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Author Details

Christopher W Bartlett
College of Medicine, The Ohio State University
2001
51
17
PMIDPaper TitleJournal TitlePublished Year
36251081Common genetic risk factors in ASD and ADHD co-occurring families.Hum Genet2023
37686052Structural Variations Contribute to the Genetic Etiology of Autism Spectrum Disorder and Language Impairments.Int J Mol Sci2023
37761888The Rosetta Phenotype Harmonization Method Facilitates Finding a Relationship Quantitative Trait Locus for a Complex Cognitive Trait.Genes (Basel)2023
37346093EARLY CONSIDERATIONS OF GENETICS IN APHASIA REHABILITATION: A NARRATIVE REVIEW.Aphasiology2023
36625779The MPRINT Hub Data, Model, Knowledge and Research Coordination Center: Bridging the gap in maternal-pediatric therapeutics research through data integration and pharmacometrics.Pharmacotherapy2023
35105355Diagnostic Evidence GAuge of Single cells (DEGAS): a flexible deep transfer learning framework for prioritizing cells in relation to disease.Genome Med2022
35893067MicroRNA and MicroRNA-Target Variants Associated with Autism Spectrum Disorder and Related Disorders.Genes (Basel)2022
30353079Outcomes following a comprehensive versus a selective approach for infants born at 22 weeks of gestation.J Perinatol2019
31546899Forming Big Datasets through Latent Class Concatenation of Imperfectly Matched Databases Features.Genes (Basel)2019
29784061Understanding developmental language disorder - the Helsinki longitudinal SLI study (HelSLI): a study protocol.BMC Psychol2018
27826669Behavioral and Molecular Genetics of Reading-Related AM and FM Detection Thresholds.Behav Genet2017
28535206Clinical exome sequencing reports: current informatics practice and future opportunities.J Am Med Inform Assoc2017
28748334Effect of Omega-3 and -6 Supplementation on Language in Preterm Toddlers Exhibiting Autism Spectrum Disorder Symptoms.J Autism Dev Disord2017
24232733Empirically Based Profiles of the Early Literacy Skills of Children With Language Impairment in Early Childhood Special Education.J Learn Disabil2015
26251232Catechol-O-methyltransferase Val158met polymorphism interacts with early experience to predict executive functions in early childhood.Dev Psychobiol2015
26379700Evidence for the multiple hits genetic theory for inherited language impairment: a case study.Front Genet2015
26702340A Review on Genomics APIs.Comput Struct Biotechnol J2015
25791271Molecular Genetic Evidence for Shared Etiology of Autism and Prodigy.Hum Hered2015
25524419An integrative analysis of regional gene expression profiles in the human brain.Methods2015
24170272A genome scan for loci shared by autism spectrum disorder and language impairment.Am J Psychiatry2014
25237388Understanding the sequence requirements of protein families: insights from the BioVis 2013 contests.BMC Proc2014
25225892Collection and extraction of saliva DNA for next generation sequencing.J Vis Exp2014
25063350Do the symptoms of language disorder align with treatment goals? An exploratory study of primary-grade students' IEPs.J Commun Disord2014
25000815Addressing the unmet need for visualizing conditional random fields in biological data.BMC Bioinformatics2014
24611799Who is afraid of math? Two sources of genetic variance for mathematical anxiety.J Child Psychol Psychiatry2014
24007414Gene-environment interplay in child psychology and psychiatry--challenges and ways forward.J Child Psychol Psychiatry2013
23909413Gene ÿ smoking interactions on human brain gene expression: finding common mechanisms in adolescents and adults.J Child Psychol Psychiatry2013
21877231Heritability across the distribution: an application of quantile regression.Behav Genet2012
23018141Evaluation of a bayesian model integration-based method for censored data.Hum Hered2012
22704665Gene ÿ gene interaction in shared etiology of autism and specific language impairment.Biol Psychiatry2012
22607587An eQTL biological data visualization challenge and approaches from the visualization community.BMC Bioinformatics2012
22365959Defining the genetic architecture of human developmental language impairment.Life Sci2012
21193955Genetic covariation underlying reading, language and related measures in a sample selected for specific language impairment.Behav Genet2011
21611176Validation of a cost-efficient multi-purpose SNP panel for disease based research.PLoS One2011
20948219Increasing genotype-phenotype model determinism: application to bivariate reading/language traits and epistatic interactions in language-impaired families.Hum Hered2010
18349700Posterior probability of linkage analysis of autism dataset identifies linkage to chromosome 16.Psychiatr Genet2008
18485327A multilocus model of the genetic architecture of autoimmune thyroid disorder, with clinical implications.Am J Hum Genet2008
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
18046759Discussing gene-gene interaction: warning--translating equations to English may result in jabberwocky.Genet Epidemiol2007
15729670Effects of updating linkage evidence across subsets of data: reanalysis of the autism genetic resource exchange data set.Am J Hum Genet2005
16451655Calculation of multipoint likelihoods using flanking marker data: a simulation study.BMC Genet2005
16451579Two novel quantitative trait linkage analysis statistics based on the posterior probability of linkage: application to the COGA families.BMC Genet2005
15892143Evaluation of the chromosome 2q37.3 gene CENTG2 as an autism susceptibility gene.Am J Med Genet B Neuropsychiatr Genet2005
15749247Three autism candidate genes: a synthesis of human genetic analysis with other disciplines.Int J Dev Neurosci2005
15133308Examination of potential overlap in autism and language loci on chromosomes 2, 7, and 13 in two independent samples ascertained for specific language impairment.Hum Hered2004
15666342The search for autism disease genes.Ment Retard Dev Disabil Res Rev2004
14696984Specific language impairment in families: evidence for co-occurrence with reading impairments.J Speech Lang Hear Res2003
12048648A major susceptibility locus for specific language impairment is located on 13q21.Am J Hum Genet2002
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Collaborators

Linda M Brzustowicz
The State University of New Jersey
Co-authored papers 16
Veronica J Vieland
The Ohio State University
Co-authored papers 12
Steven Buyske
The State University of New Jersey
Co-authored papers 8
Marco A Azaro
The State University of New Jersey
Co-authored papers 6
Liping Hou
Harrison International Peace Hospital
Co-authored papers 6
Yungui Huang
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Anne S Bassett
Institute of Medical Science, University of Toronto
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Jinchuan Xing
The State University of New Jersey
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Samuel L Wolock
Beth Israel Deaconess Medical Center
Co-authored papers 3
LaVonne A Mangin
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Alberto M Segre
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The Research Institute at Nationwide Children's Hospital
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The Abigail Wexner Research Institute, Nationwide Children's Hospital
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Joseph Piven
Oregon Health & Science University
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Jason W Bohland
University of Pittsburgh
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Val C Sheffield
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Françoise Clerget-Darpoux
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Heike Bickeb??ller
University Medical Center Goettingen
Co-authored papers 1
Lang Li
College of Medicine, The Ohio State University
Co-authored papers 1
Ellen L Goode
Mayo Clinic College of Medicine
Co-authored papers 1
Lisa J Martin
Co-authored papers 1
Jean W MacCluer
Texas Biomedical Research Institute
Co-authored papers 1
James H Millonig
Rutgers Robert Wood Johnson Medical School, The State University of New Jersey
Co-authored papers 1
Kari E North
Co-authored papers 1
William S Bush
Cleveland Institute for Computational Biology, Case Western Reserve University
Co-authored papers 1
Elizabeth R Hauser
Duke University School of Medicine
Co-authored papers 1
Martin Krzywinski
BC Cancer Research Center
Co-authored papers 1
Peter Szatmari
Hospital for Sick Children, University of Toronto
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Jared E Hayter
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Release 1.2