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Vanbellinghen Jean-François

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Main Referenced Co-authors
Beckers, Albert  (29)
Daly, Adrian  (23)
Bours, Vincent  (22)
Jaffrain-Rea, Marie-Lise (12)
Barlier, Anne (9)
Main Referenced Keywords
Humans (7); Female (6); Male (6); Adult (5); Middle Aged (4);
Main Referenced Unit & Research Centers
GIGA CRC (Cyclotron Research Center) In vivo Imaging-Aging & Memory - ULiège [BE] (1)
GIGA-I3 - Giga-Infection, Immunity and Inflammation - ULiège [BE] (1)
Main Referenced Disciplines
Endocrinology, metabolism & nutrition (29)
Genetics & genetic processes (6)
Hematology (4)
Neurology (1)
Pediatrics (1)

Publications (total 40)

The most downloaded
1130 downloads
Daly, A., Tichomirowa, M. A., Petrossians, P., Heliövaara, E., Jaffrain-Rea, M.-L., Barlier, A., Naves, L. A., Ebeling, T., Karhu, A., Raapana, A., Cazabat, L., De Menis, E., Montanana, C. F., Raverot, G., Weil, R. J., Sane, T., Maiter, D., Neggers, S., Yaneva, M., ... Beckers, A. (2010). Clinical characteristics and therapeutic responses in patients with Germ-line AIP mutations and pituitary adenomas : An international collaborative study. Journal of Clinical Endocrinology and Metabolism, 95 (11). doi:10.1210/jc.2009-2556 https://hdl.handle.net/2268/67517

The most cited

299 citations (Scopus®)

Daly, A., Tichomirowa, M. A., Petrossians, P., Heliövaara, E., Jaffrain-Rea, M.-L., Barlier, A., Naves, L. A., Ebeling, T., Karhu, A., Raapana, A., Cazabat, L., De Menis, E., Montanana, C. F., Raverot, G., Weil, R. J., Sane, T., Maiter, D., Neggers, S., Yaneva, M., ... Beckers, A. (2010). Clinical characteristics and therapeutic responses in patients with Germ-line AIP mutations and pituitary adenomas : An international collaborative study. Journal of Clinical Endocrinology and Metabolism, 95 (11). doi:10.1210/jc.2009-2556 https://hdl.handle.net/2268/67517

CASTERMANS, E., Hannon, M., Dutrieux, J., Humblet, S., Seidel, L., Cheynier, R., Willems, E., Gothot, A., Vanbellinghen, J.-F., Geenen, V., Sandmaier, B. M., Storb, R., Beguin, Y., & Baron, F. (2011). Thymic recovery after allogeneic hematopoietic cell transplantation with nonmyeloablative conditioning is limited to patients younger than 60 years of age. Haematologica, 96(2), 298-306. doi:10.3324/haematol.2010.029702
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Tichomirowa, M. A., Pellegata, N. S., Barlier, A., Daly, A., Lee, M., Marinoni, I., Theodoropoulou, M., Verhaeghe, C., Rodien, P., Naves, L. A., Jaffrain-Rea, M.-L., Rohmer, V., Estour, B., Lecomte, P., Borson-Chazot, F., Penfornis, A., Yaneva, M., Wemeau, J. L., Tabarin, A., ... Beckers, A. (2010). Cyclin dependent kinase inhibitor 1B (CDKN1B) gene mutations in FIPA. In European Neuroendocrine Association - Liège, 22-25 septembre 2010.

Tichomirowa, M. A., Barlier, A., Daly, A., Jaffrain-Rea, M.-L., Tabarin, A., Ronchi, C., Naves, L. A., Cozzi, R., Yaneva, M., Elenkova, A., Maiter, D., Caron, P., Bernabeu, I., Montanana, C. F., Sievers, C., Cogne, M., Corman, V., Halaby, G., Chabre, O., ... Beckers, A. (2010). High Prevalence of AIP Gene Mutations Following Focussed Screening in Young Patients with Sporadic Pituitary Macroadenomas. In European Neuroendocrine Association - Liège, 22-25 septembre 2010.

Beckers, A., Tichomirowa, M., Barlier, A., Daly, A., Vanbellinghen, J.-F., Tabarin, A., Jaffrain-Rea, M.-L., Ronchi, C., Cozzi, R., Yaneva, M., Elenkova, A., Maiter, D., Caron, P., Theodoropoulou, M., Sievers, C., Ferrandez Longas, A., Cognes, M., Corman, V., Halaby, G., ... Brue, T. (2010). Mutations AIP chez les jeunes patients en-dessous de 30 ans avec adénome hypophysaire agressif. In 27ème Congrès de la Société Française d'Endocrinologie - Deauville, 29 septembre - 2 octobre 2010.

Beckers, A., Tichomirowa, M., Barlier, A., Daly, A., Vanbellinghen, J.-F., Tabarin, A., Jaffrain-Rea, M.-L., Ronchi, C., Cozzi, R., Yaneva, M., Elenkova, A., Maiter, D., Caron, P., Theodoropoulou, M., Sievers, C., Ferrandez Longas, A., Cognes, M., Corman, V., Halaby, G., ... Thonnard, A.-S. (September 2010). Mutations AIP chez les jeunes patients en dessous de 30 ans avec adénome hypophysaire agressif. Annales d'Endocrinologie, 71 (5), 397.
Peer Reviewed verified by ORBi

Stratakis, C. A., Tichomirowa, M. A., Boikos, S., Azevedo, M. F., Lodish, M., Martari, M., Verma, S., Daly, A., Raygada, M., Keil, M. F., Papademetriou, J., Drori-Herishanu, L., Horvath, A., Tsang, K. M., Nesterova, M., Franklin, S., Vanbellinghen, J.-F., Bours, V., Salvatori, R., & Beckers, A. (2010). The role of germline AIP, MEN1, PRKAR1A, CDKN1B and CDKN2C mutations in causing pituitary adenomas in a large cohort of children, adolescents, and patients with genetic syndromes. Clinical Genetics. doi:10.1111/j.1399-0004.2010.01406.x
Peer Reviewed verified by ORBi

Chung, S.-K., Vanbellinghen, J.-F., Mullins, J. G. L., Robinson, A., Hantke, J., Hammond, C. L., Gilbert, D. F., Freilinger, M., Ryan, M., Kruer, M. C., Masri, A., Gurses, C., Ferrie, C., Harvey, K., Shiang, R., Christodoulou, J., Andermann, F., Andermann, E., Thomas, R. H., ... Rees, M. I. (2010). Pathophysiological mechanisms of dominant and recessive GLRA1 mutations in hyperekplexia. Journal of Neuroscience, 30 (28), 9612-20. doi:10.1523/JNEUROSCI.1763-10.2010
Peer Reviewed verified by ORBi

Baron, F., Lechanteur, C., Willems, E., Bruck, F., Baudoux, E., Seidel, L., Vanbellinghen, J.-F., Hafraoui, K., LEJEUNE, M., Gothot, A., Fillet, G., & Beguin, Y. (2010). Cotransplantation of mesenchymal stem cells might prevent death from graft-versus-host disease (GVHD) without abrogating graft-versus-tumor effects after HLA-mismatched allogeneic transplantation following nonmyeloablative conditioning. Biology of Blood and Marrow Transplantation, 16 (6), 838-47. doi:10.1016/j.bbmt.2010.01.011
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Daly, A., Tichomirowa, M. A., Petrossians, P., Heliövaara, E., Jaffrain-Rea, M.-L., Barlier, A., Naves, L. A., Ebeling, T., Karhu, A., Raapana, A., Cazabat, L., De Menis, E., Montanana, C. F., Raverot, G., Weil, R. J., Sane, T., Maiter, D., Neggers, S., Yaneva, M., ... Beckers, A. (2010). Clinical characteristics and therapeutic responses in patients with Germ-line AIP mutations and pituitary adenomas : An international collaborative study. Journal of Clinical Endocrinology and Metabolism, 95 (11). doi:10.1210/jc.2009-2556
Peer Reviewed verified by ORBi

Jaffrain-Rea, M.-L., Angelini, M., Gargano, D., Tichomirowa, M. A., Daly, A., Vanbellinghen, J.-F., D'Innocenzo, E., Barlier, A., Giangaspero, F., Esposito, V., Ventura, L., Arcella, A., Theodoropoulou, M., Naves, L. A., Fajardo, C., Zacharieva, S., Rohmer, V., Brue, T., Gulino, A., ... Beckers, A. (September 2009). Expression of aryl hydrocarbon receptor (AHR) and AHR-interacting protein in pituitary adenomas: pathological and clinical implications. Endocrine-Related Cancer, 16 (3), 1029-1043. doi:10.1677/ERC-09-0094
Peer Reviewed verified by ORBi

Tichomirova, M., Daly, A., Jaffrain-Réa, M. L., Yaneva, M., Zaccharieva, S., Cozzi, R., Sievers, C., Stalla, G., Vanbellinghen, J.-F., Bours, V., & Beckers, A. (2009). High Incidence of AIP mutations in sporadic pituitary adenomas in young patients with macroadenomas. In 52 Symposium der Deutschen Gesellschaft für Endokrinologie.

Mutesa, L., Vanbellinghen, J.-F., Hellin, A.-C., Segers, K., Jamar, M., Pierquin, G., & Bours, V. (2009). Deletion of Xpter encompassing the SHOX gene and PAR1 region in familial patients with Leri-Weill Dyschondrosteosis syndrome. Genetic Counseling, 20 (1), 9-17.
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Beckers, A., Apetrii, P., Daly, A., Tichomirova, M., Vanbellinghen, J.-F., Georges, M., & Bours, V. (2009). Caractérisation clinique et génétique des adénomes hypophysaires familiaux isolés (FIPA). Revue Médicale de Liège, 64 (S1), 15-19.
Peer reviewed

Mutesa, L., Azad, A. K., Verhaeghe, C., Segers, K., Vanbellinghen, J.-F., Ngendahayo, L., Rusingiza, E. K., Mutwa, P. R., Rulisa, S., Koulischer, L., Cassiman, J.-J., Cuppens, H., & Bours, V. (2009). Genetic Analysis of Rwandan Patients With Cystic Fibrosis-Like Symptoms: Identification of Novel Cystic Fibrosis Transmembrane Conductance Regulator and Epithelial Sodium Channel Gene Variants. CHEST, 135 (5), 1233-42. doi:10.1378/chest.08-2246
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Garraux, G., VANBELLINGHEN, J.-F., JAMAR, M., BOURS, V., Moonen, G., & DIVE, D. (2009). De novo interstitial duplication 4q associated with sporadic young-onset dopa-responsive parkinsonism. Movement Disorders, 24 (Suppl. 1), 138-S139.
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Tichomirova, M. A., Daly, A., Pujol, J., Naves, L., Rodien, P., Vanbellinghen, J.-F., Jaffrain-Rea, M.-L., Rohmer, V., Estour, B., Lecomte, P., Borson-Chazot, F., Penfornis, A., Yaneva, M., Zacharieva, S., Wemeau, J. L., Vantyghem, M. C., Cicarelli, E., Colao, A., Ferrola, P., ... Beckers, A. (2009). An analysis of the role of cyclin dependant kinase inhibitor 1B (CDKN1B) gene mutations in 86 families with familial isolated pituitary adenomas (FIPA). In The Endocrine Society's 91st Annual Meeting : 10-13 juin 2009, Washington.

Tichomirova, M. A., Daly, A., Barlier, A., Jaffrain-Réa, M. L., Zacharieva, S., Elenkova, A., Yaneva, M., Naves, L., Cozzi, R., Fajardo Montanana, C., Bernabeu Moron, I., Ronchi, C., Spada, A., Sievers, C., Stalla, G. K., Halaby, G., Vanbellinghen, J.-F., Bours, V., & Beckers, A. (2009). High Incidence of AIP mutations in sporadic pituitary adenomas in young patients with macroadenomas. In The Endocrine Society's 91st Annual Meeting : 10-13 juin 2009, Washington.

Fajardo Montanana, C., Daly, A., Tichomirova, M. A., Vanbellinghen, J.-F., Jaffrain-Réa, M. L., Trescoli Serrano, C., Riesgo Suarez, P., Gomez Vela, J., Tenes, S., Bours, V., & Beckers, A. (2009). TSH-secreting pituitary adenoma in a male patient with a novel missense AIP mutation. In The Endocrine Society's 91st Annual Meeting : 10-13 juin 2009, Washington.

Willems, E.* , Baron, F.* , Baudoux, E., Wanten, N., Seidel, L., Vanbellinghen, J.-F., Herens, C., Gothot, A., Frere, P., Bonnet, C., Hafraoui, K., Vanstraelen, G., Fillet, G., & Beguin, Y. (2009). Non-myeloablative transplantation with CD8-depleted or unmanipulated peripheral blood stem cells: a phase II randomized trial. Leukemia, 23 (3), 608-10. doi:10.1038/leu.2008.248
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* These authors have contributed equally to this work.

Yaneva, M., Daly, A., Tichomirowa, M. A., Vanbellinghen, J.-F., Hagelstein, M.-T., Bours, V., Zacharieva, S., & Beckers, A. (2008). Aryl Hydrocarbon Receptor interacting Protein Gene Mutations in Bulgarian FIPA and Young Sporadic Pituitary Adenoma Patients. In ENDO 2008: 90th Annual Meeting of the Endocrine Society - Abstract book (pp. 735 (P3-520).

Arafa, M., Kridelka, F., Mathias, V., Vanbellinghen, J.-F., Renard, I., Foidart, J.-M., Boniver, J., & Delvenne, P. (2008). High frequency of RASSF1A and RARb2 gene promoter methylation in morphologically normal endometrium adjacent to endometrioid adenocarinoma. Histopathology, 53 (5), 525-532. doi:10.1111/j.1365-2559.2008.03147.x
Peer Reviewed verified by ORBi

Mutesa, L., Pierquin, G., Segers, K., Vanbellinghen, J.-F., Gahimbare, L., & Bours, V. (2008). Spinocerebellar ataxia type 2 (SCA2): clinical features and genetic analysis. Journal of Tropical Pediatrics, 54 (5), 350-2. doi:10.1093/tropej/fmn034
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Castermans, E.* , Baron, F.* , Willems, E., Schaaf-Lafontaine, N., Meuris, N., Gothot, A., Vanbellinghen, J.-F., Herens, C., Seidel, L., Geenen, V., Cheynier, R., & Beguin, Y. (2008). Evidence for neo-generation of T cells by the thymus after non-myeloablative conditioning. Haematologica, 93 (2), 240-7. doi:10.3324/haematol.11708
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* These authors have contributed equally to this work.

Daly, A., Tichomirowa, M. A., Ebeling, T. M. L., Vierimaa, O., Cazabat, L., Jaffrain-Rea, M.-L., Naves, L. A., Eloranta, E., Salmela, P. I., Vanbellinghen, J.-F., Yaneva, M., Zacharieva, S., Barlier, A., Emy, P., Mura, A., Popelier, M., Fajardo, M. C., Sabate, M. I., Guitelman, M., ... Beckers, A. (2008). An International, Collaborative Study of the Disease Characteristics and Response to Therapy in 60 Pituitary Adenoma Patients with Aryl Hydrocarbon Receptor Interacting Protein (AIP) Gene Mutations. In ENDO 2008: 90th Annual Meeting of the Endocrine Society - Abstract book (pp. 91 (OR8-4).

Beckers, A., Vanbellinghen, J.-F., Boikos, S., Martari, M., Verma, S., Daly, A., Raygada, M., Kei, M. F., Papademetriou, J., Drori-Herishanu, L., Horvath, A., Nesterova, M., Tichomirova, M. A., Bours, V., Marx, S., Agarwal, S. K., Salvatori, R., & Stratakis, C. A. (2008). Germline AIP, MEN1, PRKAR1A, CDKN1B (p27Kip1) and CDKN2C (p18INK4c) gene mutations in a large cohort of pediatric patients with pituitary adenomas occurring in isolation or with associated syndromic features. In ENDO 2008: 90th Annual Meeting of the Endocrine Society - Abstract book (pp. 142 (OR38-1).

Fajardo Montanaña, C., Daly, A., Tichomirowa, M. A., Vanbellinghen, J.-F., Theororopoulou, M., Trescoli Serrano, C., Riesgo Suarez, P., Gomez Vela, J., Hagelstein, M.-T., Bours, V., & Beckers, A. (2008). Occurrence of AIP Mutations in Sporidic Pituitary Adenomas and Familial Isolated Pituitary Adenomas Kindreds in Valencia, Spain. In ENDO 2008: 90th Annual Meeting of the Endocrine Society - Abstract book (pp. 803 (P3-775).

Ansaneli Naves, L., Ferreira Azevedo, M., Faria de Castro, L., Magalhães Gonzaga, M., Augusto Casulari, L., Cunha Vencio, S. A., Daly, A., Tichomirowa, M. A., Vanbellinghen, J.-F., Bours, V., & Beckers, A. (2008). Genetic Causes of Pituitary Adenmas; Focus on the Roe of AIF Status in Multiple Tumor Types. In ENDO 2008: 90th Annual Meeting of the Endocrine Society - Abstract book (pp. 323 (P1-561).

Jaffrain-Rea, M. L., Spilioti, C., Vanbellinghen, J.-F., Daly, A., Gargano, D., D'Innocenzi, E., Giangaspero, F., Tichomirowa, M. A., Esposito, V., Ventura, I., Naves, I. A., Alesse, E., & Beckers, A. (2008). Aryl Hydrocarbon receptor interacting protein (AIP) expression in human pituitary adenomas. In 10th European Congress of Endocrinology - Abstract book (pp. 454).

Jaffrain-Rea, M.-L., Gargano, D., D'Innocenzo, E., Vanbellinghen, J.-F., Spilioti, C., Daly, A., Giangaspero, F., Tichomirova, M. A., Esposito, V., Ventura, L., Naves, L. A., Alesse, E., & Beckers, A. (2008). Aryl Hydrocarbon Receptor (AHR) and AHR Interacting Protein (AIP) expression in human GH/PRL-secreting pituitary adenomas. In Italian Congress of Endocrinology - Giornate Endocrinologiche Pisane GEP 2008 : Pisa 2008.

Naves, L. A., Daly, A., Vanbellinghen, J.-F., Casulari, L. A., Spilioti, C., Magalhaes, A. V., Azevedo, M. F., Giacomini, L. A., Nascimento, P. P., Nunes, R. O., Rosa, J. W. C., Jaffrain-Rea, M.-L., Bours, V., & Beckers, A. (October 2007). Variable pathological and clinical features of a large Brazilian family harboring a mutation in the aryl hydrocarbon receptor-interacting protein gene. European Journal of Endocrinology, 157 (4), 383-391. doi:10.1530/EJE-07-0533
Peer Reviewed verified by ORBi

Daly, A., Vanbellinghen, J.-F., Khoo, S. K., Jaffrain-Rea, M.-L., Naves, L. A., Guitelman, M. A., Murat, A., Emy, P., Gimenez-Roqueplo, A.-P., Tamburrano, G., Raverot, G., Barlier, A., De Herder, W., Penfornis, A., Ciccarelli, E., Estour, B., Lecomte, P., Gatta, B., Chabre, O., ... Beckers, A. (May 2007). Aryl hydrocarbon receptor-interacting protein gene mutations in familial isolated pituitary adenomas: analysis in 73 families. Journal of Clinical Endocrinology and Metabolism, 92 (5), 1891-1896. doi:10.1210/jc.2006-2513
Peer Reviewed verified by ORBi

Daly, A., Vanbellinghen, J.-F., & Beckers, A. (2007). Characteristics of familial isolated pituitary adenomas (FIPA) - Review. Expert Review of Endocrinology and Metabolism, 2 (6), 725-733. doi:10.1586/17446651.2.6.725
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Barlier, A., Vanbellinghen, J.-F., Daly, A., Silvy, M., Jaffrain-Rea, M.-L., Trouillas, J., Tamagno, G., Cazabat, L., Bours, V., Brue, T., Enjalbert, A., & Beckers, A. (2007). Mutations in the aryl hydrocarbon receptor interacting protein gene are not highly prevalent among subjects with sporadic pituitary adenomas. Journal of Clinical Endocrinology and Metabolism, 92 (5), 1952-5. doi:10.1210/jc.2006-2702
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Boemer, F., Vanbellinghen, J.-F., Bours, V., & Schoos, R. (2006). Screening for sickle cell disease on dried blood: a new approach evaluated on 27,000 Belgian newborns. Journal of Medical Screening, 13 (3), 132-136. doi:10.1258/096914106778440644
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Betea, D., Valdes Socin, H. G., Vanbellinghen, J.-F., & Beckers, A. (2003). Néoplasie endocrinienne multiple de type 1 : De la clinique au gène. Feuillets de Biologie, 44 (250), 39-48.

Valdes Socin, H. G., Poncin, J., Vanbellinghen, J.-F., Jaffrain Rea, M. L., Tamburrano, G., Delemer, B., Rohmer, V., Levasseur, S., Stevens, V., Stevenaert, A., Teh, B., & Beckers, A. (2002). Familial Pituitary tumors. In Neuroendocrinologica : Dalla Riserca di base alla Clinica (pp. 24-28).

Valdes Socin, H. G., Poncin, J., Vanbellinghen, J.-F., Jaffrain-Réa, M. L., Tamburrano, G., Delemer, B., Levasseur, S., Teh, B., Stevenaert, A., & Beckers, A. (2001). Les adénomes hypophysaires familiaux isolés non liés aux syndromes MEN1 et carney Complex : Etude multicentrique. In Annales d'Endocrinologie : XIXe Congrès de la Société Française d'Endocrinologie - Abstract book (pp. 322 (C016) (Vol.62 N°4, cahier 1).

Vanbellinghen, J.-F., Beckers, A., & Poncin, J. (1999). Preliminary characterization of the promoter and CIS-regulatory elements of the MEN1 gene. In 81st Annual Meeting of the Endocrine society (pp. 345).

Vanbellinghen, J.-F., Beckers, A., & Poncin, J. (1999). Preliminary characterization of the promoter and CIS-regulatory elements of the MEN1 gene. In 7th International workshop on Multiple Endocrine Neoplasia - Abstract book (pp. 196).

Vanbellinghen, J.-F., Beckers, A., & Poncin, J. (1999). Preliminary characterization of the promoter and CIS-regulatory elements of the MEN1 gene. In The 6th International Pituitary Congress - Abstract book (pp. 40).

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