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You searched for: Author/Creator Panchagnula, Shreyas

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1. 116 Exome Sequencing Uncovers Molecular Determinants of Trigeminal Neuralgia. Issue Volume 65:Issue CN(2018)Supplement 1 (16th August 2018)

2. 125 De Novo Mutations in Genes Regulating Neural Stem Cell Fate in Human Congenital Hydrocephalus. Issue Volume 65:Issue CN(2018)Supplement 1 (16th August 2018)

4. Exome Sequencing Defines the Molecular Pathogenesis of Vein of Galen Malformation. (1st September 2019)

5. Exome Sequencing Defines the Molecular Pathogenesis of Vein of Galen Malformation. (September 2019)

6. Integrative Genomics Implicates Genetic Disruption of Prenatal Neurogenesis in Congenital Hydrocephalus. (16th November 2020)

7. PTEN mutations in autism spectrum disorder and congenital hydrocephalus: developmental pleiotropy and therapeutic targets. Issue 12 (December 2021)

8. Symptomatic Arachnoid Cysts are Associated With Mutations in Chromatin Remodeling Genes. (16th November 2020)