Pages that link to "Q59812154"
Jump to navigation
Jump to search
The following pages link to Douglas F. Easton (Q59812154):
Displaying 50 items.
- DNA glycosylases involved in base excision repair may be associated with cancer risk in BRCA1 and BRCA2 mutation carriers (Q21144874) (← links)
- Common variation in EMSY and risk of breast and ovarian cancer: a case-control study using HapMap tagging SNPs (Q21260438) (← links)
- Sexual activity and prostate cancer risk in men diagnosed at a younger age (Q21558581) (← links)
- The rs10993994 risk allele for prostate cancer results in clinically relevant changes in microseminoprotein-beta expression in tissue and urine (Q21562160) (← links)
- Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case Series unselected for family history: a combined analysis of 22 studies (Q24531993) (← links)
- After BRCA1 and BRCA2-what next? Multifactorial segregation analyses of three-generation, population-based Australian families affected by female breast cancer (Q24535695) (← links)
- Linkage analysis of chromosome 1q markers in 136 prostate cancer families. The Cancer Research Campaign/British Prostate Group U.K. Familial Prostate Cancer Study Collaborators (Q24538779) (← links)
- Lymphoid tumours and breast cancer in ataxia telangiectasia; substantial protective effect of residual ATM kinase activity against childhood tumours (Q24597674) (← links)
- International network of cancer genome projects (Q24611474) (← links)
- A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation (Q24613870) (← links)
- PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene (Q24615080) (← links)
- Genome-wide association studies identify four ER negative-specific breast cancer risk loci (Q24622610) (← links)
- Epigenetic analysis leads to identification of HNF1B as a subtype-specific susceptibility gene for ovarian cancer (Q24633316) (← links)
- Genome-wide association study identifies novel breast cancer susceptibility loci (Q24645441) (← links)
- Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants (Q24646663) (← links)
- Polymorphism in the IL18 gene and epithelial ovarian cancer in non-Hispanic white women (Q24648412) (← links)
- Interactions between genes involved in the antioxidant defence system and breast cancer risk (Q24652651) (← links)
- Identification of common variants in the SHBG gene affecting sex hormone-binding globulin levels and breast cancer risk in postmenopausal women (Q24653491) (← links)
- Common breast cancer-predisposition alleles are associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers (Q24655824) (← links)
- Common genetic variation in candidate genes and susceptibility to subtypes of breast cancer (Q24658131) (← links)
- Mutations in the gene encoding the Sigma 2 subunit of the adaptor protein 1 complex, AP1S2, cause X-linked mental retardation (Q24671723) (← links)
- Genetic linkage analysis in familial breast and ovarian cancer: results from 214 families. The Breast Cancer Linkage Consortium (Q24671905) (← links)
- Mutations in ZDHHC9, which encodes a palmitoyltransferase of NRAS and HRAS, cause X-linked mental retardation associated with a Marfanoid habitus (Q24682652) (← links)
- The androgen receptor CAG repeat polymorphism and modification of breast cancer risk in BRCA1 and BRCA2 mutation carriers (Q24797305) (← links)
- Common ERBB2 polymorphisms and risk of breast cancer in a white British population: a case-control study (Q24797594) (← links)
- How many more breast cancer predisposition genes are there? (Q24800566) (← links)
- Familial risks of breast cancer (Q24802759) (← links)
- BRCA1 and BRCA2 mutations in a population-based study of male breast cancer (Q24803673) (← links)
- Network-Based Integration of GWAS and Gene Expression Identifies a HOX-Centric Network Associated with Serous Ovarian Cancer Risk (Q26799669) (← links)
- Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk (Q27008356) (← links)
- Do MDM2 SNP309 and TP53 R72P interact in breast cancer susceptibility? A large pooled series from the breast cancer association consortium (Q27851413) (← links)
- Association between BRCA1 and BRCA2 mutations and survival in women with invasive epithelial ovarian cancer (Q27851709) (← links)
- Germline BRCA mutations are associated with higher risk of nodal involvement, distant metastasis, and poor survival outcomes in prostate cancer (Q27852185) (← links)
- A germline mutation in the androgen receptor gene in two brothers with breast cancer and Reifenstein syndrome (Q28208102) (← links)
- No evidence for an association between Saitohin Q7R polymorphism and Alzheimer's disease (Q28211288) (← links)
- Low-penetrance susceptibility to breast cancer due to CHEK2(*)1100delC in noncarriers of BRCA1 or BRCA2 mutations (Q28215462) (← links)
- Common polymorphisms in the prostaglandin pathway genes and their association with breast cancer susceptibility and survival (Q28237788) (← links)
- Inhibition of mTOR induces autophagy and reduces toxicity of polyglutamine expansions in fly and mouse models of Huntington disease (Q28261987) (← links)
- Overexpression of RAD51 occurs in aggressive prostatic cancer (Q28267299) (← links)
- Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair (Q28267893) (← links)
- Multiple newly identified loci associated with prostate cancer susceptibility (Q28268180) (← links)
- Interim analysis of the incidence of breast cancer in the Royal Marsden Hospital tamoxifen randomised chemoprevention trial (Q28277066) (← links)
- Mutations in CUL4B, which encodes a ubiquitin E3 ligase subunit, cause an X-linked mental retardation syndrome associated with aggressive outbursts, seizures, relative macrocephaly, central obesity, hypogonadism, pes cavus, and tremor (Q28284058) (← links)
- Familial cylindromatosis (turban tumour syndrome) gene localised to chromosome 16q12-q13: evidence for its role as a tumour suppressor gene (Q28284637) (← links)
- Hyaluronan-mediated motility receptor gene single nucleotide polymorphisms and risk of breast cancer (Q28303249) (← links)
- A Cross-Cancer Genetic Association Analysis of the DNA Repair and DNA Damage Signaling Pathways for Lung, Ovary, Prostate, Breast, and Colorectal Cancer (Q28384141) (← links)
- Candidate locus analysis of the TERT-CLPTM1L cancer risk region on chromosome 5p15 identifies multiple independent variants associated with endometrial cancer risk (Q28385765) (← links)
- Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations (Q28388475) (← links)
- Genome-Wide Meta-Analyses of Breast, Ovarian, and Prostate Cancer Association Studies Identify Multiple New Susceptibility Loci Shared by at Least Two Cancer Types (Q28388497) (← links)
- Cross Cancer Genomic Investigation of Inflammation Pathway for Five Common Cancers: Lung, Ovary, Prostate, Breast, and Colorectal Cancer (Q28396029) (← links)