Cora M. Taylor - The University of Tennessee

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论文共 52 篇作者统计合作学者相似作者

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Improvement of Variant Reclassification in Genetic Neurodevelopmental Conditions

Michelle Kowanda,Rebecca Sheedy Smith, Jamie Atondo,Catherine Kentros, Elisheva Kleinman,Lauren Kasparson Walsh,Gerhard Schratt,Cora M. Taylor,Wendy K. Chung.

Genetics in Medicine Openpp.101845, (2024)

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Genetic Modifiers and Ascertainment Drive Variable Expressivity of Complex Disorders

Matthew Jensen,Corrine Smolen,Anastasia Tyryshkina,Lucilla Pizzo,Deepro Banerjee, Matthew Oetjens,Hermela Shimelis,Cora M Taylor,Vijay Kumar Pounraja,Hyebin Song,Laura Rohan,Emily Huber,Laila El Khattabi,Ingrid van de Laar,Rafik Tadros,Connie Bezzina,Marjon van Slegtenhorst,Janneke Kammeraad,Paolo Prontera,Jean-Hubert Caberg, Harry Fraser, Siddhartha Banka,Anke Van Dijck,Charles Schwartz,Els Voorhoeve,Patrick Callier,Anne-Laure Mosca-Boidron,Nathalie Marle,Mathilde Lefebvre,Kate Pope,Penny Snell,Amber Boys,Paul J Lockhart,Myla Ashfaq,Elizabeth McCready, Margaret Nowacyzk,Lucia Castiglia,Ornella Galesi,Emanuela Avola,Teresa Mattina,Marco Fichera, Maria Grazia Bruccheri,Giuseppa Maria Luana Mandarà,Francesca Mari,Flavia Privitera,Ilaria Longo,Aurora Curró,Alessandra Renieri,Boris Keren,Perrine Charles,Silvestre Cuinat,Mathilde Nizon,Olivier Pichon,Claire Bénéteau,Radka Stoeva,Dominique Martin-Coignard, Sophia Blesson,Cedric Le Caignec,Sandra Mercier,Marie Vincent,Christa Martin,Katrin Mannik,Alexandre Reymond,Laurence Faivre,Erik Sistermans,R Frank Kooy,David J Amor,Corrado Romano,Joris Andrieux,Santhosh Girirajan

medRxiv the preprint server for health sciences (2024)

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Marissa Weyer Mitchel,Stefanie Turner,Lauren K Walsh,Rebecca I Torene, Scott M Myers,Cora M Taylor

Research square (2024)

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P152: Seizure Severity Across Neurogenetic Conditions in Simons Searchlight*

Michelle Kowanda, Katina Calakos,LeeAnne Green Snyder,Catherine Kentros,Jennifer Bain,Siddharth Srivastava,Tristan Sands,Gerhard Schratt,Cora Taylor,Wendy Chung

Genetics in Medicine Open (2024): 101049

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P612: Improvement of Variant Reclassification in Genetic Neurodevelopmental Conditions: Simons Searchlight Research Registry

Michelle Kowanda,Rebecca Sheedy Smith, Jamie Lundy,Catherine Kentros, Elisheva Kleinman,Lauren Kasparson Walsh,Gerhard Schratt,Cora Taylor,Wendy Chung

Genetics in Medicine Open (2024): 101518

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Phenotypic Shift in Copy Number Variants: Evidence in 16p11.2 Duplication Syndrome

Cora M. Taylor,Brenda M. Finucane,Andres Moreno-De-Luca,Lauren K. Walsh,Christa Lese Martin,David H. Ledbetter

GENETICS IN MEDICINE（2023）

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Neurodevelopmental Phenotypes Associated with Pathogenic Variants in SLC6A1

Ashley Kahen,Haluk Kavus,Alexa Geltzeiler,Catherine Kentros,Cora Taylor,Elizabeth Brooks,LeeAnne Green Snyder,Wendy Chung

JOURNAL OF MEDICAL GENETICS（2022）

引用16浏览0WOS引用

Availability of Services and Caregiver Burden: Supporting Individuals with Neurogenetic Conditions During the COVID-19 Pandemic

Michelle Kowanda, Lindsey Cartner,Catherine Kentros,Alexa R. Geltzeiler, Kaitlyn E. Singer, W. Curtis Weaver, Christopher D. Lehman, Simone Smith,Rebecca Sheedy Smith,Lauren Kasparson Walsh,Katharine Diehl, Natalie Nagpal,Elizabeth Brooks,Caroline M. Mebane,Ashley L. Wilson,Alison R. Marvin,L. Casey White,J. Kiely Law, William Jensen,Amy M. Daniels,Jennifer Tjernagel,LeeAnne Green Snyder,Cora M. Taylor,Wendy K. Chung

JOURNAL OF CHILD NEUROLOGY（2021）

引用14浏览0WOS引用

DELETERIOUS "SHIFT" IN FUNCTIONAL PERFORMANCE EXPLAINS CLINICAL VARIABILITY IN RARE GENETIC NEURODEVELOPMENTAL PSYCHIATRIC DISORDERS

David Ledbetter,Brenda Finucane,Cora Taylor, Andres Morena de Luca,Scott Myers,Christa Martin

EUROPEAN NEUROPSYCHOPHARMACOLOGY（2021）

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