Roberto Mendoza‐Londono

8.7k total citations
85 papers, 2.1k citations indexed

About

Roberto Mendoza‐Londono is a scholar working on Genetics, Molecular Biology and Oncology. According to data from OpenAlex, Roberto Mendoza‐Londono has authored 85 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 53 papers in Genetics, 40 papers in Molecular Biology and 10 papers in Oncology. Recurrent topics in Roberto Mendoza‐Londono's work include Genomic variations and chromosomal abnormalities (21 papers), Connective tissue disorders research (13 papers) and Genomics and Rare Diseases (12 papers). Roberto Mendoza‐Londono is often cited by papers focused on Genomic variations and chromosomal abnormalities (21 papers), Connective tissue disorders research (13 papers) and Genomics and Rare Diseases (12 papers). Roberto Mendoza‐Londono collaborates with scholars based in Canada, United States and France. Roberto Mendoza‐Londono's co-authors include Lucie Dupuis, Svetlana A. Yatsenko, Christian R. Marshall, Richard A. Lewis, Stephen W. Scherer, Dimitri J. Stavropoulos, Leena Ala‐Kokko, Marjorie Withers, Claudia M.B. Carvalho and Patricia Robbins‐Furman and has published in prestigious journals such as Journal of Clinical Investigation, SHILAP Revista de lepidopterología and Biochemistry.

In The Last Decade

Roberto Mendoza‐Londono

79 papers receiving 2.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Roberto Mendoza‐Londono Canada 26 1.2k 1.0k 258 174 166 85 2.1k
Beyhan Tüysüz Türkiye 24 988 0.8× 1.4k 1.4× 244 0.9× 231 1.3× 126 0.8× 139 2.5k
Bruno Leheup France 29 758 0.6× 1.1k 1.1× 171 0.7× 239 1.4× 225 1.4× 97 2.2k
Mohnish Suri United Kingdom 24 736 0.6× 1.2k 1.2× 171 0.7× 200 1.1× 137 0.8× 82 2.2k
Bertrand Isidor France 26 908 0.8× 1.3k 1.3× 112 0.4× 157 0.9× 138 0.8× 112 2.1k
Armand Bottani Switzerland 24 1.3k 1.1× 1.2k 1.2× 222 0.9× 178 1.0× 88 0.5× 62 2.2k
Rika Kosaki Japan 25 846 0.7× 1.3k 1.2× 185 0.7× 297 1.7× 236 1.4× 113 2.3k
Éliane Chouery Lebanon 29 621 0.5× 1.7k 1.7× 224 0.9× 188 1.1× 87 0.5× 130 2.8k
Yasemin Alanay Türkiye 26 1.0k 0.9× 994 1.0× 321 1.2× 370 2.1× 92 0.6× 108 2.1k
M.H. Breuning Netherlands 29 1.3k 1.1× 1.1k 1.1× 204 0.8× 201 1.2× 171 1.0× 60 2.6k
Diana Baralle United Kingdom 24 761 0.7× 1.8k 1.8× 149 0.6× 106 0.6× 145 0.9× 84 2.7k

Countries citing papers authored by Roberto Mendoza‐Londono

Since Specialization
Citations

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

Fields of papers citing papers by Roberto Mendoza‐Londono

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Roberto Mendoza‐Londono. 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 Roberto Mendoza‐Londono. The network helps show where Roberto Mendoza‐Londono may publish in the future.

Co-authorship network of co-authors of Roberto Mendoza‐Londono

This figure shows the co-authorship network connecting the top 25 collaborators of Roberto Mendoza‐Londono. A scholar is included among the top collaborators of Roberto Mendoza‐Londono 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 Roberto Mendoza‐Londono. Roberto Mendoza‐Londono 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.
Ungar, Wendy J., Christian R. Marshall, Robin Z. Hayeems, et al.. (2025). A microcosting and cost consequence analysis from a randomized controlled trial comparing genome sequencing with exome sequencing for genetic diagnosis. Genetics in Medicine. 28(2). 101561–101561. 1 indexed citations
2.
Gonorazky, Hernán, et al.. (2022). PURA syndrome: neuromuscular junction manifestations with potential therapeutic implications. Neuromuscular Disorders. 32(10). 842–844. 6 indexed citations
3.
Hayeems, Robin Z., David Dimmock, David Bick, et al.. (2020). Clinical utility of genomic sequencing: a measurement toolkit. npj Genomic Medicine. 5(1). 56–56. 46 indexed citations
4.
Deshwar, Ashish R., Malte Spielmann, Roberto Mendoza‐Londono, et al.. (2019). Disruption of the PTHLH regulatory landscape results in features consistent with hyperparathyroid disease. American Journal of Medical Genetics Part A. 179(4). 663–667. 2 indexed citations
5.
Sabatini, Peter, et al.. (2018). Stable transmission of an unbalanced chromosome 21 derived from chromoanasynthesis in a patient with a SYNGAP1 likely pathogenic variant. Molecular Cytogenetics. 11(1). 50–50. 9 indexed citations
6.
Costain, Gregory, Rebekah Jobling, Susan Walker, et al.. (2018). Periodic reanalysis of whole-genome sequencing data enhances the diagnostic advantage over standard clinical genetic testing. European Journal of Human Genetics. 26(5). 740–744. 65 indexed citations
7.
Mendoza‐Londono, Roberto, Somayyeh Fahiminiya, Jacek Majewski, et al.. (2015). Recessive Osteogenesis Imperfecta Caused by Missense Mutations in SPARC. The American Journal of Human Genetics. 96(6). 979–985. 95 indexed citations
8.
Mendoza‐Londono, Roberto, Lucie Dupuis, Pekka Kannus, et al.. (2015). MG-109 Revisiting a clinical diagnosis 15 years later with the aid of whole exome sequencing: Osteopetrosis versus harderophorphyria. Clinical Genetics. A4.1–A4. 1 indexed citations
9.
Mullegama, Sureni V., Christian R. Marshall, Anath C. Lionel, et al.. (2011). Severe intellectual disability and autistic features associated with microduplication 2q23.1. European Journal of Human Genetics. 20(4). 398–403. 27 indexed citations
10.
Yang, Tao, Roberto Mendoza‐Londono, Jianning Tao, et al.. (2010). E-selectin ligand–1 regulates growth plate homeostasis in mice by inhibiting the intracellular processing and secretion of mature TGF-β. Journal of Clinical Investigation. 120(7). 2474–2485. 25 indexed citations
11.
Gahunia, Harpal K., Paul Babyn, Susan Kirsch, & Roberto Mendoza‐Londono. (2009). Imaging ofSHOX-Associated Anomalies. Seminars in Musculoskeletal Radiology. 13(3). 236–254. 10 indexed citations
12.
Goobie, Sharan, Jeroen Knijnenburg, David Fitzpatrick, et al.. (2008). Molecular and clinical characterization of de novo and familial cases with microduplication 3q29: guidelines for copy number variation case reporting. Cytogenetic and Genome Research. 123(1-4). 65–78. 30 indexed citations
13.
Purandare, Smita M., Roberto Mendoza‐Londono, Svetlana A. Yatsenko, et al.. (2008). De novo three‐way chromosome translocation 46,XY,t(4;6;21)(p16;p21.1;q21) in a male with cleidocranial dysplasia. American Journal of Medical Genetics Part A. 146A(4). 453–458. 10 indexed citations
14.
Napierala, Dobrawa, Keiko Wakui, Connie Chen, et al.. (2005). Mutations and promoter SNPs in RUNX2, a transcriptional regulator of bone formation. Molecular Genetics and Metabolism. 86(1-2). 257–268. 50 indexed citations
15.
Yatsenko, Svetlana A., et al.. (2004). Attenuated phenotype in a child with trisomy for 1q due to unbalanced X;1 translocation [46,X,der(X),t(X;1)(q28;q32.1)]. American Journal of Medical Genetics Part A. 128A(1). 72–77. 9 indexed citations
16.
Yatsenko, Svetlana A., Roberto Mendoza‐Londono, John W. Belmont, & Lisa G. Shaffer. (2003). Omphalocele in trisomy 3q: further delineation of phenotype. Clinical Genetics. 64(5). 404–413. 20 indexed citations
17.
Mendoza‐Londono, Roberto. (2003). SABE CUÁNTO LE CUESTA LA ROTACIÓN DE PERSONAL. SHILAP Revista de lepidopterología. 48(48). 104–109. 1 indexed citations
18.
Brunetti‐Pierri, Nicola, Roberto Mendoza‐Londono, Maulik R. Shah, Lefkothea Karaviti, & Brendan Lee. (2003). von Voss‐Cherstvoy syndrome with transient thrombocytopenia and normal psychomotor development. American Journal of Medical Genetics Part A. 126A(3). 299–302. 5 indexed citations
19.
Mendoza‐Londono, Roberto, et al.. (1990). DNase I susceptibility of bent DNA and its alteration by ditercalinium and distamycin. Biochemistry. 29(21). 5035–5043. 11 indexed citations
20.
García‐Cruz, Diana, et al.. (1990). A distinct dysmorphic syndrome with congenital glaucoma and probable autosomal recessive inheritance. Ophthalmic Paediatrics and Genetics. 11(1). 35–40. 4 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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