Correction: A longitudinal footprint of genetic epilepsies using automated electronic medical record interpretation.

Journal

Genetics in medicine : official journal of the American College of Medical Genetics
ISSN: 1530-0366
Titre abrégé: Genet Med
Pays: United States
ID NLM: 9815831

Informations de publication

Date de publication:
Nov 2020
Historique:
pubmed: 6 9 2020
medline: 6 9 2020
entrez: 5 9 2020
Statut: ppublish

Résumé

An amendment to this paper has been published and can be accessed via a link at the top of the paper.

Identifiants

DOI: 10.1038/s41436-020-00953-6 PMID: 32887940 PMC: PMC7962580
pubmed: 32887940
doi: 10.1038/s41436-020-00953-6
pii: S1098-3600(21)00794-2
pmc: PMC7962580
doi:

Types de publication

Published Erratum

Langues

eng

Sous-ensembles de citation

IM

Pagination

1921-1922

Subventions

Organisme : NICHD NIH HHS
ID : P50 HD105354
Pays : United States
Organisme : NICHD NIH HHS
ID : U54 HD086984
Pays : United States

Commentaires et corrections

Type : ErratumFor

Auteurs

Shiva Ganesan (S)

Division of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
The Epilepsy NeuroGenetics Initiative (ENGIN), Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Department of Biomedical and Health Informatics (DBHi), Children's Hospital of Philadelphia, Philadelphia, PA, USA.

Peter D Galer (PD)

Division of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
The Epilepsy NeuroGenetics Initiative (ENGIN), Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Department of Biomedical and Health Informatics (DBHi), Children's Hospital of Philadelphia, Philadelphia, PA, USA.

Katherine L Helbig (KL)

Division of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
The Epilepsy NeuroGenetics Initiative (ENGIN), Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Department of Biomedical and Health Informatics (DBHi), Children's Hospital of Philadelphia, Philadelphia, PA, USA.

Sarah E McKeown (SE)

Division of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
The Epilepsy NeuroGenetics Initiative (ENGIN), Children's Hospital of Philadelphia, Philadelphia, PA, USA.

Margaret O'Brien (M)

Division of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Department of Biomedical and Health Informatics (DBHi), Children's Hospital of Philadelphia, Philadelphia, PA, USA.

Alexander K Gonzalez (AK)

The Epilepsy NeuroGenetics Initiative (ENGIN), Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Department of Biomedical and Health Informatics (DBHi), Children's Hospital of Philadelphia, Philadelphia, PA, USA.

Alex S Felmeister (AS)

Department of Biomedical and Health Informatics (DBHi), Children's Hospital of Philadelphia, Philadelphia, PA, USA.

Pouya Khankhanian (P)

Department of Neurology, University of Pennsylvania, Perelman School of Medicine, Philadelphia, PA, USA.

Colin A Ellis (CA)

The Epilepsy NeuroGenetics Initiative (ENGIN), Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Department of Biomedical and Health Informatics (DBHi), Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Department of Neurology, University of Pennsylvania, Perelman School of Medicine, Philadelphia, PA, USA.

Ingo Helbig (I)

Division of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA, USA. helbigi@email.chop.edu.
The Epilepsy NeuroGenetics Initiative (ENGIN), Children's Hospital of Philadelphia, Philadelphia, PA, USA. helbigi@email.chop.edu.
Department of Biomedical and Health Informatics (DBHi), Children's Hospital of Philadelphia, Philadelphia, PA, USA. helbigi@email.chop.edu.
Department of Neurology, University of Pennsylvania, Perelman School of Medicine, Philadelphia, PA, USA. helbigi@email.chop.edu.
ORCID: 0000-0001-8486-0558

Classifications MeSH