Lista de obras -

A candidate regulatory variant at the TREM gene cluster associates with decreased Alzheimer's disease risk and increased TREML1 and TREM2 brain gene expression

artículo científico publicado en 2016

Abnormal expression of homeobox genes and transthyretin in C9ORF72 expansion carriers

artículo científico publicado en 2017

Amplification of 9p24.1 in diffuse large B-cell lymphoma identifies a unique subset of cases that resemble primary mediastinal large B-cell lymphoma

artículo científico publicado en 2019

BAP1 dependent expression of long non-coding RNA NEAT-1 contributes to sensitivity to gemcitabine in cholangiocarcinoma

scientific article published on 25 January 2017

Circulating Extracellular RNA Markers of Liver Regeneration

artículo científico publicado en 2016

Conserved brain myelination networks are altered in Alzheimer's and other neurodegenerative diseases

artículo científico publicado en 2017

Differences in genomic abnormalities among African individuals with monoclonal gammopathies using calculated ancestry

article

Discovery and prioritization of somatic mutations in diffuse large B-cell lymphoma (DLBCL) by whole-exome sequencing

artículo científico publicado en 2012

Early life sun exposure, vitamin D-related gene variants, and risk of non-Hodgkin lymphoma.

artículo científico publicado en 2012

Extensive transcriptomic study emphasizes importance of vesicular transport in C9orf72 expansion carriers

scientific article published on 08 October 2019

Genetically predicted longer telomere length is associated with increased risk of B-cell lymphoma subtypes

artículo científico publicado en 2016

Genome-wide analyses as part of the international FTLD-TDP whole-genome sequencing consortium reveals novel disease risk factors and increases support for immune dysfunction in FTLD

scientific article published on 09 February 2019

Genome-wide association study identifies multiple susceptibility loci for diffuse large B cell lymphoma

artículo científico publicado en 2014

Germline copy number variation and ovarian cancer survival

artículo científico publicado en 2012

Host genetic variation in tumor necrosis factor and nuclear factor-κB pathways and overall survival in mantle cell lymphoma: A discovery and replication study

artículo científico publicado en 2019

Human Pegivirus infection and lymphoma risk and prognosis: a North American study

artículo científico publicado en 2018

Human whole genome genotype and transcriptome data for Alzheimer's and other neurodegenerative diseases

artículo científico publicado en 2016

Identification of novel variants in colorectal cancer families by high-throughput exome sequencing

artículo científico publicado en 2013

In-depth clinico-pathological examination of RNA foci in a large cohort of C9ORF72 expansion carriers

artículo científico publicado en 2017

Late-onset Alzheimer disease risk variants mark brain regulatory loci

artículo científico publicado en 2015

Loss of TNFAIP3 enhances MYD88-driven signaling in non-Hodgkin lymphoma

artículo científico publicado en 2018

Lupus-related single nucleotide polymorphisms and risk of diffuse large B-cell lymphoma

artículo científico publicado en 2017

MYC dysregulation in the progression of multiple myeloma

artículo científico publicado en 2019

Mapping of the IRF8 gene identifies a 3'UTR variant associated with risk of chronic lymphocytic leukemia but not other common non-Hodgkin lymphoma subtypes

artículo científico publicado en 2013

PatternCNV: a versatile tool for detecting copy number changes from exome sequencing data.

artículo científico publicado en 2014

Systematic analysis of dark and camouflaged genes reveals disease-relevant genes hiding in plain sight

article

Systematic analysis of dark and camouflaged genes: disease-relevant genes hiding in plain sight: Supplemental figures

article

TYROBP genetic variants in early-onset Alzheimer's disease

artículo científico publicado en 2016

Targeting of inflammatory pathways with R2CHOP in high-risk DLBCL

artículo científico publicado en 2020

The CCND1 c.870G risk allele is enriched in individuals of African ancestry with plasma cell dyscrasias

artículo científico publicado en 2020

Lista de obras de

A candidate regulatory variant at the TREM gene cluster associates with decreased Alzheimer's disease risk and increased TREML1 and TREM2 brain gene expression

Abnormal expression of homeobox genes and transthyretin in C9ORF72 expansion carriers

Amplification of 9p24.1 in diffuse large B-cell lymphoma identifies a unique subset of cases that resemble primary mediastinal large B-cell lymphoma

BAP1 dependent expression of long non-coding RNA NEAT-1 contributes to sensitivity to gemcitabine in cholangiocarcinoma

Circulating Extracellular RNA Markers of Liver Regeneration

Conserved brain myelination networks are altered in Alzheimer's and other neurodegenerative diseases

Differences in genomic abnormalities among African individuals with monoclonal gammopathies using calculated ancestry

Discovery and prioritization of somatic mutations in diffuse large B-cell lymphoma (DLBCL) by whole-exome sequencing

Early life sun exposure, vitamin D-related gene variants, and risk of non-Hodgkin lymphoma.

Extensive transcriptomic study emphasizes importance of vesicular transport in C9orf72 expansion carriers

Genetically predicted longer telomere length is associated with increased risk of B-cell lymphoma subtypes

Genome-wide analyses as part of the international FTLD-TDP whole-genome sequencing consortium reveals novel disease risk factors and increases support for immune dysfunction in FTLD

Genome-wide association study identifies multiple susceptibility loci for diffuse large B cell lymphoma

Germline copy number variation and ovarian cancer survival

Host genetic variation in tumor necrosis factor and nuclear factor-κB pathways and overall survival in mantle cell lymphoma: A discovery and replication study

Human Pegivirus infection and lymphoma risk and prognosis: a North American study

Human whole genome genotype and transcriptome data for Alzheimer's and other neurodegenerative diseases

Identification of novel variants in colorectal cancer families by high-throughput exome sequencing

In-depth clinico-pathological examination of RNA foci in a large cohort of C9ORF72 expansion carriers

Late-onset Alzheimer disease risk variants mark brain regulatory loci

Loss of TNFAIP3 enhances MYD88-driven signaling in non-Hodgkin lymphoma

Lupus-related single nucleotide polymorphisms and risk of diffuse large B-cell lymphoma

MYC dysregulation in the progression of multiple myeloma

Mapping of the IRF8 gene identifies a 3'UTR variant associated with risk of chronic lymphocytic leukemia but not other common non-Hodgkin lymphoma subtypes

PatternCNV: a versatile tool for detecting copy number changes from exome sequencing data.

Systematic analysis of dark and camouflaged genes reveals disease-relevant genes hiding in plain sight

Systematic analysis of dark and camouflaged genes: disease-relevant genes hiding in plain sight: Supplemental figures

TYROBP genetic variants in early-onset Alzheimer's disease

Targeting of inflammatory pathways with R2CHOP in high-risk DLBCL

The CCND1 c.870G risk allele is enriched in individuals of African ancestry with plasma cell dyscrasias