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Nature Genetics
|
March 2, 2011
Mutations in origin recognition complex gene ORC4 cause Meier-Gorlin syndrome
Duane L Guernsey, Makoto Matsuoka, Haiyan Jiang, et al.
American Journal of Human Genetics
|
July 6, 2010
Mutations in centrosomal protein CEP152 in primary microcephaly families linked to MCPH4
Duane L Guernsey, Haiyan Jiang, Julie Hussin, et al.
Journal of Neurosurgery. Pediatrics
|
October 19, 2023
Machine learning models for predicting seizure outcome after MR-guided laser interstitial thermal therapy in children
Omar Yossofzai, Scellig S D Stone, Joseph R Madsen, et al.
Epilepsy & Behavior : E&B
|
August 8, 2025
Immediate-use rescue medication and the epilepsy monitoring unit: experiences from an expert panel
Evelyn K Shih, Brin E Freund, Michael R Sperling, et al.
Epilepsia Open
|
October 20, 2022
Predictors of outcomes after surgery for medically intractable insular epilepsy: A systematic review and individual participant data meta-analysis
Sami Obaid, Jia-Shu Chen, George M Ibrahim, et al.
Epilepsia
|
February 2, 2026
Characterizing early behavioral and social-emotional problems in young children with SCN1A+ Dravet syndrome: Findings from the ENVISION prospective natural history study
Ingrid E Scheffer, M Scott Perry, Joseph Sullivan, et al.
Epilepsia
|
December 6, 2020
FBXO28 causes developmental and epileptic encephalopathy with profound intellectual disability
Amy L Schneider, Candace T Myers, Alison M Muir, et al.
Epilepsia
|
November 18, 2025
Cognitive stagnation and executive function deficits in young children with SCN1A+ Dravet syndrome: Detailed characterization of onset, progression, and impact in the ENVISION natural history study
Joseph Sullivan, M Scott Perry, Ingrid E Scheffer, et al.
Epilepsia
|
December 4, 2023
Severe communication delays are independent of seizure burden and persist despite contemporary treatments in SCN1A+ Dravet syndrome: Insights from the ENVISION natural history study
M Scott Perry, Ingrid E Scheffer, Joseph Sullivan, et al.
Molecular Cell
|
October 12, 2021
NRF1 association with AUTS2-Polycomb mediates specific gene activation in the brain
Sanxiong Liu, Kimberly A Aldinger, Chi Vicky Cheng, et al.
Page
of 15
Search research articles
Search
Showing results (121-130 of 150) with videos related to
Sort By:
Page
of 15
Nature Genetics
|
March 2, 2011
Mutations in origin recognition complex gene ORC4 cause Meier-Gorlin syndrome
Duane L Guernsey, Makoto Matsuoka, Haiyan Jiang, et al.
American Journal of Human Genetics
|
July 6, 2010
Mutations in centrosomal protein CEP152 in primary microcephaly families linked to MCPH4
Duane L Guernsey, Haiyan Jiang, Julie Hussin, et al.
Journal of Neurosurgery. Pediatrics
|
October 19, 2023
Machine learning models for predicting seizure outcome after MR-guided laser interstitial thermal therapy in children
Omar Yossofzai, Scellig S D Stone, Joseph R Madsen, et al.
Epilepsy & Behavior : E&B
|
August 8, 2025
Immediate-use rescue medication and the epilepsy monitoring unit: experiences from an expert panel
Evelyn K Shih, Brin E Freund, Michael R Sperling, et al.
Epilepsia Open
|
October 20, 2022
Predictors of outcomes after surgery for medically intractable insular epilepsy: A systematic review and individual participant data meta-analysis
Sami Obaid, Jia-Shu Chen, George M Ibrahim, et al.
Epilepsia
|
February 2, 2026
Characterizing early behavioral and social-emotional problems in young children with SCN1A+ Dravet syndrome: Findings from the ENVISION prospective natural history study
Ingrid E Scheffer, M Scott Perry, Joseph Sullivan, et al.
Epilepsia
|
December 6, 2020
FBXO28 causes developmental and epileptic encephalopathy with profound intellectual disability
Amy L Schneider, Candace T Myers, Alison M Muir, et al.
Epilepsia
|
November 18, 2025
Cognitive stagnation and executive function deficits in young children with SCN1A+ Dravet syndrome: Detailed characterization of onset, progression, and impact in the ENVISION natural history study
Joseph Sullivan, M Scott Perry, Ingrid E Scheffer, et al.
Epilepsia
|
December 4, 2023
Severe communication delays are independent of seizure burden and persist despite contemporary treatments in SCN1A+ Dravet syndrome: Insights from the ENVISION natural history study
M Scott Perry, Ingrid E Scheffer, Joseph Sullivan, et al.
Molecular Cell
|
October 12, 2021
NRF1 association with AUTS2-Polycomb mediates specific gene activation in the brain
Sanxiong Liu, Kimberly A Aldinger, Chi Vicky Cheng, et al.
Page
of 15