2023 - Research.com Medicine in Australia Leader Award
2023 - Research.com Neuroscience in Australia Leader Award
2023 - Research.com Genetics in Australia Leader Award
2022 - Research.com Best Female Scientist Award
2022 - Research.com Neuroscience in Australia Leader Award
2022 - Research.com Genetics and Molecular Biology in Australia Leader Award
2018 - Fellow of the Royal Society, United Kingdom
2014 - Fellow of the Australian Academy of Science
2014 - Prime Minister's Prize for Science, Australia For their contribution to the study of epilepsy, its diagnosis, management and treatment
2014 - Fellow of the Australian Academy of Health and Medical Science
Her primary areas of study are Epilepsy, Genetics, Generalized epilepsy, Mutation and Generalized epilepsy with febrile seizures plus. Her Epilepsy study integrates concerns from other disciplines, such as Internal medicine, Pediatrics and SCN1B. Her Genetics research is multidisciplinary, relying on both Childhood absence epilepsy and Bioinformatics.
The Generalized epilepsy study combines topics in areas such as Genetic architecture and Dravet syndrome. Ingrid E. Scheffer focuses mostly in the field of Mutation, narrowing it down to topics relating to Endocrinology and, in certain cases, Autosomal dominant nocturnal frontal lobe epilepsy. Her research integrates issues of GABRG2, Neurological disorder and Exon in her study of Generalized epilepsy with febrile seizures plus.
The scientist’s investigation covers issues in Epilepsy, Genetics, Pediatrics, Dravet syndrome and Epilepsy syndromes. Her work in Epilepsy covers topics such as Internal medicine which are related to areas like Endocrinology. Mutation, Gene, Exome sequencing, Proband and Genetic heterogeneity are subfields of Genetics in which her conducts study.
Her study looks at the intersection of Pediatrics and topics like Intellectual disability with Autism. Her Dravet syndrome research is multidisciplinary, incorporating elements of Anesthesia and SCN1B. She studied SCN1B and Generalized epilepsy with febrile seizures plus that intersect with Myoclonic epilepsy.
Ingrid E. Scheffer mostly deals with Epilepsy, Pediatrics, Genetics, Dravet syndrome and Clinical neurology. Ingrid E. Scheffer has researched Epilepsy in several fields, including Encephalopathy, Intellectual disability and Cohort. She has included themes like Status epilepticus, Retrospective cohort study, Epileptic encephalopathy, Epileptic spasms and Etiology in her Pediatrics study.
Her work on Genetics deals in particular with Gene, Exome sequencing, Missense mutation, Phenotype and Proband. Her research investigates the connection between Missense mutation and topics such as Disease that intersect with problems in Computational biology. The study incorporates disciplines such as Anesthesia, Sleep disorder, Sleep Wake Disorders, Cannabidiol and Internal medicine in addition to Dravet syndrome.
Ingrid E. Scheffer mainly focuses on Epilepsy, Dravet syndrome, Pediatrics, Genetics and Gene. Her Epilepsy study improves the overall literature in Psychiatry. Ingrid E. Scheffer interconnects Adverse effect, Internal medicine, Quality of life, Physical therapy and Sedation in the investigation of issues within Dravet syndrome.
Her research in Pediatrics intersects with topics in Sleep in non-human animals, Sleep disorder, Sleep Wake Disorders, Status epilepticus and Genetic testing. Her work investigates the relationship between Genetic testing and topics such as SCN1B that intersect with problems in Generalized epilepsy, Genetic epilepsy, Genetic architecture and Childhood absence epilepsy. Her Genome, Proband and Allele study in the realm of Gene connects with subjects such as Biomarker.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Revised Terminology and Concepts for Organization of Seizures and Epilepsies: Report of the ILAE Commission on Classification and Terminology, 2005-2009
Anne T. Berg;Anne T. Berg;Samuel F. Berkovic;Martin J. Brodie;Jeffrey Buchhalter.
ILAE Official Report: A practical clinical definition of epilepsy
Robert S. Fisher;Carlos Acevedo;Alexis Arzimanoglou;Alicia Bogacz.
ILAE classification of the epilepsies: Position paper of the ILAE Commission for Classification and Terminology.
Ingrid E. Scheffer;Samuel Berkovic;Giuseppe Capovilla;Mary B. Connolly.
Operational classification of seizure types by the International League Against Epilepsy: position paper of the ILAE Commission for Classification and Terminology
Robert S. Fisher;J. Helen Cross;Jacqueline A. French;Norimichi Higurashi.
A Definition and Classification of Status epilepticus--Report of the ILAE Task Force on Classification of Status Epilepticus
Eugen Trinka;Hannah Cock;Dale Hesdorffer;Andrea O. Rossetti.
Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel beta1 subunit gene SCN1B.
Robyn H. Wallace;Dao W. Wang;Rita Singh;Rita Singh;Ingrid E. Scheffer;Ingrid E. Scheffer;Ingrid E. Scheffer.
Nature Genetics (1998)
A missense mutation in the neuronal nicotinic acetylcholine receptor alpha 4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy.
Ortrud K. Steinlein;John C. Mulley;Peter Propping;Robyn H. Wallace;Robyn H. Wallace.
Nature Genetics (1995)
Analysis of shared heritability in common disorders of the brain
Verneri Anttila;Verneri Anttila;Brendan Bulik-Sullivan;Brendan Bulik-Sullivan;Hilary K. Finucane;Raymond K. Walters;Raymond K. Walters.
Trial of Cannabidiol for Drug-Resistant Seizures in the Dravet Syndrome
Orrin Devinsky;J. Helen Cross;Linda Laux;Eric Marsh.
The New England Journal of Medicine (2017)
De novo mutations in epileptic encephalopathies
Andrew S. Allen;Samuel F. Berkovic;Patrick Cossette;Norman Delanty.
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