Laia Rodriguez-Revenga (Laia Rodríguez-Revenga)

ORCID

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 16

Top Venues

Genes

Prenatal diagnosis

Genes, brain, and behavior

Journal of clinical medicine

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

Publications

Ines Agusti, Marta Méndez, Aina Borrás, Anna Goday, Marta Guimerà, Sara Peralta, Laura Ribera, Laia Rodriguez-Revenga, Dolors Manau
Prevalence of the FMR1 Gene Premutation in Young Women with a Diminished Ovarian Reserve Included in an IVF Program: Implications for Clinical Practice. Genes 15 (8) (2024)
Ines Agusti, Marta Méndez, Aina Borrás, Anna Goday, Marta Guimerà, Sara Peralta, Laura Ribera, Laia Rodriguez-Revenga, Dolors Manau
Prevalence of the FMR1 Gene Premutation in Young Women with a Diminished Ovarian Reserve Included in an IVF Program: Implications for Clinical Practice. Genes 15 (8) (2024)
Laia Rodriguez-Revenga, Alfons Nadal, Virginia Borobio, Maria Isabel Álvarez-Mora, Irene Madrigal, Montse Pauta, Antoni Borrell
A novel NONO nonsense variant in a fetus with renal abnormalities. Prenatal diagnosis 44 (1) (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)
Laia Rodriguez-Revenga, Alfons Nadal, Virginia Borobio, Maria Isabel Álvarez-Mora, Irene Madrigal, Montse Pauta, Antoni Borrell
A novel NONO nonsense variant in a fetus with renal abnormalities. Prenatal diagnosis (2023)
Maria Isabel Alvarez-Mora, Gloria Garrabou, Laura Molina-Porcel, Ruben Grillo-Risco, Francisco Garcia-Garcia, Tamara Barcos, Judith Cantó-Santos, Laia Rodriguez-Revenga
Exploration of SUMO2/3 Expression Levels and Autophagy Process in Fragile X-Associated Tremor/Ataxia Syndrome: Addressing Study Limitations and Insights for Future Research. Cells 12 (19) (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)
Laia Rodriguez-Revenga, Alfons Nadal, Virginia Borobio, Maria Isabel Álvarez-Mora, Irene Madrigal, Montse Pauta, Antoni Borrell
A novel NONO nonsense variant in a fetus with renal abnormalities. Prenatal diagnosis 44 (1) (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)
Laia Rodriguez-Revenga, Alfons Nadal, Virginia Borobio, Maria Isabel Álvarez-Mora, Irene Madrigal, Montse Pauta, Antoni Borrell
A novel NONO nonsense variant in a fetus with renal abnormalities. Prenatal diagnosis 44 (1) (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)
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)
Maria Isabel Alvarez-Mora, Petar Podlesniy, Teresa Riazuelo, Laura Molina-Porcel, Ellen Gelpi, Laia Rodriguez-Revenga
Reduced mtDNA Copy Number in the Prefrontal Cortex of C9ORF72 Patients. Molecular neurobiology 59 (2) (2022)
Laia Rodriguez-Revenga, Maria Isabel Alvarez-Mora
Special Issue: Genetics of Psychiatric Disease and the Basics of Neurobiology. Genes 13 (11) (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)
Maria I Alvarez-Mora, Petar Podlesniy, Ellen Gelpi, Renate K Hukema, Irene Madrigal, Javier Pagonabarraga, Ramon Trullas, Montserrat Mila, Laia Rodriguez-Revenga
Fragile X-associated tremor/ataxia syndrome: Regional decrease of mitochondrial DNA copy number relates to clinical manifestations. Genes, brain, and behavior 18 (5) (2019)

Laia Rodriguez-Revenga.css-eqlu8i{font-size:small;padding-left:4px;} (Laia Rodríguez-Revenga)

Publication Activity (10 Years)

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Laia Rodriguez-Revenga (Laia Rodríguez-Revenga)