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Daniel Burgess

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Matthew N Bainbridge; Daniel L Burgess; Thomas J Albert; John L Jefferies; Donna M Muzny; Irene Newsham; Min Wang; Yuanqing Wu; Richard A Gibbs
Targeted enrichment beyond the consensus coding DNA sequence exome reveals exons with higher variant densities.
Matthew N Bainbridge; Min Wang; Daniel L Burgess; Christie Kovar; Matthew J Rodesch; Mark D'Ascenzo; Jacob Kitzman; Yuan-Qing Wu; Irene Newsham; Richmond Todd; Jeffrey A Jeddeloh; Donna M Muzny; Thomas J Albert; Richard A Gibbs
Whole exome capture in solution with 3 Gbp of data.
Maureen G Price; Jong W Yoo; Daniel L Burgess; Fang Deng; Richard A Hrachovy; James D Frost; Jeffrey L Noebels
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.

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All Publications

2011: Matthew N Bainbridge; Daniel L Burgess; Thomas J Albert; John L Jefferies; Donna M Muzny; Irene Newsham; Min Wang; Yuanqing Wu; Richard A Gibbs
Targeted enrichment beyond the consensus coding DNA sequence exome reveals exons with higher variant densities.
Genome biology 2011;12(7):R68.
2010: Matthew N Bainbridge; Min Wang; Daniel L Burgess; Christie Kovar; Matthew J Rodesch; Mark D'Ascenzo; Jacob Kitzman; Yuan-Qing Wu; Irene Newsham; Richmond Todd; Jeffrey A Jeddeloh; Donna M Muzny; Thomas J Albert; Richard A Gibbs
Whole exome capture in solution with 3 Gbp of data.
Genome biology 2010;11(6):R62.
2009: Maureen G Price; Jong W Yoo; Daniel L Burgess; Fang Deng; Richard A Hrachovy; James D Frost; Jeffrey L Noebels
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 2009;29(27):8752-63.
2006: Fang Deng; Maureen G Price; Caleb F Davis; Mayra Mori; Daniel L Burgess
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 2006;26(30):7875-84.
2005: Maureen G Price; Caleb F Davis; Fang Deng; Daniel L Burgess
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 2005;280(20):19711-20.
2005: Daniel L Burgess
Neonatal epilepsy syndromes and GEFS+: mechanistic considerations.
Epilepsia 2005;46 Suppl 10():51-8.
2004: Mayra Mori; Daniel L Burgess; LA Gefrides; PERRY FOREMAN; J T Opferman; Stanley J Korsmeyer; Esper A. Cavalheiro; Md G Naffah-Mazzacoratti; Jeffrey L Noebels
Expression of apoptosis inhibitor protein Mcl1 linked to neuroprotection in CNS neurons.
Cell death and differentiation 2004;11(11):1223-33.
2004: Miriam H Meisler; Nicholas W Plummer; Daniel L Burgess; David A Buchner; Leslie K Sprunger
Allelic mutations of the sodium channel SCN8A reveal multiple cellular and physiological functions.
Genetica 2004;122(1):37-45.
2002: Yi Zhang; Mayra Mori; Daniel L Burgess; Jeffrey L Noebels
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 2002;22(15):6362-71.
2001: Heidi A Heilstedt; Daniel L Burgess; Anne E Anderson; A Chedrawi; Barbara Z Tharp; O Lee; Catherine D Kashork; D E Starkey; YQ Wu; Jeffrey L Noebels; Lisa Shaffer; Stuart K Shapira
Loss of the potassium channel beta-subunit gene, KCNAB2, is associated with epilepsy in patients with 1p36 deletion syndrome.
Epilepsia 2001;42(9):1103-11.
2001: Daniel L Burgess
Listen carefully: positional cloning of an audiogenic seizure mutation may yield Frings benefits.
Neuron 2001;31(4):507-8.
2001: Daniel L Burgess; LA Gefrides; PERRY FOREMAN; Jeffrey L Noebels
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 2001;71(3):339-50.
2000: Tohru Matsuura; T Yamagata; Daniel L Burgess; A Rasmussen; Raji P Grewal; Kei Watase; Mehrdad Khajavi; AE McCall; Caleb F Davis; Lan Zu; Madhureeta Achari; Stef pulst; E Alonso; Jeffrey L Noebels; David L Nelson; Huda Y Zoghbi; Tetsuo Ashizawa
Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10.
Nature genetics 2000;26(2):191-4.
2000: Daniel L Burgess; Jeffrey L Noebels
Calcium channel defects in models of inherited generalized epilepsy.
Epilepsia 2000;41(8):1074-5.
2000: Daniel L Burgess; Tohru Matsuura; Tetsuo Ashizawa; Jeffrey L Noebels
Genetic localization of the Ca2+ channel gene CACNG2 near SCA10 on chromosome 22q13.
Epilepsia 2000;41(1):24-7.
1999: Daniel L Burgess; Caleb F Davis; LA Gefrides; Jeffrey L Noebels
Identification of three novel Ca(2+) channel gamma subunit genes reveals molecular diversification by tandem and chromosome duplication.
Genome research 1999;9(12):1204-13.
1999: Daniel L Burgess; Jeffrey L Noebels
Single gene defects in mice: the role of voltage-dependent calcium channels in absence models.
Epilepsy research 1999;36(2-3):111-22.
1999: Daniel L Burgess; Jeffrey L Noebels
Voltage-dependent calcium channel mutations in neurological disease.
Annals of the New York Academy of Sciences 1999;868():199-212.
1999: Daniel L Burgess; G H Biddlecome; S I McDonough; Maria E Diaz; Carolyn A Zilinski; Bruce P Bean; K P Campbell; Jeffrey L Noebels
beta subunit reshuffling modifies N- and P/Q-type Ca2+ channel subunit compositions in lethargic mouse brain.
Molecular and cellular neurosciences 1999;13(4):293-311.
1998: Nicholas W Plummer; J Galt; Julie M Jones; Daniel L Burgess; Leslie K Sprunger; David C Kohrman; Miriam H Meisler
Exon organization, coding sequence, physical mapping, and polymorphic intragenic markers for the human neuronal sodium channel gene SCN8A.
Genomics 1998;54(2):287-96.
1997: Daniel L Burgess; Julie M Jones; Miriam H Meisler; Jeffrey L Noebels
Mutation of the Ca2+ channel beta subunit gene Cchb4 is associated with ataxia and seizures in the lethargic (lh) mouse.
Cell 1997;88(3):385-92.
1996: Daniel L Burgess; Jill A Rafael-Fortney; Miriam H Meisler; Jeffrey S Chamberlain
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 1996;7(8):623-4.
1996: Andrew J Griffith; Daniel L Burgess; David C Kohrman; J Yu; J Blaschak; S Blanton; Michael Boehnke; J T Hecht; J Overhauser; Miriam H Meisler
Localization of the homolog of a mouse craniofacial mutant to human chromosome 18q11 and evaluation of linkage to human CLP and CPO.
Genomics 1996;34(3):299-303.
1996: Andrew J Griffith; G L Radice; Daniel L Burgess; David C Kohrman; Gwenn M Hansen; Monica J Justice; K R Johnson; M T Davisson; Miriam H Meisler
Location of the 9257 and ataxia mutations on mouse chromosome 18.
Mammalian genome : official journal of the International Mammalian Genome Society 1996;7(6):417-9.
1995: Daniel L Burgess; David C Kohrman; J Galt; Nicholas W Plummer; Julie M Jones; B Spear; Miriam H Meisler
Mutation of a new sodium channel gene, Scn8a, in the mouse mutant 'motor endplate disease'.
Nature genetics 1995;10(4):461-5.
1995: David C Kohrman; Nicholas W Plummer; T Schuster; Julie M Jones; W Jang; Daniel L Burgess; J Galt; B T Spear; Miriam H Meisler
Insertional mutation of the motor endplate disease (med) locus on mouse chromosome 15.
Genomics 1995;26(2):171-7.
1994: C N Ting; David C Kohrman; Daniel L Burgess; A Boyle; Richard A Altschuler; G Gholizadeh; Linda C Samuelson; W Jang; Miriam H Meisler
Insertional mutation on mouse chromosome 18 with vestibular and craniofacial abnormalities.
Genetics 1994;136(1):247-54.
1993: C N Ting; Daniel L Burgess; Jeffrey S Chamberlain; T P Keith; K Falls; Miriam H Meisler
Phosphoenolpyruvate carboxykinase (GTP): characterization of the human PCK1 gene and localization distal to MODY on chromosome 20.
Genomics 1993;16(3):698-706.
1992: Jerome L Gorski; E N Burright; E L Reyner; P N Goodfellow; Daniel L Burgess
Isolation of DNA markers from a region between incontinentia pigmenti 1 (IP1) X-chromosomal translocation breakpoints by a comparative PCR analysis of a radiation hybrid subclone mapping panel.
Genomics 1992;14(3):649-56.