Anna Rajab

4.8k total citations
58 papers, 1.9k citations indexed

About

Anna Rajab is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Anna Rajab has authored 58 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Molecular Biology, 28 papers in Genetics and 9 papers in Cell Biology. Recurrent topics in Anna Rajab's work include Genomics and Rare Diseases (9 papers), Connective tissue disorders research (7 papers) and Nuclear Structure and Function (7 papers). Anna Rajab is often cited by papers focused on Genomics and Rare Diseases (9 papers), Connective tissue disorders research (7 papers) and Nuclear Structure and Function (7 papers). Anna Rajab collaborates with scholars based in Oman, United Kingdom and Germany. Anna Rajab's co-authors include Stefan Mundlos, Michael A. Patton, Peter Nürnberg, Michael Quinn Patton, Mohsen Karbasiyan, Ali R. Afzal, Christiane Fenske, Victoria A. Murday, Navaratnam Elanko and Steven Jeffery and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and PLoS ONE.

In The Last Decade

Anna Rajab

57 papers receiving 1.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Anna Rajab Oman 23 1.2k 628 454 180 170 58 1.9k
Wafaa Eyaid Saudi Arabia 25 1.5k 1.3× 889 1.4× 459 1.0× 255 1.4× 108 0.6× 55 2.4k
Stavit A. Shalev Israel 29 1.8k 1.5× 709 1.1× 378 0.8× 126 0.7× 124 0.7× 88 2.6k
Noriyuki Azuma Japan 28 1.5k 1.2× 644 1.0× 215 0.5× 147 0.8× 148 0.9× 139 2.6k
Kaya Bilgüvar United States 27 992 0.8× 532 0.8× 284 0.6× 128 0.7× 122 0.7× 78 2.0k
Beyhan Tüysüz Türkiye 24 1.4k 1.1× 988 1.6× 469 1.0× 171 0.9× 136 0.8× 139 2.5k
Diana Baralle United Kingdom 24 1.8k 1.5× 761 1.2× 426 0.9× 84 0.5× 153 0.9× 84 2.7k
Vincent El Ghouzzi France 27 1.1k 0.9× 1.0k 1.7× 233 0.5× 185 1.0× 113 0.7× 44 2.1k
Mohnish Suri United Kingdom 24 1.2k 1.0× 736 1.2× 260 0.6× 180 1.0× 94 0.6× 82 2.2k
Eissa Faqeih Saudi Arabia 28 1.5k 1.2× 920 1.5× 238 0.5× 136 0.8× 98 0.6× 80 2.2k
David Geneviève France 24 1.3k 1.1× 1.1k 1.8× 233 0.5× 202 1.1× 168 1.0× 80 2.3k

Countries citing papers authored by Anna Rajab

Since Specialization
Citations

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

Fields of papers citing papers by Anna Rajab

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anna Rajab

This figure shows the co-authorship network connecting the top 25 collaborators of Anna Rajab. A scholar is included among the top collaborators of Anna Rajab 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 Anna Rajab. Anna Rajab 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.
Bradshaw, Tyler WA, Erik J. Soderblom, Anna Rajab, et al.. (2021). Genetic disruption of WASHC4 drives endo-lysosomal dysfunction and cognitive-movement impairments in mice and humans. eLife. 10. 29 indexed citations
2.
Rajab, Anna, et al.. (2015). Cytogenetic studies of 1232 patients with different sexual development abnormalities from the Sultanate of Oman. Reproductive BioMedicine Online. 32(2). 162–169. 7 indexed citations
3.
Al‐Maawali, Almundher, Brenda J. Barry, Anna Rajab, et al.. (2015). Novel loss‐of‐function variants in DIAPH1 associated with syndromic microcephaly, blindness, and early onset seizures. American Journal of Medical Genetics Part A. 170(2). 435–440. 37 indexed citations
4.
Squitieri, Ferdinando, et al.. (2014). K13 First Middle Eastern Focus On Research And Assistance On Huntington Disease In Oman. Journal of Neurology Neurosurgery & Psychiatry. 85(Suppl 1). A83–A83. 2 indexed citations
5.
Derivery, Emmanuel, Hongbo Hu, Masoud Garshasbi, et al.. (2011). Identification of a novel candidate gene for non-syndromic autosomal recessive intellectual disability: the WASH complex member SWIP. Human Molecular Genetics. 20(13). 2585–2590. 62 indexed citations
6.
Rajab, Anna, Volker Straub, Liza McCann, et al.. (2010). Fatal Cardiac Arrhythmia and Long-QT Syndrome in a New Form of Congenital Generalized Lipodystrophy with Muscle Rippling (CGL4) Due to PTRF-CAVIN Mutations. PLoS Genetics. 6(3). e1000874–e1000874. 181 indexed citations
7.
Manzini, M. Chiara, Anna Rajab, Thomas M. Maynard, et al.. (2009). Developmental and degenerative features in a complicated spastic paraplegia. Annals of Neurology. 67(4). 516–525. 27 indexed citations
8.
Rajab, Anna, et al.. (2009). Cytogenetic studies in couples with recurrent miscarriage in the Sultanate of Oman. Reproductive BioMedicine Online. 18(3). 424–429. 36 indexed citations
9.
Kornak, Uwe, Ellen Reynders, Aikaterini Dimopoulou, et al.. (2008). Mutations in the a2-subunit of the v-type H+-ATPase impair Golgi function and cause a novel congenital disorder of glycosylation with cutix laxa. Medizinische Genetik. 20(1).
10.
Kornak, Uwe, Ellen Reynders, Aikaterini Dimopoulou, et al.. (2007). Impaired glycosylation and cutis laxa caused by mutations in the vesicular H+-ATPase subunit ATP6V0A2. Nature Genetics. 40(1). 32–34. 259 indexed citations
11.
Hoffmann, Katrin, Juliane Müller, Sigmar Stricker, et al.. (2006). Escobar Syndrome Is a Prenatal Myasthenia Caused by Disruption of the Acetylcholine Receptor Fetal γ Subunit. The American Journal of Human Genetics. 79(2). 303–312. 100 indexed citations
12.
Ganesh, Anuradha, Darryl Nishimura, Eleanor Rattenberry, et al.. (2006). Autozygosity mapping of Bardet–Biedl syndrome to 12q21.2 and confirmation of FLJ23560 as BBS10. European Journal of Human Genetics. 15(2). 173–178. 22 indexed citations
13.
Rajab, Anna, et al.. (2005). Common Autosomal Recessive Diseases in Oman Derived from a Hospital-Based Registry. Public Health Genomics. 8(1). 27–30. 22 indexed citations
14.
Hennies, Hans Christian, Anita Rauch, Wenke Seifert, et al.. (2004). Allelic Heterogeneity in the COH1 Gene Explains Clinical Variabilityin Cohen Syndrome. The American Journal of Human Genetics. 75(1). 138–145. 55 indexed citations
15.
Rajab, Anna, M A Patton, & B Modell. (2000). Study of hemoglobinopathies in Oman through a national register.. PubMed. 21(12). 1168–72. 27 indexed citations
16.
Afzal, Ali R., Anna Rajab, Christiane Fenske, et al.. (2000). Autosomal recessive Robinow syndrome is allelic to dominant brachydactyly type B and caused by loss of function mutations in ROR2. Journal of Medical Genetics. 37. 2 indexed citations
17.
Afzal, Ali R., Anna Rajab, Christiane Fenske, et al.. (2000). Linkage of recessive Robinow syndrome to a 4 cM interval on chromosome 9q22. Human Genetics. 106(3). 351–354. 16 indexed citations
18.
Rajab, Anna & Michael A. Patton. (1999). Analysis of the Population Structure in Oman. Public Health Genomics. 2(1). 23–25. 9 indexed citations
19.
Rajab, Anna, et al.. (1999). Neural Tube Defects. Tropical Doctor. 29(4). 235–237. 1 indexed citations
20.
Soliman, Ashraf, et al.. (1998). Defective Growth Hormone (GH) secretion and short-term treatment in Noonan syndrome. The Indian Journal of Pediatrics. 65(5). 741–749. 5 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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