All papers authored by Sara Lewis
Refreshing results…
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Sara A. Lewis ,
Somayeh Bakhtiari,
Sandra Hinz Nordlie,
Alex Pagnozzi,
Helen Magee,
Stephanie Efthymiou ,
Jennifer A. Heim,
Patricia Cornejo,
Maha S. Zaki,
Najwa Anwar,
Shazia Maqbool,
Fatima Rahman,
Derek E. Neilson,
Anusha Vemuri
and 45 other authors
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Maya Chopra,
Julie S. Cohen,
Jennifer Bain,
Bhooma Aravamuthan,
Jason B. Carmel,
Michael C. Fahey,
Reeval Segel,
Richard F. Wintle ,
Michael Zech,
Halie May,
Nahla Haque,
Darcy Fehlings,
Siddharth Srivastava,
Michael C. Kruer
Clinical actionability of genetic findings in cerebral palsy
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Somayeh Bakhtiari,
Jacob Forstrom,
Allan Bayat ,
Frédéric Bilan ,
Gwenaël Le Guyader,
Ebba Alkhunaizi ,
Hilary Vernon ,
Sergio R. Padilla-Lopez,
Michael C. Kruer
Download from doi.org
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Sheetal Shetty,
Sean Gamble,
Jennifer Heim,
Ningning Zhao,
Gideon Stitt,
Matthew Pankratz,
Tara Mangum,
Iris Marku,
Robert B. Rosenberg,
Angus A. Wilfong,
Michael C. Fahey,
Sukhan Kim,
Scott J. Myers,
Brian Appavu
and 1 other authors
Intrathecal magnesium delivery for Mg++-insensitive NMDA receptor activity due to GRIN1 mutation
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Daniel Cameron,
Phillip Demarest,
Anika Nabila,
Junfei Zhao,
Paul Bergin,
Casie Reed,
Makiko Yamada,
Alex Pagnozzi,
Caroline Nava,
Emilie Bourel-Ponchel,
Derek E. Neilson
and 10 other authors
A transposase-derived gene required for human brain development
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Sara A. Lewis ,
Michael C. Kruer,
Annapurna Poduri
Underrepresentation of the term cerebral palsy in clinical genetics databases
Download from onlinelibrary.wiley.com
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Somayeh Bakhtiari,
Jennifer Heim,
Patricia Cornejo,
James Liu,
Aris Huang,
Andrew Musmacker,
Sheng Chih Jin,
Kaya Bilguvar ,
Sergio R. Padilla-Lopez,
Michael C. Kruer
Mutation in ZDHHC15 Leads to Hypotonic Cerebral Palsy, Autism, Epilepsy, and Intellectual Disability
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Sheetal Shetty,
Bryce A. Wilson,
Aris J. Huang,
Sheng Chih Jin,
Hayley Smithers-Sheedy,
Michael C. Fahey,
Michael C. Kruer
Insights From Genetic Studies of Cerebral Palsy
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Sara A. Lewis ,
Somayeh Bakhtiari,
Xue Zeng ,
Michael C. Sierant ,
Sheetal Shetty,
Sandra M. Nordlie ,
Aureliane Elie,
Mark A. Corbett ,
Bethany Y. Norton,
Clare L. van Eyk ,
Shozeb Haider ,
Brandon S. Guida,
Helen Magee,
James Liu
and 62 other authors
Author Correction: Mutations disrupting neuritogenesis genes confer risk for cerebral palsy
Download from www.nature.com
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Sara A. Lewis ,
Somayeh Bakhtiari,
Xue Zeng ,
Michael C. Sierant ,
Sheetal Shetty,
Sandra M. Nordlie ,
Aureliane Elie,
Mark A. Corbett ,
Bethany Y. Norton,
Clare L. van Eyk ,
Shozeb Haider ,
Brandon S. Guida,
Helen Magee,
James Liu
and 62 other authors
Mutations disrupting neuritogenesis genes confer risk for cerebral palsy
Download from www.nature.com
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Brandon Guida,
Matthew Troester,
Sotirios Keros,
Andrea Meredith ,
Michael C. Kruer
Cataplexy in patients harboring the KCNMA1 p.N999S mutation
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Katherine L. Helbig ,
Candace T. Myers,
Marcello Scala,
Robert Huether,
Sara Lewis ,
Tyler N. Kruer,
Brandon S. Guida,
Somayeh Bakhtiari,
Joy Sebe,
Sha Tang,
Heather Stickney,
Sehribani Ulusoy Oktay,
Ashwin A. Bhandiwad,
Keri Ramsey
and 30 other authors
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Andres Moreno-De-Luca ,
Michael Fahey,
Richard J. Leventer,
Sarah McIntyre ,
Hilla Ben-Pazi ,
Mark Corbett,
Xiaoyang Wang,
Gareth Baynam,
Darcy Fehlings,
Manju A. Kurian,
Changlian Zhu,
Kate Himmelmann,
Hayley Smithers-Sheedy
and 13 other authors
Genetic or Other Causation Should Not Change the Clinical Diagnosis of Cerebral Palsy
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