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Patient-control association study of substance P-related genes in unipolar and bipolar affective disorders.
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- International Journal of Neuropsychopharmacology, 2005, v. 8, n. 4, p. 505, doi. 10.1017/s1461145705005444
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- Article
NR4A2: Effects of an “Orphan” Receptor on Sustained Attention in a Schizophrenic Population.
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- Schizophrenia Bulletin, 2013, v. 39, n. 3, p. 555
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- Article
No evidence for GNAS copy number variants in patients with features of Albright's hereditary osteodystrophy and abnormal platelet Gs activity.
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- Journal of Human Genetics, 2012, v. 57, n. 4, p. 277, doi. 10.1038/jhg.2012.1
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- Article
miRVaS: a tool to predict the impact of genetic variants on miRNAs.
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- Nucleic Acids Research, 2016, v. 44, n. 3, p. 1, doi. 10.1093/nar/gkv921
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- Article
A genome wide survey supports the involvement of large copy number variants in schizophrenia with and without intellectual disability.
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2013, v. 162B, n. 8, p. 847, doi. 10.1002/ajmg.b.32189
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- Article
Identification of Rare Copy Number Variants in High Burden Schizophrenia Families.
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2013, v. 162B, n. 3, p. 273, doi. 10.1002/ajmg.b.32146
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- Article
Rare Copy Number Variants in Neuropsychiatric Disorders: Specific Phenotype or Not?
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2012, v. 159B, n. 7, p. 812, doi. 10.1002/ajmg.b.32088
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- Article
Identification of a CACNA2D4 Deletion in Late Onset Bipolar Disorder Patients and Implications for the Involvement of Voltage-Dependent Calcium Channels in Psychiatric Disorders.
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2012, v. 159B, n. 4, p. 465, doi. 10.1002/ajmg.b.32053
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- Article
Optimized filtering reduces the error rate in detecting genomic variants by short-read sequencing.
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- Nature Biotechnology, 2012, v. 30, n. 1, p. 61, doi. 10.1038/nbt.2053
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- Article
P3-162: Increased variability of the tau gene MAPT due to genomic instability
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- 2006
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- Abstract
O2-02-08: Duplication of the APP locus in a Dutch family with early-onset Alzheimer dementia
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- 2006
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- Abstract
P3-162: Increased variability of the tau gene MAPT due to genomic instability
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- 2006
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- Publication type:
- Abstract
O2-02-08: Duplication of the APP locus in a Dutch family with early-onset Alzheimer dementia
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- 2006
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- Abstract
Genetic variation in the KIF1B locus influences susceptibility to multiple sclerosis.
- Published in:
- Nature Genetics, 2008, v. 40, n. 12, p. 1402, doi. 10.1038/ng.251
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- Article
Mutations in SEPT9 cause hereditary neuralgic amyotrophy.
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- Nature Genetics, 2005, v. 37, n. 10, p. 1044, doi. 10.1038/ng1649
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- Article
VEGF is a modifier of amyotrophic lateral sclerosis in mice and humans and protects motoneurons against ischemic death.
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- Nature Genetics, 2003, v. 34, n. 4, p. 383, doi. 10.1038/ng1211
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- Article
The skin microbiome of caspase-14-deficient mice shows mild dysbiosis.
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- Experimental Dermatology, 2014, v. 23, n. 8, p. 561, doi. 10.1111/exd.12458
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- Article
Sequencing of DISC1 Pathway Genes Reveals Increased Burden of Rare Missense Variants in Schizophrenia Patients from a Northern Swedish Population.
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- PLoS ONE, 2011, v. 6, n. 8, p. 1, doi. 10.1371/journal.pone.0023450
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- Article
The Relationship between the Val158Met Catechol-o-Methyltransferase (COMT) Polymorphism and Irritable Bowel Syndrome.
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- PLoS ONE, 2011, v. 6, n. 3, p. 1, doi. 10.1371/journal.pone.0018035
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- Article
Genome-wide linkage of febrile seizures and epilepsy to the FEB4 locus at 5q14.3-q23.1 and no MASS1 mutation.
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- Human Genetics, 2006, v. 118, n. 5, p. 618, doi. 10.1007/s00439-005-0077-x
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- Article
The TNFRSF6 gene is not implicated in familial early-onset Alzheimer's disease.
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- Human Genetics, 2001, v. 108, n. 6, p. 552, doi. 10.1007/s004390100508
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- Article
Genetic variants in microRNA genes: impact on microRNA expression, function, and disease.
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- Frontiers in Genetics, 2015, p. 1, doi. 10.3389/fgene.2015.00186
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- Article
A genome-wide search for linkage to allergic rhinitis in Danish sib-pair families.
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- European Journal of Human Genetics, 2012, v. 20, n. 9, p. 965, doi. 10.1038/ejhg.2012.46
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- Article
Serotonin transporter 5HTTLPR polymorphism and affective disorders: no evidence of association in a large European multicenter study.
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- European Journal of Human Genetics, 2004, v. 12, n. 5, p. 377, doi. 10.1038/sj.ejhg.5201149
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- Article
Parametric and nonparametric genome scan analyses for human handedness.
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- European Journal of Human Genetics, 2003, v. 11, n. 10, p. 779, doi. 10.1038/sj.ejhg.5201048
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- Article
European combined analysis of the CTG18.1 and the ERDA1 CAG/CTG repeats in bipolar disorder.
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- European Journal of Human Genetics, 2002, v. 10, n. 4, p. 276, doi. 10.1038/sj.ejhg.5200803
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- Article
No evidence for the involvement of CAG/CTG repeats from within 18q21.33–q23 in bipolar disorder.
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- European Journal of Human Genetics, 2000, v. 8, n. 5, p. 385, doi. 10.1038/sj.ejhg.5200469
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- Article
Genetic refinement and physical mapping of a chromosome 18q candidate region for bipolar disorder.
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- European Journal of Human Genetics, 1999, v. 7, n. 4, p. 427, doi. 10.1038/sj.ejhg.5200318
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- Article
Glucocorticoid Receptor Gene-Based SNP Analysis in Patients with Recurrent Major Depression.
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- Neuropsychopharmacology, 2006, v. 31, n. 3, p. 620, doi. 10.1038/sj.npp.1300898
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- Article
The genomics of major psychiatric disorders in a large pedigree from Northern Sweden.
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- Translational Psychiatry, 2019, v. 9, n. 1, p. 1, doi. 10.1038/s41398-019-0414-9
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- Article
SNPbox: web-based high-throughput primer design from gene to genome.
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- Nucleic Acids Research, 2004, v. 32, n. suppl 2, p. w170, doi. 10.1093/nar/gkh369
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- Article
A novel locus for dementia with Lewy bodies: a clinically and genetically heterogeneous disorder.
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- Brain: A Journal of Neurology, 2007, v. 130, n. 9, p. 2277, doi. 10.1093/brain/awm167
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- Article
APP duplication is sufficient to cause early onset Alzheimer's dementia with cerebral amyloid angiopathy.
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- Brain: A Journal of Neurology, 2006, v. 129, n. 11, p. 2977, doi. 10.1093/brain/awl203
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- Article
BioGraph: unsupervised biomedical knowledge discovery via automated hypothesis generation.
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- Genome Biology, 2011, v. 12, n. 6, p. 1, doi. 10.1186/gb-2011-12-6-r57
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- Article
Expression Profiling of Endocrine-Disrupting Compounds Using a Customized Cyprinus carpio cDNA Microarray.
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- Toxicological Sciences, 2006, v. 93, n. 2, p. 298, doi. 10.1093/toxsci/kfl057
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- Article
A qPCR Assay to Detect and Quantify Shiga Toxin-Producing E. coli (STEC) in Cattle and on Farms: A Potential Predictive Tool for STEC Culture-Positive Farms.
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- Toxins, 2014, v. 6, n. 4, p. 1201, doi. 10.3390/toxins6041201
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- Article
Schizophrenia-Associated MIR204 Regulates Noncoding RNAs and Affects Neurotransmitter and Ion Channel Gene Sets.
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- PLoS ONE, 2015, v. 10, n. 12, p. 1, doi. 10.1371/journal.pone.0144428
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- Article
Evidence for the involvement of the glucocorticoid receptor gene in bipolar disorder in an isolated northern Swedish population.
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- Bipolar Disorders, 2011, v. 13, n. 7/8, p. 614, doi. 10.1111/j.1399-5618.2011.00960.x
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- Article
miRNA genes and the brain: implications for psychiatric disorders.
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- Human Mutation, 2010, v. 31, n. 11, p. 1195, doi. 10.1002/humu.21344
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- Article
Searching genetic risk factors for schizophrenia and bipolar disorder: learn from the past and back to the future.
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- Human Mutation, 2009, v. 30, n. 8, p. 1139, doi. 10.1002/humu.21042
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- Article
Relative contribution of simple mutations vs. copy number variations in five Parkinson disease genes in the Belgian population.
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- Human Mutation, 2009, v. 30, n. 7, p. 1054, doi. 10.1002/humu.21007
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- Article
Simultaneous mutation and copy number variation (CNV) detection by multiplex PCR-based GS-FLX sequencing.
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- Human Mutation, 2009, v. 30, n. 3, p. 472, doi. 10.1002/humu.20873
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- Article
Chasing genes for mood disorders and schizophrenia in genetically isolated populations.
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- Human Mutation, 2007, v. 28, n. 12, p. 1156, doi. 10.1002/humu.20582
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- Article
Microdeletions involving the SCN1A gene may be common in SCN1A-mutation-negative SMEI patients.
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- Human Mutation, 2006, v. 27, n. 9, p. 914, doi. 10.1002/humu.20350
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- Article
Major affective disorders and schizophrenia: a common molecular signature?
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- Human Mutation, 2006, v. 27, n. 9, p. 833, doi. 10.1002/humu.20369
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- Article
SCAMP5, NBEA and AMISYN: three candidate genes for autism involved in secretion of large dense-core vesicles.
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- Human Molecular Genetics, 2010, v. 19, n. 7, p. 1368, doi. 10.1093/hmg/ddq013
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- Article
Strong evidence that GNB1L is associated with schizophrenia.
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- Human Molecular Genetics, 2008, v. 17, n. 4, p. 555, doi. 10.1093/hmg/ddm330
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- Article
High-density SNP haplotyping suggests altered regulation of tau gene expression in progressive supranuclear palsy.
- Published in:
- Human Molecular Genetics, 2005, v. 14, n. 21, p. 3281, doi. 10.1093/hmg/ddi361
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- Article
Genomic architecture of human 17q21 linked to frontotemporal dementia uncovers a highly homologous family of low-copy repeats in the tau region.
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- Human Molecular Genetics, 2005, v. 14, n. 13, p. 1753, doi. 10.1093/hmg/ddi182
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- Article
Less Cognitive and Neurological Deficits in Schizophrenia Patients Carrying Risk Variant in ZNF804A.
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- Neuropsychobiology, 2012, v. 66, n. 3, p. 158, doi. 10.1159/000339731
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- Article