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Items: 1 to 20 of 98


Validity of probands' reports and self-reports of essential tremor: Data from a large family study in North America.

Louis ED, Hernandez N, Sebastian AA, Clark LN, Ottman R.

J Neurol Sci. 2018 Oct 15;393:45-50. doi: 10.1016/j.jns.2018.08.006. Epub 2018 Aug 6.


Return of individual results in epilepsy genomic research: A view from the field.

Ottman R, Freyer C, Mefford HC, Poduri A, Lowenstein DH; Epilepsy Return of Results Workshop Participants.

Epilepsia. 2018 Sep;59(9):1635-1642. doi: 10.1111/epi.14530. Epub 2018 Aug 10.


Transient, Isolated Head Tremor in "Unaffected" Individuals: Is Essential Tremor an Even More Prevalent Disease Than We Suppose?

Louis ED, Meyers JH, Cristal AD, Patel A, Tinaz S, Pullman SL, Clark LN, Ottman R, Factor-Litvak P.

Front Neurol. 2018 Jul 13;9:570. doi: 10.3389/fneur.2018.00570. eCollection 2018.


Familial aggregation of major depressive disorder in an African-American community.

Murphy E, Gangwisch JE, Matsunaga JT, Ottman R.

Depress Anxiety. 2018 Jul;35(7):674-684. doi: 10.1002/da.22775. Epub 2018 May 21.


Genetic Testing Preferences of Individuals in Families with Essential Tremor.

Naranjo KV, Park J, Chen KP, Hernandez N, Clark LN, Ottman R, Louis ED.

Tremor Other Hyperkinet Mov (N Y). 2018 Mar 27;8:545. doi: 10.7916/D8B296RK. eCollection 2018.


Knowledge about Essential Tremor: A Study of Essential Tremor Families.

Cristal AD, Chen KP, Hernandez NC, Factor-Litvak P, Clark LN, Ottman R, Louis ED.

Front Neurol. 2018 Jan 26;9:27. doi: 10.3389/fneur.2018.00027. eCollection 2018.


Mood disorders in familial epilepsy: A test of shared etiology.

Insel BJ, Ottman R, Heiman GA.

Epilepsia. 2018 Feb;59(2):431-439. doi: 10.1111/epi.13985. Epub 2018 Jan 10.


Utility of EEG Activation Procedures in Epilepsy: A Population-Based Study.

Baldin E, Hauser WA, Buchhalter JR, Hesdorffer DC, Ottman R.

J Clin Neurophysiol. 2017 Nov;34(6):512-519. doi: 10.1097/WNP.0000000000000371.


Application of rare variant transmission disequilibrium tests to epileptic encephalopathy trio sequence data.

Epi4K Consortium; EuroEPINOMICS-RES Consortium; Epilepsy Phenome Genome Project.

Eur J Hum Genet. 2017 Jun;25(7):894-899. doi: 10.1038/ejhg.2017.61. Epub 2017 May 17.


Action Tremor Asymmetry Profile Does Not Aggregate in Families with Essential Tremor.

Louis ED, Hernandez N, Chen KP, Naranjo KV, Park J, Clark LN, Ottman R.

Front Neurol. 2017 Apr 19;8:148. doi: 10.3389/fneur.2017.00148. eCollection 2017.


Polygenic risk scores in familial Alzheimer disease.

Tosto G, Bird TD, Tsuang D, Bennett DA, Boeve BF, Cruchaga C, Faber K, Foroud TM, Farlow M, Goate AM, Bertlesen S, Graff-Radford NR, Medrano M, Lantigua R, Manly J, Ottman R, Rosenberg R, Schaid DJ, Schupf N, Stern Y, Sweet RA, Mayeux R.

Neurology. 2017 Mar 21;88(12):1180-1186. doi: 10.1212/WNL.0000000000003734. Epub 2017 Feb 17.


Familial Aggregation of the Cerebellar Signs in Familial Essential Tremor.

Louis ED, Hernandez N, Chen KP, Naranjo KV, Park J, Clark LN, Ottman R.

Tremor Other Hyperkinet Mov (N Y). 2017 Jan 13;7:439. doi: 10.7916/D8KK9C8Q. eCollection 2017.


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

Epi4K consortium; Epilepsy Phenome/Genome Project.

Lancet Neurol. 2017 Feb;16(2):135-143. doi: 10.1016/S1474-4422(16)30359-3.


De Novo Mutations in Synaptic Transmission Genes Including DNM1 Cause Epileptic Encephalopathies.

EuroEPINOMICS-RES Consortium. Electronic address:; Epilepsy Phenome/Genome Project; Epi4K Consortium; EuroEPINOMICS-RES Consortium.

Am J Hum Genet. 2017 Jan 5;100(1):179. doi: 10.1016/j.ajhg.2016.12.012. No abstract available.


Depression and genetic causal attribution of epilepsy in multiplex epilepsy families.

Sorge ST, Hesdorffer DC, Phelan JC, Winawer MR, Shostak S, Goldsmith J, Chung WK, Ottman R.

Epilepsia. 2016 Oct;57(10):1643-1650. doi: 10.1111/epi.13500. Epub 2016 Aug 25.


The Role of Cardiovascular Risk Factors and Stroke in Familial Alzheimer Disease.

Tosto G, Bird TD, Bennett DA, Boeve BF, Brickman AM, Cruchaga C, Faber K, Foroud TM, Farlow M, Goate AM, Graff-Radford NR, Lantigua R, Manly J, Ottman R, Rosenberg R, Schaid DJ, Schupf N, Stern Y, Sweet RA, Mayeux R; National Institute on Aging Late-Onset Alzheimer Disease/National Cell Repository for Alzheimer Disease (NIA-LOAD/NCRAD) Family Study Group.

JAMA Neurol. 2016 Oct 1;73(10):1231-1237. doi: 10.1001/jamaneurol.2016.2539.


De Novo Mutations in SLC1A2 and CACNA1A Are Important Causes of Epileptic Encephalopathies.

Epi4K Consortium.

Am J Hum Genet. 2016 Aug 4;99(2):287-98. doi: 10.1016/j.ajhg.2016.06.003. Epub 2016 Jul 28.


Definition and diagnostic criteria of sleep-related hypermotor epilepsy.

Tinuper P, Bisulli F, Cross JH, Hesdorffer D, Kahane P, Nobili L, Provini F, Scheffer IE, Tassi L, Vignatelli L, Bassetti C, Cirignotta F, Derry C, Gambardella A, Guerrini R, Halasz P, Licchetta L, Mahowald M, Manni R, Marini C, Mostacci B, Naldi I, Parrino L, Picard F, Pugliatti M, Ryvlin P, Vigevano F, Zucconi M, Berkovic S, Ottman R.

Neurology. 2016 May 10;86(19):1834-42. doi: 10.1212/WNL.0000000000002666. Epub 2016 Apr 15. Review.


Parents' interest in genetic testing of their offspring in multiplex epilepsy families.

Caminiti CB, Hesdorffer DC, Shostak S, Goldsmith J, Sorge ST, Winawer MR, Phelan JC, Chung WK, Ottman R.

Epilepsia. 2016 Feb;57(2):279-87. doi: 10.1111/epi.13287. Epub 2015 Dec 22.


Familial Aggregation and Co-Aggregation of Essential Tremor and Parkinson's Disease.

Louis ED, Clark L, Ottman R.

Neuroepidemiology. 2016;46(1):31-6. doi: 10.1159/000442021. Epub 2015 Nov 26.

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