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1. • Journal article

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   NPHS2 mutations in steroid-resistant nephrotic syndrome: A mutation update and the associated phenotypic spectrum

   Bouchireb, Karim Boyer, Olivia Gribouval, Olivier Nevo, Fabien Huynh-Cong, Evelyne Morinière, Vincent Campait, Raphaëlle Ars, Elisabet Brackman, Damien Dantal, Jacques Eckart, Philippe Gigante, Maddalena Lipska, Beata S. Liutkus, Aurélia Megarbane, André Mohsin, Nabil Ozaltin, Fatih Saleem, Moin A. Schaefer, Franz Soulami, Kenza Torra, Roser Garcelon, Nicolas Mollet, Géraldine Dahan, Karin[UCL] Antignac, Corinne (2014) Human Mutation — Vol. 35, no. 2, p. 178-186 (2014)
2. • Journal article

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   Hypermethylation of the 5' CpG island of the p14ARF flanking exon 1β in human colorectal cancer displaying a restricted pattern of p53 overexpression concomitant with increased MDM2 expression.

   Nyiraneza, Christine[UCL] Sempoux, Christine[UCL] Detry, Roger[UCL] Kartheuser, Alex[UCL] Dahan, Karin[UCL] (2012) Clinical Epigenetics — Vol. 4, no.1, p. 9 (2012)
3. • Journal article

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   Mutation Update of the CLCN5 Gene Responsible for Dent Disease 1

   Mansour-Hendili, Lamisse Blanchard, Anne Le Pottier, Nelly Roncelin, Isabelle Lourdel, Stéphane Treard, Cyrielle González, Wendy Vergara-Jaque, Ariela Morin, Gilles Colin, Estelle Holder-Espinasse, Muriel Bacchetta, Justine Baudouin, Véronique Benoit, Stéphane Bérard, Etienne Bourdat-Michel, Guylhène Bouchireb, Karim Burtey, Stéphane Cailliez, Mathilde Cardon, Gérard Cartery, Claire Champion, Gerard Chauveau, Dominique Cochat, Pierre Dahan, Karin De la Faille, Renaud Debray, François-Guillaume Dehoux, Laurenne Deschenes, Georges Desport, Estelle Devuyst, Olivier[UCL] Dieguez, Stella Emma, Francesco Fischbach, Michel Fouque, Denis Fourcade, Jacques François, Hélène Gilbert-Dussardier, Brigitte Hannedouche, Thierry Houillier, Pascal Izzedine, Hassan Janner, Marco Karras, Alexandre Knebelmann, Bertrand Lavocat, Marie-Pierre Lemoine, Sandrine Leroy, Valérie Loirat, Chantal Macher, Marie-Alice Martin-Coignard, Dominique Morin, Denis Niaudet, Patrick Nivet, Hubert Nobili, François Novo, Robert Faivre, Laurence Rigothier, Claire Roussey-Kesler, Gwenaëlle Salomon, Remi Schleich, Andreas Sellier-Leclerc, Anne-Laure Soulami, Kenza Tiple, Aurélien Ulinski, Tim Vanhille, Philippe Van Regemorter, Nicole Jeunemaître, Xavier Vargas-Poussou, Rosa (2015) Human Mutation — Vol. 36, no. 8, p. 743-752 (2015)
4. • Journal article

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   Paradoxical response to furosemide in uromodulin-associated kidney disease

   Labriola, Laura[UCL] Olinger, Eric Belge, Hendrica[UCL] Pirson, Yves[UCL] Dahan, Karin[UCL] Devuyst, Olivier[UCL] (2015) Nephrology, Dialysis, Transplantation — Vol. 30, no. 2, p. 330-335 (2015)
5. • Speech

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   PHENOTYPIC VARIABILITY IN A FAMILY WITH X-LINKED RETINITIS PIGMENTOSA: WHEN THE EYES GO WRONG, LOOK AT THE CILIA!

   Balligand, Thomas[UCL] Dahan, Karin[UCL] Lengele, Jean-Philippe[UCL] (2013) Congress of the Belgian Society of Internal Medicine — Jette
6. • Journal article

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   De Novo Atypical Haemolytic Uremic Syndrome after Kidney Transplantation.

   Devresse, Arnaud[UCL] de Meyer, Martine[UCL] Aydin, Selda[UCL] Dahan, Karin[UCL] Kanaan, Nada[UCL] (2018) Case Reports in Nephrology — Vol. 2018, p. 1727986 (2018)
7. • Journal article

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   Identification of novel and recurrent glucokinase mutations in Belgian and Luxembourg maturity onset diabetes of the young patients

   Vits, L. Beckers, D. Craen, M. de Beaufort, C. Vanfleteren, E. Dahan, Karin[UCL] Nollet, A. Vanhaverbeke, G. Imschoot, S. V. Bourguignon, J-P Beauloye, Véronique[UCL] Storm, K. Massa, G. Giri, M. Nobels, F. De Schepper, Jean-Pierre[UCL] Rooman, R. Van den Bruel, A. Mathieu, Chantal[UCL] Wuyts, W. (2006) Clinical Genetics : an international journal of genetics and molecular medicine — Vol. 70, no. 4, p. 355-9 (2006)
8. • Journal article

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   Telomere length, ATM mutation status and cancer risk in Ataxia-Telangiectasia families.

   Renault, Anne-Laure Mebirouk, Noura Cavaciuti, Eve Le Gal, Dorothée Lecarpentier, Julie d'Enghien, Catherine Dubois Laugé, Anthony Dondon, Marie-Gabrielle Labbé, Martine Lesca, Gaetan Leroux, Dominique Gladieff, Laurence Adenis, Claude Faivre, Laurence Gilbert-Dussardier, Brigitte Lortholary, Alain Fricker, Jean-Pierre Dahan, Karin[UCL] Bay, Jacques-Olivier Longy, Michel Buecher, Bruno Janin, Nicolas[UCL] Zattara, Hélène Berthet, Pascaline Combès, Audrey Coupier, Isabelle CoF-AT study collaborators Hall, Janet Stoppa-Lyonnet, Dominique Andrieu, Nadine Lesueur, Fabienne (2017) Carcinogenesis : integrative cancer research — Vol. 38, no.10, p. 994-1003 (2017)
9. • Speech

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   Detection of large rearrangements by MLPA in severe hemophilia A patients

   Lannoy, Nathalie[UCL] Abinet, Isabelle[UCL] Lambert, Catherine[UCL] Vermylen, Christiane[UCL] Dahan, Karin[UCL] Hermans, Cédric[UCL] (2009) XXII Congress of the International Society of Thrombosis and Haemostasis — (United States) Boston, MA
10. • Speech

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    Proposition for a multi-step mutation detection in haemophilia A

    Lannoy, Nathalie[UCL] Abinet, Isabelle[UCL] Verellen-Dumoulin, Christine[UCL] Vermylen, Christiane[UCL] Hermans, Cédric[UCL] Dahan, Karin[UCL] (2007) XXI Congress of the International Society on Thrombosis and Haemostasis — (Switzerland) Geneva
11. • Journal article

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    Clinical and mutational spectrum of hypoparathyroidism, deafness and renal dysplasia syndrome.

    Belge, Hendrica[UCL] Dahan, Karin Cambier, Jean-François Benoit, Valérie Morelle, Johann[UCL] Bloch, Julie Vanhille, Philippe Pirson, Yves[UCL] Demoulin, Nathalie[UCL] (2017) Nephrology, Dialysis, Transplantation — Vol. 32, no. 5, p. 830-837 (2017)
12. • Journal article

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    X-linked Alport syndrome: Natural history and genotype-phenotype correlations in girls and women belonging to 195 families: A "European community Alport syndrome concerted action" study

    Jais, JP Knebelmann, B Giatras, I De Marchi, M Rizzoni, G Renieri, A Weber, MICHEL Gross, O Netzer, KO Flinter, F Pirson, Yves[UCL] Dahan, Karin[UCL] Wieslander, J Persson, U Tryggvason, K Martin, Paula Hertz, JM Schroder, Cornelis Sanak, Marek Carvalho, MF Saus, Juan Antignac, Corinne Smeets, Hubert Gubler, Marie Claire (2003) Journal of the American Society of Nephrology — Vol. 14, no. 10, p. 2603-2610 (2003)
13. • Journal article

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    Transcriptional and functional analyses of SLC12A3 mutations: new clues for the pathogenesis of Gitelman syndrome.

    Riveira-Munoz, Eva[UCL] Chang, Qing Godefroid, Nathalie[UCL] Hoenderop, Joost G. Bindels, René J Dahan, Karin[UCL] Devuyst, Olivier[UCL] (2007) Journal of the American Society of Nephrology : JASN — Vol. 18, no. 4, p. 1271-83 (2007)
14. • Journal article

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    Genome-wide study of familial juvenile hyperuricaemic (gouty) nephropathy (FJHN) indicates a new locus, FJHN3, linked to chromosome 2p22.1-p21.

    Piret, Sian E Danoy, Patrick Dahan, Karin[UCL] Reed, Anita A C Pryce, Karena Wong, William Torres, Rosa J Puig, Juan G Müller, Thomas Kotanko, Peter Lhotta, Karl Devuyst, Olivier[UCL] Brown, Matthew A Thakker, Rajesh V (2011) Human Genetics — Vol. 129, no. 1, p. 51-8 (2011)
15. • Journal article

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    Blau syndrome associated with a CARD15/NOD2 mutation.

    Snyers, Bernadette[UCL] Dahan, Karin[UCL] (2006) American journal of ophthalmology — Vol. 142, no. 6, p. 1089-92 (2006)
16. • Speech

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    MLH1 and MSH2 mutation identification from unselected patients with colorectal cancer is facilitated by the combined analysis of microsatellite instability and immunohistochemistry.

    Dumoulin, Christine[UCL] Kartheuser, Alex[UCL] Detry, Roger[UCL] Sempoux, Christine[UCL] Dahan, Karin[UCL] Thim, VV Smaers, M Camby, P. (2000) —
17. • Journal article

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    High risk for neoplastic transformation of endometriosis in a carrier of lynch syndrome.

    Nyiraneza, Christine[UCL] Marbaix, Etienne[UCL] Galant, Christine[UCL] Sempoux, Christine[UCL] Smets, Mireille Dahan, Karin[UCL] (2010) Familial cancer — Vol. 9, no. 3, p. 383-7 (2010)
18. • Journal article

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    Gitelman syndrome and glomerular proteinuria: a link between loss of sodium-chloride cotransporter and podocyte dysfunction?

    Demoulin, Nathalie[UCL] Aydin, Selda[UCL] Cosyns, Jean-Pierre[UCL] Dahan, Karin[UCL] Cornet, Georges Auberger, Ines Loffing, Johannes Devuyst, Olivier[UCL] (2014) Nephrology, Dialysis, Transplantation — Vol. 29, no.suppl 4, p. iv117-iv120 (2014)
19. • Journal article

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    Outcome of kidney transplantation in type I oral-facial-digital syndrome

    Halleux, Delphine[UCL] Dahan, Karin[UCL] Thauvin-Robinet, Christel Aral, Bernard Pouteil-Noble, Claire Devuyst, Olivier[UCL] Pirson, Yves[UCL] (2011) Transplant International — Vol. 24, no. 6, p. e48-50 (2011)
20. • Journal article

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    A classification of ductal plate malformations based on distinct pathogenic mechanisms of biliary dysmorphogenesis

    Raynaud, Peggy[UCL] Tate, Joshua Callens, Céline Cordi, Sabine[UCL] Van Der Smissen, Patrick[UCL] Carpentier, Rodolphe[UCL] Sempoux, Christine[UCL] Devuyst, Olivier[UCL] Pierreux, Christophe[UCL] Courtoy, Pierre J.[UCL] Dahan, Karin[UCL] Delbecque, Katty Lepreux, Sébastien Pontoglio, Marco Guay-Woodford, Lisa M Lemaigre, Frédéric[UCL] (2011) Hepatology — Vol. 53, no. 6, p. 1959-1966 (2011)
21. • Journal article

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    Evolution of communication abilities after cochlear implantation in prelingually deaf children

    Gérard, Jean-Marc[UCL] Deggouj, Naima Hupin, Cloé[UCL] Buisson, Anne-Laure[UCL] Monteyne, Veronique[UCL] Lavis, C.[UCL] Dahan, Karin[UCL] Gersdorff, Michel (2010) International Journal of Pediatric Otorhinolaryngology — Vol. 74, no. 6, p. 642-648 (2010)
22. • Speech

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    Syndrome de Gitelman et protéinurie glomérulaire: à propos d'une association atypique

    Demoulin, Nathalie[UCL] Cosyns, Jean-Pierre[UCL] Cornet, C. Godefroid, Nathalie[UCL] Pirson, Yves[UCL] Jadoul, Michel[UCL] Dahan, Karin[UCL] Devuyst, Olivier[UCL] (2010) 12e Réunion commune de la Société de Néphrologie (SN) et de la Société Francophone de Dialyse (SFD) — (Belgium) Brussels
23. • Journal article

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    Eculizumab in anti-factor H antibodies associated with atypical hemolytic uremic syndrome

    Diamante Chiodini, Benedetta Adams, Brigitte Ismaili, Khalid Dahan, Karin[UCL] Khaldi, Karim Corazza, Francis Davin, Jean-Claude (2014) Pediatrics — Vol. 133, no. 6, p. e1764-e1768 (2014)
24. • Journal article

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    [Secondary hemochromatosis - Response]

    Buysschaert, Martin[UCL] Dahan, Karin[UCL] Paris, Isabelle (1999) Acta Clinica Belgica (Multilingual Edition) — Vol. 54, no. 3, p. 173-174 (1999)
25. • Speech

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    Difficult genetic counseling in a family with pathogenic BRCA2 mutation.

    Ingargiola, II Dahan, Karin[UCL] Smaers, M Van Cangh, Paul[UCL] Dumoulin, Christine[UCL] (2001) —

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