Author

Jessica Zweifach

Icahn School of Medicine at Mount SinaiORCID 0000-0001-5392-8839Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Research Focus:benchmarking· 1 Research Focus:cell type annotation· 1 Research Focus:clustering· 1 Research Focus:differential expression· 1 Assay:electronic health records· 1 Approach:experimental assay· 1 Approach:machine learning (classical)· 1

Frequent Co-Authors

Alexander KolevzoniD· 2 shared Danielle B. HalperniD· 2 shared Joseph D. BuxbaumiD· 2 shared Paige M. SiperiD· 2 shared Abigaël A. Thinakaran· 1 shared Bonnie LermaniD· 1 shared Catherine SanciminoiD· 1 shared Evan SchafferiD· 1 shared

Activity by Year

2023-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 37 mutual co-author links

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2 shared papersNeuroscience

Alexander KolevzonORCID

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2 papers

Recent·Most cited

NeurosciencebioRxivPreprintApr 10, 2026

Identifying Phelan-McDermid-Like Electrophysiological Subtypes in Autism Using EEG and Machine Learning

Shaun Kohli, Evan Schaffer, Julia Savino…·Shlomit Beker

The paper uses EEG and machine learning to identify electrophysiological subtypes in autism, finding a PMS-like subgroup in idiopathic ASD with reduced gamma-band phase-locking.

DOI 10.64898/2026.04.10.715308

humanelectronic health records

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Genetic & Genomic MedicinemedRxivPreprintApr 17, 2023

Prospective phenotyping of CHAMP1 disorder indicates that coding mutations do not act through haploinsufficiency

Tess Levy, Thariana Pichardo, Hailey Silver…·Joseph D. Buxbaum

The paper compares clinical phenotypes of CHAMP1 mutations and deletions, finding mutations cause more severe symptoms through dominant negative or gain of function mechanisms, while deletions act via haploinsufficiency.

DOI 10.1101/2023.04.17.23288527

humanexperimental assay

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