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Author Details
Full Name
Jessica M Maia
Affiliation
Institute for Genomic Medicine, Columbia University
ORCID
Career Start Year
2001
Papers
21
H Index
15
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
35413058
A genome-wide screen for variants influencing certolizumab pegol response in a moderate to severe rheumatoid arthritis population.
PLoS One
2022
34721839
BOSC 2021, the 22nd Annual Bioinformatics Open Source Conference.
F1000Res
2021
28708842
Evaluating whole genome sequence data from the Genetic Absence Epilepsy Rat from Strasbourg and its related non-epileptic strain.
PLoS One
2017
23762022
Leveraging prior information to detect causal variants via multi-variant regression.
PLoS Comput Biol
2013
22863189
Exome sequencing followed by large-scale genotyping fails to identify single rare variants of large effect in idiopathic generalized epilepsy.
Am J Hum Genet
2012
22939633
Using ERDS to infer copy-number variants in high-coverage genomes.
Am J Hum Genet
2012
22939045
Prioritizing genetic variants for causality on the basis of preferential linkage disequilibrium.
Am J Hum Genet
2012
22863191
Exome sequencing followed by large-scale genotyping suggests a limited role for moderately rare risk factors of strong effect in schizophrenia.
Am J Hum Genet
2012
21457907
A genome-wide comparison of the functional properties of rare and common genetic variants in humans.
Am J Hum Genet
2011
21803148
A whole-genome analysis of premature termination codons.
Genomics
2011
21624899
SVA: software for annotating and visualizing sequenced human genomes.
Bioinformatics
2011
20404162
Diversification in the genetic architecture of gene expression and transcriptional networks in organ differentiation of Populus.
Proc Natl Acad Sci U S A
2010
20838461
The characterization of twenty sequenced human genomes.
PLoS Genet
2010
20577567
Whole-genome sequencing of a single proband together with linkage analysis identifies a Mendelian disease gene.
PLoS Genet
2010
20598109
Screening the human exome: a comparison of whole genome and whole transcriptome sequencing.
Genome Biol
2010
20205591
Host determinants of HIV-1 control in African Americans.
J Infect Dis
2010
20398883
Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes.
Am J Hum Genet
2010
19197363
A genome-wide investigation of SNPs and CNVs in schizophrenia.
PLoS Genet
2009
19734545
A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.
Hum Mol Genet
2009
19222302
Tissue-specific genetic control of splicing: implications for the study of complex traits.
PLoS Biol
2008
11793674
The importance of connections: joining components of the Hutterite pedigree.
Genet Epidemiol
2001
1 - 21 of 21
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