Irene Madrigal

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 10

Top Venues

Genes

Journal of clinical medicine

Orphanet journal of rare diseases

Clinical genetics

Hospital Clínic de Barcelona

Universitat de Barcelona (PHD)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Hospital Clínic de Barcelona Mar 01 2012

Spain

Especialista :: Bioquímica y Genética Molecular

Centro de Investigación Biomédica en Red de Enfermedades Raras Jan 01 2007

Spain

Investigador :: Grupo U726 (Hospital Clinic de Barcelona)

Red de Centros de Genética Clínica y Molecular del Hospital Clinic de Barcelona (Instituto Carlos III)

Spain

Becaria predoctoral :: Bioquímica y Genética Molecular

Education History

Universitat de Barcelona

Spain

PHD :: Bioquímica y Genética Molecular (Hospital Clinic de Barcelona)

Universitat Autònoma de Barcelona

Spain

MSC :: Biologia Animal, Biologia Vegental y Ecologia

Publications

Victoria Ardiles-Ruesjas, Roser Viñals, Montse Pauta, Irene Madrigal, Antoni Borrell
Prenatal Screening of Chromosomal Anomalies Using Genome-Wide or Target Cell-Free DNA: Preferences and Satisfaction of Pregnant Women. Journal of clinical medicine 13 (16) (2024)
Victoria Ardiles-Ruesjas, Roser Viñals, Montse Pauta, Irene Madrigal, Antoni Borrell
Prenatal Screening of Chromosomal Anomalies Using Genome-Wide or Target Cell-Free DNA: Preferences and Satisfaction of Pregnant Women. Journal of clinical medicine 13 (16) (2024)
Maria Isabel Alvarez-Mora, Laia Rodriguez-Revenga, Meritxell Jodar, Miriam Potrony, Aurora Sanchez, Celia Badenas, Josep Oriola, José Luis Villanueva-Cañas, Esteban Muñoz, Francesc Valldeoriola, Ana Cámara, Yaroslau Compta, Mar Carreño, María Jose Martí, Raquel Sánchez-Valle, Irene Madrigal
Implementation of Exome Sequencing in Clinical Practice for Neurological Disorders. Genes 14 (4) (2023)
Maria Isabel Alvarez-Mora, Laia Rodriguez-Revenga, Meritxell Jodar, Miriam Potrony, Aurora Sanchez, Celia Badenas, Josep Oriola, José Luis Villanueva-Cañas, Esteban Muñoz, Francesc Valldeoriola, Ana Cámara, Yaroslau Compta, Mar Carreño, María Jose Martí, Raquel Sánchez-Valle, Irene Madrigal
Implementation of Exome Sequencing in Clinical Practice for Neurological Disorders. Genes 14 (4) (2023)
Irene Madrigal
Editorial for the Molecular Mechanisms in Neurodevelopmental Disorders Special Issue. Genes 14 (9) (2023)
Maria Isabel Alvarez-Mora, Laia Rodriguez-Revenga, Meritxell Jodar, Miriam Potrony, Aurora Sanchez, Celia Badenas, Josep Oriola, José Luis Villanueva-Cañas, Esteban Muñoz, Francesc Valldeoriola, Ana Cámara, Yaroslau Compta, Mar Carreño, María Jose Martí, Raquel Sánchez-Valle, Irene Madrigal
Implementation of Exome Sequencing in Clinical Practice for Neurological Disorders. Genes 14 (4) (2023)
Maria Isabel Alvarez-Mora, Laia Rodriguez-Revenga, Meritxell Jodar, Miriam Potrony, Aurora Sanchez, Celia Badenas, Josep Oriola, José Luis Villanueva-Cañas, Esteban Muñoz, Francesc Valldeoriola, Ana Cámara, Yaroslau Compta, Mar Carreño, María Jose Martí, Raquel Sánchez-Valle, Irene Madrigal
Implementation of Exome Sequencing in Clinical Practice for Neurological Disorders. Genes 14 (4) (2023)
María Isabel Álvarez-Mora, Aurora Sánchez, Laia Rodríguez-Revenga, Jordi Corominas, Raquel Rabionet, Susana Puig, Irene Madrigal
Diagnostic yield of next-generation sequencing in 87 families with neurodevelopmental disorders. Orphanet journal of rare diseases 17 (1) (2022)
Miriam Potrony, Antoni Borrell, Narcís Masoller, Alfons Nadal, Leonardo Rodriguez-Carunchio, Karmele Saez de Gordoa, Juan Francisco Quesada-Espinosa, José Luis Villanueva-Cañas, Montse Pauta, Meritxell Jodar, Irene Madrigal, Celia Badenas, Maria Isabel Alvarez-Mora, Laia Rodriguez-Revenga
Lethal Congenital Contracture Syndrome 11: A Case Report and Literature Review. Journal of clinical medicine 11 (13) (2022)
Laia Rodriguez-Revenga, Irene Madrigal, Antoni Borrell, Josep M Martinez, Joan Sabria, Lourdes Martin, Wladimiro Jimenez, Aurea Mira, Celia Badenas, Montserrat Milà
Chromosome microarray analysis should be offered to all invasive prenatal diagnostic testing following a normal rapid aneuploidy test result. Clinical genetics 98 (4) (2020)

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Publication Activity (10 Years)

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Irene Madrigal