Author details

Full Name

Montserrat PuiggrÃ²s

Affiliation

ORCID

Career Start Year

2012

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37868040	Mutational topography reflects clinical neuroblastoma heterogeneity.	Cell Genom	2023
35176773	GCAT\|Panel, a comprehensive structural variant haplotype map of the Iberian population from high-coverage whole-genome sequencing.	Nucleic Acids Res	2022
37396538	Wnt genes in colonic polyposis predisposition.	Genes Dis	2022
34644572	TIGER: The gene expression regulatory variation landscape of human pancreatic islets.	Cell Rep	2021
33893285	The impact of non-additive genetic associations on age-related complex diseases.	Nat Commun	2021
32918070	Author Correction: PGBD5 promotes site-specific oncogenic mutations in human tumors.	Nat Genet	2020
31844324	Extrachromosomal circular DNA drives oncogenic genome remodeling in neuroblastoma.	Nat Genet	2020
32107479	Publisher Correction: Extrachromosomal circular DNA drives oncogenic genome remodeling in neuroblastoma.	Nat Genet	2020
34079956	The proliferative history shapes the DNA methylome of B-cell tumors and predicts clinical outcome.	Nat Cancer	2020
33199677	Enhancer hijacking determines extrachromosomal circular MYCN amplicon architecture in neuroblastoma.	Nat Commun	2020
32584970	Genomic and epigenomic insights into the origin, pathogenesis, and clinical behavior of mantle cell lymphoma subtypes.	Blood	2020
31399598	Insight into genetic predisposition to chronic lymphocytic leukemia from integrative epigenomics.	Nat Commun	2019
29358691	Re-analysis of public genetic data reveals a rare X-chromosomal variant associated with type 2 diabetes.	Nat Commun	2018
29785028	The reference epigenome and regulatory chromatin landscape of chronic lymphocytic leukemia.	Nat Med	2018
29849136	Publisher Correction: Re-analysis of public genetic data reveals a rare X-chromosomal variant associated with type 2 diabetes.	Nat Commun	2018
28951624	Erratum: PGBD5 promotes site-specific oncogenic mutations in human tumors.	Nat Genet	2017
28504702	PGBD5 promotes site-specific oncogenic mutations in human tumors.	Nat Genet	2017
27863955	The BLUEPRINT Data Analysis Portal.	Cell Syst	2016
25024348	Somatic signature of brain-specific single nucleotide variations in sporadic Alzheimer's disease.	J Alzheimers Dis	2014
25344728	Comprehensive characterization of complex structural variations in cancer by directly comparing genome sequence reads.	Nat Biotechnol	2014
22253291	ReLA, a local alignment search tool for the identification of distal and proximal gene regulatory regions and their conserved transcription factor binding sites.	Bioinformatics	2012
23236286	Identification of novel type 2 diabetes candidate genes involved in the crosstalk between the mitochondrial and the insulin signaling systems.	PLoS Genet	2012