Cathérine Henry

2.7k total citations
23 papers, 1.0k citations indexed

About

Cathérine Henry is a scholar working on Molecular Biology, Genetics and Hematology. According to data from OpenAlex, Cathérine Henry has authored 23 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 8 papers in Genetics and 5 papers in Hematology. Recurrent topics in Cathérine Henry's work include Genomic variations and chromosomal abnormalities (5 papers), Acute Myeloid Leukemia Research (4 papers) and Prenatal Screening and Diagnostics (4 papers). Cathérine Henry is often cited by papers focused on Genomic variations and chromosomal abnormalities (5 papers), Acute Myeloid Leukemia Research (4 papers) and Prenatal Screening and Diagnostics (4 papers). Cathérine Henry collaborates with scholars based in France, United States and Australia. Cathérine Henry's co-authors include Christèle Dubourg, Claude Bendavid, Laurent Pasquier, Véronique David, Sylvie Odent, Karin Tarte, Joëlle Dulong, Jean‐Jacques Lataillade, Norbert-Claude Gorin and Hélène Rouard and has published in prestigious journals such as Blood, Molecular and Cellular Biology and Cancer Research.

In The Last Decade

Cathérine Henry

23 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Cathérine Henry France 14 504 354 262 192 157 23 1.0k
L.I. Al-Gazali United Arab Emirates 22 691 1.4× 201 0.6× 553 2.1× 178 0.9× 159 1.0× 60 1.5k
Gundula Thiel Germany 21 587 1.2× 423 1.2× 311 1.2× 139 0.7× 122 0.8× 51 1.5k
Susan Wood United States 13 421 0.8× 326 0.9× 149 0.6× 123 0.6× 92 0.6× 24 1.7k
Hossein Mossafa France 11 299 0.6× 442 1.2× 97 0.4× 177 0.9× 125 0.8× 29 846
S L Gerson United States 17 707 1.4× 532 1.5× 235 0.9× 228 1.2× 260 1.7× 42 1.3k
Denise Batista United States 21 429 0.9× 145 0.4× 510 1.9× 449 2.3× 377 2.4× 59 1.5k
Lilian Bomme Ousager Denmark 17 428 0.8× 114 0.3× 420 1.6× 186 1.0× 103 0.7× 57 1.1k
Martine LeMerrer France 14 665 1.3× 269 0.8× 725 2.8× 210 1.1× 197 1.3× 20 1.9k
Ajlan Tükün Türkiye 14 339 0.7× 374 1.1× 108 0.4× 272 1.4× 51 0.3× 54 902
Carrie Fitzpatrick United States 17 465 0.9× 97 0.3× 439 1.7× 267 1.4× 330 2.1× 33 1.3k

Countries citing papers authored by Cathérine Henry

Since Specialization
Citations

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

Fields of papers citing papers by Cathérine Henry

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Cathérine Henry

This figure shows the co-authorship network connecting the top 25 collaborators of Cathérine Henry. A scholar is included among the top collaborators of Cathérine Henry 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 Cathérine Henry. Cathérine Henry 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.
Henry, Cathérine, Naveen K. Mehta, Kavya Rakhra, et al.. (2025). CLN-619, a MICA/B monoclonal antibody that promotes innate immune cell-mediated antitumor activity. Journal for ImmunoTherapy of Cancer. 13(4). e008987–e008987. 2 indexed citations
2.
Henry, Cathérine, et al.. (2024). Abstract 5297: CLN-619, a clinical stage MICA/B-specific hIgG1 monoclonal antibody, engages multiple immune effector cells to promote anti-tumor activity. Cancer Research. 84(6_Supplement). 5297–5297. 1 indexed citations
3.
Tucker, Elena J., Linda Akloul, Erika Launay, et al.. (2022). Pseudodicentric Chromosome Originating from an X-Autosome Translocation in a Male Patient with Cryptozoospermia. Cytogenetic and Genome Research. 162(3). 124–131. 1 indexed citations
4.
Slater, Penelope J., et al.. (2022). Fifteen years of shared care for paediatric oncology, haematology and palliative patients across Queensland: The role of Regional Case Managers. Australian Journal of Rural Health. 31(3). 436–451. 3 indexed citations
5.
Petit, Arnaud, Yves Bertrand, Claire Pluchart, et al.. (2021). Therapeutic approach and outcome of children with Philadelphia chromosome‐positive acute lymphoblastic leukemia at first relapse in the era of tyrosine kinase inhibitors: An SFCE retrospective study. Pediatric Blood & Cancer. 69(2). e29441–e29441. 2 indexed citations
6.
Loget, Philippe, Sylvie Odent, G. Le Bouar, et al.. (2021). Multicolor-FISH Characterization of a Prenatal Mosaicism for a Chromosomal Rearrangement Undetected by Molecular Cytogenetics. Cytogenetic and Genome Research. 161(3-4). 143–152. 4 indexed citations
7.
Desmots, Fabienne, Mikaël Roussel, Céline Pangault, et al.. (2018). Pan-HDAC Inhibitors Restore PRDM1 Response to IL21 in CREBBP-Mutated Follicular Lymphoma. Clinical Cancer Research. 25(2). 735–746. 19 indexed citations
8.
Dagher, Julien, Frédéric Dugay, G. Verhoest, et al.. (2013). Histologic prognostic factors associated with chromosomal imbalances in a contemporary series of 89 clear cell renal cell carcinomas. Human Pathology. 44(10). 2106–2115. 20 indexed citations
9.
Launay, Erika, Cathérine Henry, Claus Meyer, et al.. (2013). MLL-SEPT5fusion transcript in infant acute myeloid leukemia with t(11;22)(q23;q11). Leukemia & lymphoma. 55(3). 662–667. 7 indexed citations
10.
Guilloton, Fabien, Gersende Caron, Cédric Menard, et al.. (2012). Mesenchymal stromal cells orchestrate follicular lymphoma cell niche through the CCL2-dependent recruitment and polarization of monocytes. Blood. 119(11). 2556–2567. 110 indexed citations
11.
Curtis, Jackie, Cathérine Henry, Andrew Watkins, et al.. (2011). Metabolic abnormalities in an early psychosis service: a retrospective, naturalistic cross-sectional study. Early Intervention in Psychiatry. 5(2). 108–114. 45 indexed citations
12.
Tarte, Karin, Julien Burlaud‐Gaillard, Jean‐Jacques Lataillade, et al.. (2009). Clinical-grade production of human mesenchymal stromal cells: occurrence of aneuploidy without transformation. Blood. 115(8). 1549–1553. 354 indexed citations
13.
Dubourg, Christèle, Claude Bendavid, Laurent Pasquier, et al.. (2007). Holoprosencephaly. Orphanet Journal of Rare Diseases. 2(1). 8–8. 234 indexed citations
14.
Bendavid, Claude, Christèle Dubourg, Laurent Pasquier, et al.. (2007). MLPA screening reveals novel subtelomeric rearrangements in holoprosencephaly. Human Mutation. 28(12). 1189–1197. 17 indexed citations
15.
Gandemer, Virginie, Anne-Gaëlle Rio, Marie de Tayrac, et al.. (2007). Five distinct biological processes and 14 differentially expressed genes characterize TEL/AML1-positive leukemia. BMC Genomics. 8(1). 385–385. 47 indexed citations
16.
Bendavid, Claude, Laurent Pasquier, Tanguy Watrin, et al.. (2006). Phenotypic variability of a 4q34 → qter inherited deletion: MRKH syndrome in the daughter, cardiac defect and Fallopian tube cancer in the mother. European Journal of Medical Genetics. 50(1). 66–72. 27 indexed citations
17.
Henry, Cathérine, Virginie Gandemer, Florence Burtin, et al.. (2005). Late ovarian relapse of TEL/AML1 positive ALL confirming that TEL deletion is a secondary event in leukemogenesis. Leukemia Research. 29(9). 1089–1094. 13 indexed citations
18.
Bendavid, Claude, Christèle Dubourg, Isabelle Gicquel, et al.. (2005). Molecular evaluation of foetuses with holoprosencephaly shows high incidence of microdeletions in the HPE genes. Human Genetics. 119(1-2). 1–8. 44 indexed citations
19.
Dubourg, Christèle, Bertrand Toutain, Catherine Hélias, et al.. (2002). Evaluation of ETF1/eRF1, mapping to 5q31, as a candidate myeloid tumor suppressor gene. Cancer Genetics and Cytogenetics. 134(1). 33–37. 20 indexed citations
20.
Lemke, Johannes R., Ilse Chudoba, Gabriele Senger, et al.. (2001). Improved definition of chromosomal breakpoints using high-resolution multicolour banding. Human Genetics. 108(6). 478–483. 17 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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