Pages that link to "Q89224652"
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The following pages link to Encarna B Gómez García (Q89224652):
Displayed 29 items.
- DNA glycosylases involved in base excision repair may be associated with cancer risk in BRCA1 and BRCA2 mutation carriers (Q21144874) (← links)
- Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk (Q27008356) (← links)
- Evaluation of Polygenic Risk Scores for Breast and Ovarian Cancer Risk Prediction in BRCA1 and BRCA2 Mutation Carriers (Q33614244) (← links)
- Candidate genetic modifiers for breast and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers (Q34963894) (← links)
- A 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 (Q35089479) (← links)
- Common breast cancer susceptibility alleles are associated with tumour subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2. (Q35889575) (← links)
- Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer (Q35957703) (← links)
- A nonsynonymous polymorphism in IRS1 modifies risk of developing breast and ovarian cancers in BRCA1 and ovarian cancer in BRCA2 mutation carriers (Q36152991) (← links)
- Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers (Q36393232) (← links)
- Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers (Q36839777) (← links)
- Colorectal cancer risk variants on 11q23 and 15q13 are associated with unexplained adenomatous polyposis (Q37467854) (← links)
- Novel BRCA1 and BRCA2 Tumor Test as Basis for Treatment Decisions and Referral for Genetic Counselling of Patients with Ovarian Carcinomas (Q37595954) (← links)
- Awareness and attitude regarding reproductive options of persons carrying a BRCA mutation and their partners. (Q38772089) (← links)
- A white raven detected by imaging (Q41156873) (← links)
- The effect of genotypes and parent of origin on cancer risk and age of cancer development in PMS2 mutation carriers (Q41642720) (← links)
- Lynch syndrome caused by germline PMS2 mutations: delineating the cancer risk (Q41685035) (← links)
- Unraveling genetic predisposition to familial or early onset gastric cancer using germline whole-exome sequencing (Q42691689) (← links)
- Professionals' knowledge, attitude and referral behaviour of preimplantation genetic diagnosis for hereditary breast and ovarian cancer (Q47192712) (← links)
- Role of germline aberrations affecting CTNNA1, MAP3K6 and MYD88 in gastric cancer susceptibility. (Q48251790) (← links)
- The BRCA2 c.68-7T > A variant is not pathogenic: A model for clinical calibration of spliceogenicity (Q49817640) (← links)
- Cancer Risks for PMS2-Associated Lynch Syndrome (Q57284561) (← links)
- Height and Body Mass Index as Modifiers of Breast Cancer Risk in BRCA1/2 Mutation Carriers: A Mendelian Randomization Study (Q57471595) (← links)
- Ovarian stimulation for IVF and risk of primary breast cancer in BRCA1/2 mutation carriers (Q89224654) (← links)
- Genetic Testing and Clinical Management Practices for Variants in Non-BRCA1/2 Breast (and Breast/Ovarian) Cancer Susceptibility Genes: An International Survey by the Evidence-Based Network for the Interpretation of Germline Mutant Alleles (ENIGMA) C (Q90089832) (← links)
- The Apparent Genetic Anticipation in PMS2-Associated Lynch Syndrome Families Is Explained by Birth-cohort Effect (Q92060065) (← links)
- Oral Contraceptive Use and Breast Cancer Risk: Retrospective and Prospective Analyses From a BRCA1 and BRCA2 Mutation Carrier Cohort Study (Q92281866) (← links)
- Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification (Q92313654) (← links)
- An alternative approach to establishing unbiased colorectal cancer risk estimation in Lynch syndrome (Q92783253) (← links)
- Mendelian randomisation study of height and body mass index as modifiers of ovarian cancer risk in 22,588 BRCA1 and BRCA2 mutation carriers (Q92860654) (← links)