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Author Details

Jessica M Maia
Institute for Genomic Medicine, Columbia University
2001
21
15
PMIDPaper TitleJournal TitlePublished Year
35413058A genome-wide screen for variants influencing certolizumab pegol response in a moderate to severe rheumatoid arthritis population.PLoS One2022
34721839BOSC 2021, the 22nd Annual Bioinformatics Open Source Conference.F1000Res2021
28708842Evaluating whole genome sequence data from the Genetic Absence Epilepsy Rat from Strasbourg and its related non-epileptic strain.PLoS One2017
23762022Leveraging prior information to detect causal variants via multi-variant regression.PLoS Comput Biol2013
22863189Exome sequencing followed by large-scale genotyping fails to identify single rare variants of large effect in idiopathic generalized epilepsy.Am J Hum Genet2012
22939633Using ERDS to infer copy-number variants in high-coverage genomes.Am J Hum Genet2012
22939045Prioritizing genetic variants for causality on the basis of preferential linkage disequilibrium.Am J Hum Genet2012
22863191Exome sequencing followed by large-scale genotyping suggests a limited role for moderately rare risk factors of strong effect in schizophrenia.Am J Hum Genet2012
21457907A genome-wide comparison of the functional properties of rare and common genetic variants in humans.Am J Hum Genet2011
21803148A whole-genome analysis of premature termination codons.Genomics2011
21624899SVA: software for annotating and visualizing sequenced human genomes.Bioinformatics2011
20404162Diversification in the genetic architecture of gene expression and transcriptional networks in organ differentiation of Populus.Proc Natl Acad Sci U S A2010
20838461The characterization of twenty sequenced human genomes.PLoS Genet2010
20577567Whole-genome sequencing of a single proband together with linkage analysis identifies a Mendelian disease gene.PLoS Genet2010
20598109Screening the human exome: a comparison of whole genome and whole transcriptome sequencing.Genome Biol2010
20205591Host determinants of HIV-1 control in African Americans.J Infect Dis2010
20398883Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes.Am J Hum Genet2010
19197363A genome-wide investigation of SNPs and CNVs in schizophrenia.PLoS Genet2009
19734545A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.Hum Mol Genet2009
19222302Tissue-specific genetic control of splicing: implications for the study of complex traits.PLoS Biol2008
11793674The importance of connections: joining components of the Hutterite pedigree.Genet Epidemiol2001
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Collaborators

Institute for Genomic Medicine, Columbia University Irving Medical Center
Co-authored papers 16
Illumina Inc. 5200 Illumina Way
Co-authored papers 15
Department of Pharmacy, Liyang People's Hospital
Co-authored papers 14
University of North Carolina at Chapel Hill.
Co-authored papers 13
Duke University
Co-authored papers 9
Imperial College London
Co-authored papers 8
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Co-authored papers 7
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Human Vaccine Institute, Duke University Medical Center Durham
Co-authored papers 4
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Duke University School of Medicine and Duke Health System
Co-authored papers 3
Hopital Universitaire de Bruxelles - Hopital Erasme
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Co-authored papers 2
Johns Hopkins University
Co-authored papers 2
Ecole Polytechnique Federale de Lausanne
Co-authored papers 2
Duke University School of Medicine, USA Veterans Affairs Medical Center
Co-authored papers 2
Genomics England Ltd.
Co-authored papers 2
Johns Hopkins University
Co-authored papers 2
School of Pharmacy and Biomolecular Sciences, Ireland FutureNeuro SFI Research Centre
Co-authored papers 2
Duke Clinical Research Institute, Duke University School of Medicine
Co-authored papers 2
FutureNeuro SFI Research Centre, The Royal College of Surgeons in Ireland
Co-authored papers 2
UCL Institute of Neurology
Co-authored papers 2
Duke University Medical Center
Co-authored papers 2
Duke University School of Medicine
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