Hasil Pencarian - Matthew Lebo

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  1. 1
    P064: Returning genomic risk for hereditary breast and ovarian cancer: Clinical outcomes through standard of care vs research return of results*

    P064: Returning genomic risk for hereditary breast and ovarian cancer: Clinical outcomes through standard of care vs research return of results* oleh Ilham Abbasi, Emma Perez, Hana Zouk, Matthew Lebo, Robert Green, Nina Gold

    Diterbitkan 2024-01-01
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  2. 2
    P578: Using the large-language model GPT4 to programmatically determine functional evidence supporting or refuting variant pathogenicity from literature*

    P578: Using the large-language model GPT4 to programmatically determine functional evidence supporting or refuting variant pathogenicity from literature* oleh Matthew Lebo, Kalotina Machini, Pranav Sriraman, Jiyeon Shin, Emma Henricks, Carly Mailly, Michael Oates, Samuel Aronson

    Diterbitkan 2024-01-01
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  3. 3
    P501: Delivery of monogenic and polygenic results to participants in the Genomic Medicine at Veterans Affairs (GenoVA) study

    P501: Delivery of monogenic and polygenic results to participants in the Genomic Medicine at Veterans Affairs (GenoVA) study oleh Morgan Danowski, Ashley Antwi, Charles Brunette, Elizabeth Harris, Preetika Kulkarni, Katharine MacIsaac, Thomas Yi, Matthew Lebo, Jason Vassy

    Diterbitkan 2024-01-01
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  4. 4
    P504: A universal filter enabling high throughput genomic screening

    P504: A universal filter enabling high throughput genomic screening oleh Kalotina Machini, Limin Hao, Hana Zook, Lisa Mahanta, Heather Mason-Suares, Anna Nagy, Heidi Rehm, Sami Amr, Matthew Lebo

    Diterbitkan 2023-01-01
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  5. 5
    P517: An automated approach to report drafting for newborn genomic sequencing in the BabySeq Project

    P517: An automated approach to report drafting for newborn genomic sequencing in the BabySeq Project oleh Anna Nagy, Eugene Mysen, Chungming Glendy Sun, Lisa Mahanta, Bethany Zettler, Alan Beggs, Ingrid Holm, Robert Green, Matthew Lebo, Hana Zouk

    Diterbitkan 2023-01-01
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  6. 6
    O31: Risk allele evidence curation, classification, and reporting: Recommendations from the ClinGen Low Penetrance/Risk Allele Working Group*

    O31: Risk allele evidence curation, classification, and reporting: Recommendations from the ClinGen Low Penetrance/Risk Allele Working Group* oleh Matthew Lebo, Marcie Steeves, Katherine Benson, Laura Conlin, Mythily Ganapathi, Vaidehi Jobanputra, Minjie Luo, Deqiong Ma, Kelly McGoldrick, Blake Palculict, Heidi Rehm, Panagiotis Sergouniotis, Samantha Schilit, Pinar Bayrak-Toydemir, Tatiana Tvrdik, Nicholas Watkins, Lauren Zec, Wenying Zhang Zhang, Ryan Schmidt

    Diterbitkan 2023-01-01
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  7. 7
    Polygenic background modifies penetrance of monogenic variants for tier 1 genomic conditions

    Polygenic background modifies penetrance of monogenic variants for tier 1 genomic conditions oleh Akl C. Fahed, Minxian Wang, Julian R. Homburger, Aniruddh P. Patel, Alexander G. Bick, Cynthia L. Neben, Carmen Lai, Deanna Brockman, Anthony Philippakis, Patrick T. Ellinor, Christopher A. Cassa, Matthew Lebo, Kenney Ng, Eric S. Lander, Alicia Y. Zhou, Sekar Kathiresan, Amit V. Khera

    Diterbitkan 2020-08-01
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  8. 8
    P436: Population genome screening identifies previously undiagnosed disease: A case series

    P436: Population genome screening identifies previously undiagnosed disease: A case series oleh Selina Casalino, Hanna Faghfoury, Navneet Aujla, David Di Iorio, Erika Frangione, Chun Yiu Jordan Fung, Gregory Morgan, Mackenzie Scott, Dawit Wolday, Saranya Arnoldo, Erin Bearss, Alexandra Binnie, Bjug Borgundvaag, Howard Chertkow, Sunakshi Chowdhary, Monica Chung, Marc Clausen, Marc Dagher, Luke Devine, Steven Friedmen, Anne-Claude Gingras, Lee Goneau, Deepanjali Kaushik, Zeeshan Khan, Elisa Lapadula, Tiffany Lu, Georgia MacDonald, Tony Mazzulli, Allison McGeer, Shelley McLeod, Chloe Mighton, Trevor Pugh, David Richardson, Jared Simpson, Seth Stern, Lisa Strug, Ahmed Taher, Iris Wong, Natasha Zarei, Elena Greenfeld, Limin Hao, Matthew Lebo, William Lane, Abdul Noor, Yvonne Bombard, Jennifer Taher, Jordan Lerner-Ellis

    Diterbitkan 2023-01-01
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  9. 9
    P574: Summary of findings from comprehensive genome sequencing performed in a healthy population cohort*

    P574: Summary of findings from comprehensive genome sequencing performed in a healthy population cohort* oleh Selina Casalino, Radhika Mahajan, Navneet Aujla, Erika Frangione, Lochana Jayachandran, Saranya Arnoldo, Erin Bearss, Alexandra Binnie, Bjug Borgundvaag, Howard Chertkow, Sunakshi Chowdhary, Marc Clausen, Marc Dagher, Luke Devine, Brendan Dickson, David Di Iorio, Chun Yiu Jordan Fung, Steven Friedman, Anne-Claude Gingras, Lee Goneau, Simona Haller, Limin Hao, Deepanjali Kaushik, Zeeshan Khan, William Lane, Elisa Lapadula, Matthew Lebo, Tiffany Lu, Georgia MacDonald, Tony Mazzulli, Allison McGeer, Shelley McLeod, Chloe Mighton, Gregory Morgan, Romina Nomigolzar, Trevor Pugh, David Richardson, Mackenzie Scott, Jared Simpson, Seth Stern, Lisa Strug, Ahmed Taher, Shilpa Thakur, Dawit Wolday, Iris Wong, Juliet Young, Natasha Zarei, Elena Greenfeld, Yvonne Bombard, Abdul Noor, Hanna Faghfoury, Jennifer Taher, Jordan Lerner-Ellis

    Diterbitkan 2024-01-01
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