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A putative RUNX1 binding site variant between SLC9A3R1 and NAT9 is associated with susceptibility to psoriasis.
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- Nature Genetics, 2003, v. 35, n. 4, p. 349, doi. 10.1038/ng1268
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- Article
Analysis of pedigree data in populations with multiple ancestries: Strategies for dealing with admixture in Caribbean Hispanic families from the ADSP.
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- Genetic Epidemiology, 2018, v. 42, n. 6, p. 500, doi. 10.1002/gepi.22133
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- Article
Combining Family- and Population-Based Imputation Data for Association Analysis of Rare and Common Variants in Large Pedigrees.
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- Genetic Epidemiology, 2014, v. 38, n. 7, p. 579, doi. 10.1002/gepi.21844
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- Article
Value of Mendelian Laws of Segregation in Families: Data Quality Control, Imputation, and Beyond.
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- Genetic Epidemiology, 2014, v. 38, p. S21, doi. 10.1002/gepi.21821
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- Article
Detection of Mendelian Consistent Genotyping Errors in Pedigrees.
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- Genetic Epidemiology, 2014, v. 38, n. 4, p. 291, doi. 10.1002/gepi.21806
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- Article
Power of Family-Based Association Designs to Detect Rare Variants in Large Pedigrees Using Imputed Genotypes.
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- Genetic Epidemiology, 2014, v. 38, n. 1, p. 1, doi. 10.1002/gepi.21776
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- Article
Inheritance Model Introduces Differential Bias in CNV Calls Between Parents and Offspring.
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- Genetic Epidemiology, 2012, v. 36, n. 5, p. 488, doi. 10.1002/gepi.21643
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- Article
Joint linkage and segregation analysis under multiallelic trait inheritance: simplifying interpretations for complex traits.
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- Genetic Epidemiology, 2010, v. 34, n. 4, p. 344, doi. 10.1002/gepi.20490
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Case-control association testing in the presence of unknown relationships.
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- Genetic Epidemiology, 2009, v. 33, n. 8, p. 668, doi. 10.1002/gepi.20418
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- Article
Combining information from linkage and association methods.
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- Genetic Epidemiology, 2009, v. 33, n. S1, p. S81, doi. 10.1002/gepi.20477
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- Article
Empirical significance values for linkage analysis: trait simulation using posterior model distributions from MCMC oligogenic segregation analysis.
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- Genetic Epidemiology, 2008, v. 32, n. 2, p. 119, doi. 10.1002/gepi.20267
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- Article
MCMC-based linkage analysis for complex traits on general pedigrees: multipoint analysis with a two-locus model and a polygenic component.
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- Genetic Epidemiology, 2007, v. 31, n. 2, p. 103, doi. 10.1002/gepi.20194
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- Article
Summary of Genetic Analysis Workshop 15: Group 9 linkage analysis of the CEPH expression data.
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- Genetic Epidemiology, 2007, v. 31, n. S1, p. S75, doi. 10.1002/gepi.20283
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- Article
Comparison of single-nucleotide polymorphisms and microsatellite markers for linkage analysis in the COGA and simulated data sets for Genetic Analysis Workshop 14: Presentation Groups 1, 2, and 3.
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- Genetic Epidemiology, 2005, v. 29, n. S1, p. S7, doi. 10.1002/gepi.20106
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Summary of Group 8: Development and extension of linkage methods.
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- Genetic Epidemiology, 2003, v. 25, n. 0, p. S64, doi. 10.1002/gepi.10286
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A score for Bayesian genome screening.
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- Genetic Epidemiology, 2003, v. 24, n. 3, p. 181, doi. 10.1002/gepi.10230
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- Article
Characteristics of genetic markers and maps for cost-effective genome screens using diallelic markers.
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- Genetic Epidemiology, 2002, v. 22, n. 3, p. 205, doi. 10.1002/gepi.0177
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- Article
Bias in multipoint linkage analysis arising from map misspecification.
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- Genetic Epidemiology, 2000, v. 19, n. 4, p. 366, doi. 10.1002/1098-2272(200012)19:4<366::AID-GEPI8>3.0.CO;2-F
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Preface.
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- Genetic Epidemiology, 1999, v. 17, p. Sxxxi, doi. 10.1002/gepi.1370170702
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Pedigree analysis package (PAP) vs. MORGAN: Model selection and hypothesis testing on a large pedigree.
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- Genetic Epidemiology, 1998, v. 15, n. 4, p. 355, doi. 10.1002/(SICI)1098-2272(1998)15:4<355::AID-GEPI3>3.0.CO;2-1
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- Article
Semiparametric estimation of major gene effects for age of onset.
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- Genetic Epidemiology, 1998, v. 15, n. 3, p. 279, doi. 10.1002/(SICI)1098-2272(1998)15:3<279::AID-GEPI6>3.0.CO;2-#
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- Article
Genetic analysis of simulated oligogenic traits in nuclear and extended pedigrees: Summary of GAW10 contributions.
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- Genetic Epidemiology, 1997, v. 14, n. 6, p. 719, doi. 10.1002/(SICI)1098-2272(1997)14:6<719::AID-GEPI28>3.0.CO;2-S
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- Article
Segregation and linkage analysis of a quantitative versus a qualitative trait in large pedigrees.
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- Genetic Epidemiology, 1997, v. 14, n. 6, p. 999, doi. 10.1002/(SICI)1098-2272(1997)14:6<999::AID-GEPI73>3.0.CO;2-F
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- Article
Pedigree analysis package vs. MIXD: Fitting the mixed model on a large pedigree.
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- Genetic Epidemiology, 1996, v. 13, n. 1, p. 91, doi. 10.1002/(SICI)1098-2272(1996)13:1<91::AID-GEPI8>3.0.CO;2-9
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- Article
Genetic analysis of Alzheimer's disease: A summary of contributions to GAW8.
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- Genetic Epidemiology, 1993, v. 10, n. 6, p. 349, doi. 10.1002/gepi.1370100604
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The Seattle Alzheimer's disease data set.
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- Genetic Epidemiology, 1993, v. 10, n. 6, p. 365, doi. 10.1002/gepi.1370100606
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Linkage between quantitative trait and marker loci: Methods using all relative pairs.
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- Genetic Epidemiology, 1993, v. 10, n. 2, p. 87, doi. 10.1002/gepi.1370100202
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- Article
Visualization of Haplotype Sharing Patterns in Pedigree Samples.
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- Human Heredity, 2014, v. 78, n. 1, p. 1, doi. 10.1159/000358171
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- Article
Estimation and Visualization of Identity-by-Descent within Pedigrees Simplifies Interpretation of Complex Trait Analysis.
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- Human Heredity, 2011, v. 72, n. 4, p. 289, doi. 10.1159/000334083
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- Article
Accounting for Epistasis in Linkage Analysis of General Pedigrees.
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- Human Heredity, 2007, v. 63, n. 2, p. 144, doi. 10.1159/000099186
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- Article
Replication of a rare risk haplotype on 1p36.33 for autism spectrum disorder.
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- Human Genetics, 2018, v. 137, n. 10, p. 807, doi. 10.1007/s00439-018-1939-3
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- Article
Genome scan for cognitive trait loci of dyslexia: Rapid naming and rapid switching of letters, numbers, and colors.
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2014, v. 165B, n. 4, p. 345, doi. 10.1002/ajmg.b.32237
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- Article
Genome Scan in Familial Late-Onset Alzheimer's Disease: A Locus on Chromosome 6 Contributes to Age-at-Onset.
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2013, v. 162B, n. 2, p. 201, doi. 10.1002/ajmg.b.32133
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- Article
Genome Scan for Spelling Deficits: Effects of Verbal IQ on Models of Transmission and Trait Gene Localization.
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- Behavior Genetics, 2011, v. 41, n. 1, p. 31, doi. 10.1007/s10519-010-9390-9
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- Article
Genome-Wide Association of Familial Late-Onset Alzheimer's Disease Replicates BIN1 and CLU and Nominates CUGBP2 in Interaction with APOE.
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- PLoS Genetics, 2011, v. 7, n. 2, p. 1, doi. 10.1371/journal.pgen.1001308
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- Article
Evaluation of locus heterogeneity and EXT1 mutations in 34 families with hereditary multiple exostoses.
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- Human Mutation, 1998, v. 11, n. 3, p. 231, doi. 10.1002/(SICI)1098-1004(1998)11:3<231::AID-HUMU8>3.0.CO;2-K
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- Article
Monte Carlo Markov chain methods and model selection in Genetic analysis.
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- Animal Biotechnology, 1997, v. 8, n. 1, p. 129, doi. 10.1080/10495399709525875
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- Article
Genetic Candidate Variants in Two Multigenerational Families with Childhood Apraxia of Speech.
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- PLoS ONE, 2016, v. 11, n. 4, p. 1, doi. 10.1371/journal.pone.0153864
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- Article
Genome Scan of a Nonword Repetition Phenotype in Families with Dyslexia: Evidence for Multiple Loci.
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- Behavior Genetics, 2008, v. 38, n. 5, p. 462, doi. 10.1007/s10519-008-9215-2
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- Article
Familial Aggregation of Dyslexia Phenotypes.
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- Behavior Genetics, 2000, v. 30, n. 5, p. 385, doi. 10.1023/A:1002700605187
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- Article
Genome-scan for IQ discrepancy in autism: evidence for loci on chromosomes 10 and 16.
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- Human Genetics, 2011, v. 129, n. 1, p. 59, doi. 10.1007/s00439-010-0899-z
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- Article
Linkage and association analyses identify a candidate region for apoB level on chromosome 4q32.3 in FCHL families.
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- Human Genetics, 2010, v. 127, n. 6, p. 705, doi. 10.1007/s00439-010-0819-2
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- Article
Genome scan for quantitative trait loci influencing HDL levels: evidence for multilocus inheritance in familial combined hyperlipidemia.
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- Human Genetics, 2005, v. 117, n. 5, p. 494, doi. 10.1007/s00439-005-1338-4
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- Article
Evidence of linkage of HDL level variation to APOC3 in two samples with different ascertainment.
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- Human Genetics, 2003, v. 113, n. 6, p. 522, doi. 10.1007/s00439-003-1006-5
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- Article
Accounting for Linkage Disequilibrium among Markers in Linkage Analysis: Impact of Haplotype Frequency Estimation and Molecular Haplotypes for a Gene in a Candidate Region for Alzheimer’s Disease.
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- Human Heredity, 2007, v. 63, n. 1, p. 26, doi. 10.1159/000098459
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- Article
Segregation Analysis of a Complex Quantitative Trait: Approaches for Identifying Influential Data Points.
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- Human Heredity, 2006, v. 61, n. 2, p. 80, doi. 10.1159/000093085
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- Article
MCMC Multilocus Lod Scores: Application of a New Approach.
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- Human Heredity, 2005, v. 59, n. 2, p. 98, doi. 10.1159/000085224
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- Article
On Estimating the Proportion of Variance in a Phenotypic Trait Attributable to a Measured Locus.
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- Human Heredity, 2001, v. 51, n. 3, p. 145, doi. 10.1159/000053335
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- Article
Linkage of Hereditary Distal Myopathy with Desmin Accumulation to 2q.
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- Human Heredity, 2000, v. 50, n. 3, p. 166, doi. 10.1159/000022908
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- Article
Association score testing for rare variants and binary traits in family data with shared controls.
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- Briefings in Bioinformatics, 2019, v. 20, n. 1, p. 245, doi. 10.1093/bib/bbx107
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- Article