María Martínez

22.9k total citations · 2 hit papers
132 papers, 4.8k citations indexed

About

María Martínez is a scholar working on Genetics, Molecular Biology and Physiology. According to data from OpenAlex, María Martínez has authored 132 papers receiving a total of 4.8k indexed citations (citations by other indexed papers that have themselves been cited), including 74 papers in Genetics, 42 papers in Molecular Biology and 23 papers in Physiology. Recurrent topics in María Martínez's work include Genetic Associations and Epidemiology (41 papers), Genetics and Neurodevelopmental Disorders (21 papers) and Genomic variations and chromosomal abnormalities (15 papers). María Martínez is often cited by papers focused on Genetic Associations and Epidemiology (41 papers), Genetics and Neurodevelopmental Disorders (21 papers) and Genomic variations and chromosomal abnormalities (15 papers). María Martínez collaborates with scholars based in France, United States and Canada. María Martínez's co-authors include Alexis Brice, Dominique Campion, Françoise Clerget‐Darpoux, Lynn R. Goldin, Christiane Penet, Thierry Frébourg, John Hardy, Thomas Gasser, Didier Hannequin and Peter Heutink and has published in prestigious journals such as The Lancet, PLoS ONE and American Journal of Psychiatry.

In The Last Decade

María Martínez

127 papers receiving 4.6k citations

Hit Papers

Imputation of sequence variants for identificati... 1999 2026 2008 2017 2011 1999 200 400 600
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.

  1. Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies
    2011 660 citations Michael A. Nalls, María Martínez et al. profile →
  2. Early-Onset Autosomal Dominant Alzheimer Disease: Prevalence, Genetic Heterogeneity, and Mutation Spectrum
    1999 544 citations Dominique Campion, Didier Hannequin et al. The American Journal of Human Genetics profile →

Peers

María Martínez
Panos Roussos United States
Kirk C. Wilhelmsen United States
Richard Haas United States
Meharvan Singh United States
Nicola Specchio Italy
Benedetta Nacmias Italy
Margaret A. Pericak‐Vance United States
Mitsuyuki Matsumoto Japan
Valentina Escott‐Price United Kingdom
Elizabeth A. Thomas United States
Panos Roussos United States
María Martínez
Citations per year, relative to María Martínez María Martínez (= 1×) peers Panos Roussos

Countries citing papers authored by María Martínez

Since Specialization
Citations

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

Fields of papers citing papers by María Martínez

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of María Martínez

This figure shows the co-authorship network connecting the top 25 collaborators of María Martínez. A scholar is included among the top collaborators of María Martínez 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 Martínez. María Martínez 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.
Martínez, María, et al.. (2025). Increased spontaneous physical activity in female MEST-deficient mice protects against diet-induced obesity. Frontiers in Endocrinology. 16. 1680158–1680158.
2.
3.
Green, William, Stephen Wood, María Martínez, et al.. (2020). Improving junior doctor medicine prescribing and patient safety: An intervention using personalised, structured, video‐enhanced feedback and deliberate practice. British Journal of Clinical Pharmacology. 86(11). 2234–2246. 9 indexed citations
4.
Martínez, María, Christine W. Duarte, J. Patrizia Stohn, et al.. (2018). Thyroid hormone influences brain gene expression programs and behaviors in later generations by altering germ line epigenetic information. Molecular Psychiatry. 25(5). 939–950. 35 indexed citations
5.
Martínez, María, Namita Multani, Cassandra Jessica Anor, et al.. (2018). Emotion Detection Deficits and Decreased Empathy in Patients with Alzheimer’s Disease and Parkinson’s Disease Affect Caregiver Mood and Burden. Frontiers in Aging Neuroscience. 10. 120–120. 54 indexed citations
6.
Nalls, Michael A., Mohamad Saad, Alastair J. Noyce, et al.. (2013). Genetic comorbidities in Parkinson's disease. Human Molecular Genetics. 23(3). 831–841. 48 indexed citations
7.
Pierre, Aude Saint, Zulma G. Vitezica, & María Martínez. (2009). A comparative study of three methods for detecting association of quantitative traits in samples of related subjects. BMC Proceedings. 3(S7). S122–S122. 3 indexed citations
8.
Kaufman, Jean‐Marc, Agnès Ostertag, Aude Saint-Pierre, et al.. (2008). Genome-Wide Linkage Screen of Bone Mineral Density (BMD) in European Pedigrees Ascertained through a Male Relative with Low BMD Values: Evidence for Quantitative Trait Loci on 17q21–23, 11q12–13, 13q12–14, and 22q11. The Journal of Clinical Endocrinology & Metabolism. 93(10). 3755–3762. 33 indexed citations
9.
Gasparin, Gustavo, Luiz Lehmann Coutinho, María Martínez, et al.. (2005). Mapeamento de QTLS para peso ao nascimento no cromossomo 14 de bovinos. Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT). 1 indexed citations
10.
Duan, Jubao, María Martínez, Alan R. Sanders, et al.. (2004). Polymorphisms in the Trace Amine Receptor 4 (TRAR4) Gene on Chromosome 6q23.2 Are Associated with Susceptibility to Schizophrenia. The American Journal of Human Genetics. 75(4). 624–638. 66 indexed citations
11.
Martínez, María, et al.. (2002). Linkage disequillbrium analysis of 6ql3-q26 schizophrenia candidate genes.. The American Journal of Human Genetics. 71(4). 473–473. 1 indexed citations
12.
Maziade, Michel, María Martínez, Benoit R. Gauthier, et al.. (1997). Childhood/early adolescence-onsetand adult-onset schizophrenia. The British Journal of Psychiatry. 170(1). 27–30. 15 indexed citations
13.
Hannequin, Didier, Dominique Campion, Alexis Brice, et al.. (1996). Génétique de la maladie d'Alzheimer. La Revue de Médecine Interne. 17(7). 545–550.
14.
Génin, Emmanuelle, María Martínez, & Françoise Clerget‐Darpoux. (1995). Posterior probability of linkage and maximal lod score. Annals of Human Genetics. 59(1). 123–132. 9 indexed citations
15.
Otterud, Brith, Wen‐Tsong Hsieh, María Martínez, et al.. (1995). Genetic mapping of adrenergic receptor genes in humans. Journal of Molecular Medicine. 73(6). 299–306. 22 indexed citations
16.
Martínez, María, Laurent Abel, & Florence Démenais. (1995). How can maximum likelihood methods reveal candidate gene effects on a quantitative trait?. Genetic Epidemiology. 12(6). 789–794. 7 indexed citations
17.
Campion, Dominique, Thierry d’Amato, Christian Bastard, et al.. (1994). Genetic study of dopamine D1, D2, and D4 receptors in schizophrenia. Psychiatry Research. 51(3). 215–230. 36 indexed citations
18.
Goldin, Lynn R., María Martínez, & Elliot S. Gershon. (1991). Sampling strategies for linkage studies. European Archives of Psychiatry and Clinical Neuroscience. 240(3). 182–187. 16 indexed citations
19.
Martínez, María, et al.. (1990). Genetic mapping of common diseases: the challenges of manic-depressive illness and schizophrenia. Trends in Genetics. 6(9). 282–286. 16 indexed citations
20.
Martínez, María. (1987). La industria del vestido en murcia (siglos XIII-XV). 3 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.

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