Original articles in indexed journals - NeuroGenomics

Runge K, Mathieu R, Bugeon S et al (including Santpere G). Disruption of NEUROD2 causes a neurodevelopmental syndrome with autistic features via cell-autonomous defects in forebrain glutamatergic neurons. Mol Psychiatry, 2021 DOI: 10.1038/s41380-021-01179-x.

2021

Original articles in indexed journals - NeuroGenomics

Santpere G, Telford M, Andrés-Benito P, Navarro A, Ferrer I. The Presence of Human Herpesvirus 6 in the Brain in Health and Disease. Biomolecules, 2020; 10(11): 1520. PMID: 33172107 . DOI: 10.3390/biom10111520.

2020

Original articles in indexed journals - NeuroGenomics

Zhen L, Tyler WA, Zeldich E, Santpere Baró G, Okamoto M, Gao T, Li M, Sestan N, Haydar TF. Transcriptional priming as a conserved mechanism of lineage diversification in the developing mouse and human neocortex. Sci Adv, 2020; 6(45):eabd2068. PMID: 33158872 . DOI: 10.1126/sciadv.abd2068.

2020

Original articles in indexed journals - NeuroGenomics

Telford M, Hughes DA, Juan D, Stoneking M, Navarro A, Santpere G. Expanding the Geographic Characterisation of Epstein-Barr Virus Variation through Gene-Based Approaches. Microorganisms, 2020;8(11):1686. PMID: 33138327 . DOI: 10.3390/microorganisms8111686.

2020

Original articles in indexed journals - NeuroGenomics

Werling DM, Pochareddy S, Choi J, An JY, Sheppard B, Peng M, Li Z, Dastmalchi C, Santpere G et al. Whole-Genome and RNA Sequencing Reveal Variation and Transcriptomic Coordination in the Developing Human Prefrontal Cortex. Cell Rep, 2020; 31(1): 107489. PMID: 32268104 . DOI: 10.1016/j.celrep.2020.03.053.

2020

Original articles in indexed journals - NeuroGenomics

Muchnik SK, Lorente-Galdos B, Santpere G, Sestan N. Modeling the Evolution of Human Brain Development Using Organoids. Cell, 2019; 179 (6), 1250-1253. PMID: 31778651 . DOI: 10.1016/j.cell.2019.10.041.

2019

Original articles in indexed journals - NeuroGenomics

Giusti-Rodríguez P, Lu L, Yang Y, Crowley CA, Liu X, Bryois J, Juric I et al (including Santpere G). Schizophrenia and a high-resolution map of the three-dimensional chromatin interactome of adult and fetal cortex. bioRxiv, 2019 DOI: 10.1101/406330.

2019

Original articles in indexed journals - NeuroGenomics

Bensaid M, Loe-Mie Y, Lepagnol-Bestel AM, Han W, Santpere G, Klarić T et al. Multi-hit autism genomic architecture evidenced from consanguineous families with involvement of FEZF2 and mutations in high-risk genes. bioRxiv, 2019 DOI: 10.1101/759480.

2019

Original articles in indexed journals - NeuroGenomics

Lorente-Galdos B, Lao O, Serra-Vidal G, et al (including Santpere G). Whole-genome sequence analysis of a Pan African set of samples reveals archaic gene flow from an extinct basal population of modern humans into sub-Saharan populations. Genome Biol, 2019; 20(1): 77. PMID: 31023378 . DOI: 10.1186/s13059-019-1684-5.

2019

Original articles in indexed journals - Evolutionary Genomics - NeuroGenomics

Santpere G, Darre F, Blanco S, Alcami A, Villoslada P, Alba MM, Navarro A. Genome-Wide Analysis of Wild-Type Epstein-Barr Virus Genomes Derived from Healthy Individuals of the 1000 Genomes Project. Genome Biol Evol, 2014; 6 (4):846-860 DOI: 10.1093/gbe/evu054 2014.

2014