Rank |
Title |
Journal |
Year |
PubWeight™‹?› |
1
|
Associations of breast cancer risk factors with tumor subtypes: a pooled analysis from the Breast Cancer Association Consortium studies.
|
J Natl Cancer Inst
|
2010
|
4.54
|
2
|
A genome-wide association study identifies a new ovarian cancer susceptibility locus on 9p22.2.
|
Nat Genet
|
2009
|
4.38
|
3
|
Genome-wide association study identifies three loci associated with melanoma risk.
|
Nat Genet
|
2009
|
3.89
|
4
|
GWAS meta-analysis and replication identifies three new susceptibility loci for ovarian cancer.
|
Nat Genet
|
2013
|
3.42
|
5
|
Genome-wide association study identifies three new melanoma susceptibility loci.
|
Nat Genet
|
2011
|
2.29
|
6
|
The NOD2 3020insC mutation and the risk of colorectal cancer.
|
Cancer Res
|
2004
|
2.01
|
7
|
A high proportion of founder BRCA1 mutations in Polish breast cancer families.
|
Int J Cancer
|
2004
|
1.96
|
8
|
Risk of breast cancer in women with a CHEK2 mutation with and without a family history of breast cancer.
|
J Clin Oncol
|
2011
|
1.94
|
9
|
Epigenetic analysis leads to identification of HNF1B as a subtype-specific susceptibility gene for ovarian cancer.
|
Nat Commun
|
2013
|
1.73
|
10
|
A genome-wide association study of upper aerodigestive tract cancers conducted within the INHANCE consortium.
|
PLoS Genet
|
2011
|
1.68
|
11
|
A novel founder CHEK2 mutation is associated with increased prostate cancer risk.
|
Cancer Res
|
2004
|
1.60
|
12
|
Early radiation exposures and BRCA1-associated breast cancer in young women from Poland.
|
Breast Cancer Res Treat
|
2008
|
1.59
|
13
|
Genetic variation at 9p22.2 and ovarian cancer risk for BRCA1 and BRCA2 mutation carriers.
|
J Natl Cancer Inst
|
2010
|
1.41
|
14
|
Identification and molecular characterization of a new ovarian cancer susceptibility locus at 17q21.31.
|
Nat Commun
|
2013
|
1.36
|
15
|
A deletion in CHEK2 of 5,395 bp predisposes to breast cancer in Poland.
|
Breast Cancer Res Treat
|
2006
|
1.34
|
16
|
Mutation analysis of MLH1 and MSH2 genes performed by denaturing high-performance liquid chromatography.
|
J Biochem Biophys Methods
|
2002
|
1.30
|
17
|
Hereditary ovarian cancer in Poland.
|
Int J Cancer
|
2003
|
1.30
|
18
|
A variant in FTO shows association with melanoma risk not due to BMI.
|
Nat Genet
|
2013
|
1.17
|
19
|
Common alleles in candidate susceptibility genes associated with risk and development of epithelial ovarian cancer.
|
Int J Cancer
|
2011
|
1.17
|
20
|
Germline 657del5 mutation in the NBS1 gene in breast cancer patients.
|
Int J Cancer
|
2003
|
1.13
|
21
|
Interplay between BRCA1 and RHAMM regulates epithelial apicobasal polarization and may influence risk of breast cancer.
|
PLoS Biol
|
2011
|
1.12
|
22
|
Mitochondrial NADH-dehydrogenase subunit 3 (ND3) polymorphism (A10398G) and sporadic breast cancer in Poland.
|
Breast Cancer Res Treat
|
2009
|
1.05
|
23
|
Germline CHEK2 mutations and colorectal cancer risk: different effects of a missense and truncating mutations?
|
Eur J Hum Genet
|
2006
|
1.02
|
24
|
BRCA1 mutations and prostate cancer in Poland.
|
Eur J Cancer Prev
|
2008
|
1.01
|
25
|
Breast cancer risk reduction associated with the RAD51 polymorphism among carriers of the BRCA1 5382insC mutation in Poland.
|
Cancer Epidemiol Biomarkers Prev
|
2003
|
0.99
|
26
|
A low selenium level is associated with lung and laryngeal cancers.
|
PLoS One
|
2013
|
0.99
|
27
|
The 3020insC allele of NOD2 predisposes to early-onset breast cancer.
|
Breast Cancer Res Treat
|
2005
|
0.99
|
28
|
Methylenetetrahydrofolate reductase polymorphisms modify BRCA1-associated breast and ovarian cancer risks.
|
Breast Cancer Res Treat
|
2006
|
0.98
|
29
|
The G84E mutation in the HOXB13 gene is associated with an increased risk of prostate cancer in Poland.
|
Prostate
|
2013
|
0.97
|
30
|
Polymorphism in the P-glycoprotein drug transporter MDR1 gene in colon cancer patients.
|
Eur J Clin Pharmacol
|
2005
|
0.96
|
31
|
BRCA1-associated breast and ovarian cancer risks in Poland: no association with commonly studied polymorphisms.
|
Breast Cancer Res Treat
|
2009
|
0.95
|
32
|
Can selenium levels act as a marker of colorectal cancer risk?
|
BMC Cancer
|
2013
|
0.93
|
33
|
Inflammatory response gene polymorphisms and their relationship with colorectal cancer risk.
|
BMC Cancer
|
2008
|
0.92
|
34
|
Comparison of genomic abnormalities between BRCAX and sporadic breast cancers studied by comparative genomic hybridization.
|
Int J Cancer
|
2005
|
0.92
|
35
|
The risk of gastric cancer in carriers of CHEK2 mutations.
|
Fam Cancer
|
2013
|
0.91
|
36
|
Germline mutation and large deletion analysis of the CDKN2A and ARF genes in families with multiple melanoma or an aggregation of malignant melanoma and breast cancer.
|
Int J Cancer
|
2004
|
0.91
|
37
|
Association of common WRAP 53 variant with ovarian cancer risk in the Polish population.
|
Mol Biol Rep
|
2012
|
0.90
|
38
|
Do BRCA1 modifiers also affect the risk of breast cancer in non-carriers?
|
Eur J Cancer
|
2008
|
0.90
|
39
|
The VEGF_936_C>T 3'UTR polymorphism reduces BRCA1-associated breast cancer risk in Polish women.
|
Cancer Lett
|
2008
|
0.89
|
40
|
Prevalence of the NOD2 3020insC mutation in aggregations of breast and lung cancer.
|
Breast Cancer Res Treat
|
2006
|
0.89
|
41
|
BRCA1 mutations and colorectal cancer in Poland.
|
Fam Cancer
|
2010
|
0.89
|
42
|
Sulforaphane-mediated induction of a phase 2 detoxifying enzyme NAD(P)H:quinone reductase and apoptosis in human lymphoblastoid cells.
|
Acta Biochim Pol
|
2004
|
0.89
|
43
|
A common nonsense mutation of the BLM gene and prostate cancer risk and survival.
|
Gene
|
2013
|
0.89
|
44
|
A six-nucleotide deletion in the CASP8 promoter is not associated with a susceptibility to breast and prostate cancers in the Polish population.
|
Breast Cancer Res Treat
|
2007
|
0.89
|
45
|
High incidence of 4153delA BRCA1 gene mutations in Lithuanian breast- and breast-ovarian cancer families.
|
Breast Cancer Res Treat
|
2005
|
0.88
|
46
|
A sex-specific association between a 15q25 variant and upper aerodigestive tract cancers.
|
Cancer Epidemiol Biomarkers Prev
|
2011
|
0.88
|
47
|
Smoking related cancers and loci at chromosomes 15q25, 5p15, 6p22.1 and 6p21.33 in the Polish population.
|
PLoS One
|
2011
|
0.88
|
48
|
Germline mutations in the CHEK2 kinase gene are associated with an increased risk of bladder cancer.
|
Int J Cancer
|
2008
|
0.88
|
49
|
The rs1447295 and DG8S737 markers on chromosome 8q24 and cancer risk in the Polish population.
|
Eur J Cancer Prev
|
2010
|
0.87
|
50
|
DNA variation in MSR1, RNASEL and E-cadherin genes and prostate cancer in Poland.
|
Urol Int
|
2007
|
0.87
|
51
|
CHEK2 mutations and HNPCC-related colorectal cancer.
|
Int J Cancer
|
2010
|
0.87
|
52
|
CDKN2A-positive breast cancers in young women from Poland.
|
Breast Cancer Res Treat
|
2006
|
0.87
|
53
|
Synergistic interaction of variants in CHEK2 and BRCA2 on breast cancer risk.
|
Breast Cancer Res Treat
|
2008
|
0.87
|
54
|
Pathology of breast cancer in women with constitutional CHEK2 mutations.
|
Breast Cancer Res Treat
|
2005
|
0.86
|
55
|
CHEK2 germline mutations correlate with recurrence rate in patients with superficial bladder cancer.
|
Ann Acad Med Stetin
|
2008
|
0.85
|
56
|
Polymorphisms in nucleotide excision repair genes and susceptibility to colorectal cancer in the Polish population.
|
Mol Biol Rep
|
2014
|
0.85
|
57
|
The 3' untranslated region C > T polymorphism of prohibitin is a breast cancer risk modifier in Polish women carrying a BRCA1 mutation.
|
Breast Cancer Res Treat
|
2006
|
0.85
|
58
|
Clinical characteristics of laryngeal cancer in BRCA-1 mutation carriers.
|
Anticancer Res
|
2009
|
0.85
|
59
|
Fine mapping of genetic susceptibility loci for melanoma reveals a mixture of single variant and multiple variant regions.
|
Int J Cancer
|
2014
|
0.84
|
60
|
Exploring the link between germline and somatic genetic alterations in breast carcinogenesis.
|
PLoS One
|
2010
|
0.83
|
61
|
Germline 657del5 mutation in the NBS1 gene in patients with malignant melanoma of the skin.
|
Melanoma Res
|
2003
|
0.83
|
62
|
Association between early-onset breast and laryngeal cancers.
|
Breast Cancer Res Treat
|
2005
|
0.83
|
63
|
CDH1 gene mutations do not contribute in hereditary diffuse gastric cancer in Poland.
|
Fam Cancer
|
2010
|
0.83
|
64
|
PARS PLANA VITRECTOMY IN ADVANCED CASES OF VON HIPPEL-LINDAU EYE DISEASE.
|
Retina
|
2016
|
0.82
|
65
|
Direct-to-patient BRCA1 testing: the Twoj Styl experience.
|
Breast Cancer Res Treat
|
2006
|
0.82
|
66
|
Cancer Familial Aggregation (CFA) and G446A polymorphism in ARLTS1 gene.
|
Breast Cancer Res Treat
|
2006
|
0.81
|
67
|
BARD1 and breast cancer in Poland.
|
Breast Cancer Res Treat
|
2007
|
0.81
|
68
|
Gene Expression Profiling in Hereditary, BRCA1-linked Breast Cancer: Preliminary Report.
|
Hered Cancer Clin Pract
|
2006
|
0.80
|
69
|
Antigens HLA-G, sHLA- G and sHLA- class I in reproductive failure.
|
Folia Histochem Cytobiol
|
2007
|
0.80
|
70
|
Rarity of germline 1100delC mutation in CHK2 in patients with malignant melanoma of the skin.
|
Melanoma Res
|
2004
|
0.80
|
71
|
The association between the interleukin-1 polymorphisms and gastric cancer risk depends on the family history of gastric carcinoma in the study population.
|
Am J Gastroenterol
|
2006
|
0.80
|
72
|
Clinical characteristics of tumors derived from colorectal cancer patients who harbor the tumor necrosis factor alpha-1031T/T and NOD2 3020insC polymorphism.
|
Cancer Epidemiol
|
2009
|
0.80
|
73
|
Genetic heterogeneity of 8q24 region in susceptibility to cancer.
|
J Natl Cancer Inst
|
2009
|
0.80
|
74
|
The presence of prostate cancer at biopsy is predicted by a number of genetic variants.
|
Int J Cancer
|
2013
|
0.79
|
75
|
Case report of a woman with monoclonal gammapathy and papillary thyroid carcinoma, diagnosed because of detection of CHEK2 (I157T) mutation in genetic examinations.
|
Endokrynol Pol
|
2010
|
0.78
|
76
|
Identification of patients at high risk of psychological distress after BRCA1 genetic testing.
|
Genet Test Mol Biomarkers
|
2009
|
0.78
|
77
|
Polymorphic variants in VAX1 gene (rs7078160) and BMP4 gene (rs762642) and the risk of non-syndromic orofacial clefts in the Polish population.
|
Dev Period Med
|
2014
|
0.78
|
78
|
Ovarian cancer of endometrioid type as part of the MSH6gene mutation phenotype.
|
J Hum Genet
|
2002
|
0.78
|
79
|
Low-risk Genes and Multi-organ Cancer Risk in the Polish Population.
|
Hered Cancer Clin Pract
|
2006
|
0.78
|
80
|
The 3020insC NOD2 gene mutation in patients with ovarian cancer.
|
Ginekol Pol
|
2008
|
0.77
|
81
|
The variant allele of the rs188140481 polymorphism confers a moderate increase in the risk of prostate cancer in Polish men.
|
Eur J Cancer Prev
|
2015
|
0.77
|
82
|
Is there any relationship between BRCA1 gene mutation and pancreatic cancer development?
|
Pol Arch Med Wewn
|
2008
|
0.77
|
83
|
Population screening for cancer family syndromes in the west pomeranian region of poland.
|
Hered Cancer Clin Pract
|
2006
|
0.77
|
84
|
Consortium analysis of gene and gene-folate interactions in purine and pyrimidine metabolism pathways with ovarian carcinoma risk.
|
Mol Nutr Food Res
|
2014
|
0.77
|
85
|
Optimizing recruitment to a prostate cancer surveillance program among male BRCA1 mutation carriers: invitation by mail or by telephone.
|
Hered Cancer Clin Pract
|
2013
|
0.77
|
86
|
Supernormal electro-oculograms in patients with neurofibromatosis type 1.
|
Hered Cancer Clin Pract
|
2004
|
0.76
|
87
|
Combined iPLEX and TaqMan assays to screen for 45 common mutations in Lynch syndrome and FAP patients.
|
J Mol Diagn
|
2009
|
0.76
|
88
|
A Lowering of Breast and Ovarian Cancer Risk in Women with a BRCA1 Mutation by Selenium Supplementation of Diet.
|
Hered Cancer Clin Pract
|
2006
|
0.76
|
89
|
Ovarian cancer risk in Polish BRCA1 mutation carriers is not associated with the prohibitin 3' untranslated region polymorphism.
|
BMC Cancer
|
2008
|
0.76
|
90
|
Double heterozygotes among breast cancer patients analyzed for BRCA1, CHEK2, ATM, NBN/NBS1, and BLM germ-line mutations.
|
Breast Cancer Res Treat
|
2014
|
0.75
|
91
|
Corrigendum: Germline RECQL mutations are associated with breast cancer susceptibility.
|
Nat Genet
|
2016
|
0.75
|
92
|
Dupuytren's disease and the risk of malignant neoplasms.
|
Hered Cancer Clin Pract
|
2014
|
0.75
|
93
|
Coverage of the genetic background of breast cancer in the polish population.
|
Hered Cancer Clin Pract
|
2006
|
0.75
|
94
|
A case of carotid body paraganglioma and haemangioblastoma of the spinal cord in a patient with the N131K missense mutation in the VHL gene.
|
Neurol Sci
|
2011
|
0.75
|
95
|
Nuclear Pedigree Criteria for the Identification of Individuals Suspected to be at Risk of an Inherited Predisposition to Renal Cancer.
|
Hered Cancer Clin Pract
|
2005
|
0.75
|
96
|
Corrigendum: Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer.
|
Nat Genet
|
2017
|
0.75
|
97
|
Mutations in the von hippel-lindau tumour suppressor gene in central nervous system hemangioblastomas.
|
Hered Cancer Clin Pract
|
2004
|
0.75
|
98
|
Nuclear pedigree criteria for the identification of individuals suspected to be at risk of an inherited predisposition to gastric cancer.
|
Hered Cancer Clin Pract
|
2004
|
0.75
|
99
|
BRCA1 founder mutations compared to ovarian cancer in Belarus.
|
Fam Cancer
|
2014
|
0.75
|
100
|
Familial association of laryngeal, lung, stomach and early-onset breast cancer.
|
Breast Cancer Res Treat
|
2007
|
0.75
|
101
|
Retinal dysfunction in eyes of patients with BRCA1 gene mutation.
|
Klin Oczna
|
2005
|
0.75
|
102
|
Possible association of the BRCA2 gene C5972T variant with gastric cancer: a study on Polish population.
|
Pol Arch Med Wewn
|
2015
|
0.75
|
103
|
Selenium as marker for cancer risk and prevention.
|
Pol Przegl Chir
|
2012
|
0.75
|
104
|
Clinical and epidemiological features of familial laryngeal cancer in Poland.
|
Cancer Detect Prev
|
2007
|
0.75
|
105
|
Ovarian cystadenoma as a characteristic feature of families with hereditary ovarian cancers unassociated with BRCA1 and BRCA2 mutations.
|
J Appl Genet
|
2004
|
0.75
|
106
|
Clinical characteristics of hereditary ovarian cancer (HOC) in Poland.
|
Ginekol Pol
|
2002
|
0.75
|
107
|
Electroretinographic changes in eyes of patients with BRCA1 gene mutation.
|
Ophthalmic Res
|
2003
|
0.75
|
108
|
Retinal function in the von Hippel-Lindau disease.
|
Doc Ophthalmol
|
2003
|
0.75
|
109
|
Electroretinographic changes in the inner retinal layers of the retained eyes of patients with sporadic unilateral retinoblastoma.
|
Ophthalmic Genet
|
2002
|
0.75
|
110
|
Usefulness of polymorphic markers in exclusion of BRCA1/BRCA2 mutations in families with aggregation of breast/ovarian cancers.
|
J Appl Genet
|
2003
|
0.75
|
111
|
Genotyping by induced Förster Resonance Energy Transfer(iFRET) mechanism and simultaneous mutation scanning.
|
Hum Mutat
|
2013
|
0.75
|
112
|
Population Screening of CHEK2 Mutations in Poland.
|
Hered Cancer Clin Pract
|
2006
|
0.75
|
113
|
[HLA-G alleles and risk of early pregnancy loss].
|
Ann Acad Med Stetin
|
2008
|
0.75
|
114
|
Electro-oculographic and electroretinographic studies in HNPCC gene mutation carriers.
|
Ophthalmic Res
|
2003
|
0.75
|
115
|
Modest association of malignant melanoma with the rs910873 and rs1885120 markers on chromosome 20: a population-based study.
|
Melanoma Res
|
2010
|
0.75
|
116
|
Pleomorphic adenoma of salivary glands does not appear to be a BRCA-1-dependent tumour in a Polish cohort.
|
Anticancer Res
|
2008
|
0.75
|