Search Results - "Mandell, Jessica" :: K.UTB vyhledávací portál | TBU Library Retrieval Portal

Population-based screening for breast and ovarian cancer risk due to BRCA1 and BRCA2

Population-based screening for breast and ovarian cancer risk due to BRCA1 and BRCA2

by Gabai-Kapara, Efrat, Lahad, Amnon, Kaufman, Bella, Friedman, Eitan, Segev, Shlomo, Renbaum, Paul, Beeri, Rachel, Gal, Moran, Grinshpun-Cohen, Julia, Djemal, Karen, Mandell, Jessica B., Lee, Ming K., Beller, Uziel, Catane, Raphael, King, Mary-Claire, Levy-Lahad, Ephrat
Published in Proceedings of the National Academy of Sciences - PNAS (30.09.2014)

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Detection of inherited mutations for breast and ovarian cancer using genomic capture and massively parallel sequencing

Detection of inherited mutations for breast and ovarian cancer using genomic capture and massively parallel sequencing

by Walsh, Tom, Lee, Ming K., Casadei, Silvia, Thornton, Anne M., Stray, Sunday M., Pennil, Christopher, Nord, Alex S., Mandell, Jessica B., Swisher, Elizabeth M., King, Mary-Claire
Published in Proceedings of the National Academy of Sciences - PNAS (13.07.2010)

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CRISPR–Cas9/long-read sequencing approach to identify cryptic mutations in BRCA1 and other tumour suppressor genes

CRISPR–Cas9/long-read sequencing approach to identify cryptic mutations in BRCA1 and other tumour suppressor genes

by Walsh, Tom, Casadei, Silvia, Munson, Katherine M, Eng, Mary, Mandell, Jessica B, Gulsuner, Suleyman, King, Mary-Claire
Published in Journal of medical genetics (01.12.2021)

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Contribution of Inherited Mutations in the BRCA2-Interacting Protein PALB2 to Familial Breast Cancer

Contribution of Inherited Mutations in the BRCA2-Interacting Protein PALB2 to Familial Breast Cancer

by CASADEI, Silvia, NORQUIST, Barbara M, WALSH, Tom, STRAY, Sunday, MANDELL, Jessica B, LEE, Ming K, STAMATOYANNOPOULOS, John A, KING, Mary-Claire
Published in Cancer research (Chicago, Ill.) (15.03.2011)

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Parenting in matched pairs of women of color experiencing intimate partner violence and living with and without HIV

Parenting in matched pairs of women of color experiencing intimate partner violence and living with and without HIV

by Thurston, Idia B., Howell, Kathryn H., Kaufman, Caroline C., Mandell, Jessica E., Decker, Kristina M.
Published in Journal of traumatic stress (01.10.2021)

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Long-read DNA and cDNA sequencing identify cancer-predisposing deep intronic variation in tumor-suppressor genes

Long-read DNA and cDNA sequencing identify cancer-predisposing deep intronic variation in tumor-suppressor genes

by Gulsuner, Suleyman, AbuRayyan, Amal, Mandell, Jessica B, Lee, Ming K, Bernier, Greta V, Norquist, Barbara M, Pierce, Sarah B, King, Mary-Claire, Walsh, Tom
Published in Genome research (13.09.2024)

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Intersectional Epistemologies of Ignorance: How Behavioral and Social Science Research Shapes What We Know, Think We Know, and Don't Know About U.S. Black Men's Sexualities

Intersectional Epistemologies of Ignorance: How Behavioral and Social Science Research Shapes What We Know, Think We Know, and Don't Know About U.S. Black Men's Sexualities

by Bowleg, Lisa, del Río-González, Ana María, Holt, Sidney L., Pérez, Carolin, Massie, Jenné S., Mandell, Jessica E., A. Boone, Cheriko
Published in The Journal of sex research (13.06.2017)

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Association of Genetic Diagnoses for Childhood-Onset Hearing Loss With Cochlear Implant Outcomes

Association of Genetic Diagnoses for Childhood-Onset Hearing Loss With Cochlear Implant Outcomes

by Carlson, Ryan J, Walsh, Tom, Mandell, Jessica B, Aburayyan, Amal, Lee, Ming K, Gulsuner, Suleyman, Horn, David L, Ou, Henry C, Sie, Kathleen C Y, Mancl, Lisa, Rubinstein, Jay, King, Mary-Claire
Published in JAMA otolaryngology-- head & neck surgery (01.03.2023)

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Characterization of splice-altering mutations in inherited predisposition to cancer

Characterization of splice-altering mutations in inherited predisposition to cancer

by Casadei, Silvia, Gulsuner, Suleyman, Shirts, Brian H., Mandell, Jessica B., Kortbawi, Hannah M., Norquist, Barbara S., Swisher, Elizabeth M., Lee, Ming K., Goldberg, Yael, O’Connor, Robert, Tan, Zheng, Pritchard, Colin C., King, Mary-Claire, Walsha, Tom
Published in Proceedings of the National Academy of Sciences - PNAS (26.12.2019)

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Developmental Assets, Defiance, and Caregiver Communication among Black Adolescents with High Body Weights

Developmental Assets, Defiance, and Caregiver Communication among Black Adolescents with High Body Weights

by Mandell, Jessica E., Howell, Kathryn H., Thurston, Idia B.
Published in Journal of child and family studies (01.04.2022)

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Breast and Ovarian Cancer Risks Due to Inherited Mutations in BRCA1 and BRCA2

Breast and Ovarian Cancer Risks Due to Inherited Mutations in BRCA1 and BRCA2

by King, Mary-Claire, Marks, Joan H., Mandell, Jessica B., The New York Breast Cancer Study Group
Published in Science (American Association for the Advancement of Science) (24.10.2003)

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Genomic analysis of inherited breast cancer among Palestinian women: Genetic heterogeneity and a founder mutation in TP53

Genomic analysis of inherited breast cancer among Palestinian women: Genetic heterogeneity and a founder mutation in TP53

by Lolas Hamameh, Suhair, Renbaum, Paul, Kamal, Lara, Dweik, Dima, Salahat, Mohammad, Jaraysa, Tamara, Abu Rayyan, Amal, Casadei, Silvia, Mandell, Jessica B., Gulsuner, Suleyman, Lee, Ming K., Walsh, Tom, King, Mary‐Claire, Levy‐Lahad, Ephrat, Kanaan, Moein
Published in International journal of cancer (15.08.2017)

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Spectrum of Mutations in BRCA1, BRCA2, CHEK2, and TP53 in Families at High Risk of Breast Cancer

Spectrum of Mutations in BRCA1, BRCA2, CHEK2, and TP53 in Families at High Risk of Breast Cancer

by Walsh, Tom, Casadei, Silvia, Coats, Kathryn Hale, Swisher, Elizabeth, Stray, Sunday M, Higgins, Jake, Roach, Kevin C, Mandell, Jessica, Lee, Ming K, Ciernikova, Sona, Foretova, Lenka, Soucek, Pavel, King, Mary-Claire
Published in JAMA : the journal of the American Medical Association (22.03.2006)

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Genetic Predisposition to Breast Cancer Due to Mutations Other Than BRCA1 and BRCA2 Founder Alleles Among Ashkenazi Jewish Women

Genetic Predisposition to Breast Cancer Due to Mutations Other Than BRCA1 and BRCA2 Founder Alleles Among Ashkenazi Jewish Women

by Walsh, Tom, Mandell, Jessica B, Norquist, Barbara M, Casadei, Silvia, Gulsuner, Suleyman, Lee, Ming K, King, Mary-Claire
Published in JAMA oncology (01.12.2017)

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Spirituality and Parenting among Women Experiencing Intimate Partner Violence

Spirituality and Parenting among Women Experiencing Intimate Partner Violence

by Kaufman, Caroline C., Howell, Kathryn H., Mandell, Jessica E., Hasselle, Amanda H., Thurston, Idia B.
Published in Journal of family violence (01.02.2021)

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Demographic factors, personal life experiences, and types of intimate partner violence

Demographic factors, personal life experiences, and types of intimate partner violence

by Napier, Taylor R, Howell, Kathryn H, Maye, Caitlyn E, Jamison, Lacy E, Mandell, Jessica E, Thurston, Idia B
Published in Psychological trauma (01.02.2023)

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Functional and genomic approaches reveal an ancient CHEK2 allele associated with breast cancer in the Ashkenazi Jewish population

Functional and genomic approaches reveal an ancient CHEK2 allele associated with breast cancer in the Ashkenazi Jewish population

by Shaag, Avraham, Walsh, Tom, Renbaum, Paul, Kirchhoff, Tomas, Nafa, Khedoudja, Shiovitz, Stacey, Mandell, Jessica B., Welcsh, Piri, Lee, Ming K., Ellis, Nathan, Offit, Kenneth, Levy-Lahad, Ephrat, King, Mary-Claire
Published in Human molecular genetics (15.02.2005)

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Garrod's fourth inborn error of metabolism solved by the identification of mutations causing pentosuria

Garrod's fourth inborn error of metabolism solved by the identification of mutations causing pentosuria

by Pierce, Sarah B, Spurrell, Cailyn H, Mandell, Jessica B, Lee, Ming K, Zeligson, Sharon, Bereman, Michael S, Stray, Sunday M, Fokstuen, Siv, MacCoss, Michael J, Levy-Lahad, Ephrat, King, Mary-Claire, Motulsky, Arno G
Published in Proceedings of the National Academy of Sciences - PNAS (08.11.2011)

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Next generation sequencing to identify inherited mutations in all breast cancer genes in three breast cancer cohorts

Next generation sequencing to identify inherited mutations in all breast cancer genes in three breast cancer cohorts

by Bernier, Greta, MD, Mandell, Jessica, MS, Walsh, Tomas, PhD, Casadei, Silvia, PhD, Swisher, Elizabeth, MD, King, Mary-Claire, PhD
Published in Journal of the American College of Surgeons (01.09.2013)

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Infantile onset spinocerebellar ataxia caused by compound heterozygosity for Twinkle mutations and modeling of Twinkle mutations causing recessive disease

Infantile onset spinocerebellar ataxia caused by compound heterozygosity for Twinkle mutations and modeling of Twinkle mutations causing recessive disease

by Pierce, Sarah B, Gulsuner, Suleyman, Stapleton, Gail A, Walsh, Tom, Lee, Ming K, Mandell, Jessica B, Morales, Augusto, Klevit, Rachel E, King, Mary-Claire, Rogers, R Curtis
Published in Cold Spring Harbor molecular case studies (01.07.2016)

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