Fatimah Rahman

1.2k total citations
9 papers, 439 citations indexed

About

Fatimah Rahman is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Genetics. According to data from OpenAlex, Fatimah Rahman has authored 9 papers receiving a total of 439 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 2 papers in Pediatrics, Perinatology and Child Health and 2 papers in Genetics. Recurrent topics in Fatimah Rahman's work include RNA regulation and disease (2 papers), Employee Performance and Motivation (1 paper) and Neonatal and fetal brain pathology (1 paper). Fatimah Rahman is often cited by papers focused on RNA regulation and disease (2 papers), Employee Performance and Motivation (1 paper) and Neonatal and fetal brain pathology (1 paper). Fatimah Rahman collaborates with scholars based in United Kingdom, France and Tunisia. Fatimah Rahman's co-authors include Eamonn R. Maher, Shanaz Pasha, Esther Meyer, Louise Tee, Wolf Reik, John R.W. Yates, C. Geoffrey Woods, Derek Lim, Neil V. Morgan and Dominic McMullan and has published in prestigious journals such as Journal of Clinical Investigation, The American Journal of Human Genetics and PLoS Genetics.

In The Last Decade

Fatimah Rahman

7 papers receiving 414 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Fatimah Rahman United Kingdom	7	278	209	132	69	45	9	439
Bruno Passet France	14	494 1.8×	133 0.6×	77 0.6×	83 1.2×	31 0.7×	45	666
Andrew Fedoriw United States	12	681 2.4×	294 1.4×	126 1.0×	24 0.3×	71 1.6×	14	764
Ligia Mateiu Belgium	12	285 1.0×	157 0.8×	98 0.7×	18 0.3×	24 0.5×	29	480
Keiji Hirabayashi Japan	12	252 0.9×	146 0.7×	31 0.2×	68 1.0×	52 1.2×	18	436
Emilie Ait‐Yahya France	7	171 0.6×	151 0.7×	42 0.3×	39 0.6×	114 2.5×	18	366
Michele Traversa Italy	11	183 0.7×	232 1.1×	45 0.3×	23 0.3×	20 0.4×	16	393
Tomasz M. Kuliński Poland	14	648 2.3×	213 1.0×	83 0.6×	19 0.3×	13 0.3×	17	707
Anne Bergmann United States	10	394 1.4×	289 1.4×	124 0.9×	26 0.4×	20 0.4×	15	484
Diana Alcantara United Kingdom	9	274 1.0×	192 0.9×	29 0.2×	54 0.8×	17 0.4×	11	426
Ko–ichiro Yoshiura Japan	12	304 1.1×	251 1.2×	107 0.8×	24 0.3×	16 0.4×	22	505

Countries citing papers authored by Fatimah Rahman

Since Specialization

Citations

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

Fields of papers citing papers by Fatimah Rahman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Fatimah Rahman

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

All Works

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9 of 9 papers shown

Rahman, Fatimah, et al.. (2022). Pengaruh Proactive Personality Terhadap Kepuasan Kerja Pegawai di Lembaga Pemasyarakatan Kelas IIB Klaten. Jurnal Ilmiah Manajemen Kesatuan. 10(3). 445–460. 1 indexed citations

Rahman, Fatimah. (2021). Implementasi Pembinaan Kepribadian Melalui Kesadaran Beragama Terhadap Narapidana Lanjut Usia. 15(1). 1–10.

Morgan, Neil V., Sarah Goddard, Tony S. Cardno, et al.. (2011). Mutation in the TCRα subunit constant gene (TRAC) leads to a human immunodeficiency disorder characterized by a lack of TCRαβ+ T cells. Journal of Clinical Investigation. 121(2). 695–702. 55 indexed citations

Meyer, Esther, Christopher J. Ricketts, Neil V. Morgan, et al.. (2010). Mutations in FLVCR2 Are Associated with Proliferative Vasculopathy and Hydranencephaly-Hydrocephaly Syndrome (Fowler Syndrome). The American Journal of Human Genetics. 86(3). 471–478. 46 indexed citations

Meyer, Esther, Michel Michaelides, Louise Tee, et al.. (2010). Nonsense mutation in TMEM126A causing autosomal recessive optic atrophy and auditory neuropathy.. PubMed. 16. 650–64. 39 indexed citations

Shuib, Salwati, Dominic McMullan, Eleanor Rattenberry, et al.. (2009). Microarray based analysis of 3p25‐p26 deletions (3p‐ syndrome). American Journal of Medical Genetics Part A. 149A(10). 2099–2105. 76 indexed citations

Meyer, Esther, Derek Lim, Shanaz Pasha, et al.. (2009). Germline Mutation in NLRP2 (NALP2) in a Familial Imprinting Disorder (Beckwith-Wiedemann Syndrome). PLoS Genetics. 5(3). e1000423–e1000423. 183 indexed citations

Meyer, Esther, Fatimah Rahman, Shanaz Pasha, et al.. (2009). Initiation codon mutation in betaB1-crystallin (CRYBB1) associated with autosomal recessive nuclear pulverulent cataract.. PubMed. 15. 1014–9. 24 indexed citations

Gamé, Laurence, Helen Banks, Nicola Cooley, et al.. (2005). MiMiR: a comprehensive solution for storage, annotation and exchange of microarray data. BMC Bioinformatics. 6(1). 268–268. 15 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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