Author

Allan Schornagel

GGZ Delfland

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetic & Genomic Medicine· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:variant calling· 2 Assay:whole-exome sequencing· 2 Assay:whole-genome sequencing· 2

Frequent Co-Authors

Herbert M. LachmaniD· 2 shared Janet L. CunninghamiD· 2 shared Peter J. van der SpekiD· 2 shared Alberto SpaliceiD· 1 shared Andreea M. Serban· 1 shared Anjana SoorajkumariD· 1 shared Deyou ZhengiD· 1 shared Dhanya Vettiatil· 1 shared

Activity by Year

2022-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Herbert M. LachmanORCID

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2 papers

Recent·Most cited

Ultrarare Variants in DNA Damage Repair and Mitochondrial Genes in Pediatric Acute-Onset Neuropsychiatric Syndrome and Acute Behavioral Regression in Neurodevelopmental Disorders

Dhanya Vettiatil, Anjana Soorajkumar, Robert A. Dubin, Erika Pedrosa, Allan Schornagel, John Shearer Lambert, Isadora Pinheiro Costa, Joseph McDonald, Sigrid M.A. Swagemakers, Peter J. van der Spek, Jennifer Frankovich, Janet L. Cunningham, Herbert M. Lachman

The paper identifies ultrarare variants in DNA damage repair and mitochondrial genes in pediatric neuropsychiatric syndromes and neurodevelopmental disorders, linking them to innate immune pathways and gut microbiome homeostasis.

Developmental Neuroscience · Feb 9, 2026Peer-reviewedGenetic & Genomic Medicine

Identification of ultra-rare genetic variants in Pediatric Acute Onset Neuropsychiatric Syndrome (PANS) by exome and whole genome sequencing

Rosario Rich Trifiletti, Herbert M. Lachman, Olivia R. Manusama, Deyou Zheng, Alberto Spalice, Pietro Chiurazzi, Allan Schornagel, Andreea M. Serban, Rogier van Wijck, Janet L. Cunningham, Sigrid M. A. Swagemakers, Peter J. van der Spek

This study identifies ultra-rare genetic variants in PANS patients through exome and whole genome sequencing, revealing candidate genes involved in both immune and neuronal pathways.

Scientific Reports · Jun 30, 2022Peer-reviewedGenetic & Genomic Medicine