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Reasons for non-response in observational pharmacogenetic research.
- Published in:
- Pharmacoepidemiology & Drug Safety, 2009, v. 18, n. 8, p. 665, doi. 10.1002/pds.1764
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- Publication type:
- Article
Suggestive linkage to chromosome 19 in a large Cuban family with late-onset Parkinson's disease.
- Published in:
- Movement Disorders, 2003, v. 18, n. 11, p. 1240, doi. 10.1002/mds.10534
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- Publication type:
- Article
CYP2D6 polymorphism in Parkinson's disease: The Rotterdam study.
- Published in:
- Movement Disorders, 2001, v. 16, n. 2, p. 290, doi. 10.1002/mds.1041
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- 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
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- Publication type:
- Article
The TNFRSF6 gene is not implicated in familial early-onset Alzheimer's disease.
- Published in:
- Human Genetics, 2001, v. 108, n. 6, p. 552, doi. 10.1007/s004390100508
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- Publication type:
- Article
Heritability and Genome-Wide Association Analyses of Human Gait Suggest Contribution of Common Variants.
- Published in:
- 2016
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- Publication type:
- journal article
Common variants at 2q11.2, 8q21.3, and 11q13.2 are associated with major mood disorders.
- Published in:
- Translational Psychiatry, 2017, p. 1, doi. 10.1038/s41398-017-0019-0
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- 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
Early Age at Menopause is Associated with Increased risk of Dementia and Mortality in Women with Down Syndrome.
- Published in:
- Journal of Alzheimer's Disease, 2010, v. 19, n. 2, p. 545, doi. 10.3233/JAD-2010-1247
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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
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- Publication type:
- Article
Gut Microbiota Composition Is Related to AD Pathology.
- Published in:
- Frontiers in Immunology, 2022, v. 13, p. 1, doi. 10.3389/fimmu.2021.794519
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- Publication type:
- Article
Linkage analysis and whole exome sequencing identify a novel candidate gene in a Dutch multiple sclerosis family.
- Published in:
- Multiple Sclerosis Journal, 2019, v. 25, n. 7, p. 909, doi. 10.1177/1352458518777202
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- Publication type:
- Article
Gut microbiome-wide association study of depressive symptoms.
- Published in:
- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-34502-3
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- Publication type:
- Article
The effects of a moderate physical activity intervention on physical fitness and cognition in healthy elderly with low levels of physical activity: a randomized controlled trial.
- Published in:
- Alzheimer's Research & Therapy, 2023, v. 15, n. 1, p. 1, doi. 10.1186/s13195-022-01123-3
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- Publication type:
- Article
Complement Factor H Polymorphism, Complement Activators, and Risk of Age-Related Macular Degeneration.
- Published in:
- JAMA: Journal of the American Medical Association, 2006, v. 296, n. 3, p. 301, doi. 10.1001/jama.296.3.301
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- Publication type:
- Article
Head Trauma and the Risk of Alzheimer's Disease.
- Published in:
- American Journal of Epidemiology, 1992, v. 135, n. 7, p. 775, doi. 10.1093/oxfordjournals.aje.a116364
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- Publication type:
- Article
SERUM COPPER AND ZINC AND THE RISK OF DEATH FROM CANCER AND CARDIOVASCULAR DISEASE.
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- American Journal of Epidemiology, 1988, v. 128, n. 2, p. 352, doi. 10.1093/oxfordjournals.aje.a114975
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- Publication type:
- Article
Allelic variants of cytochrome P450 2C9 modify the interaction between nonsteroidal anti-inflammatory drugs and coumarin anticoagulants
- Published in:
- Clinical Pharmacology & Therapeutics, 2005, v. 77, n. 6, p. 479, doi. 10.1016/j.clpt.2005.02.009
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- Publication type:
- Article
Search for Early Pancreatic Cancer Blood Biomarkers in Five European Prospective Population Biobanks Using Metabolomics.
- Published in:
- Endocrinology, 2019, v. 160, n. 7, p. 1731, doi. 10.1210/en.2019-00165
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- Publication type:
- Article
Genetic factors and insulin secretion: gene variants in the IGF genes.
- Published in:
- 2004
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- Publication type:
- journal article
A genome-wide search for genes involved in type 2 diabetes in a recently genetically isolated population from the Netherlands.
- Published in:
- 2003
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- Publication type:
- journal article
A genome-wide search for linkage-disequilibrium with type 1 diabetes in a recent genetically isolated population from the Netherlands.
- Published in:
- 2002
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- Publication type:
- journal article
Automated workflow-based exploitation of pathway databases provides new insights into genetic associations of metabolite profiles.
- Published in:
- BMC Genomics, 2013, v. 14, n. 1, p. 1, doi. 10.1186/1471-2164-14-865
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- Publication type:
- Article
Genetic Complexities of Cerebral Small Vessel Disease, Blood Pressure, and Dementia.
- Published in:
- JAMA Network Open, 2024, v. 7, n. 5, p. e2412824, doi. 10.1001/jamanetworkopen.2024.12824
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- Publication type:
- Article
Leveraging Health Linkage Data From the UK Biobank—With Great Power Comes Great Responsibility—Reply.
- Published in:
- JAMA Psychiatry, 2023, v. 80, n. 10, p. 1077, doi. 10.1001/jamapsychiatry.2023.2969
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- Publication type:
- Article
Genome-wide association study of frontotemporal dementia identifies a C9ORF72 haplotype with a median of 12-G4C2 repeats that predisposes to pathological repeat expansions.
- Published in:
- Translational Psychiatry, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41398-021-01577-3
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- 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
Source of variant Creutzfeldt-Jakob disease outside United Kingdom.
- Published in:
- 2007
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- Publication type:
- journal article
Genetic susceptibility to multiple sclerosis: Brain structure and cognitive function in the general population.
- Published in:
- Multiple Sclerosis Journal, 2017, v. 23, n. 13, p. 1697, doi. 10.1177/1352458516682104
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- Publication type:
- Article
Exome sequencing and functional analyses suggest that SIX6 is a gene involved in an altered proliferation–differentiation balance early in life and optic nerve degeneration at old age.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 5, p. 1320, doi. 10.1093/hmg/ddt522
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- Publication type:
- Article
Genetic influences on plasma CFH and CFHR1 concentrations and their role in susceptibility to age-related macular degeneration.
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- Human Molecular Genetics, 2013, v. 22, n. 23, p. 4857, doi. 10.1093/hmg/ddt336
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- Publication type:
- Article
Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive error.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 13, p. 2754
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- Publication type:
- Article
Large common deletions associate with mortality at old age.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 21, p. 4290, doi. 10.1093/hmg/ddr340
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- Publication type:
- Article
The PCLO gene and depressive disorders: replication in a population-based study.
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- Human Molecular Genetics, 2010, v. 19, n. 4, p. 731, doi. 10.1093/hmg/ddp529
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- Publication type:
- Article
Genetic evidence for a role of adiponutrin in the metabolism of apolipoprotein B-containing lipoproteins.
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- Human Molecular Genetics, 2009, v. 18, n. 23, p. 4669, doi. 10.1093/hmg/ddp424
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- Publication type:
- Article
Genome-wide association meta-analysis for total serum bilirubin levels.
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- Human Molecular Genetics, 2009, v. 18, n. 14, p. 2700, doi. 10.1093/hmg/ddp202
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- Publication type:
- Article
Identification of a common variant at the NOS1AP locus strongly associated to QT-interval duration.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 2, p. 347
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- Publication type:
- Article
Identification of DIO2 as a new susceptibility locus for symptomatic osteoarthritis.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 12, p. 1867, doi. 10.1093/hmg/ddn082
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- Publication type:
- Article
Genome-based prediction of common diseases: advances and prospects.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. R2, p. R166, doi. 10.1093/hmg/ddn250
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- Publication type:
- Article
Heritability of the shape of subcortical brain structures in the general population.
- Published in:
- Nature Communications, 2016, v. 7, n. 12, p. 13738, doi. 10.1038/ncomms13738
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- Publication type:
- Article
A high-quality human reference panel reveals the complexity and distribution of genomic structural variants.
- Published in:
- Nature Communications, 2016, v. 7, n. 10, p. 12989, doi. 10.1038/ncomms12989
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- Publication type:
- Article
Genome-wide association study for acute otitis media in children identifies FNDC1 as disease contributing gene.
- Published in:
- Nature Communications, 2016, v. 7, n. 9, p. 12792, doi. 10.1038/ncomms12792
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- Publication type:
- Article
Prenatal exposure to the 1944–45 Dutch ‘hunger winter’ and addiction later in life.
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- Addiction, 2008, v. 103, n. 3, p. 433, doi. 10.1111/j.1360-0443.2007.02084.x
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- Publication type:
- Article
Standard process-oriented workflow introduces pre-analytical error when used in large study sample batches.
- Published in:
- 2018
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- Publication type:
- Letter to the Editor
Genome-wide association analysis on five isolated populations identifies variants of the HLA-DOA gene associated with white wine liking.
- Published in:
- European Journal of Human Genetics, 2015, v. 23, n. 12, p. 1717, doi. 10.1038/ejhg.2015.34
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- Publication type:
- Article
The dystrophin gene and cognitive function in the general population.
- Published in:
- European Journal of Human Genetics, 2015, v. 23, n. 6, p. 837, doi. 10.1038/ejhg.2014.183
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- Publication type:
- Article
Identifying genetic risk variants for coronary heart disease in familial hypercholesterolemia: an extreme genetics approach.
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- European Journal of Human Genetics, 2015, v. 23, n. 3, p. 381, doi. 10.1038/ejhg.2014.101
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- Publication type:
- Article
Improved imputation quality of low-frequency and rare variants in European samples using the 'Genome of The Netherlands'.
- Published in:
- European Journal of Human Genetics, 2014, v. 22, n. 11, p. 1321, doi. 10.1038/ejhg.2014.19
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- Publication type:
- Article
The sex-specific associations of the aromatase gene with Alzheimer's disease and its interaction with IL10 in the Epistasis Project.
- Published in:
- European Journal of Human Genetics, 2014, v. 22, n. 2, p. 216, doi. 10.1038/ejhg.2013.116
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- Publication type:
- Article
Low-density lipoprotein receptor mutations generate synthetic genome-wide associations.
- Published in:
- European Journal of Human Genetics, 2013, v. 21, n. 5, p. 563, doi. 10.1038/ejhg.2012.207
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- Publication type:
- Article