Hind Dehbi

440 total citations
47 papers, 291 citations indexed

About

Hind Dehbi is a scholar working on Molecular Biology, Hematology and Genetics. According to data from OpenAlex, Hind Dehbi has authored 47 papers receiving a total of 291 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 13 papers in Hematology and 12 papers in Genetics. Recurrent topics in Hind Dehbi's work include Chronic Myeloid Leukemia Treatments (9 papers), Glutathione Transferases and Polymorphisms (6 papers) and Drug Transport and Resistance Mechanisms (6 papers). Hind Dehbi is often cited by papers focused on Chronic Myeloid Leukemia Treatments (9 papers), Glutathione Transferases and Polymorphisms (6 papers) and Drug Transport and Resistance Mechanisms (6 papers). Hind Dehbi collaborates with scholars based in Morocco, Mali and Kuwait. Hind Dehbi's co-authors include Sellama Nadifi, Yaya Kassogué, Saïd Benchekroun, Nadia El Kadmiri, Ahmed Belmouden, Fouzia Radouani, Omar Abidi, Brehima Diakité, H. Jouhadi and Asmâa Quessar and has published in prestigious journals such as SHILAP Revista de lepidopterología, Medicine and Tumor Biology.

In The Last Decade

Hind Dehbi

40 papers receiving 285 citations

Peers

Hind Dehbi

ONCOL

HEMAT

GENET

Szymon Zmorzyński Poland

J Mayans Spain

Lidija K. Gorsic United States

Luisa Ronzoni Italy

Zhongli Chen Netherlands

Liora Z. Strichman-Almashanu United States

Vladimír Mihál Czechia

B Chen China

Elizabeth McDonough United States

Elizabeth Weisiger United States

Szymon Zmorzyński Poland

Hind Dehbi

119 ×0.8

45 ×0.6

ONCOL

55 ×0.9

HEMAT

51 ×1.0

27 ×0.7

GENET

Citations per year, relative to Hind Dehbi Hind Dehbi (= 1×) peers Szymon Zmorzyński

Countries citing papers authored by Hind Dehbi

Since Specialization

Citations

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

Fields of papers citing papers by Hind Dehbi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hind Dehbi

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

All Works

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20 of 20 papers shown

Dehbi, Hind, et al.. (2023). t(1;4) translocation in a child with acute lymphoblastic leukemia: a case report. Journal of Medical Case Reports. 17(1). 537–537. 1 indexed citations

Dehbi, Hind, et al.. (2022). Risk factors for breast cancer in women: an update review. Medical Oncology. 39(12). 197–197. 41 indexed citations

Dehbi, Hind, et al.. (2021). The impact of ABCB1 gene polymorphism (C3435T) and its expression on response to Donepezil in Moroccan patients with Alzheimer's disease. Gene Reports. 26. 101443–101443.

Dehbi, Hind, et al.. (2021). Analysis of CYP1B1 gene mutations in primary congenital glaucoma patients. European Journal of Ophthalmology. 31(6). 2796–2807. 10 indexed citations

Kayesh, Mohammad Enamul Hoque, Haya Altawalah, Shuko Murakami, et al.. (2021). Blocking neddylation elicits antiviral effect against hepatitis B virus replication. Molecular Biology Reports. 49(1). 403–412. 4 indexed citations

Kettani, A. El, et al.. (2020). 13q interstitial deletion in a moroccan child with hereditary retinoblastoma and intellectual disability: A case report. Annals of Medicine and Surgery. 60. 334–337. 1 indexed citations

Nadifi, Sellama, et al.. (2020). Genetic Polymorphisms of Glutathione S-Transferase and Risk of Acute Myeloid Leukemia: Case-Control Study and Meta-Analysis. SHILAP Revista de lepidopterología. 11(2). 127–139. 2 indexed citations

Nadifi, Sellama, et al.. (2019). MDR1 gene polymorphisms and acute myeloid leukemia AML susceptibility in A Moroccan adult population: A case-control study and meta-analysis. Current Research in Translational Medicine. 68(1). 29–35. 2 indexed citations

Abbad, Anass, et al.. (2018). Genetics of breast cancer in African populations: a literature review. PubMed. 3. e8–e8. 21 indexed citations

10.

Nadifi, Sellama, et al.. (2018). Genetics of Glioblastoma in Moroccan population: Review of literature. IBRO Reports. 5. 133–136. 1 indexed citations

11.

Nadifi, Sellama, et al.. (2017). Association of Glutathione S-transferase Genes (M1 and T1) with the Risk of Acute Myeloid Leukemia in a Moroccan Population. SHILAP Revista de lepidopterología. 6 indexed citations

12.

Dehbi, Hind, et al.. (2016). Intra-familial phenotypic variability in a Moroccan family with hearing loss and palmoplantar keratoderma (PPK). Current Research in Translational Medicine. 64(2). 61–64. 4 indexed citations

13.

Charoute, Hicham, Sellama Nadifi, Mostafa Kabine, et al.. (2016). Update of the spectrum of GJB2 gene mutations in 152 Moroccan families with autosomal recessive nonsyndromic hearing loss. European Journal of Medical Genetics. 59(6-7). 325–329. 21 indexed citations

14.

Kassogué, Yaya, et al.. (2016). Association between ABCB1 C3435T polymorphism and breast cancer risk: a Moroccan case-control study and meta-analysis. BMC Genetics. 17(1). 126–126. 16 indexed citations

15.

Kassogué, Yaya, et al.. (2015). Lack of Association of Multidrug Resistance Gene-1 Polymorphisms with Treatment Outcome in Chronic Myeloid Leukemia Patients Treated with Imatinib. SHILAP Revista de lepidopterología. 6(4). 229–235. 1 indexed citations

16.

Kottwitz, Denise, Hind Dehbi, Sellama Nadifi, et al.. (2015). Evaluation of a novel multiplex RT-qPCR assay for the quantification of leukemia-associated BCR-ABL1 translocation. International Journal of Hematology. 102(3). 335–341. 2 indexed citations

17.

Kassogué, Yaya, et al.. (2015). Association of glutathione S-transferase (GSTM1 and GSTT1) genes with chronic myeloid leukemia. SpringerPlus. 4(1). 210–210. 15 indexed citations

18.

Dehbi, Hind, et al.. (2013). FLT3-ITD Incidence and FLT-D835 Mutations in Acute Myeloid Leukemia Patients with Normal Karyotype in Morocco: A Preliminary Study. SHILAP Revista de lepidopterología. 4(1). 1–5. 4 indexed citations

19.

Kassogué, Yaya, et al.. (2013). Genotype Variability and Haplotype Frequency of MDR1 ( ABCB1 ) Gene Polymorphism in Morocco. DNA and Cell Biology. 32(10). 582–588. 18 indexed citations

20.

Kassogué, Yaya, et al.. (2013). Functional polymorphism of CYP2B6 G15631T is associated with hematologic and cytogenetic response in chronic myeloid leukemia patients treated with imatinib. Medical Oncology. 31(1). 782–782. 18 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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