María‐Isabel Tejada

3.7k total citations
46 papers, 758 citations indexed

About

María‐Isabel Tejada is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, María‐Isabel Tejada has authored 46 papers receiving a total of 758 indexed citations (citations by other indexed papers that have themselves been cited), including 38 papers in Genetics, 19 papers in Molecular Biology and 12 papers in Cognitive Neuroscience. Recurrent topics in María‐Isabel Tejada's work include Genetics and Neurodevelopmental Disorders (27 papers), Genomic variations and chromosomal abnormalities (19 papers) and Autism Spectrum Disorder Research (12 papers). María‐Isabel Tejada is often cited by papers focused on Genetics and Neurodevelopmental Disorders (27 papers), Genomic variations and chromosomal abnormalities (19 papers) and Autism Spectrum Disorder Research (12 papers). María‐Isabel Tejada collaborates with scholars based in Spain, United States and Netherlands. María‐Isabel Tejada's co-authors include Cristina Martínez-Bouzas, Elena Beristain, José-Ramón Rueda, Javier Ballesteros, Gemma Llort, Ana B. de la Hoz, Montserrat Milà, Miguel de la Hoya, Feliciano J. Ramos and Laia Rodríguez‐Revenga and has published in prestigious journals such as SHILAP Revista de lepidopterología, PEDIATRICS and Cochrane Database of Systematic Reviews.

In The Last Decade

María‐Isabel Tejada

44 papers receiving 729 citations

Peers

Countries citing papers authored by María‐Isabel Tejada

Since Specialization

Citations

This map shows the geographic impact of María‐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 María‐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 María‐Isabel Tejada more than expected).

Fields of papers citing papers by María‐Isabel Tejada

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of María‐Isabel Tejada

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	A global analysis of the reconstitution of PTEN function by translational readthrough ofPTENpathogenic premature termination codons 2021 ·Human Mutation ·(unknown), (unknown), (unknown), Laura Amo, Isabel Rodríguez‐Escudero, (unknown), Asier Erramuzpe, Jesús M. Cortés, María‐Isabel Tejada, Marı́a Molina, Caroline E. Nunes‐Xavier, José I. López, Vı́ctor J. Cid, Rafael Pulido	13
2	Targeted Next-Generation Sequencing in Patients with Suggestive X-Linked Intellectual Disability 2020 ·Genes ·(unknown), Ana B. de la Hoz, Olatz Villate, Isabel Llano‐Rivas, (unknown), Itxaso Martì, Míriam Guitart, Elisabeth Gabau, Fernando Andrade, Blanca Gener, María‐Isabel Tejada	18
3	Effect of AGG Interruptions on FMR1 Maternal Transmissions 2020 ·Frontiers in Molecular Biosciences ·Olatz Villate, Jesús Ibarluzea, (unknown), Ana B. de la Hoz, Laia Rodríguez‐Revenga, Silvia Izquierdo Álvarez, María‐Isabel Tejada	13
4	Hereditary Spastic Paraplegia and Intellectual Disability: Clinicogenetic Lessons From a Family Suggesting a Dual Genetics Diagnosis 2020 ·Frontiers in Neurology ·Sergio Aguilera, Ana B. de la Hoz, (unknown), (unknown), (unknown), Olatz Villate, (unknown), (unknown), I G Gurtubay, Guiomar Pérez de Nanclares, Arrate Pereda, María‐Isabel Tejada	1
5	Analysis of Lynch Syndrome Mismatch Repair Genes in Women with Endometrial Cancer 2016 ·Oncology ·(unknown), (unknown), Leire Andrés, Elena Aguirre, Judith Balmañà, Pilar Blay, Gemma Llort, Santiago González-Santiago, (unknown), María‐Isabel Tejada, Cristina Martínez-Bouzas	16
6	Guía clínica de las enfermedades asociadas al gen FMR1: síndrome X frágil, insuficiencia ovárica primaria y síndrome de temblor-ataxia 2013 ·Medicina Clínica ·Montserrat Milà, Feliciano J. Ramos, María‐Isabel Tejada	7
7	Intermediate FMR1 alleles and cognitive and/or behavioural phenotypes 2011 ·European Journal of Human Genetics ·Irene Madrigal, Mar Xunclà, María‐Isabel Tejada, Francisco Martı́nez, Isabel Fernández-Carvajal, Luis A. Pérez‐Jurado, Laia Rodríguez‐Revenga, Montserrat Milà	14
8	Folic acid for fragile X syndrome 2011 ·Cochrane Database of Systematic Reviews ·José-Ramón Rueda, Javier Ballesteros, (unknown), María‐Isabel Tejada, Iván Solà	8
9	Genome-wide Linkage Scan Reveals Three Putative Breast-Cancer-Susceptibility Loci 2009 ·The American Journal of Human Genetics ·Juan Manuel Rosa-Rosa, Guillermo Pita, Miguel Urioste, Gemma Llort, Joan Brunet, Conxi Lázaro, Ignacio Blanco, Teresa Ramón y Cajal, Orland Dı́ez, Miguel de la Hoya, Trinidad Caldés, María‐Isabel Tejada, Anna González‐Neira, Javier Benı́tez	25
10	Systematic review of pharmacological treatments in fragile X syndrome 2009 ·BMC Neurology ·José-Ramón Rueda, Javier Ballesteros, María‐Isabel Tejada	25
11	A study on MSH2 and MLH1 mutations in hereditary nonpolyposis colorectal cancer families from the Basque Country, describing four new germline mutations 2009 ·Familial Cancer ·Cristina Martínez-Bouzas, Elena Beristain, E Ojembarrena, José Errasti, (unknown), (unknown), María‐Isabel Tejada	4
12	Analysis of the molecular parameters that could predict the risk of manifesting premature ovarian failure in female premutation carriers of fragile X syndrome 2008 ·Menopause The Journal of The North American Menopause Society ·María‐Isabel Tejada, (unknown), Amaia Bilbao, Cristina Martínez-Bouzas, Elena Beristain, (unknown), María A. Ramos-Arroyo, (unknown), (unknown), (unknown), Feliciano J. Ramos	45
13	Risk of cognitive impairment in female premutation carriers of fragile X premutation: Analysis by means of robust segmented linear regression models 2008 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·(unknown), Berta Ibáñez, (unknown), Feliciano J. Ramos, (unknown), (unknown), (unknown), (unknown), Ángel Alonso, Cristina Martínez-Bouzas, Elena Beristain, María‐Isabel Tejada	16
14	Analysis of FANCB and FANCN/PALB2 Fanconi Anemia genes in BRCA1/2-negative Spanish breast cancer families 2008 ·Breast Cancer Research and Treatment ·María J. García, María Victoria Fernández, Ana Osório, Alicia Barroso, Gemma Llort, Conxi Lázaro, Ignacio Blanco, Trinidad Caldés, Miguel de la Hoya, Teresa Ramón y Cajal, Carmen Alonso, María‐Isabel Tejada, Carlos Román, Luis A. Díaz‐Robles, Miguel Urioste, Javier Benı́tez	68
15	X-chromosome tiling path array detection of copy number variants in patients with chromosome X-linked mental retardation 2007 ·BMC Genomics ·Irene Madrigal, Laia Rodríguez‐Revenga, Lluı́s Armengol, Eva González‐Roca, (unknown), Célia Bádenas, Aurora Sánchez, Francisco Martı́nez, Míriam Guitart, Isabel Fernández-Carvajal, (unknown), María‐Isabel Tejada, (unknown), Xavier Estivill, Montserrat Milà	48
16	Analysis of FMR1 gene expression in female premutation carriers using robust segmented linear regression models 2007 ·RNA ·(unknown), Berta Ibáñez, Miguel Mínguez, Manel Poch, (unknown), Arantza Sanz-Parra, Cristina Martínez-Bouzas, Elena Beristain, María‐Isabel Tejada	42
17	Screening for large rearrangements of the BRCA2 gene in Spanish families with breast/ovarian cancer 2006 ·Breast Cancer Research and Treatment ·Sara Gutiérrez‐Enríquez, Miguel de la Hoya, Cristina Martínez-Bouzas, (unknown), Teresa Ramón y Cajal, Gemma Llort, Ignacio Blanco, Elena Beristain, Eduardo Díaz‐Rubio, Carmen Alonso, María‐Isabel Tejada, Trinidad Caldés, Orland Dı́ez	38
18	Factors associated with premature chromosome condensation (PCC) following In Vitro Fertilization 1992 ·Journal of Assisted Reproduction and Genetics ·María‐Isabel Tejada, (unknown), (unknown), (unknown)	14
19	Chromosome studies in human unfertilized oocytes and uncleaved zygotes after treatment with gonadotropin-releasing hormone analogs 1991 ·Fertility and Sterility ·María‐Isabel Tejada, Rosario Mendoza, Beatriz Corcóstegui, (unknown)	19
20	Deletion of chromosome 4: 46,XY, del (4) (q31.3) after gamete intrafallopian transfer and in vitro fertilization-embryo transfer 1990 ·Fertility and Sterility ·María‐Isabel Tejada, Rosario Mendoza, (unknown), (unknown), Francisco Escudero, (unknown)	3

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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