• 1209 Citations
  • 7 h-Index
20032018
If you made any changes in Pure, your changes will be visible here soon.

Publications 2003 2018

  • 1209 Citations
  • 7 h-Index
  • 12 Article
  • 2 Chapter
  • 1 Comment/debate
2018
2 Citations (Scopus)

Comparative sensitivity of quantitative EEG (QEEG) spectrograms for detecting seizure subtypes

Goenka, A., Boro, A. D. & Yozawitz, E. G., Feb 1 2018, In : Seizure. 55, p. 70-75 6 p.

Research output: Contribution to journalArticle

Electroencephalography
Seizures
2017

Assessing quantitative EEG spectrograms to identify non-epileptic events

Goenka, A., Boro, A. D. & Yozawitz, E. G., Sep 1 2017, In : Epileptic Disorders. 19, 3, p. 299-306 8 p.

Research output: Contribution to journalArticle

Electroencephalography
Seizures
Epilepsy
Systems Integration
Sensitivity and Specificity
1 Citation (Scopus)

Erratum: De Novo Mutations in Synaptic Transmission Genes Including DNM1 Cause Epileptic Encephalopathies (American Journal of Human Genetics (2014) 95(4) (360–370)(S0002929714003838)(10.1016/j.ajhg.2014.08.013))

Appenzeller, S., Balling, R., Barisic, N., Baulac, S., Caglayan, H., Craiu, D., De Jonghe, P., Depienne, C., Dimova, P., Djémié, T., Gormley, P., Guerrini, R., Helbig, I., Hjalgrim, H., Hoffman-Zacharska, D., Jähn, J., Klein, K. M., Koeleman, B., Komarek, V., Krause, R. & 111 others, Kuhlenbäumer, G., Leguern, E., Lehesjoki, A. E., Lemke, J. R., Lerche, H., Linnankivi, T., Marini, C., May, P., Møller, R. S., Muhle, H., Pal, D., Palotie, A., Pendziwiat, M., Robbiano, A., Roelens, F., Rosenow, F., Selmer, K., Serratosa, J. M., Sisodiya, S., Stephani, U., Sterbova, K., Striano, P., Suls, A., Talvik, T., von Spiczak, S., Weber, Y., Weckhuysen, S., Zara, F., Abou-Khalil, B., Alldredge, B. K., Andermann, E., Andermann, F., Amrom, D., Bautista, J. F., Berkovic, S. F., Bluvstein, J., Boro, A., Cascino, G., Consalvo, D., Crumrine, P., Devinsky, O., Dlugos, D., Epstein, M. P., Fiol, M., Fountain, N. B., French, J., Friedman, D., Geller, E. B., Glauser, T., Glynn, S., Haas, K., Haut, S. R., Hayward, J., Helmers, S. L., Joshi, S., Kanner, A., Kirsch, H. E., Knowlton, R. C., Kossoff, E. H., Kuperman, R., Kuzniecky, R., Lowenstein, D. H., McGuire, S. M., Motika, P. V., Novotny, E. J., Ottman, R., Paolicchi, J. M., Parent, J., Park, K., Poduri, A., Sadleir, L., Scheffer, I. E., Shellhaas, R. A., Sherr, E., Shih, J. J., Singh, R., Sirven, J., Smith, M. C., Sullivan, J., Thio, L. L., Venkat, A., Vining, E. P. G., Von Allmen, G. K., Weisenberg, J. L., Widdess-Walsh, P., Winawer, M. R., Allen, A. S., Berkovic, S. F., Cossette, P., Delanty, N., Dlugos, D., Eichler, E. E., Epstein, M. P., Glauser, T., Goldstein, D. B., Han, Y., Heinzen, E. L., Johnson, M. R., Kuzniecky, R., Lowenstein, D. H., Marson, A. G., Mefford, H. C., Nieh, S. E., O'Brien, T. J., Ottman, R., Petrou, S., Petrovski, S., Poduri, A., Ruzzo, E. K., Scheffer, I. E. & Sherr, E., Jan 5 2017, In : American Journal of Human Genetics. 100, 1, p. 179 1 p.

Research output: Contribution to journalComment/debate

Medical Genetics
Brain Diseases
Synaptic Transmission
Names
Epilepsy
74 Citations (Scopus)

Ultra-rare genetic variation in common epilepsies: a case-control sequencing study

Allen, A. S., Bellows, S. T., Berkovic, S. F., Bridgers, J., Burgess, R., Cavalleri, G., Chung, S. K., Cossette, P., Delanty, N., Dlugos, D., Epstein, M. P., Freyer, C., Goldstein, D. B., Heinzen, E. L., Hildebrand, M. S., Johnson, M. R., Kuzniecky, R., Lowenstein, D. H., Marson, A. G., Mayeux, R. & 66 others, Mebane, C., Mefford, H. C., O'Brien, T. J., Ottman, R., Petrou, S., Petrovski, S., Pickrell, W. O., Radtke, R. A., Rees, M. I., Regan, B. M., Ren, Z., Scheffer, I. E., Sills, G. J., Thomas, R. H., Wang, Q., Abou-Khalil, B., Alldredge, B. K., Amrom, D., Andermann, E., Andermann, F., Bautista, J. F., Bluvstein, J., Boro, A., Cascino, G. D., Consalvo, D., Crumrine, P., Devinsky, O., Fiol, M., Fountain, N. B., French, J., Friedman, D., Geller, E. B., Glauser, T., Glynn, S., Haas, K., Haut, S. R., Hayward, J., Helmers, S. L., Joshi, S., Kanner, A., Kirsch, H. E., Knowlton, R. C., Kossoff, E. H., Kuperman, R., Motika, P. V., Novotny, E. J., Paolicchi, J. M., Parent, J. M., Park, K., Poduri, A., Sadleir, L. G., Shellhaas, R. A., Sherr, E. H., Shih, J. J., Shinnar, S., Singh, R. K., Sirven, J., Smith, M. C., Sullivan, J., Thio, L. L., Venkat, A., Vining, E. P. G., Von Allmen, G. K., Weisenberg, J. L., Widdess-Walsh, P. & Winawer, M. R., Feb 1 2017, In : The Lancet Neurology. 16, 2, p. 135-143 9 p.

Research output: Contribution to journalArticle

Case-Control Studies
Epilepsy
Partial Epilepsy
Generalized Epilepsy
Genes
2015
6 Citations (Scopus)

ILAE type 3 hippocampal sclerosis in patients with anti-GAD - Related epilepsy

Glover, R. L., De Niro, L. V., LaSala, P. A., Weidenheim, K. M., Graber, J. J. & Boro, A. D., 2015, In : Neurology: Neuroimmunology and NeuroInflammation. 2, 4, e122.

Research output: Contribution to journalArticle

Glutamate Decarboxylase
Sclerosis
Epilepsy
Stiff-Person Syndrome
Cerebellar Ataxia
1 Citation (Scopus)

Periodic epileptiform discharges clarified for the nonneurologist intensivist

Lahiri, S., Boro, A. D., Shiloh, A. L., Milstein, M. J. & Savel, R. H., Oct 11 2015, In : Journal of Intensive Care Medicine. 30, 7, p. 385-391 7 p.

Research output: Contribution to journalArticle

Terminology
Intensive Care Units
Electroencephalography
Seizures
5 Citations (Scopus)

Phenotypic and imaging features of FLNA-negative patients with bilateral periventricular nodular heterotopia and epilepsy

for the EPGP Investigators, Oct 1 2015, In : Epilepsy and Behavior. 51, p. 321-327 7 p.

Research output: Contribution to journalArticle

Periventricular Nodular Heterotopia
Epilepsy
Seizures
Malformations of Cortical Development
Choristoma
2014
227 Citations (Scopus)

De novo mutations in synaptic transmission genes including DNM1 cause epileptic encephalopathies

EuroEPINOMICS-RES Consortium, Epilepsy Phenome/Genome Project & Epi4K Consortium, 2014, In : American Journal of Human Genetics. 95, 4, p. 360-370 11 p.

Research output: Contribution to journalArticle

Brain Diseases
Synaptic Transmission
Mutation
Genes
Exome
2013
775 Citations (Scopus)

De novo mutations in epileptic encephalopathies

Allen, A. S., Berkovic, S. F., Cossette, P., Delanty, N., Dlugos, D., Eichler, E. E., Epstein, M. P., Glauser, T., Goldstein, D. B., Han, Y., Heinzen, E. L., Hitomi, Y., Howell, K. B., Johnson, M. R., Kuzniecky, R., Lowenstein, D. H., Lu, Y. F., Madou, M. R. Z., Marson, A. G., Mefford, H. C. & 51 others, Esmaeeli Nieh, S., O'Brien, T. J., Ottman, R., Petrovski, S., Poduri, A., Ruzzo, E. K., Scheffer, I. E., Sherr, E. H., Yuskaitis, C. J., Abou-Khalil, B., Alldredge, B. K., Bautista, J. F., Boro, A. D., Cascino, G. D., Consalvo, D., Crumrine, P., Devinsky, O., Fiol, M., Fountain, N. B., French, J., Friedman, D., Geller, E. B., Glynn, S., Haut, S. R., Hayward, J., Helmers, S. L., Joshi, S., Kanner, A., Kirsch, H. E., Knowlton, R. C., Kossoff, E. H., Kuperman, R., McGuire, S. M., Motika, P. V., Novotny, E. J., Paolicchi, J. M., Parent, J. M., Park, K., Shellhaas, R. A., Shih, J. J., Singh, R., Sirven, J., Smith, M. C., Sullivan, J., Lin Thio, L., Venkat, A., Vining, E. P. G., Von Allmen, G. K., Weisenberg, J. L., Widdess-Walsh, P. & Winawer, M. R., 2013, In : Nature. 501, 7466, p. 217-221 5 p.

Research output: Contribution to journalArticle

Brain Diseases
Mutation
Genes
Exome
Infantile Spasms
10 Citations (Scopus)

Lennox-Gastaut syndrome of unknown cause: Phenotypic characteristics of patients in the Epilepsy Phenome/Genome Project

Widdess-Walsh, P., Dlugos, D., Fahlstrom, R., Joshi, S., Shellhaas, R., Boro, A. D., Sullivan, J. & Geller, E., Nov 2013, In : Epilepsia. 54, 11, p. 1898-1904 7 p.

Research output: Contribution to journalArticle

Epilepsy
Genome
Electroencephalography
Parents
Seizures
2008
28 Citations (Scopus)

Value of routine screening for bone demineralization in an urban population of patients with epilepsy

Lado, F., Spiegel, R., Masur, J. H., Boro, A. D. & Haut, S. R., Feb 2008, In : Epilepsy Research. 78, 2-3, p. 155-160 6 p.

Research output: Contribution to journalArticle

Urban Population
Physiologic Calcification
Epilepsy
Bone Density
Bone and Bones
2006
1 Citation (Scopus)

Basic Principles of Electroencephalography

Ettinger, A. B., Boro, A. D., Holmes, G. L. & Moshe, S. L., 2006, Clinical Neurophysiology of Infancy, Childhood, and Adolescence. Elsevier Inc., p. 3-45 43 p.

Research output: Chapter in Book/Report/Conference proceedingChapter

Electroencephalography

The Diagnosis of Brain Death

Boro, A. D. & Moshe, S. L., 2006, Clinical Neurophysiology of Infancy, Childhood, and Adolescence. Elsevier Inc., p. 401-411 11 p.

Research output: Chapter in Book/Report/Conference proceedingChapter

Brain Death
2004
18 Citations (Scopus)

A novel nonpharmacologic treatment for photosensitive epilepsy: A report of three patients tested with blue cross-polarized glasses

Kepecs, M. R., Boro, A. D., Haut, S. R., Kepecs, G. & Moshe, S. L., Sep 2004, In : Epilepsia. 45, 9, p. 1158-1162 5 p.

Research output: Contribution to journalArticle

Reflex Epilepsy
Blue Cross Blue Shield Insurance Plans
Lenses
Glass
Electroencephalography
2003
61 Citations (Scopus)

Medical comorbidities in the treatment of epilepsy

Boro, A. D. & Haut, S. R., Oct 2003, In : Epilepsy and Behavior. 4, SUPPL. 2

Research output: Contribution to journalArticle

Comorbidity
Epilepsy
Psychotic Disorders
Seizures
Therapeutics