Grants per year
Personal profile
Education/Academic qualification
Cell & Molecular Biology, PhD, University of Michigan
… → 2013
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Dive into the research topics where Jeffrey D Calhoun is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
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Massively parallel reporter assays to reveal noncoding variant contribution in epilepsy
Citizens United for Research in Epilepsy
11/1/22 → 10/31/23
Project: Research project
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Resolving missense variants of uncertain significance in TSC2
9/1/22 → 8/31/23
Project: Research project
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Target validation of thalamic T-type calcium channels in a mouse model of Dravet Syndrome
Calhoun, J. D. & Kearney, J. A.
Dravet Syndrome Foundation, Inc.
1/1/17 → 12/31/17
Project: Research project
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mTORC1 functional assay reveals SZT2 loss-of-function variants and a founder in-frame deletion
Calhoun, J. D., Aziz, M. C., Happ, H. C., Gunti, J., Gleason, C., Mohamed, N., Zeng, K., Hiller, M., Bryant, E., Mithal, D. S., Bellinski, I., Kinsley, L., Grimmel, M., Schwaibold, E. M. C., Smith-Hicks, C., Chassevent, A., Scala, M., Accogli, A., Torella, A., Striano, P., & 9 others, Jun 1 2022, In: Brain. 145, 6, p. 1939-1948 10 p.Research output: Contribution to journal › Article › peer-review
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Whole-exome sequencing and adrenocorticotropic hormone therapy in individuals with infantile spasms
the WES Support Group, May 2022, In: Developmental Medicine and Child Neurology. 64, 5, p. 633-640 8 p.Research output: Contribution to journal › Article › peer-review
1 Scopus citations -
A single-center, retrospective analysis of genotype-phenotype correlations in children with Dravet syndrome
Gertler, T. S., Calhoun, J. & Laux, L., Feb 2020, In: Seizure. 75, p. 1-6 6 p.Research output: Contribution to journal › Article › peer-review
Open Access5 Scopus citations -
CACNA1H variants are not a cause of monogenic epilepsy
Calhoun, J. D., Huffman, A. M., Bellinski, I., Kinsley, L., Bachman, E., Gerard, E., Kearney, J. A. & Carvill, G. L., Jun 1 2020, In: Human mutation. 41, 6, p. 1138-1144 7 p.Research output: Contribution to journal › Article › peer-review
Open Access9 Scopus citations -
Corrigendum to “A single-center, retrospective analysis of genotype–phenotype correlations in children with Dravet syndrome” [Seizure: Eur. J. Epilepsy 75 (2020) 1–6] (Seizure: European Journal of Epilepsy (2020) 75 (1–6), (S1059131119304467), (10.1016/j.seizure.2019.12.009))
Gertler, T. S., Calhoun, J. & Laux, L., Aug 2020, In: Seizure. 80, p. 281 1 p.Research output: Contribution to journal › Comment/debate › peer-review
Open Access