Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Deepika Nathan"'
Autor:
Tyler Landrith, Bing Li, Ashley A. Cass, Blair R. Conner, Holly LaDuca, Danielle B. McKenna, Kara N. Maxwell, Susan Domchek, Nichole A. Morman, Christopher Heinlen, Deborah Wham, Cathryn Koptiuch, Jennie Vagher, Ragene Rivera, Ann Bunnell, Gayle Patel, Jennifer L. Geurts, Morgan M. Depas, Shraddha Gaonkar, Sara Pirzadeh-Miller, Rebekah Krukenberg, Meredith Seidel, Robert Pilarski, Meagan Farmer, Khateriaa Pyrtel, Kara Milliron, John Lee, Elizabeth Hoodfar, Deepika Nathan, Amanda C. Ganzak, Sitao Wu, Huy Vuong, Dong Xu, Aarani Arulmoli, Melissa Parra, Lily Hoang, Bhuvan Molparia, Michele Fennessy, Susanne Fox, Sinead Charpentier, Julia Burdette, Tina Pesaran, Jessica Profato, Brandon Smith, Ginger Haynes, Emily Dalton, Joy Rae-Radecki Crandall, Ruth Baxter, Hsiao-Mei Lu, Brigette Tippin-Davis, Aaron Elliott, Elizabeth Chao, Rachid Karam
Publikováno v:
npj Precision Oncology, Vol 4, Iss 1, Pp 1-9 (2020)
Abstract Germline variants in tumor suppressor genes (TSGs) can result in RNA mis-splicing and predisposition to cancer. However, identification of variants that impact splicing remains a challenge, contributing to a substantial proportion of patient
Externí odkaz:
https://doaj.org/article/50f2e0c212b24359a87e5f0fd59980ac
Autor:
Danielle C. Sample, N. Jewel Samadder, Lisa M. Pappas, Kenneth M. Boucher, Wade S. Samowitz, Therese Berry, Michelle Westover, Deepika Nathan, Priyanka Kanth, Kathryn R. Byrne, Randall W. Burt, Deborah W. Neklason
Publikováno v:
BMC Gastroenterology, Vol 18, Iss 1, Pp 1-8 (2018)
Abstract Background Patients with familial adenomatous polyposis (FAP) frequently undergo colectomy to reduce the 70 to 90% lifetime risk of colorectal cancer. After risk-reducing colectomy, duodenal cancer and complications from duodenal surgeries a
Externí odkaz:
https://doaj.org/article/ef08b6ae678041c8914dcf606b6811d8
Autor:
Gayle Patel, Morgan M Depas, Lily Hoang, Rob Pilarski, Brigette Tippin Davis, Elizabeth Hoodfar, Cara S. Dresbold, Olivia L. Tan, Meagan Farmer, Danielle Menashe, Samantha Stachowiak, Deborah Wham, Khateriaa Pyrtel, Sandra B. Jenkinson, Tiffani Demarco, Sara Pirzadeh-Miller, Elizabeth C. Chao, Danielle McKenna, Catherine Koptiuch, Jessica Profato, Rebekah C. Krukenberg, Jennifer L. Geurts, John G. Lee, Shraddha Gaonkar, Jen Moore, Nichole A. Morman, Danielle Dondanville, Deepika Nathan, Rachid Karam, Meredith Seidel, Holly LaDuca, Amal Yussuf, Kara J. Milliron, Carolyn Horton, Jill S. Dolinsky, Diane Samad, Cassie Garcia
Publikováno v:
Cancer Research. 80:P6-08
BACKGROUND: Germline genetic testing is routinely incorporated into clinical care for breast cancer patients to inform management decisions and reduce risk for developing subsequent cancers. While the diagnostic yield of cancer genetic testing has in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a50932ad25e8a5992a3fd2a38eb880ba
https://doi.org/10.1158/1538-7445.sabcs19-p6-08-08
https://doi.org/10.1158/1538-7445.sabcs19-p6-08-08
Autor:
Meagan Farmer, Brandon Smith, Kara N. Maxwell, Brigette Tippin-Davis, Julia Burdette, Danielle McKenna, Ashley A. Cass, Sinead Charpentier, Sitao Wu, Emily Dalton, Melissa Parra, Susanne Fox, Aaron Elliott, Holly LaDuca, Cathryn Koptiuch, Susan M. Domchek, Elizabeth Hoodfar, Robert Pilarski, Dong Xu, Khateriaa Pyrtel, Kara J. Milliron, Michele Fennessy, Gayle Patel, Lily Hoang, Morgan M Depas, Tina Pesaran, Rachid Karam, Meredith Seidel, Ann Bunnell, Huy Gia Vuong, Deborah Wham, Bing Li, Ragene Rivera, Jennie Vagher, Nichole A. Morman, Aarani Arulmoli, Sara Pirzadeh-Miller, Hsiao-Mei Lu, Jessica Profato, Joy Rae-Radecki Crandall, Elizabeth C. Chao, Ruth Baxter, Shraddha Gaonkar, Ginger Haynes, Amanda Ganzak, Deepika Nathan, Jennifer L. Geurts, Blair R. Conner, Tyler Landrith, Rebekah Krukenberg, John J. Lee, Christopher Heinlen, Bhuvan Molparia
Publikováno v:
npj Precision Oncology, Vol 4, Iss 1, Pp 1-9 (2020)
NPJ Precision Oncology
NPJ Precision Oncology
Germline variants in tumor suppressor genes (TSGs) can result in RNA mis-splicing and predisposition to cancer. However, identification of variants that impact splicing remains a challenge, contributing to a substantial proportion of patients with su
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d16807d808110f22b027a699b83d981
https://doi.org/10.1038/s41698-020-0109-y
https://doi.org/10.1038/s41698-020-0109-y
Publikováno v:
Journal of genetic counselingREFERENCES. 29(3)
This study was designed to observe whether disparities exist between ethnicities in reporting a family history of cancer in a cancer genetic counseling clinic. Four hundred sixty-nine pedigrees collected between 2015 to 2017 from a cancer clinic at t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::95c28aacf3387134aef515a65a3619fc
https://pubmed.ncbi.nlm.nih.gov/32222057
https://pubmed.ncbi.nlm.nih.gov/32222057
Autor:
Therese Berry, Wade S. Samowitz, Michelle Westover, Kathryn R. Byrne, Deepika Nathan, Kenneth M. Boucher, N. Jewel Samadder, Randall W. Burt, Danielle Sample, Lisa Pappas, Priyanka Kanth, Deborah W. Neklason
Publikováno v:
BMC Gastroenterology, Vol 18, Iss 1, Pp 1-8 (2018)
BMC Gastroenterology
BMC Gastroenterology
Background Patients with familial adenomatous polyposis (FAP) frequently undergo colectomy to reduce the 70 to 90% lifetime risk of colorectal cancer. After risk-reducing colectomy, duodenal cancer and complications from duodenal surgeries are the ma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::98bc004fe8b069d0a423eb145bf3470d
https://doi.org/10.1186/s12876-018-0841-8
https://doi.org/10.1186/s12876-018-0841-8
Autor:
David Malkin, Ana Novokmet, Judy Garber, Phuong L. Mai, Kim E. Nichols, Deepika Nathan, Robert B. Lindell, Sharon E. Plon, Sharon A. Savage, Carol A. Ford, Lisa Diller, Nicolette M. Chun, Joshua D. Schiffman, Kristin Zelley, Andrea Farkas Patenaude, Sarah Scollon, Melissa A. Alderfer, James M. Ford
Publikováno v:
Cancer. 121:286-293
BACKGROUND Li-Fraumeni syndrome is a rare genetic cancer predisposition syndrome caused by germline TP53 mutations. Up to 20% of mutation carriers develop cancer during childhood. The benefits of TP53 mutation testing of children are a matter of deba
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c76a9040307d5c491250027f04a86454
https://doi.org/10.1002/cncr.29027
https://doi.org/10.1002/cncr.29027
Autor:
Melissa A, Alderfer, Kristin, Zelley, Robert B, Lindell, Ana, Novokmet, Phuong L, Mai, Judy E, Garber, Deepika, Nathan, Sarah, Scollon, Nicolette M, Chun, Andrea F, Patenaude, James M, Ford, Sharon E, Plon, Joshua D, Schiffman, Lisa R, Diller, Sharon A, Savage, David, Malkin, Carol A, Ford, Kim E, Nichols
Publikováno v:
Cancer. 121(2)
Li-Fraumeni syndrome is a rare genetic cancer predisposition syndrome caused by germline TP53 mutations. Up to 20% of mutation carriers develop cancer during childhood. The benefits of TP53 mutation testing of children are a matter of debate and know
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::287f87d19948b87c6a4b0821b6489916
https://pubmed.ncbi.nlm.nih.gov/25223899
https://pubmed.ncbi.nlm.nih.gov/25223899
Autor:
Amanda Gammon, Wade S. Samowitz, Lindsey Martineau, Curt H. Hagedorn, Marc S. Greenblatt, Kory Jasperson, Wendy McKinnon, Laurel Smith, Elena G. Strait, Cristina Christenson, Randall W. Burt, Lisa Pappas, Deborah W. Neklason, John F. Valentine, Tom Greene, Megan Keener, Scott K. Kuwada, Mikaela Larson, Marjan Champine, Michelle W. Done, Wendy Kohlmann, Kathryn R. Byrne, Danielle Sample, David A. Jones, Priyanka Kanth, Sean V. Tavtigian, Patrick M. Lynch, Therese Berry, John C. Fang, N. Jewel Samadder, Kenneth M. Boucher, Deepika Nathan
Publikováno v:
Gastrointestinal Endoscopy. 81:AB148
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7cdc9acbfc31be10743e1bc7eb804283
https://doi.org/10.1016/j.gie.2015.03.1238
https://doi.org/10.1016/j.gie.2015.03.1238