Author

Samantha A. Schrier Vergano

Children's NationalORCID 0000-0001-9194-0644Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 2 Organism:human· 2 Approach:statistical model· 2 Assay:DNA methylation· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

A. Kuechler· 1 shared A. Petersen· 1 shared A. Vaknin-Dembinsky· 1 shared A. Waheeb· 1 shared Adam JacksoniD· 1 shared Alexander J.M. DingemansiD· 1 shared Alexander P.A. StegmanniD· 1 shared Alexandre ReymondiD· 1 shared

Activity by Year

2021-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetics

A. Kuechler

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2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintOct 23, 2026

EpiSignaLR: an open resource for genome-wide episignature analysis from methylation-aware short- and long-read sequencing

Sophia B Gibson, Miranda Pg Zalusky, Joy Goffena…·Danny E. Miller

The paper develops EpiSignaLR, a resource for genome-wide episignature analysis using methylation-aware sequencing data, identifying DMRs and classifiers for three neurodevelopmental disorders.

DOI 10.64898/2026.10.21.26366070

humanDNA methylation

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GeneticsThe American Journal of Human GeneticsPeer-reviewedJan 28, 2021

Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction

Joery den Hoed, Elke de Boer, Norine Voisin…·Lisenka E.L.M. Vissers

The paper identifies mutation-specific pathophysiological mechanisms in SATB1 variants causing distinct neurodevelopmental disorders.

52 citationstop 2%

humanstatistical model

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