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Journal Articles

in Neurogenetics
 21-40 of 317 Articles
JAMA Psychiatry | 
Original Article |  April 01, 2013
FKBP5 and Attention Bias for Threat:  Associations With Hippocampal Function and Shape
Negar Fani, PhD; David Gutman, MD, PhD; Erin B. Tone, PhD; et al.
JAMA Psychiatry. 2013;70(4):392-400. doi:10.1001/2013.jamapsychiatry.210.
INCLUDES: , Supplemental Content
JAMA Ophthalmology | 
Research Letters |  April 01, 2013
Ophthalmic Artery Ischemic Syndrome Associated With Neurofibromatosis and Moyamoya Syndrome
Matthew T. Witmer, MD; Richard Levy, MD; Kaleb Yohay, MD; et al.
JAMA Ophthalmol. 2013;131(4):538-539. doi:10.1001/jamaophthalmol.2013.2902.
JAMA Ophthalmology | 
Research Letters |  April 01, 2013
Novel Maculopathy in Patients With Spinocerebellar Ataxia Type 1 Autofluorescence Findings and Functional Characteristics
Veronika Vaclavik, MD; François-Xavier Borruat, MD; Aude Ambresin, MD; et al.
JAMA Ophthalmol. 2013;131(4):536-538. doi:10.1001/jamaophthalmol.2013.1127.
JAMA Neurology | 
Original Contribution |  March 01, 2013
Posterior Cingulate Glucose Metabolism, Hippocampal Glucose Metabolism, and Hippocampal Volume in Cognitively Normal, Late-Middle-Aged Persons at 3 Levels of Genetic Risk for Alzheimer Disease
Hillary D. Protas, PhD; Kewei Chen, PhD; Jessica B. S. Langbaum, PhD; et al.
JAMA Neurol. 2013;70(3):320-325. doi:10.1001/2013.jamaneurol.286.
JAMA Neurology | 
Editorial |  March 01, 2013
Apolipoprotein E, Neurodegeneration, and Alzheimer Disease
William Jagust, MD
JAMA Neurol. 2013;70(3):299-300. doi:10.1001/jamaneurol.2013.726.
JAMA Neurology | 
Neurological Review |  March 01, 2013
Mechanisms of Protein Seeding in Neurodegenerative Diseases
Lary C. Walker, PhD; Marc I. Diamond, MD; Karen E. Duff, PhD; et al.
JAMA Neurol. 2013;70(3):304-310. doi:10.1001/jamaneurol.2013.1453.
JAMA Psychiatry | 
Original Article |  March 01, 2013
Implication of a Rare Deletion at Distal 16p11.2 in Schizophrenia
Saurav Guha, PhD; Elliott Rees, MRes; Ariel Darvasi, PhD; et al.
JAMA Psychiatry. 2013;70(3):253-260. doi:10.1001/2013.jamapsychiatry.71.
INCLUDES: , Supplemental Content
JAMA Neurology | 
Original Contribution |  March 01, 2013
Distinct Clinical Characteristics of C9orf72 Expansion Carriers Compared With GRN, MAPT, and Nonmutation Carriers in a Flanders-Belgian FTLD Cohort
Tim Van Langenhove, MD; Julie van der Zee, PhD; Ilse Gijselinck, PhD; et al.
JAMA Neurol. 2013;70(3):365-373. doi:10.1001/2013.jamaneurol.181.
INCLUDES: , Supplemental Content
JAMA Neurology | 
Correspondence |  March 01, 2013
Parkinsonism and Cancer
Glen E. Kisby, PhD; Peter S. Spencer, PhD, FRCPath
JAMA Neurol. 2013;70(3):414-415. doi:10.1001/jamaneurol.2013.1283.
JAMA Neurology | 
Original Contribution |  February 01, 2013
Cerebellar Ataxia, Hemiplegic Migraine, and Related Phenotypes Due to a CACNA1A Missense Mutation:  12-Year Follow-up of a Large Portuguese Family
José Barros, MD; Joana Damásio, MD; Assunção Tuna, MD, Msc; et al.
JAMA Neurol. 2013;70(2):235-240. doi:10.1001/jamaneurol.2013.591.
INCLUDES: , Supplemental Content
JAMA Neurology | 
Original Contribution |  February 01, 2013
SOD1 in Cerebral Spinal Fluid as a Pharmacodynamic Marker for Antisense Oligonucleotide Therapy
Leah Winer, BA; Dushyanth Srinivasan, BA; Seung Chun, BA; et al.
JAMA Neurol. 2013;70(2):201-207. doi:10.1001/jamaneurol.2013.593.
INCLUDES: CME , Supplemental Content
JAMA Neurology | 
Original Contribution |  February 01, 2013
APOE ϵ4 Increases Risk for Dementia in Pure Synucleinopathies
Debby Tsuang, MD, MSc; James B. Leverenz, MD; Oscar L. Lopez, MD; et al.
JAMA Neurol. 2013;70(2):223-228. doi:10.1001/jamaneurol.2013.600.
JAMA Neurology | 
Observation |  February 01, 2013
Mitochondrial Cardioencephalomyopathy Due to a Novel SCO2 Mutation in a Brazilian Patient:  Case Report and Literature Review
Juliana Gurgel-Giannetti, MD, PhD; Guilherme Oliveira, PhD; Geraldo Brasileiro Filho, MD, PhD; et al.
JAMA Neurol. 2013;70(2):258-261. doi:10.1001/jamaneurol.2013.595.
JAMA Neurology | 
Correspondence |  February 01, 2013
Evolution and Animal Models
Lawrence A. Hansen, MD; Ray Greek, MD
JAMA Neurol. 2013;70(2):271-272. doi:10.1001/2013.jamaneurol.458.
JAMA Ophthalmology | 
Small Case Series |  February 01, 2013
Association Between Uveal Melanoma and Myotonic Dystrophy:  A Series of 3 Cases
Juan P. Velazquez-Martin, MD; Charles J. Pavlin, MD, FRCSC; E. Rand Simpson, MD, FRCSC
JAMA Ophthalmol. 2013;131(2):246-249. doi:10.1001/jamaophthalmol.2013.581.
JAMA Psychiatry | 
Original Article |  January 01, 2013
A Prospective Study of Autistic-Like Traits in Unaffected Siblings of Probands With Autism Spectrum Disorder
Stelios Georgiades, MA; Peter Szatmari, MD; Lonnie Zwaigenbaum, MD; et al.
JAMA Psychiatry. 2013;70(1):42-48. doi:10.1001/2013.jamapsychiatry.1.
INCLUDES: , Supplemental Content
JAMA Neurology | 
Original Contribution |  January 01, 2013
A Trial of Scheduled Deep Brain Stimulation for Tourette Syndrome:  Moving Away From Continuous Deep Brain Stimulation Paradigms
Michael S. Okun, MD; Kelly D. Foote, MD; Samuel S. Wu, PhD; et al.
JAMA Neurol. 2013;70(1):85-94. doi:10.1001/jamaneurol.2013.580.
INCLUDES: , Supplemental Content
JAMA Neurology | 
Original Contribution |  January 01, 2013
Glycine Receptor Autoimmune Spectrum With Stiff-Man Syndrome Phenotype
Andrew McKeon, MD; Eugenia Martinez-Hernandez, MD; Eric Lancaster, MD, PhD; et al.
JAMA Neurol. 2013;70(1):44-50. doi:10.1001/jamaneurol.2013.574.
JAMA Neurology | 
Images in Neurology |  January 01, 2013
Neurologic and Vascular Abnormalities in Klippel-Trenaunay-Weber Syndrome
Dimitri Renard, MD; Chantal Campello, MD; Guillaume Taieb, MD; et al.
JAMA Neurol. 2013;70(1):127-128. doi:10.1001/jamaneurol.2013.587.
JAMA Neurology | 
Clinical Trials |  January 01, 2013
A Randomized, Double-blind, Placebo-Controlled Study of Latrepirdine in Patients With Mild to Moderate Huntington Disease
HORIZON Investigators of the Huntington Study Group and European Huntington's Disease Network*
JAMA Neurol. 2013;70(1):25-33. doi:10.1001/2013.jamaneurol.382.

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From The JAMA Network
JAMA Neurology
Original Contribution  |  June 10, 2013
Fragile X–Associated Tremor/Ataxia Syndrome:  Influence of the FMR1 Gene on Motor Fiber Tracts in Males With Normal and Premutation Alleles
Jun Yi Wang, PhD; David Hessl, PhD; Andrea Schneider, PhD; et al.
JAMA Neurology
Neurological Review  |  April 9, 2013
Understanding Neurological Disease Mechanisms in the Era of Epigenetics
Irfan A. Qureshi, MD; Mark F. Mehler, MD
JAMA Neurology
Neurological Review  |  April 9, 2013
An Inflection Point in Gene Discovery Efforts for Neurodegenerative Diseases:  From Syndromic Diagnoses Toward Endophenotypes and the Epigenome
Philip L. De Jager, MD; David A. Bennett, MD
JAMA Neurology
Original Contribution  |  April 15, 2013
C9orf72 Hexanucleotide Repeat Expansions in Clinical Alzheimer Disease
Matthew Harms, MD; Bruno A. Benitez, MD; Nigel Cairns, PhD; et al.
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