Publications by authors named "Jessica Maia"

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Construction and validity of an educational video on rapid HIV testing for young black people.
Nikaelly Pinheiro Mota, Marli Teresinha Gimeniz Galvão, Nuno Damácio de Carvalho Félix, Renata Karina Reis, Ivana Cristina Vieira de Lima Maia, Juliana Cunha Maia, Jéssica Karen de Oliveira Maia

Rev Bras Enferm· October 2025

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BOSC 2023, the 24th annual Bioinformatics Open Source Conference.
Nomi L Harris, Christopher J Fields, Karsten Hokamp, Jérémy Just, Radhika Khetani, Jessica Maia

F1000Res· December 2023

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Validation of a Guideline for Nurses Taking Care of Patients With Liver Cirrhosis in the Context of COVID-19 in the Emergency Department.
Jéssica Costa Maia, Kátia Cilene Godinho Bertoncello, Sabrina da Silva de Souza, Melissa Orlandi Honório Locks, Sabrina Regina Martins

Gastroenterol Nurs· March 2023

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Educational technologies for HIV prevention in black people: scope review.
Nikaelly Pinheiro Mota, Jéssica Karen de Oliveira Maia, Wilson Jorge Correia Pinto Abreu, Marli Teresinha Gimeniz Galvão

Rev Gaucha Enferm· January 2023

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A genome-wide screen for variants influencing certolizumab pegol response in a moderate to severe rheumatoid arthritis population.
Ian R White, Sarah E Kleinstein, Christophe Praet, Chris Chamberlain, Duncan McHale, Jessica M Maia

PLoS One· April 2022

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BOSC 2021, the 22nd Annual Bioinformatics Open Source Conference.
Nomi L Harris, Peter J A Cock, Christopher J Fields, Karsten Hokamp, Jessica Maia

F1000Res· November 2021

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The 21st annual Bioinformatics Open Source Conference (BOSC 2020, part of BCC2020).
Nomi L Harris, Peter J A Cock, Christopher J Fields, Karsten Hokamp, Jessica Maia

F1000Res· October 2020

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Evaluating whole genome sequence data from the Genetic Absence Epilepsy Rat from Strasbourg and its related non-epileptic strain.
Pablo M Casillas-Espinosa, Kim L Powell, Mingfu Zhu, C Ryan Campbell, Jessica M Maia

PLoS One· September 2017

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Leveraging prior information to detect causal variants via multi-variant regression.
Nanye Long, Samuel P Dickson, Jessica M Maia, Hee Shin Kim, Qianqian Zhu

PLoS Comput Biol· January 2014

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Prioritizing genetic variants for causality on the basis of preferential linkage disequilibrium.
Qianqian Zhu, Dongliang Ge, Erin L Heinzen, Samuel P Dickson, Thomas J Urban, Jessica M Maia

Am J Hum Genet· September 2012

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Using ERDS to infer copy-number variants in high-coverage genomes.
Mingfu Zhu, Anna C Need, Yujun Han, Dongliang Ge, Jessica M Maia

Am J Hum Genet· September 2012

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Exome sequencing followed by large-scale genotyping fails to identify single rare variants of large effect in idiopathic generalized epilepsy.
Erin L Heinzen, Chantal Depondt, Gianpiero L Cavalleri, Elizabeth K Ruzzo, Nicole M Walley, Jessica M Maia

Am J Hum Genet· August 2012

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Exome sequencing followed by large-scale genotyping suggests a limited role for moderately rare risk factors of strong effect in schizophrenia.
Anna C Need, Joseph P McEvoy, Massimo Gennarelli, Erin L Heinzen, Dongliang Ge, Jessica M Maia

Am J Hum Genet· August 2012

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A whole-genome analysis of premature termination codons.
Elizabeth T Cirulli, Erin L Heinzen, Fred S Dietrich, Kevin V Shianna, Abanish Singh, Jessica M Maia

Genomics· November 2011

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SVA: software for annotating and visualizing sequenced human genomes.
Dongliang Ge, Elizabeth K Ruzzo, Kevin V Shianna, Min He, Kimberly Pelak, Jessica M Maia

Bioinformatics· July 2011

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A genome-wide comparison of the functional properties of rare and common genetic variants in humans.
Qianqian Zhu, Dongliang Ge, Jessica M Maia, Mingfu Zhu, Slave Petrovski

Am J Hum Genet· April 2011

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Screening the human exome: a comparison of whole genome and whole transcriptome sequencing.
Elizabeth T Cirulli, Abanish Singh, Kevin V Shianna, Dongliang Ge, Jason P Smith, Jessica M Maia

Genome Biol· September 2010

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The characterization of twenty sequenced human genomes.
Kimberly Pelak, Kevin V Shianna, Dongliang Ge, Jessica M Maia, Mingfu Zhu

PLoS Genet· September 2010

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Whole-genome sequencing of a single proband together with linkage analysis identifies a Mendelian disease gene.
Nara L M Sobreira, Elizabeth T Cirulli, Dimitrios Avramopoulos, Elizabeth Wohler, Gretchen L Oswald, Jessica M Maia

PLoS Genet· June 2010

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Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes.
Erin L Heinzen, Rodney A Radtke, Thomas J Urban, Gianpiero L Cavalleri, Chantal Depondt, Jessica M Maia

Am J Hum Genet· May 2010

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Diversification in the genetic architecture of gene expression and transcriptional networks in organ differentiation of Populus.
Derek R Drost, Catherine I Benedict, Arthur Berg, Evandro Novaes, Carolina R D B Novaes, Jessica M Maia

Proc Natl Acad Sci U S A· May 2010

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Host determinants of HIV-1 control in African Americans.
Kimberly Pelak, David B Goldstein, Nicole M Walley, Jacques Fellay, Dongliang Ge, Jessica M Maia

J Infect Dis· April 2010

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A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.
Anna C Need, Deborah K Attix, Jill M McEvoy, Elizabeth T Cirulli, Kristen L Linney, Jessica M Maia

Hum Mol Genet· December 2009

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A genome-wide investigation of SNPs and CNVs in schizophrenia.
Anna C Need, Dongliang Ge, Michael E Weale, Jessica Maia, Sheng Feng

PLoS Genet· February 2009

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Tissue-specific genetic control of splicing: implications for the study of complex traits.
Erin L Heinzen, Dongliang Ge, Kenneth D Cronin, Jessica M Maia, Kevin V Shianna

PLoS Biol· December 2008

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