Articles with public access mandates - Ruth OttmanLearn more
Not available anywhere: 9
De novo mutations in epileptic encephalopathies
Nature 501 (7466), 217-221, 2013
Mandates: US National Institutes of Health
Epilepsy in children with attention-deficit/hyperactivity disorder
SM Davis, SK Katusic, WJ Barbaresi, J Killian, AL Weaver, R Ottman, ...
Pediatric neurology 42 (5), 325-330, 2010
Mandates: US National Institutes of Health
Concordance for Parkinson's disease in twins: A 20‐year update
SM Goldman, K Marek, R Ottman, C Meng, K Comyns, P Chan, J Ma, ...
Annals of neurology 85 (4), 600-605, 2019
Mandates: US National Institutes of Health
Validity of probands' reports and self-reports of essential tremor: data from a large family study in North America
ED Louis, N Hernandez, AA Sebastian, LN Clark, R Ottman
Journal of the Neurological Sciences 393, 45-50, 2018
Mandates: US National Institutes of Health
Patient characteristics and antiseizure medication pathways in newly diagnosed epilepsy: Feasibility and pilot results using the common data model in a single-center electronic …
M Spotnitz, A Ostropolets, VG Castano, K Natarajan, GJ Waldman, ...
Epilepsy & Behavior 129, 108630, 2022
Mandates: US National Institutes of Health
Knowledge and beliefs about epilepsy genetics among Hispanic and non‐Hispanic patients
S Trujillo, JB Wetmore, IA Camarillo, S Misiewicz, H May, H Choi, K Siegel, ...
Epilepsia 64 (9), 2443-2453, 2023
Mandates: US National Institutes of Health
Essential Tremor Families With Heterogeneous Motor Phenomenology:“Mixed Motor Disorder”
ED Louis, NC Hernandez, R Ottman, LN Clark
Neurology: Clinical Practice, 2021
Mandates: US National Institutes of Health
Familial aggregation of seizure outcomes in four familial epilepsy cohorts
CA Ellis, D Tu, KL Oliver, HC Mefford, WA Hauser, J Buchhalter, ...
Epilepsia, 2024
Mandates: National Health and Medical Research Council, Australia
The role of copy number variants in the genetic architecture of common familial epilepsies
Epi4K Consortium, EP Almanza Fuerte, J Nguyen, M Mehaffey, A Sulovari, ...
Epilepsia 65 (3), 792-804, 2024
Mandates: Howard Hughes Medical Institute
Available somewhere: 107
Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease
E Sidransky, MA Nalls, JO Aasly, J Aharon-Peretz, G Annesi, ER Barbosa, ...
New England Journal of Medicine 361 (17), 1651-1661, 2009
Mandates: US National Institutes of Health
De novo mutations in synaptic transmission genes including DNM1 cause epileptic encephalopathies
S Appenzeller, R Balling, N Barisic, S Baulac, H Caglayan, D Craiu, ...
The American Journal of Human Genetics 95 (4), 360-370, 2014
Mandates: US National Institutes of Health
Definition and diagnostic criteria of sleep-related hypermotor epilepsy
P Tinuper, F Bisulli, JH Cross, D Hesdorffer, P Kahane, L Nobili, F Provini, ...
Neurology 86 (19), 1834-1842, 2016
Mandates: National Institute for Health Research, UK
Cognitive performance of GBA mutation carriers with early-onset PD: The CORE-PD study
RN Alcalay, E Caccappolo, H Mejia-Santana, MX Tang, L Rosado, ...
Neurology 78 (18), 1434-1440, 2012
Mandates: US National Institutes of Health
Genetic testing in the epilepsies—report of the ILAE Genetics Commission
R Ottman, S Hirose, S Jain, H Lerche, I Lopes‐Cendes, JL Noebels, ...
Epilepsia 51 (4), 655-670, 2010
Mandates: US National Institutes of Health
De novo mutations in SLC1A2 and CACNA1A are important causes of epileptic encephalopathies
CT Myers, JM McMahon, AL Schneider, S Petrovski, AS Allen, GL Carvill, ...
The American Journal of Human Genetics 99 (2), 287-298, 2016
Mandates: US National Institutes of Health
The characterization of twenty sequenced human genomes
K Pelak, KV Shianna, D Ge, JM Maia, M Zhu, JP Smith, ET Cirulli, J Fellay, ...
PLoS genetics 6 (9), e1001111, 2010
Mandates: US National Institutes of Health
Familial risk of epilepsy: a population-based study
AL Peljto, C Barker-Cummings, VM Vasoli, CL Leibson, WA Hauser, ...
Brain 137 (3), 795-805, 2014
Mandates: US National Institutes of Health
Frequency of known mutations in early-onset Parkinson disease: implication for genetic counseling: the consortium on risk for early onset Parkinson disease study
RN Alcalay, E Caccappolo, H Mejia-Santana, MX Tang, L Rosado, ...
Archives of neurology 67 (9), 1116-1122, 2010
Mandates: US National Institutes of Health
How many people in the USA have essential tremor? Deriving a population estimate based on epidemiological data
ED Louis, R Ottman
Tremor and other hyperkinetic movements 4, 2014
Mandates: US National Institutes of Health
Ultra-rare genetic variation in common epilepsies: a case-control sequencing study
AS Allen, ST Bellows, SF Berkovic, J Bridgers, R Burgess, G Cavalleri, ...
The Lancet Neurology 16 (2), 135-143, 2017
Mandates: US National Institutes of Health, UK Medical Research Council
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