J. Maia

发表

Using ERDS to infer copy-number variants in high-coverage genomes.

K. Shianna, D. Ge, A. Need, 2012, American journal of human genetics.

Screening the human exome: a comparison of whole genome and whole transcriptome sequencing

David B Goldstein, James J Goedert, Jason P Smith, 2010, Genome Biology.

Tissue-Specific Genetic Control of Splicing: Implications for the Study of Complex Traits

K. Shianna, D. Ge, D. Goldstein, 2008, PLoS biology.

The Characterization of Twenty Sequenced Human Genomes

Elizabeth T. Cirulli, Jacques Fellay, David B. Goldstein, 2010, PLoS genetics.

Whole-Genome Sequencing of a Single Proband Together with Linkage Analysis Identifies a Mendelian Disease Gene

Elizabeth T. Cirulli, Jonathan Pevsner, David B. Goldstein, 2010, PLoS genetics.

A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.

Gail Clement, Gail P. Clement, Greg Gibson, 2009, Human molecular genetics.

Exome sequencing followed by large-scale genotyping fails to identify single rare variants of large effect in idiopathic generalized epilepsy.

K. Shianna, D. Ge, A. Need, 2012, American journal of human genetics.

A genome-wide comparison of the functional properties of rare and common genetic variants in humans.

Qianqian Zhu, Slave Petrovski, Samuel P. Dickson, 2011, American journal of human genetics.

Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes.

Michael R. Johnson, Josemir W Sander, P. Matthews, 2010, American journal of human genetics.

A Genome-Wide Investigation of SNPs and CNVs in Schizophrenia

David B. Goldstein, Lefkos T. Middleton, Hans-Jürgen Möller, 2009, PLoS genetics.

Diversification in the genetic architecture of gene expression and transcriptional networks in organ differentiation of Populus

Evandro Novaes, Arthur Berg, John S. Yap, 2010, Proceedings of the National Academy of Sciences.

Exome sequencing followed by large-scale genotyping suggests a limited role for moderately rare risk factors of strong effect in schizophrenia.

Jari Tiihonen, Herbert Y Meltzer, David B Goldstein, 2012, American journal of human genetics.

SVA: software for annotating and visualizing sequenced human genomes

Elizabeth T. Cirulli, Min He, Dongliang Ge, 2011, Bioinform..

Host determinants of HIV-1 control in African Americans.

K. Shianna, D. Ge, D. Goldstein, 2010, The Journal of infectious diseases.

A genome-wide screen for variants influencing certolizumab pegol response in a moderate to severe rheumatoid arthritis population

J. Maia, P. Shea, T. Urban, 2022, PloS one.

Prioritizing genetic variants for causality on the basis of preferential linkage disequilibrium.

Qianqian Zhu, David B Goldstein, K. Shianna, 2012, American journal of human genetics.

Correction: A Genome-Wide Investigation of SNPs and CNVs in Schizophrenia

D. Rujescu, P. Muglia, C. Francks, 2009, PLoS Genetics.

A whole-genome analysis of premature termination codons.

K. Shianna, D. Goldstein, J. Goedert, 2011, Genomics.

Evaluating whole genome sequence data from the Genetic Absence Epilepsy Rat from Strasbourg and its related non-epileptic strain

Pablo M. Casillas-Espinosa, S. Petrovski, Mingfu Zhu, 2017, PLoS ONE.

Studies in Theoretical Biology: A Collection of Undergraduate Research

Carlos Castillo-Chavez, Jaime Astacio, DelMar Briere, 1996 .

The Importance of Connections: Joining Components of the Hutterite Pedigree

E. Wijsman, M. Bogdan, A. Leutenegger, 2001, Genetic epidemiology.

BOSC 2021, the 22nd Annual Bioinformatics Open Source Conference

Christopher J. Fields, K. Hokamp, N. Harris, 2021, F1000Research.

Leveraging Prior Information to Detect Causal Variants via Multi-Variant Regression

Qianqian Zhu, Andrew S. Allen, Jessica M. Maia, 2013, PLoS Comput. Biol..

Screening the human exome: a comparison of whole genome and whole transcriptome sequencing

K. Shianna, J. Goedert, J. Maia, 2010, Genome Biology.