Pain perception is altered by a nucleotide polymorphism in SCN9A von Reimann, Frank, Cox, James J, Belfer, Inna, Diatchenko, Luda, Zaykin, Dmitri V, McHale, Duncan P, Drenth, Joost P.H, Dai, Feng, Wheeler, Jerry, Sanders, Frances, Wood, Linda, Wu, Tian-Xia, Karppinen, Jaro, Nikolajsen, Lone, Männikkö, Minna, Max, Mitchell B, Kiselycznyk, Carly, Poddar, Minakshi, te Morsche, Rene H.M, Smith, Shad, Gibson, Dustin, Kelempisioti, Anthi, Maixner, William, Gribble, Fiona M, Woods, C. Geoffrey

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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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Novel GANAB variants associated with polycystic liver disease von van de Laarschot, Liyanne F M, Te Morsche, René H M, Hoischen, Alexander, Venselaar, Hanka, Roelofs, Hennie M, Cnossen, Wybrich R, Banales, Jesus M, Roepman, Ronald, Drenth, Joost P H

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Functional profiles of SCN9A variants in dorsal root ganglion neurons and superior cervical ganglion neurons correlate with autonomic symptoms in small fibre neuropathy von CHONGYANG HAN, HOEIJMAKERS, Janneke G. J, WAXMAN, Stephen G, SHUJUN LIU, GERRITS, Monique M, TE MORSCHE, Rene H. M, LAURIA, Giuseppe, DIB-HAJJ, Sulayman D, DRENTH, Joost P. H, FABER, Catharina G, MERKIES, Ingemar S. J

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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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ddPCR enables rapid detection of bloodstream infections in patients on home parenteral nutrition: A prospective cohort study von Gillis, Veerle E.L.M., Dalloyaux, Daisy, te Morsche, Rene H.M., van Ingen, Jakko, Sir, Özcan, Rovers, Chantal P., Wouters, Yannick, Wanten, Geert J.A.

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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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Common single nucleotide polymorphisms in transient receptor potential melastatin type 6 increase the risk for proton pump inhibitor-induced hypomagnesemia: a case–control study von Hess, Mark W, de Baaij, Jeroen H.F, Broekman, Mark M.T.J, Bisseling, Tanya M, Haarhuis, Bertram J.T, Tan, Adriaan C.I.T.L, te Morsche, René H.M, Hoenderop, Joost G.J, Bindels, René J.M, Drenth, Joost P.H

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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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Pasireotide does not improve efficacy of aspiration sclerotherapy in patients with large hepatic cysts, a randomized controlled trial von Wijnands, Titus F. M., Gevers, Tom J. G., Lantinga, Marten A., te Morsche, René H., Schultze Kool, Leo J., Drenth, Joost P. H.

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Alternative splicing may contribute to time-dependent manifestation of inherited erythromelalgia von Choi, Jin-Sung, Cheng, Xiaoyang, Foster, Edmund, Leffler, Andreas, Tyrrell, Lynda, te Morsche, Rene H. M., Eastman, Emmanuella M., Jansen, Henry J., Huehne, Kathrin, Nau, Carla, Dib-Hajj, Sulayman D., Drenth, Joost P. H., Waxman, Stephen G.

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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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Barrett associated MHC and FOXF1 variants also increase esophageal carcinoma risk von Dura, Polat, Veen, Elke M., Salomon, Jody, 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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