Primary tumor sidedness has an impact on prognosis and treatment outcome in metastatic colorectal cancer: results from two randomized first-line panitumumab studies
Boeckx, N., Koukakis, R., Op de Beeck, K., Rolfo, C., Van Camp, G., Siena, S., Tabernero, J., Douillard, J.-Y., André, T., Peeters, M.
Published in Annals of oncology (01.08.2017)
Published in Annals of oncology (01.08.2017)
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Hotspot DAXX, PTCH2 and CYFIP2 mutations in pancreatic neuroendocrine neoplasms
Vandamme, T, Beyens, M, Boons, G, Schepers, A, Kamp, K, Biermann, K, Pauwels, P, De Herder, W W, Hofland, L J, Peeters, M, Van Camp, G, Op de Beeck, K
Published in Endocrine-related cancer (01.01.2019)
Published in Endocrine-related cancer (01.01.2019)
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Broadening the phenotype of LRP2 mutations: a new mutation in LRP2 causes a predominantly ocular phenotype suggestive of Stickler syndrome
Schrauwen, I., Sommen, M., Claes, C., Pinner, J., Flaherty, M., Collins, F., Van Camp, G.
Published in Clinical genetics (01.09.2014)
Published in Clinical genetics (01.09.2014)
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Journal Article
KCNQ4: a gene for age-related hearing impairment?
Van Eyken, E., Van Laer, L., Fransen, E., Topsakal, V., Lemkens, N., Laureys, W., Nelissen, N., Vandevelde, A., Wienker, T., Van De Heyning, P., Van Camp, G.
Published in Human mutation (01.10.2006)
Published in Human mutation (01.10.2006)
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Structure and evolution of the squamate major histocompatibility complex as revealed by two Anolis lizard genomes
Card, Daren C., Van Camp, Andrew G., Santonastaso, Trenten, Jensen-Seaman, Michael I., Anthony, Nicola M., Edwards, Scott V.
Published in Frontiers in genetics (08.11.2022)
Published in Frontiers in genetics (08.11.2022)
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Journal Article
Candidate Gene Association Study for Noise‐induced Hearing Loss in Two Independent Noise‐exposed Populations
Konings, A., Van Laer, L., Wiktorek‐Smagur, A., Rajkowska, E., Pawelczyk, M., Carlsson, P. I., Bondeson, M. L., Dudarewicz, A., Vandevelde, A., Fransen, E., Huyghe, J., Borg, E., Sliwinska‐Kowalska, M., Van Camp, G.
Published in Annals of human genetics (01.03.2009)
Published in Annals of human genetics (01.03.2009)
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Journal Article
A common founder for the 35delG GJB2 gene mutation in connexin 26 hearing impairment
VAN LAER, L, COUCKE, P, FRANSEN, E, ROWLAND, J, CUCCI, R. A, SMITH, R. J. H, VAN CAMP, G, MUELLER, R. F, CAETHOVEN, G, FLOTHMANN, K, PRASAD, S. D, CHAMBERLIN, G. P, HOUSEMAN, M, TAYLOR, G. R, VAN DE HEYNING, C. M
Published in Journal of medical genetics (01.08.2001)
Published in Journal of medical genetics (01.08.2001)
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Journal Article
Mutation analysis of TMC1 identifies four new mutations and suggests an additional deafness gene at loci DFNA36 and DFNB7/11
Hilgert, N, Alasti, F, Dieltjens, N, Pawlik, B, Wollnik, B, Uyguner, O, Delmaghani, S, Weil, D, Petit, C, Danis, E, Yang, T, Pandelia, E, Petersen, MB, Goossens, D, Favero, JD, Sanati, MH, Smith, RJH, Van Camp, G
Published in Clinical genetics (01.09.2008)
Published in Clinical genetics (01.09.2008)
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Involvement of T-cell receptor-β alterations in the development of otosclerosis linked to OTSC2
Schrauwen, I, Venken, K, Vanderstraeten, K, Thys, M, Hendrickx, J-J, Fransen, E, Van Laer, L, Govaerts, P J, Verstreken, M, Schatteman, I, Stinissen, P, Hellings, N, Van Camp, G
Published in Genes and immunity (01.04.2010)
Published in Genes and immunity (01.04.2010)
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Journal Article
Search for a genetic cause in children with unilateral isolated microtia and congenital aural atresia
Mortier, J., van den Ende, J., Declau, F., Vercruysse, H., Wuyts, W., Van Camp, G., Vanderveken, O., Boudewyns, An
Published in European archives of oto-rhino-laryngology (01.02.2023)
Published in European archives of oto-rhino-laryngology (01.02.2023)
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Journal Article
Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing loss
Scott, DA, Kraft, ML, Carmi, R, Ramesh, A, Elbedour, K, Yairi, Y, Srisailapathy, C. R. Srikumari, Rosengren, SS, Markham, AF, Mueller, RF, Lench, NJ, Van Camp, G, Smith, RJH, Sheffield, VC
Published in Human mutation (1998)
Published in Human mutation (1998)
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P038 Early detection of breast cancer in liquid biopsies using DNA methylation markers
Neefs, I., Tjalma, W., Ibrahim, J., Croes, L., Peeters, M., Van Camp, G., de Beeck, K. Op
Published in Breast (Edinburgh) (01.04.2023)
Published in Breast (Edinburgh) (01.04.2023)
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Heart failure with preserved ejection fraction or non-cardiac dyspnea in paroxysmal atrial fibrillation: The role of left atrial strain
Katbeh, A., De Potter, T., Geelen, P., Di Gioia, G., Kodeboina, M., Balogh, Z., Albano, M., Vanderheyden, M., Bartunek, J., Barbato, E., Van Camp, G., Penicka, M.
Published in International journal of cardiology (15.01.2021)
Published in International journal of cardiology (15.01.2021)
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The prognostic value of KRAS, NRAS, BRAF and DNA mismatch repair (MMR) status in left- and right-sided metastatic colorectal cancer (mCRC): A Belgian population-based study
Janssens, K., van Camp, G., Op de Beeck, K., Fransen, E., Calay, F., van Damme, N., Peeters, M.
Published in Annals of oncology (01.10.2018)
Published in Annals of oncology (01.10.2018)
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Mitral regurgitation in patients with aortic stenosis undergoing valve replacement
Unger, P, Dedobbeleer, C, Van Camp, G, Plein, D, Cosyns, B, Lancellotti, P
Published in Heart (01.01.2010)
Published in Heart (01.01.2010)
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