Walid Al‐Achkar

744 citations
52 papers · 359 · h-index 11

Impact in

  • Hematology top 5%
    • Chronic Myeloid Leukemia Treatments
    • Iron Metabolism and Disorders
    • Acute Myeloid Leukemia Research
  • Genetics top 5%
    • Chronic Lymphocytic Leukemia Research
    • Hemoglobinopathies and Related Disorders
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities

Papers in

    • Chronic Myeloid Leukemia Treatments 23
    • Acute Myeloid Leukemia Research 12
    • Iron Metabolism and Disorders 4
    • Chronic Lymphocytic Leukemia Research 15
    • Hemoglobinopathies and Related Disorders 4

Walid Al‐Achkar

49 papers receiving 353 citations

Peers

Walid Al‐Achkar
Comparison fields: 5 of 51
  • Hematology 199
  • Genetics 160
  • Rheumatology 65
  • Sensory Systems 14
  • Reproductive Medicine 24
Replace Purificação Tavares with:
Purificação Tavares Portugal
Frédéric Bilan France
Atsushi Manabe Japan
Patrick Morice France
Stella J. Nylund Finland
K Ohyashiki Japan
G. Nozari United States
Amal Arachiche United States
Arthavan Selvanathan Australia
Walid Al‐Achkar relative to Purificação Tavares Portugal Purificação Tavares's profile →
Citations per field
00.5×
Purificação Tavares · 1×
Citations per year

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-authors

The 10 scholars most cited alongside Walid Al‐Achkar, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Walid Al‐Achkar Line = papers co-authored together Walid Al‐Achkar links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 52 papers — load more, or switch the sort, to bring in the rest.

#Work
1
A complex translocation t(5;9;22) in Philadelphia cells involving the short arm of chromosome 5 in a case of chronic myelogenous leukemia.
200737
2 198825
3 201425
4 201823
5 201419
6 201718
7 201215
8 201414
9
Correlation of p210 BCR-ABL transcript variants with clinical, parameters and disease outcome in 45 chronic myeloid leukemia patients.
201613
10 201212
11 201310
12 201310
13 201410
14 20129
15 20169
16 20168
17 20187
18 20137
19 20106
20 20106

About Walid Al‐Achkar

Walid Al‐Achkar is a scholar working on Hematology, Genetics, Public Health, Environmental and Occupational Health, Molecular Biology and Rheumatology, having authored 52 papers that have together received 359 indexed citations. Recurring topics across this work include Chronic Myeloid Leukemia Treatments (23 papers), Chronic Lymphocytic Leukemia Research (15 papers), Acute Lymphoblastic Leukemia research (13 papers), Acute Myeloid Leukemia Research (12 papers), Eosinophilic Disorders and Syndromes (11 papers), Prenatal Screening and Diagnostics (5 papers), Hemoglobinopathies and Related Disorders (4 papers) and Iron Metabolism and Disorders (4 papers). The work is most often cited by research in Hematology (199 citations), Genetics (160 citations), Rheumatology (65 citations), Sensory Systems (14 citations) and Reproductive Medicine (24 citations). Walid Al‐Achkar has collaborated with scholars based in Syria, Germany and Portugal. Frequent co-authors include Abdulsamad Wafa, Thomas Liehr, Hossam Murad, Laure Sabatier, Bernard Dutrillaux, Elisabeth Klein, Rouben Aroutiounian, Isabel M. Carreira, Joana Barbosa Melo and Marwan Alhalabi. Their work appears in journals such as Molecular Cytogenetics, International Journal of Pediatric Otorhinolaryngology, Gene, Medical Oncology and Mutation research. Fundamental and molecular mechanisms of mutagenesis.

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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