M. Y. El‐Khalifa

506 total citations
11 papers, 363 citations indexed

About

M. Y. El‐Khalifa is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, M. Y. El‐Khalifa has authored 11 papers receiving a total of 363 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 4 papers in Pediatrics, Perinatology and Child Health and 3 papers in Molecular Biology. Recurrent topics in M. Y. El‐Khalifa's work include Prenatal Screening and Diagnostics (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Genomics and Rare Diseases (2 papers). M. Y. El‐Khalifa is often cited by papers focused on Prenatal Screening and Diagnostics (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Genomics and Rare Diseases (2 papers). M. Y. El‐Khalifa collaborates with scholars based in Kuwait and United States. M. Y. El‐Khalifa's co-authors include S A Al-Awadi, Talaat I. Farag, Ahmad S. Teebi, Mohamed Moussa, Kamal K. Naguib, Gamal A. Hosny, John M. Opitz, James F. Reynolds, A. Cuschieri and Abdulla Al‐Ansari and has published in prestigious journals such as Journal of Medical Genetics, American Journal of Medical Genetics and Clinical Genetics.

In The Last Decade

M. Y. El‐Khalifa

11 papers receiving 340 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
M. Y. El‐Khalifa Kuwait 8 125 110 86 79 49 11 363
Mona S. Awadalla Australia 14 98 0.8× 79 0.7× 105 1.2× 26 0.3× 41 0.8× 20 595
Ghada El‐Kamah Egypt 10 82 0.7× 49 0.4× 142 1.7× 54 0.7× 40 0.8× 46 364
Mahmoud Aarabi United States 11 207 1.7× 34 0.3× 196 2.3× 214 2.7× 17 0.3× 20 541
Virginia J. Baldwin Canada 12 70 0.6× 48 0.4× 185 2.2× 312 3.9× 13 0.3× 22 623
Celia D. Delozier United States 9 154 1.2× 23 0.2× 90 1.0× 81 1.0× 65 1.3× 14 312
L. Zahed Lebanon 14 219 1.8× 95 0.9× 97 1.1× 263 3.3× 76 1.6× 31 495
Firouz Khamsi Canada 16 49 0.4× 24 0.2× 120 1.4× 108 1.4× 31 0.6× 26 725
Estela G. Toraño Spain 9 82 0.7× 32 0.3× 292 3.4× 49 0.6× 18 0.4× 9 431
Anjeung Kang Switzerland 9 100 0.8× 26 0.2× 138 1.6× 284 3.6× 21 0.4× 11 463
M. Benabadji Algeria 12 80 0.6× 213 1.9× 118 1.4× 71 0.9× 194 4.0× 46 496

Countries citing papers authored by M. Y. El‐Khalifa

Since Specialization
Citations

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

Fields of papers citing papers by M. Y. El‐Khalifa

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by M. Y. El‐Khalifa. 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 M. Y. El‐Khalifa. The network helps show where M. Y. El‐Khalifa may publish in the future.

Co-authorship network of co-authors of M. Y. El‐Khalifa

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

All Works

11 of 11 papers shown
1.
Lubani, M. M., et al.. (1990). Prevalence of congenital adrenal hyperplasia in Kuwait. European Journal of Pediatrics. 149(6). 391–392. 18 indexed citations
2.
Farag, Talaat I., Ahmad S. Teebi, Kamal K. Naguib, et al.. (1989). Clustering of Major Chromosomal Abnormalities among Unselected Sterile Men in Kuwait. Medical Principles and Practice. 1(4). 232–235. 1 indexed citations
3.
Farag, Talaat I., Vamshi K. Rao, M. Y. El‐Khalifa, et al.. (1989). Autosomal Recessive Duchenne-Like Muscular Dystrophy in Arabs. Medical Principles and Practice. 1(2). 96–101. 2 indexed citations
4.
El‐Khalifa, M. Y., et al.. (1989). Mental Retardation and Phenotypic Abnormalities Associated with Apparently Balanced Translocation Involving Chromosomes 2, 3 and 7. Medical Principles and Practice. 1(2). 115–117. 1 indexed citations
5.
Teebi, Ahmad S., S A Al-Awadi, Talaat I. Farag, Kamal K. Naguib, & M. Y. El‐Khalifa. (1987). Phenylketonuria in Kuwait and Arab countries. European Journal of Pediatrics. 146(1). 59–60. 17 indexed citations
6.
Al-Awadi, S A, Talaat I. Farag, R. Usha, et al.. (1986). Interstitial deletion of the long arm of chromosome 1 [del(1)(q32q42)]. American Journal of Medical Genetics. 23(4). 931–933. 7 indexed citations
7.
Al-Awadi, S A, Kamal K. Naguib, Mohamed Moussa, et al.. (1986). The effect of consanguineous marriages on reproductive wastage. Clinical Genetics. 29(5). 384–388. 85 indexed citations
8.
Al-Awadi, S A, Talaat I. Farag, Ahmad S. Teebi, et al.. (1985). Primary hypogonadism and partial alopecia in three sibs with Müllerian hypoplasia in the affected females. American Journal of Medical Genetics. 22(3). 619–622. 27 indexed citations
9.
Al-Awadi, S A, et al.. (1985). Consanguinity among the Kuwaiti population. Clinical Genetics. 27(5). 483–486. 136 indexed citations
10.
Al-Awadi, S A, et al.. (1985). Profound limb deficiency, thoracic dystrophy, unusual facies, and normal intelligence: a new syndrome.. Journal of Medical Genetics. 22(1). 36–38. 37 indexed citations
11.
Al-Awadi, S A, Talaat I. Farag, Kamal K. Naguib, et al.. (1984). Spondyloepiphyseal dysplasia tarda with progressive arthropathy.. Journal of Medical Genetics. 21(3). 193–196. 32 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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