Christian Herens

1.7k total citations
35 papers, 877 citations indexed

About

Christian Herens is a scholar working on Molecular Biology, Genetics and Hematology. According to data from OpenAlex, Christian Herens has authored 35 papers receiving a total of 877 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 10 papers in Genetics and 10 papers in Hematology. Recurrent topics in Christian Herens's work include Chronic Lymphocytic Leukemia Research (8 papers), Genomic variations and chromosomal abnormalities (7 papers) and Prenatal Screening and Diagnostics (6 papers). Christian Herens is often cited by papers focused on Chronic Lymphocytic Leukemia Research (8 papers), Genomic variations and chromosomal abnormalities (7 papers) and Prenatal Screening and Diagnostics (6 papers). Christian Herens collaborates with scholars based in Belgium, Germany and United Kingdom. Christian Herens's co-authors include Alain Verloès, Mauricette Jamar, Laurence de Leval, Lucienne Michaux, L Koulischer, Esther Oliva, Robert A. Soslow, Frank Speleman, Vincent Bours and Heidi Van Limbergen and has published in prestigious journals such as Proceedings of the National Academy of Sciences, American Journal of Obstetrics and Gynecology and Journal of Investigative Dermatology.

In The Last Decade

Christian Herens

34 papers receiving 846 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Christian Herens Belgium 16 295 275 201 178 106 35 877
Denise Batista United States 21 510 1.7× 429 1.6× 201 1.0× 145 0.8× 165 1.6× 59 1.5k
Hon Fong L. Mark United States 15 237 0.8× 263 1.0× 89 0.4× 85 0.5× 105 1.0× 54 668
Emanuela Maserati Italy 21 486 1.6× 332 1.2× 423 2.1× 152 0.9× 53 0.5× 60 1.1k
Martine Jotterand Switzerland 15 131 0.4× 311 1.1× 692 3.4× 258 1.4× 74 0.7× 35 986
Kumi Nakazaki Japan 10 315 1.1× 543 2.0× 209 1.0× 143 0.8× 130 1.2× 34 996
Antonella Minelli Italy 17 568 1.9× 232 0.8× 231 1.1× 396 2.2× 34 0.3× 46 1.2k
TS Ganesan United Kingdom 14 70 0.2× 319 1.2× 215 1.1× 191 1.1× 169 1.6× 23 942
Anne E. Wiktor United States 22 410 1.4× 547 2.0× 263 1.3× 185 1.0× 122 1.2× 55 1.5k
Eileen Boye United States 17 187 0.6× 429 1.6× 165 0.8× 114 0.6× 132 1.2× 21 1.2k
Sandra Hing United Kingdom 16 211 0.7× 408 1.5× 76 0.4× 47 0.3× 160 1.5× 24 916

Countries citing papers authored by Christian Herens

Since Specialization
Citations

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

Fields of papers citing papers by Christian Herens

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Christian Herens

This figure shows the co-authorship network connecting the top 25 collaborators of Christian Herens. A scholar is included among the top collaborators of Christian Herens 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 Christian Herens. Christian Herens 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.
Somja, Joan, Bettina Bisig, Christophe Bonnet, et al.. (2014). Peripheral T-cell lymphoma with t(6;14)(p25;q11.2) translocation presenting with massive splenomegaly. Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin. 464(6). 735–41. 7 indexed citations
2.
Josse, Claire, et al.. (2010). Systematic Chromosomal Aberrations Found in Murine Bone Marrow-Derived Mesenchymal Stem Cells. Stem Cells and Development. 19(8). 1167–1173. 44 indexed citations
3.
Könings, Peter, Katrina Rack, Mauricette Jamar, et al.. (2009). Improved detection of chromosomal abnormalities in chronic lymphocytic leukemia by conventional cytogenetics using CpG oligonucleotide and interleukin‐2 stimulation: A Belgian multicentric study. Genes Chromosomes and Cancer. 48(10). 843–853. 36 indexed citations
4.
Lambert, Frédéric, Pierre Heimann, Christian Herens, Alain Chariot, & Vincent Bours. (2007). A Case of FIP1L1-PDGFRA-Positive Chronic Eosinophilic Leukemia with a Rare FIP1L1 Breakpoint. Journal of Molecular Diagnostics. 9(3). 414–419. 8 indexed citations
5.
Oliva, Esther, Laurence de Leval, Robert A. Soslow, & Christian Herens. (2007). High Frequency of JAZF1-JJAZ1 Gene Fusion in Endometrial Stromal Tumors With Smooth Muscle Differentiation by Interphase FISH Detection. The American Journal of Surgical Pathology. 31(8). 1277–1284. 59 indexed citations
6.
Thielen, Caroline, Christian Herens, Marie France Fassotte, et al.. (2006). Establishment and characterisation of two novel human KSHV‐ and EBV‐negative Burkitt cell lines, GAL‐01 and GAL‐02, from a primary lymphomatous effusion. European Journal Of Haematology. 77(4). 318–326. 1 indexed citations
7.
8.
Detry, Olivier, Arnaud De Roover, Laurence de Leval, et al.. (2005). Transmission of An Undiagnosed Sarcoma to Recipients of Kidney and Liver Grafts Procured in a Non-Heart Beating Donor. Liver Transplantation. 11(6). 696–699. 11 indexed citations
9.
Herens, Christian, et al.. (2003). Deletion (6)(p22p25) is a recurrent anomaly of thymoma: report of a second case and review of the literature. Cancer Genetics and Cytogenetics. 146(1). 66–69. 6 indexed citations
10.
Baron, Frédéric, Étienne Baudoux, Pascale Frère, et al.. (2002). Nonmyeloablative Stem Cell Transplantation with CD8-Depleted or CD34-Selected Peripheral Blood Stem Cells. Journal of Hematotherapy & Stem Cell Research. 11(2). 301–314. 17 indexed citations
11.
Baron, Frédéric, Pascale Frère, Christian Herens, Georges Fillet, & Yves Béguin. (2002). Combination of nonmyeloablative stem cell transplantation and Imatinib in accelerated phase CML.. PubMed. 87(12). ECR43–ECR43. 1 indexed citations
12.
Herens, Christian, et al.. (2001). Translocation (16;17)(q22;p13) is a recurrent anomaly of aneurysmal bone cysts. Cancer Genetics and Cytogenetics. 127(1). 83–84. 36 indexed citations
13.
Verloès, Alain, Y. Gillerot, Lionel Van Maldergem, et al.. (2001). Major decrease in the incidence of trisomy 21 at birth in south Belgium: mass impact of triple test?. European Journal of Human Genetics. 9(1). 1–4. 37 indexed citations
14.
Riegel, Mariluce, Alessandra Baumer, Mauricette Jamar, et al.. (2001). Submicroscopic terminal deletions and duplications in retarded patients with unclassified malformation syndromes. Human Genetics. 109(3). 286–294. 76 indexed citations
15.
Michaux, Lucienne, Iwona Włodarska, Michel Stul, et al.. (2000). MLL amplification in myeloid leukemias: A study of 14 cases with multiple copies of 11q23. Genes Chromosomes and Cancer. 29(1). 40–47. 21 indexed citations
16.
Dewé, Walthère, et al.. (2000). A Four-Parameter Index of Marrow Dysplasia Has Predictive Value for Survival in Myelodysplastic Syndromes. Leukemia & lymphoma. 36(5-6). 485–496. 13 indexed citations
17.
Herens, Christian, et al.. (1999). Translocation (2;3)(p21;q26) as the Sole Anomaly in a Case of Primary Myelofibrosis. Cancer Genetics and Cytogenetics. 110(1). 62–64. 3 indexed citations
18.
Koulischer, L, et al.. (1997). Genetic risk in natural and medically assisted procreation.. PubMed. 3(3). 164–71. 12 indexed citations
19.
Verloès, Alain, et al.. (1995). A prenatal trisomy 21 screening program using α-fetoprotein, human chorionic gonadotropin, and free estriol assays on maternal dried blood. American Journal of Obstetrics and Gynecology. 172(1). 167–174. 22 indexed citations
20.
Hustinx, Roland, et al.. (1993). Monosomy 11q: Report of two familial cases and review of the literature. American Journal of Medical Genetics. 47(3). 312–317. 15 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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