V. Vieland

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Aliases
Veronica J. Vieland, Veronica Vieland, Veronica j. Vieland, V Vieland, V J Vieland, V. Vieland, V. J. Vieland, V.j. Vieland, Veronica J Vieland, Veronica Janis Vieland
Publication record
180 papers · 14,232 citations · H-index 41

PAPERS

The effect of ascertainment on penetrance estimates for rare variants: Implications for establishing pathogenicity and for genetic counselling
20234 citationsauthor #3
Digital Digital Genetic Analysis Workshop 14: Microsatellite and single- Genetic Analysis Workshop 14: Microsatellite and single-nucleotide polymorphism marker loci for genome-wide scans nucleotide polymorphism marker loci for genome-wide scans
20221 citationsauthor #19
The PPLD has advantages over conventional regression methods in application to moderately sized genome-wide association studies
20213 citationsauthor #1
Candidate gene modifiers of dystrophinopathy identified by the uniform application of genome-wide datasets to novel GWAS-identified loci
20212 citationsauthor #11
A genome-wide association analysis of loss of ambulation in dystrophinopathy patients suggests multiple candidate modifiers of disease severity
20219 citationsauthor #12
A new linear regression-like residual for survival analysis, with application to genome wide association studies of time-to-event data
20206 citationsauthor #1
Segregating patterns of copy number variations in extended autism spectrum disorder (ASD) pedigrees
202010 citationsauthor #17
No evidence amalgamation without evidence measurement
201914 citationsauthor #1
M15 ENHANCING ACCESS TO DATA AT THE NATIONAL INSTITUTE OF HEALTH REPOSITORY AND GENOMICS RESOURCE
20190 citationsauthor #13
No evidence amalgamation without evidence measurement
20180 citationsauthor #1
Validation of a microRNA target site polymorphism in H3F3B that is potentially associated with a broad schizophrenia phenotype
20186 citationsauthor #7
A genome-wide linkage study of autism spectrum disorder and the broad autism phenotype in extended pedigrees
201827 citationsauthor #12
Absolutely Zero Evidence
20180 citationsauthor #1
Long‐range genomic regulators of THBS1 and LTBP4 modify disease severity in duchenne muscular dystrophy
201847 citationsauthor #2
Supplementary Material for: The Value of Regenotyping Older Linkage Data Sets with Denser Marker Panels
20170 citationsauthor #1
Measurement of Statistical Evidence: Picking Up Where Hacking and Others Left Off
20172 citationsauthor #1
Information Loss in Binomial Data Due to Data Compression
20175 citationsauthor #2
Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia
2017532 citationsauthor #25
A single nucleotide polymorphism in the dimethylarginine dimethylaminohydrolase gene is associated with lower risk of pulmonary hypertension in bronchopulmonary dysplasia
201623 citationsauthor #6
Measurement of Statistical Evidence: Picking Up Where Hacking (et al.) Left Off
20160 citationsauthor #1
Statistical Evidence Measured on a Properly Calibrated Scale for Multinomial Hypothesis Comparisons
201610 citationsauthor #1
Joint Analysis of Psychiatric Disorders Increases Accuracy of Risk Prediction for Schizophrenia, Bipolar Disorder, and Major Depressive Disorder
2015225 citationsauthor #345
Towards a New Information-Dynamic Framework for Measuring Evidence in Biology
20150 citationsauthor #1
Contents Vol. 78, 2014
20150 citationsauthor #28
Statistical Evidence Measured on a Properly Calibrated Scale across Nested and Non-nested Hypothesis Comparisons
20152 citationsauthor #1
Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways
2015747 citationsauthor #339
Using extended pedigrees to identify novel autism spectrum disorder (ASD) candidate genes
201518 citationsauthor #22
Bronchopulmonary Dysplasia‐associated Pulmonary Hypertension and Mutations in the DDAH1 Gene
20150 citationsauthor #3
PEDSnet: a National Pediatric Learning Health System
2014217 citationsauthor #11
The Autism Simplex Collection: an international, expertly phenotyped autism sample for genetic and phenotypic analyses
201435 citationsauthor #23
Correction: In Silico Modeling of Itk Activation Kinetics in Thymocytes Suggests Competing Positive and Negative IP4 Mediated Feedbacks Increase Robustness
20142 citationsauthor #8
Meta-Analysis of Repository Data: Impact of Data Regularization on NIMH Schizophrenia Linkage Results
20144 citationsauthor #7
Next-generation linkage and association methods applied to hypertension: a multifaceted approach to the analysis of sequence data
20146 citationsauthor #4
Pedigrees, Sequential Sampling†
20140 citationsauthor #1
Evidence, Temperature, and the Laws of Thermodynamics
20144 citationsauthor #1
Using extended pedigrees to identify novel autism spectrum disorder (ASD) candidate genes
20140 citationsauthor #22
The impact of the metabotropic glutamate receptor and other gene family interaction networks on autism
201458 citationsauthor #70
Oral 1731-3 - Biomarkers in the arginine metabolome predict pulmonary hypertension in patients with bronchopulmonary dysplasia
20140 citationsauthor #4
Revisiting schizophrenia linkage data in the NIMH Repository: reanalysis of regularized data across multiple studies.
20149 citationsauthor #1
Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders
2014911 citationsauthor #101
The Value of Regenotyping Older Linkage Data Sets with Denser Marker Panels
20146 citationsauthor #1
A genome-wide linkage and association study of musical aptitude identifies loci containing genes related to inner ear development and neurocognitive functions
201479 citationsauthor #7
In Silico Modeling of Itk Activation Kinetics in Thymocytes Suggests Competing Positive and Negative IP4 Mediated Feedbacks Increase Robustness
20138 citationsauthor #8
Measurement of statistical evidence on an absolute scale following thermodynamic principles
20130 citationsauthor #1
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
20132,194 citationsauthor #339
SRGAP1 is a candidate gene for papillary thyroid carcinoma susceptibility.
201375 citationsauthor #26
Cell responses only partially shape cell-to-cell variations in protein abundances in Escherichia coli chemotaxis
201314 citationsauthor #3
Data-driven quantification of the robustness and sensitivity of cell signaling networks
20135 citationsauthor #3
Employing MCMC under the PPL framework to analyze sequence data in large pedigrees
20137 citationsauthor #3
How do cell responses shape cell-to-cell variations in protein abundances: A case study using Escherichia coli chemotaxis
20130 citationsauthor #3
A molecular genetic study of autism and related phenotypes in extended pedigrees
201328 citationsauthor #2
A molecular genetic study of autism and related phenotypes in extended pedigrees
20131 citationsauthor #2
Competing positive and negative feedbacks mediated by PH domain ligand interactions regulate Itk activation kinetics in T Cells (178.3)
20120 citationsauthor #9
Measurement of statistical evidence on an absolute scale following thermodynamic principles
20127 citationsauthor #1
Individual common variants exert weak effects on the risk for autism spectrum disorders
2012367 citationsauthor #135
Front & Back Matter
20120 citationsauthor #1
Front & Back Matter
20120 citationsauthor #1
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder
2011198 citationsauthor #120
Next-Generation Linkage Analysis
20114 citationsauthor #1
Poster: High-performance computing for mapping disease-related genes
20110 citationsauthor #4
Measurement of Evidence and Evidence of Measurement
201111 citationsauthor #1
Novel method for combined linkage and genome-wide association analysis finds evidence of distinct genetic architecture for two subtypes of autism
201123 citationsauthor #1
KELVIN: A Software Package for Rigorous Measurement of Statistical Evidence in Human Genetics
201137 citationsauthor #1
Contents Vol. 72, 2011
20110 citationsauthor #5
A genome-wide scan for common alleles affecting risk for autism
2010600 citationsauthor #162
Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability
2010100 citationsauthor #18
Combined linkage and linkage disequilibrium analysis of a motor speech phenotype within families ascertained for autism risk loci
201015 citationsauthor #4
Expected Monotonicity – A Desirable Property for Evidence Measures?
20106 citationsauthor #2
Association statistics under the PPL framework
201018 citationsauthor #2
Functional impact of global rare copy number variation in autism spectrum disorders
20102,031 citationsauthor #173
Using projection and 2D plots to visually reveal genetic mechanisms of complex human disorders
20094 citationsauthor #4
Identification of a schizophrenia-associated functional noncoding variant in NOS1AP.
200975 citationsauthor #13
Fast and Accurate Calculation of a Computationally Intensive Statistic for Mapping Disease Genes
200911 citationsauthor #3
Posterior probability of linkage analysis of autism dataset identifies linkage to chromosome 16
20089 citationsauthor #2
A multilocus model of the genetic architecture of autoimmune thyroid disorder, with clinical implications.
200836 citationsauthor #1
Contents Vol. 66, 2008
20080 citationsauthor #12
Subject Index Vol. 66, 2008
20080 citationsauthor #12
MLIP: using multiple processors to compute the posterior probability of linkage
20085 citationsauthor #3
Practical Considerations for Dividing Data into Subsets Prior to PPL Analysis
200811 citationsauthor #2
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
20071,389 citationsauthor #17
Extracting disease risk profiles from expression data for linkage analysis: application to prostate cancer
20077 citationsauthor #33
Discussing gene‐gene interaction: Warning — translating equations to English may result in Jabberwocky
20078 citationsauthor #2
Rapid computation of large numbers of LOD scores in linkage analysis through polynomial expression of genetic likelihoods
20075 citationsauthor #3
MLIP: A Multiprocessor Linkage Analysis System
20071 citationsauthor #3
Exploiting gene × gene interaction in linkage analysis
200714 citationsauthor #6
Accumulating quantitative trait linkage evidence across multiple datasets using the posterior probability of linkage
200726 citationsauthor #2
Two-stage approach for identifying single-nucleotide polymorphisms associated with rheumatoid arthritis using random forests and Bayesian networks
200725 citationsauthor #33
Fast Computation of Human Genetic Linkage
20074 citationsauthor #5
Genetic Analysis Workshop 15: gene expression analysis and approaches to detecting multiple functional loci
20078 citationsauthor #24
Acknowledgement to the Reviewers
20060 citationsauthor #84
A Posterior Probability of Linkage-Based Re-Analysis of Schizophrenia Data Yields Evidence of Linkage to Chromosomes 1 and 17
200619 citationsauthor #5
The Incorporation of Prior Genomic Information Does Not Necessarily Improve the Performance of Bayesian Linkage Methods: An Example Involving Sex-Specific Recombination and the Two-Point PPL
20068 citationsauthor #2
Thermometers: Something for Statistical Geneticists to Think about
200643 citationsauthor #1
Contents Vol. 60, 2005
20060 citationsauthor #16
Privacy-Preserving Data Set Union
20064 citationsauthor #3
Subject Index Vol. 60, 2005
20060 citationsauthor #16
Ascertainment bias in linkage analysis: Comments on Ginsburg et al.
20054 citationsauthor #1
Pedigrees, Sequential Sampling
20050 citationsauthor #1
The Posterior Probability of Linkage Allowing for Linkage Disequilibrium and a New Estimate of Disequilibrium between a Trait and a Marker
200528 citationsauthor #4
Genetic Analysis Workshop 14: microsatellite and single-nucleotide polymorphism marker loci for genome-wide scans
200513 citationsauthor #19

TIMELINE

1982 0 citations

1987 0 citations

1988 1 citations

1990 185 citations

1991 167 citations

1992 170 citations

1993 90 citations

1994 0 citations

1995 24 citations

1996 177 citations

1997 48 citations

1998 817 citations

1999 471 citations

2000 100 citations

2001 666 citations

2002 398 citations

2003 114 citations

2004 123 citations

2005 196 citations

2006 74 citations

2007 1,487 citations

2008 61 citations

2009 90 citations

2010 2,770 citations

2011 273 citations

2012 374 citations

2013 2,332 citations

2014 1,331 citations

2015 992 citations

2016 33 citations

2017 539 citations

2018 80 citations

2019 14 citations

2020 16 citations

2021 14 citations

2022 1 citations

2023 4 citations

Unknown 0 citations

V. Vieland

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