Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.


The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page


My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1950 2
1958 1
1959 1
1972 1
1976 1
1981 1
2003 1
2004 2
2008 1
2009 1
2010 1
2011 1
2012 2
2014 1
2016 1
2017 2
2018 2
2019 2
2020 4
2021 1
2022 3
2023 2
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

31 results

Results by year

Filters applied: . Clear all
Page 1
Turf battles.
Calhoun JD. Calhoun JD. AJR Am J Roentgenol. 1981 Apr;136(4):857-8. doi: 10.2214/ajr.136.4.857. AJR Am J Roentgenol. 1981. PMID: 6784496 No abstract available.
Infantile coxa vara.
Calhoun JD, Pierret G. Calhoun JD, et al. Am J Roentgenol Radium Ther Nucl Med. 1972 Jul;115(3):561-8. doi: 10.2214/ajr.115.3.561. Am J Roentgenol Radium Ther Nucl Med. 1972. PMID: 5038637 No abstract available.
CACNA1H variants are not a cause of monogenic epilepsy.
Calhoun JD, Huffman AM, Bellinski I, Kinsley L, Bachman E, Gerard E, Kearney JA, Carvill GL. Calhoun JD, et al. Hum Mutat. 2020 Jun;41(6):1138-1144. doi: 10.1002/humu.24017. Epub 2020 Apr 14. Hum Mutat. 2020. PMID: 32227660 Free PMC article.
Epilepsy Genetics: What Once Was Rare, Is Now Common.
Calhoun JD, Carvill GL. Calhoun JD, et al. Epilepsy Curr. 2020 Jun 19;20(4):221-223. doi: 10.1177/1535759720933232. eCollection 2020 Jul-Aug. Epilepsy Curr. 2020. PMID: 34025233 Free PMC article. No abstract available.
Long-read sequencing and profiling of RNA-binding proteins reveals the pathogenic mechanism of aberrant splicing of an SCN1A poison exon in epilepsy.
Happ HC, Schneider PN, Hong JH, Goes E, Bandouil M, Biar CG, Ramamurthy A, Reese F, Engel K, Weckhuysen S, Scheffer IE, Mefford HC, Calhoun JD, Carvill GL. Happ HC, et al. Among authors: calhoun jd. bioRxiv [Preprint]. 2023 May 4:2023.05.04.538282. doi: 10.1101/2023.05.04.538282. bioRxiv. 2023. PMID: 37205386 Free PMC article. Preprint.
mTORC1 functional assay reveals SZT2 loss-of-function variants and a founder in-frame deletion.
Calhoun JD, Aziz MC, Happ HC, Gunti J, Gleason C, Mohamed N, Zeng K, Hiller M, Bryant E, Mithal DS, Bellinski I, Kinsley L, Grimmel M, Schwaibold EMC, Smith-Hicks C, Chassevent A, Scala M, Accogli A, Torella A, Striano P, Capra V, Bird LM, Ben-Sahra I, Ekhilevich N, Hershkovitz T, Weiss K, Millichap J, Gerard EE, Carvill GL. Calhoun JD, et al. Brain. 2022 Jun 30;145(6):1939-1948. doi: 10.1093/brain/awab451. Brain. 2022. PMID: 35773235 Free PMC article.
Spectrum of KV 2.1 Dysfunction in KCNB1-Associated Neurodevelopmental Disorders.
Kang SK, Vanoye CG, Misra SN, Echevarria DM, Calhoun JD, O'Connor JB, Fabre KL, McKnight D, Demmer L, Goldenberg P, Grote LE, Thiffault I, Saunders C, Strauss KA, Torkamani A, van der Smagt J, van Gassen K, Carson RP, Diaz J, Leon E, Jacher JE, Hannibal MC, Litwin J, Friedman NR, Schreiber A, Lynch B, Poduri A, Marsh ED, Goldberg EM, Millichap JJ, George AL Jr, Kearney JA. Kang SK, et al. Among authors: calhoun jd. Ann Neurol. 2019 Dec;86(6):899-912. doi: 10.1002/ana.25607. Epub 2019 Oct 24. Ann Neurol. 2019. PMID: 31600826 Free PMC article.
Gene expression profiling in a mouse model of Dravet syndrome.
Hawkins NA, Calhoun JD, Huffman AM, Kearney JA. Hawkins NA, et al. Among authors: calhoun jd. Exp Neurol. 2019 Jan;311:247-256. doi: 10.1016/j.expneurol.2018.10.010. Epub 2018 Oct 19. Exp Neurol. 2019. PMID: 30347190 Free PMC article.
31 results