Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discovery
出版年份 2016 全文链接
标题
Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discovery
作者
关键词
-
出版物
NATURE GENETICS
Volume 48, Issue 9, Pages 1071-1076
出版商
Springer Nature
发表日期
2016-07-19
DOI
10.1038/ng.3592
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注意:仅列出部分参考文献,下载原文获取全部文献信息。- Regional research priorities in brain and nervous system disorders
- (2015) Vijayalakshmi Ravindranath et al. NATURE
- No evidence that selection has been less effective at removing deleterious mutations in Europeans than in Africans
- (2015) Ron Do et al. NATURE GENETICS
- Identification of a large set of rare complete human knockouts
- (2015) Patrick Sulem et al. NATURE GENETICS
- Can the impact of human genetic variations be predicted?
- (2015) Yuval Itan et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Impairment of immunity to Candida and Mycobacterium in humans with bi-allelic RORC mutations
- (2015) S. Okada et al. SCIENCE
- H 3 M 2 : detection of runs of homozygosity from whole-exome sequencing data
- (2014) Alberto Magi et al. BIOINFORMATICS
- Consanguinity and genetic diseases in North Africa and immigrants to Europe
- (2014) W. A. Anwar et al. EUROPEAN JOURNAL OF PUBLIC HEALTH
- Detection of Runs of Homozygosity from Whole Exome Sequencing Data: State of the Art and Perspectives for Clinical, Population and Epidemiological Studies
- (2014) Tommaso Pippucci et al. HUMAN HEREDITY
- Association of a Low-Frequency Variant inHNF1AWith Type 2 Diabetes in a Latino Population
- (2014) Karol Estrada et al. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION
- Guidelines for genetic studies in single patients: lessons from primary immunodeficiencies
- (2014) Jean-Laurent Casanova et al. JOURNAL OF EXPERIMENTAL MEDICINE
- Altitude adaptation in Tibetans caused by introgression of Denisovan-like DNA
- (2014) Emilia Huerta-Sánchez et al. NATURE
- The genomic landscape of Neanderthal ancestry in present-day humans
- (2014) Sriram Sankararaman et al. NATURE
- Guidelines for investigating causality of sequence variants in human disease
- (2014) D. G. MacArthur et al. NATURE
- The deleterious mutation load is insensitive to recent population history
- (2014) Yuval B Simons et al. NATURE GENETICS
- A Genetic Atlas of Human Admixture History
- (2014) G. Hellenthal et al. SCIENCE
- Exome Sequencing Links Corticospinal Motor Neuron Disease to Common Neurodegenerative Disorders
- (2014) G. Novarino et al. SCIENCE
- Long Runs of Homozygosity Are Enriched for Deleterious Variation
- (2013) Zachary A. Szpiech et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Neanderthal and Denisova genetic affinities with contemporary humans: Introgression versus common ancestral polymorphisms
- (2013) Robert K. Lowery et al. GENE
- Apparent Variation in Neanderthal Admixture among African Populations is Consistent with Gene Flow from Non-African Populations
- (2013) Shuoguo Wang et al. Genome Biology and Evolution
- RefSeq: an update on mammalian reference sequences
- (2013) Kim D. Pruitt et al. NUCLEIC ACIDS RESEARCH
- Gene flow from North Africa contributes to differential human genetic diversity in southern Europe
- (2013) L. R. Botigue et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Autozygome Sequencing Expands the Horizon of Human Knockout Research and Provides Novel Insights into Human Phenotypic Variation
- (2013) Ahmed B. Alsalem et al. PLoS Genetics
- Reconstructing the Population Genetic History of the Caribbean
- (2013) Andrés Moreno-Estrada et al. PLoS Genetics
- Genomic Patterns of Homozygosity in Worldwide Human Populations
- (2012) Trevor J. Pemberton et al. AMERICAN JOURNAL OF HUMAN GENETICS
- A program for annotating and predicting the effects of single nucleotide polymorphisms, SnpEff
- (2012) Pablo Cingolani et al. FLY
- Patterns and rates of exonic de novo mutations in autism spectrum disorders
- (2012) Benjamin M. Neale et al. NATURE
- A High-Coverage Genome Sequence from an Archaic Denisovan Individual
- (2012) M. Meyer et al. SCIENCE
- A Systematic Survey of Loss-of-Function Variants in Human Protein-Coding Genes
- (2012) D. G. MacArthur et al. SCIENCE
- Genomic Ancestry of North Africans Supports Back-to-Africa Migrations
- (2012) Brenna M. Henn et al. PLoS Genetics
- Inference of Population Splits and Mixtures from Genome-Wide Allele Frequency Data
- (2012) Joseph K. Pickrell et al. PLoS Genetics
- The variant call format and VCFtools
- (2011) P. Danecek et al. BIOINFORMATICS
- Consanguinity around the world: what do the genomic data of the HGDP-CEPH diversity panel tell us?
- (2011) Anne-Louise Leutenegger et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- A framework for variation discovery and genotyping using next-generation DNA sequencing data
- (2011) Mark A DePristo et al. NATURE GENETICS
- Erratum: Hereditary spastic paraplegias: membrane traffic and the motor pathway
- (2011) Craig Blackstone et al. NATURE REVIEWS NEUROSCIENCE
- Population Genetic Structure of the People of Qatar
- (2010) Haley Hunter-Zinck et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Robust relationship inference in genome-wide association studies
- (2010) Ani Manichaikul et al. BIOINFORMATICS
- Fast and accurate long-read alignment with Burrows–Wheeler transform
- (2010) Heng Li et al. BIOINFORMATICS
- BEDTools: a flexible suite of utilities for comparing genomic features
- (2010) Aaron R. Quinlan et al. BIOINFORMATICS
- Comparative assessment of methods for estimating individual genome-wide homozygosity-by-descent from human genomic data
- (2010) Ozren Polašek et al. BMC GENOMICS
- The genome-wide structure of the Jewish people
- (2010) Doron M. Behar et al. NATURE
- A method and server for predicting damaging missense mutations
- (2010) Ivan A Adzhubei et al. NATURE METHODS
- ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data
- (2010) K. Wang et al. NUCLEIC ACIDS RESEARCH
- A Draft Sequence of the Neandertal Genome
- (2010) R. E. Green et al. SCIENCE
- Identifying a High Fraction of the Human Genome to be under Selective Constraint Using GERP++
- (2010) Eugene V. Davydov et al. PLoS Computational Biology
- Prevalence of hereditary ataxia and spastic paraplegia in southeast Norway: a population-based study
- (2009) A. K. Erichsen et al. BRAIN
- Fast model-based estimation of ancestry in unrelated individuals
- (2009) D. H. Alexander et al. GENOME RESEARCH
- Consanguinity and reproductive health among Arabs
- (2009) Ghazi O Tadmouri et al. Reproductive Health
- Worldwide Human Relationships Inferred from Genome-Wide Patterns of Variation
- (2008) J. Z. Li et al. SCIENCE
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