Item Type | Name |
Concept
|
Alleles
|
Concept
|
Amino Acid Sequence
|
Concept
|
Analysis of Variance
|
Concept
|
Base Sequence
|
Concept
|
Genes, Immunoglobulin
|
Concept
|
Crossing Over, Genetic
|
Concept
|
DNA Mutational Analysis
|
Concept
|
DNA, Recombinant
|
Concept
|
Genes, Dominant
|
Concept
|
Genetics
|
Concept
|
Oncogenes
|
Concept
|
Genetic Carrier Screening
|
Concept
|
Fourier Analysis
|
Concept
|
Genes, Overlapping
|
Concept
|
Multigene Family
|
Concept
|
Genetics, Population
|
Concept
|
Models, Genetic
|
Concept
|
Molecular Sequence Data
|
Concept
|
Repetitive Sequences, Nucleic Acid
|
Concept
|
Selection, Genetic
|
Concept
|
Polymorphism, Genetic
|
Concept
|
Pseudogenes
|
Concept
|
Genetic Markers
|
Concept
|
Regression Analysis
|
Concept
|
Sequence Homology, Nucleic Acid
|
Concept
|
Cluster Analysis
|
Concept
|
Transcription, Genetic
|
Concept
|
Genome
|
Concept
|
Sequence Homology, Amino Acid
|
Concept
|
Genetic Variation
|
Concept
|
Leukemia, Myeloid
|
Concept
|
Gene Library
|
Concept
|
RNA Splice Sites
|
Concept
|
Genes, BRCA2
|
Concept
|
Principal Component Analysis
|
Concept
|
Genes, Tumor Suppressor
|
Concept
|
Matched-Pair Analysis
|
Concept
|
Leukemia, Myeloid, Acute
|
Concept
|
Genomic Library
|
Concept
|
Genes, Retinoblastoma
|
Concept
|
Sequence Analysis, DNA
|
Concept
|
Genes, APC
|
Concept
|
Genes, Reporter
|
Concept
|
Consensus Sequence
|
Concept
|
Evolution, Molecular
|
Concept
|
Molecular Chaperones
|
Concept
|
Genetic Association Studies
|
Concept
|
Exome
|
Concept
|
Genetic Services
|
Concept
|
Microarray Analysis
|
Concept
|
Oligonucleotide Array Sequence Analysis
|
Concept
|
Genes, bcl-2
|
Concept
|
Genes, BRCA1
|
Concept
|
Genes, p16
|
Concept
|
Genetic Diseases, Inborn
|
Concept
|
Databases, Genetic
|
Concept
|
Promoter Regions, Genetic
|
Concept
|
Suppression, Genetic
|
Concept
|
Genetic Research
|
Concept
|
Genes, Mitochondrial
|
Concept
|
Regulatory Elements, Transcriptional
|
Concept
|
Multivariate Analysis
|
Concept
|
Survival Analysis
|
Concept
|
Genes, myc
|
Concept
|
Open Reading Frames
|
Concept
|
Meta-Analysis as Topic
|
Concept
|
Genome, Human
|
Concept
|
Genes, p53
|
Concept
|
Molecular Epidemiology
|
Concept
|
Genes, erbB-2
|
Concept
|
Genetic Heterogeneity
|
Concept
|
Transcriptome
|
Concept
|
Mendelian Randomization Analysis
|
Concept
|
Tissue Array Analysis
|
Concept
|
Genes, Neoplasm
|
Concept
|
Cloning, Molecular
|
Concept
|
Enhancer Elements, Genetic
|
Concept
|
Genetic Counseling
|
Concept
|
Genetic Testing
|
Concept
|
Genetic Linkage
|
Concept
|
Translocation, Genetic
|
Concept
|
Leukemia, Myelogenous, Chronic, BCR-ABL Positive
|
Concept
|
Discriminant Analysis
|
Concept
|
Conserved Sequence
|
Concept
|
Sequence Analysis, RNA
|
Concept
|
Genetic Predisposition to Disease
|
Concept
|
Polymorphism, Single Nucleotide
|
Concept
|
Quantitative Trait Loci
|
Concept
|
Epigenesis, Genetic
|
Concept
|
Genetic Loci
|
Academic Article
|
Clinical, morphologic, and cytogenetic characteristics of 26 patients with acute erythroblastic leukemia.
|
Academic Article
|
Genetic testing of families with hereditary diseases.
|
Academic Article
|
Recurrent germ-line BRCA1 mutations in extended African American families with early-onset breast cancer.
|
Academic Article
|
Effect of smoking on breast cancer in carriers of mutant BRCA1 or BRCA2 genes.
|
Academic Article
|
The Human Genome Project and breast cancer.
|
Academic Article
|
Expression of methylthioadenosine phosphorylase cDNA in p16-, MTAP- malignant cells: restoration of methylthioadenosine phosphorylase-dependent salvage pathways and alterations of sensitivity to inhibitors of purine de novo synthesis.
|
Academic Article
|
Genetics in clinical cancer care--the future is now.
|
Academic Article
|
Familial myeloid leukemia associated with loss of the long arm of chromosome 5.
|
Academic Article
|
Preferential loss of expression of p16(INK4a) rather than p19(ARF) in breast cancer.
|
Academic Article
|
Scaffold-associated regions in the human type I interferon gene cluster on the short arm of chromosome 9.
|
Academic Article
|
Susceptibility gene for familial acute myeloid leukemia associated with loss of 5q and/or 7q is not localized on the commonly deleted portion of 5q.
|
Academic Article
|
Pregnancy and risk of early breast cancer in carriers of BRCA1 and BRCA2.
|
Academic Article
|
Computerized analysis of mammographic parenchymal patterns for breast cancer risk assessment: feature selection.
|
Academic Article
|
Genetic testing for susceptibility to cancer. Task Force on Cancer Genetics Education.
|
Academic Article
|
Cancer genetics in oncology practice.
|
Academic Article
|
Molecular analysis of deletions of the short arm of chromosome 9 in human gliomas.
|
Academic Article
|
Sequence analysis of BRCA1 and BRCA2: correlation of mutations with family history and ovarian cancer risk.
|
Academic Article
|
Characterization of an allelic variant in the nifedipine-specific element of CYP3A4: ethnic distribution and implications for prostate cancer risk. Mutations in brief no. 191. Online.
|
Academic Article
|
Pretest prediction of BRCA1 or BRCA2 mutation by risk counselors and the computer model BRCAPRO.
|
Academic Article
|
Effect of radiotherapy after breast-conserving treatment in women with breast cancer and germline BRCA1/2 mutations.
|
Academic Article
|
Gene-expression profiles in hereditary breast cancer.
|
Academic Article
|
Computerized analysis of digitized mammograms of BRCA1 and BRCA2 gene mutation carriers.
|
Academic Article
|
Predisposition testing for inherited breast cancer.
|
Academic Article
|
The American Society of Clinical Oncology position on genetic testing: implications for health care providers: workshop no. 4.
|
Academic Article
|
Molecular-cytogenetic analysis of HER-2/neu gene in BRCA1-associated breast cancers.
|
Academic Article
|
The effect of varying spectral resolution on the quality of high spectral and spatial resolution magnetic resonance images of the breast.
|
Academic Article
|
BRCA2 T2722R is a deleterious allele that causes exon skipping.
|
Academic Article
|
Male breast cancer in Cowden syndrome patients with germline PTEN mutations.
|
Academic Article
|
FANCF methylation contributes to chemoselectivity in ovarian cancer.
|
Academic Article
|
MYC is amplified in BRCA1-associated breast cancers.
|
Academic Article
|
Bilateral prophylactic mastectomy reduces breast cancer risk in BRCA1 and BRCA2 mutation carriers: the PROSE Study Group.
|
Academic Article
|
Computerized analysis of mammographic parenchymal patterns for assessing breast cancer risk: effect of ROI size and location.
|
Academic Article
|
Oral contraceptives and the risk of breast cancer in BRCA1 and BRCA2 mutation carriers.
|
Academic Article
|
Breast cancer genetics in African Americans.
|
Academic Article
|
Identification of a 1.2 Kb cDNA fragment from a region on 9p21 commonly deleted in multiple tumor types.
|
Academic Article
|
Fourier components of inhomogeneously broadened water resonances in breast: a new source of MRI contrast.
|
Academic Article
|
Racial differences in genetic factors associated with breast cancer.
|
Academic Article
|
Age at menarche and the risk of breast cancer in BRCA1 and BRCA2 mutation carriers.
|
Academic Article
|
Colorectal cancer and race: understanding the differences in outcomes between African Americans and whites.
|
Academic Article
|
Effect of pregnancy as a risk factor for breast cancer in BRCA1/BRCA2 mutation carriers.
|
Academic Article
|
Tamoxifen and contralateral breast cancer in BRCA1 and BRCA2 carriers: an update.
|
Academic Article
|
Spontaneous and therapeutic abortions and the risk of breast cancer among BRCA mutation carriers.
|
Academic Article
|
How often do BRCA mutation carriers tell their young children of the family's risk for cancer? A study of parental disclosure of BRCA mutations to minors and young adults.
|
Academic Article
|
Genetic and functional analysis of CHEK2 (CHK2) variants in multiethnic cohorts.
|
Academic Article
|
Confronting genetic testing disparities: knowledge is power.
|
Academic Article
|
Computerized texture analysis of mammographic parenchymal patterns of digitized mammograms.
|
Academic Article
|
Effect of short-term hormone replacement therapy on breast cancer risk reduction after bilateral prophylactic oophorectomy in BRCA1 and BRCA2 mutation carriers: the PROSE Study Group.
|
Academic Article
|
Genetic testing in an ethnically diverse cohort of high-risk women: a comparative analysis of BRCA1 and BRCA2 mutations in American families of European and African ancestry.
|
Academic Article
|
Ten-year multi-institutional results of breast-conserving surgery and radiotherapy in BRCA1/2-associated stage I/II breast cancer.
|
Academic Article
|
The molecular portraits of breast tumors are conserved across microarray platforms.
|
Academic Article
|
Disparities in genetic testing: thinking outside the BRCA box.
|
Academic Article
|
Salpingo-oophorectomy and the risk of ovarian, fallopian tube, and peritoneal cancers in women with a BRCA1 or BRCA2 Mutation.
|
Academic Article
|
The I1307K APC polymorphism in Ashkenazi Jews with colorectal cancer: clinical and pathologic features.
|
Academic Article
|
BRCA1 promoter methylation in sporadic breast cancer is associated with reduced BRCA1 copy number and chromosome 17 aneusomy.
|
Academic Article
|
Phenotypic evaluation of the basal-like subtype of invasive breast carcinoma.
|
Academic Article
|
Power spectral analysis of mammographic parenchymal patterns for breast cancer risk assessment.
|
Academic Article
|
Using genetic analysis to individualize preventive measures for breast and ovarian cancers.
|
Academic Article
|
Primary structure-based function characterization of BRCT domain replicates in BRCA1.
|
Academic Article
|
Correlates of depressive symptoms among women seeking cancer genetic counseling and risk assessment at a high-risk cancer clinic.
|
Academic Article
|
Fractal analysis of mammographic parenchymal patterns in breast cancer risk assessment.
|
Academic Article
|
Genomic analysis of estrogen cascade reveals histone variant H2A.Z associated with breast cancer progression.
|
Academic Article
|
Common variants on chromosome 5p12 confer susceptibility to estrogen receptor-positive breast cancer.
|
Academic Article
|
Contralateral breast cancer in BRCA1 and BRCA2 mutation carriers.
|
Academic Article
|
Genetic polymorphisms in uridine diphospho-glucuronosyltransferase 1A1 and breast cancer risk in Africans.
|
Academic Article
|
AURKA F31I polymorphism and breast cancer risk in BRCA1 and BRCA2 mutation carriers: a consortium of investigators of modifiers of BRCA1/2 study.
|
Academic Article
|
MYC in breast tumor progression.
|
Academic Article
|
No evidence for core-binding factor CBFbeta as a leukemia predisposing factor in chromosome 16q22-linked familial AML.
|
Academic Article
|
Rapid progression of prostate cancer in men with a BRCA2 mutation.
|
Academic Article
|
Estrogen receptor status in BRCA1- and BRCA2-related breast cancer: the influence of age, grade, and histological type.
|
Academic Article
|
Learning of your parent's BRCA mutation during adolescence or early adulthood: a study of offspring experiences.
|
Academic Article
|
Clinical, morphologic, and cytogenetic characteristics of patients with lymphoid malignancies characterized by both t(14;18)(q32;q21) and t(8;14)(q24;q32) or t(8;22)(q24;q11).
|
Academic Article
|
Advances in breast cancer: pathways to personalized medicine.
|
Academic Article
|
Common breast cancer-predisposition alleles are associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers.
|
Academic Article
|
Chromosome band 16q22-linked familial AML: exclusion of candidate genes, and possible disease risk modification by NQO1 polymorphisms.
|
Academic Article
|
Complete allelic analysis of BRCA1 and BRCA2 variants in young Nigerian breast cancer patients.
|
Academic Article
|
A compact VEGF signature associated with distant metastases and poor outcomes.
|
Academic Article
|
Family history of pancreatic cancer in a high-risk cancer clinic: implications for risk assessment.
|
Academic Article
|
Genetic variation in insulin-like growth factor signaling genes and breast cancer risk among BRCA1 and BRCA2 carriers.
|
Academic Article
|
Classification and risk stratification of invasive breast carcinomas using a real-time quantitative RT-PCR assay.
|
Academic Article
|
Fourier component imaging of water resonance in the human breast provides markers for malignancy.
|
Academic Article
|
Occult ovarian cancers identified at risk-reducing salpingo-oophorectomy in a prospective cohort of BRCA1/2 mutation carriers.
|
Academic Article
|
Allelic imbalance (AI) identifies novel tissue-specific cis-regulatory variation for human UGT2B15.
|
Academic Article
|
Wnt/beta-catenin pathway activation is enriched in basal-like breast cancers and predicts poor outcome.
|
Academic Article
|
Common breast cancer susceptibility alleles and the risk of breast cancer for BRCA1 and BRCA2 mutation carriers: implications for risk prediction.
|
Academic Article
|
Interpretation of genome-wide association study results.
|
Academic Article
|
Screening RAD51C nucleotide alterations in patients with a family history of breast and ovarian cancer.
|
Academic Article
|
Identification of conserved gene expression features between murine mammary carcinoma models and human breast tumors.
|
Academic Article
|
Germline mutations in CDH1 are infrequent in women with early-onset or familial lobular breast cancers.
|
Academic Article
|
Proliferating macrophages associated with high grade, hormone receptor negative breast cancer and poor clinical outcome.
|
Academic Article
|
c-Myc activates BRCA1 gene expression through distal promoter elements in breast cancer cells.
|
Academic Article
|
Estrogen receptor alpha, BRCA1, and FANCF promoter methylation occur in distinct subsets of sporadic breast cancers.
|
Academic Article
|
Breast cancer risk associated with BRCA1 and BRCA2 in diverse populations.
|
Academic Article
|
RASSF1A polymorphism A133S is associated with early onset breast cancer in BRCA1/2 mutation carriers.
|
Academic Article
|
Uptake and timing of bilateral prophylactic salpingo-oophorectomy among BRCA1 and BRCA2 mutation carriers.
|
Academic Article
|
An exploratory analysis of HER-2 amplification and overexpression in advanced endometrial carcinoma: a Gynecologic Oncology Group study.
|
Academic Article
|
Lack of association between common single nucleotide polymorphisms in the TERT-CLPTM1L locus and breast cancer in women of African ancestry.
|
Academic Article
|
Germline mutational analysis of the C19orf62 gene in African-American women with breast cancer.
|
Academic Article
|
Evaluation of 19 susceptibility loci of breast cancer in women of African ancestry.
|
Academic Article
|
Should genetic testing for BRCA1/2 be permitted for minors? Opinions of BRCA mutation carriers and their adult offspring.
|
Academic Article
|
Genetic determinants of breast cancer risk: a review of current literature and issues pertaining to clinical application.
|
Academic Article
|
Genetic susceptibility to type 2 diabetes and breast cancer risk in women of European and African ancestry.
|
Academic Article
|
Recurrent BRCA1 and BRCA2 mutations in breast cancer patients of African ancestry.
|
Academic Article
|
Novel germline PALB2 truncating mutations in African American breast cancer patients.
|
Academic Article
|
Risk assessment and genetic testing for ovarian cancer.
|
Academic Article
|
Modification of BRCA1-Associated Breast and Ovarian Cancer Risk by BRCA1-Interacting Genes.
|
Academic Article
|
Basal-like Breast cancer DNA copy number losses identify genes involved in genomic instability, response to therapy, and patient survival.
|
Academic Article
|
When parents disclose BRCA1/2 test results: their communication and perceptions of offspring response.
|
Academic Article
|
Ancestry-shift refinement mapping of the C6orf97-ESR1 breast cancer susceptibility locus.
|
Academic Article
|
Breast and ovarian cancer risk and risk reduction in Jewish BRCA1/2 mutation carriers.
|
Academic Article
|
Risk of ipsilateral breast cancer in BRCA1 and BRCA2 mutation carriers.
|
Academic Article
|
Differential allelic expression of c.1568C > A at UGT2B15 is due to variation in a novel cis-regulatory element in the 3'UTR.
|
Academic Article
|
Performance of Lynch syndrome predictive models in a multi-center US referral population.
|
Academic Article
|
Variants at 6q21 implicate PRDM1 in the etiology of therapy-induced second malignancies after Hodgkin's lymphoma.
|
Academic Article
|
Microsatellites in the estrogen receptor (ESR1, ESR2) and androgen receptor (AR) genes and breast cancer risk in African American and Nigerian women.
|
Academic Article
|
High prevalence of BRCA1 and BRCA2 mutations in unselected Nigerian breast cancer patients.
|
Academic Article
|
DNA repair genes XPC, XPG polymorphisms: relation to the risk of colorectal carcinoma and therapeutic outcome with Oxaliplatin-based adjuvant chemotherapy.
|
Academic Article
|
Computerized analysis of mammographic parenchymal patterns on a large clinical dataset of full-field digital mammograms: robustness study with two high-risk datasets.
|
Academic Article
|
Refined mapping of genomic rearrangements involving the short arm of chromosome 9 in acute lymphoblastic leukemias and other hematologic malignancies.
|
Academic Article
|
Construction of a 2.8-megabase yeast artificial chromosome contig and cloning of the human methylthioadenosine phosphorylase gene from the tumor suppressor region on 9p21.
|
Academic Article
|
Detection of 9p deletions in leukemia cell lines by interphase fluorescence in situ hybridization with YAC-derived probes.
|
Academic Article
|
A method for screening arrayed cosmid libraries with mega insert yeast artificial chromosomes.
|
Academic Article
|
p16 alterations and deletion mapping of 9p21-p22 in malignant mesothelioma.
|
Academic Article
|
BRCA2 mutation and the risk of hematologic malignancy.
|
Academic Article
|
Breakpoint junctions of chromosome 9p deletions in two human glioma cell lines.
|
Academic Article
|
A genome-wide screen for promoter methylation in lung cancer identifies novel methylation markers for multiple malignancies.
|
Academic Article
|
A nonsynonymous polymorphism in IRS1 modifies risk of developing breast and ovarian cancers in BRCA1 and ovarian cancer in BRCA2 mutation carriers.
|
Academic Article
|
Analysis of tumor suppressor gene on human chromosome 9 in mouse x human somatic cell hybrids.
|
Academic Article
|
Correlation of cytogenetic analysis and loss of heterozygosity studies in human diffuse astrocytomas and mixed oligo-astrocytomas.
|
Academic Article
|
Structure of the human type-I interferon gene cluster determined from a YAC clone contig.
|
Academic Article
|
RAD51 135G-->C modifies breast cancer risk among BRCA2 mutation carriers: results from a combined analysis of 19 studies.
|
Academic Article
|
Genetic variation in IGFBP2 and IGFBP5 is associated with breast cancer in populations of African descent.
|
Academic Article
|
Evidence for an ancient BRCA1 mutation in breast cancer patients of Yoruban ancestry.
|
Academic Article
|
Homozygous deletions within chromosomal bands 9p21-22 in bladder cancer.
|
Academic Article
|
Mapping a putative tumor suppressor gene on chromosome 9 bands p21-p22 with microdissection probes.
|
Academic Article
|
CpG island methylation affects accessibility of the proximal BRCA1 promoter to transcription factors.
|
Academic Article
|
Searching for large genomic rearrangements of the BRCA1 gene in a Nigerian population.
|
Academic Article
|
Association of risk-reducing surgery in BRCA1 or BRCA2 mutation carriers with cancer risk and mortality.
|
Academic Article
|
Predictors of contralateral breast cancer in BRCA1 and BRCA2 mutation carriers.
|
Academic Article
|
A signature of balancing selection in the region upstream to the human UGT2B4 gene and implications for breast cancer risk.
|
Academic Article
|
Molecular analysis of colorectal tumors within a diverse patient cohort at a single institution.
|
Academic Article
|
Increased p16 levels correlate with pRb alterations in human urothelial cells.
|
Academic Article
|
Lack of evidence for a polymorphism at codon 160 of human O6-alkylguanine-DNA alkyltransferase gene in normal tissue and cancer.
|
Academic Article
|
Progesterone receptor variant increases ovarian cancer risk in BRCA1 and BRCA2 mutation carriers who were never exposed to oral contraceptives.
|
Academic Article
|
Cyclin D1 amplification and p16(MTS1/CDK4I) deletion correlate with poor prognosis in head and neck tumors.
|
Academic Article
|
Direct-to-consumer marketing of genetic tests for cancer: buyer beware.
|
Academic Article
|
The risk of ovarian cancer after breast cancer in BRCA1 and BRCA2 carriers.
|
Academic Article
|
Distinct deletions of chromosome 9p associated with melanoma versus glioma, lung cancer, and leukemia.
|
Academic Article
|
A comparison of bilateral breast cancers in BRCA carriers.
|
Academic Article
|
UDP-Glucuronosyltransferase 1A1 gene polymorphisms and total bilirubin levels in an ethnically diverse cohort of women.
|
Academic Article
|
Genetic susceptibility to breast cancer.
|
Academic Article
|
Genetic testing in diverse populations: are researchers doing enough to get out the correct message?
|
Academic Article
|
Genomewide scan for loss of heterozygosity and chromosomal amplification in breast carcinoma using single-nucleotide polymorphism arrays.
|
Academic Article
|
Parent opinions regarding the genetic testing of minors for BRCA1/2.
|
Academic Article
|
Common genetic variation at BARD1 is not associated with breast cancer risk in BRCA1 or BRCA2 mutation carriers.
|
Academic Article
|
Genetic variation in IGF2 and HTRA1 and breast cancer risk among BRCA1 and BRCA2 carriers.
|
Academic Article
|
Early onset HER2-positive breast cancer is associated with germline TP53 mutations.
|
Academic Article
|
Lack of association between common UGT2B nonsynonymous single-nucleotide polymorphisms and breast cancer in populations of African ancestry.
|
Academic Article
|
Clinical implications of ERĆ methylation on sporadic breast cancers in Chinese women.
|
Academic Article
|
Chemotherapy response and recurrence-free survival in neoadjuvant breast cancer depends on biomarker profiles: results from the I-SPY 1 TRIAL (CALGB 150007/150012; ACRIN 6657).
|
Academic Article
|
ColoSeq provides comprehensive lynch and polyposis syndrome mutational analysis using massively parallel sequencing.
|
Academic Article
|
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.
|
Academic Article
|
Fine mapping of breast cancer genome-wide association studies loci in women of African ancestry identifies novel susceptibility markers.
|
Academic Article
|
Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk.
|
Academic Article
|
A genome-wide association study of breast cancer in women of African ancestry.
|
Academic Article
|
Proposal for the clinical detection and management of patients and their family members with familial myelodysplastic syndrome/acute leukemia predisposition syndromes.
|
Academic Article
|
MicroRNA-30c targets cytoskeleton genes involved in breast cancer cell invasion.
|
Academic Article
|
Molecular phenotype predicts sensitivity of squamous cell carcinoma of the head and neck to epidermal growth factor receptor inhibition.
|
Academic Article
|
Level of awareness of mammography among women attending outpatient clinics in a teaching hospital in Ibadan, South-West Nigeria.
|
Academic Article
|
MicroRNA-30c inhibits human breast tumour chemotherapy resistance by regulating TWF1 and IL-11.
|
Academic Article
|
Genome-wide profiles of CtBP link metabolism with genome stability and epithelial reprogramming in breast cancer.
|
Academic Article
|
A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry.
|
Academic Article
|
Classification of breast lesions pre-contrast injection using water resonance lineshape analysis.
|
Academic Article
|
Inherited predisposition to breast cancer among African American women.
|
Academic Article
|
Tumor genome analysis includes germline genome: are we ready for surprises?
|
Academic Article
|
Differentiation and loss of malignant character of spontaneous pulmonary metastases in patient-derived breast cancer models.
|
Academic Article
|
Identification of six new susceptibility loci for invasive epithelial ovarian cancer.
|
Academic Article
|
National survey of US oncologists' knowledge, attitudes, and practice patterns regarding herb and supplement use by patients with cancer.
|
Academic Article
|
Candidate genetic modifiers for breast and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers.
|
Academic Article
|
Expression of polycomb targets predicts breast cancer prognosis.
|
Academic Article
|
MYC overexpression and poor prognosis in sporadic breast cancer with BRCA1 deficiency.
|
Academic Article
|
Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer.
|
Academic Article
|
Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriers.
|
Academic Article
|
DNA glycosylases involved in base excision repair may be associated with cancer risk in BRCA1 and BRCA2 mutation carriers.
|
Academic Article
|
Pilot study demonstrating potential association between breast cancer image-based risk phenotypes and genomic biomarkers.
|
Academic Article
|
A comprehensive examination of breast cancer risk loci in African American women.
|
Academic Article
|
Use of Web-based training for quality improvement between a field immunohistochemistry laboratory in Nigeria and its United States-based partner institution.
|
Academic Article
|
Development of a tiered and binned genetic counseling model for informed consent in the era of multiplex testing for cancer susceptibility.
|
Academic Article
|
An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers.
|
Academic Article
|
Effect of Oophorectomy on Survival After Breast Cancer in BRCA1 and BRCA2 Mutation Carriers.
|
Academic Article
|
Molecular Subtype-Specific Expression of MicroRNA-29c in Breast Cancer Is Associated with CpG Dinucleotide Methylation of the Promoter.
|
Academic Article
|
BRCA2 Polymorphic Stop Codon K3326X and the Risk of Breast, Prostate, and Ovarian Cancers.
|
Academic Article
|
Inherited mutations in cancer susceptibility genes are common among survivors of breast cancer who develop therapy-related leukemia.
|
Academic Article
|
Male breast cancer in BRCA1 and BRCA2 mutation carriers: pathology data from the Consortium of Investigators of Modifiers of BRCA1/2.
|
Academic Article
|
The Breast-Thyroid Cancer Link: A Systematic Review and Meta-analysis.
|
Academic Article
|
Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170.
|
Academic Article
|
Ć-catenin regulates c-Myc and CDKN1A expression in breast cancer cells.
|
Academic Article
|
Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer.
|
Academic Article
|
Building local capacity for genomics research in Africa: recommendations from analysis of publications in Sub-Saharan Africa from 2004 to 2013.
|
Academic Article
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Genetic anticipation in BRCA1/BRCA2 families after controlling for ascertainment bias and cohort effect.
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Academic Article
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Naturally occurring BRCA2 alternative mRNA splicing events in clinically relevant samples.
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Academic Article
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Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus.
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Academic Article
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Fine-Scale Mapping at 9p22.2 Identifies Candidate Causal Variants That Modify Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers.
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Academic Article
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Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus.
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Academic Article
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Genetic variants in microRNA and microRNA biogenesis pathway genes and breast cancer risk among women of African ancestry.
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Academic Article
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A continuum of admixture in the Western Hemisphere revealed by the African Diaspora genome.
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Academic Article
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Effect of BRCA germline mutations on breast cancer prognosis: A systematic review and meta-analysis.
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Academic Article
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Haplotype analyses of the c.1027C>T and c.2167_2168delAT recurrent truncating mutations in the breast cancer-predisposing gene PALB2.
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Academic Article
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Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of breast cancer risk at locus 11q22.3.
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Academic Article
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Genetic and Epigenetic Regulation of TOX3 Expression in Breast Cancer.
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Academic Article
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Inheritance of deleterious mutations at both BRCA1 and BRCA2 in an international sample of 32,295 women.
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Academic Article
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Evaluation of the Quality of Adjuvant Endocrine Therapy Delivery for Breast Cancer Care in the United States.
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Academic Article
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Building local capacity for genomics research in Africa: recommendations from analysis of publications in Sub-Saharan Africa from 2004 to 2013.
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Academic Article
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Genome-wide association studies in women of African ancestry identified 3q26.21 as a novel susceptibility locus for oestrogen receptor negative breast cancer.
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Academic Article
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Parental disclosure of genetic test results to young adults, adolescents and children.
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Academic Article
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Should genetic testing for BRCA1/2 be permitted for minors? Opinions of parents who completed BRCA1/2 testing.
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Academic Article
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Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer.
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Academic Article
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Characterizing Genetic Susceptibility to Breast Cancer in Women of African Ancestry.
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Academic Article
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Association of breast cancer risk and the mTOR pathway in women of African ancestry in 'The Root' Consortium.
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Academic Article
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Comparison of Breast Cancer Molecular Features and Survival by African and European Ancestry in The Cancer Genome Atlas.
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Academic Article
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Evaluation of Polygenic Risk Scores for Breast and Ovarian Cancer Risk Prediction in BRCA1 and BRCA2 Mutation Carriers.
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Academic Article
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Genetic variants demonstrating flip-flop phenomenon and breast cancer risk prediction among women of African ancestry.
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Academic Article
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Inherited Breast Cancer in Nigerian Women.
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Academic Article
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Genetic variation in the vitamin D related pathway and breast cancer risk in women of African ancestry in the root consortium.
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Academic Article
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Community clinical practice patterns and mortality in patients with intermediate oncotype DX recurrence scores: Who benefits from chemotherapy?
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Academic Article
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HIF-2a promotes conversion to a stem cell phenotype and induces chemoresistance in breast cancer cells by activating Wnt and Notch pathways.
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Academic Article
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LncRNA BLAT1 is Upregulated in Basal-like Breast Cancer through Epigenetic Modifications.
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Academic Article
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Randomized Noninferiority Trial of Telephone vs In-Person Disclosure of Germline Cancer Genetic Test Results.
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Academic Article
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Mutations in context: implications of BRCA testing in diverse populations.
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Academic Article
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A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer.
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Academic Article
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Genetic Ancestry May Influence the Evolutionary Trajectory of Cancers.
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Academic Article
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Genetic variation in the Hippo pathway and breast cancer risk in women of African ancestry.
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Academic Article
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Preferences for in-person disclosure: Patients declining telephone disclosure characteristics and outcomes in the multicenter Communication Of GENetic Test Results by Telephone study.
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Academic Article
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Knowledge of Genetic Counseling Among Patients With Breast Cancer and Their Relatives at a Nigerian Teaching Hospital.
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Academic Article
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Association analysis identifies 65 new breast cancer risk loci.
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Academic Article
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A meta-analysis approach with filtering for identifying gene-level gene-environment interactions.
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Academic Article
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Association of Pancreatic Cancer Susceptibility Variants with Risk of Breast Cancer in Women of European and African Ancestry.
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Academic Article
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Characterization of Nigerian breast cancer reveals prevalent homologous recombination deficiency and aggressive molecular features.
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Academic Article
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Clinical interpretation of pathogenic ATM and CHEK2 variants on multigene panel tests: navigating moderate risk.
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Academic Article
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Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations.
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Academic Article
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Intensive Surveillance with Biannual Dynamic Contrast-Enhanced Magnetic Resonance Imaging Downstages Breast Cancer in BRCA1 Mutation Carriers.
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Academic Article
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Population-dependent Intron Retention and DNA Methylation in Breast Cancer.
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Academic Article
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Efficacy of Anti-HER2 Agents in Combination With Adjuvant or Neoadjuvant Chemotherapy for Early and Locally Advanced HER2-Positive Breast Cancer Patients: A Network Meta-Analysis.
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Academic Article
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Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer.
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Academic Article
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Breast Cancer Genetics Knowledge and Testing Intentions among Nigerian Professional Women.
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Academic Article
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Cancer Susceptibility Genetic Testing in a High-Risk Cohort of Urban Ashkenazi Jewish Individuals.
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Academic Article
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Trans-ethnic predicted expression genome-wide association analysis identifies a gene for estrogen receptor-negative breast cancer.
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Academic Article
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A Transcriptome-Wide Association Study Among 97,898 Women to Identify Candidate Susceptibility Genes for Epithelial Ovarian Cancer Risk.
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Academic Article
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Assembly of a pan-genome from deep sequencing of 910 humans of African descent.
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Academic Article
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Height and Body Mass Index as Modifiers of Breast Cancer Risk in BRCA1/2 Mutation Carriers: A Mendelian Randomization Study.
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Academic Article
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Author Correction: Characterization of Nigerian breast cancer reveals prevalent homologous recombination deficiency and aggressive molecular features.
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Academic Article
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Identification of novel common breast cancer risk variants at the 6q25 locusĀ among Latinas.
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Academic Article
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Shared heritability and functional enrichment across six solid cancers.
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Academic Article
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Oophorectomy and risk of contralateral breast cancer among BRCA1 and BRCA2 mutation carriers.
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Academic Article
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Association study in African-admixed populations across the Americas recapitulates asthma risk loci in non-African populations.
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Academic Article
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N-acetyltransferase 2 enzyme genotype-phenotype discordances in both HIV-negative and HIV-positive Nigerians.
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Academic Article
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Inhibition of Copper Transport Induces Apoptosis in Triple-Negative Breast Cancer Cells and Suppresses Tumor Angiogenesis.
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Academic Article
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Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer.
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Grant
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UChicago Interdisciplinary Cancer Health Disparities SPORE
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Academic Article
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BRCA1 and BRCA2 pathogenic sequence variants in women of African origin or ancestry.
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Academic Article
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Germline variants and somatic mutation signatures of breast cancer across populations of African and European ancestry in the US and Nigeria.
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Academic Article
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The spectrum of BRCA1 and BRCA2 pathogenic sequence variants in Middle Eastern, North African, and South European countries.
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Academic Article
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Mendelian randomisation study of height and body mass index as modifiers of ovarian cancer risk in 22,588 BRCA1 and BRCA2 mutation carriers.
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Academic Article
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The Time for Mainstreaming Germline Testing for Patients With Breast Cancer Is Now.
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Academic Article
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Hematologic toxicity in BRCA1 and BRCA2 mutation carriers during chemotherapy: A retrospective matched cohort study.
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Academic Article
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USPSTF Recommendations for BRCA1 and BRCA2 Testing in the Context of a Transformative National Cancer Control Plan.
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Academic Article
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Breast Cancer Risk-Associated SNPs in the mTOR Promoter Form De Novo KLF5- and ZEB1-Binding Sites that Influence the Cellular Response to Paclitaxel.
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Academic Article
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Two truncating variants in FANCC and breast cancer risk.
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Academic Article
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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) Clinical Working Group.
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Academic Article
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Association of Genomic Domains in BRCA1 and BRCA2 with Prostate Cancer Risk and Aggressiveness.
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Academic Article
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Use and Patient-Reported Outcomes of Clinical Multigene Panel Testing for Cancer Susceptibility in the Multicenter Communication of Genetic Test Results by Telephone Study.
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Academic Article
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Cancer Risks Associated With Germline PALB2 Pathogenic Variants: An International Study of 524 Families.
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Academic Article
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Prevalence of Inherited Mutations in Breast Cancer Predisposition Genes among Women in Uganda and Cameroon.
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Academic Article
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Infrastructural Challenges Lead to Delay of Curative Radiotherapy in Nigeria.
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Academic Article
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Propensity score analysis of the prognostic value of genomic assays for breast cancer in diverse populations using the National Cancer Data Base.
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Academic Article
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Germline HOXB13 mutations p.G84E and p.R217C do not confer an increased breast cancer risk.
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Academic Article
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Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants.
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Academic Article
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Association of Event-Free and Distant Recurrence-Free Survival With Individual-Level Pathologic Complete Response in Neoadjuvant Treatment of Stages 2 and 3 Breast Cancer: Three-Year Follow-up Analysis for the I-SPY2 Adaptively Randomized Clinical Trial.
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Academic Article
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Evaluating the Effect of Medicaid Expansion on Black/White Breast Cancer Mortality Disparities: A Difference-in-Difference Analysis.
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Academic Article
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Racial disparities in survival outcomes among breast cancer patients by molecular subtypes.
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Academic Article
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Impact of post-diagnosis weight change on survival outcomes in Black and White breast cancer patients.
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Academic Article
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A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers.
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Academic Article
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Evaluating Polygenic Risk Scores for Breast Cancer in Women of African Ancestry.
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Academic Article
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Breastfeeding and the risk of epithelial ovarian cancer among women with a BRCA1 or BRCA2 mutation.
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Academic Article
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Longitudinal follow-up after telephone disclosure in the randomized COGENT study.
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Academic Article
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Precision oncology: Directing genomics and pharmacogenomics toward reducing cancer inequities.
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Academic Article
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Cross-ancestry GWAS meta-analysis identifies six breast cancer loci in African and European ancestry women.
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Academic Article
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Effects of Slide Storage on Detection of Molecular Markers by IHC and FISH in Endometrial Cancer Tissues From a Clinical Trial: An NRG Oncology/GOG Pilot Study.
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Academic Article
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The impact of site-specific digital histology signatures on deep learning model accuracy and bias.
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Academic Article
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Associations between age of menarche and genetic variation in women of African descent: genome-wide association study and polygenic score analysis.
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Academic Article
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Whole-genome analysis of Nigerian patients with breast cancer reveals ethnic-driven somatic evolution and distinct genomic subtypes.
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Academic Article
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Polygenic risk modeling for prediction of epithelial ovarian cancer risk.
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Academic Article
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Polygenic risk scores for prediction of breast cancer risk in women of African ancestry: a cross-ancestry approach.
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Academic Article
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Aggregation tests identify new gene associations with breast cancer in populations with diverse ancestry.
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Academic Article
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Cancer Genetic Services in a Low- to Middle-Income Country: Cross-Sectional Survey Assessing Willingness to Undergo and Pay for Germline Genetic Testing.
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Grant
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Basic Medical Research Training in Oncology
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Grant
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Genome-wide association study of breast cancer in the African Diaspora
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Grant
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CHARACTERIZATION OF A TUMOR SUPPRESSOR GENE ON 9P
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Grant
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Scholars in Oncology Associated Research (SOAR)
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Grant
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Africa Cancer Leaders Institute
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Grant
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Genetics of Breast Cancer in Blacks
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Grant
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International Partnership for Interdisciplinary Research Training
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Grant
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Conference and Workshop on New Frontiers in diagnosis, screening and management of inherited cancer syndromes
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Grant
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SPORE in Breast Cancer
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Grant
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Using Genomics to Reduce Breast Cancer Disparities in the African Diaspora
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Academic Article
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Prediction of Breast and Prostate Cancer Risks in Male BRCA1 and BRCA2 Mutation Carriers Using Polygenic Risk Scores.
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Academic Article
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A joint transcriptome-wide association study across multiple tissues identifies candidate breast cancer susceptibility genes.
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Academic Article
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Molecular profiling of a real-world breast cancer cohort with genetically inferred ancestries reveals actionable tumor biology differences between European ancestry and African ancestry patient populations.
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Academic Article
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Mutational spectrum of breast cancer susceptibility genes among women ascertained in a cancer risk clinic in Northeast Brazil.
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Academic Article
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Detection of germline variants in Brazilian breast cancer patients using multigene panel testing.
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Academic Article
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Profile of Pathogenic Mutations and Evaluation of Germline Genetic Testing Criteria in Consecutive Breast Cancer Patients Treated at a North Indian Tertiary Care Center.
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Academic Article
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The risks of cancer in older women with BRCA pathogenic variants: How far have we come?
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Academic Article
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Weight Gain and the Risk of Ovarian Cancer in BRCA1 and BRCA2 Mutation Carriers.
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Academic Article
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Racial/Ethnic Disparities in Telemedicine Utilization and Satisfaction Among Breast Cancer Patients During the COVID-19 Pandemic: A Mixed-Methods Analysis.
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Academic Article
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Erratum: Feasibility of cancer genetic counselling and screening in Cameroon: perceived benefits and barriers.
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Academic Article
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Feasibility of cancer genetic counselling and screening in Cameroon: perceived benefits and barriers.
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Academic Article
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Remotely Delivered Cancer Genetic Testing in the Making Genetic Testing Accessible (MAGENTA) Trial: A Randomized Clinical Trial.
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Academic Article
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Breast Cancer Germline Genetic Counseling and Testing for Populations of African Heritage Globally: A Scoping Review on Research, Practice, and Bioethical Considerations.
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