Ataf Sabir

473 total citations
19 papers, 158 citations indexed

About

Ataf Sabir is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Ataf Sabir has authored 19 papers receiving a total of 158 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Genetics, 10 papers in Molecular Biology and 3 papers in Pathology and Forensic Medicine. Recurrent topics in Ataf Sabir's work include Connective tissue disorders research (6 papers), RNA modifications and cancer (5 papers) and Genetic Syndromes and Imprinting (3 papers). Ataf Sabir is often cited by papers focused on Connective tissue disorders research (6 papers), RNA modifications and cancer (5 papers) and Genetic Syndromes and Imprinting (3 papers). Ataf Sabir collaborates with scholars based in United Kingdom, United States and Ireland. Ataf Sabir's co-authors include Trevor Cole, Elizabeth Forsythe, Denise Williams, David V. Milford, Sunayna Best, Lukas Foggensteiner, Bethan E. Hoskins, Detlef Böckenhauer, Melita Irving and Philip L. Beales and has published in prestigious journals such as SHILAP Revista de lepidopterología, Journal of the American Society of Nephrology and British Medical Bulletin.

In The Last Decade

Ataf Sabir

15 papers receiving 156 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ataf Sabir United Kingdom 7 137 97 24 15 14 19 158
Salima El Chehadeh-Djebbar France 4 154 1.1× 72 0.7× 23 1.0× 14 0.9× 10 0.7× 4 222
Bai-Lin Wu United States 6 163 1.2× 142 1.5× 51 2.1× 15 1.0× 11 0.8× 7 228
Bruna Lucheze Freire Brazil 8 133 1.0× 128 1.3× 34 1.4× 21 1.4× 28 2.0× 17 227
Gabrielle Lemire Canada 7 72 0.5× 91 0.9× 10 0.4× 15 1.0× 17 1.2× 16 165
Debbie Shears United Kingdom 4 79 0.6× 54 0.6× 8 0.3× 18 1.2× 16 1.1× 5 154
Resham Ejaz Canada 7 42 0.3× 55 0.6× 16 0.7× 17 1.1× 10 0.7× 16 132
Mehmet Tekman United Kingdom 7 47 0.3× 118 1.2× 13 0.5× 18 1.2× 7 0.5× 14 168
Christel Thauvin-Robinet France 6 69 0.5× 65 0.7× 26 1.1× 16 1.1× 6 0.4× 7 124
Helen Lord United Kingdom 7 93 0.7× 67 0.7× 17 0.7× 13 0.9× 4 0.3× 9 128

Countries citing papers authored by Ataf Sabir

Since Specialization
Citations

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

Fields of papers citing papers by Ataf Sabir

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ataf Sabir

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

All Works

19 of 19 papers shown
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Cheung, Moira, Tim Cole, Paul Arundel, et al.. (2023). Growth reference charts for children with hypochondroplasia. American Journal of Medical Genetics Part A. 194(2). 243–252. 6 indexed citations
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Sabir, Ataf, Jameela Sheikh, Alistair Calder, et al.. (2021). Diagnostic yield of rare skeletal dysplasia conditions in the radiogenomics era. BMC Medical Genomics. 14(1). 148–148. 11 indexed citations
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Paesschen, Wim Van, Ataf Sabir, Francis H. Sansbury, et al.. (2021). ERBB4 exonic deletions on chromosome 2q34 in patients with intellectual disability or epilepsy. European Journal of Human Genetics. 29(9). 1377–1383. 6 indexed citations
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Sabir, Ataf, et al.. (2021). Automated reanalysis application to assist in detecting novel gene–disease associations after genome sequencing. Genetics in Medicine. 24(4). 811–820. 5 indexed citations
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Sabir, Ataf, et al.. (2021). Automated reanalysis, a novel way to diagnose an ultra-rare condition: Fibronectin-1-related spondylometaphyseal dysplasia (SMD-FN1). Clinical Dysmorphology. 30(3). 154–158. 1 indexed citations
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Sabir, Ataf & Melita Irving. (2021). Clinical trials in skeletal dysplasia: a paradigm for treating rare diseases. British Medical Bulletin. 139(1). 16–35. 3 indexed citations
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Sabir, Ataf, et al.. (2021). A second report of recessive type COL4A1-related disorder: a novel homozygous missense variant. Clinical Dysmorphology. 30(2). 115–119. 2 indexed citations
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Sabir, Ataf, Jameela Sheikh, Vasantha Gowda, et al.. (2021). KIAA0753-related skeletal ciliopathy: a ninth case, extending the phenotype and reporting a novel variant. Clinical Dysmorphology. 30(3). 142–146. 1 indexed citations
13.
Buddhdev, Pranai, et al.. (2020). Hip displacement in Wolf–Hirschhorn syndrome: Report on three cases and review of associated musculoskeletal pathologies. American Journal of Medical Genetics Part A. 182(6). 1449–1453. 2 indexed citations
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Sabir, Ataf, et al.. (2020). Earlier detection of hypochondroplasia: A large single‐center UK case series and systematic review. American Journal of Medical Genetics Part A. 185(1). 73–82. 5 indexed citations
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Sabir, Ataf, et al.. (2019). Familial Russell–Silver Syndrome like Phenotype in the PCNA Domain of the CDKN1C Gene, a Further Case. SHILAP Revista de lepidopterología. 2019(1). 1398250–1398250. 11 indexed citations
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Sabir, Ataf & Trevor Cole. (2019). The evolving therapeutic landscape of genetic skeletal disorders. Orphanet Journal of Rare Diseases. 14(1). 300–300. 20 indexed citations
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Sabir, Ataf, Jessica Walker, & Rachel Hart. (2019). Expanding the phenotype of Filippi Syndrome: a patient with early onset puberty. Clinical Dysmorphology. 28(4). 224–226. 2 indexed citations
19.
Forsythe, Elizabeth, Sunayna Best, Bethan E. Hoskins, et al.. (2016). Risk Factors for Severe Renal Disease in Bardet–Biedl Syndrome. Journal of the American Society of Nephrology. 28(3). 963–970. 74 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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