Saad Ali

467 total citations
33 papers, 311 citations indexed

About

Saad Ali is a scholar working on Hematology, Molecular Biology and Genetics. According to data from OpenAlex, Saad Ali has authored 33 papers receiving a total of 311 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Hematology, 9 papers in Molecular Biology and 9 papers in Genetics. Recurrent topics in Saad Ali's work include Acute Myeloid Leukemia Research (10 papers), Chronic Myeloid Leukemia Treatments (8 papers) and Chronic Lymphocytic Leukemia Research (6 papers). Saad Ali is often cited by papers focused on Acute Myeloid Leukemia Research (10 papers), Chronic Myeloid Leukemia Treatments (8 papers) and Chronic Lymphocytic Leukemia Research (6 papers). Saad Ali collaborates with scholars based in Tunisia, United States and Pakistan. Saad Ali's co-authors include Moez Elloumi, Yosra Ben Youssef, Hatem Elghezal, Abderrahim Khélif, Talaha M Ali, T. Boudawara, Chahnez Triki, Dominique Récan, Leila Keskes and Ali Bahloul and has published in prestigious journals such as SHILAP Revista de lepidopterología, Neurology and Journal of neurosurgery.

In The Last Decade

Saad Ali

29 papers receiving 295 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Saad Ali Tunisia 12 130 104 102 83 81 33 311
Morten Krogh Herlin Denmark 10 61 0.5× 136 1.3× 112 1.1× 57 0.7× 9 0.1× 26 471
Sarah E. Miller United States 7 66 0.5× 119 1.1× 52 0.5× 41 0.5× 25 0.3× 21 299
Lawrence G. Leichtman United States 11 21 0.2× 129 1.2× 81 0.8× 173 2.1× 31 0.4× 14 379
Özgül M. Alper Türkiye 13 15 0.1× 160 1.5× 25 0.2× 134 1.6× 54 0.7× 35 472
Marc Müller Germany 9 96 0.7× 69 0.7× 20 0.2× 18 0.2× 71 0.9× 18 254
G. Reza Jalali United Kingdom 13 184 1.4× 191 1.8× 210 2.1× 132 1.6× 41 0.5× 16 456
P. Berlier France 10 25 0.2× 84 0.8× 52 0.5× 51 0.6× 114 1.4× 23 387
Mojdeh Naghashpour United States 10 112 0.9× 47 0.5× 23 0.2× 7 0.1× 43 0.5× 14 275
P Steuber United States 11 257 2.0× 90 0.9× 292 2.9× 28 0.3× 97 1.2× 16 481
C Richard France 8 42 0.3× 78 0.8× 66 0.6× 31 0.4× 84 1.0× 20 368

Countries citing papers authored by Saad Ali

Since Specialization
Citations

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

Fields of papers citing papers by Saad Ali

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Saad Ali

This figure shows the co-authorship network connecting the top 25 collaborators of Saad Ali. A scholar is included among the top collaborators of Saad Ali 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 Saad Ali. Saad Ali 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.
Khelil, Amel Haj, et al.. (2024). RS35705950 polymorphism of MUC5B Gene: Association with Rheumatoid Arthritis and Interstitial lung disease in Tunisian Population. La Tunisie Médicale. 102(12). 1020–1024. 1 indexed citations
2.
3.
Niazi, Muhammad Bilal Khan, et al.. (2022). Drug-Induced Liver Injury from Herbal Liver Detoxification Tea. Case Reports in Gastroenterology. 16(3). 612–617. 1 indexed citations
4.
Haider, Kamran, et al.. (2022). OUTCOME OF THE CHOICE OF WOUND CLOSURE TECHNIQUE IN EMERGENCY LAPAROTOMY. Journal of Ayub Medical College Abbottabad. 34(1). 164–168.
5.
Ali, Saad, et al.. (2015). Chronic myeloid leukemia: Relevance of cytogenetic and molecular assays. Critical Reviews in Oncology/Hematology. 97. 263–274. 35 indexed citations
6.
Bouali, Nouha, Soumaya Mougou, Jérôme Bouligand, et al.. (2015). Analysis of FMR1 gene premutation and X chromosome cytogenetic abnormalities in 100 Tunisian patients presenting premature ovarian failure. Annales d Endocrinologie. 76(6). 671–678. 9 indexed citations
7.
8.
Youssef, Yosra Ben, et al.. (2012). Analysis of the clinico-hematological relevance of the breakpoint location within M-BCR in chronic myeloid leukemia. Medical Oncology. 30(1). 348–348. 22 indexed citations
9.
Youssef, Yosra Ben, et al.. (2011). Translocation t(X;10)(p10;p10): a rare chromosomal abnormality in a new born female with acute myeloid leukemia. Medical Oncology. 29(2). 1134–1136. 1 indexed citations
10.
Pyne, Michael E., Saad Ali, Valerie Orr, et al.. (2011). Developing an Extended Genomic Engineering Approach Based on Recombineering to Knock-in Heterologous Genes to Escherichia coli Genome. Molecular Biotechnology. 51(2). 109–118. 19 indexed citations
11.
Bellâaj, Hatem, et al.. (2011). Molecular cytogenetic characterization of Philadelphia-negative rearrangements in chronic myeloid leukemia patients. Journal of Cancer Research and Clinical Oncology. 137(9). 1329–1336. 13 indexed citations
12.
Youssef, Yosra Ben, Imed Harrabi, Balkis Meddeb, et al.. (2011). Molecular cytogenetic study of derivative chromosome 9 deletion in chronic myeloid leukemia patients. Medical Oncology. 29(2). 1151–1160. 2 indexed citations
13.
Elloumi, Moez, et al.. (2009). Molecular cytogenetic characterization of variant Philadelphia translocations in chronic myeloid leukemia: genesis and deletion of derivative chromosome 9. Cancer Genetics and Cytogenetics. 194(1). 30–37. 21 indexed citations
14.
Ali, Saad, et al.. (2008). Molecular Prenatal Diagnosis of Muscular Dystrophies in Tunisia and Postnatal Follow-Up Role. Genetic Testing. 12(4). 581–586. 5 indexed citations
15.
Elghezal, Hatem, Yosra Ben Youssef, Moez Elloumi, et al.. (2008). Cytogenetic analysis of 298 newly diagnosed cases of acute lymphoblastic leukaemia in Tunisia. Hematological Oncology. 26(2). 91–97. 16 indexed citations
16.
Elghezal, Hatem, et al.. (2007). Ring chromosome 20 syndrome without deletions of the subtelomeric and CHRNA4–KCNQ2 genes loci. European Journal of Medical Genetics. 50(6). 441–445. 19 indexed citations
17.
Ali, Saad, et al.. (2005). Attitude Toward Organ Donation: A Survey in Pakistan. Artificial Organs. 29(11). 899–905. 51 indexed citations
18.
Abdelmoula, N. Bouayed, Marie‐France Portnoï, Leila Keskes, et al.. (2003). Skewed X-chromosome inactivation pattern in SRY positive XX maleness: a case report and review of literature. Annales de Génétique. 46(1). 11–18. 29 indexed citations
19.
Elghezal, Hatem, et al.. (2002). Cytogenetic analysis in 139 Tunisian patients with de novo acute myeloid leukemia. Annales de Génétique. 45(1). 29–32. 11 indexed citations
20.
Elghezal, Hatem, et al.. (2002). Cytogenetic survey of 117 Tunisian patients with de novo myelodysplastic syndrome. Annales de Génétique. 45(3). 131–135. 1 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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