Laia Pedrola

1.4k total citations
31 papers, 1.0k citations indexed

About

Laia Pedrola is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Laia Pedrola has authored 31 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 8 papers in Cellular and Molecular Neuroscience and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Laia Pedrola's work include Hereditary Neurological Disorders (8 papers), Neurological diseases and metabolism (4 papers) and Neurogenetic and Muscular Disorders Research (3 papers). Laia Pedrola is often cited by papers focused on Hereditary Neurological Disorders (8 papers), Neurological diseases and metabolism (4 papers) and Neurogenetic and Muscular Disorders Research (3 papers). Laia Pedrola collaborates with scholars based in Spain, United States and Australia. Laia Pedrola's co-authors include Francesc Palau, Ana Cuesta, Teresa Sevilla, María José Chumillas, Éric Leguern, Ignacio Marı́n, Juan J. Vílchez, F. Mayordomo, Javier Garcı́a-Planells and Xingyao Wu and has published in prestigious journals such as Nature Genetics, PLoS ONE and Neurology.

In The Last Decade

Laia Pedrola

26 papers receiving 992 citations

Peers

Countries citing papers authored by Laia Pedrola

Since Specialization

Citations

This map shows the geographic impact of Laia Pedrola's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Laia Pedrola with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Laia Pedrola more than expected).

Fields of papers citing papers by Laia Pedrola

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Laia Pedrola. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Laia Pedrola. The network helps show where Laia Pedrola may publish in the future.

Co-authorship network of co-authors of Laia Pedrola

This figure shows the co-authorship network connecting the top 25 collaborators of Laia Pedrola. A scholar is included among the top collaborators of Laia Pedrola based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Laia Pedrola. Laia Pedrola is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Genetic landscape of hereditary transthyretin amyloidosis in Spain: a multicentric retrospective study 2025 ·Amyloid ·(unknown), Alfonso Caro‐Llopis, (unknown), Mónica Rosello, Silvestre Oltra, Laia Pedrola, Sandra Monfort, (unknown), Francisco Martı́nez, Carmen Orellana	0
2	Clinical Utility of Opportunistic Genome-Wide cfDNA Prenatal Screening in Intermediate-Risk Pregnancies 2025 ·Genes ·Sebastián Menao, Laia Pedrola, Carmen Orellana, Mónica Rosello, María Pilar Arruebo, (unknown), (unknown), Beatriz Braña Marcos, J. Pascual, José Cervera, (unknown), (unknown)	0
3	Utility of Optical Genome Mapping for Accurate Detection and Fine-Mapping of Structural Variants in Elusive Rare Diseases 2025 ·International Journal of Molecular Sciences ·Carmen Orellana, Mónica Rosello, Amparo Sanchís, Laia Pedrola, (unknown), (unknown), (unknown), Esperanza Such, (unknown), Gayane Avetisyan, Francisco Martı́nez	0
4	Prenatal Genome-Wide Cell-Free DNA Screening: Three Years of Clinical Experience in a Hospital Prenatal Diagnostic Unit in Spain 2024 ·Genes ·Laia Pedrola, (unknown), (unknown), (unknown), (unknown), (unknown), José Cervera, (unknown), Carmen Orellana	2
5	Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 2 Caused by a Novel PIGA Variant Not Associated with a Skewed X-Inactivation Pattern 2024 ·Genes ·(unknown), Lourdes Cordón, Amparo Sempere, Laia Pedrola, (unknown), Silvestre Oltra, Sandra Monfort, Alfonso Caro‐Llopis, (unknown), (unknown), Mónica Rosello, Carmen Orellana, Francisco Martı́nez	0
6	Expanding the phenotype of PIGP deficiency to multiple congenital anomalies‐hypotonia‐seizures syndrome 2023 ·Clinical Genetics ·(unknown), Carmen Orellana, (unknown), Laia Pedrola, (unknown), (unknown), Purificación Marín Reina, (unknown), (unknown), Francisco Martı́nez	1
7	Hidden etiology of cerebral palsy: genetic and clinical heterogeneity and efficient diagnosis by next-generation sequencing 2020 ·Pediatric Research ·Mónica Rosello, Alfonso Caro‐Llopis, Carmen Orellana, Silvestre Oltra, (unknown), (unknown), Sandra Monfort, Laia Pedrola, Francisco Martı́nez, Miguel Tomás Vila	26
8	Whole Blood Gene Expression Reveals Specific Transcriptome Changes in Neonatal Encephalopathy 2018 ·Neonatology ·Paolo Montaldo, Myrsini Kaforou, Gabriele Pollara, David Hervás, (unknown), Joaquín Panadero, Laia Pedrola, Peter Lally, Vânia Oliveira, (unknown), Gaurav Atreja, Josephine Mendoza, Aung Soe, Santosh Pattnayak, Seetha Shankaran, Máximo Vento, Jethro Herberg, Sudhin Thayyil	15
9	New mutations found by Next-Generation Sequencing screening of Spanish patients with Nemaline Myopathy 2018 ·PLoS ONE ·(unknown), Elena Aller, (unknown), (unknown), C. C. GAY, (unknown), (unknown), (unknown), (unknown), Inmaculada Pitarch Castellano, Nuria Muelas, José Cervera, José M. Millán, Laia Pedrola	5
10	Non-invasive prediction of NAFLD severity: a comprehensive, independent validation of previously postulated serum microRNA biomarkers 2018 ·Scientific Reports ·(unknown), Isabel Conde, Alfonso Quintás‐Cardama, Laia Pedrola, (unknown), (unknown), (unknown), Salvador Benlloch, José V. Castell, Ramiro Jover	58
11	Delayed Presentation and Prolonged Survival of a Child with Surfactant Protein B Deficiency 2017 ·The Journal of Pediatrics ·(unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Laia Pedrola, Lawrence M. Nogee	15
12	El nuevo reto en oncología: la secuenciación NGS y su aplicación a la medicina de precisión 2016 ·Anales de Pediatría ·(unknown), Laia Pedrola, Pablo Berlanga, (unknown), Dolors Sánchez-Izquierdo, Adela Cañete, José Cervera, José M. Millán, Victoria Castel	3
13	De Novo Assembly and Functional Annotation of the Olive (Olea europaea) Transcriptome 2013 ·DNA Research ·(unknown), Juan José González Plaza, (unknown), Anı́bal M. Blanco, (unknown), José Manuel Rodrı́guez, Laia Pedrola, M. Dolores Sicardo, M. Luisa Hernández, Raúl de la Rosa, Angjelina Belaj, (unknown), Francisco Luque, José M. Martínez‐Rivas, David G. Pisano, Oswaldo Trelles, Victoriano Valpuesta, Carmen R. Beuzón	72
14	The transcriptome of Echinostoma caproni adults: Further characterization of the secretome and identification of new potential drug targets 2013 ·Journal of Proteomics ·Gagan Garg, Dolores Bernal, María Trelis, Javier Forment, (unknown), M. Luz Valero, Laia Pedrola, Juan F. Martínez‐Blanch, J. Guillermo Esteban, Shoba Ranganathan, Rafael Toledo, Antonio Marcilla	18
15	The Transcriptome Analysis of Strongyloides stercoralis L3i Larvae Reveals Targets for Intervention in a Neglected Disease 2012 ·PLoS neglected tropical diseases ·Antonio Marcilla, Gagan Garg, Dolores Bernal, Shoba Ranganathan, Javier Forment, (unknown), Carla Muñoz-Antolí, (unknown), Laia Pedrola, Juan F. Martínez‐Blanch, Javier Sotillo, María Trelis, Rafael Toledo, J. Guillermo Esteban	39
16	High-Throughput Sequencing of RNA Silencing-Associated Small RNAs in Olive (Olea europaea L.) 2011 ·PLoS ONE ·Livia Donaire, Laia Pedrola, Raúl de la Rosa, César Llave	53
17	Microbial Diversity in the Midguts of Field and Lab-Reared Populations of the European Corn Borer Ostrinia nubilalis 2011 ·PLoS ONE ·Eugeni Belda, Laia Pedrola, Juli Peretό, Juan F. Martínez‐Blanch, Arnau Montagud, (unknown), Javier F. Urchueguía, Daniel Ramón, Andrés Moyá, Manuel Porcar	64
18	Cell expression of GDAP1 in the nervous system and pathogenesis of Charcot‐Marie‐Tooth type 4A disease 2007 ·Journal of Cellular and Molecular Medicine ·Laia Pedrola, (unknown), (unknown), Maribel Sánchez‐Piris, Erich E. Sirkowski, Steven S. Scherer, Isabel Fariñas, Francesc Palau	63
19	A novel Met116Thr mutation in the GDAP1 gene in a Polish family with the axonal recessive Charcot–Marie–Tooth type 4 disease 2005 ·Journal of the Neurological Sciences ·Dagmara Kabzińska, Andrzej Kochański, H Drac, K Rowińska-Marcińska, Barbara Ryniewicz, Laia Pedrola, Francesc Palau, I Hausmanowa-Pétrusewicz	7
20	The gene encoding ganglioside-induced differentiation-associated protein 1 is mutated in axonal Charcot-Marie-Tooth type 4A disease 2001 ·Nature Genetics ·Ana Cuesta, Laia Pedrola, Teresa Sevilla, Javier Garcı́a-Planells, María José Chumillas, F. Mayordomo, Éric Leguern, Ignacio Marı́n, Juan J. Vílchez, Francesc Palau	262

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