Watfa Al‐Mamari

443 total citations
28 papers, 255 citations indexed

About

Watfa Al‐Mamari is a scholar working on Genetics, Cognitive Neuroscience and Molecular Biology. According to data from OpenAlex, Watfa Al‐Mamari has authored 28 papers receiving a total of 255 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 12 papers in Cognitive Neuroscience and 5 papers in Molecular Biology. Recurrent topics in Watfa Al‐Mamari's work include Genetics and Neurodevelopmental Disorders (11 papers), Autism Spectrum Disorder Research (11 papers) and Genomic variations and chromosomal abnormalities (9 papers). Watfa Al‐Mamari is often cited by papers focused on Genetics and Neurodevelopmental Disorders (11 papers), Autism Spectrum Disorder Research (11 papers) and Genomic variations and chromosomal abnormalities (9 papers). Watfa Al‐Mamari collaborates with scholars based in Oman, United Kingdom and United States. Watfa Al‐Mamari's co-authors include Amna Al‐Futaisi, Khalid Al‐Thihli, M. Mazharul Islam, Abeer Al‐Saegh, Ali Mahdi Kazem, Almundher Al‐Maawali, Mahmoud Mohamed Emam, Fathiya Al Murshedi, Fathiya Al-Murshedi and Fahad Zadjali and has published in prestigious journals such as Scientific Reports, International Journal of Molecular Sciences and Journal of Autism and Developmental Disorders.

In The Last Decade

Watfa Al‐Mamari

24 papers receiving 246 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Watfa Al‐Mamari Oman 10 112 87 48 45 35 28 255
Joana Almeida Portugal 8 184 1.6× 189 2.2× 123 2.6× 27 0.6× 32 0.9× 13 309
Lucy Wilde United Kingdom 12 144 1.3× 88 1.0× 62 1.3× 13 0.3× 40 1.1× 18 285
Barbara Haas‐Givler United States 7 239 2.1× 192 2.2× 126 2.6× 29 0.6× 22 0.6× 8 323
Stephanie J. Brewster United States 7 138 1.2× 78 0.9× 30 0.6× 13 0.3× 28 0.8× 14 215
Katy Sterling-Levis Australia 8 55 0.5× 121 1.4× 64 1.3× 37 0.8× 53 1.5× 11 323
Iain Fotheringham United Kingdom 4 255 2.3× 185 2.1× 111 2.3× 21 0.5× 42 1.2× 11 358
Sailaja Golla United States 8 127 1.1× 86 1.0× 78 1.6× 17 0.4× 17 0.5× 11 242
Elena Garayzábal Spain 9 59 0.5× 50 0.6× 51 1.1× 19 0.4× 15 0.4× 56 277
Ana Florencia Vega-Benedetti Italy 9 98 0.9× 109 1.3× 128 2.7× 13 0.3× 17 0.5× 13 338
Emily Smith United States 9 45 0.4× 64 0.7× 83 1.7× 56 1.2× 32 0.9× 22 388

Countries citing papers authored by Watfa Al‐Mamari

Since Specialization
Citations

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

Fields of papers citing papers by Watfa Al‐Mamari

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Watfa Al‐Mamari. 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 Watfa Al‐Mamari. The network helps show where Watfa Al‐Mamari may publish in the future.

Co-authorship network of co-authors of Watfa Al‐Mamari

This figure shows the co-authorship network connecting the top 25 collaborators of Watfa Al‐Mamari. A scholar is included among the top collaborators of Watfa Al‐Mamari 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 Watfa Al‐Mamari. Watfa Al‐Mamari 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.
Al‐Mamari, Watfa, et al.. (2025). Could a National Screening Program Reduce the Age of Diagnosis of Autism Spectrum Disorder?. Journal of Autism and Developmental Disorders.
2.
Gupta, Vijay, et al.. (2024). Genetic Variant Analyses Identify Novel Candidate Autism Risk Genes from a Highly Consanguineous Cohort of 104 Families from Oman. International Journal of Molecular Sciences. 25(24). 13700–13700. 2 indexed citations
3.
Al‐Mamari, Watfa, et al.. (2024). Clinical and neurobehavioral phenotype in children with autism and intragenic copy number duplications in CNTN4: Case series report. Research in autism spectrum disorders. 115. 102399–102399. 2 indexed citations
4.
Al-Murshedi, Fathiya, Khalid Al‐Thihli, Abeer Al‐Saegh, et al.. (2022). The diagnostic yield, candidate genes, and pitfalls for a genetic study of intellectual disability in 118 middle eastern families. Scientific Reports. 12(1). 18862–18862. 12 indexed citations
5.
Al‐Mamari, Watfa, et al.. (2021). Intellectual Profiles of Children with Autism Spectrum Disorder. Sultan Qaboos University medical journal. 21(3). 386–393. 8 indexed citations
6.
Al‐Mamari, Watfa, et al.. (2021). Parental Age and the Risk of Autism Spectrum Disorder in Oman. Sultan Qaboos University medical journal. 21(3). 465–471. 11 indexed citations
7.
Al‐Mamari, Watfa, et al.. (2020). Telemedicine in the Era of COVID-19 and Beyond. Sultan Qaboos University medical journal. 20(4). e277–279. 9 indexed citations
8.
Al‐Mamari, Watfa, et al.. (2019). Revisiting the Prevalence of Autism Spectrum Disorder among Omani Children: A multicentre study. Sultan Qaboos University medical journal. 19(4). e305–309. 49 indexed citations
9.
Al‐Mamari, Watfa, et al.. (2019). Further Clinical and Molecular Delineation of Xp11.22 Deletion Syndrome: A Case Report. Oman Medical Journal. 34(5). 460–463.
10.
Al‐Mamari, Watfa, et al.. (2018). LHFPL5 mutation: A rare cause of non-syndromic autosomal recessive hearing loss. European Journal of Medical Genetics. 62(12). 103592–103592. 5 indexed citations
11.
Al-Mahrezi, Abdulaziz, Amna Al‐Futaisi, & Watfa Al‐Mamari. (2016). Learning Disabilities: Opportunities and challenges in Oman. Sultan Qaboos University medical journal. 16(2). e129–131. 11 indexed citations
12.
Al‐Futaisi, Amna, et al.. (2016). Coexistence of Autism Spectrum Disorders Among Three Children with Tuberous Sclerosis Complex: Case reports and review of literature. Sultan Qaboos University medical journal. 16(4). e520–524. 3 indexed citations
13.
Al‐Mamari, Watfa, Abeer Al‐Saegh, Adila Al‐Kindy, et al.. (2015). Diagnostic Yield of Chromosomal Microarray Analysis in a Cohort of Patients with Autism Spectrum Disorders from a Highly Consanguineous Population. Journal of Autism and Developmental Disorders. 45(8). 2323–2328. 9 indexed citations
14.
Al‐Mamari, Watfa, Mahmoud Mohamed Emam, Amna Al‐Futaisi, & Ali Mahdi Kazem. (2015). Comorbidity of Learning Disorders and Attention Deficit Hyperactivity Disorder in a Sample of Omani Schoolchildren. Sultan Qaboos University medical journal. 15(4). e528–e533. 16 indexed citations
15.
Al‐Mamari, Watfa, et al.. (2015). De Novo Duplication of 7p21.1p22.2 in a Child with Autism Spectrum Disorder and Craniofacial Dysmorphism. Sultan Qaboos University medical journal. 15(3). e415–419. 3 indexed citations
16.
Al‐Mamari, Watfa, Mahmoud Mohamed Emam, Amna Al‐Futaisi, & Ali Mahdi Kazem. (2015). Comorbidity of Learning Disorders and Attention Deficit Hyperactivity Disorder in a Sample of Omani Schoolchildren. Sultan Qaboos University medical journal. 15(4). 528–533. 1 indexed citations
17.
Al‐Sinani, Siham, et al.. (2015). Novel Mutation in Wolcott–Rallison Syndrome with Variable Expression in Two Omani Siblings. Oman Medical Journal. 30(2). 138–141. 6 indexed citations
18.
Al‐Thihli, Khalid, Fathiya Al-Murshedi, Nadia Alhashmi, et al.. (2014). Consanguinity, Endogamy and Inborn Errors of Metabolism in Oman: A Cross-Sectional Study. Human Heredity. 77(1-4). 183–188. 24 indexed citations
19.
Emam, Mahmoud Mohamed, et al.. (2014). Variations in Arabic Reading Skills between Normally Achieving and at Risk for Reading Disability Students in Second and Fourth Grades. Review of European Studies. 6(3). 7 indexed citations
20.
Venugopalan, P, et al.. (2003). A child with supraventricular tachycardia and convulsions. Annals of Tropical Paediatrics. 23(1). 79–82. 3 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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