667 results on '"Yang, Xiaohong R."'
Search Results
202. Phenotypic and Histopathological Tumor Characteristics According to CDKN2A Mutation Status among Affected Members of Melanoma Families
203. Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer
204. Hoyeraal-Hreidarsson Syndrome due to PARN Mutations: Fourteen Years of Follow-Up
205. Heterogeneity of luminal breast cancer characterised by immunohistochemical expression of basal markers
206. Melanoma prone families with CDK4 germline mutation: phenotypic profile and associations with MC1R variants
207. Germline mutations in <italic>Protection of Telomeres 1</italic> in two families with Hodgkin lymphoma.
208. A comprehensive analysis of polymorphic variants in steroid hormone and insulin‐like growth factor‐1 metabolism and risk of <italic>in situ</italic> breast cancer: Results from the Breast and Prostate Cancer Cohort Consortium.
209. On the interplay of telomeres, nevi and the risk of melanoma
210. Peripheral blood immunologic phenotype of population-based breast cancer cases and matched controls
211. Abstract 5570: Heterogeneity of luminal breast cancer characterized by immunohistochemical expression of basal markers
212. Female Breast Cancer Incidence Among Asian and Western Populations: More Similar Than Expected
213. Characterization of Genomic Alterations in Radiation-Associated Breast Cancer among Childhood Cancer Survivors, Using Comparative Genomic Hybridization (CGH) Arrays
214. Tumor Intrinsic Subtype Is Reflected in Cancer-Adjacent Tissue
215. Greater absolute risk for all subtypes of breast cancer in the US than Malaysia
216. Age-related terminal duct lobular unit involution in benign tissues from Chinese breast cancer patients with luminal and triple-negative tumors.
217. Disparities of time trends and birth cohort effects on invasive breast cancer incidence in Shanghai and Hong Kong pre- and post-menopausal women.
218. Abstract C81: Differences in breast cancer incidence and survival patterns by tumor subtype and ethnicity in Sarawak, Malaysia
219. Abstract LB-288: Differential cohort effect on early- and late-onset breast cancer incidence among Chinese women in different populations
220. VTET: a variable threshold exact test for identifying disease-associated copy number variations enriched in short genomic regions
221. Association of Genetic Variants in CDK6 and XRCC1 with the Risk of Dysplastic Nevi in Melanoma-Prone Families
222. Parity-related molecular signatures and breast cancer subtypes by estrogen receptor status
223. Risks of Melanoma and Other Cancers in Melanoma-Prone Families over 4 Decades
224. Germline Variation at CDKN2Aand Associations with Nevus Phenotypes among Members of Melanoma Families
225. Breast cancer susceptibility risk associations and heterogeneity by E-cadherin tumor tissue expression
226. Prolactin Receptor Expression and Breast Cancer: Relationships with Tumor Characteristics among Pre- and Post-menopausal Women in a Population-Based Case–Control Study from Poland
227. Telomere Length and the Risk of Cutaneous Malignant Melanoma in Melanoma-Prone Families with and without CDKN2A Mutations
228. Abstract 688: Promoter methylation of death receptor decoy genes in blood and risk of melanoma in melanoma-prone families .
229. Melanoma prone families withCDK4germline mutation: phenotypic profile and associations withMC1Rvariants
230. LINE-1 methylation in peripheral blood and the risk of melanoma in melanoma-prone families with and without CDKN2A mutations
231. Risk assessment model for invasive breast cancer in Hong Kong women.
232. Emerging Concepts in Breast Cancer Risk Prediction
233. Estrogen receptor and progesterone receptor expression in normal terminal duct lobular units surrounding invasive breast cancer
234. On the Interplay of Telomeres, Nevi and the Risk of Melanoma
235. Abstract LB-336: Association of variant rs2046210 at 6q25.1 (ESR1) with breast cancer risk suggests heterogeneity by E-cadherin tumor tissue expression
236. Analysis of terminal duct lobular unit involution in luminal A and basal breast cancers
237. Peripheral blood immunologic phenotype of population-based breast cancer cases and matched controls
238. Genetic variants in DNA repair genes and the risk of cutaneous malignant melanoma in melanoma-prone families with/without CDKN2A mutations
239. Associations of Breast Cancer Risk Factors With Tumor Subtypes: A Pooled Analysis From the Breast Cancer Association Consortium Studies
240. Abstract 2779: Relationship of mammographic density with breast cancer subtypes
241. Assessment of Automated Image Analysis of Breast Cancer Tissue Microarrays for Epidemiologic Studies
242. Identifying rheumatoid arthritis susceptibility genes using high-dimensional methods
243. Expression of TGF-β signaling factors in invasive breast cancers: relationships with age at diagnosis and tumor characteristics
244. DNA Hypermethylation of ESR1 and PGR in Breast Cancer: Pathologic and Epidemiologic Associations
245. T (brachyury) gene duplication confers major susceptibility to familial chordoma
246. Mutation screening of CHD5 in melanoma-prone families linked to 1p36 revealed no deleterious coding or splice site changes
247. Linkage analysis of anti-CCP levels as dichotomized and quantitative traits using GAW15 single-nucleotide polymorphism scan of NARAC families
248. Hormonal Markers in Breast Cancer: Coexpression, Relationship with Pathologic Characteristics, and Risk Factor Associations in a Population-Based Study
249. Variation in breast cancer hormone receptor andHER2levels by etiologic factors: A population-based analysis
250. Differences in Risk Factors for Breast Cancer Molecular Subtypes in a Population-Based Study
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