V. Vieland

Veronica J Vieland, Mark W Logue, V. Vieland, 2003, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Cell responses only partially shape cell-to-cell variations in protein abundances in Escherichia coli chemotaxis

Sang-Cheol Seok, Jayajit Das, Sayak Mukherjee, 2013, Proceedings of the National Academy of Sciences.

Evaluation of the chromosome 2q37.3 gene CENTG2 as an autism susceptibility gene

J. Piven, V. Sheffield, T. Wassink, 2005, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Genetic Analysis Workshop 14: microsatellite and single-nucleotide polymorphism marker loci for genome-wide scans

N. Mendell, A. Paterson, V. Vieland, 2005, BMC Genetics.

Evidence, Temperature, and the Laws of Thermodynamics

V. Vieland, 2014, Human Heredity.

KELVIN: A Software Package for Rigorous Measurement of Statistical Evidence in Human Genetics

Ümit V. Çatalyürek, Alberto Maria Segre, V. Vieland, 2011, Human Heredity.

Heterogeneity: GAW Group 15

V. Vieland, 2005, Genetic epidemiology.

Validation of a microRNA target site polymorphism in H3F3B that is potentially associated with a broad schizophrenia phenotype

V. Vieland, S. Buyske, A. Bassett, 2018, PloS one.

Contents Vol. 59, 2005

M. Pericak-Vance, V. Vieland, D. Naiman, 2005, Human Heredity.

Investigating the numerical effects of ascertainment bias in linkage analysis: Development of methods and preliminary results

V. Vieland, S. Slager, 1997, Genetic epidemiology.

Combined linkage and linkage disequilibrium analysis of a motor speech phenotype within families ascertained for autism risk loci

V. Vieland, L. Brzustowicz, J. Flax, 2010, Journal of Neurodevelopmental Disorders.

41 THE MOLECULAR AND CELLULAR GENETICS OF AUTISM

J. Sutcliffe, J. Piven, T. Wassink, 2002 .

The consistency of the posterior probability of linkage

V. Vieland, Jian Huang, Kai Wang, 2000, Annals of human genetics.

The Null Distribution of the Heterogeneity Lod Score Does Depend on the Assumed Genetic Model for the Trait

V. Vieland, Jian Huang, 2001, Human Heredity.

Statistical evaluation of age-at-onset anticipation: a new test and evaluation of its behavior in realistic applications.

V. Vieland, J. Huang, 1998, American journal of human genetics.

A genome-wide linkage study of autism spectrum disorder and the broad autism phenotype in extended pedigrees

S. Scherer, B. Fernandez, J. Howe, 2018, Journal of Neurodevelopmental Disorders.

Practical Considerations for Dividing Data into Subsets Prior to PPL Analysis

V. Vieland, M. Govil, 2008, Human Heredity.

Accumulating quantitative trait linkage evidence across multiple datasets using the posterior probability of linkage

V. Vieland, C. Bartlett, 2007, Genetic epidemiology.

Exploiting gene × gene interaction in linkage analysis

Alberto Maria Segre, V. Vieland, J. O’Connell, 2007, BMC proceedings.

A Posterior Probability of Linkage-Based Re-Analysis of Schizophrenia Data Yields Evidence of Linkage to Chromosomes 1 and 17

V. Vieland, A. Bassett, M. Logue, 2006, Human Heredity.

A model-integrated multipoint Bayesian analysis of hypertension in the Framingham Heart Study data finds little evidence of linkage

V. Vieland, M. Logue, R. Goedken, 2003, BMC Genetics.

Genome-wide linkage analysis of blood pressure under locus heterogeneity

V. Vieland, Jian Huang, Kai Wang, 2003, BMC Genetics.

Incorporating language phenotypes strengthens evidence of linkage to autism.

S. Folstein, J. Piven, V. Sheffield, 2001, American journal of medical genetics.

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

Thomas Bourgeron, Alberto Segre, Alberto Maria Segre, 2007, Nature Genetics.

Statistical Evidence Measured on a Properly Calibrated Scale across Nested and Non-nested Hypothesis Comparisons

V. Vieland, S. Seok, 2015, Entropy.

Reply to Karunaratne and Elston

V. Vieland, S. Hodge, 1998 .

Discussing gene‐gene interaction: Warning — translating equations to English may result in Jabberwocky

V. Vieland, C. Bartlett, 2007, Genetic epidemiology.

Adolescent suicide attempters. Response to suicide-prevention programs.

V. Vieland, D. Shaffer, A. Garland, 1990, JAMA.

Is Schizophrenia Linked to Chromosome 1q?

V. Vieland, A. Bassett, E. Chow, 2002, Science.

Two-locus heterogeneity cannot be distinguished from two-locus epistasis on the basis of affected-sib-pair data.

V. Vieland, Jian Huang, 2003, American journal of human genetics.

The replication requirement

V. Vieland, 2001, Nature Genetics.

The impact of curriculum-based suicide prevention programs for teenagers.

V. Vieland, D. Shaffer, A. Garland, 1991, Journal of the American Academy of Child and Adolescent Psychiatry.

The impact of curriculum-based suicide prevention programs for teenagers: an 18-month follow-up.

V. Vieland, D. Shaffer, A. Garland, 1991, Journal of the American Academy of Child and Adolescent Psychiatry.

Candidate gene modifiers of dystrophinopathy identified by the uniform application of genome-wide datasets to novel GWAS-identified loci

V. Vieland, R. Weiss, D. Dunn, 2021, medRxiv.

The Posterior Probability of Linkage Allowing for Linkage Disequilibrium and a New Estimate of Disequilibrium between a Trait and a Marker

Jian Huang, Veronica J. Vieland, Mark W. Logue, 2005, Human Heredity.

Next-Generation Linkage Analysis

Veronica J. Vieland, V. Vieland, M. Devoto, 2011, Human Heredity.

New segregation analysis of panic disorder.

V. Vieland, A. Fyer, D. Goodman, 1996, American journal of medical genetics.

No evidence amalgamation without evidence measurement

V. Vieland, Hasok Chang, 2018, Synthese.

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

Veronica J. Vieland, Mark W. Logue, V. Vieland, 2006, Human Heredity.

Effect of allelic heterogeneity on the power of the transmission disequilibrium test

V. Vieland, S. Slager, S.L. Slager, 2000, Genetic epidemiology.

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

Christopher S. Poultney, Stephan J Sanders, Stephen J. Guter, 2017, Molecular Autism.

Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways

Laura J. Scott, Naomi R. Wray, Margaret A. Pericak-Vance, 2015, Nature Neuroscience.

Association statistics under the PPL framework

Yungui Huang, Veronica J Vieland, V. Vieland, 2010, Genetic epidemiology.

An autosomal genomic screen for autism.

S. Folstein, J. Piven, V. Sheffield, 1999, American journal of medical genetics.

Better data analysis through data exploration.

V. Vieland, S. Hodge, D. Greenberg, 1993, American journal of human genetics.

Report of the Chromosome 5 Workshop of the Sixth World Congress on Psychiatric Genetics.

V. Vieland, R. Crowe, 1999, American journal of medical genetics.

Using extended pedigrees to identify novel autism spectrum disorder (ASD) candidate genes

Daniele Merico, Joseph Piven, Veronica J. Vieland, 2014, Human Genetics.

The impact of the metabotropic glutamate receptor and other gene family interaction networks on autism

Thomas Bourgeron, Ellen M. Wijsman, Gillian Baird, 2014, Nature Communications.

The Autism Simplex Collection: an international, expertly phenotyped autism sample for genetic and phenotypic analyses

D. Pinto, S. Scherer, J. Sutcliffe, 2014, Molecular Autism.

A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder

Joseph T. Glessner, Stephen J. Guter, D. Pinto, 2011, Human Genetics.

Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability

D. Pinto, S. Scherer, J. Sutcliffe, 2010, Journal of Medical Genetics.

Evaluation of FOXP2 as an autism susceptibility gene.

S. Folstein, J. Piven, V. Sheffield, 2002, American journal of medical genetics.

Segregating patterns of copy number variations in extended autism spectrum disorder (ASD) pedigrees

John Wei, S. Scherer, B. Fernandez, 2020, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

A case of autism and uniparental disomy of chromosome 1

J. Piven, V. Sheffield, T. Wassink, 2005, Human Genetics.

Adequacy of single‐locus approximations for linkage analyses of oligogenic traits

V. Vieland, S. Hodge, G. Vogler, 1992, Genetic epidemiology.

Long‐range genomic regulators of THBS1 and LTBP4 modify disease severity in duchenne muscular dystrophy

V. Vieland, R. Weiss, D. Dunn, 2018, Annals of neurology.

A new statistical test for age‐of‐onset anticipation: Application to bipolar disorder

V. Vieland, Jian Huang, 1997, Genetic epidemiology.

Novel method for combined linkage and genome-wide association analysis finds evidence of distinct genetic architecture for two subtypes of autism

Alistair T. Pagnamenta, Veronica J. Vieland, Anthony P. Monaco, 2011, Journal of Neurodevelopmental Disorders.

Incorporating language phenotypes strengthens evidence of linkage to autism.

S. Folstein, J. Piven, V. Sheffield, 2001, American journal of medical genetics.

Posterior probability of linkage analysis of autism dataset identifies linkage to chromosome 16

J. Piven, V. Sheffield, T. Wassink, 2008, Psychiatric genetics.

Effects of updating linkage evidence across subsets of data: reanalysis of the autism genetic resource exchange data set.

Christopher W Bartlett, Rhinda Goedken, Veronica J Vieland, 2005, American journal of human genetics.

Evidence supporting WNT2 as an autism susceptibility gene.

S. Folstein, J. Piven, V. Sheffield, 2001, American journal of medical genetics.

SRGAP1 is a candidate gene for papillary thyroid carcinoma susceptibility.

Michael C. Ostrowski, V. Vieland, Huiling He, 2013, The Journal of clinical endocrinology and metabolism.

Identification of a schizophrenia-associated functional noncoding variant in NOS1AP.

Steven Buyske, Veronica J Vieland, Yungui Huang, 2009, The American journal of psychiatry.

Further evidence for the increased power of LOD scores compared with nonparametric methods.

V. Vieland, D. Greenberg, M. Durner, 1999, American journal of human genetics.

Adequacy of single-locus approximations for linkage analyses of oligogenic traits: extension to multigenerational pedigree structures.

V. Vieland, S. Hodge, D. Greenberg, 1993, Human heredity.

Revisiting schizophrenia linkage data in the NIMH Repository: reanalysis of regularized data across multiple studies.

Kimberly A. Walters, V. Vieland, T. Lehner, 2014, The American journal of psychiatry.

Examination of AVPR1a as an autism susceptibility gene

V J Vieland, S. Folstein, J. Piven, 2004, Molecular Psychiatry.

A genome-wide association analysis of loss of ambulation in dystrophinopathy patients suggests multiple candidate modifiers of disease severity

V. Vieland, R. Weiss, D. Dunn, 2021, European Journal of Human Genetics.

The emperor's new methods.

Susan E Hodge, Veronica J Vieland, V. Vieland, 2003, American journal of human genetics.

NONPARAMETRIC ESTIMATION OF MARGINAL DISTRIBUTIONS UNDER BIVARIATE TRUNCATION WITH APPLICATION TO TESTING FOR AGE-OF-ONSET ANTICIPATION

V. Vieland, Jian Huang, Kai Wang, 2001 .

A molecular genetic study of autism and related phenotypes in extended pedigrees

Kimberly A. Walters, B. Fernandez, J. Piven, 2013, Journal of Neurodevelopmental Disorders.

Examination of Potential Overlap in Autism and Language Loci on Chromosomes 2, 7, and 13 in Two Independent Samples Ascertained for Specific Language Impairment

V. Vieland, P. Tallal, C. Bartlett, 2004, Human Heredity.

Power, mode of inheritance, and type I error in LOD scores and affecteds-only methods: reply to Kruglyak.

S E Hodge, M A Spence, V J Vieland, 1998, American journal of human genetics.

Perils of gene mapping with microsatellite markers.

V. Vieland, T. Gilliam, J. Knowles, 1992, American journal of human genetics.

Affecteds-only linkage methods are not a panacea.

S E Hodge, M A Spence, V J Vieland, 1996, American journal of human genetics.

Performance comparison of two-point linkage methods using microsatellite markers flanking known disease locations

V. Vieland, M. Spence, M. Logue, 2005, BMC Genetics.

HLODs, Trait Models, and Ascertainment: Implications of Admixture for Parameter Estimation and Linkage Detection

Veronica J. Vieland, V. Vieland, M. Logue, 2002, Human Heredity.

HLODs remain powerful tools for detection of linkage in the presence of genetic heterogeneity.

Susan E Hodge, Veronica J Vieland, David A Greenberg, 2002, American journal of human genetics.

Power comparisons between the TDT and two likelihood‐based methods

V. Vieland, S. Slager, J. Huang, 2001, Genetic epidemiology.

A New Method for Computing the Multipoint Posterior Probability of Linkage

Veronica J Vieland, Mark W Logue, V. Vieland, 2004, Human Heredity.

Linkage analysis of two-locus diseases under single-locus and two-locus analysis models.

V. Vieland, J. Ott, S. Hodge, 1992, Cytogenetics and Cell Genetics.

Meta-Analysis of Repository Data: Impact of Data Regularization on NIMH Schizophrenia Linkage Results

Kimberly A. Walters, V. Vieland, T. Lehner, 2014, PloS one.

Chromosome 5 workshop.

V. Vieland, R. Crowe, 1998, Psychiatric genetics.

The PPLD has advantages over conventional regression methods in application to moderately sized genome-wide association studies

V. Vieland, S. Seok, 2021, bioRxiv.

A new linear regression-like residual for survival analysis, with application to genome wide association studies of time-to-event data

V. Vieland, S. Seok, W. Stewart, 2020, PloS one.

Bayesian linkage analysis, or: how I learned to stop worrying and love the posterior probability of linkage.

V J Vieland, V. Vieland, 1998, American journal of human genetics.

Thermometers: Something for Statistical Geneticists to Think about

Veronica J Vieland, V. Vieland, 2006, Human Heredity.

Comparison of ‘Model-Free’ and ‘Model-Based’ Linkage Statistics in the Presence of Locus Heterogeneity: Single Data Set and Multiple Data Set Applications

Jian Huang, Veronica J. Vieland, V. Vieland, 2001, Human Heredity.

Power to Detect Linkage Based on Multiple Sets of Data in the Presence of Locus Heterogeneity: Comparative Evaluation of Model-Based Linkage Methods for Affected Sib Pair Data

Jian Huang, Kai Wang, Veronica J. Vieland, 2001, Human Heredity.

No evidence amalgamation without evidence measurement

Hasok Chang, Veronica J. Vieland, V. Vieland, 2019, Synthese.

Measurement of statistical evidence on an absolute scale following thermodynamic principles

Sang-Cheol Seok, Jayajit Das, Veronica J. Vieland, 2013, Theory in Biosciences.

Information Loss in Binomial Data Due to Data Compression

Veronica J. Vieland, Susan E. Hodge, V. Vieland, 2017, Entropy.

Statistical Evidence Measured on a Properly Calibrated Scale for Multinomial Hypothesis Comparisons

Sang-Cheol Seok, Veronica J. Vieland, V. Vieland, 2016, Entropy.

Measurement of Evidence and Evidence of Measurement

Veronica J. Vieland, Susan E. Hodge, V. Vieland, 2011 .

Measurement of Statistical Evidence: Picking Up Where Hacking and Others Left Off

Veronica J. Vieland, V. Vieland, 2017, Philosophy of Science.

PEDSnet: a National Pediatric Learning Health System

Keith Marsolo, Christopher B. Forrest, Michael G. Kahn, 2014, J. Am. Medical Informatics Assoc..

A genome-wide linkage study of autism spectrum disorder and the broad autism phenotype in extended pedigrees

S. Scherer, B. Fernandez, J. Howe, 2018, Journal of Neurodevelopmental Disorders.

Next-generation linkage and association methods applied to hypertension: a multifaceted approach to the analysis of sequence data

V. Vieland, Yungui Huang, D. Greenberg, 2014, BMC Proceedings.

Using extended pedigrees to identify novel autism spectrum disorder (ASD) candidate genes

S. Scherer, J. Sutcliffe, D. Merico, 2015, Human Genetics.

The Value of Regenotyping Older Linkage Data Sets with Denser Marker Panels

Kimberly A. Walters, V. Vieland, T. Lehner, 2014, Human Heredity.

A single nucleotide polymorphism in the dimethylarginine dimethylaminohydrolase gene is associated with lower risk of pulmonary hypertension in bronchopulmonary dysplasia

V. Vieland, J. Gastier-Foster, E. Zmuda, 2016, Acta paediatrica.

Host-to-host variation of ecological interactions in polymicrobial infections

V. Vieland, C. Jayaprakash, J. Das, 2014, Physical biology.

A multilocus model of the genetic architecture of autoimmune thyroid disorder, with clinical implications.

Veronica J Vieland, Yungui Huang, V. Vieland, 2008, American journal of human genetics.

Ascertainment bias in linkage analysis: Comments on Ginsburg et al.

V. Vieland, S. Hodge, 2005, Genetic epidemiology.

The essence of single ascertainment.

S E Hodge, V J Vieland, V. Vieland, 1996, Genetics.

The problem of ascertainment for linkage analysis.

S E Hodge, V J Vieland, V. Vieland, 1996, American journal of human genetics.

Inherent intractability of the ascertainment problem for pedigree data: a general likelihood framework.

S E Hodge, V J Vieland, V. Vieland, 1995, American journal of human genetics.

Two novel quantitative trait linkage analysis statistics based on the posterior probability of linkage: application to the COGA families

V. Vieland, C. Bartlett, 2005, BMC Genetics.

Contributors and Participants

D. Cox, A. Kong, N. Mendell, 1982 .

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

Christopher S. Poultney, Stephan J Sanders, Stephen J. Guter, 2017, Molecular Autism.

A genome-wide linkage study of autism spectrum disorder and the broad autism phenotype in extended pedigrees

S. Scherer, B. Fernandez, J. Howe, 2018, Journal of Neurodevelopmental Disorders.

Employing MCMC under the PPL framework to analyze sequence data in large pedigrees

Yungui Huang, Veronica J. Vieland, Alun Thomas, 2013, Front. Genet..

A bayesian approach to replication of linkage findings

Jian Huang, Kai Wang, Veronica J. Vieland, 1999, Genetic epidemiology.

Segregation analysis of panic disorder

V. Vieland, S. Hodge, M. Weissman, 1993 .

A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder

Stephen J. Guter, D. Pinto, S. Scherer, 2011, Human Genetics.

Cell responses only partially shape cell-to-cell variations in protein abundances in Escherichia coli chemotaxis

V. Vieland, J. Das, Sayak Mukherjee, 2013, Proceedings of the National Academy of Sciences.

SRGAP1 is a candidate gene for papillary thyroid carcinoma susceptibility.

Michael C. Ostrowski, V. Vieland, Huiling He, 2013, The Journal of clinical endocrinology and metabolism.

The effect of ascertainment on penetrance estimates for rare variants: Implications for establishing pathogenicity and for genetic counselling

V. Vieland, S. Seok, Andrew D. Paterson, 2023, bioRxiv.

Where’s the Evidence?

V. Vieland, B. Wood, 1995, Human Heredity.

Two-stage approach for identifying single-nucleotide polymorphisms associated with rheumatoid arthritis using random forests and Bayesian networks

Qiong Yang, Anita L DeStefano, Kathryn L Lunetta, 2007, BMC proceedings.