Tomasz Byrski

Polish oncologist

Born 1972-01-01

Tomasz Byrski is …
instance of (P31):
humanQ5

External links are
P227GND ID1022936808
P12541Ludzie Nauki ID (new)BNTCLYWcfQs
P496ORCID iD0000-0001-9181-5026
P7293PLWABN ID9810650295705606
P3124Polish scientist ID (deprecated)107202
P3829Publons author ID2510751
P1053ResearcherIDI-2844-2014
P214VIAF ID162363407
P10832WorldCat Entities IDE39PBJfrHcBHYFb78XR4t4TvHC

P512academic degreehabilitationQ308678
doctorateQ849697
scientific professorship degreeQ55695329
P27country of citizenshipPolandQ36
P184doctoral advisorJan LubińskiQ11718282
P185doctoral studentMarek JasiówkaQ60636828
P69educated atPomeranian Medical UniversityQ694887
P108employerPomeranian Medical UniversityQ694887
P734family nameByrskiQ65515001
ByrskiQ65515001
ByrskiQ65515001
P101field of workoncologyQ162555
P735given nameTomaszQ17644435
TomaszQ17644435
AntoniQ17480899
AntoniQ17480899
P1412languages spoken, written or signedPolishQ809
P1559name in native languageTomasz Byrski
P106occupationphysicianQ39631
researcherQ1650915
oncologistQ16062369
P21sex or gendermaleQ6581097

Reverse relations

author (P50)
Q36108172A Lowering of Breast and Ovarian Cancer Risk in Women with a BRCA1 Mutation by Selenium Supplementation of Diet
Q57666866A Range of Cancers Is Associated with the rs6983267 Marker on Chromosome 8
Q43566825A common nonsense mutation of the BLM gene and prostate cancer risk and survival
Q35447197A common variant of CDKN2A (p16) predisposes to breast cancer
Q80081672A deletion in CHEK2 of 5,395 bp predisposes to breast cancer in Poland
Q61945696A high frequency of BRCA2 gene mutations in Polish families with ovarian and stomach cancer
Q34548008A high proportion of founder BRCA1 mutations in Polish breast cancer families
Q36927109A large germline deletion in the Chek2 kinase gene is associated with an increased risk of prostate cancer
Q35089479A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor-negative breast cancer in the general population
Q36152991A nonsynonymous polymorphism in IRS1 modifies risk of developing breast and ovarian cancers in BRCA1 and ovarian cancer in BRCA2 mutation carriers
Q80243539A six-nucleotide deletion in the CASP8 promoter is not associated with a susceptibility to breast and prostate cancers in the Polish population
Q79652344A survey of preventive measures among BRCA1 mutation carriers from Poland
Q71579903Abnormalities of chromosome 5q correlate with morphologic features of better prognosis in clear cell renal carcinomas
Q87587823Activity of trabectedin in germline BRCA1/2-mutated metastatic breast cancer: results of an international first-in-class phase II study
Q36594121An inherited NBN mutation is associated with poor prognosis prostate cancer
Q37056869Are two-centimeter breast cancers large or small?
Q36072765Association of PHB 1630 C>T and MTHFR 677 C>T polymorphisms with breast and ovarian cancer risk in BRCA1/2 mutation carriers: results from a multicenter study
Q113241843Association of recurrent mutations in BRCA1, BRCA2, RAD51C, PALB2, and CHEK2 with the risk of borderline ovarian tumor
Q35957703Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer
Q35022847Associations of breast cancer risk factors with tumor subtypes: a pooled analysis from the Breast Cancer Association Consortium studies
Q40521165Attitudes toward preventive oophorectomy among BRCA1 mutation carriers in Poland
Q53567982BARD1 and breast cancer in Poland.
Q54409850BRCA1 mutations and colorectal cancer in Poland.
Q43632939BRCA1 mutations and prostate cancer in Poland
Q46054315BRCA1-associated breast and ovarian cancer risks in Poland: no association with commonly studied polymorphisms
Q44949616BRCA1-positive breast cancers in young women from Poland.
Q81892020Breast cancer predisposing alleles in Poland
Q73400704Breast cancer risk reduction associated with the RAD51 polymorphism among carriers of the BRCA1 5382insC mutation in Poland
Q57666904Breast cancer susceptibility genes
Q34306552CDH1 gene mutations do not contribute in hereditary diffuse gastric cancer in Poland
Q43806333CDKN2A common variant and multi-organ cancer risk--a population-based study
Q45261315CDKN2A common variants and their association with melanoma risk: a population-based study.
Q54574835CDKN2A-positive breast cancers in young women from Poland.
Q112162492CHAPTER 22. Selenium and Cancer
Q34551970CHEK2 is a multiorgan cancer susceptibility gene
Q53362846CHEK2 mutations and HNPCC-related colorectal cancer.
Q46250042CHEK2 mutations as markers for high risk of breast cancer
Q80128998CHEK2-positive breast cancers in young Polish women
Q57666910CYP1B1 and predisposition to breast cancer in Poland
Q37222641Cancer risks in first-degree relatives of CHEK2 mutation carriers: effects of mutation type and cancer site in proband
Q73333633Characteristics of selected features of hereditary ovarian cancer in carriers of constitutional BRCA1 gene mutation
Q77447971Characterization of a familial RCC-associated t(2;3)(q33;q21) chromosome translocation
Q37249356Chemotherapy-induced amenorrhea in patients with breast cancer with a BRCA1 or BRCA2 mutation
Q59288510Cisplatin in breast cancer treatment in BRCA1 carriers
Q53088764Clinical characteristics of breast cancer in patients with an NBS1 mutation.
Q73039579Clinical characteristics of hereditary ovarian cancer (HOC) in Poland
Q79843110Clinical features of familial ovarian cancer lacking mutations in BRCA1 or BRCA2
Q37363736Clinical genetic services for familial breast cancer in Poland
Q41748948Clinical outcomes in women with breast cancer and a PALB2 mutation: a prospective cohort analysis
Q41869270Combined iPLEX and TaqMan assays to screen for 45 common mutations in Lynch syndrome and FAP patients
Q47110534Combined iPLEX and TaqMan assays to screen for 45 common mutations in Lynch syndrome and FAP patients
Q36839777Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers
Q34949394Common genetic variation at BARD1 is not associated with breast cancer risk in BRCA1 or BRCA2 mutation carriers
Q35870067Common variants at the 19p13.1 and ZNF365 loci are associated with ER subtypes of breast cancer and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers
Q34585088Common variants of DNA repair genes and malignant melanoma
Q43825646Constitutional CHEK2 mutations are associated with a decreased risk of lung and laryngeal cancers
Q45906878Copper as diagnostic marker of cancers.
Q89080190Corrigendum: Germline RECQL mutations are associated with breast cancer susceptibility
Q41839357Coverage of the genetic background of breast cancer in the polish population
Q48353045Detection of germline mutations in the BRCA1 gene by RNA-based sequencing
Q79811213Direct-to-patient BRCA1 testing: the Twoj Styl experience
Q40821559Do founder mutations characteristic of some cancer sites also predispose to pancreatic cancer?
Q80514712Early radiation exposures and BRCA1-associated breast cancer in young women from Poland
Q53316752Effect of CHEK2 missense variant I157T on the risk of breast cancer in carriers of other CHEK2 or BRCA1 mutations.
Q79986282Epistatic relationship between the cancer susceptibility genes CHEK2 and p27
Q61946721Erratum: Germline CHEK2 mutations and colorectal cancer risk: different effects of a missense and truncating mutations?
Q46236360Estrogen receptor status in CHEK2-positive breast cancers: implications for chemoprevention
Q46250083Folic acid and cancer risk in BRCA1 carriers.
Q24540270Founder mutations in the BRCA1 gene in Polish families with breast-ovarian cancer
Q77642899Founder mutations in the BRCA1 gene in west Belarusian breast-ovarian cancer families
Q57666860Genetic contribution to all cancers: the first demonstration using the model of breast cancers from Poland stratified by age at diagnosis and tumour pathology
Q35022825Genetic variation at 9p22.2 and ovarian cancer risk for BRCA1 and BRCA2 mutation carriers
Q34572576Germline CHEK2 mutations and colorectal cancer risk: different effects of a missense and truncating mutations?
Q43075069Germline MSH2 and MLH1 mutational spectrum in HNPCC families from Poland and the Baltic States
Q61945792Germline MSH2 and MLH1 mutational spectrum including large rearrangements in HNPCC families from Poland (update study)
Q41010238Germline RECQL mutations are associated with breast cancer susceptibility
Q84632533Hereditary breast and ovarian cancer
Q43683502Hereditary ovarian cancer in Poland.
Q38806848Higher antitumor activity of trabectedin in germline BRCA2 carriers with advanced breast cancer as compared to BRCA1 carriers: A subset analysis of a dedicated phase II trial
Q55717426Impact of BRCA1 mutation on survival after early onset breast cancer.
Q81425159Influence of selected lifestyle factors on breast and ovarian cancer risk in BRCA1 mutation carriers from Poland
Q42550934Integrin beta3 Leu33Pro polymorphism increases BRCA1-associated ovarian cancer risk
Q46130512Iron as diagnostic marker of cancer.
Q35119701Low penetrance breast cancer susceptibility loci are associated with specific breast tumor subtypes: findings from the Breast Cancer Association Consortium
Q81803706Low prevalence of CDKN2A/ARF mutations among early-onset cancers of breast, pancreas and malignant melanoma in Poland
Q42244979Low-risk Genes and Multi-organ Cancer Risk in the Polish Population
Q45956204Lynch syndrome mutations shared by the Baltic States and Poland.
Q61946725MC1R common variants, CDKN2A and their association with melanoma and breast cancer risk
Q46130429Magnesium as a diagnostic marker of cancer.
Q51830222Male to female ratio among offspring of BRCA1 mutation carriers.
Q34988799Management of ovarian and endometrial cancers in women belonging to HNPCC carrier families: review of the literature and results of cancer risk assessment in Polish HNPCC families
Q47133182Meeting abstracts from the Annual Conference on Hereditary Cancers 2015: Szczecin, Poland. 24-25 September, 2015.
Q50233852Meeting abstracts from the Annual Conference on Hereditary Cancers 2016: Szczecin, Poland. 14-15 September 2016.
Q79298327Methylenetetrahydrofolate reductase polymorphisms modify BRCA1-associated breast and ovarian cancer risks
Q61946734Molecular Analyses in Diagnosis of High Genetic Predispositions to Malignancies
Q36897003Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer
Q54314566Mutations predisposing to breast cancer in 12 candidate genes in breast cancer patients from Poland.
Q55403547Mutations spectrum in hereditary disorders predisposing to occurrence of intestine polyposis in Poland.
Q61946727NOD2 variants and the risk of malignant melanoma
Q46250020Neoadjuvant chemotherapy with Cisplatin in BRCA1 mutation carriers – results of treatment
Q112576545Neoadjuvant chemotherapy with dose dense MVAC is associated with improved survival after radical cystectomy compared to other cytotoxic regimens: A tertiary center experience
Q59255480Neoadjuvant therapy with cisplatin in BRCA1-positive breast cancer patients
Q61946712New EPCAM founder deletion in Polish population
Q43073995Non-random transmission of mutant alleles to female offspring of BRCA1 carriers in Poland
Q35559901Novel germline mutations in the adenomatous polyposis coli gene in Polish families with familial adenomatous polyposis
Q33327308Ovarian cancer risk in Polish BRCA1 mutation carriers is not associated with the prohibitin 3' untranslated region polymorphism
Q36280191Ovarian cancer susceptibility alleles and risk of ovarian cancer in BRCA1 and BRCA2 mutation carriers
Q54308947Ovarian cystadenoma as a characteristic feature of families with hereditary ovarian cancers unassociated with BRCA1 and BRCA2 mutations.
Q43222794Pathologic complete response rates in young women with BRCA1-positive breast cancers after neoadjuvant chemotherapy
Q38240441Pathologic complete response to neoadjuvant cisplatin in BRCA1-positive breast cancer patients
Q36132338Pathological complete response after cisplatin neoadjuvant therapy is associated with the downregulation of DNA repair genes in BRCA1-associated triple-negative breast cancers
Q46130542Pathological complete response to neoadjuvant cisplatin in BRCA1-positive breast cancer patients.
Q81601356Pathology of breast cancer in women with constitutional CHEK2 mutations
Q60585018Plasma micronutrients, trace elements, and breast cancer in BRCA1 mutation carriers: an exploratory study
Q51672667Pleomorphic adenoma of salivary glands does not appear to be a BRCA-1-dependent tumour in a Polish cohort.
Q42244986Population Screening of CHEK2 Mutations in Poland
Q42244983Population screening for cancer family syndromes in the west pomeranian region of poland
Q49787762Predictors of survival for breast cancer patients with a BRCA1 mutation.
Q61946726Prevalence of the NOD2 3020insC mutation in aggregations of breast and lung cancer
Q36494555Prognostic factors in Polish patients with BRCA1-dependent ovarian cancer
Q36512097RAD51 135G-->C modifies breast cancer risk among BRCA2 mutation carriers: results from a combined analysis of 19 studies
Q122937357Recurrent Mutations in BRCA1, BRCA2, RAD51C, PALB2 and CHEK2 in Polish Patients with Ovarian Cancer
Q45185763Recurrent mutations of BRCA1 and BRCA2 in Poland: an update
Q36538025Recurrent mutations of BRCA1, BRCA2 and PALB2 in the population of breast and ovarian cancer patients in Southern Poland
Q34579373Response to neo-adjuvant chemotherapy in women with BRCA1-positive breast cancers
Q81688258Response to neoadjuvant therapy with cisplatin in BRCA1-positive breast cancer patients
Q36924418Results of a phase II open-label, non-randomized trial of cisplatin chemotherapy in patients with BRCA1-positive metastatic breast cancer
Q51421155Risk of breast cancer in women with a CHEK2 mutation with and without a family history of breast cancer.
Q59288376Selenium (Se) and breast cancer risk
Q46250119Selenium (Se) and the risk of breast, ovarian and prostate cancers
Q46738357Selenium and genotypes as marker of risk in BRCA1 mutation carriers
Q50219543Selenium and the risk of cancer in BRCA1 carriers.
Q38359733Selenium as a marker of cancer risk and of selection for control examinations in surveillance
Q46130885Selenium as diagnostic marker of cancers.
Q38067529Selenium as marker for cancer risk and prevention
Q44732177Should all BRCA1 mutation carriers with stage I breast cancer receive chemotherapy?
Q54375866Survival from breast cancer in patients with CHEK2 mutations.
Q43425193Synergistic interaction of variants in CHEK2 and BRCA2 on breast cancer risk
Q36755366Systemic treatment for hereditary cancers: a 2012 update
Q44251009Ten-year survival in patients with BRCA1-negative and BRCA1-positive breast cancer
Q44306036The 3' untranslated region C > T polymorphism of prohibitin is a breast cancer risk modifier in Polish women carrying a BRCA1 mutation
Q33722537The 3020insC Allele of NOD2 Predisposes to Cancers of Multiple Organs
Q45114407The 3020insC allele of NOD2 predisposes to early-onset breast cancer
Q40989977The Conductivity and pH Values of Dispersions of Nanospheres for Targeted Drug Delivery in the Course of Forced Equilibrium Dialysis
Q40776729The DIRC1 gene at chromosome 2q33 spans a familial RCC-associated t(2;3)(q33;q21) chromosome translocation
Q44733776The G84E mutation in the HOXB13 gene is associated with an increased risk of prostate cancer in Poland
Q79776026The RAD51 135 G>C polymorphism modifies breast cancer and ovarian cancer risk in Polish BRCA1 mutation carriers
Q80436355The VEGF_936_C>T 3'UTR polymorphism reduces BRCA1-associated breast cancer risk in Polish women
Q91565756The diameter of metastasis in positive sentinel lymph node biopsy affects axillary tumor load in early breast cancer
Q38777240The impact of oophorectomy on survival after breast cancer in BRCA1-positive breast cancer patients
Q37613551The impact of pregnancy on breast cancer survival in women who carry a BRCA1 or BRCA2 mutation
Q36898423The incidence of leukaemia in women with BRCA1 and BRCA2 mutations: an International Prospective Cohort Study
Q40137412The presence of prostate cancer at biopsy is predicted by a number of genetic variants
Q35907001The risk of breast cancer in women with a BRCA1 mutation from North America and Poland
Q46738314The risk of breast cancer in women with a CHEK2 mutation
Q61952806The variant allele of the rs188140481 polymorphism confers a moderate increase in the risk of prostate cancer in Polish men
Q43073174Transmission of mutant alleles to female offspring of BRCA1 carriers in Poland
Q55036759Usefulness of polymorphic markers in exclusion of BRCA1/BRCA2 mutations in families with aggregation of breast/ovarian cancers.
Q33654709Variant alleles of the CYP1B1 gene are associated with colorectal cancer susceptibility
Q46512471Vitamin D receptor variants and breast cancer risk in the Polish population
Q84398671Vitamin D receptor variants and the malignant melanoma risk: a population-based study
Q46738293Why choose the treatment with cisplatin for BRCA1 breast cancers patients?
Q52570748XPD common variants and their association with melanoma and breast cancer risk.
Q46660029Zinc and breast cancer risk
Q45946070Zinc as diagnostic marker of cancers.
Q81029752[Germline mutation of BRCA1 gene in Polish families with strong aggregation of breast and/or ovarian cancer based on coding sequence analysis using the SSCP method]

Q60636828Marek Jasiówkadoctoral advisorP184
Q11718282Jan Lubińskidoctoral studentP185

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