María Caimari

513 total citations
14 papers, 232 citations indexed

About

María Caimari is a scholar working on Genetics, Endocrinology, Diabetes and Metabolism and Surgery. According to data from OpenAlex, María Caimari has authored 14 papers receiving a total of 232 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 5 papers in Endocrinology, Diabetes and Metabolism and 3 papers in Surgery. Recurrent topics in María Caimari's work include Hyperglycemia and glycemic control in critically ill and hospitalized patients (4 papers), Diabetes Management and Research (3 papers) and Diabetes and associated disorders (3 papers). María Caimari is often cited by papers focused on Hyperglycemia and glycemic control in critically ill and hospitalized patients (4 papers), Diabetes Management and Research (3 papers) and Diabetes and associated disorders (3 papers). María Caimari collaborates with scholars based in Spain, United Kingdom and Palestinian Territory. María Caimari's co-authors include Karen E. Heath, Ángel Campos‐Barros, Jesús Argente, Vicente Barrios, Francisca Díaz, Ricardo Gracía, Jesús Pozo, Gabriel Ángel Martos‐Moreno, Alfonso Hisado-Oliva and Damián Heine‐Suñer and has published in prestigious journals such as PLoS ONE, The Journal of Clinical Endocrinology & Metabolism and Diabetic Medicine.

In The Last Decade

María Caimari

14 papers receiving 228 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
María Caimari Spain 8 113 95 86 42 23 14 232
Ágnes Sallai Hungary 6 66 0.6× 46 0.5× 65 0.8× 22 0.5× 9 0.4× 18 147
Kristina Uvebrant Sweden 7 101 0.9× 52 0.5× 73 0.8× 59 1.4× 12 0.5× 9 256
R. Palmarino Italy 10 98 0.9× 66 0.7× 102 1.2× 36 0.9× 42 1.8× 40 357
Melissa A. Richard United States 9 96 0.8× 16 0.2× 179 2.1× 26 0.6× 20 0.9× 27 313
Susan Bromley United Kingdom 11 73 0.6× 55 0.6× 83 1.0× 53 1.3× 3 0.1× 15 310
Michiko Ohno Japan 8 142 1.3× 64 0.7× 113 1.3× 46 1.1× 8 0.3× 14 383
Laura Guazzarotti Italy 11 153 1.4× 124 1.3× 172 2.0× 136 3.2× 6 0.3× 21 362
Hílton Kuperman Brazil 10 158 1.4× 259 2.7× 150 1.7× 46 1.1× 3 0.1× 29 380
Jeanne E. O’Brien United States 10 142 1.3× 71 0.7× 44 0.5× 24 0.6× 10 0.4× 26 332
Lukas Soellner Germany 12 480 4.2× 68 0.7× 356 4.1× 36 0.9× 11 0.5× 22 609

Countries citing papers authored by María Caimari

Since Specialization
Citations

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

Fields of papers citing papers by María Caimari

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of María Caimari

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

All Works

14 of 14 papers shown
1.
Cobo-Stark, Patricia, Maria Antolı́n, Ariadna Campos-Martorell, et al.. (2023). Genetics and Natural History of Non-pancreatectomized Patients With Congenital Hyperinsulinism Due to Variants in ABCC8. The Journal of Clinical Endocrinology & Metabolism. 108(11). e1316–e1328. 7 indexed citations
2.
Clemente, María, Patricia Cobo-Stark, Maria Antolı́n, et al.. (2023). Genetics and natural history of non-pancreatectomised patients with congenital hyperinsulinism due to variants in ABCC8-Supplemental Data. Zenodo (CERN European Organization for Nuclear Research). 1 indexed citations
3.
Rica, Itxaso, et al.. (2017). Achievement of metabolic control among children and adolescents with type 1 diabetes in Spain. Acta Diabetologica. 54(7). 677–683. 5 indexed citations
4.
Peña, Mónica de la, Aina M. Yáñez, Josep Miquel Bauçà, et al.. (2017). Glycated hemoglobin and sleep apnea syndrome in children: beyond the apnea–hypopnea index. Sleep And Breathing. 22(1). 205–210. 5 indexed citations
5.
Malíková, Jana, Núria Camats, Mónica Fernández‐Cancio, et al.. (2014). Human NR5A1/SF-1 Mutations Show Decreased Activity on BDNF (Brain-Derived Neurotrophic Factor), an Important Regulator of Energy Balance: Testing Impact of Novel SF-1 Mutations Beyond Steroidogenesis. PLoS ONE. 9(8). e104838–e104838. 16 indexed citations
6.
Martín‐Santiago, A., et al.. (2013). Diagnostic Value of the Skin Lesions in Immune Dysregulation, Polyendocrinopathy, Enteropathy, X‐Linked Syndrome. Pediatric Dermatology. 30(6). e221–2. 13 indexed citations
7.
Gregory, Louise, Evelien Gevers, Kling Chong, et al.. (2013). Structural Pituitary Abnormalities Associated With CHARGE Syndrome. The Journal of Clinical Endocrinology & Metabolism. 98(4). E737–E743. 35 indexed citations
8.
Burguera, Bartolomé, Antoni Colom, Aina M. Yáñez, et al.. (2011). ACTYBOSS: Activity, Behavioral Therapy in Young Subjects – After-School Intervention Pilot Project on Obesity Prevention. Obesity Facts. 4(5). 400–406. 14 indexed citations
9.
Benito‐Sanz, Sara, Eva Barroso, Damián Heine‐Suñer, et al.. (2010). Clinical and Molecular Evaluation of SHOX/PAR1 Duplications in Léri-Weill Dyschondrosteosis (LWD) and Idiopathic Short Stature (ISS). The Journal of Clinical Endocrinology & Metabolism. 96(2). E404–E412. 58 indexed citations
10.
Shimomura, Kenju, et al.. (2009). The first clinical case of a mutation at residue K185 of Kir6.2 (KCNJ11): a major ATP‐binding residue. Diabetic Medicine. 27(2). 225–229. 12 indexed citations
11.
Heath, Karen E., Jesús Argente, Vicente Barrios, et al.. (2008). Primary Acid-Labile Subunit Deficiency due to RecessiveIGFALSMutations Results in Postnatal Growth Deficit Associated with Low Circulating Insulin Growth Factor (IGF)-I, IGF Binding Protein-3 Levels, and Hyperinsulinemia. The Journal of Clinical Endocrinology & Metabolism. 93(5). 1616–1624. 54 indexed citations
12.
Caimari, María, et al.. (1999). Pheochromocytoma and Clear-Cell Renal Carcinoma in a Child with von Hippel-Lindau Disease: A Patient Report. Journal of Pediatric Endocrinology and Metabolism. 12(4). 579–82. 6 indexed citations
13.
Salvador, Maria João, et al.. (1986). [Stippled epiphyses disease and alcoholic fetopathy].. PubMed. 24(4). 272–4. 1 indexed citations
14.
Caimari, María, et al.. (1986). Further observations in haemorrhagic shock and encephalopathy syndrome.. PubMed. 41(5). 469–71. 5 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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