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Familial aggregation of major depressive disorder in an African-American community.
- Published in:
- 2018
- By:
- Publication type:
- journal article
Transient, Isolated Head Tremor in "Unaffected" Individuals: Is Essential Tremor an Even More Prevalent Disease Than We Suppose?
- Published in:
- Frontiers in Neurology, 2018, p. 1, doi. 10.3389/fneur.2018.00570
- By:
- Publication type:
- Article
Parkinson Disease in Twins.
- Published in:
- JAMA: Journal of the American Medical Association, 1999, v. 282, n. 14, p. 1328, doi. 10.1001/jama.282.14.1328
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- Publication type:
- Article
Parkinson Disease in Twins.
- Published in:
- JAMA: Journal of the American Medical Association, 1999, v. 281, n. 4, p. 341, doi. 10.1001/jama.281.4.341
- By:
- Publication type:
- Article
Parents' interest in genetic testing of their offspring in multiplex epilepsy families.
- Published in:
- Epilepsia (Series 4), 2016, v. 57, n. 2, p. 279, doi. 10.1111/epi.13287
- By:
- Publication type:
- Article
Genetic causal attribution of epilepsy and its implications for felt stigma.
- Published in:
- Epilepsia (Series 4), 2015, v. 56, n. 10, p. 1542, doi. 10.1111/epi.13113
- By:
- Publication type:
- Article
Attention-deficit/hyperactivity disorder symptoms in adults with self-reported epilepsy: Results from a national epidemiologic survey of epilepsy.
- Published in:
- Epilepsia (Series 4), 2015, v. 56, n. 2, p. 218, doi. 10.1111/epi.12897
- By:
- Publication type:
- Article
Genetic testing preferences in families containing multiple individuals with epilepsy.
- Published in:
- Epilepsia (Series 4), 2014, v. 55, n. 11, p. 1705, doi. 10.1111/epi.12810
- By:
- Publication type:
- Article
Copy number variations and susceptibility to lateral temporal epilepsy: A study of 21 pedigrees.
- Published in:
- Epilepsia (Series 4), 2014, v. 55, n. 10, p. 1651, doi. 10.1111/epi.12767
- By:
- Publication type:
- Article
Yield of epileptiform electroencephalogram abnormalities in incident unprovoked seizures: A population-based study.
- Published in:
- Epilepsia (Series 4), 2014, v. 55, n. 9, p. 1389, doi. 10.1111/epi.12720
- By:
- Publication type:
- Article
SCN1A testing for epilepsy: Application in clinical practice.
- Published in:
- Epilepsia (Series 4), 2013, v. 54, n. 5, p. 946, doi. 10.1111/epi.12168
- By:
- Publication type:
- Article
Comorbidities of epilepsy: Results from the Epilepsy Comorbidities and Health (EPIC) survey.
- Published in:
- Epilepsia (Series 4), 2011, v. 52, n. 2, p. 308, doi. 10.1111/j.1528-1167.2010.02927.x
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- Publication type:
- Article
Study of the genetically complex epilepsies.
- Published in:
- Epilepsia (Series 4), 2010, v. 51, p. 57, doi. 10.1111/j.1528-1167.2010.02843.x
- By:
- Publication type:
- Article
Evaluation of depression risk in LGI1 mutation carriers.
- Published in:
- Epilepsia (Series 4), 2010, v. 51, n. 9, p. 1685, doi. 10.1111/j.1528-1167.2010.02677.x
- By:
- Publication type:
- Article
Genetic testing in the epilepsies—Report of the ILAE Genetics Commission.
- Published in:
- 2010
- By:
- Publication type:
- Report
Validation of a brief screening instrument for the ascertainment of epilepsy.
- Published in:
- Epilepsia (Series 4), 2010, v. 51, n. 2, p. 191, doi. 10.1111/j.1528-1167.2009.02274.x
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- Publication type:
- Article
Ethical, Legal, and Social Dimensions of Epilepsy Genetics.
- Published in:
- Epilepsia (Series 4), 2006, v. 47, n. 10, p. 1595, doi. 10.1111/j.1528-1167.2006.00632.x
- By:
- Publication type:
- Article
Response from Drs. Shostak and Ottman.
- Published in:
- 2006
- By:
- Publication type:
- Letter
Analysis of Genetically Complex Epilepsies.
- Published in:
- Epilepsia (Series 4), 2005, v. 46, p. 7, doi. 10.1111/j.1528-1167.2005.00350.x
- By:
- Publication type:
- Article
Recruitment of Families for Genetic Studies of Epilepsy.
- Published in:
- Epilepsia (Series 4), 2005, v. 46, n. 2, p. 290, doi. 10.1111/j.0013-9580.2005.41904.x
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- Publication type:
- Article
Evidence for Distinct Genetic Influences on Generalized and Localization-related Epilepsy.
- Published in:
- Epilepsia (Series 4), 2003, v. 44, n. 9, p. 1176, doi. 10.1046/j.1528-1157.2003.58902.x
- By:
- Publication type:
- Article
Four New Families with Autosomal Dominant Partial Epilepsy with Auditory Features: Clinical Description and Linkage to Chromosome 10q24.
- Published in:
- Epilepsia (Series 4), 2002, v. 43, n. 1, p. 60, doi. 10.1046/j.1528-1157.2002.45001.x
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- Publication type:
- Article
Progress in the Genetics of the Partial Epilepsies.
- Published in:
- Epilepsia (Series 4), 2001, v. 42, p. 24, doi. 10.1111/j.1528-1167.2001.0s005.x
- By:
- Publication type:
- Article
Study Designs for Identification of Rare Disease Variants in Complex Diseases: The Utility of Family-Based Designs.
- Published in:
- Genetics, 2011, v. 189, n. 3, p. 1061, doi. 10.1534/genetics.111.131813
- By:
- Publication type:
- Article
Dale C. Hesdorffer, PhD.
- Published in:
- Neuroepidemiology, 2024, v. 58, n. 3, p. 227, doi. 10.1159/000537950
- By:
- Publication type:
- Article
Familial Aggregation of Paget's Disease of Bone.
- Published in:
- Journal of Bone & Mineral Research, 2005, v. 20, n. 3, p. 541, doi. 10.1359/jbmr.2005.20.3.541
- By:
- Publication type:
- Article
MAPT haplotypes modify the association between head injury and risk of Alzheimer’s disease.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2015, v. 11, n. 7, p. P361, doi. 10.1016/j.jalz.2015.06.256
- By:
- Publication type:
- Article
Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features.
- Published in:
- Nature Genetics, 2002, v. 30, n. 3, p. 335, doi. 10.1038/ng832
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- Publication type:
- Article
Pygmalion in the genes? On the potentially negative impacts of polygenic scores for educational attainment.
- Published in:
- Social Psychology of Education, 2021, v. 24, n. 3, p. 789, doi. 10.1007/s11218-021-09632-z
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- Publication type:
- Article
A Method for Estimating Penetrance from Families Sampled for Linkage Analysis.
- Published in:
- Biometrics, 2006, v. 62, n. 4, p. 1081, doi. 10.1111/j.1541-0420.2006.00614.x
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- Publication type:
- Article
Familial aggregation of paget's disease of bone.
- Published in:
- Journal of Bone & Mineral Research, 1991, v. 6, n. 5, p. 495, doi. 10.1002/jbmr.5650060511
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- Publication type:
- Article
Familial cosegregation of rare genetic variants with disease in complex disorders.
- Published in:
- European Journal of Human Genetics, 2013, v. 21, n. 4, p. 444, doi. 10.1038/ejhg.2012.194
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- Publication type:
- Article
Genetic Testing Preferences of Individuals in Families with Essential Tremor.
- Published in:
- Tremor & Other Hyperkinetic Movements, 2018, p. 1, doi. 10.7916/D8B296RK
- By:
- Publication type:
- Article
Use of Recommended Neurodiagnostic Evaluation Among Patients With Drug-Resistant Epilepsy.
- Published in:
- JAMA Neurology, 2024, v. 81, n. 5, p. 499, doi. 10.1001/jamaneurol.2024.0551
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- Publication type:
- Article
The Role of Cardiovascular Risk Factors and Stroke in Familial Alzheimer Disease.
- Published in:
- JAMA Neurology, 2016, v. 73, n. 10, p. 1231, doi. 10.1001/jamaneurol.2016.2539
- By:
- Publication type:
- Article
Age-Specific Incidence Rates for Dementia and Alzheimer Disease in NIA-LOAD/NCRAD and EFIGA Families.
- Published in:
- JAMA Neurology, 2014, v. 71, n. 3, p. 315, doi. 10.1001/jamaneurol.2013.5570
- By:
- Publication type:
- Article
Genetic and developmental influences on susceptibility to epilepsy: evidence from twins.
- Published in:
- 1992
- By:
- Publication type:
- journal article
Whole genome sequencing and rare variant analysis in essential tremor families.
- Published in:
- PLoS ONE, 2019, v. 14, n. 8, p. 1, doi. 10.1371/journal.pone.0220512
- By:
- Publication type:
- Article
Use of Genetic Tests among Neurologists and Psychiatrists: Knowledge, Attitudes, Behaviors, and Needs for Training.
- Published in:
- Journal of Genetic Counseling, 2014, v. 23, n. 2, p. 156, doi. 10.1007/s10897-013-9624-0
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- Publication type:
- Article
Familial risk of epilepsy: a population-based study.
- Published in:
- Brain: A Journal of Neurology, 2014, v. 137, n. 3, p. 795, doi. 10.1093/brain/awt368
- By:
- Publication type:
- Article
Familial aggregation of seizure outcomes in four familial epilepsy cohorts.
- Published in:
- Epilepsia (Series 4), 2024, v. 65, n. 7, p. 2030, doi. 10.1111/epi.18004
- By:
- Publication type:
- Article
Knowledge and beliefs about epilepsy genetics among Hispanic and non‐Hispanic patients.
- Published in:
- Epilepsia (Series 4), 2023, v. 64, n. 9, p. 2443, doi. 10.1111/epi.17701
- By:
- Publication type:
- Article
Identification of patients with drug‐resistant epilepsy in electronic medical record data using the Observational Medical Outcomes Partnership Common Data Model.
- Published in:
- Epilepsia (Series 4), 2022, v. 63, n. 11, p. 2981, doi. 10.1111/epi.17409
- By:
- Publication type:
- Article
Reproduction and genetic causal attribution of epilepsy.
- Published in:
- Epilepsia (Series 4), 2022, v. 63, n. 9, p. 2392, doi. 10.1111/epi.17349
- By:
- Publication type:
- Article
Reproductive decision‐making in families containing multiple individuals with epilepsy.
- Published in:
- Epilepsia (Series 4), 2021, v. 62, n. 5, p. 1220, doi. 10.1111/epi.16889
- By:
- Publication type:
- Article
Diverse genetic causes of polymicrogyria with epilepsy.
- Published in:
- Epilepsia (Series 4), 2021, v. 62, n. 4, p. 973, doi. 10.1111/epi.16854
- By:
- Publication type:
- Article
Generalized, focal, and combined epilepsies in families: New evidence for distinct genetic factors.
- Published in:
- Epilepsia (Series 4), 2020, v. 61, n. 12, p. 2667, doi. 10.1111/epi.16732
- By:
- Publication type:
- Article
Genetic attribution and perceived impact of epilepsy in multiplex epilepsy families.
- Published in:
- Epilepsia (Series 4), 2019, v. 60, n. 11, p. 2286, doi. 10.1111/epi.16352
- By:
- Publication type:
- Article
Return of individual results in epilepsy genomic research: A view from the field.
- Published in:
- Epilepsia (Series 4), 2018, v. 59, n. 9, p. 1635, doi. 10.1111/epi.14530
- By:
- Publication type:
- Article
Mood disorders in familial epilepsy: A test of shared etiology.
- Published in:
- Epilepsia (Series 4), 2018, v. 59, n. 2, p. 431, doi. 10.1111/epi.13985
- By:
- Publication type:
- Article