Teresa Casals

5.7k citations

81 papers · 2.7k indexed · 1 hit paper · h-index 27

Pulmonary and Respiratory Medicine top 1%
Molecular Biology
Genetics top 2%
Genetics top 5%
Surgery top 10%

Co-authors: Xavier Estivill Virginia Nunes Miguel Chillón Lluís Bassas María Dolores Burguete Ramos Marie‐Catherine Romey Núria Morral Willy Lissens
Topics: Cystic Fibrosis Research Advances (68 papers)Neonatal Respiratory Health Research (29 papers)Congenital Ear and Nasal Anomalies (26 papers)
Cited by: Pulmonary and Respiratory Medicine Genetics Reproductive Medicine
Journals: New England Journal of Medicine Nucleic Acids Research Gut
Partner nations: Spain Italy United Kingdom

In The Last Decade

Teresa Casals

79 papers receiving 2.6k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Mutations in the Cystic Fibrosis Gene in Patients with Congenital Absence of the Vas Deferens

1995 680 citations Miguel Chillón, Teresa Casals et al. New England Journal of Medicine profile →

Peers

Countries citing papers authored by Teresa Casals

Since Specialization

Citations

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

Fields of papers citing papers by Teresa Casals

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Teresa Casals

This figure shows the co-authorship network connecting the top 25 collaborators of Teresa Casals. A scholar is included among the top collaborators of Teresa Casals 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 Teresa Casals. Teresa Casals 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	Extensive sequence analysis of CFTR , SCNN1A , SCNN1B , SCNN1G and SERPINA1 suggests an oligogenic basis for cystic fibrosis‐like phenotypes 2013 ·Clinical Genetics ·María Dolores Burguete Ramos,Daniel Trujillano,(unknown),(unknown),Stephan Ossowski,José María Manzanares,(unknown),Silvia Gärtner,Claudio Priore Oliva,(unknown),(unknown),(unknown),Xavier Estivill,Teresa Casals	17
2	GUSB and ATP2B4 are suitable reference genes for CFTR gene expression data normalization in nasal epithelium cells 2012 ·Journal of Cystic Fibrosis ·Laìa Masvidal,(unknown),Laura Ruano,Javier de Gracia,Sara Larriba,Teresa Casals	4
3	Complete ascertainment of intragenic copy number mutations (CNMs) in the CFTR gene and its implications for CNM formation at other autosomal loci 2010 ·Human Mutation ·(unknown),Jian‐Min Chen,Nadia Chuzhanova,Caroline Bénech,Teresa Casals,Milan Maçek,Thierry Bienvenu,Trudi McDevitt,Philip M. Farrell,(unknown),Taïeb Messaoud,Harry Cuppens,Garry R. Cutting,Peter D. Stenson,(unknown),Marie‐Pierre Audrézet,D.N. Cooper,Claude Férec	23
4	The p.Arg258Gly Mutation in Intracellular Loop 2 of CFTR is Associated with CFTR -Related Disorders 2009 ·Genetic Testing and Molecular Biomarkers ·Laìa Masvidal,Javier Giménez,María Dolores Burguete Ramos,Christian Domingo,Antoni Farré,L. Bassas,Teresa Casals	3
5	N-terminal CFTR missense variants severely affect the behavior of the CFTR chloride channel 2008 ·Human Mutation ·(unknown),(unknown),Sara Larriba,David de Semir,Itziar Martínez-González,(unknown),Carles Solsona,Teresa Casals,Josep M. Aran	23
6	Spectrum of mutations in CFTR in Finland: 18 years follow-up study and identification of two novel mutations 2005 ·Journal of Cystic Fibrosis ·(unknown),Sandra Bonache,Teresa Casals,(unknown),Erkki Savilahti,Juha Kere,Irma Järvelä	10
7	Molecular evaluation of CFTR sequence variants in male infertility of testicular origin 2005 ·International Journal of Andrology ·Sara Larriba,Sandra Bonache,Joaquim Sàrquella,María Dolores Burguete Ramos,Juliette Gimenez,Lluís Bassas,Teresa Casals	19
8	Different CFTR Mutational Spectrum in Alcoholic and Idiopathic Chronic Pancreatitis? 2004 ·Pancreas ·Teresa Casals,L. Aparisi,Cecilia Martínez‐Costa,(unknown),María Dolores Burguete Ramos,Josefina Móra,García Díaz,Jaume Boadas,Xavier Estivill,(unknown)	26
9	Suitability of oligonucleotide‐mediated cystic fibrosis gene repair in airway epithelial cells 2003 ·The Journal of Gene Medicine ·David de Semir,Marga Nadal,Juan R. González,Sara Larriba,(unknown),Virginia Nunes,Teresa Casals,Xavier Estivill,Josep M. Aran	5
10	Non‐viral vector‐mediated uptake, distribution, and stability of chimeraplasts in human airway epithelial cells 2002 ·The Journal of Gene Medicine ·David de Semir,Jordi Pétriz,(unknown),Sara Larriba,Virginia Nunes,Teresa Casals,Xavier Estivill,Josep M. Aran	14
11	Adenosine Triphosphate-Binding Cassette Superfamily Transporter Gene Expression in Severe Male Infertility1 2001 ·Biology of Reproduction ·Sara Larriba,Lluís Bassas,Susana Egozcue,Javier Giménez,María Dolores Burguete Ramos,(unknown),Xavier Estivill,Teresa Casals	19
12	Complex allele [-102T>A+S549R(T>G)] is associated with milder forms of cystic fibrosis than allele S549R(T>G) alone 1999 ·Human Genetics ·Marie‐Catherine Romey,Caroline Guittard,J. P. Chazalette,Philippe Frossard,K. P. Dawson,M A Patton,Teresa Casals,(unknown),Emmanuelle Girodon,G. Rault,Dominique Bozon,Fabienne Séguret,Jacques Demaille,Mireille Claustres	23
13	SSCP analysis: A blind sensitivity trial 1997 ·Human Mutation ·Albena Jordanova,Luba Kalaydjieva,Alexey Savov,Mireille Claustres,Martin Schwarz,Xavier Estivill,Dora Angelicheva,Andrea Haworth,Teresa Casals,Ivo Kremensky	60
14	Clinical characteristics of 16 cystic fibrosis patients with the missense mutation R334W, a pancreatic insufficiency mutation with variable age of onset and interfamilial clinical differences 1995 ·Human Genetics ·Xavier Estivill,(unknown),(unknown),V.S. Nunes,Teresa Casals,Luís Ortigosa,(unknown),(unknown),Jorge Ferrer,(unknown),(unknown),N. Cobos,(unknown)	26
15	Analysis of the CFTR gene in the Spanish population: SSCP-screening for 60 known mutations and identification of four new mutations (Q30X, A120T, 1812-1 G→A, and 3667de14) 1994 ·Human Mutation ·Miguel Chillón,Teresa Casals,(unknown),Virginia Nunes,Xavier Estivill	25
16	Identification of a frameshift mutation (1609delCA) in exon 10 of the CFTR gene in seven Spanish cystic fibrosis patients 1992 ·Human Mutation ·Miguel Chillón,Ana Palacio,Virginia Nunes,Teresa Casals,(unknown),Xavier Estivill	11
17	Analysis of 14 cystic fibrosis mutations in five South European populations 1991 ·Human Genetics ·Virginia Nunes,Paolo Gasparini,(unknown),Antonia Gaona,A. Bonizzato,Federica Sangiuolo,Angeliki Balassopoulou,(unknown),(unknown),Metka Ravnik‐Glavač,(unknown),Vahe Mokini,Radovan Komel,Bruno Dallapiccola,Pier Franco Pignatti,(unknown),Teresa Casals,Xavier Estivill	45
18	Mutation analysis in cystic fibrosis (II) 1990 ·New England Journal of Medicine ·Paolo Gasparini,(unknown),Giuseppe Novelli,Bruno Dallapiccola,Virginia Nunes,Teresa Casals,Xavier Estivill,Esther Fernández,Angeliki Balassopoulou,(unknown),(unknown),(unknown),Radovan Komel	17
19	Distribution of the ΔF508 mutation in 194 Spanish cystic fibrosis families 1990 ·Human Genetics ·Miguel Chillón,Virginia Nunes,Teresa Casals,(unknown),Esther Fernández,Javier Benı́tez,Xavier Estivill	11
20	Linkage disequilibrium for DNA haplotypes near the cystic fibrosis locus in two South European populations 1989 ·Human Genetics ·Xavier Estivill,Paolo Gasparini,Giuseppe Novelli,Teresa Casals,Virginia Nunes,P. Gallano,Anna Savoia,Annamaria Ruzzo,Bruno Dallapiccola,(unknown)	8

About Teresa Casals

Teresa Casals is a scholar working on Genetics, Pulmonary and Respiratory Medicine and Immunology, having authored 81 papers that have together received 2.7k indexed citations. Recurring topics across this work include Cystic Fibrosis Research Advances (68 papers), Neonatal Respiratory Health Research (29 papers) and Congenital Ear and Nasal Anomalies (26 papers). The work is most often cited by research in Pulmonary and Respiratory Medicine (1.9k citations), Genetics (501 citations) and Reproductive Medicine (161 citations). Teresa Casals has collaborated with scholars based in Spain, Italy and United Kingdom. Frequent co-authors include Xavier Estivill, Virginia Nunes, Miguel Chillón, Lluís Bassas, María Dolores Burguete Ramos, Marie‐Catherine Romey, Núria Morral, Willy Lissens, C. Verlingue and M. Claustres. Their work appears in journals such as New England Journal of Medicine, Nucleic Acids Research and Gut.

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