Teresa Vendrell

947 total citations
25 papers, 310 citations indexed

About

Teresa Vendrell is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Teresa Vendrell has authored 25 papers receiving a total of 310 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 13 papers in Genetics and 8 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Teresa Vendrell's work include Prenatal Screening and Diagnostics (7 papers), Genomic variations and chromosomal abnormalities (7 papers) and Protein Tyrosine Phosphatases (5 papers). Teresa Vendrell is often cited by papers focused on Prenatal Screening and Diagnostics (7 papers), Genomic variations and chromosomal abnormalities (7 papers) and Protein Tyrosine Phosphatases (5 papers). Teresa Vendrell collaborates with scholars based in Spain, Palestinian Territory and Japan. Teresa Vendrell's co-authors include Alberto Plaja, C. Mediano, Núria Torán, Ana Carrió, Rafael Oliva, Jordi Rosell, Ester Margarit, Anna Soler, F Ballesta and D.F.C.M. Smeets and has published in prestigious journals such as PLoS ONE, Journal of Medical Genetics and American Journal of Medical Genetics.

In The Last Decade

Teresa Vendrell

23 papers receiving 290 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Teresa Vendrell Spain 12 160 143 64 49 45 25 310
Johanna Lundin Sweden 9 216 1.4× 91 0.6× 62 1.0× 24 0.5× 65 1.4× 20 397
Josef Davidsson Sweden 11 191 1.2× 165 1.2× 82 1.3× 40 0.8× 13 0.3× 16 442
Heide Seidel Germany 14 182 1.1× 192 1.3× 32 0.5× 42 0.9× 45 1.0× 24 337
Myriam Goldstein Israel 8 209 1.3× 83 0.6× 65 1.0× 22 0.4× 19 0.4× 10 331
Claudia Dellavecchia Italy 9 153 1.0× 220 1.5× 93 1.5× 32 0.7× 39 0.9× 11 408
Jürgen Groet United Kingdom 12 213 1.3× 98 0.7× 46 0.7× 59 1.2× 8 0.2× 15 502
H. Tönnies Germany 9 110 0.7× 126 0.9× 63 1.0× 15 0.3× 29 0.6× 21 330
Hirohito Shima Japan 11 149 0.9× 140 1.0× 30 0.5× 29 0.6× 65 1.4× 29 313
Martina Ruiterkamp‐Versteeg Netherlands 7 179 1.1× 90 0.6× 30 0.5× 47 1.0× 88 2.0× 11 311
Alina Khromykh United States 10 202 1.3× 164 1.1× 36 0.6× 30 0.6× 42 0.9× 13 367

Countries citing papers authored by Teresa Vendrell

Since Specialization
Citations

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

Fields of papers citing papers by Teresa Vendrell

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Teresa Vendrell

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

All Works

20 of 20 papers shown
1.
Fernández‐Álvarez, Paula, Marta Codina‐Solà, Irene Valenzuela, et al.. (2021). A systematic study and literature review of parental somatic mosaicism of FBN1 pathogenic variants in Marfan syndrome. Journal of Medical Genetics. 59(6). 605–612. 7 indexed citations
2.
Valenzuela, Irene, Benjamín Rodríguez‐Santiago, Paula Fernández‐Álvarez, et al.. (2018). Further delineation of the phenotype caused by loss of function mutations in PRMT7. European Journal of Medical Genetics. 62(3). 182–185. 10 indexed citations
3.
Valenzuela, Irene, Paula Fernández‐Álvarez, Alberto Plaja, et al.. (2018). Further delineation of the SOX18-related Hypotrichosis, Lymphedema, Telangiectasia syndrome (HTLS). European Journal of Medical Genetics. 61(5). 269–272. 12 indexed citations
4.
Valenzuela, Irene, Paula Fernández‐Álvarez, Francina Munell, et al.. (2017). Arthrogryposis as neonatal presentation of Loeys-Dietz syndrome due to a novel TGFBR2 mutation. European Journal of Medical Genetics. 60(6). 303–307. 6 indexed citations
5.
Clemente, María, et al.. (2015). Klinefelter Syndrome with Short Stature and Microcephaly: An Unusual Combination. 84.
6.
Plaja, Alberto, Anna M. Cueto‐González, Miguel Del Campo, et al.. (2015). A Novel Recurrent Breakpoint Responsible for Rearrangements in the Williams-Beuren Region. Cytogenetic and Genome Research. 146(3). 181–186. 6 indexed citations
7.
Mondéjar, R., Francisco Solano, Ángel Pérez Sempere, et al.. (2014). Mutation Prevalence of Cerebral Cavernous Malformation Genes in Spanish Patients. PLoS ONE. 9(1). e86286–e86286. 30 indexed citations
8.
Carcavilla, Atilano, Sixto García‐Miñáur, Antonio Pérez Aytés, et al.. (2014). Síndrome cardiofaciocutáneo, un trastorno relacionado con el síndrome de Noonan: hallazgos clínicos y moleculares en 11 pacientes. Medicina Clínica. 144(2). 67–72. 3 indexed citations
9.
Lloveras, Elisabet, Teresa Vendrell, Miguel Del Campo, et al.. (2014). Intrachromosomal 3p Insertion as a Cause of Reciprocal Pure Interstitial Deletion and Duplication in Two Siblings: Further Delineation of the Emerging Proximal 3p Deletion Syndrome. Cytogenetic and Genome Research. 144(4). 290–293. 5 indexed citations
10.
Krall, Paola, Patricia Ruíz, Teresa Vendrell, et al.. (2013). Cost-effective PKHD1 genetic testing for autosomal recessive polycystic kidney disease. Pediatric Nephrology. 29(2). 223–234. 13 indexed citations
11.
Serra‐Juhé, Clara, Benjamín Rodríguez‐Santiago, Ivon Cuscó, et al.. (2012). Contribution of Rare Copy Number Variants to Isolated Human Malformations. PLoS ONE. 7(10). e45530–e45530. 18 indexed citations
12.
Ezquieta, Begoña, José L. Santomé, Atilano Carcavilla, et al.. (2012). Alteraciones de los genes de la vía RAS-MAPK en 200 pacientes españoles con síndrome de Noonan y otros síndromes neurocardiofaciocutáneos. Genotipo y cardiopatía. Revista Española de Cardiología. 65(5). 447–455. 24 indexed citations
13.
Ezquieta, Begoña, José L. Santomé, Atilano Carcavilla, et al.. (2012). Alterations in RAS-MAPK Genes in 200 Spanish Patients With Noonan and Other Neuro-Cardio-Facio-Cutaneous Syndromes. Genotype and Cardiopathy. Revista Española de Cardiología (English Edition). 65(5). 447–455. 21 indexed citations
14.
Ferreres, Joan Carles, Elena Martínez‐Sáez, Teresa Vendrell, et al.. (2008). Pathological Findings in the Complete Trisomy 9 Syndrome: Three Case Reports and Review of the Literature. Pediatric and Developmental Pathology. 11(1). 23–29. 11 indexed citations
15.
Lloveras, Elisabet, Cynthia Pérez, Françesc Solé, et al.. (2003). Two cases of tetrasomy 9p syndrome with tissue limited mosaicism. American Journal of Medical Genetics Part A. 124A(4). 402–406. 17 indexed citations
16.
Plaja, Alberto, et al.. (2001). Variegated aneuploidy related to premature centromere division (PCD) is expressed in vivo and is a cancer-prone disease. American Journal of Medical Genetics. 98(3). 216–223. 37 indexed citations
17.
Vendrell, Teresa, et al.. (2001). Apparent coexistence of a neocentromere with an alphoid classic centromere. 1(44). 52–52. 1 indexed citations
18.
Plaja, Alberto, C. Mediano, Inmaculada Farrán-Codina, et al.. (1998). Trisomy (12p) with telocentric and pseudoisodicentric chromosome formation in a fetus.. PubMed. 41(1). 52–5. 5 indexed citations
19.
Plaja, Alberto, et al.. (1994). Terminal deletion of Xp in a dysmorphic anencephalic fetus. Prenatal Diagnosis. 14(5). 410–412. 18 indexed citations
20.
Plaja, Alberto, et al.. (1994). Terminal deletion of 6p: report of a new case.. PubMed. 37(4). 196–9. 12 indexed citations

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

Breakdown of academic impact, for papers by Johanna Lundin Breakdown of academic impact, for papers by Josef Davidsson Breakdown of academic impact, for papers by Heide Seidel Breakdown of academic impact, for papers by Myriam Goldstein Breakdown of academic impact, for papers by Claudia Dellavecchia Breakdown of academic impact, for papers by Jürgen Groet Breakdown of academic impact, for papers by H. Tönnies Breakdown of academic impact, for papers by Hirohito Shima Breakdown of academic impact, for papers by Martina Ruiterkamp‐Versteeg Breakdown of academic impact, for papers by Alina Khromykh
Rankless by CCL
2026