Arcadi Navarro

Chromosomal speciation and molecular divergence--accelerated evolution in rearranged chromosomes.

Accumulating postzygotic isolation genes in parapatry: a new twist on chromosomal speciation.

Dynamics of a human interparalog gene conversion hotspot.

Positive selection in MAOA gene is human exclusive: determination of the putative amino acid change selected in the human lineage.

Chromosomal rearrangements and the genomic distribution of gene-expression divergence in humans and chimpanzees.

Geographic stratification of linkage disequilibrium: a worldwide population study in a region of chromosome 22.

Chromosomal rearrangements are associated with higher rates of molecular evolution in mammals.

Association Cluster Detector: a tool for heuristic detection of significance clusters in whole-genome scans.

The prion protein gene in humans revisited: lessons from a worldwide resequencing study.

The portability of tagSNPs across populations: a worldwide survey.

Frequent appearance of novel protein-coding sequences by frameshift translation.

Patterns and rates of intron divergence between humans and chimpanzees.

Extreme individual marker F(ST )values do not imply population-specific selection in humans: the NRG1 example.

On the association between chromosomal rearrangements and genic evolution in humans and chimpanzees.

Statistical power analysis of neutrality tests under demographic expansions, contractions and bottlenecks with recombination.

SNP analysis to results (SNPator): a web-based environment oriented to statistical genomics analyses upon SNP data.

Balancing selection is the main force shaping the evolution of innate immunity genes.

The genomic distribution of intraspecific and interspecific sequence divergence of human segmental duplications relative to human/chimpanzee chromosomal rearrangements.

Identification of a novel risk locus for multiple sclerosis at 13q31.3 by a pooled genome-wide scan of 500,000 single nucleotide polymorphisms.

Allele-specific gene expression is widespread across the genome and biological processes.

Interrogating 11 fast-evolving genes for signatures of recent positive selection in worldwide human populations.

Genoeconomics: promises and caveats for a new field.

Decay of linkage disequilibrium within genes across HGDP-CEPH human samples: most population isolates do not show increased LD.

Chromosomal speciation revisited: rearranging theory with pieces of evidence.

Selection upon genome architecture: conservation of functional neighborhoods with changing genes.

Recent human evolution has shaped geographical differences in susceptibility to disease.

Comparative and demographic analysis of orang-utan genomes.

Genome-wide association studies pipeline (GWASpi): a desktop application for genome-wide SNP analysis and management.

Gorilla genome structural variation reveals evolutionary parallelisms with chimpanzee.

Copy number variation analysis in the great apes reveals species-specific patterns of structural variation.

HeT-A_pi1, a piRNA target sequence in the Drosophila telomeric retrotransposon HeT-A, is extremely conserved across copies and species.

The genome of melon (Cucumis melo L.).

Identification of a functional variant in the KIF5A-CYP27B1-METTL1-FAM119B locus associated with multiple sclerosis.

Accelerated exon evolution within primate segmental duplications.

The genome sequencing of an albino Western lowland gorilla reveals inbreeding in the wild.

High trans-ethnic replicability of GWAS results implies common causal variants.

Great ape genetic diversity and population history.

Application of multi-SNP approaches Bayesian LASSO and AUC-RF to detect main effects of inflammatory-gene variants associated with bladder cancer risk.

Pool and conquer: new tricks for (c)old problems.

Genome-wide analysis of wild-type Epstein-Barr virus genomes derived from healthy individuals of the 1,000 Genomes Project.

Genomic analysis of the blood attributed to Louis XVI (1754-1793), king of France.

Genetic variation in the TP53 pathway and bladder cancer risk. a comprehensive analysis.

Interplay of interlocus gene conversion and crossover in segmental duplications under a neutral scenario.

Mendelian genes for Parkinson's disease contribute to the sporadic forms of the disease.

Analysis of Five Gene Sets in Chimpanzees Suggests Decoupling between the Action of Selection on Protein-Coding and on Noncoding Elements.

Genetic and Clinical Factors Associated with Chronic Postsurgical Pain after Hernia Repair, Hysterectomy, and Thoracotomy: A Two-year Multicenter Cohort Study.

The European Genome-phenome Archive of human data consented for biomedical research.

SeDuS: segmental duplication simulator.

Pharmacogenomic study in patients with multiple sclerosis: Responders and nonresponders to IFN-β.

267 Spanish Exomes Reveal Population-Specific Differences in Disease-Related Genetic Variation.

Functional Implications of Human-Specific Changes in Great Ape microRNAs.

Assessing statistical significance in multivariable genome wide association analysis.

Demographic History of the Genus Pan Inferred from Whole Mitochondrial Genome Reconstructions.

Differences in molecular evolutionary rates among microRNAs in the human and chimpanzee genomes.

Chimpanzee genomic diversity reveals ancient admixture with bonobos.

Natural Selection in the Great Apes.

Combining Multiple Hypothesis Testing with Machine Learning Increases the Statistical Power of Genome-wide Association Studies.

Properties of human disease genes and the role of genes linked to Mendelian disorders in complex disease aetiology.

Interhemispheric gene expression differences in the cerebral cortex of humans and macaque monkeys.

Transcriptional network analysis in frontal cortex in Lewy body diseases with focus on dementia with Lewy bodies.

Erratum to: Interhemispheric gene expression differences in the cerebral cortex of humans and macaque monkeys.

Genetic factors affecting EBV copy number in lymphoblastoid cell lines derived from the 1000 Genome Project samples.

Antagonistic pleiotropy and mutation accumulation influence human senescence and disease.

The impact of endogenous content, replicates and pooling on genome capture from faecal samples.

A 3-way hybrid approach to generate a new high-quality chimpanzee reference genome (Pan_tro_3.0).

NLRP3 polymorphisms and response to interferon-beta in multiple sclerosis patients.

Potential damaging mutation in LRP5 from genome sequencing of the first reported chimpanzee with the Chiari malformation.

Similar genomic proportions of copy number variation within gray wolves and modern dog breeds inferred from whole genome sequencing.

Whole genome diversity of inherited chromosomally integrated HHV-6 derived from healthy individuals of diverse geographic origin.

Author Correction: Whole genome diversity of inherited chromosomally integrated HHV-6 derived from healthy individuals of diverse geographic origin.

Replicability and Prediction: Lessons and Challenges from GWAS.

Author Correction: Potential damaging mutation in LRP5 from genome sequencing of the first reported chimpanzee with the Chiari malformation.

Biological Processes Modulating Longevity across Primates: A Phylogenetic Genome-Phenome Analysis.

Effect of Collapsed Duplications on Diversity Estimates: What to Expect.

Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences.

A pharmacogenetic study implicates in the response to Interferon-β in multiple sclerosis.

Reply to: Retesting the influences of mutation accumulation and antagonistic pleiotropy on human senescence and disease.

Genome-phenome explorer (GePhEx): a tool for the visualization and interpretation of phenotypic relationships supported by genetic evidence.

Leveraging European infrastructures to access 1 million human genomes by 2022.

Author Correction: Leveraging European infrastructures to access 1 million human genomes by 2022.

Evolutionary History, Genomic Adaptation to Toxic Diet, and Extinction of the Carolina Parakeet.

A New Risk Variant for Multiple Sclerosis at 11q23.3 Is Associated with Expansion of Circulating Regulatory T Cells.

Copy number variants and fixed duplications among 198 rhesus macaques (Macaca mulatta).

Extreme differences between human germline and tumor mutation densities are driven by ancestral human-specific deviations.

The shared genetic architecture of schizophrenia, bipolar disorder and lifespan.

Expanding the Geographic Characterisation of Epstein-Barr Virus Variation through Gene-Based Approaches.

The Presence of Human Herpesvirus 6 in the Brain in Health and Disease.

Variation in predicted COVID-19 risk among lemurs and lorises.

Variation in predicted COVID-19 risk among lemurs and lorises.

Inversions and genomic differentiation after secondary contact: When drift contributes to maintenance, not loss, of differentiation.

Epigenomic profiling of primate lymphoblastoid cell lines reveals the evolutionary patterns of epigenetic activities in gene regulatory architectures.

Genetic Predisposition to Alzheimer's Disease Is Associated with Enlargement of Perivascular Spaces in Centrum Semiovale Region.

Comparative Analysis of Mammal Genomes Unveils Key Genomic Variability for Human Life Span.

Coexpression of the discoidin domain receptor 1 gene with oligodendrocyte-related and schizophrenia risk genes in the developing and adult human brain.

The genetic impact of an Ebola outbreak on a wild gorilla population.

Single-cell Transcriptional Changes in Neurodegenerative Diseases.

Correction: Telford et al. Expanding the Geographic Characterisation of Epstein-Barr Virus Variation through Gene-Based Approaches. 2020, , 1686.

GA4GH: International policies and standards for data sharing across genomic research and healthcare.

International federation of genomic medicine databases using GA4GH standards.

Beacon v2 and Beacon networks: A "lingua franca" for federated data discovery in biomedical genomics, and beyond.

Human herpesvirus diversity is altered in HLA class I binding peptides.

Prepandemic Alzheimer Disease Biomarkers and Anxious-Depressive Symptoms During the COVID-19 Confinement in Cognitively Unimpaired Adults.

Author Correction: Comparative and demographic analysis of orang-utan genomes.

Look-alike humans identified by facial recognition algorithms show genetic similarities.

Genetically predicted telomere length and its relationship with neurodegenerative diseases and life expectancy.

Brain transcriptomic profiling reveals common alterations across neurodegenerative and psychiatric disorders.

Genetically predicted telomere length and Alzheimer's disease endophenotypes: a Mendelian randomization study.

Polygenic risk scores enhance prediction of body mass index increase in individuals with a first episode of psychosis.

Evolutionary constraint and innovation across hundreds of placental mammals.

The landscape of tolerated genetic variation in humans and primates.

The landscape of tolerated genetic variation in humans and primates.

A global catalog of whole-genome diversity from 233 primate species.

Understanding the neurological implications of acute and long COVID using brain organoids.

CAAStools: a toolbox to identify and test Convergent Amino Acid Substitutions.

Identification of constrained sequence elements across 239 primate genomes.

Genetic characterization of the ALFA study: Uncovering genetic profiles in the Alzheimer's continuum.