Jean-Pierre Bayley
Department of Human Genetics
Leiden University Medical Centre
Leiden
Netherlands
Name/email consistency: high
- SDHAF2 mutations in familial and sporadic paraganglioma and phaeochromocytoma. Bayley, J.P., Kunst, H.P., Cascon, A., Sampietro, M.L., Gaal, J., Korpershoek, E., Hinojar-Gutierrez, A., Timmers, H.J., Hoefsloot, L.H., Hermsen, M.A., Suárez, C., Hussain, A.K., Vriends, A.H., Hes, F.J., Jansen, J.C., Tops, C.M., Corssmit, E.P., de Knijff, P., Lenders, J.W., Cremers, C.W., Devilee, P., Dinjens, W.N., de Krijger, R.R., Robledo, M. Lancet Oncol. (2010)
- Sdhd and SDHD/H19 knockout mice do not develop paraganglioma or pheochromocytoma. Bayley, J.P., van Minderhout, I., Hogendoorn, P.C., Cornelisse, C.J., van der Wal, A., Prins, F.A., Teppema, L., Dahan, A., Devilee, P., Taschner, P.E. PLoS. ONE (2009)
- The first Dutch SDHB founder deletion in paraganglioma-pheochromocytoma patients. Bayley, J.P., Grimbergen, A.E., van Bunderen, P.A., van der Wielen, M., Kunst, H.P., Lenders, J.W., Jansen, J.C., Dullaart, R.P., Devilee, P., Corssmit, E.P., Vriends, A.H., Losekoot, M., Weiss, M.M. BMC Med. Genet. (2009)
- Molecular characterization of novel germline deletions affecting SDHD and SDHC in pheochromocytoma and paraganglioma patients. Bayley, J.P., Weiss, M.M., Grimbergen, A., van Brussel, B.T., Hes, F.J., Jansen, J.C., Verhoef, S., Devilee, P., Corssmit, E.P., Vriends, A.H. Endocr. Relat. Cancer (2009)
- The FH mutation database: an online database of fumarate hydratase mutations involved in the MCUL (HLRCC) tumor syndrome and congenital fumarase deficiency. Bayley, J.P., Launonen, V., Tomlinson, I.P. BMC Med. Genet. (2008)
- Mutation analysis of SDHB and SDHC: novel germline mutations in sporadic head and neck paraganglioma and familial paraganglioma and/or pheochromocytoma. Bayley, J.P., van Minderhout, I., Weiss, M.M., Jansen, J.C., Oomen, P.H., Menko, F.H., Pasini, B., Ferrando, B., Wong, N., Alpert, L.C., Williams, R., Blair, E., Devilee, P., Taschner, P.E. BMC Med. Genet. (2006)
- The SDH mutation database: an online resource for succinate dehydrogenase sequence variants involved in pheochromocytoma, paraganglioma and mitochondrial complex II deficiency. Bayley, J.P., Devilee, P., Taschner, P.E. BMC Med. Genet. (2005)
- Association between polymorphisms in the human chemokine receptor genes CCR2 and CX3CR1 and rheumatoid arthritis. Bayley, J.P., Baggen, J.M., van der Pouw-Kraan, T., Crusius, J.B., Huizinga, T.W., Verweij, C.L. Tissue. Antigens (2003)
