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Correction to: Unjustly forgotten scientist Wacław Mayzel (1847–1916)—co‑discoverer of somatic mitosis

Journal of applied genetics, 2024-09, Vol.65 (3), p.645-645

2024

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Unjustly forgotten scientist Wacław Mayzel (1847–1916)—co-discoverer of somatic mitosis

Journal of applied genetics, 2021-12, Vol.62 (4), p.639-642

2021

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Tumor genotype is an independent prognostic factor in primary gastrointestinal stromal tumors of gastric origin: a european multicenter analysis based on ConticaGIST

Clinical cancer research, 2014-12, Vol.20 (23), p.6105-6116

2014

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Albert de la Chapelle—pro memoriam

Journal of applied genetics, 2021-09, Vol.62 (3), p.455-458

2021

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Sex contribution to average age at onset of Huntington’s disease depends on the number of (CAG)n repeats

Scientific reports, 2024-07, Vol.14 (1), p.15729-9, Article 15729

2024

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Folate/homocysteine metabolism and lung cancer risk among smokers

PloS one, 2019-04, Vol.14 (4), p.e0214462

2019

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Synergy between the alteration in the N-terminal region of butyrylcholinesterase K variant and apolipoprotein E4 in late-onset Alzheimer's disease

Scientific reports, 2019-03, Vol.9 (1), p.5223, Article 5223

2019

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Routine brush cytology and fluorescence in situ hybridization for assessment of pancreatobiliary strictures

Gastrointestinal endoscopy, 2012, Vol.75 (1), p.65-73

2012

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The outcome and predictive factors of sunitinib therapy in advanced gastrointestinal stromal tumors (GIST) after imatinib failure - one institution study

BMC cancer, 2012-03, Vol.12 (1), p.107-107, Article 107

2012

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Risk criteria and prognostic factors for predicting recurrences after resection of primary gastrointestinal stromal tumor

Annals of surgical oncology, 2007-07, Vol.14 (7), p.2018-2027

2007

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Bayesian multilevel model of micro RNA levels in ovarian-cancer and healthy subjects

PloS one, 2019-08, Vol.14 (8), p.e0221764

2019

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Cancer predisposing BARD1 mutations in breast–ovarian cancer families

Breast cancer research and treatment, 2012-01, Vol.131 (1), p.89-97

2012

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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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Conversion of epidermal growth factor receptor 2 and hormone receptor expression in breast cancer metastases to the brain

Breast cancer research : BCR, 2012-08, Vol.14 (4), p.R119-R119, Article R119

2012

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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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Transcriptomic Effects of Estrogen Starvation and Induction in the MCF7 Cells. The Meta-analysis of Microarray Results

Current pharmaceutical biotechnology, 2016-01, Vol.17 (2), p.161-172

2016

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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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Association of Genes Related to Oxidative Stress with the Extent of Coronary Atherosclerosis

Life (Basel, Switzerland), 2020-09, Vol.10 (9), p.210

2020

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NADPH Oxidase Gene Polymorphism is Associated with Mortality and Cardiovascular Events in 7-Year Follow-Up

Journal of clinical medicine, 2020-05, Vol.9 (5), p.1475

2020

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High frequency of BRCA1/2 germline mutations in consecutive ovarian cancer patients in Poland

Gynecologic oncology, 2008-02, Vol.108 (2), p.433-437

2008

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Comparative Genomic Hybridization to Microarrays in Fetuses with High-Risk Prenatal Indications: Polish Experience with 7400 Pregnancies

Genes, 2022-04, Vol.13 (4), p.690

2022

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Microdeletion of Target Sites for Insulator Protein CTCF in a Chromosome 11p15 Imprinting Center in Beckwith-Wiedemann Syndrome and Wilms' Tumor

Proceedings of the National Academy of Sciences - PNAS, 2005-03, Vol.102 (11), p.4085-4090

2005

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Monitoring the Effects of Hypolipidemic Treatment in Children with Familial Hypercholesterolemia in Poland

Life (Basel, Switzerland), 2020-11, Vol.10 (11), p.270

2020

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Parental age as a risk factor for isolated congenital malformations in a Polish population

Paediatric and perinatal epidemiology, 2009-01, Vol.23 (1), p.29-40

2009

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Correction to: Unjustly forgotten scientist Wacław Mayzel (1847–1916)—co‑discoverer of somatic mitosis

Unjustly forgotten scientist Wacław Mayzel (1847–1916)—co-discoverer of somatic mitosis

Tumor genotype is an independent prognostic factor in primary gastrointestinal stromal tumors of gastric origin: a european multicenter analysis based on ConticaGIST

Albert de la Chapelle—pro memoriam

Sex contribution to average age at onset of Huntington’s disease depends on the number of (CAG)n repeats

Folate/homocysteine metabolism and lung cancer risk among smokers

Synergy between the alteration in the N-terminal region of butyrylcholinesterase K variant and apolipoprotein E4 in late-onset Alzheimer's disease

Routine brush cytology and fluorescence in situ hybridization for assessment of pancreatobiliary strictures

The outcome and predictive factors of sunitinib therapy in advanced gastrointestinal stromal tumors (GIST) after imatinib failure - one institution study

Risk criteria and prognostic factors for predicting recurrences after resection of primary gastrointestinal stromal tumor

Bayesian multilevel model of micro RNA levels in ovarian-cancer and healthy subjects

Cancer predisposing BARD1 mutations in breast–ovarian cancer families

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

Conversion of epidermal growth factor receptor 2 and hormone receptor expression in breast cancer metastases to the brain

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

Transcriptomic Effects of Estrogen Starvation and Induction in the MCF7 Cells. The Meta-analysis of Microarray Results

Novel, activating KIT -N822I mutation in familial cutaneous mastocytosis

Management of familial hypercholesterolemia in children and adolescents. Position paper of the Polish Lipid Expert Forum

Association of Genes Related to Oxidative Stress with the Extent of Coronary Atherosclerosis

NADPH Oxidase Gene Polymorphism is Associated with Mortality and Cardiovascular Events in 7-Year Follow-Up

High frequency of BRCA1/2 germline mutations in consecutive ovarian cancer patients in Poland

Comparative Genomic Hybridization to Microarrays in Fetuses with High-Risk Prenatal Indications: Polish Experience with 7400 Pregnancies

Microdeletion of Target Sites for Insulator Protein CTCF in a Chromosome 11p15 Imprinting Center in Beckwith-Wiedemann Syndrome and Wilms' Tumor

Monitoring the Effects of Hypolipidemic Treatment in Children with Familial Hypercholesterolemia in Poland

Parental age as a risk factor for isolated congenital malformations in a Polish population

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