Wayne M Jepsen (Wayne Jepsen)

ORCID

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 6

Top Venues

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

Publications

Anna Abraham, Keri Ramsey, Newell Belnap, Szabolcs Szelinger, Wayne M Jepsen, Chris Balak, Meredith Sanchez-Castillo, Marcus Naymik, Anna Bonfitto, Sampathkumar Rangasamy, Semyon Kruglyak, Matthew Huentelman, Vinodh Narayanan
FGF12 copy number variant associated with epileptic encephalopathy. Clinical genetics (2024)
Anna Abraham, Keri Ramsey, Newell Belnap, Szabolcs Szelinger, Wayne M Jepsen, Chris Balak, Meredith Sanchez-Castillo, Marcus Naymik, Anna Bonfitto, Sampathkumar Rangasamy, Semyon Kruglyak, Matthew Huentelman, Vinodh Narayanan
FGF12 copy number variant associated with epileptic encephalopathy. Clinical genetics 106 (1) (2024)
Eric Frankel, Avijit Podder, Megan Sharifi, Roshan Pillai, Newell Belnap, Keri Ramsey, Julius Dodson, Pooja Venugopal, Molly Brzezinski, Lorida Llaci, Brittany Gerald, Gabrielle Mills, Meredith Sanchez-Castillo, Chris D Balak, Szabolcs Szelinger, Wayne M Jepsen, Ashley L Siniard, Ryan Richholt, Marcus Naymik, Isabelle Schrauwen, David W Craig, Ignazio Stefano Piras, Matthew J Huentelman, Nicholas J Schork, Vinodh Narayanan, Sampathkumar Rangasamy
Genetic and Protein Network Underlying the Convergence of Rett-Syndrome-like (RTT-L) Phenotype in Neurodevelopmental Disorders. Cells 12 (10) (2023)
Wayne M Jepsen, Matthew De Both, Ashley L Siniard, Keri Ramsey, Ignazio Stefano Piras, Marcus Naymik, Adrienne Henderson, Matthew J Huentelman
Adenosine triphosphate binding cassette subfamily C member 1 (ABCC1) overexpression reduces APP processing and increases alpha- versus beta-secretase activity, in vitro. Biology open 10 (1) (2021)
Wayne M Jepsen, Keri Ramsey, Szabolcs Szelinger, Lorida Llaci, Chris Balak, Newell Belnap, Cherae Bilagody, Matthew De Both, Raj Gupta, Marcus Naymik, Richa Pandey, Ignazio S Piras, Meredith Sanchez-Castillo, Sampathkumar Rangasamy, Vinodh Narayanan, Matthew J Huentelman
Two additional males with X-linked, syndromic mental retardation carry de novo mutations in HNRNPH2. Clinical genetics 96 (2) (2019)
Matt Huentelman, Matthew De Both, Wayne M Jepsen, Ignazio S Piras, Joshua S Talboom, Mari Willeman, Eric M Reiman, John Hardy, Amanda J Myers
Common BACE2 Polymorphisms are Associated with Altered Risk for Alzheimer's Disease and CSF Amyloid Biomarkers in APOE ε4 Non-Carriers. Scientific reports 9 (1) (2019)

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Publication Activity (10 Years)

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Wayne M Jepsen (Wayne Jepsen)