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Genome-Wide Association Study of Determinants of Anti-Cyclic Citrullinated Peptide Antibody Titer in Adults with Rheumatoid Arthritis.
- Published in:
- Molecular Medicine, 2009, v. 15, n. 5/6, p. 136, doi. 10.2119/molmed.2009.00008
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- Article
Genomewide linkage study of modifiers of LRRK2-related Parkinson's disease.
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- Movement Disorders, 2011, v. 26, n. 11, p. 2039, doi. 10.1002/mds.23781
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- Article
Genomewide association study for susceptibility genes contributing to familial Parkinson disease.
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- Human Genetics, 2009, v. 124, n. 6, p. 593, doi. 10.1007/s00439-008-0582-9
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- Article
Replication of association between ELAVL4 and Parkinson disease: the GenePD study.
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- Human Genetics, 2008, v. 124, n. 1, p. 95, doi. 10.1007/s00439-008-0526-4
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- Article
Association of HSP70 and its Co-Chaperones with Alzheimer's Disease.
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- Journal of Alzheimer's Disease, 2011, v. 25, n. 1, p. 93, doi. 10.3233/JAD-2011-101560
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- Article
Bone mineral density and the risk of incident dementia: A meta‐analysis.
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- Journal of the American Geriatrics Society, 2024, v. 72, n. 1, p. 194, doi. 10.1111/jgs.18638
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- Article
Combined haplotype relative risk (CHRR): a general and simple genetic association test that combines trios and unrelated case-controls.
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- Genetic Epidemiology, 2009, v. 33, n. 1, p. 54, doi. 10.1002/gepi.20356
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- Article
Informative-Transmission Disequilibrium Test (i-TDT): combined linkage and association mapping that includes unaffected offspring as well as affected offspring.
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- Genetic Epidemiology, 2007, v. 31, n. 2, p. 115, doi. 10.1002/gepi.20195
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- Article
Data mining, neural nets, trees - Problems 2 and 3 of Genetic Analysis Workshop 15.
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- Genetic Epidemiology, 2007, v. 31, n. S1, p. S51, doi. 10.1002/gepi.20280
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- Article
Influence of Marker Heterozygosity and Genetic Heterogeneity on Fine Mapping.
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- Genetic Epidemiology, 2001, v. 21, p. S467, doi. 10.1002/gepi.2001.21.s1.s467
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- Article
Family-Based Association Tests for Qualitative and Quantitative Traits Using Single-Nucleotide Polymorphism and Microsatellite Data.
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- Genetic Epidemiology, 2001, v. 21, p. S364, doi. 10.1002/gepi.2001.21.s1.s364
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- Article
Power of concordant versus discordant sib pairs at different penetrance levels.
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- Genetic Epidemiology, 1999, v. 17, p. S679, doi. 10.1002/gepi.13701707111
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- Article
Detecting linkage for a complex disease using simulated extended pedigrees.
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- Genetic Epidemiology, 1997, v. 14, n. 6, p. 981, doi. 10.1002/(SICI)1098-2272(1997)14:6<981::AID-GEPI70>3.0.CO;2-G
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- Article
Expectation Maximization Algorithm Based Haplotype Relative Risk (EM-HRR): Test of Linkage Disequilibrium Using Incomplete Case-Parents Trios.
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- Human Heredity, 2005, v. 59, n. 3, p. 125, doi. 10.1159/000085571
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- Article
Linkage and association with pulmonary function measures on chromosome 6q27 in the Framingham Heart Study.
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- Human Molecular Genetics, 2003, v. 12, n. 21, p. 2745, doi. 10.1093/hmg/ddg311
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- Article
Genome-wide Analysis of Genetic Loci Associated With Alzheimer Disease.
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- JAMA: Journal of the American Medical Association, 2010, v. 303, n. 18, p. 1832, doi. 10.1001/jama.2010.574
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- Article
Is DFNA5 a susceptibility gene for age-related hearing impairment?
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- European Journal of Human Genetics, 2002, v. 10, n. 12, p. 883, doi. 10.1038/sj.ejhg.5200878
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- Article
Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease.
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- Nature Genetics, 2014, v. 46, n. 9, p. 989, doi. 10.1038/ng.3043
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- Article
Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease.
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- Nature Genetics, 2013, v. 45, n. 12, p. 1452, doi. 10.1038/ng.2802
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- Article
Common variants at 6q22 and 17q21 are associated with intracranial volume.
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- Nature Genetics, 2013, v. 45, n. 6, p. 713, doi. 10.1038/ng0613-713c
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- Article
Erratum: Common variants at 6q22 and 17q21 are associated with intracranial volume.
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- 2012
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- Publication type:
- Erratum
Common variants at 6q22 and 17q21 are associated with intracranial volume.
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- Nature Genetics, 2012, v. 44, n. 5, p. 539, doi. 10.1038/ng.2245
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- Article
Common variants at 12q14 and 12q24 are associated with hippocampal volume.
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- Nature Genetics, 2012, v. 44, n. 5, p. 545, doi. 10.1038/ng.2237
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- Article
Novel microRNA discovery using small RNA sequencing in post-mortem human brain.
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- BMC Genomics, 2016, v. 17, p. 1, doi. 10.1186/s12864-016-3114-3
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- Article
Evaluation of logistic regression models and effect of covariates for case-control study in RNA-Seq analysis.
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- BMC Bioinformatics, 2017, v. 18, p. 1, doi. 10.1186/s12859-017-1498-y
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- Article
Comprehensive Research Synopsis and Systematic Meta-Analyses in Parkinson's Disease Genetics: The PDGene Database.
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- PLoS Genetics, 2012, v. 8, n. 3, p. 1, doi. 10.1371/journal.pgen.1002548
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- Article
Large‐scale sequencing studies expand the known genetic architecture of Alzheimer's disease.
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- Alzheimer's & Dementia: Diagnosis, Assessment & Disease Monitoring, 2021, v. 13, n. 1, p. 1, doi. 10.1002/dad2.12255
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- Article
Frequency of familial Alzheimer's disease gene mutations within the Alzheimer Disease Sequencing Project (ADSP): Genetics/genetic factors of Alzheimer's disease.
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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.046203
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- Article
Alzheimer's disease GWAS weighted by multi‐omics and endophenotypes identifies novel risk loci: Genetics/genetic factors of Alzheimer's disease.
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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.043977
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- Article
Comparative trans‐ethnic meta‐analysis of whole exome sequencing variation for Alzheimer's disease (AD) in 18,402 individuals of the Alzheimer's Disease Sequencing Project (ADSP): Genetics/genetic factors of Alzheimer's disease.
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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.041583
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- Article
Whole genome sequence association analyses of brain volumes in the TOPMed program: Genetics: Genetics of cognitive aging, other dementia, and endophenotypes.
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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.040627
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- Article
Genetic analysis of biobank data: Familial history aggregation‐based tests (FHAT) with application to Alzheimer's disease: Genetics/genetic factors of Alzheimer's disease.
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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.038648
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- Article
O5‐02‐01: GENOME‐WIDE ASSOCIATION STUDY OF PLASMA TAU LEVELS USING HRC IMPUTATIONS IN THE FRAMINGHAM STUDY.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2019, v. 15, p. P1615, doi. 10.1016/j.jalz.2019.06.4840
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- Article
O3‐06‐01: WHOLE EXOME SEQUENCING STUDY IDENTIFIES RARE COPY NUMBER VARIATIONS FOR LATE‐ONSET ALZHEIMER'S DISEASE: THE ALZHEIMER'S DISEASE SEQUENCING PROJECT CASE‐CONTROL ANALYSIS.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2018, v. 14, p. P1025, doi. 10.1016/j.jalz.2018.06.2800
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- Article
P2‐111: INTERACTION BETWEEN ALZHEIMER'S DISEASE GENETIC RISK SCORE AND MIDLIFE PLASMA LIPID LEVELS ON ALZHEIMER 'S DISEASE IN THE FRAMINGHAM HEART STUDY.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2018, v. 14, p. P711, doi. 10.1016/j.jalz.2018.06.797
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- Article
P1‐156: GENE‐BASED ANALYSES IN WHOLE GENOME SEQUENCING OF FAMILIAL LATE‐ONSET ALZHEIMER'S DISEASE.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2018, v. 14, p. P336, doi. 10.1016/j.jalz.2018.06.160
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- Article
TOPMED WHOLE GENOME SEQUENCE (WGS) ASSOCIATIONS WITH BRAIN MRI MEASURES IN THE FRAMINGHAM STUDY.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2017, v. 13, p. P219, doi. 10.1016/j.jalz.2017.07.097
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- Article
ALZHEIMER'S DISEASE SEQUENCING PROJECT: CASE-CONTROL ANALYSES.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2017, v. 13, p. P570, doi. 10.1016/j.jalz.2017.07.186
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- Article
GENOMEWIDE LINKAGE ANALYSIS IDENTIFIES NOVEL CANDIDATE GENES FOR ALZHEIMER’S DISEASE.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2016, v. 12, p. P196, doi. 10.1016/j.jalz.2016.06.341
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- Publication type:
- Article
IDENTIFICATION OF WHOLE EXOME SEQUENCING VARIANTS ASSOCIATED WITH LATE-ONSET ALZHEIMER'S DISEASE IN THE COHORTS FOR HEART AND AGING RESEARCH IN GENOMIC EPIDEMIOLOGY (CHARGE) CONSORTIUM.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2016, v. 12, p. P197, doi. 10.1016/j.jalz.2016.06.344
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- Article
TISSUE-SPECIFIC GENOME-WIDE PREDICTIONS OF GENETICALLY REGULATED EXPRESSION IN ALZHEIMER’S DISEASE.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2016, v. 12, p. P239, doi. 10.1016/j.jalz.2016.06.426
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- Publication type:
- Article
RARE DELETERIOUS AND LOSS-OF-FUNCTION VARIANTS IN OPRL1 AND GAS2L2 CONTRIBUTE TO THE RISK OF LATE-ONSET ALZHEIMER’S DISEASE: ALZHEIMER’S DISEASE SEQUENCING PROJECT CASE-CONTROL STUDY.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2016, v. 12, p. P406, doi. 10.1016/j.jalz.2016.06.765
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- Publication type:
- Article
RARE DELETERIOUS AND LOSS-OF-FUNCTION VARIANTS IN OPRL1 AND GAS2L2 CONTRIBUTE TO THE RISK OF LATE-ONSET ALZHEIMER’S DISEASE: ALZHEIMER’S DISEASE SEQUENCING PROJECT CASE-CONTROL STUDY.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2016, v. 12, p. P163, doi. 10.1016/j.jalz.2016.06.273
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- Article
THE ALZHEIMER’S DISEASE SEQUENCING PROJECT (ADSP): DATA PRODUCTION, MANAGEMENT, AND AVAILABILITY.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2016, v. 12, p. P648, doi. 10.1016/j.jalz.2016.06.1302
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- Article
GENE EXPRESSION, PATHOLOGY AND GENETIC EPIDEMIOLOGY IN LARGE POPULATION-BASED STUDIES.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2016, v. 12, p. P267, doi. 10.1016/j.jalz.2016.06.480
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- Publication type:
- Article
Genome-wide linkage analyses of non-Hispanic white families identify novel loci for familial late-onset Alzheimer's disease.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2016, v. 12, n. 1, p. 2, doi. 10.1016/j.jalz.2015.05.020
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- Article
Association of polymorphisms in the promoter region of the PNMT gene with essential hypertension in African Americans but not in whites
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- American Journal of Hypertension, 2003, v. 16, n. 10, p. 859, doi. 10.1016/S0895-7061(03)01026-4
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- Article
Identification of a polymorphic glutamic acid stretch in the α<sub>2b</sub>-adrenergic receptor and lack of linkage with essential hypertension.
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- American Journal of Hypertension, 1999, v. 12, n. 9, p. 853, doi. 10.1016/S0895-7061(99)00070-9
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- Publication type:
- Article
Gene-Wide Analysis Detects Two New Susceptibility Genes for Alzheimer's Disease.
- Published in:
- PLoS ONE, 2014, v. 9, n. 6, p. 1, doi. 10.1371/journal.pone.0094661
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- Article
Copy Number Variation in Familial Parkinson Disease.
- Published in:
- PLoS ONE, 2011, v. 6, n. 8, p. 1, doi. 10.1371/journal.pone.0020988
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- Article