sameAs
Functional impact of global rare copy number variation in autism spectrum disordersUlcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association studyHigh-density association study of 383 candidate genes for volumetric BMD at the femoral neck and lumbar spine among older menUsing ancestry matching to combine family-based and unrelated samples for genome-wide association studiesGenome-wide association identifies multiple ulcerative colitis susceptibility lociThe heritability of IQSynaptic, transcriptional and chromatin genes disrupted in autismGenetic relationship between five psychiatric disorders estimated from genome-wide SNPsIndividual common variants exert weak effects on the risk for autism spectrum disordersA genome-wide scan for common alleles affecting risk for autismMultiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with AutismA framework for the interpretation of de novo mutation in human diseaseWhole exome sequencing reveals minimal differences between cell line and whole blood derived DNA.Common genetic variants in the CLDN2 and PRSS1-PRSS2 loci alter risk for alcohol-related and sporadic pancreatitis.Common genetic variants, acting additively, are a major source of risk for autismThe autism sequencing consortium: large-scale, high-throughput sequencing in autism spectrum disorders.Evolutionary-based association analysis using haplotype data.DAWN: a framework to identify autism genes and subnetworks using gene expression and genetics.MIRA: mutual information-based reporter algorithm for metabolic networksTesting for an unusual distribution of rare variants.On the identification of disease mutations by the analysis of haplotype similarity and goodness of fit.Transcriptional consequences of 16p11.2 deletion and duplication in mouse cortex and multiplex autism familiesTransmission/disequilibrium test meets measured haplotype analysis: family-based association analysis guided by evolution of haplotypes.Next generation analytic tools for large scale genetic epidemiology studies of complex diseasesScreen and clean: a tool for identifying interactions in genome-wide association studiesGenome-Wide Significance Levels and Weighted Hypothesis Testing.Most genetic risk for autism resides with common variation.Haplotype fine mapping by evolutionary treesDe novo insertions and deletions of predominantly paternal origin are associated with autism spectrum disorderThe power of genomic controlUsing linkage genome scans to improve power of association in genome scans.Positive Semidefinite Rank-based Correlation Matrix Estimation with Application to Semiparametric Graph Estimation.The autism-associated chromatin modifier CHD8 regulates other autism risk genes during human neurodevelopmentUnbiased methods for population-based association studies.Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci.Genomic control, a new approach to genetic-based association studies.Clustering and alignment of polymorphic sequences for HLA-DRB1 genotypingAnalysis of rare, exonic variation amongst subjects with autism spectrum disorders and population controls.Integrated model of de novo and inherited genetic variants yields greater power to identify risk genes.Candidate gene analysis of femoral neck trabecular and cortical volumetric bone mineral density in older men.
P50
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P50
description
American statistician
@en
Amerikaans onderzoekster
@nl
hulumtuese
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statisticienne américaine
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statisticiste american
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usona statistikisto
@eo
հետազոտող
@hy
name
Kathryn Roeder
@ast
Kathryn Roeder
@de
Kathryn Roeder
@en
Kathryn Roeder
@es
Kathryn Roeder
@fr
Kathryn Roeder
@nl
Kathryn Roeder
@sl
type
label
Kathryn Roeder
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Kathryn Roeder
@de
Kathryn Roeder
@en
Kathryn Roeder
@es
Kathryn Roeder
@fr
Kathryn Roeder
@nl
Kathryn Roeder
@sl
prefLabel
Kathryn Roeder
@ast
Kathryn Roeder
@de
Kathryn Roeder
@en
Kathryn Roeder
@es
Kathryn Roeder
@fr
Kathryn Roeder
@nl
Kathryn Roeder
@sl
P166
P1153
7103005216
P166
P1960
KPxl53wzvv4C
P21
P31
P4955
P496
0000-0002-8869-6254