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Reconstructing SNP allele and genotype frequencies from GWAS summary statistics

Scientific reports, 2022-05, Vol.12 (1), p.8242-22, Article 8242

2022

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Structure-informed clustering for population stratification in association studies

BMC bioinformatics, 2023-10, Vol.24 (1), p.1-411, Article 411

2023

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TeraPCA: a fast and scalable software package to study genetic variation in tera-scale genotypes

Bioinformatics, 2019-10, Vol.35 (19), p.3679-3683

2019

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Multiomic approach and Mendelian randomization analysis identify causal associations between blood biomarkers and subcortical brain structure volumes

NeuroImage (Orlando, Fla.), 2023-12, Vol.284, p.120466-120466, Article 120466

2023

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Variant Ranker: a web-tool to rank genomic data according to functional significance

BMC bioinformatics, 2017-07, Vol.18 (1), p.341-341, Article 341

2017

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Genome-wide association study reveals genetic architecture of eating behavior in pigs and its implications for humans obesity by comparative mapping

PloS one, 2013-08, Vol.8 (8), p.e71509-e71509

2013

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The genetic basis of Gilles de la Tourette Syndrome

Neuroscience and biobehavioral reviews, 2013-07, Vol.37 (6), p.1026-1039

Paschou, Peristera

2013

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Standing at the gateway to Europe--the genetic structure of Western balkan populations based on autosomal and haploid markers

PloS one, 2014-08, Vol.9 (8), p.e105090

2014

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Aeolus winds impact on volcanic ash early warning systems for aviation

Scientific reports, 2023-05, Vol.13 (1), p.7531-7531, Article 7531

2023

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Multivariate analysis of dopaminergic gene variants as risk factors of heroin dependence

PloS one, 2013-06, Vol.8 (6), p.e66592

2013

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Arrival of Paleo-Indians to the southern cone of South America: new clues from mitogenomes

PloS one, 2012-12, Vol.7 (12), p.e51311-e51311

2012

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CNVrd, a read-depth algorithm for assigning copy-number at the FCGR locus: population-specific tagging of copy number variation at FCGR3B

PloS one, 2013-04, Vol.8 (4), p.e63219-e63219

2013

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Polymorphisms of the UCP2 Gene Are Associated with Glomerular Filtration Rate in Type 2 Diabetic Patients and with Decreased UCP2 Gene Expression in Human Kidney

PloS one, 2015-07, Vol.10 (7), p.e0132938

2015

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PCA-correlated SNPs for structure identification in worldwide human populations

PLoS genetics, 2007-09, Vol.3 (9), p.1672-1686

2007

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Support of the histaminergic hypothesis in Tourette Syndrome: association of the histamine decarboxylase gene in a large sample of families

Journal of medical genetics, 2013-11, Vol.50 (11), p.760-764

2013

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Maritime route of colonization of Europe

Proceedings of the National Academy of Sciences - PNAS, 2014-06, Vol.111 (25), p.9211-9216

2014

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The Genetic Etiology of Tourette Syndrome: Large-Scale Collaborative Efforts on the Precipice of Discovery

Frontiers in neuroscience, 2016-08, Vol.10, p.351-351

2016

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PheWAS and cross-disorder analysis reveal genetic architecture, pleiotropic loci and phenotypic correlations across 11 autoimmune disorders

Frontiers in immunology, 2023-09, Vol.14, p.1147573

2023

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Inferring geographic coordinates of origin for Europeans using small panels of ancestry informative markers

PloS one, 2010-08, Vol.5 (8), p.e11892-e11892

2010

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Genetic variation of ITGB3 is associated with asthma in Chinese Han children

PloS one, 2013-02, Vol.8 (2), p.e56914-e56914

2013

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The distinctive geographic patterns of common pigmentation variants at the OCA2 gene

Scientific reports, 2020-09, Vol.10 (1), p.15433, Article 15433

2020

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Tourette syndrome research highlights from 2022 [version 1; peer review: 2 approved, 1 approved with reservations]

F1000 research, 2023, Vol.12, p.826

2023

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A miRNA binding site single-nucleotide polymorphism in the 3'-UTR region of the IL23R gene is associated with breast cancer

PloS one, 2012-12, Vol.7 (12), p.e49823-e49823

2012

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A global view of the OCA2-HERC2 region and pigmentation

Human genetics, 2012-05, Vol.131 (5), p.683-696

2012

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Tracing cattle breeds with principal components analysis ancestry informative SNPs

PloS one, 2011-04, Vol.6 (4), p.e18007-e18007

2011

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Reconstructing SNP allele and genotype frequencies from GWAS summary statistics

Structure-informed clustering for population stratification in association studies

TeraPCA: a fast and scalable software package to study genetic variation in tera-scale genotypes

Multiomic approach and Mendelian randomization analysis identify causal associations between blood biomarkers and subcortical brain structure volumes

Variant Ranker: a web-tool to rank genomic data according to functional significance

Genome-wide association study reveals genetic architecture of eating behavior in pigs and its implications for humans obesity by comparative mapping

The genetic basis of Gilles de la Tourette Syndrome

Standing at the gateway to Europe--the genetic structure of Western balkan populations based on autosomal and haploid markers

Aeolus winds impact on volcanic ash early warning systems for aviation

Multivariate analysis of dopaminergic gene variants as risk factors of heroin dependence

Arrival of Paleo-Indians to the southern cone of South America: new clues from mitogenomes

CNVrd, a read-depth algorithm for assigning copy-number at the FCGR locus: population-specific tagging of copy number variation at FCGR3B

Polymorphisms of the UCP2 Gene Are Associated with Glomerular Filtration Rate in Type 2 Diabetic Patients and with Decreased UCP2 Gene Expression in Human Kidney

PCA-correlated SNPs for structure identification in worldwide human populations

Support of the histaminergic hypothesis in Tourette Syndrome: association of the histamine decarboxylase gene in a large sample of families

Maritime route of colonization of Europe

The Genetic Etiology of Tourette Syndrome: Large-Scale Collaborative Efforts on the Precipice of Discovery

PheWAS and cross-disorder analysis reveal genetic architecture, pleiotropic loci and phenotypic correlations across 11 autoimmune disorders

Inferring geographic coordinates of origin for Europeans using small panels of ancestry informative markers

Genetic variation of ITGB3 is associated with asthma in Chinese Han children

The distinctive geographic patterns of common pigmentation variants at the OCA2 gene

Tourette syndrome research highlights from 2022 [version 1; peer review: 2 approved, 1 approved with reservations]

A miRNA binding site single-nucleotide polymorphism in the 3'-UTR region of the IL23R gene is associated with breast cancer

A global view of the OCA2-HERC2 region and pigmentation

Tracing cattle breeds with principal components analysis ancestry informative SNPs

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