Isabel Tejada

659 total citations
9 papers, 414 citations indexed

About

Isabel Tejada is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Isabel Tejada has authored 9 papers receiving a total of 414 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 4 papers in Molecular Biology and 3 papers in Cognitive Neuroscience. Recurrent topics in Isabel Tejada's work include Genetics and Neurodevelopmental Disorders (6 papers), Genomic variations and chromosomal abnormalities (4 papers) and Autism Spectrum Disorder Research (3 papers). Isabel Tejada is often cited by papers focused on Genetics and Neurodevelopmental Disorders (6 papers), Genomic variations and chromosomal abnormalities (4 papers) and Autism Spectrum Disorder Research (3 papers). Isabel Tejada collaborates with scholars based in Spain, France and United States. Isabel Tejada's co-authors include Étienne Mornet, Jack Tarleton, Dominique Heitz, Angela Barnicoat, H Malmgren, Niklas Dahl, Christopher G. Mathew, Janet L. Macpherson, François Rousseau and A Boué and has published in prestigious journals such as Human Molecular Genetics, Human Mutation and American Journal of Medical Genetics.

In The Last Decade

Isabel Tejada

8 papers receiving 406 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Isabel Tejada Spain 6 359 248 223 47 15 9 414
Marja‐Leena Väisänen Finland 8 336 0.9× 200 0.8× 203 0.9× 37 0.8× 13 0.9× 11 447
R. Willemsen Netherlands 6 254 0.7× 230 0.9× 128 0.6× 48 1.0× 15 1.0× 8 349
Mary Jacena Leigh United States 6 334 0.9× 216 0.9× 256 1.1× 37 0.8× 17 1.1× 6 444
Stela Filipovic-Sadic United States 7 511 1.4× 304 1.2× 358 1.6× 40 0.9× 25 1.7× 7 553
Gabrielle Barnby United Kingdom 5 214 0.6× 163 0.7× 184 0.8× 61 1.3× 11 0.7× 6 343
Kali Witherspoon United States 2 446 1.2× 283 1.1× 279 1.3× 35 0.7× 33 2.2× 2 568
Bert Ba de Vries Netherlands 5 270 0.8× 169 0.7× 121 0.5× 18 0.4× 9 0.6× 7 305
Louise W. Staley United States 6 369 1.0× 210 0.8× 283 1.3× 19 0.4× 12 0.8× 8 398
Aia Elise Jønch Denmark 6 306 0.9× 230 0.9× 194 0.9× 69 1.5× 23 1.5× 11 396
Allison Sumis United States 6 309 0.9× 198 0.8× 213 1.0× 34 0.7× 24 1.6× 7 350

Countries citing papers authored by Isabel Tejada

Since Specialization
Citations

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

Fields of papers citing papers by Isabel Tejada

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Isabel Tejada

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

All Works

9 of 9 papers shown
1.
2.
Martı́nez, Francisco, Isabel Martínez‐Garay, Silvestre Oltra, et al.. (2004). Localization of MRX82: A new nonsyndromic X‐linked mental retardation locus to Xq24‐q25 in a Basque family. American Journal of Medical Genetics Part A. 131A(2). 174–178. 5 indexed citations
4.
5.
Rousseau, François, Dominique Heitz, Jack Tarleton, et al.. (1994). A multicenter study on genotype-phenotype correlations in the fragile X syndrome, using direct diagnosis with probe StB12.3: the first 2,253 cases.. PubMed. 55(2). 225–37. 238 indexed citations
6.
Mornet, Étienne, et al.. (1993). Affected sibs with fragde X syndrome exhibit an age‐dependent decrease in the size of the fragile X full mutation. Clinical Genetics. 43(3). 157–159. 9 indexed citations
7.
Oudet, C, Étienne Mornet, J.L. Serre, et al.. (1993). Linkage disequilibrium between the fragile X mutation and two closely linked CA repeats suggests that fragile X chromosomes are derived from a small number of founder chromosomes.. PubMed. 52(2). 297–304. 111 indexed citations
8.
Tejada, Isabel, Étienne Mornet, Valérie Biancalana, et al.. (1992). Direct DNA analysis of fragile X syndrome in Spanish pedigrees. American Journal of Medical Genetics. 43(1-2). 282–290. 21 indexed citations
9.
Tejada, Isabel, J Boué, & S Gilgenkrantz. (1983). [Prenatal diagnosis of a male fetal carrier of fragile X chromosome by the amniotic fluid cells].. PubMed. 26(4). 247–50. 2 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

Rankless by CCL
2026