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Natalie Ginn

children's hospital of philadelphia

3H-index
11Paper Count
46Citation Count
Published Papers 4
Publication Date
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Genetic testing for familial epilepsies: Diagnostic yield and genetic findings
errEpilepsia
IF6.6
err2026-03-08
err0
errOAAI
errColin A. Ellis; Juliette Copeland; Isabella Velez; Karen L. Oliver; Hannah Shalaby; Aaron Baldwin; Caren Armstrong; Amanda Back; Brianna Berlin; Stacey Cohen; Vishnu Anand Cuddapah; Danielle deCampo; Holly Dubbs; Natalie Ginn; Alicia G. Harrison; Naomi Lewin; Laina Lusk; Eric D. Marsh; Shavonne L. Massey; Pamela Pojomovsky McDonnell; Jillian L. McKee; Xilma Ortiz-Gonzalez; Anna J. Prentice; Katie Rose Sullivan; Sarah M. Ruggiero; Mark P. Fitzgerald; Ethan M. Goldberg; Ingo Helbig
errShare
errSave
Sequence variants in HECTD1 result in a variable neurodevelopmental disorder
errAMERICAN JOURNAL OF HUMAN GENETICS
IF8.1
err2025-01-01
err0
errOAAI
errZerafati-Jahromi, Gazelle; Oxman, Elias; Hoang, Hieu D.; Charng, Wu-Lin; Kotla, Tanvitha; Yuan, Weimin; Ishibashi, Keito; Sebaoui, Sonia; Luedtke, Kathryn; Winrow, Bryce; Ganetzky, Rebecca D.; Ruiz, Anna; Manso-Basuz, Carmen; Spataro, Nino; Kannu, Peter; Athey, Taryn; Peroutka, Christina; Barnes, Caitlin; Sidlow, Richard; Anadiotis, George; Magnussen, Kari; Valenzuela, Irene; Moles-Fernandez, Alejandro; Berger, Seth; Grant, Christina L.; Vilain, Eric; Arnadottir, Gudny A.; Sulem, Patrick; Sulem, Telma S.; Stefansson, Kari; Massey, Shavonne; Ginn, Natalie; Poduri, Annapurna; D'Gama, Alissa M.; Valentine, Rozalia; Trowbridge, Sara K.; Murali, Chaya N.; Franciskovich, Rachel; Tran, Yen; Webb, Bryn D.; Keppler-Noreuil, Kim M.; Hall, April L.; Mcgivern, Bobbi; Monaghan, Kristin G.; Sacoto, Maria J. Guillen; Baldridge, Dustin; Silverman, Gary A.; Dahiya, Sonika; Turner, Tychele N.; Schedl, Tim; Corbin, Joshua G.; Pak, Stephen C.; Zohn, Irene E.; Gurnett, Christina A.
errShare
errSave
Rare dysfunctional SCN2A variants are associated with malformation of cortical development
errEPILEPSIA
IF6.6
err2024-12-21
err0
errOAAI
errClatot, Jerome; Thompson, Christopher H.; Sotardi, Susan; Jiang, Jinan; Trivisano, Marina; Balestrini, Simona; Ward, D. Isum; Ginn, Natalie; Guaragni, Brunetta; Malerba, Laura; Vakrinou, Angeliki; Sherer, Mia; Helbig, Ingo; Somarowthu, Ala; Sisodiya, Sanjay M.; Ben-Shalom, Roy; Guerrini, Renzo; Specchio, Nicola; George Jr, Alfred L.; Goldberg, Ethan M.
errShare
errSave
A KCNC1-related neurological disorder due to gain of Kv3.1 function
errANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY
IF3.9
err2022-11-23
err9
errOAAI
errClatot, Jerome; Ginn, Natalie; Costain, Gregory; Goldberg, Ethan M.
errShare
errSave

Research Directions

No research directions
Co-authors
Cooperation Journals
K
Kāri Stefánsson
H-index: 219 · Papers: 1.2K
R
Renzo Guerrini
H-index: 116 · Papers: 2.1K
P
Patrick Sulem
H-index: 111 · Papers: 377
A
Alfred L. George
H-index: 100 · Papers: 568
S
Sanjay M. Sisodiya
H-index: 99 · Papers: 577
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