Fatima Rahman

715 total citations
14 papers, 130 citations indexed

About

Fatima Rahman is a scholar working on Molecular Biology, Genetics and Emergency Medicine. According to data from OpenAlex, Fatima Rahman has authored 14 papers receiving a total of 130 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 4 papers in Genetics and 3 papers in Emergency Medicine. Recurrent topics in Fatima Rahman's work include Genomics and Rare Diseases (4 papers), Trauma and Emergency Care Studies (3 papers) and Neurogenetic and Muscular Disorders Research (2 papers). Fatima Rahman is often cited by papers focused on Genomics and Rare Diseases (4 papers), Trauma and Emergency Care Studies (3 papers) and Neurogenetic and Muscular Disorders Research (2 papers). Fatima Rahman collaborates with scholars based in United Kingdom, Pakistan and Australia. Fatima Rahman's co-authors include Paul Gissen, Eamonn R. Maher, Evangeline Wassmer, Esther Meyer, Shanaz Pasha, J. Helen Cross, Salwati Shuib, Ingrid E. Scheffer, Neil V. Morgan and John Osborne and has published in prestigious journals such as SHILAP Revista de lepidopterología, Brain and Journal of Medical Genetics.

In The Last Decade

Fatima Rahman

11 papers receiving 128 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Fatima Rahman United Kingdom 5 52 38 23 19 17 14 130
Adel Mahmoud Saudi Arabia 9 80 1.5× 42 1.1× 62 2.7× 9 0.5× 14 0.8× 27 207
Tyson L. Ware Australia 9 49 0.9× 35 0.9× 31 1.3× 29 1.5× 3 0.2× 12 203
Anne Dieux‐Coëslier France 7 99 1.9× 39 1.0× 7 0.3× 22 1.2× 15 0.9× 12 156
Monica Lodi Italy 10 42 0.8× 62 1.6× 113 4.9× 38 2.0× 4 0.2× 15 231
Ahlam A. Hamed Sudan 7 33 0.6× 19 0.5× 24 1.0× 14 0.7× 4 0.2× 15 102
Maria Antonietta Pisanti Italy 5 76 1.5× 43 1.1× 6 0.3× 11 0.6× 10 0.6× 7 135
Marlies Frank Austria 8 94 1.8× 16 0.4× 20 0.9× 13 0.7× 3 0.2× 20 196
Paige Cooper United States 6 106 2.0× 11 0.3× 5 0.2× 22 1.2× 5 0.3× 8 194
Jean‐Paul Harpey France 7 137 2.6× 63 1.7× 9 0.4× 14 0.7× 7 0.4× 7 253
Elliott H. Sherr United States 2 61 1.2× 24 0.6× 40 1.7× 7 0.4× 23 1.4× 2 115

Countries citing papers authored by Fatima Rahman

Since Specialization
Citations

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

Fields of papers citing papers by Fatima Rahman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Fatima Rahman

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

All Works

14 of 14 papers shown
1.
2.
Rahman, Fatima, Abolfazl Rad, Gabriela Oprea, et al.. (2024). Bi-allelic MYMX variants cause a syndromic congenital myopathy with recognizable facial palsy, growth restriction, and dysmorphism. European Journal of Human Genetics. 33(4). 552–555.
3.
Rahman, Fatima, et al.. (2024). Behavior Problem and Mental Health of Children Affected by Floods-2022 in Pakistan. Journal of Loss and Trauma. 30(4). 540–565. 1 indexed citations
4.
Rahman, Fatima, et al.. (2023). Parenting Practices and Aggression in Childhood Behaviour Disorders. SHILAP Revista de lepidopterología. 73(1). 74–78. 1 indexed citations
5.
Salayev, Kamran, Clarissa Rocca, Rauan Kaiyrzhanov, et al.. (2022). AP4B1-associated hereditary spastic paraplegia: Expansion of clinico-genetic phenotype and geographic range. European Journal of Medical Genetics. 65(11). 104620–104620.
6.
Maroofian, Reza, Stéphanie Efthymiou, Fatima Rahman, et al.. (2022). Consolidating the association of biallelic MAPKAPK5 pathogenic variants with a distinct syndromic neurodevelopmental disorder. Journal of Medical Genetics. 60(8). 791–796. 1 indexed citations
7.
Zaki, Maha S., Andrea Accogli, Ghayda Mirzaa, et al.. (2021). Pathogenic variants in PIDD1 lead to an autosomal recessive neurodevelopmental disorder with pachygyria and psychiatric features. European Journal of Human Genetics. 29(8). 1226–1234. 9 indexed citations
8.
Nazir, Niaman, et al.. (2020). Baseline characteristics of American Indian smokeless tobacco users participating in two pilot cessation studies. Journal of Community Health. 45(4). 812–819. 2 indexed citations
9.
Mitra, Biswadev, Annie Carter, De Villiers Smit, et al.. (2019). Proactive review by the emergency department before inter‐hospital transfer (the PREVENT study). Emergency Medicine Australasia. 32(1). 61–66. 3 indexed citations
10.
Rahman, Fatima, et al.. (2015). Indications for blood transfusion following trauma - a pilot study. Journal of emergency medicine, trauma & acute care. 2015(1). 6 indexed citations
11.
12.
Bruce, Christopher K, Fatima Rahman, Zhifeng Liu, et al.. (2010). Design and validation of a metabolic disorder resequencing microarray (BRUM1). Human Mutation. 31(7). 858–865. 13 indexed citations
13.
Kurian, Manju A., Esther Meyer, Grace Vassallo, et al.. (2010). Phospholipase C beta 1 deficiency is associated with early-onset epileptic encephalopathy. Brain. 133(10). 2964–2970. 78 indexed citations
14.
Fitzgerald, Mark, et al.. (2008). Survival following resuscitative thoracotomy for combined left ventricle and left atrium ruptures secondary to blunt trauma. Injury. 39(9). 1089–1092. 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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