Laila K. Effat

787 total citations
29 papers, 249 citations indexed

About

Laila K. Effat is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Laila K. Effat has authored 29 papers receiving a total of 249 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 7 papers in Clinical Biochemistry and 6 papers in Genetics. Recurrent topics in Laila K. Effat's work include Metabolism and Genetic Disorders (6 papers), Moyamoya disease diagnosis and treatment (4 papers) and interferon and immune responses (3 papers). Laila K. Effat is often cited by papers focused on Metabolism and Genetic Disorders (6 papers), Moyamoya disease diagnosis and treatment (4 papers) and interferon and immune responses (3 papers). Laila K. Effat collaborates with scholars based in Egypt, United States and Malaysia. Laila K. Effat's co-authors include Ghada M. H. Abdel‐Salam, Mohamed S. Abdel‐Hamid, Maha S. Zaki, Khalda Amr, Mostafa K. El Awady, Nagwa Abdallah Ismail, Amal Saad‐Hussein, Maha M. Eid, Nagwa A. Meguid and Hebatallah A. Darwish and has published in prestigious journals such as Annals of the Rheumatic Diseases, European Journal of Human Genetics and Acta Neurologica Scandinavica.

In The Last Decade

Laila K. Effat

29 papers receiving 247 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Laila K. Effat Egypt 11 139 61 47 46 38 29 249
Mahmoud F. Elsaid Qatar 12 174 1.3× 73 1.2× 55 1.2× 53 1.2× 51 1.3× 26 375
Lina Ghaloul‐Gonzalez United States 10 131 0.9× 58 1.0× 52 1.1× 12 0.3× 28 0.7× 29 254
Kent E. Kruckeberg United States 8 180 1.3× 132 2.2× 52 1.1× 17 0.4× 21 0.6× 9 350
Kalpana Gowrishankar India 10 172 1.2× 94 1.5× 8 0.2× 30 0.7× 26 0.7× 23 305
Chad Glasser United States 8 160 1.2× 65 1.1× 18 0.4× 12 0.3× 25 0.7× 13 303
Paula Grigorescu‐Sido Romania 9 138 1.0× 81 1.3× 12 0.3× 21 0.5× 124 3.3× 33 310
Katalin Szakszon Hungary 10 178 1.3× 103 1.7× 27 0.6× 13 0.3× 26 0.7× 29 276
Chin-Chang Huang Taiwan 12 88 0.6× 15 0.2× 21 0.4× 44 1.0× 14 0.4× 22 369
Ognian Kalev Austria 9 131 0.9× 40 0.7× 10 0.2× 62 1.3× 46 1.2× 22 277

Countries citing papers authored by Laila K. Effat

Since Specialization
Citations

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

Fields of papers citing papers by Laila K. Effat

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Laila K. Effat. 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 Laila K. Effat. The network helps show where Laila K. Effat may publish in the future.

Co-authorship network of co-authors of Laila K. Effat

This figure shows the co-authorship network connecting the top 25 collaborators of Laila K. Effat. A scholar is included among the top collaborators of Laila K. Effat 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 Laila K. Effat. Laila K. Effat 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.
Abdel‐Hamid, Mohamed S., et al.. (2020). Micro and Martsolf syndromes in 34 new patients: Refining the phenotypic spectrum and further molecular insights. Clinical Genetics. 98(5). 445–456. 10 indexed citations
2.
Abdel‐Salam, Ghada M. H., Hanan H. Afifi, Samira Ismail, et al.. (2020). Microcephalic osteodysplastic primordial dwarfism type II: Additional nine patients with implications on phenotype and genotype correlation. American Journal of Medical Genetics Part A. 182(6). 1407–1420. 6 indexed citations
3.
Raslan, Hala M., et al.. (2017). Endothelial nitric oxide synthase gene (T786C and G894T) polymorphisms in Egyptian patients with type 2 diabetes. Journal of Genetic Engineering and Biotechnology. 15(2). 431–436. 11 indexed citations
4.
Abdel‐Salam, Ghada M. H., Mohamed S. Abdel‐Hamid, Shaimaa Abdelsattar Mohammad, et al.. (2017). Aicardi-Goutières syndrome: unusual neuro-radiological manifestations. Metabolic Brain Disease. 32(3). 679–683. 9 indexed citations
5.
Abdel‐Hamid, Mohamed S., Manal F. Ismail, Hebatallah A. Darwish, et al.. (2016). Molecular and phenotypic spectrum of ASPM‐related primary microcephaly: Identification of eight novel mutations. American Journal of Medical Genetics Part A. 170(8). 2133–2140. 23 indexed citations
6.
Abdel‐Salam, Ghada M. H., Mohamed S. Abdel‐Hamid, Samira Ismail, et al.. (2016). Megalencephalic leukoencephalopathy with cysts in twelve Egyptian patients: novel mutations in MLC1 and HEPACAM and a founder effect. Metabolic Brain Disease. 31(5). 1171–1179. 6 indexed citations
7.
Ahmed, Rania Mohammed, et al.. (2015). Study of Vitamin D Receptor Gene Polymorphisms in Egyptian Patients with Primary Osteoporosis. 53(4). 1–11. 1 indexed citations
8.
9.
Abdel-Maksoud, Sahar M., et al.. (2014). C242T polymorphism of NADPH oxidase p22phox gene reduces the risk of coronary artery disease in a random sample of Egyptian population. Molecular Biology Reports. 41(4). 2281–2286. 12 indexed citations
10.
Amr, Khalda, et al.. (2014). Monoamine oxidase A (MAOA) gene polymorphism in offenders and psychiatric patients in an Egyptian Study. IOSR Journal of Pharmacy and Biological Sciences. 9(2). 38–42. 1 indexed citations
11.
Abdel‐Salam, Ghada M. H., Mohamed S. Abdel‐Hamid, Mahmoud Y. Issa, et al.. (2013). Further delineation of the clinical spectrum in RNU4ATAC related microcephalic osteodysplastic primordial dwarfism type I. American Journal of Medical Genetics Part A. 161(8). 1875–1881. 14 indexed citations
12.
Abdel‐Salam, Ghada M. H., Mohamed S. Abdel‐Hamid, Sahar N. Saleem, et al.. (2012). Profound microcephaly, primordial dwarfism with developmental brain malformations: A new syndrome. American Journal of Medical Genetics Part A. 158A(8). 1823–1831. 4 indexed citations
13.
Ismail, Nagwa Abdallah, et al.. (2011). A long-term study of bone mineral density in patients with phenylketonuria under diet therapy. Archives of Medical Science. 3(3). 493–500. 32 indexed citations
14.
Abdel‐Salam, Ghada M. H., Noriko Miyake, Maha M. Eid, et al.. (2011). A homozygous mutation in RNU4ATAC as a cause of microcephalic osteodysplastic primordial dwarfism type I (MOPD I) with associated pigmentary disorder. American Journal of Medical Genetics Part A. 155(11). 2885–2896. 21 indexed citations
15.
Abdel‐Salam, Ghada M. H., Laura Flores‐Sarnat, Jillian S. Parboosingh, et al.. (2010). Muenke syndrome with pigmentary disorder and probable hemimegalencephaly: An expansion of the phenotype. American Journal of Medical Genetics Part A. 155(1). 207–214. 15 indexed citations
16.
Abdel-Salam, Ahmed M. & Laila K. Effat. (2010). Preparation and evaluation of a novel therapeutic dairy-based drink for phenylketonuria.. PubMed. 2(2). 66–70. 3 indexed citations
17.
Amr, Khalda, et al.. (2003). The milder phenotype of the dystrophin gene double deletions. Acta Neurologica Scandinavica. 107(6). 400–404. 7 indexed citations
18.
Awady, Mostafa K. El, Yehia Z. Gad, Laila K. Effat, et al.. (2001). Schistosoma hematobium soluble egg antigens induce proliferation of urothelial and endothelial cells. World Journal of Urology. 19(4). 263–266. 14 indexed citations
19.
Effat, Laila K., et al.. (2000). Screening of Dystrophin Gene Deletions in Egyptian Patients with DMD/BMD Muscular Dystrophies. Disease Markers. 16(3-4). 125–129. 16 indexed citations
20.
Effat, Laila K., et al.. (1999). Haplotypes and mutations of the PAH locus in Egyptian families with PKU. European Journal of Human Genetics. 7(2). 259–262. 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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