0     

Ayyoubi AH, Fazli Besheli B, Quach MM, Gavvala JR, Goldman AM, Swamy CP, et al. Benchmarking signal quality and spatiotemporal distribution of interictal spikes in prolonged human iEEG recordings using CorTec wireless brain interchange. Sci Rep. 2024;14(1):2652. PMID: 38332136.

0     

Brunklaus A, George AL, Jr, Lal D, Heinzen EL, Goldman AM. Prophecy or empiricism? Clinical value of predicting versus determining genetic variant functions. Epilepsia. 2023;64(11):2909-13. PMID: 37562820.

0     

Goldman AM, Thio KLL. SLC35A2-related epilepsy: Global neuronal consequences of a focal disruption in glycosylation. Neurology. 2023;100(5):225-6. PMID: 36307216.

0     

Goldman AM. Oncogenic pathways provide clue to the etiology of human mesial temporal lobe epilepsy. JAMA Neurol. 2023;80(6):546-7. PMID: 37126324.

0     

Goldman AM. Can a mouse help us unravel the mysteries of CDKL5-related epilepsy? Epilepsy Curr. 2022;22(6):375-7. PMID: 36426191.

0     

Goldman AM. When seizures trigger "extreme (cardiac) makeover". Epilepsy Curr. 2022;22(3):181-3. DOI: 10.1177/15357597221085892.

0     

Van Loo KMJ, Carvill GL, Becker AJ, Conboy K, Goldman AM, Kobow K, et al. Epigenetic genes and epilepsy - Emerging mechanisms and clinical applications. Nat Rev Neurol. 2022;18(9):530-43. PMID: 35859062.

0     

Goldman AM. Peri-ictal brainstem-driven posturing and its meaning. Neurology. 2021;96(3):89-90. PMID: 33268564.

0     

Kyle JE, Stratton KG, Zink EM, Kim YM, Bloodsworth KJ, Monroe ME, et al. A resource of lipidomics and metabolomics data from individuals with undiagnosed diseases. Sci Data. 2021;8(1):114. PMID: 33883556.

0     

Massey CA, Thompson SJ, Ostrom RW, Drabek J, Sveinsson OA, Tomson T, et al. X-linked serotonin 2C receptor is associated with a non-canonical pathway for sudden unexpected death in epilepsy. Brain Commun. 2021;3(3):. PMID: 34396109.

0     

Torrealba-Acosta G, Butt H, Edmondson EA, Willaert R, Viswanathan A, Goldman AM. A neurostimulation-triggered trigeminal neuralgia-like pain: Risk factors and management. Neurol Clin Pract. 2021;11(5):e760-e762. PMID: 34840901.

0     

Goldman AM. What does a defect in N-glycosylation mean for neuronal migration and function? Neurol Genet. 2020;6(4):e490. PMID: 32754647.

0     

Kobow K, Reid CA, van Vliet EA, Becker AJ, Carvill GL, Goldman AM, et al. Epigenetics explained: A topic "primer" for the epilepsy community by the ILAE Genetics/Epigenetics Task Force. Epileptic Disord. 2020;22(2):127-41. PMID: 32301721.

0     

Mattioli F, Hayot G, Drouot N, Isidor B, Courraud J, Hinckelmann MV, et al. De novo frameshift variants in the neuronal splicing factor NOVA2 result in a common c-terminal extension and cause a severe form of neurodevelopmental disorder. Am J Hum Genet. 2020;106(4):438-52. PMID: 32197073.

0     

Nair DR, Laxer KD, Weber PB, Murro AM, Park YD, Barkley GL, et al. Nine-year prospective efficacy and safety of brain-responsive neurostimulation for focal epilepsy. Neurology. 2020;95(9):e1244-e1256. PMID: 32690786.

1

Assia Batzir N, Bhagwat PK, Eble TN, Liu P, Eng CM, Elsea SH, et al. De novo missense variant in the GTPase effector domain (GED) of DNM1L leads to static encephalopathy and seizures. Cold Spring Harb Mol Case Stud. 2019;5(3):. PMID: 30850373.

1

Marafi D, Suter B, Schultz R, Glaze D, Pavlik VN, Goldman AM. Spectrum and time course of epilepsy and the associated cognitive decline in MECP2 duplication syndrome. Neurology. 2019;92(2):e108-14. PMID: 30552298.

0     

Montier L, Haneef Z, Gavvala J, Yoshor D, North R, Verla T, et al. A somatic mutation in MEN1 gene detected in periventricular nodular heterotopia tissue obtained from depth electrodes. Epilepsia. 2019;60(10):e104-e109. PMID: 31489630.

2

Mueller SG, Bateman LM, Nei M, Goldman AM, Laxer KD. Brainstem atrophy in focal epilepsy destabilizes brainstem-brain interactions: Preliminary findings. Neuroimage Clin. 2019;23:101888. PMID: 31203171.

4

Frasier CR, Zhang H, Offord J, Dang LT, Auerbach DS, Shi H, et al. Channelopathy as a SUDEP biomarker in Dravet syndrome patient-derived cardiac myocytes. Stem Cell Reports. 2018;11(3):626-34. PMID: 30146492.

11

Mueller SG, Nei M, Bateman LM, Knowlton R, Laxer KD, Friedman D, et al. Brainstem network disruption: A pathway to sudden unexplained death in epilepsy? Hum Brain Mapp. 2018;39(12):4820-30. PMID: 30096213.

66

Geller EB, Skarpaas TL, Gross RE, Goodman RR, Barkley GL, Bazil CW, et al. Brain-responsive neurostimulation in patients with medically intractable mesial temporal lobe epilepsy. Epilepsia. 2017;58(6):994-1004. PMID: 28398014.

49

Jobst BC, Kapur R, Barkley GL, Bazil CW, Berg MJ, Bergey GK, et al. Brain-responsive neurostimulation in patients with medically intractable seizures arising from eloquent and other neocortical areas. Epilepsia. 2017;58(6):1005-14. PMID: 28387951.

62

Lam AD, Deck G, Goldman A, Eskandar EN, Noebels J, Cole AJ. Silent hippocampal seizures and spikes identified by foramen ovale electrodes in Alzheimer's disease. Nat Med. 2017;23(6):678-80. PMID: 28459436.

38

Goldman AM, Behr ER, Semsarian C, Bagnall RD, Sisodiya S, Cooper PN. Sudden unexpected death in epilepsy genetics: Molecular diagnostics and prevention. Epilepsia. 2016;57 Suppl 1:17-25. PMID: 26749013.

5

Goldman AM, LaFrance WC, Jr, Benke T, Asato M, Drane D, et al. 2014 Epilepsy Benchmarks Area IV: Limit or prevent adverse consequence of seizures and their treatment across the lifespan. Epilepsy Curr. 2016;16(3):198-205. PMID: 27330453.

230

Bergey GK, Morrell MJ, Mizrahi EM, Goldman A, King-Stephens D, Nair D, et al. Long-term treatment with responsive brain stimulation in adults with refractory partial seizures. Neurology. 2015;84(8):810-7. PMID: 25616485.

25

Goldman AM. Mechanisms of sudden unexplained death in epilepsy. Curr Opin Neurol. 2015;28(2):166-74. PMID: 25734955.

54

King-Stephens D, Mirro E, Weber PB, Laxer KD, Van Ness PC, Salanova V, et al. Lateralization of mesial temporal lobe epilepsy with chronic ambulatory electrocorticography. Epilepsia. 2015;56(6):959-67. PMID: 25988840.

0     

Goldman AM, Tuchman R. Commentary: Genetic testing in epilepsy: What do patients and families want to know? Epilepsia. 2014;55(11):1703-4. PMID: 25377513.

236

Heck CN, King-Stephens D, Massey AD, Nair DR, Jobst BC, Barkley GL, et al. Two-year seizure reduction in adults with medically intractable partial onset epilepsy treated with responsive neurostimulation: Final results of the RNS System Pivotal trial. Epilepsia. 2014;55(3):432-41. PMID: 24621228.

45

Klassen TL, Bomben VC, Patel A, Drabek J, Chen TT, Gu W, et al. High-resolution molecular genomic autopsy reveals complex sudden unexpected death in epilepsy risk profile. Epilepsia. 2014;55(2):e6-12. PMID: 24372310.

25

Chen TT, Klassen TL, Goldman AM, Marini C, Guerrini R, Noebels JL. Novel brain expression of ClC-1 chloride channels and enrichment of CLCN1 variants in epilepsy. Neurology. 2013;80(12):1078-85. PMID: 23408874.

45

Hirose S, Scheffer IE, Marini C, De Jonghe P, Andermann E, Goldman AM, et al. SCN1A testing for epilepsy: Application in clinical practice. Epilepsia. 2013;54(5):946-52. PMID: 23586701.

3

Klassen TL, Drabek J, Tomson T, Sveinsson O, von Dobeln U, Noebels JL, et al. Visual automated fluorescence electrophoresis provides simultaneous quality, quantity, and molecular weight spectra for genomic DNA from archived neonatal blood spots. J Mol Diagn. 2013;15(3):283-90. PMID: 23518217.

13

Klassen TL, von Ruden EL, Drabek J, Noebels JL, Goldman AM. Comparative analytical utility of DNA derived from alternative human specimens for molecular autopsy and diagnostics. J Mol Diagn. 2012;14(5):451-7. PMID: 22796560.

199

Klassen T, Davis C, Goldman A, Burgess D, Chen T, Wheeler D, et al. Exome sequencing of ion channel genes reveals complex profiles confounding personal risk assessment in epilepsy. Cell. 2011;145(7):1036-48. PMID: 21703448.

69

McGuire AL, Oliver JM, Slashinski MJ, Graves JL, Wang T, Kelly PA, et al. To share or not to share: a randomized trial of consent for data sharing in genome research. Genet Med. 2011;13(11):948-55. PMID: 21785360.

14

Dulay MF, Levin HS, York MK, Li X, Mizrahi EM, Goldsmith I, et al. Changes in individual and group spatial and verbal learning characteristics after anterior temporal lobectomy. Epilepsia. 2009;50(6):1385-95. PMID: 18657174.

178

Goldman AM, Glasscock E, Yoo J, Chen TT, Klassen TL, Noebels JL. Arrhythmia in heart and brain: KCNQ1 mutations link epilepsy and sudden unexplained death. Sci Transl Med. 2009;1(2):2ra6. PMID: 20368164.

79

McGuire AL, Hamilton JA, Lunstroth R, McCullough LB, Goldman A. DNA data sharing: Research participants' perspectives. Genet Med. 2008;10(1):46-53. PMID: 18197056.

53

Bi W, Yan J, Shi X, Yuva-Paylor LA, Antalffy BA, Goldman A, et al. Rai1 deficiency in mice causes learning impairment and motor dysfunction, whereas Rai1 heterozygous mice display minimal behavioral phenotypes. Hum Mol Genet. 2007;16(15):1802-13. PMID: 17517686.

0     

Goldman A, Noebels J. Invited comments on the Shostak and Ottman review. Epilepsia. 2006;47(10):1750-1; author reply 1755-6. PMID: 17054704.

24

Goldman AM, Potocki L, Walz K, Lynch JK, Glaze DG, Lupski JR, et al. Epilepsy and chromosomal rearrangements in Smith-Magenis Syndrome [del(17)(p11.2p11.2)]. J Child Neurol. 2006;21(2):93-8. PMID: 16566870.