Lista de obras - Marcin Imielinski - Dominio Público Uruguay

17q12-21 variants interact with smoke exposure as a risk factor for pediatric asthma but are equally associated with early-onset versus late-onset asthma in North Americans of European ancestry

article

A Genomic-Pathologic Annotated Risk Model to Predict Recurrence in Early-Stage Lung Adenocarcinoma

artículo científico publicado en 2020

A genome-wide meta-analysis of six type 1 diabetes cohorts identifies multiple associated loci

scientific journal article

A landscape of driver mutations in melanoma

artículo científico publicado en 2012

A pan-cancer analysis of transcriptome changes associated with somatic mutations in U2AF1 reveals commonly altered splicing events

artículo científico publicado en 2014

Analyses of non-coding somatic drivers in 2,658 cancer whole genomes

artículo científico publicado en 2020

Association analysis of the FTO gene with obesity in children of Caucasian and African ancestry reveals a common tagging SNP.

artículo científico publicado en 2008

Association of the BANK 1 R61H variant with systemic lupus erythematosus in Americans of European and African ancestry.

artículo científico publicado en 2009

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

artículo científico publicado en 2009

Breaking new ground in inflammatory bowel disease genetics: genome-wide association studies and beyond

artículo científico publicado en 2010

Common genetic variants on 5p14.1 associate with autism spectrum disorders

artículo científico publicado en 2009

Common variants at five new loci associated with early-onset inflammatory bowel disease

artículo científico publicado en 2009

Comparative genetic analysis of inflammatory bowel disease and type 1 diabetes implicates multiple loci with opposite effects

artículo científico publicado en 2010

Deep Convolutional Neural Networks Enable Discrimination of Heterogeneous Digital Pathology Images

artículo científico publicado en 2017

Deep epistasis in human metabolism

artículo científico publicado en 2010

Distinct Classes of Complex Structural Variation Uncovered across Thousands of Cancer Genome Graphs

scientific article published on 01 October 2020

Distinct patterns of somatic genome alterations in lung adenocarcinomas and squamous cell carcinomas

artículo científico publicado en 2016

Diverse genome-wide association studies associate the IL12/IL23 pathway with Crohn Disease

artículo científico publicado en 2009

Duplication of the SLIT3 locus on 5q35.1 predisposes to major depressive disorder

artículo científico publicado en 2010

Erratum: Corrigendum: Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47

scholarly article published in Nature Genetics

Erratum: Corrigendum: Signatures of mutational processes in human cancer

artículo científico publicado en 2013

Exploiting the pathway structure of metabolism to reveal high-order epistasis

artículo científico

Follow-up analysis of genome-wide association data identifies novel loci for type 1 diabetes

artículo científico publicado en 2008

Functional analysis of receptor tyrosine kinase mutations in lung cancer identifies oncogenic extracellular domain mutations of ERBB2.

artículo científico publicado en 2012

Fusion oncogenes-genetic musical chairs

scientific article published on 01 August 2018

Genetic modifiers of EGFR dependence in non-small cell lung cancer

artículo científico publicado en 2014

Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes

artículo científico publicado en 2009

Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder

artículo científico publicado en 2011

High-resolution mapping and analysis of copy number variations in the human genome: a data resource for clinical and research applications.

artículo científico publicado en 2009

High-throughput Phenotyping of Lung Cancer Somatic Mutations

artículo científico publicado en 2016

High-throughput Phenotyping of Lung Cancer Somatic Mutations

artículo científico publicado en 2017

Histone H1 loss drives lymphoma by disrupting 3D chromatin architecture ⬇️

artículo científico publicado en 2020

Identification of focally amplified lineage-specific super-enhancers in human epithelial cancers

artículo científico publicado en 2015

Impact of Lineage Plasticity to and from a Neuroendocrine Phenotype on Progression and Response in Prostate and Lung Cancers

artículo científico publicado en 2020

Insertions and Deletions Target Lineage-Defining Genes in Human Cancers

artículo científico publicado en 2017

Integrated Proteomic, Transcriptomic, and Biological Network Analysis of Breast Carcinoma Reveals Molecular Features of Tumorigenesis and Clinical Relapse ⬇️

artículo científico publicado el 12 de enero de 2012

Investigation of the locus near MC4R with childhood obesity in Americans of European and African ancestry

artículo científico publicado en 2009

Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease

artículo científico publicado en 2008

Mapping the hallmarks of lung adenocarcinoma with massively parallel sequencing

artículo científico publicado en 2012

Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47

scientific journal article

Metabolic networks analysis using convex optimization

article

Modeling cancer rearrangement landscapes.

artículo científico publicado en 2016

Mutational heterogeneity in cancer and the search for new cancer-associated genes

artículo científico publicado en 2013

Next-generation characterization of the Cancer Cell Line Encyclopedia

artículo científico publicado en 2019

ORMDL3 variants associated with asthma susceptibility in North Americans of European ancestry.

artículo científico publicado en 2008

Oncogenic and sorafenib-sensitive ARAF mutations in lung adenocarcinoma

artículo científico publicado en 2014

Patterns of somatic structural variation in human cancer genomes

artículo científico publicado en 2020

Portraits of genetic intra-tumour heterogeneity and subclonal selection across cancer types

Prostate cancer: Clinical hallmarks in whole cancer genomes

artículo científico publicado en 2017

Selective and mechanistic sources of recurrent rearrangements across the cancer genome

Shotgun Transcriptome and Isothermal Profiling of SARS-CoV-2 Infection Reveals Unique Host Responses, Viral Diversification, and Drug Interactions

artículo científico publicado en 2020

Shotgun transcriptome, spatial omics, and isothermal profiling of SARS-CoV-2 infection reveals unique host responses, viral diversification, and drug interactions

artículo científico publicado en 2021

Signatures of mutational processes in human cancer

artículo científico publicado en 2013

Strong synaptic transmission impact by copy number variations in schizophrenia

artículo científico publicado en 2010

Structural variant evolution after telomere crisis

artículo científico publicado en 2021

SvABA: genome-wide detection of structural variants and indels by local assembly.

artículo científico publicado en 2018

Systematic analysis of conservation relations in Escherichia coli genome-scale metabolic network reveals novel growth media

artículo científico publicado en 2006

Systemic Tissue and Cellular Disruption from SARS-CoV-2 Infection revealed in COVID-19 Autopsies and Spatial Omics Tissue Maps

artículo científico publicado en 2021

The cancer precision medicine knowledge base for structured clinical-grade mutations and interpretations

artículo científico publicado en 2016

The evolutionary history of 2,658 cancers

artículo científico publicado en 2020

Variants of DENND1B associated with asthma in children

artículo científico publicado en 2009

Lista de obras de Marcin Imielinski

17q12-21 variants interact with smoke exposure as a risk factor for pediatric asthma but are equally associated with early-onset versus late-onset asthma in North Americans of European ancestry

A Genomic-Pathologic Annotated Risk Model to Predict Recurrence in Early-Stage Lung Adenocarcinoma

A genome-wide meta-analysis of six type 1 diabetes cohorts identifies multiple associated loci

A landscape of driver mutations in melanoma

A pan-cancer analysis of transcriptome changes associated with somatic mutations in U2AF1 reveals commonly altered splicing events

Analyses of non-coding somatic drivers in 2,658 cancer whole genomes

Association analysis of the FTO gene with obesity in children of Caucasian and African ancestry reveals a common tagging SNP.

Association of the BANK 1 R61H variant with systemic lupus erythematosus in Americans of European and African ancestry.

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

Breaking new ground in inflammatory bowel disease genetics: genome-wide association studies and beyond

Common genetic variants on 5p14.1 associate with autism spectrum disorders

Common variants at five new loci associated with early-onset inflammatory bowel disease

Comparative genetic analysis of inflammatory bowel disease and type 1 diabetes implicates multiple loci with opposite effects

Deep Convolutional Neural Networks Enable Discrimination of Heterogeneous Digital Pathology Images

Deep epistasis in human metabolism

Distinct Classes of Complex Structural Variation Uncovered across Thousands of Cancer Genome Graphs

Distinct patterns of somatic genome alterations in lung adenocarcinomas and squamous cell carcinomas

Diverse genome-wide association studies associate the IL12/IL23 pathway with Crohn Disease

Duplication of the SLIT3 locus on 5q35.1 predisposes to major depressive disorder

Erratum: Corrigendum: Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47

Erratum: Corrigendum: Signatures of mutational processes in human cancer

Exploiting the pathway structure of metabolism to reveal high-order epistasis

Follow-up analysis of genome-wide association data identifies novel loci for type 1 diabetes

Functional analysis of receptor tyrosine kinase mutations in lung cancer identifies oncogenic extracellular domain mutations of ERBB2.

Fusion oncogenes-genetic musical chairs

Genetic modifiers of EGFR dependence in non-small cell lung cancer

Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes

Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder

High-resolution mapping and analysis of copy number variations in the human genome: a data resource for clinical and research applications.

High-throughput Phenotyping of Lung Cancer Somatic Mutations

High-throughput Phenotyping of Lung Cancer Somatic Mutations

Histone H1 loss drives lymphoma by disrupting 3D chromatin architecture ⬇️

Identification of focally amplified lineage-specific super-enhancers in human epithelial cancers

Impact of Lineage Plasticity to and from a Neuroendocrine Phenotype on Progression and Response in Prostate and Lung Cancers

Insertions and Deletions Target Lineage-Defining Genes in Human Cancers

Integrated Proteomic, Transcriptomic, and Biological Network Analysis of Breast Carcinoma Reveals Molecular Features of Tumorigenesis and Clinical Relapse ⬇️

Investigation of the locus near MC4R with childhood obesity in Americans of European and African ancestry

Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease

Mapping the hallmarks of lung adenocarcinoma with massively parallel sequencing

Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47

Metabolic networks analysis using convex optimization

Modeling cancer rearrangement landscapes.

Mutational heterogeneity in cancer and the search for new cancer-associated genes

Next-generation characterization of the Cancer Cell Line Encyclopedia

ORMDL3 variants associated with asthma susceptibility in North Americans of European ancestry.

Oncogenic and sorafenib-sensitive ARAF mutations in lung adenocarcinoma

Patterns of somatic structural variation in human cancer genomes

Portraits of genetic intra-tumour heterogeneity and subclonal selection across cancer types

Prostate cancer: Clinical hallmarks in whole cancer genomes

Selective and mechanistic sources of recurrent rearrangements across the cancer genome

Shotgun Transcriptome and Isothermal Profiling of SARS-CoV-2 Infection Reveals Unique Host Responses, Viral Diversification, and Drug Interactions

Shotgun transcriptome, spatial omics, and isothermal profiling of SARS-CoV-2 infection reveals unique host responses, viral diversification, and drug interactions

Signatures of mutational processes in human cancer

Strong synaptic transmission impact by copy number variations in schizophrenia

Structural variant evolution after telomere crisis

SvABA: genome-wide detection of structural variants and indels by local assembly.

Systematic analysis of conservation relations in Escherichia coli genome-scale metabolic network reveals novel growth media

Systemic Tissue and Cellular Disruption from SARS-CoV-2 Infection revealed in COVID-19 Autopsies and Spatial Omics Tissue Maps

The cancer precision medicine knowledge base for structured clinical-grade mutations and interpretations

The evolutionary history of 2,658 cancers

The evolutionary history of 2,658 cancers

Variants of DENND1B associated with asthma in children

iSUMO - integrative prediction of functionally relevant SUMOylation events