Identification of ultra-rare genetic variants in pediatric acute onset neuropsychiatric syndrome (PANS) by exome and whole genome sequencing

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 2045-2322

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Identification of ultra-rare genetic variants in pediatric acute onset neuropsychiatric syndrome (PANS) by exome and whole genome sequencing ; volume:12 ; number:1 ; day:30 ; month:6 ; year:2022 ; pages:1-14 ; date:12.2022
Scientific reports ; 12, Heft 1 (30.6.2022), 1-14, 12.2022

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

Contributor: SpringerLink (Online service)

DOI: 10.1038/s41598-022-15279-3

URN: urn:nbn:de:101:1-2022082110200155429313

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:27 AM CEST

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Associated

Trifiletti, Rosario
Lachman, Herbert M.
Manusama, Olivia
Zheng, Deyou
Spalice, Alberto
Chiurazzi, Pietro
Schornagel, Allan
Serban, Andreea M.
Wijck, Rogier van
Cunningham, Janet L.
Swagemakers, Sigrid
Spek, Peter J. van der
SpringerLink (Online service)

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Identification of ultra-rare genetic variants in pediatric acute onset neuropsychiatric syndrome (PANS) by exome and whole genome sequencing

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Other Objects (12)

Exome sequence analysis of rare frequency variants in Late-Onset Alzheimer Disease

Prevalence of pediatric acute-onset neuropsychiatric syndrome (PANS) in children and adolescents with eating disorders

Substantial batch effects in TCGA exome sequences undermine pan-cancer analysis of germline variants

Paediatric Acute-onset Neuropsychiatric Syndrome (PANS) and intravenous immunoglobulin (IVIG): comprehensive open-label trial in ten children

Exome variants associated with asthma and allergy

Neuropsychiatric comorbidities in adult patients with new-onset epilepsy

Identification of novel candidate variants including COL6A6 polymorphisms in early-onset atopic dermatitis using whole-exome sequencing

Neuropsychiatric involvement in juvenile-onset systemic lupus erythematosus (jSLE)

Autoantibodies and neuropsychiatric manifestations in childhood-onset systemic lupus erythematosus

Identification of copy number variants from exome sequence data

Annotation of human exome gene variants with consensus pathogenicity

Identifying rare variants from exome scans: the GAW17 experience

Exome sequence analysis of rare frequency variants in Late-Onset Alzheimer Disease

Prevalence of pediatric acute-onset neuropsychiatric syndrome (PANS) in children and adolescents with eating disorders

Substantial batch effects in TCGA exome sequences undermine pan-cancer analysis of germline variants

Paediatric Acute-onset Neuropsychiatric Syndrome (PANS) and intravenous immunoglobulin (IVIG): comprehensive open-label trial in ten children

Exome variants associated with asthma and allergy

Neuropsychiatric comorbidities in adult patients with new-onset epilepsy

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Neuropsychiatric involvement in juvenile-onset systemic lupus erythematosus (jSLE)

Autoantibodies and neuropsychiatric manifestations in childhood-onset systemic lupus erythematosus

Identification of copy number variants from exome sequence data

Annotation of human exome gene variants with consensus pathogenicity

Identifying rare variants from exome scans: the GAW17 experience

Exome sequence analysis of rare frequency variants in Late-Onset Alzheimer Disease

Prevalence of pediatric acute-onset neuropsychiatric syndrome (PANS) in children and adolescents with eating disorders

Substantial batch effects in TCGA exome sequences undermine pan-cancer analysis of germline variants

Paediatric Acute-onset Neuropsychiatric Syndrome (PANS) and intravenous immunoglobulin (IVIG): comprehensive open-label trial in ten children

Exome variants associated with asthma and allergy

Neuropsychiatric comorbidities in adult patients with new-onset epilepsy

Identification of novel candidate variants including COL6A6 polymorphisms in early-onset atopic dermatitis using whole-exome sequencing

Neuropsychiatric involvement in juvenile-onset systemic lupus erythematosus (jSLE)

Autoantibodies and neuropsychiatric manifestations in childhood-onset systemic lupus erythematosus

Identification of copy number variants from exome sequence data

Annotation of human exome gene variants with consensus pathogenicity

Identifying rare variants from exome scans: the GAW17 experience

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