J. Limon

F. Hirsch, P. Bunn, M. Varella‐Garcia, 2007, Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer.

Double minutes in two primary adenocarcinomas of the prostate.

F. Mitelman, N. Mandahl, J. Limon, 1989, Cancer genetics and cytogenetics.

Cytogenetic analysis of 57 primary prostatic adenocarcinomas

F. Mitelman, N. Mandahl, J. Limon, 1992, Genes, chromosomes & cancer.

Loss of heterozygosity at chromosomes 3p and 17p in primary non-small cell lung cancer.

R. Dziadziuszko, J. Jassem, E. Jassem, 2004, Anticancer research.

Chromosome 18q deletion syndrome with autoimmune diabetes mellitus: putative genomic loci for autoimmunity and immunodeficiency

M. Borowiec, W. Młynarski, J. Limon, 2016, Pediatric diabetes.

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

M. Banach, S. Gidding, A. Mazur, 2014, Journal of clinical lipidology.

[Management in familial hypercholesterolaemia in children and adolescents. Position of the Lipid Expert Forum].

M. Banach, A. Mazur, T. Zdrojewski, 2013, Kardiologia polska.

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

M. Stukan, P. Kozłowski, J. Limon, 2018, Cancers.

Molecular basis of familial hypercholesterolemia in Poland – update from the Polish national centre of diagnostics and treatment of familial hypercholesterolemia

A. Rynkiewicz, J. Limon, M. Gruchała, 2016 .

Clinical course of homozygous familial hypercholesterolemia during childhood: report on 4 unrelated patients with homozygous or compound heterozygous mutations in theLDLR gene

A. Wierzbicka, J. Limon, E. Pronicka, 2010, Journal of Applied Genetics.

Olanzapine-induced weight gain is associated with the −759C/T and −697G/C polymorphisms of the HTR2C gene

B. Godlewska, J. Landowski, J. Limon, 2009, The Pharmacogenomics Journal.

Calretinin and Other Mesothelioma Markers in Synovial Sarcoma: Analysis of Antigenic Similarities and Differences With Malignant Mesothelioma

A. Niezabitowski, J. Limon, J. Lasota, 2001, The American journal of surgical pathology.

Association of the ScaI atrial natriuretic peptide gene polymorphism with nonfatal myocardial infarction and extent of coronary artery disease.

A. Rynkiewicz, J. Limon, M. Gruchała, 2003, American heart journal.

Abnormally banded region in a poorly differentiated sarcoma is not correlated with amplification of c-MYC or c-MOS protooncogenes.

F. Li, A. Sandberg, J. Limon, 1988, Cancer genetics and cytogenetics.

Cytogenetic studies of adipose tissue tumors. II. Recurrent reciprocal translocation t(12;16)(q13;p11) in myxoid liposarcomas.

C. Turc‐Carel, A. Sandberg, J. Limon, 1986, Cancer genetics and cytogenetics.

Limited significance of family history for presence of BRCA1 gene mutation in Polish breast and ovarian cancer cases

M. Dąbrowska, A. Kluska, A. Bałabas, 2012, Familial Cancer.

Molecular characterization of Polish patients with familial hypercholesterolemia: novel and recurrentLDLR mutations

A. Rynkiewicz, J. Limon, E. Pronicka, 2010, Journal of Applied Genetics.

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

M. Stukan, J. Limon, M. Ratajska, 2008, Gynecologic oncology.

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

A. Rynkiewicz, J. Limon, M. Gruchała, 2020, Journal of clinical medicine.

Genomic findings in patients with clinical suspicion of 22q11.2 deletion syndrome

R. Śmigiel, M. Sasiadek, J. Limon, 2016, Journal of Applied Genetics.

Prevalence of the BLM nonsense mutation, p.Q548X, in ovarian cancer patients from Central and Eastern Europe

T. Dörk, E. Khusnutdinova, P. Hillemanns, 2014, Familial Cancer.

Lymphocytic meningitis and spinal neurocysticercosis: A case report and literature review☆

J. Limon, B. Yagüe, M. García, 2014 .

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

J. Limon, W. Biernat, I. Marek, 2012, Gastrointestinal endoscopy.

When Do Paediatric Patients with Familial Hypercholesterolemia Need Statin Therapy?*

A. Rynkiewicz, J. Limon, M. Gruchała, 2017, Developmental period medicine.

[Management of familial heterozygous hypercholesterolaemia. Position paper of the Polish Lipid Expert Forum].

M. Banach, T. Zdrojewski, J. Stȩpińska, 2013, Kardiologia polska.

Analysis of candidate genes for genotypic diagnosis in the long QT syndrome.

J. Kwiatkowska, N. Blin, J. Limon, 2004, Journal of applied genetics.

Founder BRCA1 mutations and two novel germline BRCA2 mutations in breast and/or ovarian cancer families from North‐Eastern Poland

J. Jassem, J. Limon, E. Oláh, 2000, Human mutation.

Clinical impact of molecular and cytogenetic findings in synovial sarcoma

O. Larsson, P. D. Dal Cin, R. Sciot, 2001, Genes, chromosomes & cancer.

Cytogenetic analysis and clinical significance of chromosome 7 aberrations in acute leukaemia.

A. Wozniak, J. Limon, A. Balcerska, 2003, Journal of applied genetics.

The algorithm for Alzheimer risk assessment based on APOE promoter polymorphisms

B. Godlewska, J. Limon, B. Lipska-Ziętkiewicz, 2016, Alzheimer's Research & Therapy.

Molecular genetic characterization of the EWS/ATF1 fusion gene in clear cell sarcoma of tendons and aponeuroses

O. Larsson, R. Sciot, F. Mertens, 2002, International journal of cancer.

A rare chimeric TLS/FUS-CHOP transcript in a patient with multiple liposarcomas: a case report.

R. Schneider-Stock, J. Ryś, A. Niezabitowski, 1999, Cancer Genetics and Cytogenetics.

Trisomy 13 in a case of myelodysplastic syndrome.

J. Limon, A. Hellmann, W. Baran, 1989, Cancer genetics and cytogenetics.

Cytogenetic and immunohistochemical profile of myxoid liposarcoma.

K. Mrózek, M. Debiec‐Rychter, J. Ryś, 1995, American journal of clinical pathology.

Chromosomal changes in soft-tissue sarcomas. A new diagnostic parameter.

C. Turc‐Carel, A. Sandberg, J. Limon, 1987, Archives of surgery.

Novel, activating KIT-N822I mutation in familial cutaneous mastocytosis.

A. Piskorz, M. Debiec‐Rychter, E. Jassem, 2011, Experimental hematology.

Diagnosis of Mastocytosis in Children and Adults in Daily Clinical Practice.

J. Limon, B. Nedoszytko, R. Nowicki, 2016, Acta dermato-venereologica.

Recurrent chromosome changes in two adult fibrosarcomas

K. Mrózek, M. Debiec‐Rychter, J. Limon, 1998, Genes, chromosomes & cancer.

Evidence of somatic mutations in osteoarthritis

S. Toksvig-Larsen, A. Lindstrand, F. Mitelman, 1996, Human Genetics.

Cytogenetic findings in a primary adrenocortical carcinoma.

A. Sandberg, J. Limon, R. Huben, 1987, Cancer genetics and cytogenetics.

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

A. Rynkiewicz, J. Limon, M. Gruchała, 2020, Life.

Imatinib targeted therapy for a patient with chronic eosinophilic leukemia

J. Limon, W. Prejzner, A. Hellmann, 2005 .

Mutations in the EDA gene in three unrelated families reveal no apparent correlation between phenotype and genotype in the patients with an X-linked anhidrotic ectodermal dysplasia.

J. Limon, J. Wierzba, J. Roszkiewicz, 2001, American journal of medical genetics.

Mutation in the regulatory region of the EDA gene coincides with the symptoms of anhidrotic ectodermal dysplasia.

J. Limon, W. Trzeciak, K. Kobielak, 1998, Acta biochimica Polonica.

Accumulation of chromosomal changes in human glioma progression. A cytogenetic study of 50 cases.

K. Mrózek, P. Liberski, M. Debiec‐Rychter, 1995, Cancer genetics and cytogenetics.

Patterns of keratin polypeptides in 110 biphasic, monophasic, and poorly differentiated synovial sarcomas

J. Limon, J. Lasota, M. Miettinen, 2000, Virchows Archiv.

Cytogenetic findings in two synovial sarcomas.

K. Mrózek, J. Limon, J. Jaśkiewicz, 1989, Cancer genetics and cytogenetics.

Complex tumor-specific t(X;18) in seven synovial sarcoma tumors.

R. Sciot, M. Debiec‐Rychter, J. Ryś, 2009, Cancer genetics and cytogenetics.

Karyotypic characterization of 64 nonmalignant thyroid goiters.

J. Limon, Alina Kuźniacka, A. Łachiński, 2005, Cancer genetics and cytogenetics.

Cytogenetics of uterine sarcomas: presentation of eight new cases and review of the literature.

C. Bloomfield, K. Mrózek, N. Mandahl, 1998, Gynecologic oncology.

Parachordoma: a rare sarcoma with clonal chromosomal changes.

J. Ryś, A. Niezabitowski, J. Limon, 1998, Cancer genetics and cytogenetics.

Cytogenetic findings in an embryonal sarcoma of the liver.

J. Limon, P. Czauderna, M. Iliszko, 1998, Cancer genetics and cytogenetics.

Translocation (X;1)(p11.2;q21) in a papillary renal cell carcinoma in a 14-year-old girl.

J. Limon, J. Gronwald, J. Lubiński, 1998, Cancer genetics and cytogenetics.

Characteristic karyotypic features in lacrimal and salivary gland carcinomas.

F. Mitelman, F. Mertens, N. Mandahl, 1994, British Journal of Cancer.

On the significance of trisomy 7 and sex chromosome loss in renal cell carcinoma.

F. Mitelman, K. Mrózek, N. Mandahl, 1990, Cancer genetics and cytogenetics.

Prevalence and clinical correlations of BRCA1/BRCA2 unclassified variant carriers among unselected primary ovarian cancer cases - preliminary report.

P. Devilee, J. Jassem, C. Cornelisse, 2005, European journal of cancer.

Polymorphisms of the histamine receptor (H1HR) gene are not associated with olanzapine-induced weight gain.

B. Godlewska, J. Landowski, J. Limon, 2013, Journal of clinical psychopharmacology.

Changes in expression of serine proteases HtrA1 and HtrA2 during estrogen-induced oxidative stress and nephrocarcinogenesis in male Syrian hamster.

A. Wozniak, J. Limon, J. Kobiela, 2008, Acta biochimica Polonica.

Mutational analysis in podocin-associated hereditary nephrotic syndrome in Polish patients: founder effect in the Kashubian population

M. Litwin, M. Szczepańska, F. Schaefer, 2013, Journal of Applied Genetics.

Loss of heterozygosity atBRCA1/2 loci in hereditary and sporadic ovarian cancers

M. Stukan, J. Limon, M. Ratajska, 2010, Journal of Applied Genetics.

Ring marker containing 17q and chromosome 22 in a case of dermatofibrosarcoma protuberans.

F. Mitelman, F. Mertens, N. Mandahl, 1996, Cancer genetics and cytogenetics.

Array CGH analysis in primary gastrointestinal stromal tumors: Cytogenetic profile correlates with anatomic site and tumor aggressiveness, irrespective of mutational status

J. Vermeesch, R. Sciot, L. Guillou, 2007, Genes, chromosomes & cancer.

Spectrum of NIPBL gene mutations in Polish patients with Cornelia de Lange syndrome

M. Malinowska, J. Limon, J. Wierzba, 2013, Journal of applied genetics.

Spectrum of NIPBL gene mutations in Polish patients with Cornelia de Lange syndrome

M. Malinowska, J. Limon, J. Wierzba, 2012, Journal of Applied Genetics.

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

R. Dziadziuszko, J. Jassem, W. Kozlowski, 2012, Breast Cancer Research.

Cytogenetic findings in a primary leiomyosarcoma of the prostate.

A. Sandberg, J. Limon, P. Dal Cin, 1986, Cancer genetics and cytogenetics.

Isolabeling of the long arm of the human Y chromosome demonstrated by the FPG technique

J. Limon, Z. Gibas, 1978, Chromosoma.

Trisomy of chromosome 12 in a case of thecoma of the ovary.

K. Mrózek, J. Limon, B. Nedoszytko, 1990, Gynecologic oncology.

Chromosome changes associated with spontaneous phenotypic variation of transplantable melanoma.

A. Sandberg, J. Limon, Z. Gibas, 1987, Cancer genetics and cytogenetics.

Trisomy 7, trisomy 10, and loss of the Y chromosome in short-term cultures of normal kidney tissue.

J. Cigudosa, F. Mitelman, N. Mandahl, 1990, Cytogenetics and cell genetics.

AgNOR staining in benign hyperplasia and carcinoma of the prostate

J. Limon, S. Heim, Stella Mamaeva, 1991, The Prostate.

Two mosaic cases with nonfluorescent Y chromosome analysed with Y-specific DNA probes.

K. Grzeschik, M. Debiec‐Rychter, J. Limon, 1988, American journal of medical genetics.

A case with 47,XXY,del(11)(q23) karotype-coexistence of Jacobsen and Klinefelter syndromes.

A. Wozniak, J. Limon, J. Wierzba, 2000, Genetic counseling.

Sertoli cell tumor in androgen insensitivity syndrome--a case report.

J. Jassem, J. Limon, B. Wysocka, 1999, Gynecologic oncology.

Unusual SCD in cancer cells: a phenomenon related to decreased BrdU incorporation?

A. Sandberg, J. Limon, R. Becher, 1983, Cancer genetics and cytogenetics.

An improved technique for short-term culturing of human prostatic adenocarcinoma tissue for cytogenetic analysis.

F. Mitelman, N. Mandahl, J. Limon, 1990, Cancer genetics and cytogenetics.

The induction of sister-chromatid exchanges by 9-aminoacridine derivatives. I. The relation between the yield of SCE induction and cell kinetics in cultured human lymphocytes.

J. Limon, Z. Gibas, 1979, Mutation research.

Sarcomatoid carcinoma (carcinosarcoma) of the gallbladder.

A. Niezabitowski, J. Limon, A. Wasilewska, 1998, General & diagnostic pathology.

Partial trisomy of distal 5q and partial monosomy of Xp as a result of mating between two translocation carriers: a female with a balanced translocation t(X;5)(p11;q31) and a male with a der(13;14)(q10;q10)--a case report and a family study.

A. Wozniak, J. Limon, J. Wierzba, 2002, Annales de genetique.

Root morphology of mandibular premolars in 40 patients with Turner syndrome.

J. Limon, B. Kochańska, A. Kusiak, 2005, International endodontic journal.

The frequency of occurrence of abnormal frenal attachment of lips and enamel defects in Turner syndrome.

J. Limon, B. Kochańska, A. Kusiak, 2008, Oral diseases.

X-linked anhidrotic ectodermal dysplasia and de novo t(X;1) in a female

K. Mrózek, J. Limon, M. Castrén, 1991, Human Genetics.

Cancer predisposing BARD1 mutations in breast–ovarian cancer families

Å. Borg, A. Piskorz, J. Limon, 2011, Breast Cancer Research and Treatment.

BRCA1 and BRCA2 mutation analysis in breast‐ovarian cancer families from northeastern Poland

Å. Borg, J. Limon, U. Johansson, 2003, Human mutation.

Clinical and molecular‐cytogenetic studies in seven patients with ring chromosome 18

P. Stankiewicz, J. Pilch, A. Wozniak, 2001 .

Limited significance of family history for presence of BRCA1 gene mutation in Polish breast and ovarian cancer cases

M. Dąbrowska, A. Kluska, A. Bałabas, 2012, Familial Cancer.

Prevalence of the most frequent BRCA1 mutations in Polish population

Danuta Januszkiewicz-Lewandowska, M. Dąbrowska, A. Kluska, 2011, Journal of Applied Genetics.

BRCA1 and BRCA2 point mutations and large rearrangements in breast and ovarian cancer families in Northern Poland.

Å. Borg, J. Jassem, G. Palmieri, 2008, Oncology reports.

Antagonizing functions of BARD1 and its alternatively spliced variant BARD1δ in telomere stability

I. Irminger-Finger, G. Laurent, J. Limon, 2016, Oncotarget.

Cancer predisposing BARD1 mutations affect exon skipping and are associated with overexpression of specific BARD1 isoforms.

I. Irminger-Finger, G. Laurent, P. Kozłowski, 2015, Oncology reports.

Analysis of large mutations in BARD1 in patients with breast and/or ovarian cancer: the Polish population as an example

I. Irminger-Finger, M. Stukan, P. Kozłowski, 2015, Scientific Reports.

Cancer predisposing BARD 1 mutations affect exon skipping and are associated with overexpression of specific BARD 1 isoforms

I. Irminger-Finger, G. Laurent, P. Kozłowski, 2015 .

Cell-free DNA BRAF V600E measurements during BRAF inhibitor therapy of metastatic melanoma: long-term analysis

P. Rutkowski, J. Siedlecki, J. Limon, 2020, Tumori.

Expression and significance of HER family receptors in neuroblastic tumors

W. Grajkowska, A. Wozniak, J. Limon, 2011, Clinical & Experimental Metastasis.

Rearrangement of the neoplasia‐associated gene HMGIC in synovia from patients with osteoarthritis

S. Toksvig-Larsen, A. Lindstrand, M. Höglund, 1999, Genes, chromosomes & cancer.

Comparative study of clinical characteristics of amniotic rupture sequence with and without body wall defect: further evidence for separation.

Aleksander Jamsheer, A. Latos-Bieleńska, J. Limon, 2009, Birth defects research. Part A, Clinical and molecular teratology.

Epidemiologic characteristics of amniotic band sequence with limb malformations without body wall defect: data from the Polish Registry of Congenital Malformations

A. Latos-Bieleńska, K. Kiryluk, J. Limon, 2008 .

On the significance of germline cytogenetic rearrangements at MYCN locus in neuroblastoma

J. Limon, J. Wierzba, Magdalena Koczkowska, 2013, Molecular Cytogenetics.

Expression of the c-erbB2 proto-oncogene in male breast carcinoma: lack of prognostic significance.

A. Niezabitowski, C. Welter, N. Blin, 1993, Oncology.

COLIA1-PDGFB gene fusion in dermatofibrosarcoma protuberans. molecular analysis of a case with an unusual large marker containing sequences from chromosomes 7, 8, 17, 21, and 22.

K. Mrózek, J. Limon, F. Pedeutour, 2002, Cancer genetics and cytogenetics.

Management of familial heterozygous hypercholesterolemia. Position paper of the Polish Lipid Expert Forum.

M. Banach, T. Zdrojewski, J. Stȩpińska, 2013, Polskie Archiwum Medycyny Wewnetrznej.

Detection of BRCA1/2 mutations in circulating tumor DNA from patients with ovarian cancer

M. Stukan, J. Limon, W. Biernat, 2017, Oncotarget.

Prevalence of the BLM nonsense mutation, p.Q548X, in ovarian cancer patients from Central and Eastern Europe

T. Dörk, E. Khusnutdinova, P. Hillemanns, 2015, Familial Cancer.

Improved technique for short‐term culture and cytogenetic analysis of human breast cancer

F. Mitelman, N. Mandahl, J. Limon, 1992, Genes, chromosomes & cancer.

Chromosome changes in metastatic human melanoma.

S. Sait, A. Sandberg, J. Limon, 1988, Cancer genetics and cytogenetics.

Mutational and genotype–phenotype correlation analyses in 28 Polish patients with Cornelia de Lange syndrome

P. Stankiewicz, J. Lupski, J. Limon, 2006, American journal of medical genetics. Part A.

HER2 Amplification Has no Prognostic Value in Sporadic and Hereditary Ovarian Tumours

M. Stukan, J. Limon, M. Ratajska, 2006, Hereditary cancer in clinical practice.

High frequency of telomeric associations and chromatid exchanges and breaks in human ovarian carcinoma.

K. Mrózek, J. Limon, 2008, Hereditas.

Microdeletion and IGF2 loss of imprinting in a cascade causing Beckwith-Wiedemann syndrome with Wilms' tumor

D. Housman, J. Pelletier, D. Reutzel, 2005, Nature Genetics.

Loss of heterozygosity in 73 human thyroid tumors.

M. Wiench, B. Jarzab, A. Wozniak, 2005, Neuro endocrinology letters.

Clonal chromosome aberrations are present in vivo in synovia and osteophytes from patients with osteoarthritis

S. Toksvig-Larsen, A. Lindstrand, F. Mertens, 1997, Human Genetics.

Application of high-resolution genomic profiling in the differential diagnosis of liposarcoma

J. Limon, W. Biernat, J. Lasota, 2017, Molecular Cytogenetics.

Interstitial deletion of the short arm of chromosome 3 as a primary chromosome abnormality in carcinomas of the breast

F. Mitelman, N. Mandahl, J. Limon, 1993, Genes, chromosomes & cancer.

Cytogenetics of Synovial Sarcoma: Presentation of Ten New Cases and Review of the Literature

F. Mitelman, K. Mrózek, A. Rydholm, 1991, Genes, chromosomes & cancer.

Chromosome abnormalities in bilateral breast carcinomas. Cytogenetic evaluation of the clonal origin of multiple primary tumors

F. Mitelman, N. Mandahl, A. Gerdes, 1995, Cancer.

Trisomy 12 and 4 in a thecoma of the ovary.

K. Mrózek, J. Limon, J. Emerich, 1992, Gynecologic oncology.

Translocation (6;16) in a case of granulosa cell tumor of the ovary.

J. Limon, B. Nedoszytko, A. Verhest, 1992, Cancer genetics and cytogenetics.

Aberrations of chromosome 22 and polysomy of chromosome 8 as non-random changes in clear cell sarcoma.

P. Liberski, M. Debiec‐Rychter, J. Limon, 1994, Cancer genetics and cytogenetics.

Translocation (13;22) in a hemangiopericytoma.

A. Sandberg, J. Limon, U. Rao, 1986, Cancer genetics and cytogenetics.

Prognostic implications of cytogenetic findings in kidney cancer.

M. Fernö, H. Olsson, F. Mitelman, 1997, British journal of urology.

EGFR, PIK3CA and PTEN gene status and their protein product expression in neuroblastic tumours.

W. Grajkowska, A. Wozniak, J. Limon, 2010, Folia neuropathologica.

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

E. Obersztyn, B. Wiśniowiecka-Kowalnik, M. Smyk, 2022, Genes.

Clinical and molecular-cytogenetic studies in seven patients with ring chromosome 18.

P. Stankiewicz, J. Pilch, A. Wozniak, 2001, American journal of medical genetics.

Germline MSH2 and MLH1 mutational spectrum including large rearrangements in HNPCC families from Poland (update study)

J. Kładny, A. Jakubowska, K. Safranow, 2005, Clinical genetics.

What are the current outcomes of advanced gastrointestinal stromal tumors: who are the long-term survivors treated initially with imatinib?

P. Rutkowski, M. Debiec‐Rychter, J. Siedlecki, 2013, Medical Oncology.

Clinical utility of the new American Joint Committee on Cancer staging system for gastrointestinal stromal tumors

P. Rutkowski, M. Debiec‐Rychter, J. Siedlecki, 2011, Cancer.

An open label phase II study evaluating first-line EGFR tyrosine kinase inhibitor erlotinib in non-small cell lung cancer patients with tumors showing high EGFR gene copy number

R. Dziadziuszko, J. Jassem, A. Szczesna, 2016, Oncotarget.

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

P. Krawczyk, J. Milanowski, R. Dziadziuszko, 2014, Journal of Cancer Research and Clinical Oncology.

High Resolution Melting analysis as a rapid and efficient method of screening for small mutations in the STK11 gene in patients with Peutz-Jeghers syndrome

J. Lubiński, A. Pławski, J. Limon, 2013, BMC Medical Genetics.

Cancer predisposing BARD1 mutations in breast-ovarian cancer families

M. Stukan, J. Limon, M. Matusiak, 2012, Hereditary Cancer in Clinical Practice.

A novel splicing mutation in the SLC9A3R1 gene in tumors from ovarian cancer patients.

M. Stukan, J. Limon, E. Kreimann, 2015, Oncology letters.

beta-2-adrenergic receptor gene polymorphism confers susceptibility to Graves disease.

K. Jażdżewski, S. Liyanarachchi, K. Narkiewicz, 2007, International journal of molecular medicine.

Maternal reproductive history and the risk of isolated congenital malformations.

J. Limon, B. Więckowska, A. Materna-Kiryluk, 2011, Paediatric and perinatal epidemiology.

Absence of structural rearrangements of chromosome 11 in human primary malignant melanoma.

K. Mrózek, J. Limon, B. Nedoszytko, 1992, Cancer genetics and cytogenetics.

Translocation t(4;11)(q35;p13) in an adrenocortical carcinoma.

A. Sandberg, J. Limon, P. Dal Cin, 1987, Cancer genetics and cytogenetics.

c.1810C>T Polymorphism of NTRK1Gene is associated with reduced Survival in Neuroblastoma Patients

G. Tonini, P. Scaruffi, J. Limon, 2009, BMC Cancer.

Recurrent Deletion of the Region Encoding Two (Gly-X-Y) Repeats in Patients with Anhidrotic Ectodermal Dysplasia Indicates Important Role for Collagen-Like Domain of the EDA Gene Product—Ectodysplasin-A

J. Limon, J. Roszkiewicz, W. Trzeciak, 2000 .

Recommendations for diagnostics and therapy of gastrointestinal stromal tumors (GIST) in 2010

W. Olszewski, M. Krzakowski, P. Rutkowski, 2010 .

Risk Criteria and Prognostic Factors for Predicting Recurrences After Resection of Primary Gastrointestinal Stromal Tumor

P. Rutkowski, M. Debiec‐Rychter, S. Głuszek, 2007, Annals of Surgical Oncology.

Predictive factors for long-term effects of imatinib therapy in patients with inoperable/metastatic CD117(+) gastrointestinal stromal tumors (GISTs)

P. Rutkowski, M. Debiec‐Rychter, J. Siedlecki, 2007, Journal of Cancer Research and Clinical Oncology.

Tumor Genotype Is an Independent Prognostic Factor in Primary Gastrointestinal Stromal Tumors of Gastric Origin: A European Multicenter Analysis Based on ConticaGIST

J. Blay, E. Wardelmann, R. Sciot, 2014, Clinical Cancer Research.

Clear cell sarcoma of tendons and aponeuroses with t(12;22) (q13;q12) diagnosed initially as malignant melanoma.

K. Mrózek, J. Limon, B. Nedoszytko, 1996, Cancer genetics and cytogenetics.

Granulosa cell tumors of the ovary: a karyotypic analysis

J. Limon, B. Nedoszytko, A. Verhest, 1991 .

Noninvasive assessment of endothelial function and vascular parameters in patients with familial and nonfamilial hypercholesterolemia.

A. Rynkiewicz, J. Limon, M. Gruchała, 2014, Polskie Archiwum Medycyny Wewnetrznej.

Cytogenetics of hepatoblastoma: further characterization of 1q rearrangements by fluorescence in situ hybridization: an international collaborative study.

D. Gisselsson, M. Höglund, B. Johansson, 2000, Medical and pediatric oncology.

Germline mutations in the von Hippel-Lindau (VHL) gene in patients from Poland: disease presentation in patients with deletions of the entire VHL gene

A. Jakubowska, J. Lubiński, L. Sagan, 2002, Journal of medical genetics.

Cytogenetic and proliferative potentials in meningiomas.

P. Liberski, M. Debiec‐Rychter, R. Kordek, 1999, Polish journal of pathology : official journal of the Polish Society of Pathologists.

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

Elzbieta Gajewska, A. Latos-Bieleńska, J. Limon, 2009, Paediatric and Perinatal Epidemiology.

Parachordoma--a clinicopathologic, immunohistochemical, electron microscopic, flow cytometric, and cytogenetic study.

A. Niezabitowski, J. Limon, A. Wasilewska, 1995, General & diagnostic pathology.

Folate/homocysteine metabolism and lung cancer risk among smokers

R. Dziadziuszko, J. Jassem, W. Rzyman, 2019, PloS one.

Angiotensin converting enzyme gene polymorphism is associated with severity of coronary artery disease in men with high total cholesterol levels

A. Rynkiewicz, J. Limon, M. Gruchała, 2012, Journal of Applied Genetics.

Prognostic value of KIT/PDGFRA mutations in gastrointestinal stromal tumours (GIST): Polish Clinical GIST Registry experience.

P. Sowa, A. Piskorz, P. Rutkowski, 2012, Annals of oncology : official journal of the European Society for Medical Oncology.

Epidemiology of isolated preaxial polydactyly type I: Data from the Polish Registry of Congenital Malformations (PRCM)

A. Latos-Bieleńska, J. Limon, B. Więckowska, 2013, BMC Pediatrics.

Primary leiomyosarcoma of the mesentery in two sisters: clinical and molecular characteristics.

J. Jassem, J. Limon, W. Biernat, 2013, Polish journal of pathology : official journal of the Polish Society of Pathologists.

Loss of genetic material within 1p and 19q chromosomal arms in low grade gliomas of central nervous system.

J. Limon, W. Biernat, P. Słoniewski, 2013, Folia neuropathologica.

Demonstration of two different regions of lateral asymmetry in human Y chromosomes

J. Limon, B. Kałużewski, Z. Gibas, 1979, Human Genetics.

Erratum to: Spectrum of NIPBL gene mutations in Polish patients with Cornelia de Lange syndrome

M. Malinowska, J. Limon, J. Wierzba, 2013, Journal of Applied Genetics.

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

A. Rynkiewicz, T. Bandurski, J. Limon, 2016, Atherosclerosis.

Cytogenic analysis of transplantable mouse B16 melanomas.

J. Limon, Z. Gibas, P. Mierzewski, 1985, Neoplasma.

Involvement of chromosomes 3 and 5 in renal cell carcinoma.

J. Richie, A. Sandberg, J. Limon, 1988, Cancer genetics and cytogenetics.

Coincidence of PTPN22 c.1858CC and FCRL3 ‐169CC genotypes as a biomarker of preserved residual β‐cell function in children with type 1 diabetes

J. Limon, A. Balcerska, Rafal Filipów, 2017, Pediatric diabetes.

Coincidence of PTPN 22 c . 1858 CC and FCRL 3-169 CC genotypes as a biomarker of preserved residual β-cell function in children with type 1 diabetes †

J. Limon, A. Balcerska, J. Kulczycka, 2016 .

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

D. Cysewski, J. Limon, B. Wasąg, 2019, Scientific Reports.

A case of mast cell leukaemia with exon 9 KIT mutation and good response to imatinib

A. Piskorz, J. Limon, K. Lewandowski, 2011, European journal of haematology.

Gastrointestinal stromal tumors. A multicenter experience.

E. Korobowicz, J. Stachura, J. Sygut, 2005, Polish journal of pathology : official journal of the Polish Society of Pathologists.

Influence of Cytochrome P450, ABC and SLC Gene Polymorphisms on Imatinib Therapy Outcome of Patients with Gastrointestinal Stromal Tumours (GIST).

P. Rutkowski, J. Siedlecki, A. Wozniak, 2017, Folia biologica.

A study in a Polish ataxia cohort indicates genetic heterogeneity and points to MTCL1 as a novel candidate gene

R. Płoski, M. Rydzanicz, J. Limon, 2018, Clinical genetics.

Combined analysis of P53 Arg72Pro, GSTM1 and GSTT1 gene polymorphisms as predisposing factors for non-small cell lung cancer (NSCLC) development

Å. Borg, R. Dziadziuszko, J. Jassem, 2005 .

ovarian cancer in a family with coexistence of germline nf1 and brca1 mutations case report

J. Limon, Magdalena Koczkowska, Alina Kuźniacka, 2018 .

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

A. Rynkiewicz, J. Limon, M. Gruchała, 2020, Life.

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

P. Sachadyn, J. Limon, Janusz Limon, 2015, Current pharmaceutical biotechnology.

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

P. Rutkowski, J. Siedlecki, A. Wozniak, 2012, BMC Cancer.

Novel RB1 gene constitutional mutations found in Polish patients with familial and/or bilateral retinoblastoma

A. Jakubowska, J. Lubiński, J. Limon, 2001, Human Mutation.

Mitochondrial DNA levels in Huntington disease leukocytes and dermal fibroblasts

G. Węgrzyn, J. Limon, Małgorzata Drozd, 2017, Metabolic Brain Disease.

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

D. Cysewski, J. Limon, B. Wasąg, 2019, Scientific Reports.

Different factors are responsible for predicting relapses after primary tumors resection and for imatinib treatment outcomes in gastrointestinal stromal tumors.

P. Nyckowski, P. Rutkowski, M. Debiec‐Rychter, 2007, Medical science monitor : international medical journal of experimental and clinical research.

The algorithm for Alzheimer risk assessment based on APOE promoter polymorphisms

B. Godlewska, J. Limon, B. Lipska-Ziętkiewicz, 2016, Alzheimer's Research & Therapy.

Abnormal karyotypes in three carcinomas of the gallbladder.

A. Andrén-sandberg, L. Gorunova, N. Mandahl, 1994, Cancer genetics and cytogenetics.

Recurrent chromosome translocations in liposarcoma.

C. Turc‐Carel, A. Sandberg, J. Limon, 1986, Cancer genetics and cytogenetics.

Application of high-resolution genomic profiling in the differential diagnosis of liposarcoma

J. Limon, W. Biernat, J. Lasota, 2017, Molecular Cytogenetics.

Nonrandom chromosomal aberrations and cytogenetic heterogeneity in gallbladder carcinomas

B. Johansson, L. Gorunova, J. Limon, 1999, Genes, chromosomes & cancer.

Ser9Gly polymorphism of the DRD3 gene is associated with worse premorbid social functioning and an earlier age of onset in female but not male schizophrenic patients

B. Godlewska, J. Landowski, J. Limon, 2010, Psychiatry Research.

Mutational analysis in podocin-associated hereditary nephrotic syndrome in Polish patients: founder effect in the Kashubian population

M. Litwin, M. Szczepańska, F. Schaefer, 2013, Journal of Applied Genetics.

Management of familial heterozygous hypercholesterolemia: Position Paper of the Polish Lipid Expert Forum.

M. Banach, T. Zdrojewski, J. Stȩpińska, 2013, Journal of clinical lipidology.

Adult with rare genetic disorder — principles of follow up in Cornelia de Lange Syndrome

J. Limon, J. Wierzba, Wierzba, 2010 .

Molecular genetic characterization of the EWS/ATF1 fusion gene in clear cell sarcoma of tendons and aponeuroses.

O. Larsson, R. Sciot, F. Mertens, 2002, International journal of cancer.

Chromosome aberrations, spontaneous SCE, and growth kinetics in PHA-stimulated lymphocytes of five cases with Sézary syndrome.

K. Mrózek, J. Lubiński, J. Limon, 1995, Cancer genetics and cytogenetics.

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

M. Stukan, P. Kozłowski, J. Limon, 2018, Cancers.

[Analysis of prognostic value of TP53 gene mutations in non-small cell lung cancer].

Å. Borg, R. Dziadziuszko, J. Jassem, 2005, Pneumonologia i alergologia polska.

Cornelia de Lange syndrome case due to genomic rearrangements including NIPBL.

P. Stankiewicz, Z. Xia, J. Lupski, 2010, European journal of medical genetics.

Improved detection of KIT exon 11 duplications in formalin-fixed, paraffin-embedded gastrointestinal stromal tumors.

S. Steigen, J. Limon, J. Lasota, 2007, The Journal of molecular diagnostics : JMD.

Cytogenetic and molecular findings in 75 clear cell renal cell carcinomas.

K. Mrózek, J. Lubiński, J. Limon, 2005, Oncology reports.

A novel c.C2754?>?T transition in the androgen receptor gene introduces the premature termination codon Q798X and results in a truncated form of the receptor

J. Limon, J. Turek-Plewa, M. Ignacak, 2004, Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology.

Concurrent DNA Copy‐Number Alterations and Mutations in Genes Related to Maintenance of Genome Stability in Uninvolved Mammary Glandular Tissue from Breast Cancer Patients

A. Piotrowski, A. Bogdan, Rafał Bartoszewski, 2015, Human mutation.

A case of mast cell leukaemia with exon 9 KIT mutation and good response to imatinib

A. Piskorz, J. Limon, K. Lewandowski, 2011, European journal of haematology.

Polymorphisms of the histamine receptor (H1HR) gene are not associated with olanzapine-induced weight gain.

B. Godlewska, J. Landowski, J. Limon, 2013, Journal of clinical psychopharmacology.

Consistent involvement of band 12q14 in benign lipoma

S. Leong, A. Sandberg, J. Limon, 1987 .

The occurrence of cerebellar hemangioblastoma in numerous first degree relatives with von Hippel-Lindau disease.

J. Jassem, J. Limon, B. Wysocka, 1999, Folia Neuropathologica.

Allogeneic bone marrow transplantation for hypereosinophilic syndrome: long-term follow-up with eradication of FIP1L1-PDGFRA fusion transcript

J. Limon, K. Halaburda, W. Prejzner, 2006, Bone Marrow Transplantation.