D Soekarman
Impact in
- Hematology top 5%
- Chronic Myeloid Leukemia Treatments
- Acute Myeloid Leukemia Research
- Genetics top 10%
- Chronic Lymphocytic Leukemia Research
- Genetics and Neurodevelopmental Disorders
Papers in
-
- Hedgehog Signaling Pathway Studies 2
- RNA modifications and cancer 2
- Genetics 7
- Chronic Lymphocytic Leukemia Research 5
- Genetics and Neurodevelopmental Disorders 3
- Neurogenetic and Muscular Disorders Research 2
- Co-authors
- A Hagemeijer (5 shared papers)Gerard C. Grosveld (5 shared papers)Marieke von Lindern (3 shared papers)Christa Fonatsch (2 shared papers)Bauke M. de Jong (2 shared papers)B Heinze (2 shared papers)Jean‐Pierre Fryns (5 shared papers)Claus R. Bartram (1 shared paper)
- Journals
- Blood (4 papers)Clinical Genetics (2 papers)Journal of Medical Genetics (1 paper)American Journal of Medical Genetics Part A (1 paper)Qatar medical journal (1 paper)
- Partner nations
- NetherlandsBelgiumQatar
In The Last Decade
D Soekarman
21 papers receiving 327 citations
Peers
Comparison fields: 5 of 35
- Hematology 207
- Genetics 106
- Rheumatology 45
- Oral Surgery 18
- Molecular Biology 156
Countries citing papers authored by D Soekarman
This map shows the geographic impact of D Soekarman'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 D Soekarman with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites D Soekarman more than expected).
Fields of papers citing papers by D Soekarman
This network shows the impact of papers produced by D Soekarman. 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 D Soekarman. The network helps show where D Soekarman may publish in the future.
Co-authors
The 25 scholars most cited alongside D Soekarman, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 23 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1992 | 82 | |
| 2 | 1989 | 55 | |
| 3 | A novel variant of the bcr-abl fusion product in Philadelphia chromosome-positive acute lymphoblastic leukemia. | 1990 | 45 |
| 4 | bcr-abl mRNA lacking abl exon a2 detected by polymerase chain reaction in a chronic myelogeneous leukemia patient. | 1991 | 34 |
| 5 | Dek-can rearrangement in translocation (6;9)(p23;q34). | 1992 | 27 |
| 6 | Increased head circumference and facial cleft as presenting signs of the nevoid basal-cell carcinoma syndrome. | 1991 | 20 |
| 7 | 1995 | 14 | |
| 8 | A form of non-specific mental retardation is probably caused by a microdeletion in a Belgian family | 1996 | 12 |
| 9 | Corpus callosum agenesis in Coffin-Lowry syndrome. | 1994 | 9 |
| 10 | 1994 | 8 | |
| 11 | Pfeiffer acrocephalosyndactyly syndrome in mother and son with cloverleaf skull anomaly in the child. | 1992 | 8 |
| 12 | 1993 | 7 | |
| 13 | 1992 | 4 | |
| 14 | Non-specific mental retardation is probably caused by a microdeletion in a Belgian family | 1995 | 3 |
| 15 | The Philadelphia translocation in CML and ALL: recent investigations, new detection methods. | 1990 | 2 |
| 16 | 2019 | 2 | |
| 17 | 1989 | 1 | |
| 18 | The association of hemifacial microsomia, homolateral micro/anophthalmos, hemihypotrophy, dental anomalies, submucous cleft palate, CNS malformations and hypopigmented skin lesions following Blaschko's lines in two unrelated female patients. Further evidence for a lethal mutation surviving in mosaic form in "hypomelanosis of Ito". | 1993 | 1 |
| 19 | Macrocephaly and mental retardation. The unique association with short stature, spastic paraplegia and CNS malformations. | 1993 | 1 |
| 20 | Marden-Walker phenotype: a diagnostic dilemma. | 1996 | 1 |
About D Soekarman
D Soekarman is a scholar working on Molecular Biology, Genetics, Hematology, Genetics and Public Health, Environmental and Occupational Health, having authored 23 papers that have together received 338 indexed citations. Recurring topics across this work include Chronic Myeloid Leukemia Treatments (7 papers), Chronic Lymphocytic Leukemia Research (5 papers), Acute Myeloid Leukemia Research (3 papers), Genetics and Neurodevelopmental Disorders (3 papers), Hedgehog Signaling Pathway Studies (2 papers), Acute Lymphoblastic Leukemia research (2 papers), Neurogenetic and Muscular Disorders Research (2 papers) and RNA modifications and cancer (2 papers). The work is most often cited by research in Hematology (207 citations), Genetics (106 citations), Rheumatology (45 citations), Oral Surgery (18 citations) and Molecular Biology (156 citations). D Soekarman has collaborated with scholars based in Netherlands, Belgium and Qatar. Frequent co-authors include A Hagemeijer, Gerard C. Grosveld, Marieke von Lindern, Christa Fonatsch, Bauke M. de Jong, B Heinze, Jean‐Pierre Fryns, Claus R. Bartram, Herman Van den Berghe and R. H. van Gent. Their work appears in journals such as Blood, Clinical Genetics, Journal of Medical Genetics, American Journal of Medical Genetics Part A and Qatar medical journal.
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.