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Daniel L. Burgess - Publications

Affiliations: 
Baylor College of Medicine, Houston, TX 
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29 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2011 Klassen T, Davis C, Goldman A, Burgess D, Chen T, Wheeler D, McPherson J, Bourquin T, Lewis L, Villasana D, Morgan M, Muzny D, Gibbs R, Noebels J. Exome sequencing of ion channel genes reveals complex profiles confounding personal risk assessment in epilepsy. Cell. 145: 1036-48. PMID 21703448 DOI: 10.1016/J.Cell.2011.05.025  0.574
2009 Price MG, Yoo JW, Burgess DL, Deng F, Hrachovy RA, Frost JD, Noebels JL. A triplet repeat expansion genetic mouse model of infantile spasms syndrome, Arx(GCG)10+7, with interneuronopathy, spasms in infancy, persistent seizures, and adult cognitive and behavioral impairment. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 29: 8752-63. PMID 19587282 DOI: 10.1523/JNEUROSCI.0915-09.2009  0.586
2006 Deng F, Price MG, Davis CF, Mori M, Burgess DL. Stargazin and other transmembrane AMPA receptor regulating proteins interact with synaptic scaffolding protein MAGI-2 in brain. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 26: 7875-84. PMID 16870733 DOI: 10.1523/JNEUROSCI.1851-06.2006  0.356
2006 Burgess DL. Transgenic and Gene Replacement Models of Epilepsy: Targeting Ion Channel and Neurotransmission Pathways in Mice Models of Seizures and Epilepsy. 199-222. DOI: 10.1016/B978-012088554-1/50018-9  0.303
2005 Burgess DL. Neonatal epilepsy syndromes and GEFS+: mechanistic considerations. Epilepsia. 46: 51-8. PMID 16359473 DOI: 10.1111/j.1528-1167.2005.00359.x  0.524
2005 Price MG, Davis CF, Deng F, Burgess DL. The alpha-amino-3-hydroxyl-5-methyl-4-isoxazolepropionate receptor trafficking regulator "stargazin" is related to the claudin family of proteins by Its ability to mediate cell-cell adhesion. The Journal of Biological Chemistry. 280: 19711-20. PMID 15760900 DOI: 10.1074/jbc.M500623200  0.439
2004 Meisler MH, Plummer NW, Burgess DL, Buchner DA, Sprunger LK. Allelic mutations of the sodium channel SCN8A reveal multiple cellular and physiological functions. Genetica. 122: 37-45. PMID 15619959 DOI: 10.1007/S10709-004-1441-9  0.43
2004 Mori M, Burgess DL, Gefrides LA, Foreman PJ, Opferman JT, Korsmeyer SJ, Cavalheiro EA, Naffah-Mazzacoratti MG, Noebels JL. Expression of apoptosis inhibitor protein Mcl1 linked to neuroprotection in CNS neurons. Cell Death and Differentiation. 11: 1223-33. PMID 15286683 DOI: 10.1038/Sj.Cdd.4401483  0.549
2002 Zhang Y, Mori M, Burgess DL, Noebels JL. Mutations in high-voltage-activated calcium channel genes stimulate low-voltage-activated currents in mouse thalamic relay neurons. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 22: 6362-71. PMID 12151514 DOI: 10.1523/Jneurosci.22-15-06362.2002  0.625
2002 Zhang Y, Mori M, Burgess DL, Noebels JL. Mutations in High-Voltage-Activated Calcium Channel Genes Stimulate Low-Voltage-Activated Currents in Mouse Thalamic Relay Neurons The Journal of Neuroscience. 22: 6362-6371. DOI: 10.1523/JNEUROSCI.22-15-06362.2002  0.555
2001 Heilstedt HA, Burgess DL, Anderson AE, Chedrawi A, Tharp B, Lee O, Kashork CD, Starkey DE, Wu YQ, Noebels JL, Shaffer LG, Shapira SK. Loss of the potassium channel beta-subunit gene, KCNAB2, is associated with epilepsy in patients with 1p36 deletion syndrome. Epilepsia. 42: 1103-11. PMID 11580756 DOI: 10.1046/J.1528-1157.2001.08801.X  0.642
2001 Burgess DL. Listen carefully: positional cloning of an audiogenic seizure mutation may yield Frings benefits. Neuron. 31: 507-8. PMID 11545706 DOI: 10.1016/S0896-6273(01)00400-7  0.419
2001 Burgess DL, Gefrides LA, Foreman PJ, Noebels JL. A cluster of three novel Ca2+ channel gamma subunit genes on chromosome 19q13.4: evolution and expression profile of the gamma subunit gene family. Genomics. 71: 339-50. PMID 11170751 DOI: 10.1006/geno.2000.6440  0.601
2000 Matsuura T, Yamagata T, Burgess DL, Rasmussen A, Grewal RP, Watase K, Khajavi M, McCall AE, Davis CF, Zu L, Achari M, Pulst SM, Alonso E, Noebels JL, Nelson DL, et al. Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10. Nature Genetics. 26: 191-4. PMID 11017075 DOI: 10.1038/79911  0.566
2000 Burgess DL, Noebels JL. Calcium channel defects in models of inherited generalized epilepsy. Epilepsia. 41: 1074-5. PMID 10961647 DOI: 10.1111/J.1528-1157.2000.Tb00305.X  0.59
2000 Burgess DL, Matsuura T, Ashizawa T, Noebels JL. Genetic localization of the Ca2+ channel gene CACNG2 near SCA10 on chromosome 22q13. Epilepsia. 41: 24-7. PMID 10643919 DOI: 10.1111/J.1528-1157.2000.Tb01500.X  0.63
2000 Noebels JL, Burgess DL, Qian J. Nature in the development of epilepsy Acta Neurologica Scandinavica, Supplement. 102: 11-13. DOI: 10.1034/J.1600-0404.2000.00202-6.X  0.584
1999 Burgess DL, Davis CF, Gefrides LA, Noebels JL. Identification of three novel Ca(2+) channel gamma subunit genes reveals molecular diversification by tandem and chromosome duplication. Genome Research. 9: 1204-13. PMID 10613843 DOI: 10.1101/gr.9.12.1204  0.627
1999 Burgess DL, Noebels JL. Single gene defects in mice: the role of voltage-dependent calcium channels in absence models. Epilepsy Research. 36: 111-22. PMID 10515159 DOI: 10.1016/S0920-1211(99)00045-5  0.662
1999 Burgess DL, Noebels JL. Voltage-dependent calcium channel mutations in neurological disease. Annals of the New York Academy of Sciences. 868: 199-212. PMID 10414295 DOI: 10.1111/j.1749-6632.1999.tb11287.x  0.609
1999 Burgess DL, Biddlecome GH, McDonough SI, Diaz ME, Zilinski CA, Bean BP, Campbell KP, Noebels JL. beta subunit reshuffling modifies N- and P/Q-type Ca2+ channel subunit compositions in lethargic mouse brain. Molecular and Cellular Neurosciences. 13: 293-311. PMID 10328888 DOI: 10.1006/Mcne.1999.0748  0.568
1998 Plummer NW, Galt J, Jones JM, Burgess DL, Sprunger LK, Kohrman DC, Meisler MH. Exon organization, coding sequence, physical mapping, and polymorphic intragenic markers for the human neuronal sodium channel gene SCN8A. Genomics. 54: 287-96. PMID 9828131 DOI: 10.1006/Geno.1998.5550  0.435
1997 Burgess DL, Jones JM, Meisler MH, Noebels JL. Mutation of the Ca2+ channel beta subunit gene Cchb4 is associated with ataxia and seizures in the lethargic (lh) mouse. Cell. 88: 385-92. PMID 9039265 DOI: 10.1016/S0092-8674(00)81877-2  0.628
1996 Griffith AJ, Burgess DL, Kohrman DC, Yu J, Blaschak J, Blanton SH, Boehnke M, Hecht JT, Overhauser J, Meisler MH. Localization of the homolog of a mouse craniofacial mutant to human chromosome 18q11 and evaluation of linkage to human CLP and CPO. Genomics. 34: 299-303. PMID 8786128 DOI: 10.1006/Geno.1996.0290  0.375
1996 Burgess DL, Rafael JA, Meisler MH, Chamberlain JS. Dlgh1, a mouse homolog of the drosophila discs-large gene, is located on chromosome 16. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 7: 623-4. PMID 8678991 DOI: 10.1007/S003359900187  0.386
1996 Griffith AJ, Radice GL, Burgess DL, Kohrman DC, Hansen GM, Justice MJ, Johnson KR, Davisson MT, Meisler MH. Location of the 9257 and ataxia mutations on mouse chromosome 18. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 7: 417-9. PMID 8662222 DOI: 10.1007/S003359900124  0.389
1995 Burgess DL, Kohrman DC, Galt J, Plummer NW, Jones JM, Spear B, Meisler MH. Mutation of a new sodium channel gene, Scn8a, in the mouse mutant 'motor endplate disease'. Nature Genetics. 10: 461-5. PMID 7670495 DOI: 10.1038/Ng0895-461  0.469
1995 Kohrman DC, Plummer NW, Schuster T, Jones JM, Jang W, Burgess DL, Galt J, Spear BT, Meisler MH. Insertional mutation of the motor endplate disease (med) locus on mouse chromosome 15. Genomics. 26: 171-7. PMID 7601440 DOI: 10.1016/0888-7543(95)80198-U  0.388
1993 Ting CN, Burgess DL, Chamberlain JS, Keith TP, Falls K, Meisler MH. Phosphoenolpyruvate carboxykinase (GTP): characterization of the human PCK1 gene and localization distal to MODY on chromosome 20. Genomics. 16: 698-706. PMID 8325643 DOI: 10.1006/Geno.1993.1250  0.395
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