Whole-exome sequencing reveals LRP5 mutations and canonical Wnt signaling associated with hepatic cystogenesis von Cnossen, Wybrich R., te Morsche, René H. M., Hoischen, Alexander, Gilissen, Christian, Chrispijn, Melissa, Venselaar, Hanka, Mehdi, Soufi, Bergmann, Carsten, Veltman, Joris A., Drenth, Joost P. H.

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Over-expression of COX-2 mRNA in colorectal cancer von Roelofs, Hennie M J, Te Morsche, Rene H M, van Heumen, Bjorn W H, Nagengast, Fokko M, Peters, Wilbert H M

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Droplet digital polymerase chain reaction for rapid broad‐spectrum detection of bloodstream infections von Wouters, Yannick, Dalloyaux, Daisy, Christenhusz, Anke, Roelofs, Hennie M. J., Wertheim, Heiman F., Bleeker‐Rovers, Chantal P., Morsche, René H., Wanten, Geert J. A.

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Exploring the innate immune response in polycystic liver disease von Duijzer, Renée, Dalloyaux, Daisy, Boerrigter, Melissa M., Lemmers, Heidi, Dijkstra, Helga, van Emst, Liesbeth, te Morsche, René H.M., Jaeger, Martin, Joosten, Leo A.B., Drenth, Joost P.H.

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Chymotrypsin C (CTRC) variants that diminish activity or secretion are associated with chronic pancreatitis von Nickel, Renate, Sahin-Tóth, Miklós, Ózsvári, Béla, Gress, Thomas M, Truninger, Kaspar, Macek, Milan, Landt, Olfert, Büning, Carsten, Berg, Thomas, Witt, Heiko, Kovacs, Peter, Puhl, Gero, Pfützer, Roland, Groneberg, David Alexander, Kage, Andreas, Hegyi, Péter, Wiedenmann, Bertram, Bhatia, Eesh, Blüher, Matthias, Schmidt, Hartmut, te Morsche, René HM, Bödeker, Hans, Stumvoll, Michael, Teich, Niels, Schulz, Hans-Ulrich, Szmola, Richárd, Ockenga, Johann, Mössner, Joachim, Keim, Volker, Rosendahl, Jonas, Löhr, Matthias, Choudhuri, Gourdas, Drenth, Joost PH, Witt, Ulrike

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NaV1.7 Gain-of-Function Mutations as a Continuum: A1632E Displays Physiological Changes Associated with Erythromelalgia and Paroxysmal Extreme Pain Disorder Mutations and Produces... von Estacion, M, Dib-Hajj, S. D, Benke, P. J, te Morsche, Rene H. M, Eastman, E. M, Macala, L. J, Drenth, J. P. H, Waxman, S. G

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SCN9A Mutations Define Primary Erythermalgia as a Neuropathic Disorder of Voltage Gated Sodium Channels von Drenth, Joost P.H., te Morsche, Rene H.M., Guillet, Gerard, Taieb, Alain, Lee Kirby, R., Jansen, Jan B.M.J.

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Contribution of Genetic and Clinical Risk Factors to Development of Candidemia in Patients Receiving Home Parenteral Nutrition von Wouters, Yannick, Roelofs, Hennie M. J., Netea, Mihai G., te Morsche, René H. M., Wanten, Geert J. A.

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Germline mutations in PRKCSH are associated with autosomal dominant polycystic liver disease von Drenth, Joost P.H, te Morsche, Rene H.M, Smink, Renate, Bonifacino, Juan S, Jansen, Jan B.M.J

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Common variants in glyoxalase I do not increase chronic pancreatitis risk von Kaune, Tom, Hollenbach, Marcus, Keil, Bettina, Chen, Jian-Min, Masson, Emmanuelle, Becker, Carla, Damm, Marko, Ruffert, Claudia, Grützmann, Robert, Hoffmeister, Albrecht, Te Morsche, Rene H M, Cavestro, Giulia Martina, Zuppardo, Raffaella Alessia, Saftoiu, Adrian, Malecka-Panas, Ewa, Głuszek, Stanislaw, Bugert, Peter, Lerch, Markus M, Weiss, Frank Ulrich, Zou, Wen-Bin, Liao, Zhuan, Hegyi, Peter, Drenth, Joost Ph, Riedel, Jan, Férec, Claude, Scholz, Markus, Kirsten, Holger, Tóth, Andrea, Ewers, Maren, Witt, Heiko, Griesmann, Heidi, Michl, Patrick, Rosendahl, Jonas

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Chromosomal abnormalities in hepatic cysts point to novel polycystic liver disease genes von Wills, Edgar S, Cnossen, Wybrich R, Veltman, Joris A, Woestenenk, Rob, Steehouwer, Marloes, Salomon, Jody, Te Morsche, René H M, Huch, Meritxell, Hehir-Kwa, Jayne Y, Banning, Martijn J, Pfundt, Rolph, Roepman, Ronald, Hoischen, Alexander, Drenth, Joost P H

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Polymorphisms in the insulin-like growth factor axis are associated with gastrointestinal cancer von Ong, Jennie, Salomon, Jody, te Morsche, Rene H M, Roelofs, Hennie M J, Witteman, Ben J M, Dura, Polat, Lacko, Martin, Peters, Wilbert H M

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Infliximab Exerts No Direct Hepatotoxic Effect on HepG2 Cells In Vitro von de Vries, Hilbert S., de Heij, Tineke, Roelofs, Henie M. J., te Morsche, Rene H. M., Peters, Wilbert H. M., de Jong, Dirk J.

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Genetic polymorphism in the conjugating enzyme UGT1A1 and the risk of head and neck cancer von Lacko, Martin, Roelofs, Hennie M.J., te Morsche, Rene H.M., Voogd, Adri C., Ophuis, Michel B. Oude, Peters, Wilbert H.M., Manni, Johannes J.

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Celecoxib and tauro-ursodeoxycholic acid co-treatment inhibits cell growth in familial adenomatous polyposis derived LT97 colon adenoma cells von van Heumen, Bjorn W.H., Roelofs, Hennie M.J., te Morsche, René H.M., Marian, Brigitte, Nagengast, Fokko M., Peters, Wilbert H.M.

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The functional -765G→C polymorphism of the COX-2 gene may reduce the risk of developing crohn's disease von de Vries, Hilbert S, te Morsche, Rene H M, van Oijen, Martijn G H, Nagtegaal, Iris D, Peters, Wilbert H M, de Jong, Dirk J

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High enzyme activity UGT1A1 or low activity UGT1A8 and UGT2B4 genotypes increase esophageal cancer risk von DURA, Polat, SALOMON, Jody, TE MORSCHE, Rene H. M, ROELOFS, Hennie M. J, KRISTINSSON, Jon O, WOBBES, Theo, WITTEMAN, Ben J. M, TAN, Adriaan C. I. T. L, DRENTH, Joost P. H, PETERS, Wilbert H. M

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COX-2 polymorphisms -765G-->C and -1195A-->G and colorectal cancer risk von Hoff, Juliët H, te Morsche, Rene H M, Roelofs, Hennie M J, van der Logt, Elise M J, Nagengast, Fokko M, Peters, Wilbert H M

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COX-2 polymorphisms and the risk for head and neck cancer in white patients von Peters, Wilbert H. M., Lacko, Martin, te Morsche, Rene H. M., Voogd, Adri C., Oude Ophuis, Michael B., Manni, Johannes J.

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The C50T polymorphism of the cyclooxygenase-1 gene and the risk of thrombotic events during low-dose therapy with acetyl salicylic acid von Clappers, Nick, van Oijen, Martijn G. H., Sundaresan, Santosh, Brouwer, Marc A., te Morsche, Rene H. M., Keuper, Wessel, Peters, Wilbert H. M., Drenth, Joost P . H., Verheugt, Freek W. A.

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