Pages that link to "Q87001219"
Jump to navigation
Jump to search
The following pages link to Margaret A. Tucker (Q87001219):
Displaying 50 items.
- Detectable clonal mosaicism and its relationship to aging and cancer (Q23916196) (← links)
- Imputation and subset-based association analysis across different cancer types identifies multiple independent risk loci in the TERT-CLPTM1L region on chromosome 5p15.33 (Q23924183) (← links)
- Characterization of large structural genetic mosaicism in human autosome (Q24169697) (← links)
- Analysis of heritability and shared heritability based on genome-wide association studies for thirteen cancer types (Q24170413) (← links)
- Associations of 9p21 variants with cutaneous malignant melanoma, nevi, and pigmentation phenotypes in melanoma-prone families with and without CDKN2A mutations (Q24630954) (← links)
- A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma (Q24657797) (← links)
- Female chromosome X mosaicism is age-related and preferentially affects the inactivated X chromosome (Q27908479) (← links)
- Mutational analysis of the BRCA1-interacting genes ZNF350/ZBRK1 and BRIP1/BACH1 among BRCA1 and BRCA2-negative probands from breast-ovarian cancer families and among early-onset breast cancer cases and reference individuals (Q28188416) (← links)
- A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer (Q28303909) (← links)
- Genetic polymorphisms in the 9p21 region associated with risk of multiple cancers (Q28383262) (← links)
- Genome-wide association study confirms lung cancer susceptibility loci on chromosomes 5p15 and 15q25 in an African-American population (Q28383750) (← links)
- Meta-analysis of genome-wide association studies identifies multiple lung cancer susceptibility loci in never-smoking Asian women (Q28385292) (← links)
- Impact of occupational carcinogens on lung cancer risk in a general population (Q28386338) (← links)
- Lung cancer and occupation in a population-based case-control study (Q28393149) (← links)
- Mosaic loss of chromosome Y is associated with common variation near TCL1A (Q28393244) (← links)
- Rare Germline Copy Number Variations and Disease Susceptibility in Familial Melanoma (Q28394958) (← links)
- Common genetic variants in the 9p21 region and their associations with multiple tumours (Q28396581) (← links)
- Joint analysis of three genome-wide association studies of esophageal squamous cell carcinoma in Chinese populations (Q28396727) (← links)
- The 5p15.33 locus is associated with risk of lung adenocarcinoma in never-smoking females in Asia (Q28397565) (← links)
- Genome-wide scan of 29,141 African Americans finds no evidence of directional selection since admixture (Q28655044) (← links)
- Genome-wide association study identifies two susceptibility loci for osteosarcoma (Q28659642) (← links)
- Genome-wide association analysis identifies new lung cancer susceptibility loci in never-smoking women in Asia (Q28943345) (← links)
- Multiple loci identified in a genome-wide association study of prostate cancer (Q28943507) (← links)
- Genome-wide association study of prostate cancer identifies a second risk locus at 8q24 (Q29614925) (← links)
- A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry (Q30416161) (← links)
- The landscape of recombination in African Americans (Q30428393) (← links)
- Telomere length and the risk of cutaneous malignant melanoma in melanoma-prone families with and without CDKN2A mutations (Q31131061) (← links)
- Environment And Genetics in Lung cancer Etiology (EAGLE) study: an integrative population-based case-control study of lung cancer (Q33341194) (← links)
- Potential excess mortality in BRCA1/2 mutation carriers beyond breast, ovarian, prostate, and pancreatic cancers, and melanoma (Q33416772) (← links)
- Phase I metabolic genes and risk of lung cancer: multiple polymorphisms and mRNA expression (Q33455775) (← links)
- Cancer screening practices of adult survivors of retinoblastoma at risk of second cancers (Q33575528) (← links)
- A new statistic and its power to infer membership in a genome-wide association study using genotype frequencies (Q33577138) (← links)
- Risk of cataract extraction among adult retinoblastoma survivors (Q33638053) (← links)
- Rare missense variants in POT1 predispose to familial cutaneous malignant melanoma (Q33751971) (← links)
- Refining the prostate cancer genetic association within the JAZF1 gene on chromosome 7p15.2. (Q33835331) (← links)
- A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1). (Q34085748) (← links)
- Geographical variation in the penetrance of CDKN2A mutations for melanoma (Q34134115) (← links)
- Fine mapping of 14q24.1 breast cancer susceptibility locus (Q34158088) (← links)
- A shared susceptibility locus in PLCE1 at 10q23 for gastric adenocarcinoma and esophageal squamous cell carcinoma (Q34162606) (← links)
- Risk of subsequent malignant neoplasms in long-term hereditary retinoblastoma survivors after chemotherapy and radiotherapy (Q34260518) (← links)
- Risk of new cancers after radiotherapy in long-term survivors of retinoblastoma: an extended follow-up (Q34407554) (← links)
- On the interplay of telomeres, nevi and the risk of melanoma (Q34540748) (← links)
- Common single nucleotide polymorphisms in genes related to immune function and risk of papillary thyroid cancer (Q34631671) (← links)
- Fine mapping of a region of chromosome 11q13 reveals multiple independent loci associated with risk of prostate cancer (Q35056055) (← links)
- Large-scale fine mapping of the HNF1B locus and prostate cancer risk (Q35119669) (← links)
- Common genetic variants related to genomic integrity and risk of papillary thyroid cancer (Q35193949) (← links)
- Two susceptibility loci identified for prostate cancer aggressiveness (Q35575585) (← links)
- Lack of germline PALB2 mutations in melanoma-prone families with CDKN2A mutations and pancreatic cancer (Q35627634) (← links)
- Genetic variants in DNA repair genes and the risk of cutaneous malignant melanoma in melanoma‐prone families with/without CDKN2A mutations (Q35742829) (← links)
- Improved imputation of common and uncommon SNPs with a new reference set. (Q35747559) (← links)