Lista de obras - Bogdan Pasaniuc - Dominio Público Uruguay

A Bayesian Framework for Multiple Trait Colo-calization from Summary Association Statistics.

artículo científico publicado en 2018

A Genetic Population Isolate in The Netherlands Showing Extensive Haplotype Sharing and Long Regions of Homozygosity

artículo científico publicado en 2017

A multi-stage genome-wide association study of uterine fibroids in African Americans

artículo científico publicado en 2017

A multivariate Bernoulli model to predict DNaseI hypersensitivity status from haplotype data

artículo científico publicado en 2015

A spatial haplotype copying model with applications to genotype imputation

artículo científico publicado en 2014

A transcriptome-wide association study of high-grade serous epithelial ovarian cancer identifies new susceptibility genes and splice variants

scientific article published on 01 May 2019

Accurate estimation of SNP-heritability from biobank-scale data irrespective of genetic architecture

scientific article published on 29 July 2019

Accurate estimation of expression levels of homologous genes in RNA-seq experiments.

artículo científico publicado en 2011

Admixture mapping identifies a locus on 6q25 associated with breast cancer risk in US Latinas

artículo científico publicado en 2012

Amerindian-specific regions under positive selection harbour new lipid variants in Latinos

artículo científico publicado en 2014

Analysis of Latino populations from GALA and MEC studies reveals genomic loci with biased local ancestry estimation

artículo científico publicado en 2013

Analysis of case-control association studies with known risk variants

artículo científico publicado en 2012

Atlas of prostate cancer heritability in European and African-American men pinpoints tissue-specific regulation

artículo científico publicado en 2016

Author Correction: Large-scale transcriptome-wide association study identifies new prostate cancer risk regions

scientific article published in Nature Communications

Colocalization of GWAS and eQTL Signals Detects Target Genes

artículo científico publicado en 2016

Combining effects from rare and common genetic variants in an exome-wide association study of sequence data

artículo científico publicado en 2011

Contrasting the Genetic Architecture of 30 Complex Traits from Summary Association Data

artículo científico publicado en 2016

Credible learning of hydroxychloroquine and dexamethasone effects on COVID-19 mortality outside of randomized trials ⬇️

artículo científico publicado en 2020

Dissecting the genetics of complex traits using summary association statistics ⬇️

artículo científico publicado en 2016

Drug-Induced Epigenomic Plasticity Reprograms Circadian Rhythm Regulation to Drive Prostate Cancer toward Androgen Independence

artículo científico publicado en 2022

Enhanced localization of genetic samples through linkage-disequilibrium correction

artículo científico publicado en 2013

Enhanced methods for local ancestry assignment in sequenced admixed individuals

artículo científico publicado en 2014

Enhanced methods to detect haplotypic effects on gene expression

artículo científico publicado en 2017

Enhanced statistical tests for GWAS in admixed populations: assessment using African Americans from CARe and a Breast Cancer Consortium

artículo científico publicado en 2011

Erratum to: A multi-stage genome-wide association study of uterine fibroids in African Americans

artículo científico publicado en 2017

Estimation of regional polygenicity from GWAS provides insights into the genetic architecture of complex traits

artículo científico publicado en 2021

Extremely low-coverage sequencing and imputation increases power for genome-wide association studies

artículo científico publicado en 2012

Fast and accurate imputation of summary statistics enhances evidence of functional enrichment

artículo científico publicado en 2014

Fast and accurate inference of local ancestry in Latino populations

artículo científico publicado en 2012

Fine-mapping of lipid regions in global populations discovers ethnic-specific signals and refines previously identified lipid loci

artículo científico publicado en 2016

Genome-wide comparison of African-ancestry populations from CARe and other cohorts reveals signals of natural selection

artículo científico publicado en 2011

Genotype error detection using Hidden Markov Models of haplotype diversity.

artículo científico publicado en 2008

Highly Scalable Genotype Phasing by Entropy Minimization

artículo científico publicado en 2006

Highly scalable genotype phasing by entropy minimization.

artículo científico publicado en 2008

IBD genetics: focus on (dys) regulation in immune cells and the epithelium.

artículo científico publicado en 2014

Identification of causal genes for complex traits

artículo científico publicado en 2015

Identifying causal variants at loci with multiple signals of association

artículo científico publicado en 2014

Improved methods for multi-trait fine mapping of pleiotropic risk loci

artículo científico publicado en 2016

Inference of locus-specific ancestry in closely related populations

artículo científico publicado en 2009

Informed conditioning on clinical covariates increases power in case-control association studies

artículo científico publicado en 2012

Inhibition of activated pericentromeric SINE/Alu repeat transcription in senescent human adult stem cells reinstates self-renewal

artículo científico publicado en 2011

Integrating Gene Expression with Summary Association Statistics to Identify Genes Associated with 30 Complex Traits

artículo científico publicado en 2017

Integrating functional data to prioritize causal variants in statistical fine-mapping studies

artículo científico publicado en 2014

Integrative approaches for large-scale transcriptome-wide association studies

artículo científico publicado en 2016

Large-scale transcriptome-wide association study identifies new prostate cancer risk regions

artículo científico publicado en 2018

Leveraging Functional-Annotation Data in Trans-ethnic Fine-Mapping Studies

artículo científico publicado en 2015

Leveraging Functional-Annotation Data in Trans-ethnic Fine-Mapping Studies

Leveraging ancestry to improve causal variant identification in exome sequencing for monogenic disorders

artículo científico publicado en 2015

Leveraging genetic variability across populations for the identification of causal variants.

artículo científico publicado en 2010

Leveraging local ancestry to detect gene-gene interactions in genome-wide data

artículo científico publicado en 2015

Leveraging population admixture to characterize the heritability of complex traits

artículo científico publicado en 2014

Leveraging reads that span multiple single nucleotide polymorphisms for haplotype inference from sequencing data

artículo científico publicado en 2013

Local Genetic Correlation Gives Insights into the Shared Genetic Architecture of Complex Traits

artículo científico publicado en 2017

Methods for fine-mapping with chromatin and expression data.

artículo científico publicado en 2018

Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores

artículo científico publicado en 2015

New approaches to disease mapping in admixed populations

artículo científico publicado en 2011

Opportunities and challenges for transcriptome-wide association studies

artículo científico publicado en 2019

Partitioning gene-level contributions to complex-trait heritability by allele frequency identifies disease-relevant genes

artículo científico publicado en 2022

Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases

artículo científico publicado en 2014

Polygenic enrichment distinguishes disease associations of individual cells in single-cell RNA-seq data

artículo científico publicado en 2022

Prior diagnoses and medications as risk factors for COVID-19 in a Los Angeles Health System

artículo científico publicado en 2020

Probabilistic fine-mapping of transcriptome-wide association studies

artículo científico publicado en 2019

Prostate Cancer Susceptibility in Men of African Ancestry at 8q24

artículo científico publicado en 2016

Publisher Correction: Shared heritability and functional enrichment across six solid cancers

scientific article published on 23 September 2019

Quantifying missing heritability at known GWAS loci

artículo científico publicado en 2013

Shared heritability and functional enrichment across six solid cancers

artículo científico publicado en 2019

Shared heritability and functional enrichment across six solid cancers

Spatial localization of recent ancestors for admixed individuals

artículo científico publicado en 2014

The contribution of rare variation to prostate cancer heritability

artículo científico publicado en 2015

Transcriptome-wide association study of breast cancer risk by estrogen-receptor status

artículo científico publicado en 2020

Transcriptome-wide association study of schizophrenia and chromatin activity yields mechanistic disease insights

article

Using extended genealogy to estimate components of heritability for 23 quantitative and dichotomous traits

artículo científico publicado en 2013

Using population admixture to help complete maps of the human genome

artículo científico publicado en 2013

Whole-exome sequencing of over 4100 men of African ancestry and prostate cancer risk

artículo científico publicado en 2015

Widespread Allelic Heterogeneity in Complex Traits

artículo científico publicado en 2017

Lista de obras de Bogdan Pasaniuc

A Bayesian Framework for Multiple Trait Colo-calization from Summary Association Statistics.

A Genetic Population Isolate in The Netherlands Showing Extensive Haplotype Sharing and Long Regions of Homozygosity

A multi-stage genome-wide association study of uterine fibroids in African Americans

A multivariate Bernoulli model to predict DNaseI hypersensitivity status from haplotype data

A spatial haplotype copying model with applications to genotype imputation

A transcriptome-wide association study of high-grade serous epithelial ovarian cancer identifies new susceptibility genes and splice variants

Accurate estimation of SNP-heritability from biobank-scale data irrespective of genetic architecture

Accurate estimation of expression levels of homologous genes in RNA-seq experiments.

Admixture mapping identifies a locus on 6q25 associated with breast cancer risk in US Latinas

Amerindian-specific regions under positive selection harbour new lipid variants in Latinos

Analysis of Latino populations from GALA and MEC studies reveals genomic loci with biased local ancestry estimation

Analysis of case-control association studies with known risk variants

Atlas of prostate cancer heritability in European and African-American men pinpoints tissue-specific regulation

Author Correction: Large-scale transcriptome-wide association study identifies new prostate cancer risk regions

Colocalization of GWAS and eQTL Signals Detects Target Genes

Combining effects from rare and common genetic variants in an exome-wide association study of sequence data

Contrasting the Genetic Architecture of 30 Complex Traits from Summary Association Data

Credible learning of hydroxychloroquine and dexamethasone effects on COVID-19 mortality outside of randomized trials ⬇️

Dissecting the genetics of complex traits using summary association statistics ⬇️

Drug-Induced Epigenomic Plasticity Reprograms Circadian Rhythm Regulation to Drive Prostate Cancer toward Androgen Independence

Enhanced localization of genetic samples through linkage-disequilibrium correction

Enhanced methods for local ancestry assignment in sequenced admixed individuals

Enhanced methods to detect haplotypic effects on gene expression

Enhanced statistical tests for GWAS in admixed populations: assessment using African Americans from CARe and a Breast Cancer Consortium

Erratum to: A multi-stage genome-wide association study of uterine fibroids in African Americans

Estimation of regional polygenicity from GWAS provides insights into the genetic architecture of complex traits

Extremely low-coverage sequencing and imputation increases power for genome-wide association studies

Fast and accurate imputation of summary statistics enhances evidence of functional enrichment

Fast and accurate inference of local ancestry in Latino populations

Fine-mapping of lipid regions in global populations discovers ethnic-specific signals and refines previously identified lipid loci

Genome-wide comparison of African-ancestry populations from CARe and other cohorts reveals signals of natural selection

Genotype error detection using Hidden Markov Models of haplotype diversity.

Highly Scalable Genotype Phasing by Entropy Minimization

Highly scalable genotype phasing by entropy minimization.

IBD genetics: focus on (dys) regulation in immune cells and the epithelium.

Identification of causal genes for complex traits

Identifying causal variants at loci with multiple signals of association

Improved methods for multi-trait fine mapping of pleiotropic risk loci

Inference of locus-specific ancestry in closely related populations

Informed conditioning on clinical covariates increases power in case-control association studies

Inhibition of activated pericentromeric SINE/Alu repeat transcription in senescent human adult stem cells reinstates self-renewal

Integrating Gene Expression with Summary Association Statistics to Identify Genes Associated with 30 Complex Traits

Integrating functional data to prioritize causal variants in statistical fine-mapping studies

Integrative approaches for large-scale transcriptome-wide association studies

Large-scale transcriptome-wide association study identifies new prostate cancer risk regions

Leveraging Functional-Annotation Data in Trans-ethnic Fine-Mapping Studies

Leveraging Functional-Annotation Data in Trans-ethnic Fine-Mapping Studies

Leveraging ancestry to improve causal variant identification in exome sequencing for monogenic disorders

Leveraging genetic variability across populations for the identification of causal variants.

Leveraging local ancestry to detect gene-gene interactions in genome-wide data

Leveraging population admixture to characterize the heritability of complex traits

Leveraging reads that span multiple single nucleotide polymorphisms for haplotype inference from sequencing data

Local Genetic Correlation Gives Insights into the Shared Genetic Architecture of Complex Traits

Methods for fine-mapping with chromatin and expression data.

Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores

New approaches to disease mapping in admixed populations

Opportunities and challenges for transcriptome-wide association studies

Partitioning gene-level contributions to complex-trait heritability by allele frequency identifies disease-relevant genes

Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases

Polygenic enrichment distinguishes disease associations of individual cells in single-cell RNA-seq data

Prior diagnoses and medications as risk factors for COVID-19 in a Los Angeles Health System

Probabilistic fine-mapping of transcriptome-wide association studies

Prostate Cancer Susceptibility in Men of African Ancestry at 8q24

Publisher Correction: Shared heritability and functional enrichment across six solid cancers

Quantifying missing heritability at known GWAS loci

Shared heritability and functional enrichment across six solid cancers

Shared heritability and functional enrichment across six solid cancers

Spatial localization of recent ancestors for admixed individuals

The contribution of rare variation to prostate cancer heritability

Transcriptome-wide association study of breast cancer risk by estrogen-receptor status

Transcriptome-wide association study of schizophrenia and chromatin activity yields mechanistic disease insights

Using extended genealogy to estimate components of heritability for 23 quantitative and dichotomous traits

Using population admixture to help complete maps of the human genome

Whole-exome sequencing of over 4100 men of African ancestry and prostate cancer risk

Widespread Allelic Heterogeneity in Complex Traits