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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

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31 results

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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.
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.
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.
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.
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.
Precision medicine for developmental and epileptic encephalopathies in Africa-strategies for a resource-limited setting.
Esterhuizen AI, Tiffin N, Riordan G, Wessels M, Burman RJ, Aziz MC, Calhoun JD, Gunti J, Amiri EE, Ramamurthy A, Bamshad MJ; University of Washington Centre for Mendelian Genomics (UW-CMG); Mefford HC, Ramesar R, Wilmshurst JM, Carvill GL. Esterhuizen AI, et al. Among authors: calhoun jd. Genet Med. 2023 Feb;25(2):100333. doi: 10.1016/j.gim.2022.11.002. Epub 2022 Dec 8. Genet Med. 2023. PMID: 36480001 Free 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.
31 results