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Author Details
Full Name
Peter D Galer
Affiliation
Children's Hospital of Philadelphia
ORCID
Career Start Year
2016
Papers
19
H Index
11
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37100502
Enriching representation learning using 53 million patient notes through human phenotype ontology embedding.
Artif Intell Med
2023
37723282
Loss of Grin2a causes a transient delay in the electrophysiological maturation of hippocampal parvalbumin interneurons.
Commun Biol
2023
37077567
Investigating the genetic contribution in febrile infection-related epilepsy syndrome and refractory status epilepticus.
Front Neurol
2023
35190816
Assessing the landscape of STXBP1-related disorders in 534 individuals.
Brain
2022
35460582
Computational analysis of neurodevelopmental phenotypes: Harmonization empowers clinical discovery.
Hum Mutat
2022
35514061
Visits of concern in child neurology telemedicine.
Dev Med Child Neurol
2022
35190834
Extracting seizure frequency from epilepsy clinic notes: a machine reading approach to natural language processing.
J Am Med Inform Assoc
2022
33264411
The Human Phenotype Ontology in 2021.
Nucleic Acids Res
2021
33731876
Computational analysis of 10,860 phenotypic annotations in individuals with SCN2A-related disorders.
Genet Med
2021
34031551
Phenotypic homogeneity in childhood epilepsies evolves in gene-specific patterns across 3251 patient-years of clinical data.
Eur J Hum Genet
2021
33949685
Modeling seizures in the Human Phenotype Ontology according to contemporary ILAE concepts makes big phenotypic data tractable.
Epilepsia
2021
32518152
Analyzing 2,589 child neurology telehealth encounters necessitated by the COVID-19 pandemic.
Neurology
2020
32773773
A longitudinal footprint of genetic epilepsies using automated electronic medical record interpretation.
Genet Med
2020
32887940
Correction: A longitudinal footprint of genetic epilepsies using automated electronic medical record interpretation.
Genet Med
2020
32853554
Semantic Similarity Analysis Reveals Robust Gene-Disease Relationships in Developmental and Epileptic Encephalopathies.
Am J Hum Genet
2020
32666661
Whole-exome and HLA sequencing in Febrile infection-related epilepsy syndrome.
Ann Clin Transl Neurol
2020
31393404
Mapping the knowledge structure and trends of epilepsy genetics over the past decade: A co-word analysis based on medical subject headings terms.
Medicine (Baltimore)
2019
31368773
The Effect of Vitamin D Supplementation on Attention-Deficit/Hyperactivity Disorder: A Systematic Review and Meta-Analysis of Randomized Controlled Trials.
J Child Adolesc Psychopharmacol
2019
26340655
The Associations Between Pain-related Beliefs, Pain Intensity, and Patient Functioning: Hypnotizability as a Moderator.
Clin J Pain
2016
1 - 19 of 19
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Alex S Felmeister
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Ganna Balagura
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Tim Jeske
Dr. von Hauner Children's Hospital
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1
Christoph Klein
Kinderklinik und Kinderpoliklinik der Ludwig-Maximilians-Universitat Munchen
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1
Rebecca L Peters
American College of Medical Genetics and Genomics (ACMG)
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American College of Medical Genetics and Genomics (ACMG)
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Christina K Rapp
Ludwig-Maximilians University, German Center for Lung Research (DZL)
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Gareth Baynam
King Edward Memorial Hospital
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Fabian Hauck
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Matthias Griese
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