Maria Rigau
Maria Rigau
MRC-LMS Postdoctoral Research Scientist
Verified email at
Cited by
Cited by
Integrated analysis of whole-exome sequencing and transcriptome profiling in males with autism spectrum disorders
M Codina-Solà, B Rodríguez-Santiago, A Homs, J Santoyo, M Rigau, ...
Molecular autism 6 (1), 1-16, 2015
Intronic CNVs and gene expression variation in human populations
M Rigau, D Juan, A Valencia, D Rico
PLoS genetics 15 (1), e1007902, 2019
Loose ends: almost one in five human genes still have unresolved coding status
F Abascal, D Juan, I Jungreis, L Martinez, M Rigau, JM Rodriguez, ...
Nucleic acids research 46 (14), 7070-7084, 2018
Solid‐phase peptide synthesis using acetonitrile as a solvent in combination with PEG‐based resins
GA Acosta, M del Fresno, M Paradis‐Bas, M Rigau‐DeLlobet, S Cote, ...
Journal of Peptide Science: An Official Publication of the European Peptide …, 2009
Degradable Glycine‐Based Photo‐Polymerizable Polyphosphazenes for Use as Scaffolds for Tissue Regeneration
S Rothemund, TB Aigner, A Iturmendi, M Rigau, B Husár, F Hildner, ...
Macromolecular bioscience 15 (3), 351-363, 2015
Three-dimensional connectivity and chromatin environment mediate the activation efficiency of mammalian DNA replication origins
K Jodkowska, V Pancaldi, R Almeida, M Rigau, O Graña-Castro, ...
BioRxiv, 644971, 2019
A catalogue of 863 Rett-syndrome-causing MECP2 mutations and lessons learned from data integration
F Ehrhart, A Jacobsen, M Rigau, M Bosio, R Kaliyaperumal, JFJ Laros, ...
Scientific data 8 (1), 10, 2021
Emerging mechanisms and dynamics of three-dimensional genome organisation at zygotic genome activation
E Ing-Simmons, M Rigau, JM Vaquerizas
Current Opinion in Cell Biology 74, 37-46, 2022
Look-alike humans identified by facial recognition algorithms show genetic similarities
RS Joshi, M Rigau, CA García-Prieto, MC de Moura, D Piñeyro, S Moran, ...
Cell Reports 40 (8), 111257, 2022
Intronic CNVs cause gene expression variation in human population
M Rigau, D Juan, A Valencia, D Rico
bioRxiv., 171165, 2018
Rare disease research workflow using multilayer networks elucidates the molecular determinants of severity in Congenital Myasthenic Syndromes
I Núòez-Carpintero, E O'Connor, M Rigau, M Bosio, Y Azuma, A Topf, ...
bioRxiv, 2023.01. 19.524736, 2023
3D chromatin connectivity underlies replication origin efficiency in mouse embryonic stem cells
K Jodkowska, V Pancaldi, M Rigau, R Almeida, JM Fernández-Justel, ...
Nucleic Acids Research 50 (21), 12149-12165, 2022
Widespread population variability of intron size in evolutionary old genes: implications for gene expression variability: Intronic CNVs and gene regulation
M Rigau, D Juan, A Valencia, D Rico
bioRxiv, 171165, 2017
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