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Correction: Prediction of mortality in very low birth weight neonates in Spain

PloS one, 2023-05, Vol.18 (5), p.e0285353-e0285353

2023

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Rare disease research workflow using multilayer networks elucidates the molecular determinants of severity in Congenital Myasthenic Syndromes

Nature communications, 2024-02, Vol.15 (1), p.1227-1227, Article 1227

2024

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Continual learning for predictive maintenance: Overview and challenges

Intelligent systems with applications, 2023-09, Vol.19, p.200251, Article 200251

2023

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Prediction of mortality in very low birth weight neonates in Spain

PloS one, 2020-07, Vol.15 (7), p.e0235794-e0235794

2020

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Efficient and flexible Integration of variant characteristics in rare variant association studies using integrated nested Laplace approximation

PLoS computational biology, 2021-02, Vol.17 (2), p.e1007784

2021

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Tracking of Antibiotic Resistance Transfer and Rapid Plasmid Evolution in a Hospital Setting by Nanopore Sequencing

mSphere, 2020-08, Vol.5 (4)

2020

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A catalogue of 863 Rett-syndrome-causing MECP2 mutations and lessons learned from data integration

Scientific data, 2021-01, Vol.8 (1), p.10-10, Article 10

2021

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LRBA Deficiency in a Patient With a Novel Homozygous Mutation Due to Chromosome 4 Segmental Uniparental Isodisomy

Frontiers in immunology, 2018-10, Vol.9, p.2397-2397

2018

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Predicción de mortalidad en recién nacidos prematuros. Revisión sistemática actualizada

Anales de pediatría (Barcelona, Spain : 2003), 2020-07, Vol.93 (1), p.24-33

2020

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The landscape of expression and alternative splicing variation across human traits

Cell genomics, 2023-01, Vol.3 (1), p.100244, Article 100244

2023

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Characterization of a Clinically and Biologically Defined Subgroup of Patients with Autism Spectrum Disorder and Identification of a Tailored Combination Treatment

Biomedicines, 2024-05, Vol.12 (5), p.991

2024

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Foraging success is differently affected by local climate in two syntopic forest-dwelling salamanders

Ethology, ecology & evolution, 2023-07, Vol.35 (4), p.424-433

2023

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Allele balance bias identifies systematic genotyping errors and false disease associations

Human mutation, 2019-01, Vol.40 (1), p.115-126

2019

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FGFR Inhibition Overcomes Resistance to EGFR-targeted Therapy in Epithelial-like Cutaneous Carcinoma

Clinical cancer research, 2021-03, Vol.27 (5), p.1491-1504

2021

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Prediction of mortality in premature neonates. An updated systematic review

Anales de Pediatría, 2020-07, Vol.93 (1), p.24-33

2020

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Les services sociaux dans le marché intérieur : à la frontière entre compétitivité et solidarité

Revue française des affaires sociales, 2012-06 (1), p.130-149

Bosio, Mattia

2012

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eDiVA—Classification and prioritization of pathogenic variants for clinical diagnostics

Human mutation, 2019-07, Vol.40 (7), p.865-878

2019

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Social services in the internal market: at the boundary between competitiveness and solidarity

Revue française des affaires sociales, 2012-01, Vol.1, p.130-149

Bosio, Mattia

2012

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Allele balance bias identifies systematic genotyping errors and false disease associations

Human mutation, 2018-10

2018

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A De Novo Nonsense Mutation in MAGEL2 in a Patient Initially Diagnosed as Opitz-C: Similarities Between Schaaf-Yang and Opitz-C Syndromes

Scientific reports, 2017-03, Vol.7 (1), p.44138-44138, Article 44138

2017

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Differential expression of long non‐coding RNAs are related to proliferation and histological diversity in follicular lymphomas

British journal of haematology, 2019-02, Vol.184 (3), p.373-383

2019

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Survival among children with “Lethal” congenital contracture syndrome 11 caused by novel mutations in the gliomedin gene (GLDN)

Human mutation, 2017-11, Vol.38 (11), p.1477-1484

2017

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Prediction of mortality in premature neonates. An updated systematic review

Anales de Pediatría, 2020-07, Vol.93 (1), p.24-33

2020

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Prediction of mortality in premature neonates. An updated systematic review

Anales de Pediatría, 2020-07, Vol.93 (1), p.24-33

2020

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Differential expression of long non‐coding RNA s are related to proliferation and histological diversity in follicular lymphomas

British journal of haematology, 2019-02, Vol.184 (3), p.373-383

2019

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Correction: Prediction of mortality in very low birth weight neonates in Spain

Rare disease research workflow using multilayer networks elucidates the molecular determinants of severity in Congenital Myasthenic Syndromes

Continual learning for predictive maintenance: Overview and challenges

Prediction of mortality in very low birth weight neonates in Spain

Efficient and flexible Integration of variant characteristics in rare variant association studies using integrated nested Laplace approximation

Tracking of Antibiotic Resistance Transfer and Rapid Plasmid Evolution in a Hospital Setting by Nanopore Sequencing

A catalogue of 863 Rett-syndrome-causing MECP2 mutations and lessons learned from data integration

LRBA Deficiency in a Patient With a Novel Homozygous Mutation Due to Chromosome 4 Segmental Uniparental Isodisomy

Predicción de mortalidad en recién nacidos prematuros. Revisión sistemática actualizada

The landscape of expression and alternative splicing variation across human traits

Characterization of a Clinically and Biologically Defined Subgroup of Patients with Autism Spectrum Disorder and Identification of a Tailored Combination Treatment

Foraging success is differently affected by local climate in two syntopic forest-dwelling salamanders

Allele balance bias identifies systematic genotyping errors and false disease associations

FGFR Inhibition Overcomes Resistance to EGFR-targeted Therapy in Epithelial-like Cutaneous Carcinoma

Prediction of mortality in premature neonates. An updated systematic review

Les services sociaux dans le marché intérieur : à la frontière entre compétitivité et solidarité

eDiVA—Classification and prioritization of pathogenic variants for clinical diagnostics

Social services in the internal market: at the boundary between competitiveness and solidarity

Allele balance bias identifies systematic genotyping errors and false disease associations

A De Novo Nonsense Mutation in MAGEL2 in a Patient Initially Diagnosed as Opitz-C: Similarities Between Schaaf-Yang and Opitz-C Syndromes

Differential expression of long non‐coding RNAs are related to proliferation and histological diversity in follicular lymphomas

Survival among children with “Lethal” congenital contracture syndrome 11 caused by novel mutations in the gliomedin gene (GLDN)

Prediction of mortality in premature neonates. An updated systematic review

Prediction of mortality in premature neonates. An updated systematic review

Differential expression of long non‐coding RNA s are related to proliferation and histological diversity in follicular lymphomas

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