| Year |
Citation |
Score |
| 2020 |
Bouza AA, Philippe JM, Edokobi N, Pinsky AM, Offord J, Calhoun JD, Lopez-Florán M, Lopez-Santiago LF, Jenkins PM, Isom LL. Sodium channel β1 subunits are post-translationally modified by tyrosine phosphorylation, S-palmitoylation, and regulated intramembrane proteolysis. The Journal of Biological Chemistry. PMID 32503841 DOI: 10.1074/Jbc.Ra120.013978 |
0.578 |
|
| 2019 |
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, et al. Spectrum of K 2.1 Dysfunction in KCNB1-Associated Neurodevelopmental Disorders. Annals of Neurology. PMID 31600826 DOI: 10.1002/Ana.25607 |
0.366 |
|
| 2017 |
Lamar T, Vanoye CG, Calhoun J, Wong JC, Dutton SB, Jorge BS, Velinov M, Escayg A, Kearney JA. SCN3A deficiency associated with increased seizure susceptibility. Neurobiology of Disease. PMID 28235671 DOI: 10.1016/J.Nbd.2017.02.006 |
0.319 |
|
| 2016 |
Calhoun JD, Hawkins NA, Zachwieja NJ, Kearney JA. Cacna1g is a genetic modifier of epilepsy caused by mutation of voltage-gated sodium channel Scn2a. Epilepsia. PMID 27112236 DOI: 10.1111/Epi.13390 |
0.315 |
|
| 2014 |
Calhoun JD, Isom LL. The role of non-pore-forming β subunits in physiology and pathophysiology of voltage-gated sodium channels. Handbook of Experimental Pharmacology. 221: 51-89. PMID 24737232 DOI: 10.1007/978-3-642-41588-3_4 |
0.684 |
|
| 2012 |
Chen C, Calhoun JD, Zhang Y, Lopez-Santiago L, Zhou N, Davis TH, Salzer JL, Isom LL. Identification of the cysteine residue responsible for disulfide linkage of Na+ channel α and β2 subunits. The Journal of Biological Chemistry. 287: 39061-9. PMID 22992729 DOI: 10.1074/Jbc.M112.397646 |
0.68 |
|
| 2012 |
Yang M, Kozminski DJ, Wold LA, Modak R, Calhoun JD, Isom LL, Brackenbury WJ. Therapeutic potential for phenytoin: targeting Na(v)1.5 sodium channels to reduce migration and invasion in metastatic breast cancer. Breast Cancer Research and Treatment. 134: 603-15. PMID 22678159 DOI: 10.1007/S10549-012-2102-9 |
0.643 |
|
| 2012 |
Nguyen HM, Calhoun JD, Isom LL, Goldin AL, Chandy GK. Modulation of Kv1 Voltage-Gated Potassium Channels by Sodium Channel Beta Subunits Biophysical Journal. 102: 687a. DOI: 10.1016/J.Bpj.2011.11.3733 |
0.665 |
|
| 2011 |
Patino GA, Brackenbury WJ, Bao Y, Lopez-Santiago LF, O'Malley HA, Chen C, Calhoun JD, Lafrenière RG, Cossette P, Rouleau GA, Isom LL. Voltage-gated Na+ channel β1B: a secreted cell adhesion molecule involved in human epilepsy. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 31: 14577-91. PMID 21994374 DOI: 10.1523/Jneurosci.0361-11.2011 |
0.519 |
|
| 2010 |
Brackenbury WJ, Calhoun JD, Chen C, Miyazaki H, Nukina N, Oyama F, Ranscht B, Isom LL. Functional reciprocity between Na+ channel Nav1.6 and beta1 subunits in the coordinated regulation of excitability and neurite outgrowth. Proceedings of the National Academy of Sciences of the United States of America. 107: 2283-8. PMID 20133873 DOI: 10.1073/Pnas.0909434107 |
0.662 |
|
| 2009 |
Chioni AM, Brackenbury WJ, Calhoun JD, Isom LL, Djamgoz MB. A novel adhesion molecule in human breast cancer cells: voltage-gated Na+ channel beta1 subunit. The International Journal of Biochemistry & Cell Biology. 41: 1216-27. PMID 19041953 DOI: 10.1016/J.Biocel.2008.11.001 |
0.613 |
|
| 2008 |
Schmalhofer WA, Calhoun J, Burrows R, Bailey T, Kohler MG, Weinglass AB, Kaczorowski GJ, Garcia ML, Koltzenburg M, Priest BT. ProTx-II, a selective inhibitor of NaV1.7 sodium channels, blocks action potential propagation in nociceptors. Molecular Pharmacology. 74: 1476-84. PMID 18728100 DOI: 10.1124/mol.108.047670 |
0.375 |
|
| Low-probability matches (unlikely to be authored by this person) |
| 2017 |
Calhoun JD, Hawkins NA, Zachwieja NJ, Kearney JA. Cacna1g is a genetic modifier of epilepsy in a mouse model of Dravet syndrome. Epilepsia. PMID 28556246 DOI: 10.1111/Epi.13811 |
0.297 |
|
| 2023 |
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. Long-read sequencing and profiling of RNA-binding proteins reveals the pathogenic mechanism of aberrant splicing of an poison exon in epilepsy. Biorxiv : the Preprint Server For Biology. PMID 37205386 DOI: 10.1101/2023.05.04.538282 |
0.214 |
|
| 2020 |
Calhoun JD, Huffman AM, Bellinski I, Kinsley L, Bachman E, Gerard E, Kearney JA, Carvill GL. CACNA1H variants are not a cause of monogenic epilepsy. Human Mutation. PMID 32227660 DOI: 10.1002/Humu.24017 |
0.189 |
|
| 2022 |
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, et al. mTORC1 functional assay reveals SZT2 loss-of-function variants and a founder in-frame deletion. Brain : a Journal of Neurology. 145: 1939-1948. PMID 35773235 DOI: 10.1093/brain/awab451 |
0.186 |
|
| 2004 |
Calhoun JD, Rao RR, Warrenfeltz S, Rekaya R, Dalton S, McDonald J, Stice SL. Transcriptional profiling of initial differentiation events in human embryonic stem cells. Biochemical and Biophysical Research Communications. 323: 453-64. PMID 15369773 DOI: 10.1016/j.bbrc.2004.08.117 |
0.175 |
|
| 2018 |
Hawkins NA, Calhoun JD, Huffman AM, Kearney JA. Gene expression profiling in a mouse model of Dravet syndrome. Experimental Neurology. PMID 30347190 DOI: 10.1016/J.Expneurol.2018.10.010 |
0.172 |
|
| 2018 |
Calhoun JD, Carvill GL. Unravelling the genetic architecture of autosomal recessive epilepsy in the genomic era. Journal of Neurogenetics. 1-18. PMID 30247086 DOI: 10.1080/01677063.2018.1513509 |
0.158 |
|
| 2003 |
Calhoun JD, Lambert NA, Mitalipova MM, Noggle SA, Lyons I, Condie BG, Stice SL. Differentiation of rhesus embryonic stem cells to neural progenitors and neurons. Biochemical and Biophysical Research Communications. 306: 191-7. PMID 12788087 DOI: 10.1016/S0006-291X(03)00937-9 |
0.152 |
|
| 2017 |
Calhoun JD, Vanoye CG, Kok F, George AL, Kearney JA. Characterization of a KCNB1 variant associated with autism, intellectual disability, and epilepsy. Neurology. Genetics. 3: e198. PMID 29264390 DOI: 10.1212/Nxg.0000000000000198 |
0.151 |
|
| 2020 |
Gertler TS, Calhoun J, Laux L. 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. PMID 32414541 DOI: 10.1016/J.Seizure.2020.04.004 |
0.147 |
|
| 2004 |
Rao RR, Calhoun JD, Qin X, Rekaya R, Clark JK, Stice SL. Comparative transcriptional profiling of two human embryonic stem cell lines. Biotechnology and Bioengineering. 88: 273-86. PMID 15493035 DOI: 10.1002/Bit.20245 |
0.136 |
|
| 2020 |
Bryant EM, Millichap JJ, Spinelli E, Calhoun JD, Miller C, Giannelli J, Wolak J, Sanders V, Carvill GL, Charrow J. Oligosaccharyltransferase complex-congenital disorders of glycosylation: A novel congenital disorder of glycosylation. American Journal of Medical Genetics. Part A. PMID 32267060 DOI: 10.1002/Ajmg.A.61553 |
0.127 |
|
| 2019 |
Gertler TS, Calhoun J, Laux L. A single-center, retrospective analysis of genotype-phenotype correlations in children with Dravet syndrome. Seizure. 75: 1-6. PMID 31864146 DOI: 10.1016/J.Seizure.2019.12.009 |
0.12 |
|
| 2020 |
Calhoun JD, Carvill GL. Epilepsy Genetics: What Once Was Rare, Is Now Common. Epilepsy Currents. 20: 221-223. PMID 34025233 DOI: 10.1177/1535759720933232 |
0.115 |
|
| 1976 |
Schoultz TW, Morrison JR, Calhoun JD. Atlas of the human brain for use in diagnosis by computer-assisted tomography. Surgical Neurology. 5: 255-66. PMID 1265639 |
0.087 |
|
| 2022 |
Esterhuizen AI, Tiffin N, Riordan G, Wessels M, Burman RJ, Aziz MC, Calhoun JD, Gunti J, Amiri EE, Ramamurthy A, Bamshad MJ, Mefford HC, Ramesar R, Wilmshurst JM, Carvill GL. Precision medicine for developmental and epileptic encephalopathies in Africa-strategies for a resource-limited setting. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 36480001 DOI: 10.1016/j.gim.2022.11.002 |
0.083 |
|
| 1972 |
Calhoun JD, Pierret G. Infantile coxa vara. The American Journal of Roentgenology, Radium Therapy, and Nuclear Medicine. 115: 561-8. PMID 5038637 |
0.081 |
|
| 1992 |
Calhoun JD, Brglez F. A Framework and Method for Hierarchical Test Generation Ieee Transactions On Computer-Aided Design of Integrated Circuits and Systems. 11: 45-67. DOI: 10.1109/43.108618 |
0.07 |
|
| 1958 |
BUCHMAN JA, CALHOUN JD. Colloid carcinoma of the colon in children. The American Surgeon. 24: 280-6. PMID 13521279 |
0.029 |
|
| 1950 |
MESCHAN I, SCURGGS JB, CALHOUN JD. The study of convulsive fractures of the dorsal spine following electric shock therapy in psychotic patients. The Journal of the Arkansas Medical Society. 46: 167-70. PMID 15405067 |
0.025 |
|
| 1950 |
MESCHAN I, SCRUGGS JB, CALHOUN JD. Convulsive fractures of the dorsal spine following electric-shock therapy. Radiology. 54: 180-93, illust. PMID 15403701 DOI: 10.1148/54.2.180 |
0.024 |
|
| 1959 |
CALHOUN JD, THOMPSON SB. Vertebra plana in children produced by xanthomatous disease. The American Journal of Roentgenology, Radium Therapy, and Nuclear Medicine. 82: 482-9. PMID 13806943 |
0.02 |
|
| 1981 |
Calhoun JD. Turf battles. Ajr. American Journal of Roentgenology. 136: 857-8. PMID 6784496 DOI: 10.2214/ajr.136.4.857 |
0.01 |
|
| 1950 |
Meschan I, Calhoun JD. Bronchopulmonary hypogenesis: Diagnosis in the living Southern Medical Journal. 43: 1038-1042. |
0.01 |
|
| Hide low-probability matches. |