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Secondary chronic myeloid leukemia in a patient with CALR and ASXL1-mutated primary myelofibrosis

International journal of hematology, 2022-09, Vol.116 (3), p.442-445

2022

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APPLE trial: Feasibility and activity of AZD9291 (osimertinib) treatment on Positive PLasma T790M in EGFR mutant NSCLC patients. EORTC 1613

Clinical lung cancer, 2017-09, Vol.18 (5), p.583-588

2017

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The oncogene AAMDC links PI3K-AKT-mTOR signaling with metabolic reprograming in estrogen receptor-positive breast cancer

Nature communications, 2021-03, Vol.12 (1), p.1920-22, Article 1920

2021

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Overall Survival From the EORTC LCG-1613 APPLE Trial of Osimertinib Versus Gefitinib Followed by Osimertinib in Advanced EGFR -Mutant Non-Small-Cell Lung Cancer

Journal of clinical oncology, 2024-04, Vol.42 (12), p.1350-1356

2024

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Colonic Adenocarcinomas Harboring NTRK Fusion Genes: A Clinicopathologic and Molecular Genetic Study of 16 Cases and Review of the Literature

The American journal of surgical pathology, 2020-02, Vol.44 (2), p.162-173

2020

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Molecular characterization of two novel intronic variants of NIPBL gene detected in unrelated Cornelia de Lange syndrome patients

BMC medical genetics, 2019-01, Vol.20 (1), p.1-1, Article 1

2019

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Frequency and clinicopathologic profile of PIK3CA mutant GISTs: molecular genetic study of 529 cases

Modern pathology, 2016-03, Vol.29 (3), p.275-282

2016

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Mechanisms of resistance to imatinib mesylate in gastrointestinal stromal tumors and activity of the PKC412 inhibitor against imatinib-resistant mutants

Gastroenterology (New York, N.Y. 1943), 2005-02, Vol.128 (2), p.270-279

2005

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The genome of Dasychira pudibunda nucleopolyhedrovirus (DapuNPV) reveals novel genetic connection between baculoviruses infecting moths of the Lymantriidae family

BMC genomics, 2015-10, Vol.16 (1), p.759-759, Article 759

2015

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Genetic Mosaicism in a Group of Patients With Cornelia de Lange Syndrome

Frontiers in pediatrics, 2019-05, Vol.7, p.203-203

2019

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The kinase inhibitor TKI258 is active against the novel CUX1-FGFR1 fusion detected in a patient with T-lymphoblastic leukemia/lymphoma and t(7;8)(q22;p11)

Haematologica (Roma), 2011-06, Vol.96 (6), p.922-926

2011

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Spectrum and Prevalence of Pathogenic Variants in Ovarian Cancer Susceptibility Genes in a Group of 333 Patients

Cancers, 2018-11, Vol.10 (11), p.442

2018

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The Role of Butyrylcholinesterase and Iron in the Regulation of Cholinergic Network and Cognitive Dysfunction in Alzheimer's Disease Pathogenesis

International journal of molecular sciences, 2021-02, Vol.22 (4), p.2033

2021

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Assessment of Subclinical Atherosclerosis Using Computed Tomography Calcium Scores in Patients with Familial and Nonfamilial Hypercholesterolemia

Journal of Atherosclerosis and Thrombosis, 2016/05/02, Vol.23(5), pp.588-595

2016

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Colorectal Adenocarcinomas Harboring ALK Fusion Genes: A Clinicopathologic and Molecular Genetic Study of 12 Cases and Review of the Literature

The American journal of surgical pathology, 2020-09, Vol.44 (9), p.1224-1234

2020

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Efficacy of clinical diagnostic criteria for familial hypercholesterolemia genetic testing in Poland

Atherosclerosis, 2016-06, Vol.249, p.52-58

2016

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Butyrylcholinesterase Protein Ends in the Pathogenesis of Alzheimer's Disease-Could BCHE Genotyping Be Helpful in Alzheimer's Therapy?

Biomolecules (Basel, Switzerland), 2019-10, Vol.9 (10), p.592

2019

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Mosaic Intronic NIPBL Variant in a Family With Cornelia de Lange Syndrome

Frontiers in genetics, 2018-07, Vol.9, p.255-255

2018

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Novel, activating KIT -N822I mutation in familial cutaneous mastocytosis

Experimental hematology, 2011-08, Vol.39 (8), p.859-865.e2

2011

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Diagnosis of Mastocytosis in Children and Adults in Daily Clinical Practice

Acta dermato-venereologica, 2016-03, Vol.96 (3), p.292-297

2016

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Diagnosis and treatment of patients with breast cancer and mutation in the BRCA1/2 genes

Oncology in Clinical Practice, 2024-06, Vol.20 (3), p.222-228

2024

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Genomic Profiling Identifies Putative Pathogenic Alterations in NSCLC Brain Metastases

JTO clinical and research reports, 2022-12, Vol.3 (12), p.100435-100435, Article 100435

2022

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The efficacy of EGFR gene mutation testing in various samples from non-small cell lung cancer patients: a multicenter retrospective study

Journal of cancer research and clinical oncology, 2015-01, Vol.141 (1), p.61-68

2015

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Mutations in gastrointestinal stromal tumors - a population-based study from Northern Norway

APMIS : acta pathologica, microbiologica et immunologica Scandinavica, 2007-04, Vol.115 (4), p.289-298

2007

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Secondary chronic myeloid leukemia in a patient with CALR and ASXL1-mutated primary myelofibrosis

APPLE trial: Feasibility and activity of AZD9291 (osimertinib) treatment on Positive PLasma T790M in EGFR mutant NSCLC patients. EORTC 1613

The oncogene AAMDC links PI3K-AKT-mTOR signaling with metabolic reprograming in estrogen receptor-positive breast cancer

Overall Survival From the EORTC LCG-1613 APPLE Trial of Osimertinib Versus Gefitinib Followed by Osimertinib in Advanced EGFR -Mutant Non-Small-Cell Lung Cancer

Colonic Adenocarcinomas Harboring NTRK Fusion Genes: A Clinicopathologic and Molecular Genetic Study of 16 Cases and Review of the Literature

Molecular characterization of two novel intronic variants of NIPBL gene detected in unrelated Cornelia de Lange syndrome patients

Frequency and clinicopathologic profile of PIK3CA mutant GISTs: molecular genetic study of 529 cases

Alterations in key signaling pathways in sinonasal tract melanoma. A molecular genetics and immunohistochemical study of 90 cases and comprehensive review of the literature

Mechanisms of resistance to imatinib mesylate in gastrointestinal stromal tumors and activity of the PKC412 inhibitor against imatinib-resistant mutants

The genome of Dasychira pudibunda nucleopolyhedrovirus (DapuNPV) reveals novel genetic connection between baculoviruses infecting moths of the Lymantriidae family

Genetic Mosaicism in a Group of Patients With Cornelia de Lange Syndrome

The kinase inhibitor TKI258 is active against the novel CUX1-FGFR1 fusion detected in a patient with T-lymphoblastic leukemia/lymphoma and t(7;8)(q22;p11)

Spectrum and Prevalence of Pathogenic Variants in Ovarian Cancer Susceptibility Genes in a Group of 333 Patients

The Role of Butyrylcholinesterase and Iron in the Regulation of Cholinergic Network and Cognitive Dysfunction in Alzheimer's Disease Pathogenesis

Assessment of Subclinical Atherosclerosis Using Computed Tomography Calcium Scores in Patients with Familial and Nonfamilial Hypercholesterolemia

Colorectal Adenocarcinomas Harboring ALK Fusion Genes: A Clinicopathologic and Molecular Genetic Study of 12 Cases and Review of the Literature

Efficacy of clinical diagnostic criteria for familial hypercholesterolemia genetic testing in Poland

Butyrylcholinesterase Protein Ends in the Pathogenesis of Alzheimer's Disease-Could BCHE Genotyping Be Helpful in Alzheimer's Therapy?

Mosaic Intronic NIPBL Variant in a Family With Cornelia de Lange Syndrome

Novel, activating KIT -N822I mutation in familial cutaneous mastocytosis

Diagnosis of Mastocytosis in Children and Adults in Daily Clinical Practice

Diagnosis and treatment of patients with breast cancer and mutation in the BRCA1/2 genes

Genomic Profiling Identifies Putative Pathogenic Alterations in NSCLC Brain Metastases

The efficacy of EGFR gene mutation testing in various samples from non-small cell lung cancer patients: a multicenter retrospective study

Mutations in gastrointestinal stromal tumors - a population-based study from Northern Norway

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