Ravi Savarirayan

12.7k total citations · 3 hit papers
171 papers, 5.5k citations indexed

About

Ravi Savarirayan is a scholar working on Genetics, Molecular Biology and Rheumatology. According to data from OpenAlex, Ravi Savarirayan has authored 171 papers receiving a total of 5.5k indexed citations (citations by other indexed papers that have themselves been cited), including 122 papers in Genetics, 65 papers in Molecular Biology and 28 papers in Rheumatology. Recurrent topics in Ravi Savarirayan's work include Connective tissue disorders research (82 papers), Neonatal Respiratory Health Research (16 papers) and Genomic variations and chromosomal abnormalities (12 papers). Ravi Savarirayan is often cited by papers focused on Connective tissue disorders research (82 papers), Neonatal Respiratory Health Research (16 papers) and Genomic variations and chromosomal abnormalities (12 papers). Ravi Savarirayan collaborates with scholars based in Australia, United States and United Kingdom. Ravi Savarirayan's co-authors include Zornitza Stark, Andrea Superti‐Furga, Valérie Cormier‐Daire, John F. Bateman, David Sillence, Sheila Unger, Geert Mortier, Gen Nishimura, Matthew L. Warman and Christine M Hall and has published in prestigious journals such as New England Journal of Medicine, Nature Communications and Nature Genetics.

In The Last Decade

Ravi Savarirayan

167 papers receiving 5.3k citations

Hit Papers

align trajectories

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.

Nosology and classification of genetic skeletal disorders: 2010 revision

2011 450 citations Matthew L. Warman, Valérie Cormier‐Daire et al. American Journal of Medical Genetics Part A profile →
Nosology and classification of genetic skeletal disorders: 2019 revision

2019 379 citations Geert Mortier, Valérie Cormier‐Daire et al. American Journal of Medical Genetics Part A profile →
Nosology and classification of genetic skeletal disorders: 2015 revision

2015 367 citations Luisa Bonafé, Valérie Cormier‐Daire et al. American Journal of Medical Genetics Part A profile →

Peers

Ravi Savarirayan

GENET

RHEUM

SURGE

ONCOL

Gen Nishimura Japan

Deborah Krakow United States

Ralph S. Lachman United States

Sheila Unger Switzerland

Laurence Legeai‐Mallet France

Beat Steinmann Switzerland

Martine Le Merrer France

Ilkka Kaitila Finland

Michael J. Dixon United Kingdom

Kenjiro Kosaki Japan

Gen Nishimura Japan

Ravi Savarirayan

3.7k ×1.2

GENET

3.6k ×1.5

1.2k ×1.2

RHEUM

781 ×1.2

SURGE

828 ×1.5

ONCOL

Citations per year, relative to Ravi Savarirayan Ravi Savarirayan (= 1×) peers Gen Nishimura

Countries citing papers authored by Ravi Savarirayan

Since Specialization

Citations

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

Fields of papers citing papers by Ravi Savarirayan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ravi Savarirayan

This figure shows the co-authorship network connecting the top 25 collaborators of Ravi Savarirayan. A scholar is included among the top collaborators of Ravi Savarirayan 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 Ravi Savarirayan. Ravi Savarirayan 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

Cheung, Moira, Deborah M. Eastwood, Mohamad Maghnie, et al.. (2024). Meeting report from the 3rd ISCBH-ERN BOND Achondroplasia Workshop on Long Bone Pathology in Children with Achondroplasia, Salzburg, Austria 22nd June 2024. Bone. 190. 117268–117268. 2 indexed citations

Savarirayan, Ravi, William R. Wilcox, Paul Harmatz, et al.. (2024). P131: Persistence of growth-promoting effects in infants and toddlers with achondroplasia: Results from a phase II extension study with vosoritide*. SHILAP Revista de lepidopterología. 2. 101028–101028. 1 indexed citations

Billich, Natassja, et al.. (2023). A scoping review of nutrition issues and management strategies in individuals with skeletal dysplasia. Genetics in Medicine. 25(10). 100920–100920. 2 indexed citations

Ferdinand, Angeline, Jeromey Temple, Yin Paradies, et al.. (2021). Culturally competent communication in Indigenous disability assessment: a qualitative study. International Journal for Equity in Health. 20(1). 68–68. 7 indexed citations

Fredwall, Svein O., Cecilie F. Rustad, Heidi B. Eggesbø, et al.. (2020). High prevalence of symptomatic spinal stenosis in Norwegian adults with achondroplasia: a population-based study. Orphanet Journal of Rare Diseases. 15(1). 123–123. 33 indexed citations

Irving, Melita, Joel Charrow, Valérie Cormier‐Daire, et al.. (2018). Vosoritide for Children with Achondroplasia: A 30 Month Update from an Ongoing Phase 2 Clinical Trial. Hormone Research in Paediatrics. 89.

Bonafé, Luisa, Valérie Cormier‐Daire, Christine M Hall, et al.. (2015). Nosology and classification of genetic skeletal disorders: 2015 revision. American Journal of Medical Genetics Part A. 167(12). 2869–2892. 367 indexed citations breakdown →

White, Klane K., Viviana Bompadre, Michael J. Goldberg, et al.. (2015). Best practices in the evaluation and treatment of foramen magnum stenosis in achondroplasia during infancy. American Journal of Medical Genetics Part A. 170(1). 42–51. 51 indexed citations

Hendriksz, Christian J., Kenneth I. Berger, Roberto Giugliani, et al.. (2014). International guidelines for the management and treatment of Morquio A syndrome. American Journal of Medical Genetics Part A. 167(1). 11–25. 93 indexed citations

10.

Cullinane, Fiona, et al.. (2014). Midtrimester pregnancy loss and cervical incompetence—Is there an association with connective tissue laxity?. Open Journal of Obstetrics and Gynecology. 4(1). 28–32. 3 indexed citations

11.

Banka, Siddharth, Damien Lederer, Valérie Benoît, et al.. (2014). Novel KDM6A (UTX) mutations and a clinical and molecular review of the X‐linked Kabuki syndrome (KS2). Clinical Genetics. 87(3). 252–258. 91 indexed citations

12.

Warman, Matthew L., Valérie Cormier‐Daire, Christine M Hall, et al.. (2011). Nosology and classification of genetic skeletal disorders: 2010 revision. American Journal of Medical Genetics Part A. 155(5). 943–968. 450 indexed citations breakdown →

13.

Kannus, Pekka, Melita Irving, Salim Aftimos, & Ravi Savarirayan. (2011). Two Novel COL2A1 Mutations Associated with a Legg-Calvé-Perthes Disease-like Presentation. Clinical Orthopaedics and Related Research. 469(6). 1785–1790. 36 indexed citations

14.

Stark, Zornitza, et al.. (2011). Isolated hypogonadotropic hypogonadism with SOX2 mutation and anophthalmia/microphthalmia in offspring. European Journal of Human Genetics. 19(7). 753–756. 27 indexed citations

15.

Stark, Zornitza, Monique M. Ryan, Ion Cristian Cirstea, et al.. (2011). Two novel germline KRAS mutations: expanding the molecular and clinical phenotype. Clinical Genetics. 81(6). 590–594. 23 indexed citations

16.

Dimasi, David P., Kathryn P. Burdon, Alex W. Hewitt, et al.. (2010). Candidate gene study to investigate the genetic determinants of normal variation in central corneal thickness.. PubMed. 16. 562–9. 14 indexed citations

17.

Kannus, Pekka, Ravi Savarirayan, Linda Ozoemena, Susan M. White, & John A. McGrath. (2006). Rapp–Hodgkin ectodermal dysplasia syndrome: The clinical and molecular overlap with Hay–Wells syndrome. American Journal of Medical Genetics Part A. 140A(8). 887–891. 13 indexed citations

18.

White, Susan M., Elizabeth M. Thompson, Alexa Kidd, et al.. (2004). Growth, behavior, and clinical findings in 27 patients with Kabuki (Niikawa–Kuroki) syndrome. American Journal of Medical Genetics Part A. 127A(2). 118–127. 66 indexed citations

19.

Lucia, S. P., Alessandra Pangrazio, Cristina Sobacchi, et al.. (2004). TCIRG1-dependent recessive osteopetrosis: Mutation analysis, functional identification of the splicing defects, andin vitro rescue by U1 snRNA. Human Mutation. 24(3). 225–235. 80 indexed citations

20.

Savarirayan, Ravi, Elizabeth Thompson, & Jozef Gécz. (2003). Spondyloepiphyseal dysplasia tarda (SEDL, MIM #313400). European Journal of Human Genetics. 11(9). 639–642. 22 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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