| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1101004775 |
| P356 | DOI | 10.1186/S12885-018-4112-4 |
| P2888 | exact match | https://scigraph.springernature.com/pub.10.1186/s12885-018-4112-4 |
| P932 | PMC publication ID | 5809862 |
| P698 | PubMed publication ID | 29433565 |
| P50 | author | Nirmala D Sirisena | Q59160849 |
| Adebowale A. Adeyemo | Q37390255 | ||
| P2093 | author name string | Vajira H W Dissanayake | |
| Nilakshi Samaranayake | |||
| Nilaksha Neththikumara | |||
| Anchala I Kuruppu | |||
| P2860 | cites work | Double-Strand Break Repair Gene Polymorphisms and Risk of Breast or Ovarian Cancer | Q57265812 |
| Prohibitin 3′ untranslated region polymorphism and breast cancer risk in Australian women | Q57265866 | ||
| Polymorphisms in RAD51, XRCC2, and XRCC3 Are Not Related to Breast Cancer Risk | Q57420865 | ||
| Single nucleotide polymorphism in prohibitin 3' untranslated region and breast-cancer susceptibility | Q73936455 | ||
| XRCC2 Arg188His polymorphism is not directly associated with breast cancer risk: evidence from 37,369 subjects | Q82759643 | ||
| Functional Analysis of Missense Variants in the Putative Breast Cancer Susceptibility Gene XRCC2. | Q39730889 | ||
| Identification of novel susceptibility markers for the risk of overall breast cancer as well as subtypes defined by hormone receptor status in the Chinese population | Q40591033 | ||
| Genetic variants in FGFR2 and TNRC9 genes are associated with breast cancer risk in Pakistani women | Q40602866 | ||
| Prohibitin expression is associated with high grade breast cancer but is not a driver of amplification at 17q21.33. | Q42449247 | ||
| A comprehensive haplotype analysis of CYP19 and breast cancer risk: the Multiethnic Cohort | Q44307819 | ||
| Sample size requirements for association studies of gene-gene interaction | Q46177453 | ||
| Do BRCA1 modifiers also affect the risk of breast cancer in non-carriers? | Q46205547 | ||
| Common single-nucleotide polymorphisms in DNA double-strand break repair genes and breast cancer risk | Q46209474 | ||
| Lack of association between prohibitin 3' untranslated region C-->T polymorphism and breast cancer in a Turkish population | Q46583777 | ||
| Tumor suppression by the prohibitin gene 3'untranslated region RNA in human breast cancer | Q47616977 | ||
| Importance of ATM gene as a susceptible trait: predisposition role of D1853N polymorphism in breast cancer. | Q48234883 | ||
| A potential role for the XRCC2 R188H polymorphic site in DNA-damage repair and breast cancer | Q48303260 | ||
| Mutational analysis of prohibitin--a highly conserved gene in Indian female breast cancer cases. | Q51287924 | ||
| Breast cancer risk and common single nucleotide polymorphisms in homologous recombination DNA repair pathway genes XRCC2, XRCC3, NBS1 and RAD51. | Q53355024 | ||
| Single nucleotide polymorphism D1853N of the ATM gene may alter the risk for breast cancer. | Q54547212 | ||
| Polymorphisms in DNA double-strand break repair genes and risk of breast cancer: two population-based studies in USA and Poland, and meta-analyses | Q57250685 | ||
| Global cancer statistics | Q22241238 | ||
| A note on exact tests of Hardy-Weinberg equilibrium | Q24531633 | ||
| Genome-wide association study identifies novel breast cancer susceptibility loci | Q24645441 | ||
| PLINK: a tool set for whole-genome association and population-based linkage analyses | Q24677407 | ||
| Identification of a functional genetic variant at 16q12.1 for breast cancer risk: results from the Asia Breast Cancer Consortium | Q28474694 | ||
| Large-scale genotyping identifies 41 new loci associated with breast cancer risk | Q29416989 | ||
| Variants in the ATM gene associated with a reduced risk of contralateral breast cancer | Q30438940 | ||
| Genetic polymorphisms of selected DNA repair genes, estrogen and progesterone receptor status, and breast cancer risk | Q33217205 | ||
| Genetic polymorphisms in the DNA repair genes XRCC1, XRCC2 and XRCC3 and risk of breast cancer in Cyprus | Q33314347 | ||
| Novel sequence variants and a high frequency of recurrent polymorphisms in BRCA1 gene in Sri Lankan breast cancer patients and at risk individuals | Q33355677 | ||
| Prohibitin expression deregulation in gastric cancer is associated with the 3' untranslated region 1630 C>T polymorphism and copy number variation | Q33690194 | ||
| Analysis of BRCA1and BRCA2 large genomic rearrangements in Sri Lankan familial breast cancer patients and at risk individuals | Q33755042 | ||
| E-cadherin polymorphisms and breast cancer susceptibility: a report from the Shanghai Breast Cancer Study | Q33869447 | ||
| XRCC2 rs3218536 polymorphism decreases the sensitivity of colorectal cancer cells to poly(ADP-ribose) polymerase 1 inhibitor | Q33967571 | ||
| The association between ATM D1853N polymorphism and breast cancer susceptibility: a meta-analysis | Q34114256 | ||
| Variants in DNA double-strand break repair genes and breast cancer susceptibility | Q34129771 | ||
| The association between ATM IVS 22-77 T>C and cancer risk: a meta-analysis | Q34140207 | ||
| Genetic and functional analysis of CHEK2 (CHK2) variants in multiethnic cohorts | Q34960835 | ||
| RAD51, XRCC3, and XRCC2 mutation screening in Finnish breast cancer families | Q35502165 | ||
| Association of Genetic Polymorphisms in CDH1 and CTNNB1 with Breast Cancer Susceptibility and Patients' Prognosis among Chinese Han Women | Q35748901 | ||
| Association 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 | Q36072765 | ||
| Novel sequence variants and common recurrent polymorphisms of BRCA2 in Sri Lankan breast cancer patients and a family with BRCA1 mutations | Q36230861 | ||
| Lack of an association between XRCC2 R188H polymorphisms and breast cancer: an update meta-analysis involving 35,422 subjects | Q36317693 | ||
| XRCC2 and XRCC3 gene polymorphism and risk of pancreatic cancer | Q36498727 | ||
| Prediction of breast cancer risk based on profiling with common genetic variants | Q36583004 | ||
| Identification of a BRCA2-specific modifier locus at 6p24 related to breast cancer risk | Q36720814 | ||
| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | sporadic breast cancer | Q18557808 |
| P304 | page(s) | 180 | |
| P577 | publication date | 2018-02-13 | |
| P1433 | published in | BMC Cancer | Q326300 |
| P1476 | title | Genetic determinants of sporadic breast cancer in Sri Lankan women. | |
| P478 | volume | 18 |
| Q92348397 | Electrophoretic mobility shift assays implicate XRCC2:rs3218550C>T as a potential low-penetrant susceptibility allele for sporadic breast cancer |
| Q55500887 | Genetic Variants Associated with Clinicopathological Profiles in Sporadic Breast Cancer in Sri Lankan Women. |
| Q92030506 | Genotype data for single nucleotide polymorphism markers in sporadic breast cancer related genes in a Sri Lankan case-control cohort of postmenopausal women |
| Q58765654 | Relative normalized luciferase activity for the recombinant vector constructs carrying the ancestral and variant alleles for XRCC2:rs3218550 and PHB:rs6917 |
Search more.