C Herens

515 total citations
19 papers, 219 citations indexed

About

C Herens is a scholar working on Genetics, Molecular Biology and Hematology. According to data from OpenAlex, C Herens has authored 19 papers receiving a total of 219 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 7 papers in Molecular Biology and 7 papers in Hematology. Recurrent topics in C Herens's work include Genomic variations and chromosomal abnormalities (9 papers), Acute Myeloid Leukemia Research (4 papers) and Prenatal Screening and Diagnostics (3 papers). C Herens is often cited by papers focused on Genomic variations and chromosomal abnormalities (9 papers), Acute Myeloid Leukemia Research (4 papers) and Prenatal Screening and Diagnostics (3 papers). C Herens collaborates with scholars based in Belgium, India and United States. C Herens's co-authors include Alain Verloès, H. Barbason, Bruce Poppe, A Hagemeijer, Frank Speleman, Jan Cools, Nicole Dastugue, Barbara Cauwelier, Anne De Paepe and Lionel Van Maldergem and has published in prestigious journals such as Journal of Clinical Oncology, Blood and British Journal of Haematology.

In The Last Decade

C Herens

19 papers receiving 210 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
C Herens Belgium	8	86	67	63	48	44	19	219
Stella J. Nylund Finland	7	89 1.0×	38 0.6×	172 2.7×	32 0.7×	33 0.8×	11	289
P. Guanciali Franchi Italy	6	17 0.2×	110 1.6×	86 1.4×	33 0.7×	38 0.9×	9	242
Johannes Ihle Germany	9	55 0.6×	71 1.1×	105 1.7×	19 0.4×	13 0.3×	14	244
Yuichiro Semba Japan	12	60 0.7×	39 0.6×	203 3.2×	33 0.7×	41 0.9×	35	305
Asuka Kamio Japan	6	81 0.9×	51 0.8×	245 3.9×	22 0.5×	26 0.6×	8	274
Siân Morgan United Kingdom	8	39 0.5×	117 1.7×	107 1.7×	25 0.5×	25 0.6×	16	304
Maria Patrizia Bicocchi Italy	12	169 2.0×	124 1.9×	189 3.0×	45 0.9×	18 0.4×	24	420
Vincent Leymarie France	6	95 1.1×	27 0.4×	56 0.9×	37 0.8×	52 1.2×	16	226
M. J. Grégoire France	7	155 1.8×	92 1.4×	232 3.7×	11 0.2×	32 0.7×	14	302
Shu‐Chin Chien Taiwan	10	13 0.2×	73 1.1×	84 1.3×	29 0.6×	29 0.7×	32	309

Countries citing papers authored by C Herens

Since Specialization

Citations

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

Fields of papers citing papers by C Herens

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of C Herens

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

All Works

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19 of 19 papers shown

Duhoux, François P., Geneviève Ameye, Iwona Włodarska, et al.. (2011). PRDM16 (1p36) translocations define a distinct entity of myeloid malignancies with poor prognosis but may also occur in lymphoid malignancies.. Journal of Clinical Oncology. 29(15_suppl). 6531–6531. 5 indexed citations

Castermans, Emilie, Frédéric Baron, E. Willems, et al.. (2008). Evidence for neo-generation of T cells by the thymus after non-myeloablative conditioning. Haematologica. 93(2). 240–247. 25 indexed citations

Cauwelier, Barbara, Nicole Dastugue, Jan Cools, et al.. (2006). Molecular cytogenetic study of 126 unselected T-ALL cases reveals high incidence of TCRβ locus rearrangements and putative new T-cell oncogenes. Leukemia. 20(7). 1238–1244. 44 indexed citations

Baron, Frédéric, Étienne Baudoux, Pascale Frère, et al.. (2003). Low T-cell chimerism is not followed by graft rejection after nonmyeloablative stem cell transplantation (NMSCT) with CD34-selected PBSC. Bone Marrow Transplantation. 32(8). 829–834. 3 indexed citations

Koulischer, L, et al.. (2000). Inv(12)(q15q24). Cancer Genetics and Cytogenetics. 121(2). 206–207. 1 indexed citations

Herens, C, et al.. (2000). Deletion of the 5′‐ABL region: a recurrent anomaly detected by fluorescence in situ hybridization in about 10% of Philadelphia‐positive chronic myeloid leukaemia patients. British Journal of Haematology. 110(1). 214–216. 37 indexed citations

Michaux, Lucienne, Judith Dierlamm, Michel Stul, et al.. (1998). Amplification of chromosome 11q23 involving the MLL gene is recurrently observed in myeloid leukemias.. Blood. 92(10). 1 indexed citations

Verloès, Alain, Cynthia J. Curry, C Herens, et al.. (1998). Juvenile rheumatoid arthritis and del(22q11) syndrome: a non-random association.. Journal of Medical Genetics. 35(11). 943–947. 20 indexed citations

Barbason, H., et al.. (1996). Importance of cell kinetics rhythmicity for the control of cell proliferation and carcinogenesis in rat liver (review).. PubMed. 9(6). 539–48. 18 indexed citations

10.

Herens, C, Serge Massart, Boumediene Bouzahzah, L Koulischer, & H. Barbason. (1995). Nuclear lesions during rat hepatocarcinogenesis. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 329(2). 161–171. 3 indexed citations

11.

Herens, C, et al.. (1995). Nuclear lesions during rat hepatocarcinogenesis. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 329(2). 153–159. 1 indexed citations

12.

Herens, C, et al.. (1992). Cytogenetic changes in hepatocarcinomas from rats treated with chronic exposure to diethylnitrosamine. Cancer Genetics and Cytogenetics. 60(1). 45–52. 11 indexed citations

13.

Verloès, Alain, et al.. (1992). Combined 10pter-->p11 and 18pter-->q11 trisomy in a 7-year-old child.. PubMed. 3(3). 155–9. 2 indexed citations

14.

Avni, Fred E., et al.. (1991). Ring chromosome 9 in a newborn male presenting with facial dysmorphia, hypospadias and skeletal abnormalities.. PubMed. 2(2). 123–7. 4 indexed citations

15.

Herens, C, et al.. (1990). Trisomy 20q. A new case and further phenotypic delineation. Clinical Genetics. 37(5). 363–366. 18 indexed citations

16.

Herens, C, Geneviève Pierquin, Alain Verloès, J P Schaaps, & J Frédéric. (1989). Mosaicism of 46,XX/47,XX,+9/47,XX,+?mar in the same amniotic fluid with apparent loss of one cell line after delivery. Prenatal Diagnosis. 9(5). 373–375. 5 indexed citations

17.

Verloès, Alain, et al.. (1989). Roberts-SC phocomelia syndrome with exencephaly.. PubMed. 32(3). 169–70. 3 indexed citations

18.

Pierquin, Geneviève, C Herens, J Frédéric, et al.. (1988). Partial trisomy 20q due to paternal t(8;20) translocation: Case report and review of the literature. Clinical Genetics. 33(5). 386–389. 15 indexed citations

19.

Verloès, Alain, C Herens, C Lambotte, & J Frédéric. (1987). Chromosome 22 mosaic monosomy (46,XY/45,XY,-22).. PubMed. 30(3). 178–9. 3 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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