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The National Israeli Registry for Oculo-Pharyngeal Muscular Dystrophy (IsrO-PMD): rationale and design.
- Published in:
- Journal of Rare Diseases, 2023, v. 2, n. 1, p. 1, doi. 10.1007/s44162-023-00020-z
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- Article
Relationship between Rgs2 gene expression level and anxiety and depression-like behaviour in a mutant mouse model: serotonergic involvement.
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- International Journal of Neuropsychopharmacology, 2012, v. 15, n. 9, p. 1307, doi. 10.1017/S1461145711001453
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- Article
DOCK4 and CEACAM21 as novel schizophrenia candidate genes in the Jewish population.
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- International Journal of Neuropsychopharmacology, 2012, v. 15, n. 4, p. 459, doi. 10.1017/S1461145711000903
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- Article
Oxytocin and vasopressin genes are significantly associated with schizophrenia in a large Arab-Israeli pedigree.
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- International Journal of Neuropsychopharmacology, 2012, v. 15, n. 3, p. 309, doi. 10.1017/S1461145711001374
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- Article
Association of the dopamine receptor interacting protein gene, NEF3, with early response to antipsychotic medication.
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- International Journal of Neuropsychopharmacology, 2007, v. 10, n. 3, p. 321, doi. 10.1017/S1461145706006651
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- Article
Perspective: Identification of genetic variants associated with dopaminergic compensatory mechanisms in early Parkinson's disease.
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- Frontiers in Systems Neuroscience, 2013, v. 7, p. 1, doi. 10.3389/fnins.2013.00052
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- Article
GALC variants affect galactosylceramidase enzymatic activity and risk of Parkinson's disease.
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- Brain: A Journal of Neurology, 2023, v. 146, n. 5, p. 1859, doi. 10.1093/brain/awac413
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- Article
Targeted sequencing of Parkinson's disease loci genes highlights SYT11, FGF20 and other associations.
- Published in:
- 2021
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- Publication type:
- journal article
Genetic modifiers of risk and age at onset in GBA associated Parkinson's disease and Lewy body dementia.
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- Brain: A Journal of Neurology, 2020, v. 143, n. 1, p. 234, doi. 10.1093/brain/awz350
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- Article
Genetic modifiers of risk and age at onset in GBA associated Parkinson's disease and Lewy body dementia.
- Published in:
- 2019
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- Publication type:
- journal article
The Israel National Brain Repository.The establishment and uniqueness of the first brain bank in Israel.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2023, v. 19, n. 22, p. 1, doi. 10.1002/alz.079606
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- Article
Blood DNA methylation biomarkers for cognitive decline in older adults with type 2 diabetes.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2023, v. 19, p. 1, doi. 10.1002/alz.065120
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- Article
The National Israel Brain Repository: Characterizing those who sign and do not sign intent to autopsy.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2023, v. 19, p. 1, doi. 10.1002/alz.064443
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- Publication type:
- Article
No evidence for association of Alzheimer's disease risk loci with the rate of cognitive decline among elderly with type 2 diabetes.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2021, v. 17, n. 3, p. 1, doi. 10.1002/alz.050081
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- Article
The COMT rs4680 polymorphism is associated with rate of cognitive decline in older adults with type 2 diabetes: Biomarkers (non‐neuroimaging) / Longitudinal change over time.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2020, v. 16, n. 11, p. 1, doi. 10.1002/alz.045227
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- Article
TYPE 2 DIABETES GENETIC RISK VARIANTS WITHIN TCF7L2 ARE ASSOCIATED WITH SMALLER AMYGDALAR VOLUME AMONG DIABETIC ELDERLY PATIENTS.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2017, v. 13, p. P294, doi. 10.1016/j.jalz.2017.06.204
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- Article
The Alzheimer's disease risk loci bin1 is associated with poorer episodic memory performance in cognitively normal type 2 diabetes elderly.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2015, v. 11, n. 7, p. P769, doi. 10.1016/j.jalz.2015.06.1715
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- Article
Diabetes and alzheimer's-associated genes affect differently the association of glycemic control with cognitive function.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2014, v. 10, p. P222, doi. 10.1016/j.jalz.2014.04.309
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- Publication type:
- Article
The yield of chromosomal microarray testing for cases of abnormal fetal head circumference.
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- Journal of Perinatal Medicine, 2020, v. 48, n. 6, p. 553, doi. 10.1515/jpm-2020-0048
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- Article
The Melanocortin 1 Receptor (Mc1r) Variants Do Not Account for the Co-occurrence of Parkinson's Disease and Malignant Melanoma.
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- Journal of Molecular Neuroscience, 2014, v. 54, n. 4, p. 820, doi. 10.1007/s12031-014-0425-1
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- Publication type:
- Article
Do Tardive Dyskinesia and l-Dopa Induced Dyskinesia Share Common Genetic Risk Factors? An Exploratory Study.
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- Journal of Molecular Neuroscience, 2013, v. 51, n. 2, p. 380, doi. 10.1007/s12031-013-0020-x
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- Publication type:
- Article
Association of the Type 2 Diabetes Mellitus Susceptibility Gene, TCF7L2, with Schizophrenia in an Arab-Israeli Family Sample.
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- PLoS ONE, 2012, v. 7, n. 1, p. 1, doi. 10.1371/journal.pone.0029228
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- Article
Identification of a homozygous VRK1 mutation in two patients with adult-onset distal hereditary motor neuropathy.
- Published in:
- 2020
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- Publication type:
- journal article
The Yield of Chromosomal Microarray in Pregnancies Complicated with Fetal Growth Restriction Can Be Predicted According to Clinical Parameters.
- Published in:
- 2021
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- Publication type:
- journal article
A porphobilinogen deaminase (PBGD) Ran-binding protein interaction is implicated in nuclear trafficking of PBGD in differentiating glioma cells.
- Published in:
- Oncogene, 2003, v. 22, n. 34, p. 5221, doi. 10.1038/sj.onc.1206723
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- Article
Alzheimer's Disease Polygenic Risk Score Is Not Associated With Cognitive Decline Among Older Adults With Type 2 Diabetes.
- Published in:
- Frontiers in Aging Neuroscience, 2022, v. 14, p. 1, doi. 10.3389/fnagi.2022.853695
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- Article
Publisher Correction: TCF7L2 polymorphisms are associated with amygdalar volume in elderly individuals with Type 2 Diabetes.
- Published in:
- 2020
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- Correction Notice
TCF7L2 polymorphisms are associated with amygdalar volume in elderly individuals with Type 2 Diabetes.
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- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-48899-3
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- Publication type:
- Article
Evaluation of Diagnostic Yield in Fetal Whole-Exome Sequencing: A Report on 45 Consecutive Families.
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- Frontiers in Genetics, 2019, p. 1, doi. 10.3389/fgene.2019.00425
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- Publication type:
- Article
Evaluation of Diagnostic Yield in Fetal Whole-Exome Sequencing: A Report on 45 Consecutive Families.
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- Frontiers in Genetics, 2019, p. N.PAG, doi. 10.3389/fgene.2019.00425
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- Publication type:
- Article
Identification of new schizophrenia susceptibility loci in an ethnically homogeneous, family-based, Arab-Israeli sample.
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- FASEB Journal, 2011, v. 25, n. 11, p. 4011, doi. 10.1096/fj.11-184937
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- Article
Ser77Tyr transthyretin amyloidosis in Israel: Initial manifestations and diagnostic features.
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- Annals of Clinical & Translational Neurology, 2023, v. 10, n. 4, p. 553, doi. 10.1002/acn3.51741
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- Article
Early and late manifestations of neuropathy due to HSPB1 mutation in the Jewish Iranian population.
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- Annals of Clinical & Translational Neurology, 2021, v. 8, n. 6, p. 1260, doi. 10.1002/acn3.51362
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- Publication type:
- Article
Association of the ZFPM2 gene with antipsychotic-induced parkinsonism in schizophrenia patients.
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- Psychopharmacology, 2012, v. 220, n. 3, p. 519, doi. 10.1007/s00213-011-2499-6
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- Article
Erratum to: Association of the ZFPM2 gene with antipsychotic-induced parkinsonism in schizophrenia patients.
- Published in:
- 2012
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- Publication type:
- Correction Notice
Genome-wide association study of antipsychotic-induced parkinsonism severity among schizophrenia patients.
- Published in:
- Psychopharmacology, 2009, v. 206, n. 3, p. 491, doi. 10.1007/s00213-009-1627-z
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- Publication type:
- Article
Prenatal diagnosis for de novo mutations: Experience from a tertiary center over a 10‐year period.
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- Molecular Genetics & Genomic Medicine, 2019, v. 7, n. 4, p. N.PAG, doi. 10.1002/mgg3.573
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- Publication type:
- Article
Investigation of the HSPG2 Gene in Tardive Dyskinesia – New Data and Meta-Analysis.
- Published in:
- Frontiers in Pharmacology, 2018, p. N.PAG, doi. 10.3389/fphar.2018.00974
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- Publication type:
- Article
Exercise induced muscle blood flow is decreased in Charcot–Marie–Tooth disease type 1 polyneuropathy: a power Doppler analysis.
- Published in:
- European Journal of Neurology, 2023, v. 30, n. 7, p. 1991, doi. 10.1111/ene.15789
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- Publication type:
- Article
Association of Rare Variants in ARSA with Parkinson's Disease.
- Published in:
- Movement Disorders, 2023, v. 38, n. 10, p. 1806, doi. 10.1002/mds.29521
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- Article
Analysis of Heterozygous PRKN Variants and Copy‐Number Variations in Parkinson's Disease.
- Published in:
- Movement Disorders, 2021, v. 36, n. 1, p. 178, doi. 10.1002/mds.28299
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- Publication type:
- Article
Vici syndrome in Israel: Clinical and molecular insights.
- Published in:
- Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2022.991721
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- Publication type:
- Article
Pharmacogenetics of antipsychotic-induced movement disorders as a resource for better understanding Parkinson's disease modifier genes.
- Published in:
- Frontiers in Neurology, 2015, v. 6, p. 1, doi. 10.3389/fneur.2015.00027
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- Publication type:
- Article
The role of exposure to pesticides in the etiology of Parkinson's disease: a <sup>18</sup>F-DOPA positron emission tomography study.
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- Journal of Neural Transmission, 2019, v. 126, n. 2, p. 159, doi. 10.1007/s00702-018-1951-8
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- Publication type:
- Article
The impact of early versus late levodopa administration.
- Published in:
- Journal of Neural Transmission, 2017, v. 124, n. 4, p. 471, doi. 10.1007/s00702-016-1669-4
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- Publication type:
- Article
Long-term Variability in Glycemic Control Is Associated With White Matter Hyperintensities in APOE4 Genotype Carriers With Type 2 Diabetes.
- Published in:
- 2016
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- Publication type:
- journal article
Adult-onset Alexander disease among patients of Jewish Syrian descent.
- Published in:
- Neurogenetics, 2023, v. 24, n. 4, p. 303, doi. 10.1007/s10048-023-00732-w
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- Publication type:
- Article
Evidence for association of the GLI2 gene with tardive dyskinesia in patients with chronic schizophrenia.
- Published in:
- Movement Disorders, 2010, v. 25, n. 16, p. 2809, doi. 10.1002/mds.23377
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- Publication type:
- Article
Are rare heterozygous SYNJ1 variants associated with Parkinson's disease?
- Published in:
- NPJ Parkinson's Disease, 2024, v. 10, n. 1, p. 1, doi. 10.1038/s41531-024-00809-9
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- Publication type:
- Article
Ethnicity/culture modulates the relationships of the haptoglobin (Hp) 1-1 phenotype with cognitive function in older individuals with type 2 diabetes.
- Published in:
- 2016
- By:
- Publication type:
- journal article