Samantha Schrier Vergano

22PUBLICATIONS
99CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)NeurogeneticsCryptographyGene mappingMedical infection agents (incl. prions)
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Publications (22)

|Jan 20, 2024
ARID2, a milder cause of Coffin-Siris Syndrome? Broadening the phenotype with 17 additional individuals.

Samantha A Schrier Vergano

|Jul 27, 2023
Landscape of mSWI/SNF chromatin remodeling complex perturbations in neurodevelopmental disorders.

Alfredo M Valencia, Akshay Sankar, Pleuntje J van der Sluijs

|Sep 30, 2022
Epilepsy in Coffin-Siris syndrome: A report from the international CSS registry and review of the literature.

Michael Ciliberto, Karen Skjei, Ashley Vasko

|Jul 07, 2022
Evidence for an association between Coffin-Siris syndrome and congenital diaphragmatic hernia.

Yoel Gofin, Xiaonan Zhao, Amanda Gerard

|May 11, 2022
Heterozygous variants in PRPF8 are associated with neurodevelopmental disorders.

Lauren O'Grady, Samantha A Schrier Vergano, Trevor L Hoffman

|Mar 07, 2022
Exome and RNA-Seq analyses of an incomplete penetrance variant in USP9X in female-specific syndromic intellectual disability.

Dong Li, Michael E March, Tiancheng Wang

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