Isabel Tejada
Impact in
- Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Cognitive Neuroscience top 10%
- Autism Spectrum Disorder Research
Papers in
- Genetics 6
- Genetics and Neurodevelopmental Disorders 6
- Genomic variations and chromosomal abnormalities 4
- Genomics and Rare Diseases 1
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- Retinal Development and Disorders 2
- Epigenetics and DNA Methylation 1
- Co-authors
- Étienne Mornet (4 shared papers)H Malmgren (1 shared paper)Niklas Dahl (1 shared paper)Dominique Heitz (1 shared paper)Jack Tarleton (1 shared paper)François Rousseau (1 shared paper)Angela Barnicoat (1 shared paper)Janet L. Macpherson (1 shared paper)
In The Last Decade
Isabel Tejada
9 papers receiving 408 citations
Peers
Comparison fields: 5 of 44
- Genetics 350
- Cognitive Neuroscience 202
- Molecular Biology 232
- Cellular and Molecular Neuroscience 47
- Developmental Neuroscience 4
Countries citing papers authored by Isabel Tejada
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
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-authors
The 25 scholars most cited alongside Isabel Tejada, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | A multicenter study on genotype-phenotype correlations in the fragile X syndrome, using direct diagnosis with probe StB12.3: the first 2,253 cases. | 1994 | 238 |
| 2 | 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. | 1993 | 110 |
| 3 | 1992 | 21 | |
| 4 | 1994 | 20 | |
| 5 | 1993 | 9 | |
| 6 | 1996 | 8 | |
| 7 | 2004 | 5 | |
| 8 | [Prenatal diagnosis of a male fetal carrier of fragile X chromosome by the amniotic fluid cells]. | 1983 | 2 |
| 9 | 2024 | 1 |
About Isabel Tejada
Isabel Tejada is a scholar working on Genetics, Molecular Biology, Cognitive Neuroscience, Cellular and Molecular Neuroscience and Social Psychology, having authored 9 papers that have together received 414 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (6 papers), Genomic variations and chromosomal abnormalities (4 papers), Autism Spectrum Disorder Research (3 papers), Retinal Development and Disorders (2 papers), Photoreceptor and optogenetics research (2 papers), Epigenetics and DNA Methylation (1 paper), Genomics and Rare Diseases (1 paper) and Bat Biology and Ecology Studies (1 paper). The work is most often cited by research in Genetics (350 citations), Cognitive Neuroscience (202 citations), Molecular Biology (232 citations), Cellular and Molecular Neuroscience (47 citations) and Developmental Neuroscience (4 citations). Isabel Tejada has collaborated with scholars based in Spain, France and Canada. Frequent co-authors include Étienne Mornet, H Malmgren, Niklas Dahl, Dominique Heitz, Jack Tarleton, François Rousseau, Angela Barnicoat, Janet L. Macpherson, Christopher G. Mathew and A Boué. Their work appears in journals such as Clinical Genetics, Human Molecular Genetics, Human Mutation, Revista Peruana de Biología and American Journal of Medical Genetics Part A.
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.