檢索結果 - Jennifer Ivanovich
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Psychosocial and Clinical Factors Associated with Family Communication of Cancer Genetic Test Results among Women Diagnosed with Breast Cancer at a Young Age 由 Ashley Elrick, Sato Ashida, Jennifer Ivanovich, Sarah Lyons, Barbara B. Biesecker, Melody S. Goodman, Kimberly A. Kaphingst
出版 2016Artigo -
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Predictive DNA Testing and Prophylactic Thyroidectomy in Patients at Risk for Multiple Endocrine Neoplasia Type 2A 由 Samuel A. Wells, Doina David, Koji Toshima, Louis P. Dehner, Cheryl M. Coffin, S. Bruce Dowton, Jennifer Ivanovich, Mary K. DeBenedettl, William G. Dilley, Jeffrey F. Moley, Jeffrey A. Norton, Helen Donis-Keller
出版 1994Artigo -
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TERC and TERT gene mutations in patients with bone marrow failure and the significance of telomere length measurements 由 Hong-Yan Du, Elena Pumbo, Jennifer Ivanovich, Ping An, Richard T. Maziarz, Ulrike M. Reiss, Deborah Chirnomas, Akiko Shimamura, Adrianna Vlachos, Jeffrey M. Lipton, Rakesh K. Goyal, Frederick D. Goldman, David B. Wilson, Philip J. Mason, Monica Bessler
出版 2008Artigo -
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Germline PTEN Promoter Mutations and Deletions in Cowden/Bannayan-Riley-Ruvalcaba Syndrome Result in Aberrant PTEN Protein and Dysregulation of the Phosphoinositol-3-Kinase/Akt Pat... 由 Xiao-Ping Zhou, Kristin Waite, Robert Pilarski, Heather Hampel, Magali Fernandez, Cindy Bos, Majed Dasouki, Gerald L. Feldman, Lois A. Greenberg, Jennifer Ivanovich, Ellen Matloff, Annette R. Patterson, Mary Ella Pierpont, Donna Russo, Najah T. Nassif, Charis Eng
出版 2003Artigo -
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<i>DICER1</i> Mutations in Familial Pleuropulmonary Blastoma 由 D. Ashley Hill, Jennifer Ivanovich, John R. Priest, Christina A. Gurnett, Louis P. Dehner, David M. Desruisseau, Jason A. Jarzembowski, Kathryn A. Wikenheiser‐Brokamp, Brian K. Suarez, Alison J. Whelan, Gretchen M. Williams, Dawn Bracamontes, Yoav H. Messinger, Paul J. Goodfellow
出版 2009Artigo -
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Temporal order of RNase IIIb and loss-of-function mutations during development determines phenotype in DICER1 syndrome: a unique variant of the two-hit tumor suppression model 由 Mark A. Brenneman, Amanda Field, Jiandong Yang, Gretchen M. Williams, Leslie Doros, Christopher Rossi, Kris Ann P. Schultz, Avi Z. Rosenberg, Jennifer Ivanovich, Joyce Turner, Heather Gordish‐Dressman, Douglas R. Stewart, Weiying Yu, Anne K. Harris, Peter Schoettler, Paul J. Goodfellow, Louis P. Dehner, Yoav H. Messinger, D. Ashley Hill
出版 2015Pré-impressão -
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Temporal order of RNase IIIb and loss-of-function mutations during development determines phenotype in pleuropulmonary blastoma / DICER1 syndrome: a unique variant of the two-hit t... 由 Mark A. Brenneman, Amanda Field, Jiandong Yang, Gretchen M. Williams, Leslie Doros, Christopher Rossi, Kris Ann P. Schultz, Avi Z. Rosenberg, Jennifer Ivanovich, Joyce Turner, Heather Gordish‐Dressman, Douglas R. Stewart, Weiying Yu, Anne K. Harris, Peter Schoettler, Paul J. Goodfellow, Louis P. Dehner, Yoav H. Messinger, D. Ashley Hill
出版 2018Pré-impressão -
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NCCN Guidelines® Insights: Breast Cancer Screening and Diagnosis, Version 1.2023 由 Therese B. Bevers, Bethany L. Niell, Jennifer L. Baker, Debbie L. Bennett, Ermelinda Bonaccio, Melissa Camp, Sona A. Chikarmane, Emily F. Conant, Mohammad Eghtedari, Meghan R. Flanagan, Jeffrey Hawley, Mark A. Helvie, Linda Hodgkiss, Tamarya L. Hoyt, Jennifer Ivanovich, Maxine S. Jochelson, Swati Kulkarni, Rachael Lancaster, Caitlin Mauer, Jessica E. Maxwell, Bhavika Patel, Mark D. Pearlman, Liane E. Philpotts, Donna Plecha, Jennifer K. Plichta, Shadi Aminololama Shakeri, Mary Lou Smith, Clarie L. Streibert, Roberta M. Strigel, Lusine Tumyan, Nicole Winkler, Dulcy E. Wolverton, Mary Anne Bergman, Rashmi Kumar, Katie Stehman
出版 2023Artigo -
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DNA sequencing of a cytogenetically normal acute myeloid leukaemia genome 由 Timothy J. Ley, Elaine R. Mardis, Li Ding, Bob Fulton, Michael D. McLellan, Ken Chen, David J. Dooling, Brian H. Dunford-Shore, Sean McGrath, Matthew T. Hickenbotham, Lisa L. Cook, Rachel M. Abbott, David E. Larson, Dan Koboldt, Craig Pohl, Scott M. Smith, Amy Hawkins, Scott Abbott, Devin P. Locke, LaDeana Hillier, Tracie L. Miner, Lucinda Fulton, Vincent Magrini, Todd Wylie, Jarret Glasscock, Joshua J. Conyers, Nathan Sander, Xiaoqi Shi, John R. Osborne, Patrick Minx, David Gordon, Asif Chinwalla, Yu Zhao, Rhonda E. Ries, Jacqueline E. Payton, Peter Westervelt, Michael H. Tomasson, Mark A. Watson, Jack Baty, Jennifer Ivanovich, Sharon E. Heath, William D. Shannon, Rakesh Nagarajan, Matthew J. Walter, Daniel C. Link, Timothy A. Graubert, John F. DiPersio, Richard K. Wilson
出版 2008Artigo -
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Genome remodelling in a basal-like breast cancer metastasis and xenograft 由 Li Ding, Matthew J. Ellis, Shunqiang Li, David E. Larson, Ken Chen, John W. Wallis, Christopher Harris, Michael D. McLellan, Robert S. Fulton, Lucinda Fulton, Rachel M. Abbott, Jeremy Hoog, David J. Dooling, Daniel C. Koboldt, Heather K. Schmidt, Joelle Kalicki, Qunyuan Zhang, Lei Chen, Ling Lin, Michael C. Wendl, Joshua F. McMichael, Vincent Magrini, Lisa Cook, Sean McGrath, Tammi L. Vickery, Elizabeth L. Appelbaum, Katherine DeSchryver, Sherri R. Davies, Therese Guintoli, Lin Li, Robert J. Crowder, Tao Yu, Jacqueline Snider, Scott M. Smith, Adam F. Dukes, Gabriel E. Sanderson, Craig Pohl, Kim D. Delehaunty, Catrina C. Fronick, Kimberley A. Pape, Jerry S. Reed, Jody S. Robinson, Jennifer S. Hodges, William Schierding, Nathan D. Dees, Dong Shen, Devin P. Locke, Madeline E. Wiechert, James M. Eldred, Josh B. Peck, Benjamin J. Oberkfell, Justin T. Lolofie, Feiyu Du, Amy Hawkins, Michelle D. O’Laughlin, Kelly E. Bernard, Mark Cunningham, Glendoria Elliott, Mark Mason, Dominic M. Thompson, Jennifer Ivanovich, Paul J. Goodfellow, Charles M. Perou, George M. Weinstock, Rebecca Aft, Mark A. Watson, Timothy J. Ley, Richard K. Wilson, Elaine R. Mardis
出版 2010Artigo -
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Genome-wide association study identifies 25 known breast cancer susceptibility loci as risk factors for triple-negative breast cancer 由 Kristen S. Purrington, Susan Slager, Diana Eccles, Drakoulis Yannoukakos, Peter A. Fasching, Penelope Miron, Jane Carpenter, Jenny Chang‐Claude, Nicholas G. Martin, Grant W. Montgomery, Vessela Kristensen, Hoda Anton‐Culver, Paul J. Goodfellow, William Tapper, Sajjad Rafiq, Susan M. Gerty, Lorraine Durcan, Irene Konstantopoulou, Florentia Fostira, Athanassios Vratimos, Paraskevi Apostolou, Irene Konstanta, Vassiliki Kotoula, Sotiris Lakis, Meletios Α. Dimopoulos, Dimosthenis Skarlos, Dimitrios Pectasides, George Fountzilas, Matthias W. Beckmann, Alexander Hein, Matthias Ruebner, Arif B. Ekici, Arndt Hartmann, R. Schulz-Wendtland, Stefan P. Renner, Wolfgang Janni, Brigitte Rack, Christoph Scholz, Julia Neugebauer, Ulrich Andergassen, Michael P. Lux, Lothar Haeberle, Christine L. Clarke, Nirmala Pathmanathan, Anja Rudolph, Dieter Flesch‐Janys, Stefan Nickels, Janet E. Olson, James N. Ingle, Curtis Olswold, Seth W. Slettedahl, Jeanette E. Eckel‐Passow, S. Keith Anderson, Daniel W. Visscher, Victoria Cafourek, Hugues Sicotte, Naresh Prodduturi, Elisabete Weiderpass, Leslie Bernstein, Argyrios Ziogas, Jennifer Ivanovich, Graham G. Giles, Laura Baglietto, Melissa C. Southey, Veli-Matti Kosma, H.-P. Fischer, Malcolm Reed, Simon S. Cross, Sandra Deming-Halverson, Martha J. Shrubsole, Qiuyin Cai, Xiao‐Ou Shu, Mary B. Daly, JoEllen Weaver, Eric A. Ross, Jennifer R. Klemp, Priyanka Sharma, Diana Torres, Thomas Rüdiger, Heidrun Wölfing, Hans-Ulrich Ulmer, Asta Försti, Thaer Khoury, Shicha Kumar, Robert Pilarski, Charles L. Shapiro, Dario Greco, Päivi Heikkilä, Kristiina Aittomäki, Carl Blomqvist, Astrid Irwanto, Jianjun Liu, V. Shane Pankratz, Xianshu Wang, Gianluca Severi, Graham J. Mann, Douglas F. Easton, Per Hall, Hiltrud Brauch, Angela Cox
出版 2013Artigo -
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A common variant at the TERT-CLPTM1L locus is associated with estrogen receptor–negative breast cancer 由 Christopher A. Haiman, Gary K. Chen, Celine M. Vachon, Federico Canzian, Alison M. Dunning, Robert C. Millikan, Xianshu Wang, Foluso O. Ademuyiwa, Shahana Ahmed, Christine B. Ambrosone, Laura Baglietto, Rosemary L. Balleine, Elisa V. Bandera, Matthias W. Beckmann, Christine D. Berg, Leslie Bernstein, Carl Blomqvist, William J. Blot, Hiltrud Brauch, Julie E. Buring, Lisa A. Carey, Jane Carpenter, Jenny Chang‐Claude, Stephen J. Chanock, Daniel I. Chasman, Christine L. Clarke, Angela Cox, Simon S. Cross, Sandra L. Deming, Robert B. Diasio, Meletios Α. Dimopoulos, W. Ryan Driver, Thomas Dünnebier, Lorraine Durcan, Diana Eccles, Christopher K. Edlund, Arif B. Ekici, Peter A. Fasching, Heather Spencer Feigelson, Dieter Flesch‐Janys, Florentia Fostira, Asta Försti, George Fountzilas, Susan M. Gerty, Graham G. Giles, Andrew K. Godwin, Paul J. Goodfellow, Nikki Graham, Dario Greco, Ute Hamann, Susan E. Hankinson, Arndt Hartmann, Rebecca Hein, Judith Heinz, Andrea Holbrook, Robert N. Hoover, Jennifer J. Hu, David J. Hunter, Sue A. Ingles, Astrid Irwanto, Jennifer Ivanovich, Esther M. John, Nicola Johnson, Arja Jukkola‐Vuorinen, Rudolf Kaaks, Yon‐Dschun Ko, Laurence N. Kolonel, Irene Konstantopoulou, Veli-Matti Kosma, Swati Kulkarni, Diether Lambrechts, Adam M. Lee, Loı̈c Le Marchand, Timothy G. Lesnick, Jianjun Liu, Sara Lindström, Graham J. Mann, Sara Margolin, Nicholas G. Martin, Penelope Miron, Grant W. Montgomery, Heli Nevanlinna, Stephan Nickels, Sarah J. Nyante, Curtis Olswold, Julie R. Palmer, Harsh B. Pathak, Dimitrios Pectasides, Charles M. Perou, Julian Peto, Paul D.P. Pharoah, Loreall Pooler, Michael F. Press, Katri Pylkäs, Timothy R. Rebbeck, Jorge L. Rodriguez‐Gil, Lynn Rosenberg, Eric A. Ross, Thomas Rüdiger, Isabel dos–Santos–Silva
出版 2011Artigo
相關主題
Biology
Genetics
Gene
Medicine
Mutation
Internal medicine
Breast cancer
Cancer
Cancer research
Germline mutation
Germline
Allele
Genome
Oncology
Pathology
DNA sequencing
Disease
Environmental health
Family medicine
Genetic counseling
Genetic testing
Genome-wide association study
Genotype
Missense mutation
Molecular biology
Odds ratio
Population
Single-nucleotide polymorphism
Triple-negative breast cancer
Whole genome sequencing