Walid Al‐Achkar

744 total citations
52 papers, 359 citations indexed

About

Walid Al‐Achkar is a scholar working on Hematology, Genetics and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Walid Al‐Achkar has authored 52 papers receiving a total of 359 indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Hematology, 21 papers in Genetics and 15 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Walid Al‐Achkar's work include Chronic Myeloid Leukemia Treatments (23 papers), Chronic Lymphocytic Leukemia Research (15 papers) and Acute Lymphoblastic Leukemia research (13 papers). Walid Al‐Achkar is often cited by papers focused on Chronic Myeloid Leukemia Treatments (23 papers), Chronic Lymphocytic Leukemia Research (15 papers) and Acute Lymphoblastic Leukemia research (13 papers). Walid Al‐Achkar collaborates with scholars based in Syria, Germany and Portugal. Walid Al‐Achkar's co-authors include Abdulsamad Wafa, Thomas Liehr, Hossam Murad, Laure Sabatier, Bernard Dutrillaux, Elisabeth Klein, Rouben Aroutiounian, Isabel M. Carreira, Marwan Alhalabi and Joana Barbosa Melo and has published in prestigious journals such as SHILAP Revista de lepidopterología, Gene and Mutation research. Fundamental and molecular mechanisms of mutagenesis.

In The Last Decade

Walid Al‐Achkar

49 papers receiving 353 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Walid Al‐Achkar Syria 11 199 160 108 65 63 52 359
Atsushi Manabe Japan 10 113 0.6× 38 0.2× 123 1.1× 16 0.2× 18 0.3× 22 395
Patrick Morice France 11 238 1.2× 211 1.3× 100 0.9× 31 0.5× 55 0.9× 20 394
Stella J. Nylund Finland 7 89 0.4× 32 0.2× 172 1.6× 19 0.3× 33 0.5× 11 289
K Ohyashiki Japan 8 207 1.0× 54 0.3× 209 1.9× 43 0.7× 98 1.6× 11 377
Frédéric Bilan France 11 30 0.2× 94 0.6× 151 1.4× 19 0.3× 9 0.1× 25 355
Purificação Tavares Portugal 9 64 0.3× 74 0.5× 107 1.0× 25 0.4× 12 0.2× 18 301
Arthavan Selvanathan Australia 7 98 0.5× 22 0.1× 88 0.8× 21 0.3× 128 2.0× 22 290
Walid Al Achkar Syria 8 41 0.2× 33 0.2× 134 1.2× 13 0.2× 26 0.4× 16 237
Marina Manvelyan Germany 13 23 0.1× 36 0.2× 190 1.8× 23 0.4× 36 0.6× 22 402

Countries citing papers authored by Walid Al‐Achkar

Since Specialization
Citations

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

Fields of papers citing papers by Walid Al‐Achkar

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Walid Al‐Achkar. 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 Walid Al‐Achkar. The network helps show where Walid Al‐Achkar may publish in the future.

Co-authorship network of co-authors of Walid Al‐Achkar

This figure shows the co-authorship network connecting the top 25 collaborators of Walid Al‐Achkar. A scholar is included among the top collaborators of Walid Al‐Achkar 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 Walid Al‐Achkar. Walid Al‐Achkar 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.
Wafa, Abdulsamad, et al.. (2021). Frequency of FLT3 Internal Tandem Duplications in Adult Syrian Patients with Acute Myeloid Leukemia and Normal Karyotype. Asian Pacific Journal of Cancer Prevention. 22(10). 3245–3251. 4 indexed citations
2.
Wafa, Abdulsamad, et al.. (2020). A new childhood ALL case with an extremely complex karyotype and acute spontaneous tumor lysis syndrome. Molecular Cytogenetics. 13(1). 44–44.
3.
Wafa, Abdulsamad, et al.. (2020). An acquired stable variant of a dicentric dic(9;20) and complex karyotype in a Syrian childhood B-acute lymphoblastic leukemia case. Molecular Cytogenetics. 13(1). 29–29. 1 indexed citations
4.
Al‐Achkar, Walid, et al.. (2018). Investigation of the mtDNA mutations in Syrian families with non-syndromic sensorineural hearing loss. International Journal of Pediatric Otorhinolaryngology. 113. 110–114. 7 indexed citations
5.
Al‐Achkar, Walid, et al.. (2016). First report of prevalence c.IVS1+1G>A and del (GJB6-13S1854) mutations in Syrian families with non-syndromic sensorineural hearing loss. International Journal of Pediatric Otorhinolaryngology. 92. 82–87. 9 indexed citations
6.
Wafa, Abdulsamad, et al.. (2015). Deletion 9p23 to 9p11.1 as sole additional abnormality in a Philadelphia positive chronic myeloid leukemia in blast crisis: a rare event. Molecular Cytogenetics. 8(1). 59–59. 2 indexed citations
7.
Al‐Achkar, Walid, et al.. (2014). Influence of CYP1A1, GST polymorphisms and susceptibility risk of chronic myeloid leukemia in Syrian population. Medical Oncology. 31(5). 889–889. 19 indexed citations
8.
Murad, Hossam, et al.. (2014). Molecular Update of β-Thalassemia Mutations in the Syrian Population: Identification of Rare β-Thalassemia Mutations. Hemoglobin. 38(4). 272–276. 25 indexed citations
9.
Murad, Hossam, et al.. (2013). Mutation spectrum of phenylketonuria in Syrian population: Genotype–phenotype correlation. Gene. 528(2). 241–247. 10 indexed citations
10.
Al‐Achkar, Walid, et al.. (2013). A unique case of female pseudohermaphroditism with 21-hydroxylase deficiency and small supernumerary marker chromosome 7. Molecular Medicine Reports. 7(5). 1545–1548.
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Al‐Achkar, Walid, et al.. (2012). Detailed analysis of an idic(Y)(q11.21) in a mosaic karyotype. Molecular Medicine Reports. 6(2). 293–296. 5 indexed citations
14.
Al‐Achkar, Walid, et al.. (2012). A chronic myeloid leukemia case with a unique variant Philadelphia translocation: t(9;22;21)(q34;q11;p12). Oncology Letters. 3(5). 1027–1029. 9 indexed citations
15.
Al‐Achkar, Walid, et al.. (2012). Cytogenetic abnormalities and Y-chromosome microdeletions in infertile Syrian males. Biomedical Reports. 1(2). 275–279. 15 indexed citations
16.
Al‐Achkar, Walid, Abdulsamad Wafa, & Thomas Liehr. (2011). Complex translocation involving four chromosomes in a novel Philadelphia-positive chronic myeloid leukemia case. Oncology Letters. 2(2). 273–276. 1 indexed citations
17.
Al‐Achkar, Walid, et al.. (2011). A new case of de novo translocation (12;17;18)(q21.2;q22;q21.1) and cranio‐cerebello‐cardiac (3C) syndrome. American Journal of Medical Genetics Part A. 155(3). 648–651. 2 indexed citations
18.
Al‐Achkar, Walid, et al.. (2011). Biclonal myelodysplastic syndrome involving six chromosomes and monoallelic loss of RB1 - A rare case. Molecular Cytogenetics. 4(1). 16–16. 3 indexed citations
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Al‐Achkar, Walid, et al.. (2007). A complex translocation t(5;9;22) in Philadelphia cells involving the short arm of chromosome 5 in a case of chronic myelogenous leukemia.. PubMed. 26(3). 411–5. 37 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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