Mohammad Shboul

2.0k total citations
34 papers, 513 citations indexed

About

Mohammad Shboul is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Mohammad Shboul has authored 34 papers receiving a total of 513 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 14 papers in Genetics and 5 papers in Genetics. Recurrent topics in Mohammad Shboul's work include Connective tissue disorders research (4 papers), Craniofacial Disorders and Treatments (4 papers) and Nuclear Structure and Function (3 papers). Mohammad Shboul is often cited by papers focused on Connective tissue disorders research (4 papers), Craniofacial Disorders and Treatments (4 papers) and Nuclear Structure and Function (3 papers). Mohammad Shboul collaborates with scholars based in Jordan, Singapore and Austria. Mohammad Shboul's co-authors include Bruno Reversade, Hane Lee, Stanley F. Nelson, Hanan Hamamy, Carine Bonnard, Yan Ling Chong, Sudipto Roy, Feng Zhou, Barry Merriman and Osama H. Ababneh and has published in prestigious journals such as Nature Genetics, SHILAP Revista de lepidopterología and Blood.

In The Last Decade

Mohammad Shboul

30 papers receiving 507 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mohammad Shboul Jordan 13 358 178 81 67 53 34 513
Zi Yan United States 14 439 1.2× 159 0.9× 56 0.7× 62 0.9× 45 0.8× 34 657
Mariam Al‐Mureikhi Qatar 12 334 0.9× 280 1.6× 98 1.2× 45 0.7× 32 0.6× 18 591
Davor Lessel Germany 17 523 1.5× 181 1.0× 72 0.9× 37 0.6× 50 0.9× 44 733
Pelin Özlem Şimşek‐Kiper Türkiye 14 377 1.1× 326 1.8× 70 0.9× 57 0.9× 29 0.5× 99 662
Elisa Pisaneschi Italy 12 346 1.0× 258 1.4× 96 1.2× 41 0.6× 16 0.3× 41 579
Deborah Morrogh United Kingdom 9 247 0.7× 299 1.7× 83 1.0× 34 0.5× 25 0.5× 13 542
Nadine Jalkh Lebanon 13 541 1.5× 238 1.3× 34 0.4× 49 0.7× 90 1.7× 38 751
Paul Gontarz United States 14 507 1.4× 96 0.5× 43 0.5× 46 0.7× 62 1.2× 25 655
Adi Mory Israel 15 245 0.7× 147 0.8× 66 0.8× 38 0.6× 18 0.3× 40 592
Ita Costello United Kingdom 15 796 2.2× 108 0.6× 59 0.7× 81 1.2× 60 1.1× 18 898

Countries citing papers authored by Mohammad Shboul

Since Specialization
Citations

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

Fields of papers citing papers by Mohammad Shboul

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mohammad Shboul

This figure shows the co-authorship network connecting the top 25 collaborators of Mohammad Shboul. A scholar is included among the top collaborators of Mohammad Shboul 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 Mohammad Shboul. Mohammad Shboul 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.
Shboul, Mohammad, et al.. (2024). Association between vitamin D metabolism gene polymorphisms and schizophrenia. Biomedical Reports. 21(3). 134–134. 1 indexed citations
2.
Shboul, Mohammad, et al.. (2024). Plasma miRNAs as potential biomarkers for schizophrenia in a Jordanian cohort. Non-coding RNA Research. 9(2). 350–358. 5 indexed citations
3.
Shboul, Mohammad, et al.. (2024). The Ser434Phe Androgen Receptor Gene Mutation Does Not Affect Fertility but is Associated with Increased Prolactin. The Application of Clinical Genetics. Volume 17. 143–149.
4.
Shboul, Mohammad, et al.. (2024). Case report: Dihydropyridine receptor (CACNA1S) congenital myopathy, a novel phenotype with early onset periodic paralysis. Frontiers in Neurology. 15. 1359479–1359479.
5.
6.
Kaissi, Ali Al, et al.. (2021). Infantile Systemic Hyalinosis. SHILAP Revista de lepidopterología. 18(4). 224–230. 5 indexed citations
7.
8.
Kaissi, Ali Al, Vladimir Kenis, Mohammad Shboul, et al.. (2020). Tomographic Study of the Malformation Complex in Correlation With the Genotype in Patients With Robinow Syndrome: Review Article. Journal of Investigative Medicine High Impact Case Reports. 8. 2737376923–2737376923. 6 indexed citations
9.
Masri, Amira, Mohammad Shboul, Nathalie Escande‐Beillard, et al.. (2019). Congenital insensitivity to pain with anhidrosis syndrome: A series from Jordan. Clinical Neurology and Neurosurgery. 189. 105636–105636. 14 indexed citations
10.
Shboul, Mohammad, et al.. (2019). Recessive mutation in GALNT3 causes hyperphosphatemic familial tumoral calcinosis associated with chronic recurrent multifocal osteomyelitis. The Turkish Journal of Pediatrics. 61(1). 130–133. 4 indexed citations
11.
Chia, Poh Hui, Franklin L. Zhong, Shinsuke Niwa, et al.. (2018). A homozygous loss-of-function CAMK2A mutation causes growth delay, frequent seizures and severe intellectual disability. eLife. 7. 44 indexed citations
12.
Tian, Jing, Cong Liu, Chih‐Wei Chou, et al.. (2018). Deficiency of lrp4 in zebrafish and human LRP4 mutation induce aberrant activation of Jagged–Notch signaling in fin and limb development. Cellular and Molecular Life Sciences. 76(1). 163–178. 22 indexed citations
13.
Shboul, Mohammad, Paul Roschger, Rudolf Ganger, et al.. (2018). Bone matrix hypermineralization associated with low bone turnover in a case of Nasu-Hakola disease. Bone. 123. 48–55. 7 indexed citations
14.
Shboul, Mohammad, Zhihao Wang, Zhaojie Lyu, et al.. (2018). Novel frame shift mutation in ERCC6 leads to a severe form of Cockayne syndrome with postnatal growth failure and early death. Medicine. 97(33). e11636–e11636. 10 indexed citations
15.
Trott, Jamie, Sheena L. M. Ong, Drew M. Titmarsh, et al.. (2017). Long-Term Culture of Self-renewing Pancreatic Progenitors Derived from Human Pluripotent Stem Cells. Stem Cell Reports. 8(6). 1675–1688. 50 indexed citations
16.
Shboul, Mohammad, Valério Taverniti, Carine Bonnard, et al.. (2015). Loss of the scavenger mRNA decapping enzyme DCPS causes syndromic intellectual disability with neuromuscular defects. Human Molecular Genetics. 24(11). 3163–3171. 25 indexed citations
17.
Jodoin, Jeanne N., Todd R. Albrecht, Sarah May, et al.. (2013). Nuclear-localized Asunder regulates cytoplasmic dynein localization via its role in the Integrator complex. Molecular Biology of the Cell. 24(18). 2954–2965. 19 indexed citations
18.
Jodoin, Jeanne N., et al.. (2012). Human Asunder promotes dynein recruitment and centrosomal tethering to the nucleus at mitotic entry. Molecular Biology of the Cell. 23(24). 4713–4724. 18 indexed citations
19.
Dajani, Rana, et al.. (2012). Prevalence of coagulation factor II G20210A and factor V G1691A Leiden polymorphisms in Chechans, a genetically isolated population in Jordan. Molecular Biology Reports. 39(9). 9133–9138. 6 indexed citations
20.
Bonnard, Carine, Mohammad Shboul, Hane Lee, et al.. (2012). Mutations in IRX5 impair craniofacial development and germ cell migration via SDF1. Nature Genetics. 44(6). 709–713. 53 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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