Projects per year
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Dive into the research topics where Sheryl R. Haut is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
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Recent external collaboration on country/territory level. Dive into details by clicking on the dots or
Grants
- 2 Finished
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IMPACT OF SEIZURE CLUSTERING ON ADULT EPILESPY
National Institute of Neurological Disorders and Stroke
9/21/00 → 8/31/04
Project: Research project
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Association of ultra-rare coding variants with genetic generalized epilepsy: A case–control whole exome sequencing study
Canadian Epilepsy Network, Epi4K Consortium, Epilepsy Phenome/Genome Project, EpiPGX Consortium & EuroEPINOMICS-CoGIE Consortium, Mar 2022, In: Epilepsia. 63, 3, p. 723-735 13 p.Research output: Contribution to journal › Article › peer-review
Open Access1 Scopus citations -
Epilepsy-related stigma and attitudes: Systematic review of screening instruments and interventions - Report by the International League Against Epilepsy Task Force on Stigma in Epilepsy
Austin, J. K., Birbeck, G., Parko, K., Kwon, C. S., Fernandes, P. T., Braga, P., Fiest, K. M., Ali, A., Cross, J. H., de Boer, H., Dua, T., Haut, S. R., Jacoby, A., Lorenzetti, D. L., Mifsud, J., Moshé, S. L., Tripathi, M., Wiebe, S. & Jette, N., Mar 2022, In: Epilepsia. 63, 3, p. 598-628 31 p.Research output: Contribution to journal › Article › peer-review
1 Scopus citations -
Systematic review of frequency of felt and enacted stigma in epilepsy and determining factors and attitudes toward persons living with epilepsy—Report from the International League Against Epilepsy Task Force on Stigma in Epilepsy
Kwon, C. S., Jacoby, A., Ali, A., Austin, J., Birbeck, G. L., Braga, P., Cross, J. H., de Boer, H., Dua, T., Fernandes, P. T., Fiest, K. M., Goldstein, J., Haut, S., Lorenzetti, D., Mifsud, J., Moshe, S., Parko, K. L., Tripathi, M., Wiebe, S. & Jette, N., Mar 2022, In: Epilepsia. 63, 3, p. 573-597 25 p.Research output: Contribution to journal › Article › peer-review
3 Scopus citations -
Association of SLC32A1 Missense Variants With Genetic Epilepsy With Febrile Seizures Plus
Heron, S. E., Regan, B. M., Harris, R. V., Gardner, A. E., Coleman, M. J., Bennett, M. F., Grinton, B. E., Helbig, K. L., Sperling, M. R., Haut, S., Geller, E. B., Widdess-Walsh, P., Pelekanos, J. T., Bahlo, M., Petrovski, S., Heinzen, E. L., Hildebrand, M. S., Corbett, M. A., Scheffer, I. E., Gécz, J. & 1 others, , May 4 2021, In: Neurology. 96, 18, p. e2251-e2260Research output: Contribution to journal › Article › peer-review
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Diverse genetic causes of polymicrogyria with epilepsy
Epilepsy Phenome/Genome Project, Epi4K Consortium, Apr 2021, In: Epilepsia. 62, 4, p. 973-983 11 p.Research output: Contribution to journal › Article › peer-review
5 Scopus citations