Xavier Estivill

90.8k citations

510 papers · 22.2k indexed · 2 hit papers · h-index 76

Impact in

Sensory Systems top 0.05%
- Hearing, Cochlea, Tinnitus, Genetics
Genetics top 0.1%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities

Papers in

Sensory Systems 31
- Hearing, Cochlea, Tinnitus, Genetics 31
Genetics 150
- Genetics and Neurodevelopmental Disorders 51
- Genomic variations and chromosomal abnormalities 48

Co-authors: Raquel Rabionet Lluı́s Armengol Mónica Gratacòs Paolo Gasparini Eulàlia Martı́Virginia Nunes Juan R. González Teresa Casals
Journals: Human Genetics (57 papers)Human Mutation (44 papers)Human Molecular Genetics (19 papers)Genomics (15 papers)Journal of Medical Genetics (12 papers)
Partner nations: Spain United States United Kingdom

In The Last Decade

Xavier Estivill

506 papers receiving 21.7k citations

Hit Papers

align trajectories log scale

SNPassoc: an R package to perform whole genome association studies 2007 · 630 citations

Peers

Countries citing papers authored by Xavier Estivill

Since Specialization

Citations

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

Fields of papers citing papers by Xavier Estivill

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Xavier Estivill, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Xavier Estivill Line = papers co-authored together Xavier Estivill links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Dysregulation of the Wnt signaling pathway in South African patients with diffuse systemic sclerosis Clinical Rheumatology ·Jacqueline Frost, Xavier Estivill, Michèle Ramsay, Mohammed Tikly	2018	15
2	Deregulation of key signaling pathways involved in oocyte maturation in FMR1 premutation carriers with Fragile X-associated primary ovarian insufficiency Gene ·(unknown), Laia Rodríguez‐Revenga, Irene Madrigal, Francisco García‐García, M. Durán, Joaquı́n Dopazo, Xavier Estivill, Montserrat Milà	2015	10
3	Extensive sequence analysis of CFTR , SCNN1A , SCNN1B , SCNN1G and SERPINA1 suggests an oligogenic basis for cystic fibrosis‐like phenotypes Clinical Genetics ·María Dolores Burguete Ramos, Daniel Trujillano, Rut Olivar, Fernando Sotillo, Stephan Ossowski, José María Manzanares, Juliana Martins Barbosa da Silva Costa, Silvia Gärtner, Claudio Priore Oliva, E.C. Quintana, Mercedes González, C Vázquez, Xavier Estivill, Teresa Casals	2013	17
4	MicroRNA expression profiling in blood from fragile X‐associated tremor/ataxia syndrome patients Genes Brain & Behavior ·María Isabel Álvarez‐Mora, Laia Rodríguez‐Revenga, Irene Madrigal, F. Torres‐Silva, Elisabet Mateu-Huertas, Esther Lizano, Marc R. Friedländer, Eulàlia Martı́, Xavier Estivill, Montserrat Milà	2013	23
5	PeSV-Fisher: Identification of Somatic and Non-Somatic Structural Variants Using Next Generation Sequencing Data PLoS ONE ·Geòrgia Escaramís, Cristian Tornador, Laia Bassaganyas, Raquel Rabionet, José M. C. Tubío, Alexander Martinez‐Fundichely, Mario Cáceres, Marta Gut, Stephan Ossowski, Xavier Estivill	2013	15
6	Screening for the presence of FMR1 premutation alleles in women with fibromyalgia Gene ·Laia Rodríguez‐Revenga, Irene Madrigal, Josep Blanch‐Rubió, Dei M. Elurbe, Elisa Docampo, Antonio Collado, Javier Vidal, Jordi Carbonell, Xavier Estivill, Montserrat Milà	2012	9
7	Técnicas de Reflexión Estratégica: <i>Search Conference Momentum</i> El Profesional de la Informacion ·Toni Blanco, Joan Casals, Joan Frígols, Elisa Stinus, Xavier Estivill, Alfons Stinus	2011	0
8	A myriad of miRNA variants in control and Huntington’s disease brain regions detected by massively parallel sequencing Nucleic Acids Research ·Eulàlia Martı́, Lorena Pantano, Mónica Báñez-Coronel, Franc Llorens, Elena Miñones-Moyano, Sílvia Porta, Lauro Sumoy, Isidró Ferrer, Xavier Estivill	2010	238
9	A brain-derived neurotrophic factor (BDNF) haplotype is associated with antidepressant treatment outcome in mood disorders The Pharmacogenomics Journal ·Mónica Gratacòs, Virginia Soria, Mikel Urretavizcaya, Juan R. González, José Manuel Crespo, Mónica Bayés, Rafael de Cid, José M. Menchón, J. Vallejo, Xavier Estivill	2007	76
10	Different CFTR Mutational Spectrum in Alcoholic and Idiopathic Chronic Pancreatitis? Pancreas ·Teresa Casals, L. Aparisi, Cecilia Martínez‐Costa, (unknown), María Dolores Burguete Ramos, Josefina Móra, García Díaz, Jaume Boadas, Xavier Estivill, Antoni Farr	2004	26
11	Adenosine Triphosphate-Binding Cassette Superfamily Transporter Gene Expression in Severe Male Infertility1 Biology of Reproduction ·Sara Larriba, Lluís Bassas, Susana Egozcue, Javier Giménez, María Dolores Burguete Ramos, Oscar Briceño, Xavier Estivill, Teresa Casals	2001	19
12	Association Study of the Chromosomal Region Containing the FCER2 Gene Suggests It Has a Regulatory Role in Atopic Disorders American Journal of Respiratory and Critical Care Medicine ·Tarja Laitinen, Vesa Ollikainen, Conxi Lázaro, Paula Kauppi, Rafael de Cid, Josep M. Antó, Xavier Estivill, Heikki Lokki, Heikki Mannila, Lauri A. Laitinen, Juha Kere	2000	33
13	CDKN2A mutations in Spanish cutaneous malignant melanoma families and patients with multiple melanomas and other neoplasia Journal of Medical Genetics ·Anna Ruiz, Susana Puig, Josep Malvehy, Conxi Lázaro, Michael Lynch, A M Gimenez-Arnau, L. Puig, J Sánchez-Conejo, Xavier Estivill, T Castel	1999	41
14	[An analysis of 6 Leber mutations in 31 individuals with optic atrophy. A study of its transmission in 5 families]. PubMed ·Montse Gómez Zaera, Antoni Barrientos, Luís Arias, Isabel Rojas, Jorge Arruga, Xavier Estivill, Jordi Casademont, Virginia Nunes	1999	1
15	Mitochondrial DNA LHON mutations in alcoholic patients developing amblyopia Alcoholism Clinical and Experimental Research ·Montse Gómez Zaera, Óscar Miró, Luís Arias, Antoni Barrientos, Isabel Rojas, Jordi Arruga, Xavier Estivill, Jordi Casademont, Virginia Nunes	1999	3
16	Role of UEV-1, an Inactive Variant of the E2 UbiquitinConjugating Enzymes, in In Vitro Differentiation and Cell Cycle Behavior of HT-29-M6 Intestinal Mucosecretory Cells Molecular and Cellular Biology ·Elena Sancho, Maya R. Vilà, Luis Sánchez‐Pulido, Juan José Lozano, Rosanna Paciucci, Marga Nadal, Margaret Fox, Clare B. Harvey, Brenda Bercovich, Nourredine Loukili, Aaron Ciechanover, Stanley L. Lin, Ferrán Sanz, Xavier Estivill, Alfonso Valencia, Timothy M. Thomson	1998	111
17	[Molecular analysis of the IT15 gene in 79 Spanish families with Huntington's disease: diagnostic confirmation and presymptomatic diagnosis]. PubMed ·Aurora Sánchez, Montserrat Milà, Sergi Castellvı́-Bel, Matilde Calopa, D. E. Genis, Dolores Jiménez, Xavier Estivill	1997	3
18	HLA Class II Genes in Soybean Epidemic Asthma Patients American Journal of Respiratory and Critical Care Medicine ·Joan B. Soriano, Guadalupe Ercilla, Jordi Sunyer, Francisco X. Real, Conxi Lázaro, Marı́a J. Rodrigo, Xavier Estivill, Josep Roca, Robert Rodriguez-Roisín, Ferrán Morell, Josep M. Antó	1997	26
19	Genomic organization of TUPLE1/HIRA: Alternative splice products of the same gene UCL Discovery (University College London) ·Roser Llevadot, Peter Scambler, Xavier Estivill, Melanie Pritchard	1996	1
20	Mutation analysis in cystic fibrosis (II) New England Journal of Medicine ·Paolo Gasparini, P. F. Pignatti, Giuseppe Novelli, Bruno Dallapiccola, Virginia Nunes, Teresa Casals, Xavier Estivill, Esther Fernández, Angeliki Balassopoulou, Δημήτρης Λουκόπουλος, J. Javinha, Lidija Simova, Radovan Komel	1990	17

About Xavier Estivill

Xavier Estivill is a scholar working on Sensory Systems, Genetics, Molecular Biology, Genetics and Pulmonary and Respiratory Medicine, having authored 510 papers that have together received 22.2k indexed citations. Recurring topics across this work include Cystic Fibrosis Research Advances (87 papers), Genetics and Neurodevelopmental Disorders (51 papers), Genomic variations and chromosomal abnormalities (48 papers), Neonatal Respiratory Health Research (36 papers), Mitochondrial Function and Pathology (31 papers), Hearing, Cochlea, Tinnitus, Genetics (31 papers), Autism Spectrum Disorder Research (30 papers) and Tracheal and airway disorders (27 papers). The work is most often cited by research in Sensory Systems (2.2k citations), Genetics (4.9k citations), Molecular Biology (10.6k citations), Endocrine and Autonomic Systems (1.0k citations) and Cancer Research (2.1k citations). Xavier Estivill has collaborated with scholars based in Spain, United States and United Kingdom. Frequent co-authors include Raquel Rabionet, Lluı́s Armengol, Mónica Gratacòs, Paolo Gasparini, Eulàlia Martı́, Virginia Nunes, Juan R. González, Teresa Casals, Josep M. Mercader and Isidró Ferrer. Their work appears in journals such as Human Genetics, Human Mutation, Human Molecular Genetics, Genomics and Journal of Medical Genetics.

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.

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