Improved method for determining lipase von L. SCHELLONG, R. ZIELENSKI, U. PRINZING

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Defining the disease liability of variants in the cystic fibrosis transmembrane conductance regulator gene von Sosnay, Patrick R, Siklosi, Karen R, Van Goor, Fredrick, Kaniecki, Kyle, Yu, Haihui, Sharma, Neeraj, Ramalho, Anabela S, Amaral, Margarida D, Dorfman, Ruslan, Zielenski, Julian, Masica, David L, Karchin, Rachel, Millen, Linda, Thomas, Philip J, Patrinos, George P, Corey, Mary, Lewis, Michelle H, Rommens, Johanna M, Castellani, Carlo, Penland, Christopher M, Cutting, Garry R

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Genetic Modifiers of Lung Disease in Cystic Fibrosis von Drumm, Mitchell L, Konstan, Michael W, Schluchter, Mark D, Handler, Allison, Pace, Rhonda, Zou, Fei, Zariwala, Maimoona, Fargo, David, Xu, Airong, Dunn, John M, Darrah, Rebecca J, Dorfman, Ruslan, Sandford, Andrew J, Corey, Mary, Zielenski, Julian, Durie, Peter, Goddard, Katrina, Yankaskas, James R, Wright, Fred A, Knowles, Michael R

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Consensus on the use and interpretation of cystic fibrosis mutation analysis in clinical practice von Castellani, C, Cuppens, H, Macek, M, Cassiman, J.J, Kerem, E, Durie, P, Tullis, E, Assael, B.M, Bombieri, C, Brown, A, Casals, T, Claustres, M, Cutting, G.R, Dequeker, E, Dodge, J, Doull, I, Farrell, P, Ferec, C, Girodon, E, Johannesson, M, Kerem, B, Knowles, M, Munck, A, Pignatti, P.F, Radojkovic, D, Rizzotti, P, Schwarz, M, Stuhrmann, M, Tzetis, M, Zielenski, J, Elborn, J.S

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Recommendations for the classification of diseases as CFTR-related disorders von Bombieri, C, Claustres, M, De Boeck, K, Derichs, N, Dodge, J, Girodon, E, Sermet, I, Schwarz, M, Tzetis, M, Wilschanski, M, Bareil, C, Bilton, D, Castellani, C, Cuppens, H, Cutting, G.R, Drevínek, P, Farrell, P, Elborn, J.S, Jarvi, K, Kerem, B, Kerem, E, Knowles, M, Macek, M, Munck, A, Radojkovic, D, Seia, M, Sheppard, D.N, Southern, K.W, Stuhrmann, M, Tullis, E, Zielenski, J, Pignatti, P.F, Ferec, C

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Type of CFTR Mutation Determines Risk of Pancreatitis in Patients With Cystic Fibrosis von Ooi, Chee Y, Dorfman, Ruslan, Cipolli, Marco, Gonska, Tanja, Castellani, Carlo, Keenan, Katherine, Freedman, Steven D, Zielenski, Julian, Berthiaume, Yves, Corey, Mary, Schibli, Susanne, Tullis, Elizabeth, Durie, Peter R

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Do common in silico tools predict the clinical consequences of amino-acid substitutions in the CFTR gene? von Dorfman, R, Nalpathamkalam, T, Taylor, C, Gonska, T, Keenan, K, Yuan, XW, Corey, M, Tsui, L-C, Zielenski, J, Durie, P

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Genetic Modifiers of Liver Disease in Cystic Fibrosis von Bartlett, Jaclyn R, Friedman, Kenneth J, Ling, Simon C, Pace, Rhonda G, Bell, Scott C, Bourke, Billy, Castaldo, Giuseppe, Castellani, Carlo, Cipolli, Marco, Colombo, Carla, Colombo, John L, Debray, Dominique, Fernandez, Adriana, Lacaille, Florence, Macek, Milan, Rowland, Marion, Salvatore, Francesco, Taylor, Christopher J, Wainwright, Claire, Wilschanski, Michael, Zemková, Dana, Hannah, William B, Phillips, M. James, Corey, Mary, Zielenski, Julian, Dorfman, Ruslan, Wang, Yunfei, Zou, Fei, Silverman, Lawrence M, Drumm, Mitchell L, Wright, Fred A, Lange, Ethan M, Durie, Peter R, Knowles, Michael R, Gene Modifier Study Group, for the

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Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13.2 von Wright, Fred A, Strug, Lisa J, Doshi, Vishal K, Commander, Clayton W, Blackman, Scott M, Sun, Lei, Berthiaume, Yves, Cutler, David, Cojocaru, Andreea, Collaco, J Michael, Corey, Mary, Dorfman, Ruslan, Goddard, Katrina, Green, Deanna, Kent, Jack W, Lange, Ethan M, Lee, Seunggeun, Li, Weili, Luo, Jingchun, Mayhew, Gregory M, Naughton, Kathleen M, Pace, Rhonda G, Paré, Peter, Rommens, Johanna M, Sandford, Andrew, Stonebraker, Jaclyn R, Sun, Wei, Taylor, Chelsea, Vanscoy, Lori L, Zou, Fei, Blangero, John, Zielenski, Julian, O'Neal, Wanda K, Drumm, Mitchell L, Durie, Peter R, Knowles, Michael R, Cutting, Garry R

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Multiple apical plasma membrane constituents are associated with susceptibility to meconium ileus in individuals with cystic fibrosis von Sun, Lei, Rommens, Johanna M, Corvol, Harriet, Li, Weili, Li, Xin, Chiang, Theodore A, Lin, Fan, Dorfman, Ruslan, Busson, Pierre-François, Parekh, Rashmi V, Zelenika, Diana, Blackman, Scott M, Corey, Mary, Doshi, Vishal K, Henderson, Lindsay, Naughton, Kathleen M, O'Neal, Wanda K, Pace, Rhonda G, Stonebraker, Jaclyn R, Wood, Sally D, Wright, Fred A, Zielenski, Julian, Clement, Annick, Drumm, Mitchell L, Boëlle, Pierre-Yves, Cutting, Garry R, Knowles, Michael R, Durie, Peter R, Strug, Lisa J

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Role of Cystic Fibrosis Transmembrane Conductance Regulator in Patients With Chronic Sinopulmonary Disease von Gonska, Tanja, MD, Choi, Perry, MD, Stephenson, Anne, MD, PhD, Ellis, Lynda, RN, Martin, Sheelagh, RN, Solomon, Melinda, MD, Dupuis, Annie, PhD, Dorfman, Ruslan, MBA, PhD, Zielenski, Julian, PhD, Ooi, Chee Y., MBBS, Weiser, William, MD, Durie, Peter R., MD, Tullis, Elizabeth, MD, FCCP

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Cystic fibrosis modifier genes related to Pseudomonas aeruginosa infection von Park, J E, Yung, R, Stefanowicz, D, Shumansky, K, Akhabir, L, Durie, P R, Corey, M, Zielenski, J, Dorfman, R, Daley, D, Sandford, A J

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Detection of a cystic fibrosis modifier locus for meconium ileus on human chromosome 19q13 von Zielenski, Julian, Bal, Jerzy, Cutting, Garry R, Macek, Milan, Palacio, Ana, Ferec, Claude, Larriba, Sara, Marshall, Bruce C, Krebsova, Alice, Markiewicz, Danuta, Casals, Teresa, Claustres, Mirreille, Durie, Peter, Tsui, Lap-Chee, Corey, Mary, Langfelder-Schwind, Elinor, Rozmahel, Richard, DeCelie-Germana, J, Nowakowska, Aleksandra, Mercier, Bernard, Estivill, Xavier, Aznarez, Isabel

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TLR5 as an anti-inflammatory target and modifier gene in cystic fibrosis von Blohmke, Christoph J, Park, Julie, Hirschfeld, Aaron F, Victor, Rachel E, Schneiderman, Julia, Stefanowicz, Dorota, Chilvers, Mark A, Durie, Peter R, Corey, Mary, Zielenski, Julian, Dorfman, Ruslan, Sandford, Andrew J, Daley, Denise, Turvey, Stuart E

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The cystic fibrosis transmembrane conductance regulator gene and ion channel function in patients with idiopathic pancreatitis von BISHOP, Michele D, FREEDMAN, Steven D, KORTAN, Paul, HABER, Gregory, ROSS, Christine, TZOUNTZOURIS, John, STEELE, Leslie, RAY, Peter N, TSUI, Lap-Chee, DURIE, Peter R, ZIELENSKI, Julian, AHMED, Najma, DUPUIS, Annie, MARTIN, Sheelagh, ELLIS, Lynda, SHEA, Julie, HOPPER, Isobel, COREY, Mary

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Increased prevalence of CFTR mutations and variants and decreased chloride secretion in primary sclerosing cholangitis von SHETH, Sunil, SHEA, Julie C, ZIELENSKI, Julian, FREEDMAN, Steven D, BISHOP, Michele D, CHOPRA, Sanjiv, REGAN, Meredith M, MALMBERG, Emily, WALKER, Carolyn, RICCI, Ryan, TSUI, Lap-Chee, DURIE, Peter R

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Modulatory effect of the SLC9A3 gene on susceptibility to infections and pulmonary function in children with cystic fibrosis von Dorfman, Ruslan, Taylor, Chelsea, Lin, Fan, Sun, Lei, Sandford, Andrew, Paré, Peter, Berthiaume, Yves, Corey, Mary, Durie, Peter, Zielenski, Julian

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Adsorption of nucleic acids to a solid phase von ZIELENSKI RALF,GEISSLER KLAUS DR.,WALTER THOMAS DR

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Evaluation of the Disease Liability of CFTR Variants von Sosnay, Patrick R., Castellani, Carlo, Corey, Mary, Dorfman, Ruslan, Zielenski, Julian, Karchin, Rachel, Penland, Christopher M., Cutting, Garry R.

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Primary Sclerosing Cholangitis in Childhood is Associated with Abnormalities in Cystic Fibrosis–Mediated Chloride Channel Function von Pall, Harpreet, MD, Zielenski, Julian, PhD, Jonas, Maureen M., MD, DaSilva, Deborah A., RN, Potvin, Kimberly M, Yuan, Xiao-Wei, MSc, Huang, Qiuju, MD, Freedman, Steven D., MD, PhD

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