Hatem El‐Shanti

6.0k total citations
84 papers, 2.7k citations indexed

About

Hatem El‐Shanti is a scholar working on Molecular Biology, Genetics and Rheumatology. According to data from OpenAlex, Hatem El‐Shanti has authored 84 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 48 papers in Molecular Biology, 34 papers in Genetics and 18 papers in Rheumatology. Recurrent topics in Hatem El‐Shanti's work include Inflammasome and immune disorders (24 papers), Genetics and Neurodevelopmental Disorders (12 papers) and Osteomyelitis and Bone Disorders Research (9 papers). Hatem El‐Shanti is often cited by papers focused on Inflammasome and immune disorders (24 papers), Genetics and Neurodevelopmental Disorders (12 papers) and Osteomyelitis and Bone Disorders Research (9 papers). Hatem El‐Shanti collaborates with scholars based in United States, Jordan and Qatar. Hatem El‐Shanti's co-authors include Polly J. Ferguson, Hasan A. Majeed, Kamel Ajlouni, Mohammed El‐Khateeb, Nadim Jarrah, Marwan K. Tayeh, Jamil Al-Alami, Xinyu Bing, Andrew C. Lidral and Azhar S. Daoud and has published in prestigious journals such as The Lancet, Nature Genetics and SHILAP Revista de lepidopterología.

In The Last Decade

Hatem El‐Shanti

82 papers receiving 2.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Hatem El‐Shanti United States 28 1.7k 618 604 553 475 84 2.7k
Anne E. Hughes United Kingdom 26 1.0k 0.6× 311 0.5× 371 0.6× 741 1.3× 198 0.4× 59 3.0k
Thomas A. Davis United States 30 760 0.4× 344 0.6× 721 1.2× 470 0.8× 414 0.9× 73 3.1k
Sutada Lotinun United States 32 2.2k 1.3× 346 0.6× 338 0.6× 291 0.5× 201 0.4× 70 3.8k
Maria Hoeltzenbein Germany 23 899 0.5× 794 1.3× 420 0.7× 722 1.3× 272 0.6× 54 2.8k
Pawel Zerr Germany 31 1.6k 0.9× 243 0.4× 338 0.6× 662 1.2× 308 0.6× 39 3.4k
Maja Di Rocco Italy 34 1.5k 0.9× 860 1.4× 778 1.3× 205 0.4× 232 0.5× 147 3.6k
May Christine V. Malicdan United States 29 1.5k 0.9× 544 0.9× 188 0.3× 212 0.4× 157 0.3× 126 2.6k
Anna Spada Italy 46 2.6k 1.6× 1.4k 2.3× 337 0.6× 190 0.3× 1.2k 2.5× 172 7.0k
Marina Colombi Italy 31 1.1k 0.6× 1.8k 3.0× 489 0.8× 140 0.3× 477 1.0× 181 3.7k
Francesca Gori United States 29 2.1k 1.3× 478 0.8× 306 0.5× 155 0.3× 313 0.7× 68 3.9k

Countries citing papers authored by Hatem El‐Shanti

Since Specialization
Citations

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

Fields of papers citing papers by Hatem El‐Shanti

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hatem El‐Shanti

This figure shows the co-authorship network connecting the top 25 collaborators of Hatem El‐Shanti. A scholar is included among the top collaborators of Hatem El‐Shanti 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 Hatem El‐Shanti. Hatem El‐Shanti 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.
Chandra, Bharatendu, Cristina M. Justice, Anthony M. Musolf, et al.. (2022). TBX3 and EFNA4 Variant in a Family with Ulnar-Mammary Syndrome and Sagittal Craniosynostosis. Genes. 13(9). 1649–1649. 2 indexed citations
2.
El‐Shanti, Hatem, et al.. (2018). Congenital glucose‐galactose malabsorption: A case report with a novel SLC5A1 mutation. Clinical Case Reports. 7(1). 51–53. 4 indexed citations
3.
Platt, Daniel E., Essa Hariri, Pascale Salameh, et al.. (2017). Type II diabetes mellitus and hyperhomocysteinemia: a complex interaction. Diabetology & Metabolic Syndrome. 9(1). 19–19. 20 indexed citations
4.
Ahram, Dina, et al.. (2017). A chromosomal microdeletion of 15q in a female patient with epilepsy, ID , and autism spectrum disorder: a case report. Clinical Case Reports. 5(6). 1013–1017. 4 indexed citations
5.
Hadj‐Rabia, S., Gaëlle Brideau, Yasser Al‐Sarraj, et al.. (2017). Multiplex epithelium dysfunction due to CLDN10 mutation: the HELIX syndrome. Genetics in Medicine. 20(2). 190–201. 68 indexed citations
6.
Platt, Daniel E., Michella Ghassibe‐Sabbagh, Pascale Salameh, et al.. (2015). Caffeine Impact on Metabolic Syndrome Components Is Modulated by a CYP1A2 Variant. Annals of Nutrition and Metabolism. 68(1). 1–11. 19 indexed citations
7.
Taha, Rowaida Z., et al.. (2015). Overlap of Familial Mediterranean Fever and Hyper-IgD Syndrome in an Arabic Kindred. Journal of Clinical Immunology. 35(3). 249–253. 14 indexed citations
8.
Kambouris, Marios, Rachid C. Maroun, Tawfeg Ben‐Omran, et al.. (2014). Mutations in zinc finger 407 [ZNF407] cause a unique autosomal recessive cognitive impairment syndrome. Orphanet Journal of Rare Diseases. 9(1). 80–80. 16 indexed citations
9.
Ghassibe‐Sabbagh, Michella, Mary Deeb, Angelique K. Salloum, et al.. (2014). Multivariate epidemiologic analysis of type 2 diabetes mellitus risks in the Lebanese population. Diabetology & Metabolic Syndrome. 6(1). 89–89. 22 indexed citations
10.
Ahram, Dina, T. Shawn Sato, Marwan K. Tayeh, et al.. (2009). A Homozygous Mutation in ADAMTSL4 Causes Autosomal-Recessive Isolated Ectopia Lentis. The American Journal of Human Genetics. 84(2). 274–278. 101 indexed citations
11.
Milhavet, Florian, Laurence Cuisset, Hal M. Hoffman, et al.. (2008). The infevers autoinflammatory mutation online registry: update with new genes and functions. Human Mutation. 29(6). 803–808. 199 indexed citations
12.
El‐Shanti, Hatem, et al.. (2006). A distinct autosomal recessive ataxia maps to chromosome 12in an inbred family from Jordan. Brain and Development. 28(6). 353–357. 6 indexed citations
13.
El‐Shanti, Hatem, Hasan A. Majeed, & Mohammed El‐Khateeb. (2006). Familial Mediterranean fever in Arabs. The Lancet. 367(9515). 1016–1024. 99 indexed citations
14.
El‐Shanti, Hatem, Kwanghyuk Lee, Attya Bhatti, et al.. (2005). Novel sequence variants in the TMIE gene in families with autosomal recessive nonsyndromic hearing impairment. Journal of Molecular Medicine. 84(3). 226–231. 19 indexed citations
15.
Majeed, Hasan A., et al.. (2005). The Spectrum of Familial Mediterranean Fever Gene Mutations in Arabs: Report of a Large Series. Seminars in Arthritis and Rheumatism. 34(6). 813–818. 61 indexed citations
16.
Al-Alami, Jamil, et al.. (2003). Familial Mediterranean fever mutation frequencies and carrier rates among a mixed Arabic population.. PubMed. 24(10). 1055–9. 49 indexed citations
17.
Wang, Kun, Elizabeth Pugh, Kimberly F. Doheny, et al.. (2001). Homozygosity Mapping Places the Acrodermatitis Enteropathica Gene on Chromosomal Region 8q24.3. The American Journal of Human Genetics. 68(4). 1055–1060. 69 indexed citations
18.
Majeed, Hasan A., et al.. (2001). The syndrome of chronic recurrent multifocal osteomyelitis and congenital dyserythropoietic anaemia. Report of a new family and a review. European Journal of Pediatrics. 160(12). 705–710. 82 indexed citations
19.
El‐Shanti, Hatem, Andrew C. Lidral, Nadim Jarrah, Lawrence J. Druhan, & Kamel Ajlouni. (2000). Homozygosity Mapping Identifies an Additional Locus for Wolfram Syndrome on Chromosome 4q. The American Journal of Human Genetics. 66(4). 1229–1236. 102 indexed citations
20.
Al-Alami, Jamil, et al.. (1999). Fine Mapping of Progressive Pseudorheumatoid Dysplasia: A Tool for Heterozygote Identification. Genetic Testing. 3(4). 329–333. 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Anne E. Hughes Breakdown of academic impact, for papers by Thomas A. Davis Breakdown of academic impact, for papers by Sutada Lotinun Breakdown of academic impact, for papers by Maria Hoeltzenbein Breakdown of academic impact, for papers by Pawel Zerr Breakdown of academic impact, for papers by Maja Di Rocco Breakdown of academic impact, for papers by May Christine V. Malicdan Breakdown of academic impact, for papers by Anna Spada Breakdown of academic impact, for papers by Marina Colombi Breakdown of academic impact, for papers by Francesca Gori
Rankless by CCL
2026