Irene Madrigal

2.4k total citations
83 papers, 1.3k citations indexed

About

Irene Madrigal is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Irene Madrigal has authored 83 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 58 papers in Genetics, 36 papers in Molecular Biology and 18 papers in Cognitive Neuroscience. Recurrent topics in Irene Madrigal's work include Genetics and Neurodevelopmental Disorders (41 papers), Genomic variations and chromosomal abnormalities (31 papers) and Autism Spectrum Disorder Research (18 papers). Irene Madrigal is often cited by papers focused on Genetics and Neurodevelopmental Disorders (41 papers), Genomic variations and chromosomal abnormalities (31 papers) and Autism Spectrum Disorder Research (18 papers). Irene Madrigal collaborates with scholars based in Spain, Netherlands and Poland. Irene Madrigal's co-authors include Montserrat Milà, Laia Rodríguez‐Revenga, Célia Bádenas, Mar Xunclà, María Isabel Álvarez‐Mora, Javier Pagonabarraga, Aurora Sánchez, Jaime Kulisevsky, Beatriz Gόmez and Xavier Estivill and has published in prestigious journals such as Neurology, The American Journal of Human Genetics and International Journal of Cancer.

In The Last Decade

Irene Madrigal

82 papers receiving 1.3k citations

Peers

Countries citing papers authored by Irene Madrigal

Since Specialization

Citations

This map shows the geographic impact of Irene Madrigal'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 Irene Madrigal with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Irene Madrigal more than expected).

Fields of papers citing papers by Irene Madrigal

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Irene Madrigal. 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 Irene Madrigal. The network helps show where Irene Madrigal may publish in the future.

Co-authorship network of co-authors of Irene Madrigal

This figure shows the co-authorship network connecting the top 25 collaborators of Irene Madrigal. A scholar is included among the top collaborators of Irene Madrigal 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 Irene Madrigal. Irene Madrigal is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	A novel NONO nonsense variant in a fetus with renal abnormalities 2023 ·Prenatal Diagnosis ·Laia Rodríguez‐Revenga, Alfons Nadal, V. Borobio, María Isabel Álvarez‐Mora, Irene Madrigal, Montse Pauta, A. Borrell	1
2	Evaluation of AQP4 functional variants and its association with fragile X-associated tremor/ataxia syndrome 2023 ·Frontiers in Aging Neuroscience ·(unknown), Míriam Potrony, (unknown), David J. Cutler, María Isabel Álvarez‐Mora, (unknown), (unknown), Joan Anton Puig‐Butillé, Marta Rubio, Irene Madrigal, Susana Puig, Emily G. Allen, Laia Rodríguez‐Revenga	3
3	The Contribution of QF-PCR and Pathology Studies in the Diagnosis of Diandric Triploidy/Partial Mole 2021 ·Diagnostics ·(unknown), Montse Pauta, Célia Bádenas, Irene Madrigal, Alfons Nadal, (unknown), A. Borrell	2
4	Chromosome microarray analysis should be offered to all invasive prenatal diagnostic testing following a normal rapid aneuploidy test result 2020 ·Clinical Genetics ·Laia Rodríguez‐Revenga, Irene Madrigal, A. Borrell, Josep M. Martínez, J. Sabrià, (unknown), Wladimiro Jiménez, Áurea Mira, Célia Bádenas, Montserrat Milà	8
5	Fragile X‐associated tremor/ataxia syndrome: Regional decrease of mitochondrial DNA copy number relates to clinical manifestations 2019 ·Genes Brain & Behavior ·María Isabel Álvarez‐Mora, Petar Podlesniy, Ellen Gelpí, Renate K. Hukema, Irene Madrigal, Javier Pagonabarraga, Ramón Trullás, Montserrat Milà, Laia Rodríguez‐Revenga	11
6	Fragile X syndrome: An overview and update of the FMR1 gene 2017 ·Clinical Genetics ·Montserrat Milà, María Isabel Álvarez‐Mora, Irene Madrigal, Laia Rodríguez‐Revenga	74
7	Comprehensive molecular testing in patients with high functioning autism spectrum disorder 2016 ·Mutation research. Fundamental and molecular mechanisms of mutagenesis ·María Isabel Álvarez‐Mora, Rosa Calvo, (unknown), Irene Madrigal, Inés Quintela, Jorge Amigo, (unknown), M Linder-Lucht, (unknown), Ãngel Carracedo, Montserrat Milà, Laia Rodríguez‐Revenga	22
8	Impaired Mitochondrial Function and Dynamics in the Pathogenesis of FXTAS 2016 ·Molecular Neurobiology ·(unknown), Laia Rodríguez‐Revenga, Irene Madrigal, Mariona Guitart‐Mampel, Glòria Garrabou, Montserrat Milà	47
9	Deregulation of key signaling pathways involved in oocyte maturation in FMR1 premutation carriers with Fragile X-associated primary ovarian insufficiency 2015 ·Gene ·(unknown), Laia Rodríguez‐Revenga, Irene Madrigal, Francisco García‐García, (unknown), Joaquı́n Dopazo, Xavier Estivill, Montserrat Milà	10
10	MicroRNA expression profiling in blood from fragile X‐associated tremor/ataxia syndrome patients 2013 ·Genes Brain & Behavior ·María Isabel Álvarez‐Mora, Laia Rodríguez‐Revenga, Irene Madrigal, (unknown), (unknown), Esther Lizano, Marc R. Friedländer, Eulàlia Martı́, Xavier Estivill, Montserrat Milà	23
11	Screening for the presence of FMR1 premutation alleles in women with fibromyalgia 2012 ·Gene ·Laia Rodríguez‐Revenga, Irene Madrigal, (unknown), Dei M. Elurbe, Elisa Docampo, Antonio Collado, (unknown), Jordi Carbonell, Xavier Estivill, Montserrat Milà	9
12	Intermediate FMR1 alleles and cognitive and/or behavioural phenotypes 2011 ·European Journal of Human Genetics ·Irene Madrigal, Mar Xunclà, María‐Isabel Tejada, Francisco Martı́nez, Isabel Fernández-Carvajal, Luis A. Pérez‐Jurado, Laia Rodríguez‐Revenga, Montserrat Milà	14
13	Novel MLH1 duplication identified in Colombian families with Lynch syndrome 2011 ·Genetics in Medicine ·(unknown), María D. Giraldez, (unknown), Heleen van der Klift, Jenifer Muñoz, Francesc Balaguer, Teresa Ocaña, Irene Madrigal, Angela M. Jones, (unknown), Alejandro Velez-Zea, Ian Tomlinson, Montserrat Milà, Juul Wijnen, Luis G. Carvajal‐Carmona, Antoni Castells, Sergi Castellvı́-Bel	12
14	Motor and mental dysfunction in mother–daughter transmitted FXTAS 2010 ·Neurology ·Laia Rodríguez‐Revenga, Javier Pagonabarraga, Beatriz Gómez‐Ansón, (unknown), Irene Madrigal, Mar Xunclà, Jaime Kulisevsky, Montserrat Milà	20
15	Síndrome de temblor y ataxia asociado a síndrome del cromosoma X frágil: un nuevo tipo de ataxia cerebelosa asociada a los portadores del síndrome del cromosoma X frágil 2009 ·Medicina Clínica ·Montserrat Milà, Irene Madrigal, Jaime Kulisevsky, Javier Pagonabarraga, Beatriz Gόmez, Aurora Sánchez, Laia Rodríguez‐Revenga	3
16	Screening for FXTAS in 95 Spanish Patients Negative for Huntington Disease 2008 ·Genetic Testing ·Laia Rodríguez‐Revenga, (unknown), Aurora Sánchez, Montserrat Pujol, Beatriz Gómez‐Ansón, Célia Bádenas, (unknown), Irene Madrigal, Montserrat Milà	12
17	X-chromosome tiling path array detection of copy number variants in patients with chromosome X-linked mental retardation 2007 ·BMC Genomics ·Irene Madrigal, Laia Rodríguez‐Revenga, Lluı́s Armengol, Eva González‐Roca, (unknown), Célia Bádenas, Aurora Sánchez, Francisco Martı́nez, Míriam Guitart, Isabel Fernández-Carvajal, (unknown), María‐Isabel Tejada, (unknown), Xavier Estivill, Montserrat Milà	48
18	MLPA as first screening method for the detection of microduplications and microdeletions in patients with X-linked mental retardation 2007 ·Genetics in Medicine ·Irene Madrigal, Laia Rodríguez‐Revenga, Célia Bádenas, Aurora Sánchez, Francisco Martı́nez, Isabel Fernández, Miguel Fernández‐Burriel, Montserrat Milà	23
19	46,XY,18q+/46,XY,18q− mosaicism in a fragile X prenatal diagnosis 2005 ·Prenatal Diagnosis ·Laia Rodríguez‐Revenga, Célia Bádenas, Irene Madrigal, Aurora Sánchez, Anna Soler, Ana Carrió, Montserrat Milà	4
20	Coamplified and overexpressed genes at ERBB2 locus in gastric cancer 2004 ·International Journal of Cancer ·Asta Varis, Alexander Zaika, Pauli Puolakkainen, Bálint Nagy, Irene Madrigal, Arto Kokkola, (unknown), Päivi Kärkkäinen, Christopher A. Moskaluk, (unknown), Sakari Knuutila	47

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

Explore authors with similar magnitude of impact