Torthaí cuardaigh - Mohamed Abozaid
- 1 - 3 toradh as 3 á dtaispeáint
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1
AI chatbots show promise but limitations on UK medical exam questions: a comparative performance study de réir Mohammed Ahmed Sadeq, Reem Mohamed Farouk Ghorab, Mohamed Hady Ashry, Ahmed Mohamed Abozaid, Haneen A. Banihani, Moustafa Salem, Mohammed Tawfiq Abu Aisheh, Saad Abuzahra, Marina Ramzy Mourid, Mohamad Monif Assker, Mohammed Ayyad, Mostafa Hossam El Din Moawad
Foilsithe / Cruthaithe 2024Artigo -
2
Functional analysis and clinical classification of 462 germline BRCA2 missense variants affecting the DNA binding domain de réir 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
Foilsithe / Cruthaithe 2024Artigo -
3
Functional evaluation and clinical classification of BRCA2 variants de réir 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
Foilsithe / Cruthaithe 2025Artigo
Uirlisí cuardaigh:
Ábhair a bhaineann le hábhar
Biology
Computational biology
Gene
Genetic testing
Genetics
Germline
Missense mutation
Mutation
Artificial intelligence
Computer science
ENCODE
Family medicine
Genome
Genomics
In silico
Language model
Loss function
Medical education
Medical genetics
Medicine
Perplexity
Phenotype
Psychology
Specialty