Author details

Full Name

Pau Navarro

Affiliation

ORCID

Career Start Year

2000

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
36918541	Genetic architecture of spatial electrical biomarkers for cardiac arrhythmia and relationship with cardiovascular disease.	Nat Commun	2023
37034613	Unraveling Neuro-Proteogenomic Landscape and Therapeutic Implications for Human Behaviors and Psychiatric Disorders.	Res Sq	2023
36711749	Phenome-wide analysis identifies parent-of-origin effects on the human methylome associated with changes in the rate of aging.		2023
36824751	Genetic mechanisms of 184 neuro-related proteins in human plasma.	medRxiv	2023
37189164	Phenome-wide analyses identify an association between the parent-of-origin effects dependent methylome and the rate of aging in humans.		2023
35303797	Effect of genotyping strategies on the sustained benefit of single-step genomic BLUP over multiple generations.	Genetics Selection Evolution	2022
35953587	A multi-tissue atlas of regulatory variants in cattle.	Nature Genetics	2022
36050321	Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways.	Nat Commun	2022
36532132	The impact of SNP density on quantitative genetic analyses of body size traits in a wild population of Soay sheep.		2022
35332118	Genetic regulation of post-translational modification of two distinct proteins.	Nature Communications	2022
35069690	SNP and Haplotype Regional Heritability Mapping (SNHap-RHM): Joint Mapping of Common and Rare Variation Affecting Complex Traits.	Frontiers in Genetics	2021
33558525	Publisher Correction: Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.	Nat Commun	2021
33402679	Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.	Nat Commun	2021
34857772	Mapping the serum proteome to neurological diseases using whole genome sequencing.	Nat Commun	2021
34499657	Genome-wide methylation data improves dissection of the effect of smoking on body mass index.	PLoS Genetics	2021
34883445	Lifestyle and Genetic Factors Modify Parent-of-Origin Effects on the Human Methylome.	eBioMedicine	2021
31696970	Genomic regions influencing intramuscular fat in divergently selected rabbit lines.	Animal Genetics	2020
31043600	Publisher Correction: Parent of origin genetic effects on methylation in humans are common and influence complex trait variation.	Nat Commun	2019
30918249	Parent of origin genetic effects on methylation in humans are common and influence complex trait variation.	Nat Commun	2019
31481615	The genetic landscape of Scotland and the Isles.	Proc Natl Acad Sci U S A	2019
29321673	Genomic analysis of family data reveals additional genetic effects on intelligence and personality.	Molecular Psychiatry	2018
29563569	Haplotype Heritability Mapping Method Uncovers Missing Heritability of Complex Traits.	Scientific Reports	2018
29170203	Identification of a novel locus on chromosome 2q13, which predisposes to clinical vertebral fractures independently of bone density.	Ann Rheum Dis	2018
28153336	Genome-wide Regional Heritability Mapping Identifies a Locus Within the TOX2 Gene Associated With Major Depressive Disorder.	Biol Psychiatry	2017
28986520	Regional variation in health is predominantly driven by lifestyle rather than genetics.	Nature Communications	2017
28380033	Antagonistic genetic correlations for milking traits within the genome of dairy cattle.	PLoS ONE	2017
28898252	Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis.	PLoS Med	2017
28448500	Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults.	PLoS Genet	2017
28443625	Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits.	Nat Commun	2017
28832619	Correction: Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults.	PLoS Genet	2017
28436984	Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk.	Nat Genet	2017
30093824	The effect of increasing lifespan and recycling rate on carbon storage in wood products from theoretical model to application for the European wood sector.	Mitigation and Adaptation Strategies for Global Change	2017
27422368	A Combined Pathway and Regional Heritability Analysis Indicates NETRIN1 Pathway Is Associated With Major Depressive Disorder.	Biol Psychiatry	2017
28270201	Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants.	Genome Med	2017
28196069	Correction: Pedigree- and SNP-Associated Genetics and Recent Environment are the Major Contributors to Anthropometric and Cardiometabolic Trait Variation.	PLoS Genetics	2017
27838479	Shared Genetics and Couple-Associated Environment Are Major Contributors to the Risk of Both Clinical and Self-Declared Depression.	eBioMedicine	2016
26836320	Pedigree- and SNP-Associated Genetics and Recent Environment are the Major Contributors to Anthropometric and Cardiometabolic Trait Variation.	PLoS Genetics	2016
26868669	Erratum to: Genetic determination of height-mediated mate choice.		2016
26781582	Genetic determination of height-mediated mate choice.		2016
26824792	Modelling carbon stocks and fluxes in the wood product sector: a comparative review.	Global Change Biology	2016
27036123	Meta-analysis of 49â¿¿549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levels.	J Med Genet	2016
26561523	A meta-analysis of 120 246 individuals identifies 18 new loci for fibrinogen concentration.	Hum Mol Genet	2016
26696135	Regional heritability mapping method helps explain missing heritability of blood lipid traits in isolated populations.	Heredity	2016
26242864	Multicohort analysis of the maternal age effect on recombination.	Nat Commun	2015
28721259	Fine mapping the <i>CETP</i> region reveals a common intronic insertion associated to HDL-C.	NPJ Aging Mech Dis	2015
25918167	Genomic prediction of complex human traits: relatedness, trait architecture and predictive meta-models.	Human Molecular Genetics	2015
25811787	Modulation of genetic associations with serum urate levels by body-mass-index in humans.	PLoS One	2015
26131930	Directional dominance on stature and cognition inÂ diverse human populations.	Nature	2015
26048416	Recent genomic heritage in Scotland.	BMC Genomics	2015
26635082	Sixteen new lung function signals identified through 1000 Genomes Project reference panel imputation.	Nat Commun	2015