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Sharon N. Teraoka

Sharon N. Teraoka,University of Virginia,Genetics & Genealogy,Oncology,Anatomy

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Sharon N. Teraoka

University of Virginia

Publications: 17 | Citations: 310

Fields: Genetics & Genealogy, Oncology, Anatomy

Collaborated with 94 co-authors from 1996 to 2011 | Cited by 1390 authors

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Publications (17)

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Risk of contralateral breast cancer associated with common variants in BRCA1 and BRCA2 : potential modifying effect of BRCA1/BRCA2 mutation carrier status (Citations: 1)

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Journal: Breast Cancer Research and Treatment - BREAST CANCER RES TREAT , vol. 127, no. 3, pp. 819-829, 2011

Radiation Exposure, the ATM Gene, and Contralateral Breast Cancer in the Women's Environmental Cancer and Radiation Epidemiology Study (Citations: 8)

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Journal: Journal of The National Cancer Institute - J NAT CANCER INST , vol. 102, no. 7, pp. 475-483, 2010

Population-Based Study of the Risk of Second Primary Contralateral Breast Cancer Associated With Carrying a Mutation in BRCA1 or BRCA2 (Citations: 6)

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Journal: Journal of Clinical Oncology - J CLIN ONCOL , vol. 28, no. 14, pp. 2404-2410, 2010

Characterization of BRCA1 and BRCA2 deleterious mutations and variants of unknown clinical significance in unilateral and bilateral breast cancer: the WECARE study (Citations: 5)

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Journal: Human Mutation - HUM MUTAT , vol. 31, no. 3, pp. E1200-E1240, 2010

Adjuvant systemic therapy for breast cancer in BRCA1/BRCA2 mutation carriers in a population-based study of risk of contralateral breast cancer (Citations: 2)

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Journal: Breast Cancer Research and Treatment - BREAST CANCER RES TREAT , vol. 123, no. 2, pp. 491-498, 2010

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Citations (310 times by 263 publications)

Full-Exon Pyrosequencing Screening of BRCA Germline Mutations in Mexican Women with Inherited Breast and Ovarian Cancer

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Journal: PLOS One , vol. 7, no. 5, 2012

Multimodel assessment of BRCA1 mutations in Taiwanese (ethnic Chinese) women with early-onset, bilateral or familial breast cancer

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Journal: Journal of Human Genetics - J HUM GENET , vol. 57, no. 2, pp. 130-138, 2012

The dual effect of the lupus-associated polymorphism rs10516487 on BANK1 gene expression and protein localization

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Journal: Genes and Immunity - GENES IMMUN , vol. 13, no. 2, pp. 129-138, 2012

Rare, evolutionarily unlikely missense substitutions in CHEK2 contribute to breast cancer susceptibility: results from a breast cancer family registry case-control mutation-screening study (Citations: 2)

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Journal: Breast Cancer Research - BREAST CANCER RES , vol. 13, no. 1, pp. R6-12, 2011

Risk of contralateral breast cancer associated with common variants in BRCA1 and BRCA2 : potential modifying effect of BRCA1/BRCA2 mutation carrier status (Citations: 1)

, , , , , , , , , , , http://academic.research.microsoft.com/io.ashx?type=5&id=47939129&selfId1=5371770&selfId2=0&maxNumber=12&query=

Journal: Breast Cancer Research and Treatment - BREAST CANCER RES TREAT , vol. 127, no. 3, pp. 819-829, 2011

Comments

Co-authors (94)

Journals (10)

Keywords (58)

Sharon N. Teraoka,University of Virginia,Genetics & Genealogy,Oncology,Anatomy

Publications (17)

BibTeX | RIS | RefWorks Download

Risk of contralateral breast cancer associated with common variants in BRCA1 and BRCA2 : potential modifying effect of BRCA1/BRCA2 mutation carrier status (Citations: 1)

Radiation Exposure, the ATM Gene, and Contralateral Breast Cancer in the Women's Environmental Cancer and Radiation Epidemiology Study (Citations: 8)

Population-Based Study of the Risk of Second Primary Contralateral Breast Cancer Associated With Carrying a Mutation in BRCA1 or BRCA2 (Citations: 6)

Characterization of BRCA1 and BRCA2 deleterious mutations and variants of unknown clinical significance in unilateral and bilateral breast cancer: the WECARE study (Citations: 5)

Adjuvant systemic therapy for breast cancer in BRCA1/BRCA2 mutation carriers in a population-based study of risk of contralateral breast cancer (Citations: 2)

Citations (310 times by 263 publications)

Full-Exon Pyrosequencing Screening of BRCA Germline Mutations in Mexican Women with Inherited Breast and Ovarian Cancer

Multimodel assessment of BRCA1 mutations in Taiwanese (ethnic Chinese) women with early-onset, bilateral or familial breast cancer

The dual effect of the lupus-associated polymorphism rs10516487 on BANK1 gene expression and protein localization

Rare, evolutionarily unlikely missense substitutions in CHEK2 contribute to breast cancer susceptibility: results from a breast cancer family registry case-control mutation-screening study (Citations: 2)

Risk of contralateral breast cancer associated with common variants in BRCA1 and BRCA2 : potential modifying effect of BRCA1/BRCA2 mutation carrier status (Citations: 1)


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Co-authors (94)

Journals (10)

Keywords (58)

Sharon N. Teraoka,University of Virginia,Genetics & Genealogy,Oncology,Anatomy

Publications (17) BibTeX | RIS | RefWorks Download

Risk of contralateral breast cancer associated with common variants in BRCA1 and BRCA2 : potential modifying effect of BRCA1/BRCA2 mutation carrier status (Citations: 1)

Radiation Exposure, the ATM Gene, and Contralateral Breast Cancer in the Women's Environmental Cancer and Radiation Epidemiology Study (Citations: 8)

Population-Based Study of the Risk of Second Primary Contralateral Breast Cancer Associated With Carrying a Mutation in BRCA1 or BRCA2 (Citations: 6)

Characterization of BRCA1 and BRCA2 deleterious mutations and variants of unknown clinical significance in unilateral and bilateral breast cancer: the WECARE study (Citations: 5)

Adjuvant systemic therapy for breast cancer in BRCA1/BRCA2 mutation carriers in a population-based study of risk of contralateral breast cancer (Citations: 2)

Citations (310 times by 263 publications)

Full-Exon Pyrosequencing Screening of BRCA Germline Mutations in Mexican Women with Inherited Breast and Ovarian Cancer

Multimodel assessment of BRCA1 mutations in Taiwanese (ethnic Chinese) women with early-onset, bilateral or familial breast cancer

The dual effect of the lupus-associated polymorphism rs10516487 on BANK1 gene expression and protein localization

Rare, evolutionarily unlikely missense substitutions in CHEK2 contribute to breast cancer susceptibility: results from a breast cancer family registry case-control mutation-screening study (Citations: 2)

Risk of contralateral breast cancer associated with common variants in BRCA1 and BRCA2 : potential modifying effect of BRCA1/BRCA2 mutation carrier status (Citations: 1)

Publications (17)

BibTeX | RIS | RefWorks Download