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Contribution of constitutional BRCA1 promoter methylation to early-onset and familial breast cancer patients from Pakistan.
- Published in:
- Breast Cancer Research & Treatment, 2023, v. 202, n. 2, p. 377, doi. 10.1007/s10549-023-07068-x
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- Publication type:
- Article
Native American ancestry and breast cancer risk in Colombian and Mexican women: ruling out potential confounding through ancestry-informative markers.
- Published in:
- Breast Cancer Research, 2023, v. 25, n. 1, p. 1, doi. 10.1186/s13058-023-01713-5
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- Publication type:
- Article
Ovarian cancer pathology characteristics as predictors of variant pathogenicity in BRCA1 and BRCA2.
- Published in:
- British Journal of Cancer, 2023, v. 128, n. 12, p. 2283, doi. 10.1038/s41416-023-02263-5
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- Publication type:
- Article
DNA methylation biomarkers for noninvasive detection of triple‐negative breast cancer using liquid biopsy.
- Published in:
- International Journal of Cancer, 2023, v. 152, n. 5, p. 1025, doi. 10.1002/ijc.34337
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- Publication type:
- Article
Prevalence of FANCM germline variants in BRCA1/2 negative breast and/or ovarian cancer patients from Pakistan.
- Published in:
- Familial Cancer, 2023, v. 22, n. 1, p. 31, doi. 10.1007/s10689-022-00304-1
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- Publication type:
- Article
Correction: PredictCBC-2.0: a contralateral breast cancer risk prediction model developed and validated in ~ 200,000 patients.
- Published in:
- 2022
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- Publication type:
- corrected article
PredictCBC-2.0: a contralateral breast cancer risk prediction model developed and validated in ~ 200,000 patients.
- Published in:
- 2022
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- Publication type:
- journal article
Chasing the origin of 23 recurrent BRCA1 mutations in Pakistani breast and ovarian cancer patients.
- Published in:
- International Journal of Cancer, 2022, v. 151, n. 3, p. 402, doi. 10.1002/ijc.34016
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- Publication type:
- Article
Prevalence of BRCA1 and BRCA2 Germline Mutations in Patients of African Descent with Early-Onset and Familial Colombian Breast Cancer.
- Published in:
- Oncologist, 2022, v. 27, n. 2, p. e151, doi. 10.1093/oncolo/oyab026
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- Publication type:
- Article
Epigenetic quantification of circulating immune cells in peripheral blood of triple-negative breast cancer patients.
- Published in:
- Clinical Epigenetics, 2021, v. 13, n. 1, p. 1, doi. 10.1186/s13148-021-01196-1
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- Publication type:
- Article
Correction to: Prevalence of RECQL germline variants in Pakistani early-onset and familial breast cancer patients.
- Published in:
- 2021
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- Publication type:
- Correction Notice
Prevalence of RECQL germline variants in Pakistani early-onset and familial breast cancer patients.
- Published in:
- Hereditary Cancer in Clinical Practice, 2020, v. 18, n. 1, p. 1, doi. 10.1186/s13053-020-00159-6
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- Publication type:
- Article
Genetic Variability in the microRNA Binding Sites of BMPR1B, TGFBR1, IQGAP1, KRAS, SETD8 and RYR3 and Risk of Breast Cancer in Colombian Women.
- Published in:
- OncoTargets & Therapy, 2020, v. 13, p. 12281, doi. 10.2147/OTT.S274431
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- Publication type:
- Article
DNA methylation of the long intergenic noncoding RNA 299 gene in triple-negative breast cancer: results from a prospective study.
- Published in:
- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-68506-0
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- Publication type:
- Article
Spectrum and prevalence of BRCA1/2 germline mutations in Pakistani breast cancer patients: results from a large comprehensive study.
- Published in:
- Hereditary Cancer in Clinical Practice, 2019, v. 17, n. 1, p. N.PAG, doi. 10.1186/s13053-019-0125-5
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- Publication type:
- Article
Prevalence of PALB2 Germline Mutations in Early-onset and Familial Breast/Ovarian Cancer Patients from Pakistan.
- Published in:
- Cancer Research & Treatment, 2019, v. 51, n. 3, p. 992, doi. 10.4143/crt.2018.356
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- Publication type:
- Article
Low Prevalence of the Four Common Colombian Founder Mutations in BRCA1 and BRCA2 in Early‐Onset and Familial Afro‐Colombian Patients with Breast Cancer.
- Published in:
- Oncologist, 2019, v. 24, n. 7, p. e475, doi. 10.1634/theoncologist.2018-0346
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- Publication type:
- Article
Interaction between genetic ancestry and common breast cancer susceptibility variants in Colombian women.
- Published in:
- International Journal of Cancer, 2019, v. 144, n. 9, p. 2181, doi. 10.1002/ijc.32023
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- Publication type:
- Article
Tissue-Specific Down-Regulation of the Long Non-Coding RNAs PCAT18 and LINC01133 in Gastric Cancer Development.
- Published in:
- International Journal of Molecular Sciences, 2018, v. 19, n. 12, p. 3881, doi. 10.3390/ijms19123881
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- Publication type:
- Article
Mutational spectrum in a worldwide study of 29,700 families with <italic>BRCA1</italic> or <italic>BRCA2</italic> mutations.
- Published in:
- Human Mutation, 2018, v. 39, n. 5, p. 593, doi. 10.1002/humu.23406
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- Publication type:
- Article
Gene-environment interactions involving functional variants: Results from the Breast Cancer Association Consortium.
- Published in:
- International Journal of Cancer, 2017, v. 141, n. 9, p. 1830, doi. 10.1002/ijc.30859
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- Publication type:
- Article
Imputation of missing genotypes within LD-blocks relying on the basic coalescent and beyond: consideration of population growth and structure.
- Published in:
- BMC Genomics, 2017, v. 18, p. 1, doi. 10.1186/s12864-017-4208-2
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- Publication type:
- Article
Contribution of BRCA1 large genomic rearrangements to early-onset and familial breast/ovarian cancer in Pakistan.
- Published in:
- Breast Cancer Research & Treatment, 2017, v. 161, n. 2, p. 191, doi. 10.1007/s10549-016-4044-0
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- Publication type:
- Article
High prevalence and predominance of BRCA1 germline mutations in Pakistani triple-negative breast cancer patients.
- Published in:
- 2016
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- Publication type:
- journal article
A novel deleterious c.2656G>T MSH2 germline mutation in a Pakistani family with a phenotypic overlap of hereditary breast and ovarian cancer and Lynch syndrome.
- Published in:
- Hereditary Cancer in Clinical Practice, 2016, v. 14, p. 1, doi. 10.1186/s13053-016-0056-3
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- Publication type:
- Article
Genes associated with histopathologic features of triple negative breast tumors predict molecular subtypes.
- Published in:
- Breast Cancer Research & Treatment, 2016, v. 157, n. 1, p. 117, doi. 10.1007/s10549-016-3775-2
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- Publication type:
- Article
Inbreeding and homozygosity in breast cancer survival.
- Published in:
- Scientific Reports, 2015, p. 16467, doi. 10.1038/srep16467
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- Publication type:
- Article
Association between the BsmI Polymorphism in the Vitamin D Receptor Gene and Breast Cancer Risk: Results from a Pakistani Case-Control Study.
- Published in:
- PLoS ONE, 2015, v. 10, n. 10, p. 1, doi. 10.1371/journal.pone.0141562
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- Publication type:
- Article
Absence of the FANCM c.5101C>T mutation in BRCA1/2-negative triple-negative breast cancer patients from Pakistan.
- Published in:
- 2015
- By:
- Publication type:
- Letter
Assessment of variation in immunosuppressive pathway genes reveals TGFBR2 to be associated with prognosis of estrogen receptor-negative breast cancer after chemotherapy.
- Published in:
- Breast Cancer Research, 2015, v. 17, n. 1, p. 1, doi. 10.1186/s13058-015-0522-2
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- Publication type:
- Article
Tailored Selection of Study Individuals to be Sequenced in Order to Improve the Accuracy of Genotype Imputation.
- Published in:
- Genetic Epidemiology, 2015, v. 39, n. 2, p. 114, doi. 10.1002/gepi.21873
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- Publication type:
- Article
Assessment of variation in immunosuppressive pathway genes reveals TGFBR2 to be associated with prognosis of estrogen receptor-negative breast cancer after chemotherapy.
- Published in:
- 2015
- By:
- Publication type:
- journal article
Practical investigation of the performance of robust logistic regression to predict the genetic risk of hypertension.
- Published in:
- BMC Proceedings, 2014, v. 9, n. Supplement 5, p. 1, doi. 10.1186/1753-6561-8-S1-S65
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- Publication type:
- Article
Deleterious RAD51C germline mutations rarely predispose to breast and ovarian cancer in Pakistan.
- Published in:
- Breast Cancer Research & Treatment, 2014, v. 145, n. 3, p. 775, doi. 10.1007/s10549-014-2972-0
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- Publication type:
- Article
Systematic Pathway Enrichment Analysis of a Genome-Wide Association Study on Breast Cancer Survival Reveals an Influence of Genes Involved in Cell Adhesion and Calcium Signaling on the Patients’ Clinical Outcome.
- Published in:
- PLoS ONE, 2014, v. 9, n. 6, p. 1, doi. 10.1371/journal.pone.0098229
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- Publication type:
- Article
Estrogen Receptor Alpha and Nuclear Factor Y Coordinately Regulate the Transcription of the SUMO-Conjugating <i>UBC9</i> Gene in MCF-7 Breast Cancer Cells.
- Published in:
- PLoS ONE, 2013, v. 8, n. 9, p. 1, doi. 10.1371/journal.pone.0075695
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- Publication type:
- Article
Night work and breast cancer estrogen receptor status - results from the German GENICA study.
- Published in:
- Scandinavian Journal of Work, Environment & Health, 2013, v. 39, n. 5, p. 448, doi. 10.5271/sjweh.3360
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- Publication type:
- Article
Constitutional CHEK2 mutations are infrequent in early-onset and familial breast/ovarian cancer patients from Pakistan.
- Published in:
- BMC Cancer, 2013, v. 13, n. 1, p. 1, doi. 10.1186/1471-2407-13-312
- By:
- Publication type:
- Article
Exploring the association between genetic variation in the SUMO isopeptidase gene USPL1 and breast cancer through integration of data from the population-based GENICA study and external genetic databases.
- Published in:
- International Journal of Cancer, 2013, v. 133, n. 2, p. 362, doi. 10.1002/ijc.28040
- By:
- Publication type:
- Article
Constitutional CHEK2 mutations are infrequent in early-onset and familial breast/ovarian cancer patients from Pakistan.
- Published in:
- 2013
- By:
- Publication type:
- journal article
Evaluation of chromosome 6p22 as a breast cancer risk modifier locus in a follow-up study of BRCA2 mutation carriers.
- Published in:
- 2012
- By:
- Publication type:
- Report
Prevalence of TP53 germ line mutations in young Pakistani breast cancer patients.
- Published in:
- Familial Cancer, 2012, v. 11, n. 2, p. 307, doi. 10.1007/s10689-012-9509-7
- By:
- Publication type:
- Article
The postmenopausal hormone replacement therapy-related breast cancer risk is decreased in women carrying the CYP2C19*17 variant.
- Published in:
- 2012
- By:
- Publication type:
- Letter
Single nucleotide polymorphisms in the 20q13 amplicon genes in relation to breast cancer risk and clinical outcome.
- Published in:
- Breast Cancer Research & Treatment, 2011, v. 130, n. 3, p. 905, doi. 10.1007/s10549-011-1600-5
- By:
- Publication type:
- Article
Identification of the deleterious 2080insA BRCA1 mutation in a male renal cell carcinoma patient from a family with multiple cancer diagnoses from Pakistan.
- Published in:
- 2011
- By:
- Publication type:
- Letter
The earwax-associated SNP c.538G>A (G180R) in ABCC11 is not associated with breast cancer risk in Europeans.
- Published in:
- 2011
- By:
- Publication type:
- Report
No association of polymorphisms in the cell polarity gene SCRIB with breast cancer risk.
- Published in:
- Breast Cancer Research & Treatment, 2011, v. 127, n. 1, p. 259, doi. 10.1007/s10549-010-1194-3
- By:
- Publication type:
- Article
The CYP17A1 −34T > C polymorphism and breast cancer risk in BRCA1 and BRCA2 mutation carriers.
- Published in:
- Breast Cancer Research & Treatment, 2011, v. 126, n. 2, p. 521, doi. 10.1007/s10549-010-1123-5
- By:
- Publication type:
- Article
Polymorphisms of the nuclear receptor pregnane X receptor and organic anion transporter polypeptides 1A2, 1B1, 1B3, and 2B1 are not associated with breast cancer risk.
- Published in:
- Breast Cancer Research & Treatment, 2011, v. 125, n. 2, p. 563, doi. 10.1007/s10549-010-1046-1
- By:
- Publication type:
- Article
Combined UGT1A1 and UGT1A6 genotypes together with a stressful life event increase breast cancer risk.
- Published in:
- 2011
- By:
- Publication type:
- Letter