comparable to ETV6-breakapart Analysis for Differentiating Between Papillary Cystic Variants of Acinic Cell Carcinoma and Mammary Analogue Secretory Carcinoma

Klinefelter's Syndrome with Maternal Uniparental Disomy X, Interstitial Xp22.31 Deletion, X-linked Ichthyosis, and Severe Central Nervous System Regression

AluY-mediated germline deletion, duplication and somatic stem cell reversion in UBE2T defines a new subtype of Fanconi anemia

Positive cell-free fetal DNA testing for trisomy 13 reveals confined placental mosaicism

Independent Prognostic Significance of Monosomy 17 and Impact of Karyotype Complexity in Monosomal Karyotype/Complex Karyotype Acute Myeloid Leukemia: Results from Four ECOG-ACRIN Prospective Therapeutic Trials

Pretransplant HLA typing revealed loss of heterozygosity in the major histocompatibility complex in a patient with acute myeloid leukemia

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