Shahida Moosa

841 total citations
29 papers, 169 citations indexed

About

Shahida Moosa is a scholar working on Genetics, Molecular Biology and Rheumatology. According to data from OpenAlex, Shahida Moosa has authored 29 papers receiving a total of 169 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Genetics, 15 papers in Molecular Biology and 5 papers in Rheumatology. Recurrent topics in Shahida Moosa's work include Connective tissue disorders research (6 papers), Genomics and Rare Diseases (5 papers) and Bone and Dental Protein Studies (4 papers). Shahida Moosa is often cited by papers focused on Connective tissue disorders research (6 papers), Genomics and Rare Diseases (5 papers) and Bone and Dental Protein Studies (4 papers). Shahida Moosa collaborates with scholars based in South Africa, Germany and Japan. Shahida Moosa's co-authors include Bernd Wollnik, Peter Nürnberg, Virginia Fano, Janine Altmüller, Hölger Thiele, Lindsay Lambie, Ida Vogel, Yun Li, Gökhan Yigit and Arnold L. Christianson and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS Genetics and Seminars in Cell and Developmental Biology.

In The Last Decade

Shahida Moosa

20 papers receiving 168 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Shahida Moosa South Africa 10 96 91 18 17 16 29 169
Nadja Kokalj Vokač Slovenia 8 79 0.8× 62 0.7× 11 0.6× 27 1.6× 19 1.2× 27 179
Hugo Hernán Abarca-Barriga Peru 7 86 0.9× 88 1.0× 9 0.5× 11 0.6× 11 0.7× 30 159
Zita Halász Hungary 8 131 1.4× 164 1.8× 11 0.6× 9 0.5× 20 1.3× 20 267
John Hutson Australia 4 149 1.6× 119 1.3× 12 0.7× 17 1.0× 15 0.9× 6 201
Manisha Goyal India 8 48 0.5× 46 0.5× 5 0.3× 17 1.0× 16 1.0× 43 147
Beth A. Torchia United States 7 139 1.4× 281 3.1× 14 0.8× 13 0.8× 35 2.2× 11 369
Stefano Petrocchi Italy 8 84 0.9× 129 1.4× 18 1.0× 12 0.7× 31 1.9× 15 236
Peikuan Cong China 8 75 0.8× 62 0.7× 13 0.7× 7 0.4× 8 0.5× 12 168
Anne‐Sophie Jourdain France 6 99 1.0× 50 0.5× 15 0.8× 10 0.6× 11 0.7× 9 154
Thaís Kataoka Homma Brazil 10 144 1.5× 148 1.6× 8 0.4× 11 0.6× 31 1.9× 19 292

Countries citing papers authored by Shahida Moosa

Since Specialization
Citations

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

Fields of papers citing papers by Shahida Moosa

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Shahida Moosa

This figure shows the co-authorship network connecting the top 25 collaborators of Shahida Moosa. A scholar is included among the top collaborators of Shahida Moosa 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 Shahida Moosa. Shahida Moosa 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.
Yépez, Vicente A., et al.. (2025). RNA Sequencing for Rare Disease Diagnosis in a South African Family: A Novel Exon Elongation Event in OFD1 . American Journal of Medical Genetics Part A. 200(4). 985–988.
2.
Moosa, Shahida, et al.. (2025). Advancing genetic counselling in Southern Africa. Saudi Medical Journal. 46(4). 335–344.
3.
Javanmardi, Behnam, Tzung‐Chien Hsieh, Silvan Mertes, et al.. (2025). GestaltGAN: synthetic photorealistic portraits of individuals with rare genetic disorders. European Journal of Human Genetics. 33(3). 377–382. 4 indexed citations
4.
Sjöström, Elisabeth Stoltz, Ange‐Line Bruel, Christophe Philippe, et al.. (2024). Exploring the Cognitive and Behavioral Aspects of Shprintzen‐Goldberg Syndrome; a Novel Cohort and Literature Review. Clinical Genetics. 107(3). 328–334.
5.
Duong, Dat, Ping Hu, Behnam Javanmardi, et al.. (2024). Comparison of clinical geneticist and computer visual attention in assessing genetic conditions. PLoS Genetics. 20(2). e1011168–e1011168. 2 indexed citations
6.
Moosa, Shahida, et al.. (2024). Utility of next generation sequencing in paediatric neurological disorders: experience from South Africa. European Journal of Human Genetics. 32(10). 1314–1318.
7.
Zöllner, Ekkehard Werner, et al.. (2023). Genetic basis of osteogenesis imperfecta from a single tertiary centre in South Africa. European Journal of Human Genetics. 32(10). 1285–1290.
8.
Moosa, Shahida, et al.. (2023). Case report: Enamel renal syndrome: a case series from sub-Saharan Africa. SHILAP Revista de lepidopterología. 4. 1228760–1228760. 2 indexed citations
9.
Toorn, Ronald van, et al.. (2023). Adar-associated Aicardi Goutières syndrome in a child with bilateral striatal necrosis and recurrent episodes of transaminitis. BMJ Case Reports. 16(3). e252436–e252436. 1 indexed citations
10.
Jacob, Prince, Cecilie F. Rustad, V. Reid Sutton, et al.. (2023). Clinical, genetic and structural delineation of RPL13-related spondyloepimetaphyseal dysplasia suggest extra-ribosomal functions of eL13. npj Genomic Medicine. 8(1). 39–39. 1 indexed citations
11.
Wollnik, Bernd, et al.. (2023). B3GALT6-linkeropathy: Three illustrative patients spanning the disease spectrum. European Journal of Medical Genetics. 66(10). 104829–104829. 1 indexed citations
12.
Moosa, Shahida, et al.. (2022). A rare case of tuberous sclerosis complex-associated renal cell carcinoma. South African Journal of Radiology. 26(1). 2406–2406. 1 indexed citations
13.
14.
15.
Moosa, Shahida, et al.. (2018). Uncommon IFITM5 mutation associated with severe skeletal deformity in osteogenesis imperfecta. Annals of Human Genetics. 82(6). 477–481. 13 indexed citations
16.
Moosa, Shahida, Janine Altmüller, Filippo Beleggia, et al.. (2016). Smith–Kingsmore syndrome: A third family with the MTOR mutation c.5395G>A p.(Glu1799Lys) and evidence for paternal gonadal mosaicism. American Journal of Medical Genetics Part A. 173(1). 264–267. 13 indexed citations
17.
Moosa, Shahida, María Gabriela Obregón, Janine Altmüller, et al.. (2016). Novel IFT122 mutations in three Argentinian patients with cranioectodermal dysplasia: Expanding the mutational spectrum. American Journal of Medical Genetics Part A. 170(5). 1295–1301. 17 indexed citations
18.
Moosa, Shahida, et al.. (2013). Thyroid dysfunction in a cohort of South African children with Down syndrome. South African Medical Journal. 103(12). 966–966. 12 indexed citations
19.
Moosa, Shahida & Gen Nishimura. (2013). Pseudoachondroplasia: Report on a South African family. SHILAP Revista de lepidopterología. 17(2). 65–67. 1 indexed citations
20.
Moosa, Shahida, Lindsay Lambie, & Amanda Krause. (2012). Sirenomelia. Clinical Dysmorphology. 21(3). 124–130. 9 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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