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The role of body mass index, insulin, and adiponectin in the relation between fat distribution and bone mineral density.
- Published in:
- 2010
- By:
- Publication type:
- journal article
Transforming activity of polyoma virus middle-T antigen probed by site-directed mutagenesis.
- Published in:
- Nature, 1983, v. 304, n. 5925, p. 456, doi. 10.1038/304456a0
- By:
- Publication type:
- Article
Association of HSP70 and its Co-Chaperones with Alzheimer's Disease.
- Published in:
- Journal of Alzheimer's Disease, 2011, v. 25, n. 1, p. 93, doi. 10.3233/JAD-2011-101560
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- Publication type:
- Article
A Study of the SORL1 Gene in Alzheimer's Disease and Cognitive Function.
- Published in:
- Journal of Alzheimer's Disease, 2009, v. 18, n. 1, p. 51, doi. 10.3233/JAD-2009-1137
- By:
- Publication type:
- Article
Congenital dyserythropoietic anemia type II: molecular analysis and expression of the SEC23B gene.
- Published in:
- 2011
- By:
- Publication type:
- journal article
Association of heat shock proteins with Parkinson's disease.
- Published in:
- 2011
- By:
- Publication type:
- Letter
Heritabilities, apolipoprotein E, and effects of inbreeding on plasma lipids in a genetically isolated population: The Erasmus Rucphen Family Study.
- Published in:
- European Journal of Epidemiology, 2007, v. 22, n. 2, p. 99, doi. 10.1007/s10654-006-9103-0
- By:
- Publication type:
- Article
Phenotypic Subtypes in Attention Deficit Hyperactivity Disorder in an Isolated Population.
- Published in:
- European Journal of Epidemiology, 2005, v. 20, n. 9, p. 789, doi. 10.1007/s10654-005-0366-7
- By:
- Publication type:
- Article
Synaptic ionotropic glutamate receptors and plasticity are developmentally altered in the CA1 field of Fmr1 knockout mice.
- Published in:
- Journal of Physiology, 2009, v. 587, n. 4, p. 787, doi. 10.1113/jphysiol.2008.160929
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- Publication type:
- Article
Migraine is not associated with enhanced atherosclerosis.
- Published in:
- Cephalalgia, 2013, v. 33, n. 4, p. 228, doi. 10.1177/0333102412466966
- By:
- Publication type:
- Article
Replication of CD58 and CLEC16A as genome-wide significant risk genes for multiple sclerosis.
- Published in:
- Journal of Human Genetics, 2009, v. 54, n. 11, p. 676, doi. 10.1038/jhg.2009.96
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- Publication type:
- Article
Fragile X syndrome: From protein function to therapy.
- Published in:
- American Journal of Medical Genetics. Part A, 2013, v. 161A, n. 11, p. 2809, doi. 10.1002/ajmg.a.36241
- By:
- Publication type:
- Article
Complex craniosynostosis is associated with the 2p15p16.1 microdeletion syndrome.
- Published in:
- American Journal of Medical Genetics. Part A, 2013, v. 161A, n. 2, p. 244, doi. 10.1002/ajmg.a.35632
- By:
- Publication type:
- Article
Genome-wide linkage analysis of serum creatinine in three isolated European populations.
- Published in:
- Kidney International, 2009, v. 76, n. 3, p. 297, doi. 10.1038/ki.2009.135
- By:
- Publication type:
- Article
Ablation of Fmrp in adult neural stem cells disrupts hippocampus-dependent learning.
- Published in:
- Nature Medicine, 2011, v. 17, n. 5, p. 559, doi. 10.1038/nm.2336
- By:
- Publication type:
- Article
Whole genome sequencing of late-onset Alzheimer's disease patients from genetic isolate.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2015, v. 11, n. 7, p. P250, doi. 10.1016/j.jalz.2015.07.309
- By:
- Publication type:
- Article
Phosphosphingolipid levels are associated with cognitive function and level of education in healthy subjects
- Published in:
- 2012
- By:
- Publication type:
- Abstract
Genome-wide linkage screen of cognitive function identifies susceptible chromosomal regions
- Published in:
- 2010
- By:
- Publication type:
- Abstract
The GAB2 gene and the risk of Alzheimer's disease: Replication and meta-analysis
- Published in:
- 2009
- By:
- Publication type:
- Abstract
P1-309: Evidence for interaction between the Cholesteryl ester transfer protein (CETP) gene and APOE in late onset Alzheimer’s disease
- Published in:
- 2006
- By:
- Publication type:
- Abstract
O2-02-03: Linkage-based full genome scan for late onset Alzheimer’s disease in a genetically isolated population
- Published in:
- 2006
- By:
- Publication type:
- Abstract
P1-309: Evidence for interaction between the Cholesteryl ester transfer protein (CETP) gene and APOE in late onset Alzheimer’s disease
- Published in:
- 2006
- By:
- Publication type:
- Abstract
O2-02-03: Linkage-based full genome scan for late onset Alzheimer’s disease in a genetically isolated population
- Published in:
- 2006
- By:
- Publication type:
- Abstract
Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaque.
- Published in:
- Nature Genetics, 2011, v. 43, n. 10, p. 940, doi. 10.1038/ng.920
- By:
- Publication type:
- Article
Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies.
- Published in:
- Nature Genetics, 2009, v. 41, n. 11, p. 1199, doi. 10.1038/ng.446
- By:
- Publication type:
- Article
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
- By:
- Publication type:
- Article
Magnitude and distribution of linkage disequilibrium in population isolates and implications for genome-wide association studies.
- Published in:
- Nature Genetics, 2006, v. 38, n. 5, p. 556, doi. 10.1038/ng1770
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- Publication type:
- Article
A mutation in SLC11A3 is associated with autosomal dominant hemochromatosis.
- Published in:
- Nature Genetics, 2001, v. 28, n. 3, p. 213, doi. 10.1038/90038
- By:
- Publication type:
- Article
Abundant kif21b is associated with accelerated progression in neurodegenerative diseases.
- Published in:
- Acta Neuropathologica Communications, 2014, v. 2, n. 1, p. 1, doi. 10.1186/s40478-014-0144-4
- By:
- Publication type:
- Article
The Challenges of Genome-Wide Interaction Studies: Lessons to Learn from the Analysis of HDL Blood Levels.
- Published in:
- PLoS ONE, 2014, v. 9, n. 10, p. 1, doi. 10.1371/journal.pone.0109290
- By:
- Publication type:
- Article
Dopaminergic Neuronal Loss and Dopamine-Dependent Locomotor Defects in Fbxo7-Deficient Zebrafish.
- Published in:
- PLoS ONE, 2012, v. 7, n. 11, p. 1, doi. 10.1371/journal.pone.0048911
- By:
- Publication type:
- Article
Loss of Nuclear Activity of the FBXO7 Protein in Patients with Parkinsonian-Pyramidal Syndrome (PARK15).
- Published in:
- PLoS ONE, 2011, v. 6, n. 2, p. 1, doi. 10.1371/journal.pone.0016983
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- Publication type:
- Article
Array-Based FMR1 Sequencing and Deletion Analysis in Patients with a Fragile X Syndrome-Like Phenotype.
- Published in:
- PLoS ONE, 2010, v. 5, n. 3, p. 1, doi. 10.1371/journal.pone.0009476
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- Publication type:
- Article
Association between Type 2 Diabetes Loci and Measures of Fatness.
- Published in:
- PLoS ONE, 2010, v. 5, n. 1, p. 1, doi. 10.1371/journal.pone.0008541
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- Publication type:
- Article
Genetic Factors Influence the Clustering of Depression among Individuals with Lower Socioeconomic Status.
- Published in:
- PLoS ONE, 2009, v. 4, n. 3, p. 1, doi. 10.1371/journal.pone.0005069
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- Publication type:
- Article
Isolation of mouse neuritic mRNAs.
- Published in:
- Journal of Molecular Histology, 2006, v. 37, n. 1/2, p. 79, doi. 10.1007/s10735-006-9036-7
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- Publication type:
- Article
Prospects of TAT-Mediated Protein Therapy for Fragile X Syndrome.
- Published in:
- Journal of Molecular Histology, 2004, v. 35, n. 4, p. 389, doi. 10.1023/B:HIJO.0000039841.22959.3c
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- Publication type:
- Article
FXTAS: A progressive neurologic syndrome associated with fragile X premutation.
- Published in:
- Current Neurology & Neuroscience Reports, 2005, v. 5, n. 5, p. 405, doi. 10.1007/s11910-005-0065-5
- By:
- Publication type:
- Article
Epistatic Effect of Cholesteryl Ester Transfer Protein and Hepatic Lipase on Serum High-Density Lipoprotein Cholesterol Levels.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2007, v. 92, n. 7, p. 2680, doi. 10.1210/jc.2007-0269
- By:
- Publication type:
- Article
Cyclin-dependent kinase 5 is associated with risk for Alzheimer’s disease in a Dutch population-based study.
- Published in:
- Journal of Neurology, 2008, v. 255, n. 5, p. 655, doi. 10.1007/s00415-008-0770-5
- By:
- Publication type:
- Article
Linking DJ-1 to neurodegeneration offers novel insights for understanding the pathogenesis of Parkinson’s disease.
- Published in:
- Journal of Molecular Medicine, 2004, v. 82, n. 3, p. 163, doi. 10.1007/s00109-003-0512-1
- By:
- Publication type:
- Article
Heritabilities, proportions of heritabilities explained by GWAS findings, and implications of cross-phenotype effects on PR interval.
- Published in:
- Human Genetics, 2015, v. 134, n. 11/12, p. 1211, doi. 10.1007/s00439-015-1595-9
- By:
- Publication type:
- Article
Common DNA variants predict tall stature in Europeans.
- Published in:
- Human Genetics, 2014, v. 133, n. 5, p. 587, doi. 10.1007/s00439-013-1394-0
- By:
- Publication type:
- Article
Linkage analysis for plasma amyloid beta levels in persons with hypertension implicates Aβ-40 levels to presenilin 2.
- Published in:
- Human Genetics, 2012, v. 131, n. 12, p. 1869, doi. 10.1007/s00439-012-1210-2
- By:
- Publication type:
- Article
A new syndrome with noncompaction cardiomyopathy, bradycardia, pulmonary stenosis, atrial septal defect and heterotaxy with suggestive linkage to chromosome 6p.
- Published in:
- Human Genetics, 2008, v. 122, n. 6, p. 595, doi. 10.1007/s00439-007-0436-x
- By:
- Publication type:
- Article
Evidence for novel loci for late-onset Parkinson’s disease in a genetic isolate from the Netherlands.
- Published in:
- Human Genetics, 2006, v. 119, n. 1/2, p. 51, doi. 10.1007/s00439-005-0108-7
- By:
- Publication type:
- Article
Chasing genes in Alzheimer’s and Parkinson’s disease.
- Published in:
- Human Genetics, 2004, v. 114, n. 5, p. 413, doi. 10.1007/s00439-004-1097-7
- By:
- Publication type:
- Article
Timing of the absence of FMR1 expression in full mutation chorionic villi.
- Published in:
- Human Genetics, 2002, v. 110, n. 6, p. 601, doi. 10.1007/s00439-002-0723-5
- By:
- Publication type:
- Article
A fragile X case with an amplification/deletion mosaic pattern.
- Published in:
- Human Genetics, 2000, v. 106, n. 3, p. 366, doi. 10.1007/s004390000256
- By:
- Publication type:
- Article
A Combined Linkage and Exome Sequencing Analysis for Electrocardiogram Parameters in the Erasmus Rucphen Family Study.
- Published in:
- Frontiers in Genetics, 2016, v. 7, p. 1, doi. 10.3389/fgene.2016.00190
- By:
- Publication type:
- Article