Sandra Deming-Halverson

researcher

Sandra Deming-Halverson is …
instance of (P31):
humanQ5

P735given nameSandraQ1474819
SandraQ1474819
P106occupationresearcherQ1650915
P5008on focus list of Wikimedia projectWikiProject COVID-19Q87748614
P21sex or genderfemaleQ6581072

Reverse relations

author (P50)
Q40597341A Meta-analysis of Multiple Myeloma Risk Regions in African and European Ancestry Populations Identifies Putatively Functional Loci
Q35755874A common variant at the TERT-CLPTM1L locus is associated with estrogen receptor-negative breast cancer
Q37109758A genome-wide association study of breast cancer in women of African ancestry
Q30416161A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry
Q36435849A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11.
Q37205864APOBEC3 deletion polymorphism is associated with breast cancer risk among women of European ancestry
Q34619821Associations of hormone-related factors with breast cancer risk according to hormone receptor status among white and African American women
Q64921568Chronic antibiotic use during adulthood and weight change in the Sister Study.
Q34379032Common non-synonymous SNPs associated with breast cancer susceptibility: findings from the Breast Cancer Association Consortium
Q46958735Correction: Evaluating Genome-Wide Association Study-Identified Breast Cancer Risk Variants in African-American Women.
Q30432415Enhanced statistical tests for GWAS in admixed populations: assessment using African Americans from CARe and a Breast Cancer Consortium
Q34022151Evaluating 17 breast cancer susceptibility loci in the Nashville breast health study
Q34339783Evaluating genome-wide association study-identified breast cancer risk variants in African-American women
Q37594336FGF receptor genes and breast cancer susceptibility: results from the Breast Cancer Association Consortium
Q35524465Fine-mapping identifies two additional breast cancer susceptibility loci at 9q31.2.
Q34903062Fine-scale mapping of the 5q11.2 breast cancer locus reveals at least three independent risk variants regulating MAP3K1.
Q37367871Fine-scale mapping of the FGFR2 breast cancer risk locus: putative functional variants differentially bind FOXA1 and E2F1.
Q36742577Functional variants at the 11q13 risk locus for breast cancer regulate cyclin D1 expression through long-range enhancers
Q33589487Genes associated with histopathologic features of triple negative breast tumors predict molecular subtypes
Q34378972Genetic variation in mitotic regulatory pathway genes is associated with breast tumor grade
Q35996692Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer
Q24622610Genome-wide association studies identify four ER negative-specific breast cancer risk loci
Q29417100Genome-wide association study identifies 25 known breast cancer susceptibility loci as risk factors for triple-negative breast cancer
Q37045108Genome-wide association study of age at menarche in African-American women
Q28655044Genome-wide scan of 29,141 African Americans finds no evidence of directional selection since admixture
Q37523423High use of complementary and alternative medicine among a large cohort of women with a family history of breast cancer: the Sister Study
Q35102646Identification and characterization of novel associations in the CASP8/ALS2CR12 region on chromosome 2 with breast cancer risk
Q28474694Identification of a functional genetic variant at 16q12.1 for breast cancer risk: results from the Asia Breast Cancer Consortium
Q31036626Identification, replication, and fine-mapping of Loci associated with adult height in individuals of african ancestry
Q37679492Interactions of hormone replacement therapy, body weight, and bilateral oophorectomy in breast cancer risk
Q29416989Large-scale genotyping identifies 41 new loci associated with breast cancer risk
Q34428438Local breast cancer spatial patterning: a tool for community health resource allocation to address local disparities in breast cancer mortality
Q30977635Methodological Considerations in Estimation of Phenotype Heritability Using Genome-Wide SNP Data, Illustrated by an Analysis of the Heritability of Height in a Large Sample of African Ancestry Adults
Q36897003Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer
Q30374367No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer.
Q47143943PHIP - a novel candidate breast cancer susceptibility locus on 6q14.1.
Q36583004Prediction of breast cancer risk based on profiling with common genetic variants
Q34870700Replication and functional genomic analyses of the breast cancer susceptibility locus at 6q25.1 generalize its importance in women of chinese, Japanese, and European ancestry
Q94552258The COronavirus Pandemic Epidemiology (COPE) Consortium: A Call to Action
Q47553137The Sister Study Cohort: Baseline Methods and Participant Characteristics
Q30428393The landscape of recombination in African Americans
Q34034263Use of nonsteroidal anti-inflammatory drugs and reduced breast cancer risk among overweight women
Q42654606Validity of self-reported breast cancer characteristics in a nationwide cohort of women with a family history of breast cancer

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