Profil bibliographique

Priya Vaidiswaran

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

13Publications signalées

475Citations signalées

2Affiliations récentes

Institutions déclarées

Fox Chase Cancer Center Temple University Health System

Domaines associés

Genomics and Rare DiseasesEpilepsy research and treatmentGenetics and Neurodevelopmental DisordersGenomic variations and chromosomal abnormalitiesGenetic Associations and Epidemiology

Publications récentes

2026 conference-abstractOpenAlex

Identification of high-grade neuroendocrine carcinoma (HGNEC) biology across tumor types through transcriptomic profiling and validation in lung cancer.

Yatian Yang, N. Gandhi, Andrew Elliott, Priya Vaidiswaran et autres

0 citationsJournal of Clinical Oncology

Accès ouvert 2026 otherOpenAlex

Immunotherapy Induced T cell dynamics in Non-Small Cell Lung Cancer (NSCLC)

Priya Vaidiswaran

0 citationsCalifornia Digital Library

Accès ouvert 2024 articleOpenAlex

Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes

Siwei Chen, Bassel Abou‐Khalil, Zaid Afawi, Quratulain Zulfiqar Ali et autres

63 citationsNature Neuroscience

Accès ouvert 2024 articleOpenAlex

Clinical signatures of genetic epilepsies precede diagnosis in electronic medical records of 32,000 individuals

Peter D. Galer, Shridhar Parthasarathy, Julie Xian, Jillian L. McKee et autres

9 citationsGenetics in Medicine

Accès ouvert 2024 preprintOpenAlex

Optimizing clinical interpretability of functional evidence in epilepsy-related ion channel variants

Shridhar Parthasarathy, Stacey Cohen, Eryn Fitch, Priya Vaidiswaran et autres

1 citationbioRxiv (Cold Spring Harbor Laboratory)

Accès ouvert 2023 reviewOpenAlex

GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture

Remi Stevelink, Ciarán Campbell, Siwei Chen, Bassel Abou‐Khalil et autres

225 citationsNature Genetics

Accès ouvert 2023 articleOpenAlex

Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals

Ludovica Montanucci, David Lewis‐Smith, Ryan L. Collins, Lisa‐Marie Niestroj et autres

59 citationsNature Communications

Accès ouvert 2023 preprintOpenAlex

Clinical Signatures of Genetic Epilepsies Precede Diagnosis in Electronic Medical Records of 32,000 Individuals

Peter D. Galer, Shridhar Parthasarathy, Julie Xian, Jillian L. McKee et autres

0 citationsSSRN Electronic Journal

Accès ouvert 2021 articleOpenAlex

Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals

Joshua E. Motelow, Gundula Povysil, Ryan S. Dhindsa, Kate E. Stanley et autres

4 citationsThe American Journal of Human Genetics

Accès ouvert 2021 articleOpenAlex

Modeling seizures in the Human Phenotype Ontology according to contemporary ILAE concepts makes big phenotypic data tractable

David Lewis‐Smith, Peter D. Galer, Ganna Balagura, Hugh Kearney et autres

25 citationsEpilepsia

Accès ouvert 2021 articleOpenAlex

Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals

Joshua E. Motelow, Gundula Povysil, Ryan S. Dhindsa, Kate E. Stanley et autres

60 citationsThe American Journal of Human Genetics

Accès ouvert 2020 articleOpenAlex

Whole‐exome and HLA sequencing in Febrile infection‐related epilepsy syndrome

Ingo Helbig, Giulia Barcia, Manuela Pendziwiat, Shiva Ganesan et autres

29 citationsAnnals of Clinical and Translational Neurology

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