| Title | Author(s) | Year | View Count |
 | A systematic analysis of intronic sequences downstream of 5′ splice sites reveals a widespread role for U-rich motifs and TIA1/TIAL1 proteins in alternative splicing regulation | Aznarez, I; Barash, Y; Shai, O; He, D; Zielenski, J; Tsui, LC; Parkinson, J; Frey, BJ; Rommens, JM; Blencowe, BJ | 2008 | 358 |
 | Exon skipping through the creation of a putative exonic splicing silencer as a consequence of the cystic fibrosis mutation R553X | Aznarez, I; Zielenski, J; Rommens, JM; Blencowe, BJ; Tsui, LC | 2007 | 176 |
| Characterization of disease-associated mutations affecting an exonic splicing enhancer and two cryptic splice sites in exon 13 of the cystic fibrosis transmembrane conductance regulator gene | Aznarez, I; Chan, EM; Zielenski, J; Blencowe, BJ; Tsui, LC | 2003 | 747 |
| CFTR mutation detection by multiplex heteroduplex (mHET) analysis on MDE gel. | Zielenski, J; Aznarez, I; Onay, T; Tzounzouris, J; Markiewicz, D; Tsui, LC | 2002 | 91 |
| Cystic fibrosis in Uruguay | Luzardo, G; Aznarez, I; Crispino, B; Mimbacas, A; Martínez, L; Poggio, R; Zielenski, J; Tsui, LC; Cardoso, H | 2002 | 453 |
 | Characterization of a novel 21-kb deletion, CFTRdele2,3(21 kb), in the CFTR gene: A cystic fibrosis mutation of Slavic origin common in Central and East Europe | Dörk, T; Macek Jr, M; Mekus, F; Tümmler, B; Tzountzouris, J; Casals, T; Krebsová, A; Koudová, M; Sakmaryová, I; Macek Sr, M; Vávrová, V; Zemková, D; Ginter, E; Petrova, NV; Ivaschenko, T; Baranov, V; Witt, M; Pogorzelski, A; Bal, J; Zékanowsky, C; Wagner, K; Stuhrmann, M; Bauer, I; Seydewitz, HH; Neumann, T; Jakubiczka, S; Kraus, C; Thamm, B; Nechiporenko, M; Livshits, L; Mosse, N; Tsukerman, G; Kadási, L; RavnikGlavač, M; Glavač, D; Komel, R; Vouk, K; Kučinskas, V; Krumina, A; Teder, M; Kocheva, S; Efremov, GD; Onay, T; Kirdar, B; Malone, G; Schwarz, M; Zhou, Z; Friedman, KJ; Carles, S; Claustres, M; Bozon, D; Verlingue, C; Férec, C; Tzetis, M; Kanavakis, E; Cuppens, H; Bombieri, C; Pignatti, PF; Sangiuolo, F; Jordanova, A; Kusic, J; Radojkovič, D; Sertić, J; Richter, D; Rukavina, AS; Bjorck, E; Strandvik, B; Cardoso, H; Montgomery, M; Nakielna, B; Hughes, D; Estivill, X; Aznarez, I; Tullis, E; Tsui, LC; Zielenski, J | 2000 | 449 |
| Analysis of mutations in the CFTR gene in patients diagnosed with cystic fibrosis in Poland | Analiza mutacji w genie CFTR u pacjentów z rozpoznana mukowiscydoza w Polsce. | Aznarez, I; Bal, J; Casals, T; Estivill, X; Moral, N; Sands, D; Nunes, V; SobczyńskaTomaszewska, A; Tsui, LC; Zielenski, J | 2000 | 306 |
| Detection of a cystic fibrosis modifier locus for meconium ileus on human chromosome 19q13 [3] | Zielenski, J; Corey, M; Rozmahel, R; Markiewicz, D; Aznarez, I; Casals, T; Larriba, S; Mercier, B; Cutting, GR; Krebsova, A; Macek M, Jr; Langfelder Schwind, E; Marshall, BC; DecelieGermana, J; Claustres, M; Palacio, A; Bal, J; Nowakowska, A; Ferec, C; Estivill, X; Durie, P; Tsui, LC | 1999 | 118 |
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