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Author Details

Veronica J Vieland
The Ohio State University
1990
113
35
PMIDPaper TitleJournal TitlePublished Year
36935420A genome-wide association analysis of loss of ambulation in dystrophinopathy patients suggests multiple candidate modifiers of disease severity.Eur J Hum Genet2023
37733810The effect of ascertainment on penetrance estimates for rare variants: Implications for establishing pathogenicity and for genetic counselling.PLoS One2023
34550985The PPLD has advantages over conventional regression methods in application to moderately sized genome-wide association studies.PLoS One2021
32372567Segregating patterns of copy number variations in extended autism spectrum disorder (ASD) pedigrees.Am J Med Genet B Neuropsychiatr Genet2020
32365095A new linear regression-like residual for survival analysis, with application to genome wide association studies of time-to-event data.PLoS One2020
29529098Validation of a microRNA target site polymorphism in H3F3B that is potentially associated with a broad schizophrenia phenotype.PLoS One2018
29890955A genome-wide linkage study of autism spectrum disorder and the broad autism phenotype in extended pedigrees.J Neurodev Disord2018
30014611Long-range genomic regulators of THBS1 and LTBP4 modify disease severity in duchenne muscular dystrophy.Ann Neurol2018
26663142A single nucleotide polymorphism in the dimethylarginine dimethylaminohydrolase gene is associated with lower risk of pulmonary hypertension in bronchopulmonary dysplasia.Acta Paediatr2016
24614497A genome-wide linkage and association study of musical aptitude identifies loci containing genes related to inner ear development and neurocognitive functions.Mol Psychiatry2015
25432440Using extended pedigrees to identify novel autism spectrum disorder (ASD) candidate genes.Hum Genet2015
24170318Revisiting schizophrenia linkage data in the NIMH Repository: reanalysis of regularized data across multiple studies.Am J Psychiatry2014
25473880Host-to-host variation of ecological interactions in polymicrobial infections.Phys Biol2014
25519364Next-generation linkage and association methods applied to hypertension: a multifaceted approach to the analysis of sequence data.BMC Proc2014
25392729The Autism Simplex Collection: an international, expertly phenotyped autism sample for genetic and phenotypic analyses.Mol Autism2014
25358903Evidence, temperature, and the laws of thermodynamics.Hum Hered2014
24969307The value of regenotyping older linkage data sets with denser marker panels.Hum Hered2014
24768552Convergence of genes and cellular pathways dysregulated in autism spectrum disorders.Am J Hum Genet2014
24821737PEDSnet: a National Pediatric Learning Health System.J Am Med Inform Assoc2014
24919409Arginase I gene single-nucleotide polymorphism is associated with decreased risk of pulmonary hypertension in bronchopulmonary dysplasia.Acta Paediatr2014
24454738Meta-analysis of repository data: impact of data regularization on NIMH schizophrenia linkage results.PLoS One2014
23539728SRGAP1 is a candidate gene for papillary thyroid carcinoma susceptibility.J Clin Endocrinol Metab2013
24093601A molecular genetic study of autism and related phenotypes in extended pedigrees.J Neurodev Disord2013
24066087In silico modeling of Itk activation kinetics in thymocytes suggests competing positive and negative IP4 mediated feedbacks increase robustness.PLoS One2013
24167288Cell responses only partially shape cell-to-cell variations in protein abundances in Escherichia coli chemotaxis.Proc Natl Acad Sci U S A2013
24164951Data-driven quantification of the robustness and sensitivity of cell signaling networks.Phys Biol2013
23933821Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs.Nat Genet2013
23626600Employing MCMC under the PPL framework to analyze sequence data in large pedigrees.Front Genet2013
23463577Measurement of statistical evidence on an absolute scale following thermodynamic principles.Theory Biosci2013
21996756A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder.Hum Genet2012
22843504Individual common variants exert weak effects on the risk for autism spectrum disorders.Hum Mol Genet2012
20972252Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability.J Med Genet2011
22189470KELVIN: a software package for rigorous measurement of statistical evidence in human genetics.Hum Hered2011
22189464Next-generation linkage analysis.Hum Hered2011
21484201Novel method for combined linkage and genome-wide association analysis finds evidence of distinct genetic architecture for two subtypes of autism.J Neurodev Disord2011
21422761Where's the evidence?Hum Hered2011
20663923A genome-wide scan for common alleles affecting risk for autism.Hum Mol Genet2010
21125004Combined linkage and linkage disequilibrium analysis of a motor speech phenotype within families ascertained for autism risk loci.J Neurodev Disord2010
21058335Association statistics under the PPL framework.Genet Epidemiol2010
20531469Functional impact of global rare copy number variation in autism spectrum disorders.Nature2010
20664208Expected monotonicity--a desirable property for evidence measures?Hum Hered2010
19255043Identification of a schizophrenia-associated functional noncoding variant in NOS1AP.Am J Psychiatry2009
19432537Fast and accurate calculation of a computationally intensive statistic for mapping disease genes.J Comput Biol2009
18349700Posterior probability of linkage analysis of autism dataset identifies linkage to chromosome 16.Psychiatr Genet2008
18541055MLIP: using multiple processors to compute the posterior probability of linkage.BMC Bioinformatics2008
18485327A multilocus model of the genetic architecture of autoimmune thyroid disorder, with clinical implications.Am J Hum Genet2008
18612207Practical considerations for dividing data into subsets prior to PPL analysis.Hum Hered2008
17123305Accumulating quantitative trait linkage evidence across multiple datasets using the posterior probability of linkage.Genet Epidemiol2007
18466565Exploiting gene x gene interaction in linkage analysis.BMC Proc2007
18466438Genetic Analysis Workshop 15: gene expression analysis and approaches to detecting multiple functional loci.BMC Proc2007
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Collaborators

Joseph Piven
Oregon Health & Science University
Co-authored papers 16
Yungui Huang
Research Institute at Nationwide Childrens Hospital, University of Iowa
Co-authored papers 14
Peter Szatmari
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Co-authored papers 12
Christopher W Bartlett
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Co-authored papers 12
Andrew D Paterson
The Hospital for Sick Children
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Sang-Cheol Seok
Mathematical Medicine LLC
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Val C Sheffield
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James S Sutcliffe
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Co-authored papers 10
David A Greenberg
Abigail Wexner Research Institute, Nationwide Children's Hospital
Co-authored papers 10
Linda M Brzustowicz
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Ann Thompson
McMaster University
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Bridget A Fernandez
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Monash University
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Louise Gallagher
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John I Nurnberger
Stark Neurosciences Research Institute, Indiana University School of Medicine
Co-authored papers 7
Alistair T Pagnamenta
NIHR Biomedical Research Centre, University of Oxford
Co-authored papers 7
Hilary Coon
Co-authored papers 7
Daniel H Geschwind
University of California los angeles
Co-authored papers 7
Christine M Freitag
Co-authored papers 7
Sabine M Klauck
Co-authored papers 7
Edwin H Cook
Co-authored papers 7
Marion Leboyer
INSERM U
Co-authored papers 6
Eftichia Duketis
Co-authored papers 6
Gerard D Schellenberg
Co-authored papers 6
Agatino Battaglia
Co-authored papers 6
Release 1.2