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European journal of cardiovascular nursing : journal of the Working Group on Cardiovascular Nursing of the European Society of Cardiology, 2021-11, Vol.20 (8), p.767

2021

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Platform evaluation for rapid genotyping of CYP2C9 and VKORC1 alleles

Personalized medicine, 2009-07, Vol.6 (4), p.449-457

2009

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Selection of a Platform for Mutation Detection

Current Protocols in Human Genetics, 2008-01, Vol.56 (1), p.7.15.1-7.15.30

2008

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EGFR Mutation Is a Better Predictor of Response to Tyrosine Kinase Inhibitors in Non-Small Cell Lung Carcinoma Than FISH, CISH, and Immunohistochemistry

American journal of clinical pathology, 2010-06, Vol.133 (6), p.922-934

2010

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Further insight into the markers of methotrexate resistance in childhood acute lymphoblastic leukemia patients

Personalized medicine, 2008-07, Vol.5 (4), p.325-329

2008

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Correspondence regarding genetic assessment following increased nuchal translucency and normal karyotype

Prenatal diagnosis, 2012-06, Vol.32 (6), p.607-608

2012

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The Creating an Optimal Warfarin Nomogram (CROWN) Study

Thrombosis and haemostasis, 2012-01, Vol.107 (1), p.59

2012

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First-Line Gefitinib in Patients With Advanced Non–Small-Cell Lung Cancer Harboring Somatic EGFR Mutations

Germline gain-of-function mutations in SOS1 cause Noonan syndrome

A restricted spectrum of NRAS mutations causes Noonan syndrome

The Impact of Initial Gefitinib or Erlotinib versus Chemotherapy on Central Nervous System Progression in Advanced Non-Small Cell Lung Cancer with EGFR Mutations

EGFR mutations are detected comparably in cytologic and surgical pathology specimens of nonsmall cell lung cancer

Exon 19 Deletion Mutations of Epidermal Growth Factor Receptor Are Associated with Prolonged Survival in Non–Small Cell Lung Cancer Patients Treated with Gefitinib or Erlotinib

The Introduction of Systematic Genomic Testing for Patients with Non–Small-Cell Lung Cancer

A Rapid and Sensitive Enzymatic Method for Epidermal Growth Factor Receptor Mutation Screening

The spectrum of FBN1, TGFβR1, TGFβR2 and ACTA2 variants in 594 individuals with suspected Marfan Syndrome, Loeys–Dietz Syndrome or Thoracic Aortic Aneurysms and Dissections (TAAD)

Mucinous Differentiation Correlates with Absence of EGFR Mutation and Presence of KRAS Mutation in Lung Adenocarcinomas with Bronchioloalveolar Features

Response to Treatment and Survival of Patients with Non‐Small Cell Lung Cancer Undergoing Somatic EGFR Mutation Testing

Germline TP53 Mutations in Patients With Early-Onset Colorectal Cancer in the Colon Cancer Family Registry

The GeneInsight suite: a platform to support laboratory and provider use of DNA-based genetic testing

Phase I Study of Gefitinib Plus Celecoxib in Recurrent or Metastatic Squamous Cell Carcinoma of the Head and Neck

Epidermal Growth Factor Receptor Mutation Testing in the Care of Lung Cancer Patients

Genetics and Genomics in the Practice of Medicine

Pharmacogenomics of lung cancer: with a view to address EGFR-targeted therapies

1032 Prevalence of Germline TP53 Mutations in 510 Population and Clinic-Based Cases of Colorectal Cancer Diagnosed Under Age 40

Feeling understood for the first time: experiences of participation in rehabilitation after out-of-hospital sudden cardiac arrest

Platform evaluation for rapid genotyping of CYP2C9 and VKORC1 alleles

Selection of a Platform for Mutation Detection

EGFR Mutation Is a Better Predictor of Response to Tyrosine Kinase Inhibitors in Non-Small Cell Lung Carcinoma Than FISH, CISH, and Immunohistochemistry

Further insight into the markers of methotrexate resistance in childhood acute lymphoblastic leukemia patients

Correspondence regarding genetic assessment following increased nuchal translucency and normal karyotype

The Creating an Optimal Warfarin Nomogram (CROWN) Study

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