Wen‐Han Tan
发表
G. Carvill,
H. Mefford,
P. Striano,
2018,
Epilepsia.
Meghan T. Miller,
J. Hipp,
A. Rotenberg,
2019,
Biological Psychiatry.
A. Pagnamenta,
J. Lupski,
J. Meiler,
2020,
medRxiv.
Ethan M. Goldberg,
Zara,
Silvana,
2021
.
Rodney C. Samaco,
E. Storch,
W. Goodman,
2022,
American journal on intellectual and developmental disabilities.
F. Duffy,
Yiping Shen,
David T. Miller,
2014,
Annals of neurology.
Ethan M. Goldberg,
S. Scherer,
J. Howe,
2021,
medRxiv.
K. Maski,
S. Kothare,
K. Krishnamoorthy,
2010,
Epilepsy & Behavior.
I. Campbell,
Sarah E. Sheppard,
Wen‐Han Tan,
2021,
Scientific Reports.
J. Hipp,
L. Bird,
M. Keute,
2021,
Biological psychiatry global open science.
J. Hipp,
A. Rotenberg,
L. Bird,
2021,
Pediatric neurology.
D. J. Driscoll,
Hye-Seung Lee,
W. Kaufmann,
2021,
Pediatric neurology.
Clinical heterogeneity associated with KCNA1 mutations include cataplexy and nonataxic presentations
Meghan C Towne,
C. Brownstein,
A. Beggs,
2015,
neurogenetics.
E. M. DeGennaro,
Sarah E. Gould,
David R. Murdock,
2023,
Proceedings of the National Academy of Sciences of the United States of America.
M. Daly,
J. Korn,
J. Thakuria,
2008,
Journal of Medical Genetics.
Kimberly A. Parkerson,
Meghan T. Miller,
J. Hipp,
2023,
Journal of Neurodevelopmental Disorders.
Disruption of MBD5 contributes to a spectrum of psychopathology and neurodevelopmental abnormalities
J. Gusella,
C. Morton,
M. Talkowski,
2014,
Molecular Psychiatry.
L. Bird,
R. Hundley,
S. Peters,
2023,
Journal of autism and developmental disorders.
Joshua M. Korn,
M. Daly,
J. Thakuria,
2008,
Journal of Medical Genetics.
Disruption of MBD5 contributes to a spectrum of psychopathology and neurodevelopmental abnormalities
J. Gusella,
C. Morton,
M. Talkowski,
2014,
Molecular Psychiatry.
L. Bird,
R. Burdine,
Cesar Ochoa-Lubinoff,
2023,
Quality of Life Research.