Jair Tenorio

3.9k total citations
76 papers, 943 citations indexed

About

Jair Tenorio is a scholar working on Molecular Biology, Pulmonary and Respiratory Medicine and Genetics. According to data from OpenAlex, Jair Tenorio has authored 76 papers receiving a total of 943 indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Molecular Biology, 29 papers in Pulmonary and Respiratory Medicine and 28 papers in Genetics. Recurrent topics in Jair Tenorio's work include Pulmonary Hypertension Research and Treatments (27 papers), Genomic variations and chromosomal abnormalities (13 papers) and Genetic Syndromes and Imprinting (10 papers). Jair Tenorio is often cited by papers focused on Pulmonary Hypertension Research and Treatments (27 papers), Genomic variations and chromosomal abnormalities (13 papers) and Genetic Syndromes and Imprinting (10 papers). Jair Tenorio collaborates with scholars based in Spain, United States and Netherlands. Jair Tenorio's co-authors include Pablo Lapunzina, Pedro Arias, Víctor Martínez‐Glez, Víctor L. Ruiz‐Pérez, Julián Nevado, Pilar Escribano Subías, Gema Gordo, Julián Palomino Doza, Sixto García‐Miñáur and Karen E. Heath and has published in prestigious journals such as Nucleic Acids Research, Journal of Clinical Oncology and SHILAP Revista de lepidopterología.

In The Last Decade

Jair Tenorio

63 papers receiving 932 citations

Peers

Jair Tenorio
Mette Gaustadnes Denmark
Malu Zandbergen Netherlands
Daniel Ng United States
Toshihiro Shimizu Japan
Bernhard Bielesz Austria
Yuko Shima Japan
Emilia Cirillo Italy
Thiruvur Niranjan United States
Elena Pardi Italy
Maria Lombardi Netherlands
Mette Gaustadnes Denmark
Jair Tenorio
Citations per year, relative to Jair Tenorio Jair Tenorio (= 1×) peers Mette Gaustadnes

Countries citing papers authored by Jair Tenorio

Since Specialization
Citations

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

Fields of papers citing papers by Jair Tenorio

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jair Tenorio

This figure shows the co-authorship network connecting the top 25 collaborators of Jair Tenorio. A scholar is included among the top collaborators of Jair Tenorio 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 Jair Tenorio. Jair Tenorio 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.
Rodríguez‐Antolín, Carlos, et al.. (2025). A Novel Deep Intronic Variant in NSD1 Causing Sotos Syndrome. American Journal of Medical Genetics Part A. 197(8). e64074–e64074. 1 indexed citations
2.
Nevado, Julián, Raquel Blanco-Lago, Adolfo Hernández, et al.. (2025). Clinician-Based Functional Scoring and Genomic Insights for Prognostic Stratification in Wolf–Hirschhorn Syndrome. Genes. 16(7). 820–820.
3.
Batzir, Nurit Assia, Julián Nevado, Jair Tenorio, et al.. (2025). N-terminal truncating variants in CACNB1 cause a new congenital muscular disorder. European Journal of Human Genetics. 34(3). 314–323.
4.
Tenorio, Jair, Rita María Regojo, Jane Juusola, et al.. (2024). Non‐immune hydrops fetalis is associated with bi‐allelic pathogenic variants in the MYB Binding Protein 1a ( MYBBP1A ) gene. Clinical Genetics. 106(6). 713–720.
5.
Arias, Pedro, Steven D. Klein, Julián Nevado, et al.. (2024). Phenotypic spectrum and tumor risk in Simpson‐Golabi‐Behmel syndrome: Case series and comprehensive literature review. American Journal of Medical Genetics Part A. 194(12). e63840–e63840. 4 indexed citations
6.
Simón, Rogelio, Daniel Natera‐de Benito, Jair Tenorio, et al.. (2024). A Novel Missense Variant in the NKX2-1 Homeodomain Prevents Transcriptional Rescue by TAZ. Thyroid. 34(7). 942–948.
7.
8.
Montani, David, Christina A. Eichstaedt, Catharina Belge, et al.. (2023). Conseil génétique et dépistage de l’hypertension artérielle pulmonaire – consensus du Consortium international pour les études génétiques dans l’HTAP – version française. Revue des Maladies Respiratoires. 40(9-10). 838–852. 1 indexed citations
9.
Hernández, Adolfo, et al.. (2023). Cognitive–Behavioral Profile in Pediatric Patients with Syndrome 5p-; Genotype–Phenotype Correlationships. Genes. 14(8). 1628–1628. 3 indexed citations
10.
11.
Marín, María Jesús del Cerro, María Álvarez-Fuente, Víctor Manuel Becerra‐Muñoz, et al.. (2023). Seven Additional Patients with SOX17 Related Pulmonary Arterial Hypertension and Review of the Literature. Genes. 14(10). 1965–1965. 2 indexed citations
12.
Franco‐Gonzalez, Juan Felipe, Daniel Morales‐Cano, Edgar Fernández-Malavé, et al.. (2023). Novel Loss-of-Function KCNA5 Variants in Pulmonary Arterial Hypertension. American Journal of Respiratory Cell and Molecular Biology. 69(2). 147–158. 6 indexed citations
13.
Mussa, Alessandro, Pablo Lapunzina, Jair Tenorio, et al.. (2023). Adult experiences in Beckwith–Wiedemann syndrome. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 193(2). 116–127. 2 indexed citations
14.
15.
Eichstaedt, Christina A., Catharina Belge, Wendy K. Chung, et al.. (2022). Genetic counselling and testing in pulmonary arterial hypertension: a consensus statement on behalf of the International Consortium for Genetic Studies in PAH. European Respiratory Journal. 61(2). 2201471–2201471. 23 indexed citations
16.
Hernández‐González, Ignacio, Manuel López‐Meseguer, Pablo Lapunzina, et al.. (2022). Usefulness of genetics for clinical reclassification and refinement of prognostic stratification in pulmonary arterial hypertension. Revista Española de Cardiología (English Edition). 76(6). 460–467. 1 indexed citations
17.
Fernández‐Burriel, Miguel, et al.. (2021). TBL1XR1 associated intellectual disability, a new missense variant with dysmorphic features plus autism: Expanding the phenotypic spectrum. Clinical Genetics. 99(6). 812–817. 9 indexed citations
18.
Martínez‐Glez, Víctor, Jair Tenorio, Julián Nevado, et al.. (2020). A six-attribute classification of geneticmosaicism. Genetics in Medicine. 22(11). 1743–1757. 42 indexed citations
19.
Monteagudo, Ana, José Ramón Hernández Mora, Carlos Simón, et al.. (2020). The role of ZFP57 and additional KRAB-zinc finger proteins in the maintenance of human imprinted methylation and multi-locus imprinting disturbances. Nucleic Acids Research. 48(20). 11394–11407. 33 indexed citations
20.
Gordo, Gema, Jair Tenorio, Pedro Arias, et al.. (2017). mTOR mutations in Smith‐Kingsmore syndrome: Four additional patients and a review. Clinical Genetics. 93(4). 762–775. 29 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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