标题
Haploinsufficiency predictions without study bias
作者
关键词
-
出版物
NUCLEIC ACIDS RESEARCH
Volume 43, Issue 15, Pages e101-e101
出版商
Oxford University Press (OUP)
发表日期
2015-05-23
DOI
10.1093/nar/gkv474
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- A Proteome-Scale Map of the Human Interactome Network
- (2014) Thomas Rolland et al. CELL
- Bias tradeoffs in the creation and analysis of protein–protein interaction networks
- (2014) Jesse Gillis et al. Journal of Proteomics
- Synaptic, transcriptional and chromatin genes disrupted in autism
- (2014) Silvia De Rubeis et al. NATURE
- The role of de novo mutations in the genetics of autism spectrum disorders
- (2014) Michael Ronemus et al. NATURE REVIEWS GENETICS
- Phenotype Ontologies and Cross-Species Analysis for Translational Research
- (2014) Peter N. Robinson et al. PLoS Genetics
- The Roles of FMRP-Regulated Genes in Autism Spectrum Disorder: Single- and Multiple-Hit Genetic Etiologies
- (2013) Julia Steinberg et al. AMERICAN JOURNAL OF HUMAN GENETICS
- The Genotype-Tissue Expression (GTEx) project
- (2013) John Lonsdale et al. NATURE GENETICS
- Interpretation of Genomic Variants Using a Unified Biological Network Approach
- (2013) Ekta Khurana et al. PLoS Computational Biology
- From Mouse to Human: Evolutionary Genomics Analysis of Human Orthologs of Essential Genes
- (2013) Benjamin Georgi et al. PLoS Genetics
- Genic Intolerance to Functional Variation and the Interpretation of Personal Genomes
- (2013) Slavé Petrovski et al. PLoS Genetics
- Patterns and rates of exonic de novo mutations in autism spectrum disorders
- (2012) Benjamin M. Neale et al. NATURE
- De novo mutations revealed by whole-exome sequencing are strongly associated with autism
- (2012) Stephan J. Sanders et al. NATURE
- Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations
- (2012) Brian J. O’Roak et al. NATURE
- De Novo Gene Disruptions in Children on the Autistic Spectrum
- (2012) Ivan Iossifov et al. NEURON
- COXPRESdb: a database of comparative gene coexpression networks of eleven species for mammals
- (2012) Takeshi Obayashi et al. NUCLEIC ACIDS RESEARCH
- A Systematic Survey of Loss-of-Function Variants in Human Protein-Coding Genes
- (2012) D. G. MacArthur et al. SCIENCE
- Genes and biological processes commonly disrupted in rare and heterogeneous developmental delay syndromes
- (2010) Tamim H. Shaikh et al. HUMAN MOLECULAR GENETICS
- Characterising and Predicting Haploinsufficiency in the Human Genome
- (2010) Ni Huang et al. PLoS Genetics
- Origins and functional impact of copy number variation in the human genome
- (2009) Donald F. Conrad et al. NATURE
- Identification of human haploinsufficient genes and their genomic proximity to segmental duplications
- (2008) Vinh T Dang et al. EUROPEAN JOURNAL OF HUMAN GENETICS
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