Matthew S Lebo (M S Lebo, Matthew Lebo, Mathew S Lebo)

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2015-2023
Publications (10 Years): 12

Top Topics

Genome Wide Association Study

Hypertrophic Cardiomyopathy

Structural Basis

Top Venues

Genetics in medicine : official journal of the American College of Medical Genetics

Nature medicine

NPJ genomic medicine

Molecular genetics & genomic medicine

This page only lists publications with an associated author ORCID identifier.

Publications

Satoshi Koyama, Ying Wang, Kaavya Paruchuri, M D Mesbah Uddin, So Mi Jemma Cho, Sarah M Urbut, Sara Haidermota, Whitney E Hornsby, Robert C Green, Mark J Daly, Benjamin M Neale, Patrick T Ellinor, Jordan W Smoller, Matthew S Lebo, Elizabeth W Karlson, Alicia R Martin, Pradeep Natarajan
Decoding Genetics, Ancestry, and Geospatial Context for Precision Health. medRxiv : the preprint server for health sciences (2023)
Limin Hao, Peter Kraft, Gabriel F Berriz, Elizabeth D Hynes, Christopher Koch, Prathik Korategere V Kumar, Shruti S Parpattedar, Marcie Steeves, Wanfeng Yu, Ashley A Antwi, Charles A Brunette, Morgan Danowski, Manish K Gala, Robert C Green, Natalie E Jones, Anna C F Lewis, Steven A Lubitz, Pradeep Natarajan, Jason L Vassy, Matthew S Lebo
Development of a clinical polygenic risk score assay and reporting workflow. Nature medicine 28 (5) (2022)
L Lazo de la Vega, W Yu, K Machini, C A Austin-Tse, L Hao, C L Blout Zawatsky, H Mason-Suares, R C Green, H L Rehm, Matthew S Lebo
A framework for automated gene selection in genomic applications. Genetics in medicine : official journal of the American College of Medical Genetics 23 (10) (2021)
Seyedeh M Zekavat, Shu-Hong Lin, Alexander G Bick, Aoxing Liu, Kaavya Paruchuri, Chen Wang, M D Mesbah Uddin, Yixuan Ye, Zhaolong Yu, Xiaoxi Liu, Yoichiro Kamatani, Romit Bhattacharya, James Paul Pirruccello, Akhil Pampana, Po-Ru Loh, Puja Kohli, Steven A McCarroll, Krzysztof Kiryluk, Benjamin M Neale, Iuliana Ionita-Laza, Eric A Engels, Derek W Brown, Jordan W Smoller, Robert C Green, Elizabeth W Karlson, Matthew S Lebo, Patrick T Ellinor, Scott T Weiss, Mark J Daly, null null, null null, Chikashi C Terao, Hongyu Zhao, Benjamin L Ebert, Muredach P Reilly, Andrea Ganna, Mitchell J Machiela, Giulio Genovese, Pradeep Natarajan
Hematopoietic mosaic chromosomal alterations increase the risk for diverse types of infection. Nature medicine 27 (6) (2021)
Leora Witkowski, Mitchell W Dillon, Elissa Murphy, Matthew S Lebo, Heather Mason-Suares
Expanding the Noonan spectrum/RASopathy NGS panel: Benefits of adding NF1 and SPRED1. Molecular genetics & genomic medicine 8 (4) (2020)
Christian R Marshall, Shimul Chowdhury, Ryan J Taft, Matthew S Lebo, Jillian G Buchan, Steven M Harrison, Ross Rowsey, Eric W Klee, Pengfei Liu, Elizabeth A Worthey, Vaidehi Jobanputra, David P Dimmock, Hutton M Kearney, David Bick, Shashikant Kulkarni, Stacie L Taylor, John W Belmont, Dimitri J Stavropoulos, Niall J Lennon, null null
Best practices for the analytical validation of clinical whole-genome sequencing intended for the diagnosis of germline disease. NPJ genomic medicine 5 (2020)
Akl C Fahed, Minxian Wang, Julian R Homburger, Aniruddh Pradip Patel, Alexander G Bick, Cynthia L Neben, Carmen Lai, Deanna Brockman, Anthony Philippakis, Patrick T Ellinor, Christopher A Cassa, Matthew S Lebo, Kenney Ng, Eric S Lander, Alicia Y Zhou, Sekar Kathiresan, Amit V Khera
Polygenic background modifies penetrance of monogenic variants for tier 1 genomic conditions. Nature communications 11 (1) (2020)
Ozlem Senol-Cosar, Ryan J Schmidt, Emily Qian, Derick Hoskinson, Heather Mason-Suares, Birgit H Funke, Matthew S Lebo
Considerations for clinical curation, classification, and reporting of low-penetrance and low effect size variants associated with disease risk. Genetics in medicine : official journal of the American College of Medical Genetics 21 (12) (2019)
Heather Mason-Suares, Diana Toledo, Jean Gekas, Katherine A Lafferty, Naomi Meeks, M Cristina Pacheco, David Sharpe, Thomas E Mullen, Matthew S Lebo
Juvenile myelomonocytic leukemia-associated variants are associated with neo-natal lethal Noonan syndrome. European journal of human genetics : EJHG 25 (4) (2017)
Ozge Ceyhan-Birsoy, Kalotina Machini, Matthew S Lebo, Timothy W Yu, Pankaj B Agrawal, Richard B Parad, Ingrid A Holm, Amy McGuire, Robert C Green, Alan H Beggs, Heidi L Rehm
A curated gene list for reporting results of newborn genomic sequencing. Genetics in medicine : official journal of the American College of Medical Genetics 19 (7) (2017)
Sami S Amr, Saeed H Al Turki, Matthew S Lebo, Mahdi Sarmady, Michael J Bamshad, Ahmad N Abou Tayoun
Using large sequencing data sets to refine intragenic disease regions and prioritize clinical variant interpretation. Genetics in medicine : official journal of the American College of Medical Genetics 19 (5) (2016)
Diana L Mandelker, Ryan J Schmidt, Arunkanth Ankala, Kristin McDonald Gibson, Mark Bowser, Himanshu Sharma, Elizabeth D Hynes, Madhuri Hegde, Avni Santani, Matthew S Lebo, Birgit Funke
Navigating highly homologous genes in a molecular diagnostic setting: a resource for clinical next-generation sequencing. Genetics in medicine : official journal of the American College of Medical Genetics 18 (12) (2016)
Ahmed A Alfares, Melissa A Kelly, Gregory McDermott, Birgit H Funke, Matthew S Lebo, Samantha B Baxter, Jun Shen, Heather M McLaughlin, Eugene H Clark, Larry J Babb, Stephanie W Cox, Steven R DePalma, Carolyn Y Ho, J G Seidman, Christine E Seidman, Michael J Bamshad
Results of clinical genetic testing of 2,912 probands with hypertrophic cardiomyopathy: expanded panels offer limited additional sensitivity. Genetics in medicine : official journal of the American College of Medical Genetics 17 (11) (2015)