Որոնման արդյունքները - Marcy E. Richardson
- Ցուցադրվում են 1 - 17 արդյունքները 17
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Universal Germline Panel Testing for Individuals With Pheochromocytoma and Paraganglioma Produces High Diagnostic Yield Carolyn Horton, Holly LaDuca, Ashley Deckman, Kate Durda, Michelle Jackson, Marcy E. Richardson, Yuan Tian, Amal Yussuf, Kory Jasperson, Tobias Else
Հրապարակվել է 2022Artigo -
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Rare <i>BRIP1</i> Missense Alleles Confer Risk for Ovarian and Breast Cancer Cassandra L. Moyer, Jennifer Ivanovich, Jessica L. Gillespie, Rachel Doberstein, Marc R. Radke, Marcy E. Richardson, Scott H. Kaufmann, Elizabeth M. Swisher, Paul J. Goodfellow
Հրապարակվել է 2019Artigo -
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Closing the gap: Systematic integration of multiplexed functional data resolves variants of uncertain significance in BRCA1, TP53, and PTEN Shawn Fayer, Carolyn Horton, Jennifer N. Dines, Alan F. Rubin, Marcy E. Richardson, Kelly McGoldrick, Felicia Hernandez, Tina Pesaran, Rachid Karam, Brian H. Shirts, Douglas M. Fowler, Lea M. Starita
Հրապարակվել է 2021Artigo -
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Targeted DNA demethylation and activation of endogenous genes using programmable TALE-TET1 fusion proteins Morgan L. Maeder, James Angstman, Marcy E. Richardson, Samantha J Linder, Vincent Cascio, Shengdar Q. Tsai, Quan Ho, Jeffry D. Sander, Deepak Reyon, B Bernstein, J Costello, Miles Wilkinson, J. Keith Joung
Հրապարակվել է 2013Artigo -
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Diagnostic Outcomes of Concurrent DNA and RNA Sequencing in Individuals Undergoing Hereditary Cancer Testing Carolyn Horton, Lily Hoang, Heather Zimmermann, Colin C. Young, Jessica Grzybowski, Kate Durda, Huy Gia Vuong, David Burks, Ashley Cass, Holly LaDuca, Marcy E. Richardson, Steven M. Harrison, Elizabeth Chao, Rachid Karam
Հրապարակվել է 2023Artigo -
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Differences in Cancer Phenotypes Among Frequent <i>CHEK2</i> Variants and Implications for Clinical Care—Checking <i>CHEK2</i> Brittany Bychkovsky, Nihat Buğra Ağaoğlu, Carolyn Horton, Jing Zhou, Amal Yussuf, Parichehr Hemyari, Marcy E. Richardson, Colin C. Young, Holly LaDuca, Deborah L. McGuinness, Rochelle Scheib, Judy E. Garber, Huma Q. Rana
Հրապարակվել է 2022Artigo -
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Strong functional data for pathogenicity or neutrality classify BRCA2 DNA-binding-domain variants of uncertain significance Marcy E. Richardson, Chunling Hu, Kun Y. Lee, Holly LaDuca, Kelly Fulk, Kate Durda, Ashley Deckman, David E. Goldgar, Álvaro N.A. Monteiro, Rohan Gnanaolivu, Steven N. Hart, Eric C. Polley, Elizabeth Chao, Tina Pesaran, Fergus J. Couch
Հրապարակվել է 2021Artigo -
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The Homeobox Transcription Factor RHOX10 Drives Mouse Spermatogonial Stem Cell Establishment H. C. Song, Anilkumar Bettegowda, Blue B. Lake, A ZHAO, David Skarbrevik, Eric Babajanian, Meena Sukhwani, Eleen Y. Shum, Mimi H. Phan, Terra‐Dawn M. Plank, Marcy E. Richardson, Madhuvanthi Ramaiah, Vaishnavi Sridhar, Dirk G. de Rooij, Kyle E. Orwig, Kun Zhang, Miles Wilkinson
Հրապարակվել է 2016Artigo -
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BRCA1 frameshift variants leading to extended incorrect protein C termini Thales C. Nepomuceno, Tzeh Keong Foo, Marcy E. Richardson, John Michael O. Rañola, Jamie Weyandt, Matthew J. Varga, Amaya Alarcon, Diana Gutiérrez, Anna von Wachenfeldt, Daniel Eriksson, Raymond H. Kim, Susan Randall Armel, Edwin S. Iversen, Fergus J. Couch, Åke Borg, Bing Xia, Marcelo A. Carvalho, Álvaro N.A. Monteiro
Հրապարակվել է 2023Artigo -
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Integration of functional assay data results provides strong evidence for classification of hundreds of BRCA1 variants of uncertain significance Paulo C. Lyra, Thales C. Nepomuceno, Marcele Lorentz Mattos de Souza, Géssica F. Machado, Mariana Friedrich Veloso, Taciane Barbosa Henriques, Diandra Zipinotti dos Santos, Iuly G. Ribeiro, Roberto Silva Ribeiro, Letícia Batista Azevedo Rangel, Marcy E. Richardson, Edwin S. Iversen, David E. Goldgar, Fergus J. Couch, Marcelo A. Carvalho, Álvaro N.A. Monteiro
Հրապարակվել է 2020Artigo -
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Assessment of Diagnostic Outcomes of RNA Genetic Testing for Hereditary Cancer Rachid Karam, Blair R. Conner, Holly LaDuca, Kelly McGoldrick, Kate Krempely, Marcy E. Richardson, Heather Zimmermann, Stephanie Gutierrez, Patrick Reineke, Lily Hoang, Kyle Allen, Amal Yussuf, Suzette Farber-Katz, Huma Q. Rana, Samantha Culver, John Lee, Sarah Nashed, Deborah Toppmeyer, Debra L. Collins, Ginger Haynes, Tina Pesaran, Jill S. Dolinsky, Brigette Tippin Davis, Aaron Elliott, Elizabeth Chao
Հրապարակվել է 2019Artigo -
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Functional analysis and clinical classification of 462 germline BRCA2 missense variants affecting the DNA binding domain Chunling Hu, Huaizhi Huang, Jie Na, Carolyn A. Lumby, Mohamed Abozaid, Megan Holdren, T. Jagan Mohan Rao, Rachid Karam, Tina Pesaran, Jamie Weyandt, Christen M. Csuy, Christina Seelaus, Colin C. Young, Kelly Fulk, Zahra Heidari, Paulo C. Lyra, Ronan E. Couch, Benjamin Persons, Eric C. Polley, Rohan Gnanaolivu, Nicholas J. Boddicker, Álvaro N.A. Monteiro, Siddhartha Yadav, Susan M. Domchek, Marcy E. Richardson, Fergus J. Couch
Հրապարակվել է 2024Artigo -
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Gene-specific ACMG/AMP classification criteria for germline APC variants: Recommendations from the ClinGen InSiGHT Hereditary Colorectal Cancer/Polyposis Variant Curation Expert Pa... Isabel Spier, Xiaoyu Yin, Marcy E. Richardson, Marta Pineda, Andreas Laner, Deborah Ritter, Julie Boyle, Pilar Mur, Thomas van Overeem Hansen, Xuemei Shi, Khalid Mahmood, John‐Paul Plazzer, Elisabet Ognedal, Margareta Nordling, Susan M. Farrington, Gou Yamamoto, Stéphanie Baert‐Desurmont, Alexandra Martins, Ester Borràs, Carli M.J. Tops, Erica Webb, Victoria Beshay, Maurizio Genuardi, Tina Pesaran, Gabriel Capellà, Sean V. Tavtigian, Andrew Latchford, Ian M. Frayling, Sharon E. Plon, Marc S. Greenblatt, Finlay Macrae, Stefan Aretz
Հրապարակվել է 2023Artigo -
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Evidence-based recommendations for gene-specific ACMG/AMP variant classification from the ClinGen ENIGMA BRCA1 and BRCA2 Variant Curation Expert Panel Michael T. Parsons, Miguel de la Hoya, Marcy E. Richardson, Emma Tudini, Michael G. Anderson, Windy Berkofsky‐Fessler, Sandrine M. Caputo, Raymond C. Chan, Melissa Cline, Bing Feng, Cristina Fortuño, E. Gómez, Johanna Hadler, Susan Hiraki, Megan Holdren, Claude Houdayer, Kathleen S. Hruska, Paul A. James, Rachid Karam, Huei San Leong, Alexandra Martins, Arjen R. Mensenkamp, Álvaro N.A. Monteiro, Vaishnavi Nathan, Robert O’Connor, Inge Søkilde Pedersen, Tina Pesaran, Paolo Radice, Gunnar Schmidt, Melissa C. Southey, Sean V. Tavtigian, Bryony A. Thompson, Amanda E. Toland, Clare Turnbull, Maartje J. Vogel, Jamie Weyandt, George A. R. Wiggins, Lauren Zec, Fergus J. Couch, Logan C. Walker, Maaike P.G. Vreeswijk, David E. Goldgar, Amanda B. Spurdle
Հրապարակվել է 2024Artigo -
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Functional evaluation and clinical classification of BRCA2 variants Huaizhi Huang, Chunling Hu, Jie Na, Steven N. Hart, Rohan Gnanaolivu, Mohamed Abozaid, Tara Rao, Yohannes A. Tecleab, Christine B. Ambrosone, Song Yao, Amy Trentham-Dietz, A. Heather Eliassen, Lauren R. Teras, Alpa V. Patel, Christopher A. Haiman, Esther M. John, Elena Martínez, James V. Lacey, Dale P. Sandler, Clarice R. Weinberg, Julie R. Palmer, Celine M. Vachon, Janet E. Olson, Kathryn J. Ruddy, Hoda Anton Culver, Jeffrey N. Weitzel, Peter Kraft, Tina Pesaran, Paulo C. Lyra, Rachid Karam, Siddhartha Yadav, Katherine L. Nathanson, Susan M. Domchek, Miguel de la Hoya, Mark E. Robson, Miika Mehine, Chaitanya Bandlamudi, Diana Mandelker, Álvaro N.A. Monteiro, Edwin S. Iversen, Nicholas J. Boddicker, Wenan Chen, Marcy E. Richardson, Fergus J. Couch
Հրապարակվել է 2025Artigo
Որոնման գործիքներ:
Առնչվող խորագիր
Biology
Genetics
Gene
Medicine
Computational biology
Mutation
Internal medicine
Bioinformatics
Cancer
Genetic testing
Germline mutation
Germline
Phenotype
Oncology
Computer science
Gene expression
Missense mutation
Breast cancer
CHEK2
Colorectal cancer
DNA methylation
Family history
Homeobox
Loss function
Ovarian cancer
Pathology
Allele
Allele frequency
Apoptosis
Cancer research