Ayesha Muhammad

Publication Activity (10 Years)

Years Active: 2022-2024
Publications (10 Years): 10

Top Topics

Genome Wide Association

Angiotensin Converting Enzyme

Top Venues

Circulation. Genomic and precision medicine

bioRxiv : the preprint server for biology

European heart journal

Clinical and translational science

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

Publications

Joanne G Ma, Matthew J O'Neill, Ebony Richardson, Kate L Thomson, Jodie Ingles, Ayesha Muhammad, Joseph F Solus, Giovanni E Davogustto, Katherine C Anderson, M Benjamin Shoemaker, Andrew Ben Stergachis, Brendan J Floyd, Kyla E Dunn, Victoria N Parikh, Henry ChubbW, Mark J Perrin, Dan M Roden, Jamie I Vandenberg, Chai-Ann Ng, Andrew M Glazer
Multisite Validation of a Functional Assay to Adjudicate SCN5A Brugada Syndrome-Associated Variants. Circulation. Genomic and precision medicine 17 (4) (2024)
Joanne G Ma, Matthew J O'Neill, Ebony Richardson, Kate L Thomson, Jodie Ingles, Ayesha Muhammad, Joseph F Solus, Giovanni E Davogustto, Katherine C Anderson, M Benjamin Shoemaker, Andrew Ben Stergachis, Brendan J Floyd, Kyla E Dunn, Victoria N Parikh, Henry ChubbW, Mark J Perrin, Dan M Roden, Jamie I Vandenberg, Chai-Ann Ng, Andrew M Glazer
Multisite Validation of a Functional Assay to Adjudicate SCN5A Brugada Syndrome-Associated Variants. Circulation. Genomic and precision medicine 17 (4) (2024)
Joanne G Ma, Matthew J O'Neill, Ebony Richardson, Kate L Thomson, Jodie Ingles, Ayesha Muhammad, Joseph F Solus, Giovanni E Davogustto, Katherine C Anderson, M Benjamin Shoemaker, Andrew Ben Stergachis, Brendan J Floyd, Kyla E Dunn, Victoria N Parikh, Henry ChubbW, Mark J Perrin, Dan M Roden, Jamie I Vandenberg, Chai-Ann Ng, Andrew M Glazer
Multisite Validation of a Functional Assay to Adjudicate SCN5A Brugada Syndrome-Associated Variants. Circulation. Genomic and precision medicine (2024)
Joanne G Ma, Matthew J O'Neill, Ebony Richardson, Kate L Thomson, Jodie Ingles, Ayesha Muhammad, Joseph F Solus, Giovanni E Davogustto, Katherine C Anderson, M Benjamin Shoemaker, Andrew Ben Stergachis, Brendan J Floyd, Kyla E Dunn, Victoria N Parikh, Henry ChubbW, Mark J Perrin, Dan M Roden, Jamie I Vandenberg, Chai-Ann Ng, Andrew M Glazer
Multisite Validation of a Functional Assay to Adjudicate SCN5A Brugada Syndrome-Associated Variants. Circulation. Genomic and precision medicine 17 (4) (2024)
Joanne G Ma, Matthew J O'Neill, Ebony Richardson, Kate L Thomson, Jodie Ingles, Ayesha Muhammad, Joseph F Solus, Giovanni E Davogustto, Katherine C Anderson, M Benjamin Shoemaker, Andrew Ben Stergachis, Brendan J Floyd, Kyla E Dunn, Victoria N Parikh, Henry ChubbW, Mark J Perrin, Dan M Roden, Jamie I Vandenberg, Chai-Ann Ng, Andrew M Glazer
Multisite Validation of a Functional Assay to Adjudicate SCN5A Brugada Syndrome-Associated Variants. Circulation. Genomic and precision medicine (2024)
Ayesha Muhammad, Maria E Calandranis, Bian Li, Tao Yang, Daniel J Blackwell, M Lorena Harvey, Jeremy E Smith, Ashli E Chew, Anthony Capra, Kenneth A Matreyek, Douglas M Fowler, Dan M Roden, Andrew M Glazer
High-throughput functional mapping of variants in an arrhythmia gene, KCNE1 , reveals novel biology. bioRxiv : the preprint server for biology (2023)
Ayesha Muhammad, Maria E Calandranis, Bian Li, Tao Yang, Daniel J Blackwell, M Lorena Harvey, Jeremy E Smith, Ashli E Chew, Anthony Capra, Kenneth A Matreyek, Douglas M Fowler, Dan M Roden, Andrew M Glazer
High-throughput functional mapping of variants in an arrhythmia gene, KCNE1 , reveals novel biology. bioRxiv : the preprint server for biology (2023)
Morgan L Shannon, Ayesha Muhammad, Nathan T James, Michael L Williams, Joseph Breeyear, Todd Edwards, Jonathan D Mosley, Leena Choi, Prince Kannankeril, Sara L Van Driest
Variant-Based Heritability Assessment of Dexmedetomidine and Fentanyl Clearance in Pediatric Patients. Clinical and translational science (2023)
Ayesha Muhammad, Maria E Calandranis, Bian Li, Tao Yang, Daniel J Blackwell, M Lorena Harvey, Jeremy E Smith, Ashli E Chew, Anthony Capra, Kenneth A Matreyek, Douglas M Fowler, Dan M Roden, Andrew M Glazer
High-throughput functional mapping of variants in an arrhythmia gene, KCNE1 , reveals novel biology. bioRxiv : the preprint server for biology (2023)
Jonas Ghouse, Vinicius Tragante, Ayesha Muhammad, Gustav Ahlberg, Morten W Skov, Dan M Roden, Ingileif Jónsdóttir, Laura Andreasen, Pia Rengtved Lundegaard, Linea C Trudsø, Karina Banasik, Søren Brunak, Sisse Rye Ostrowski, null null, Christian Torp-Pedersen, Ole V Pedersen, Erik Sørensen, Lars Valeur Køber, Kasper Iversen, Unnur Thorsteinsdottir, Gudmundur Thorgeirsson, Henrik Ullum, Daniel F Gudbjartsson, Jonathan D Mosley, Hilma Hólm, Kári Stefánsson, Henning Bundgaard, Morten Salling Olesen
Polygenic risk score for ACE-inhibitor-associated cough based on the discovery of new genetic loci. European heart journal 43 (45) (2022)