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Shridhar Parthasarathy

Showing results (11-20 of 24) with videos related to

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Medrxiv : the Preprint Server for Health Sciences|May 7, 2024
The clinical and genetic spectrum of paediatric speech and language disorders in 52,143 individualsJan Magielski, Sarah M Ruggiero, Julie Xian, et al.
Neurology|April 14, 2025
Deciphering the Natural History of <i>SCN8A</i>-Related DisordersJan H Magielski, Stacey Cohen, Michael C Kaufman, et al.
Medrxiv : the Preprint Server for Health Sciences|July 10, 2023
Early life seizures and epileptic spasms in <i>STXBP1</i>-related disordersKim M Thalwitzer, Julie Xian, Danielle deCampo, et al.
Epilepsia|January 27, 2024
Early life seizures and epileptic spasms in STXBP1-related disordersKim M Thalwitzer, Julie Xian, Danielle de Campo, et al.
Brain : a Journal of Neurology|October 16, 2024
The clinical and genetic spectrum of paediatric speech and language disordersJan H Magielski, Sarah M Ruggiero, Julie Xian, et al.
Nature Communications|July 20, 2023
Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individualsLudovica Montanucci, David Lewis-Smith, Ryan L Collins, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 18, 2021
Computational analysis of 10,860 phenotypic annotations in individuals with SCN2A-related disordersKatherine Crawford, Julie Xian, Katherine L Helbig, et al.
Biorxiv : the Preprint Server for Biology|March 31, 2025
Phenotypic analysis of 11,125 trio exomes in neurodevelopmental disordersShiva Ganesan, Sarah M Ruggiero, Shridhar Parthasarathy, et al.
Medrxiv : the Preprint Server for Health Sciences|April 20, 2026
DNM1-related disorder is characterized by recurrent variants and phenotypic homogeneityAlicia G Harrison, Shiva Ganesan, Hongbo M Xie, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 16, 2024
Clinical signatures of genetic epilepsies precede diagnosis in electronic medical records of 32,000 individualsPeter D Galer, Shridhar Parthasarathy, Julie Xian, et al.
Pageof 3

Showing results (11-20 of 24) with videos related to

Sort By:
Pageof 3
Medrxiv : the Preprint Server for Health Sciences|May 7, 2024
The clinical and genetic spectrum of paediatric speech and language disorders in 52,143 individualsJan Magielski, Sarah M Ruggiero, Julie Xian, et al.
Neurology|April 14, 2025
Deciphering the Natural History of <i>SCN8A</i>-Related DisordersJan H Magielski, Stacey Cohen, Michael C Kaufman, et al.
Medrxiv : the Preprint Server for Health Sciences|July 10, 2023
Early life seizures and epileptic spasms in <i>STXBP1</i>-related disordersKim M Thalwitzer, Julie Xian, Danielle deCampo, et al.
Epilepsia|January 27, 2024
Early life seizures and epileptic spasms in STXBP1-related disordersKim M Thalwitzer, Julie Xian, Danielle de Campo, et al.
Brain : a Journal of Neurology|October 16, 2024
The clinical and genetic spectrum of paediatric speech and language disordersJan H Magielski, Sarah M Ruggiero, Julie Xian, et al.
Nature Communications|July 20, 2023
Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individualsLudovica Montanucci, David Lewis-Smith, Ryan L Collins, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 18, 2021
Computational analysis of 10,860 phenotypic annotations in individuals with SCN2A-related disordersKatherine Crawford, Julie Xian, Katherine L Helbig, et al.
Biorxiv : the Preprint Server for Biology|March 31, 2025
Phenotypic analysis of 11,125 trio exomes in neurodevelopmental disordersShiva Ganesan, Sarah M Ruggiero, Shridhar Parthasarathy, et al.
Medrxiv : the Preprint Server for Health Sciences|April 20, 2026
DNM1-related disorder is characterized by recurrent variants and phenotypic homogeneityAlicia G Harrison, Shiva Ganesan, Hongbo M Xie, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 16, 2024
Clinical signatures of genetic epilepsies precede diagnosis in electronic medical records of 32,000 individualsPeter D Galer, Shridhar Parthasarathy, Julie Xian, et al.
Pageof 3