Grants per year
Personal profile
Expertise related to UN Sustainable Development Goals
In 2015, UN member states agreed to 17 global Sustainable Development Goals (SDGs) to end poverty, protect the planet and ensure prosperity for all. This person’s work contributes towards the following SDG(s):
Education/Academic qualification
Cell & Molecular Biology, PhD, University of Michigan
… → 2013
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Collaborations and top research areas from the last five years
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Scalable assays to resolve variants of uncertain significance in TSC2
Calhoun, J. D. (PD/PI)
TSC Alliance Endowment Fund, Inc.
12/1/24 → 11/30/26
Project: Research project
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Poison exons in epilepsy and neurodevelopment
Carvill, G. L. (PD/PI) & Calhoun, J. D. (Co-Investigator)
National Institute of Neurological Disorders and Stroke
6/1/24 → 5/31/29
Project: Research project
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Leveraging predictive models to design high-throughput assays to resolve variants of uncertain significance (VUS) in SYNGAP1
Carvill, G. L. (PD/PI), Carvill, G. L. (PD/PI), Calhoun, J. D. (Co-Investigator) & Calhoun, J. D. (Co-Investigator)
2/1/24 → 7/31/25
Project: Research project
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Deep mutational scanning of CHD2 for variant interpretation in neurodevelopmental disorders
Carvill, G. L. (PD/PI) & Calhoun, J. D. (Co-PD/PI)
National Institute of Neurological Disorders and Stroke
9/15/23 → 8/31/25
Project: Research project
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Massively parallel reporter assays to reveal noncoding variant contribution in epilepsy
Calhoun, J. D. (PD/PI)
Citizens United for Research in Epilepsy
11/1/22 → 4/30/24
Project: Research project
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Antisense oligonucleotides modulate aberrant inclusion of poison exons in SCN1A-related Dravet syndrome
Tang, S., Stamberger, H., Calhoun, J. D., Weckhuysen, S. & Carvill, G. L., Apr 8 2025, In: JCI Insight. 10, 7, e188014.Research output: Contribution to journal › Article › peer-review
Open Access1 Scopus citations -
Precision medicine for developmental and epileptic encephalopathies in Africa—strategies for a resource-limited setting
University of Washington Centre for Mendelian Genomics (UW-CMG), Feb 2023, In: Genetics in Medicine. 25, 2, 100333.Research output: Contribution to journal › Article › peer-review
Open Access8 Scopus citations -
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
Open Access4 Scopus citations -
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
7 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 Access14 Scopus citations