M
Małgorzata Mizerska-Wasiak
Researcher at Medical University of Warsaw
Publications - 55
Citations - 1263
Małgorzata Mizerska-Wasiak is an academic researcher from Medical University of Warsaw. The author has contributed to research in topics: Nephropathy & Proteinuria. The author has an hindex of 11, co-authored 49 publications receiving 863 citations. Previous affiliations of Małgorzata Mizerska-Wasiak include University of Warsaw.
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Journal ArticleDOI
Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens
Krzysztof Kiryluk,Yifu Li,Francesco Scolari,Simone Sanna-Cherchi,Murim Choi,Miguel Verbitsky,David Fasel,Sneh Lata,Sindhuri Prakash,Samantha Shapiro,Clara Fischman,Holly J. Snyder,Gerald B. Appel,Claudia Izzi,Battista Fabio Viola,Nadia Dallera,Lucia Del Vecchio,Cristina Barlassina,Erika Salvi,Francesca Bertinetto,Antonio Amoroso,Silvana Savoldi,Marcella Rocchietti,Alessandro Amore,Licia Peruzzi,Rosanna Coppo,Maurizio Salvadori,Pietro Ravani,Riccardo Magistroni,Gian Marco Ghiggeri,Gianluca Caridi,Monica Bodria,Francesca Lugani,Landino Allegri,Marco Delsante,Mariarosa Maiorana,Andrea Magnano,Giovanni M. Frascà,Emanuela Boer,Giuliano Boscutti,Claudio Ponticelli,Renzo Mignani,Carmelita Marcantoni,Domenico Di Landro,Domenico Santoro,Antonello Pani,Rosaria Polci,Sandro Feriozzi,Silvana Chicca,Marco Galliani,Maddalena Gigante,Loreto Gesualdo,Pasquale Zamboli,Giovanni Giorgio Battaglia,Maurizio Garozzo,Dita Maixnerova,Vladimir Tesar,Frank Eitner,Thomas Rauen,Jürgen Floege,Tibor Kovács,Judit Nagy,Krzysztof Mucha,Leszek Pączek,Marcin Zaniew,Małgorzata Mizerska-Wasiak,Maria Roszkowska-Blaim,Krzysztof Pawlaczyk,Daniel P. Gale,Jonathan Barratt,Lise Thibaudin,François Berthoux,Guillaume Canaud,Anne Boland,Marie Metzger,Ulf Panzer,Hitoshi Suzuki,Shin Goto,Ichiei Narita,Yasar Caliskan,Jingyuan Xie,Ping Hou,Nan Chen,Hong Zhang,Robert J. Wyatt,Jan Novak,Bruce A. Julian,John Feehally,Bénédicte Stengel,Daniele Cusi,Richard P. Lifton,Ali G. Gharavi +91 more
TL;DR: A genome-wide association study of IgA nephropathy (IgAN), the most common form of glomerulonephritis, with discovery and follow-up in 20,612 individuals of European and East Asian ancestry is performed, suggesting a possible role for host–intestinal pathogen interactions in shaping the genetic landscape of IgAN.
Journal ArticleDOI
The MEST score provides earlier risk prediction in lgA nephropathy
Sean J. Barbour,Sean J. Barbour,Gabriela Espino-Hernandez,Heather N. Reich,Rosanna Coppo,Ian S.D. Roberts,John Feehally,Andrew M. Herzenberg,Daniel C. Cattran,Nuket Bavbek,Terry Cook,Stéphan Troyanov,C. Alpers,Alessandro Amore,Jonathan Barratt,F. Berthoux,S. Bonsib,Jan A. Bruijn,V. D’Agati,Giuseppe D'Amico,Steven N. Emancipator,F. Emmal,Franco Ferrario,Fernando C. Fervenza,Sandrine Florquin,Agnes B. Fogo,Colin C. Geddes,Hermann Josef Groene,Mark Haas,Prue Hill,Ronald J. Hogg,S. Hsu,Tracy E. Hunley,Michelle Hladunewich,Caroline E. Jennette,Kensuke Joh,Bruce A. Julian,Tetsuya Kawamura,F. Lai,C. Leung,L. Li,P. Li,Z. Liu,Alfonso Eirin Massat,Bruce Mackinnon,Sergio Mezzano,Federico Schena,Yasuhiko Tomino,Patrick D. Walker,H. Wang,Jan J. Weening,N Yoshikawa,Hong Zhang,R. Coppo,Dan Cattran,H.T. Cook,J. Feehally,I. Roberts,V. Tesar,Dita Maixnerova,Sigrid Lundberg,Loreto Gesualdo,Francesco Emma,L. Fuiano,Giulietta Beltrame,Cristiana Rollino,Rc,Roberta Camilla,Licia Peruzzi,Manuel Praga,Sandro Feriozzi,Rosaria Polci,G. Segoloni,Loredana Colla,Antonello Pani,A. Angioi,L. Piras,Jf,Giovanni Cancarini,Sara Ravera,Magdalena Durlik,Elisabetta Moggia,J. Ballarin,S. Di Giulio,F. Pugliese,I. Serriello,Yasar Caliskan,Mehmet Sukru Sever,Isin Kilicaslan,Francesco Locatelli,L. Del Vecchio,Jack F.M. Wetzels,H. Peters,Ulla Berg,F. Carvalho,A.C. da Costa Ferreira,Milena Maggio,A. Wiecek,M. Ots-Rosenberg,Riccardo Magistroni,Rezan Topaloglu,Yelda Bilginer,Marco D'Amico,Maria Stangou,F. Giacchino,Dimitris Goumenos,Pantelitsa Kalliakmani,Miltiadis Gerolymos,Krešimir Galešić,Kostas C. Siamopoulos,Olga Balafa,Marco Galliani,Piero Stratta,Marco Quaglia,Roberto Bergia,Raffaella Cravero,Maurizio Salvadori,L. Cirami,Bengt Fellström,H. Kloster Smerud,T. Stellato,Jesús Egido,C. Martin,J. Floege,Frank Eitner,Antonio Lupo,Patrizia Bernich,P. Menè,M. Morosetti,C. van Kooten,Ton J. Rabelink,M. Reinders,J.M. Boria Grinyo,Stefano Cusinato,Luisa Benozzi,Silvana Savoldi,C. Licata,Małgorzata Mizerska-Wasiak,G. Martina,A. Messuerotti,A. Dal Canton,Ciro Esposito,C. Migotto,G. Triolo,Filippo Mariano,Claudio Pozzi,R. Boero,Shubha Bellur,Gianna Mazzucco,Costantinos Giannakakis,Eva Honsova,B. Sundelin,A.M. Di Palma,E. Gutiérrez,Anna Maria Asunis,Regina Tardanico,Agnieszka Perkowska-Ptasińska,J. Arce Terroba,M. Fortunato,Aphroditi Pantzaki,Yasemin Ozluk,Eric J. Steenbergen,Magnus Söderberg,Z. Riispere,L. Furci,Diclehan Orhan,David Kipgen,Donatella Casartelli,D. Galesic Ljubanovic,Hariklia Gakiopoulou,E. Bertoni,P. Cannata Ortiz,Henryk Karkoszka,Hermann-Josef Groene,A. Stoppacciaro,Ingeborg M. Bajema,X. Fulladosa Oliveras,J. Maldyk,E. Ioachim +178 more
TL;DR: Combining the MEST score with cross-sectional clinical data at biopsy provides earlier risk prediction in IgAN than current best methods, which requires clinical data over 2 years of follow-up.
Journal ArticleDOI
The copy number variation landscape of congenital anomalies of the kidney and urinary tract
Miguel Verbitsky,Rik Westland,Alejandra Perez,Krzysztof Kiryluk,Qingxue Liu,Priya Krithivasan,Adele Mitrotti,David Fasel,Ekaterina Batourina,Matthew G. Sampson,Monica Bodria,Max Werth,Charlly Kao,Jeremiah Martino,Valentina P Capone,Asaf Vivante,Asaf Vivante,Shirlee Shril,Byum Hee Kil,Maddalena Marasa,Jun Zhang,Young Ji Na,Tze Y Lim,Dina Ahram,Patricia L. Weng,Erin L. Heinzen,Alba Carrea,Giorgio Piaggio,Loreto Gesualdo,Valeria Manca,Giuseppe Masnata,Maddalena Gigante,Daniele Cusi,Claudia Izzi,Francesco Scolari,Joanna A.E. van Wijk,Marijan Saraga,Domenico Santoro,Giovanni Conti,Pasquale Zamboli,Hope White,Dorota Drozdz,Katarzyna Zachwieja,Monika Miklaszewska,Marcin Tkaczyk,Daria Tomczyk,Anna Krakowska,Przemysław Sikora,Tomasz Jarmoliński,Maria K Borszewska-Kornacka,Robert Pawluch,Maria Szczepańska,Piotr Adamczyk,Małgorzata Mizerska-Wasiak,Grażyna Krzemień,Agnieszka Szmigielska,Marcin Zaniew,Mark G Dobson,John M Darlow,Prem Puri,David E. Barton,David E. Barton,Susan L. Furth,Bradley A. Warady,Zoran Gucev,Vladimir J Lozanovski,Vladimir J Lozanovski,Velibor Tasic,Isabella Pisani,Landino Allegri,Lida Rodas,Josep M. Campistol,Cécile Jeanpierre,Shumyle Alam,Pasquale Casale,Pasquale Casale,Craig S. Wong,Fangming Lin,Débora Marques de Miranda,Eduardo A. Oliveira,Ana Cristina Simões-e-Silva,Jonathan Barasch,Brynn Levy,Nan Wu,Nan Wu,Friedhelm Hildebrandt,Gian Marco Ghiggeri,Anna Latos-Bielenska,Anna Materna-Kiryluk,Feng Zhang,Hakon Hakonarson,Virginia E. Papaioannou,Cathy Mendelsohn,Ali G. Gharavi,Simone Sanna-Cherchi +94 more
TL;DR: Genome-wide analysis of copy number variants in 2,824 cases across the phenotypic spectrum of CAKUT sheds light on the genomic architecture of disease and identifies TBX6 as a driver forCAKUT subphenotypes in the 16p11.2 microdeletion syndrome.
Journal ArticleDOI
Genetic Drivers of Kidney Defects in the DiGeorge Syndrome.
Esther Lopez-Rivera,Yangfan P. Liu,Miguel Verbitsky,Blair R. Anderson,Valentina P Capone,Edgar A. Otto,Zhonghai Yan,Adele Mitrotti,Jeremiah Martino,Nicholas J Steers,David Fasel,Katarina Vukojević,Rong Deng,Silvia E. Racedo,Qingxue Liu,Max Werth,Rik Westland,Asaf Vivante,Gabriel Makar,Gabriel Makar,Monica Bodria,Matthew G. Sampson,Christopher E. Gillies,Virginia Vega-Warner,Mariarosa Maiorana,Donald Petrey,Barry Honig,Vladimir J Lozanovski,Rémi Salomon,Rémi Salomon,Laurence Heidet,Wassila Carpentier,Dominique Gaillard,Alba Carrea,Loreto Gesualdo,Daniele Cusi,Claudia Izzi,Francesco Scolari,Joanna A.E. van Wijk,Adela Arapović,Mirna Saraga-Babić,Marijan Saraga,Nenad Kunac,Ali Samii,Donna M. McDonald-McGinn,Terrence B. Crowley,Elaine H. Zackai,Dorota Drozdz,Monika Miklaszewska,Marcin Tkaczyk,Przemysław Sikora,Maria Szczepańska,Małgorzata Mizerska-Wasiak,Grażyna Krzemień,Agnieszka Szmigielska,Marcin Zaniew,John M Darlow,Prem Puri,David E. Barton,David E. Barton,Emilio Casolari,Susan L. Furth,Bradley A. Warady,Zoran Gucev,Hakon Hakonarson,Hana Flögelová,Velibor Tasic,Anna Latos-Bielenska,Anna Materna-Kiryluk,Landino Allegri,Craig S. Wong,Iain A. Drummond,V. D’Agati,Akira Imamoto,Jonathan Barasch,Friedhelm Hildebrandt,Krzysztof Kiryluk,Richard P. Lifton,Bernice E. Morrow,Cécile Jeanpierre,Virginia E. Papaioannou,Gian Marco Ghiggeri,Ali G. Gharavi,Nicholas Katsanis,Simone Sanna-Cherchi +84 more
TL;DR: A recurrent 370‐kb deletion at the 22q11.2 locus is identified as a driver of kidney defects in the DiGeorge syndrome and in sporadic congenital kidney and urinary tract anomalies.
Journal ArticleDOI
Prevalence of Hypertension in Children with Early-Stage ADPKD
Laura Massella,Djalila Mekahli,Dusan Paripovic,Larisa Prikhodina,Nathalie Godefroid,Anna Niemirska,Ayşe Ağbaş,Karolina Kalicka,Augustina Jankauskiene,Małgorzata Mizerska-Wasiak,Alberto Caldas Afonso,Rémi Salomon,Georges Deschênes,Gema Ariceta,Z. Birsin Özçakar,Ana Teixeira,Ali Duzova,Jérôme Harambat,Tomáš Seeman,Gabriela Hrčková,Adrian Lungu,Svetlana Papizh,Amira Peco-Antic,Stéphanie De Rechter,Ugo Giordano,Marietta Kirchner,Teresa Lutz,Franz Schaefer,Olivier Devuyst,Olivier Devuyst,Elke Wühl,Francesco Emma +31 more
TL;DR: High prevalence of hypertension in children with autosomal dominant polycystic kidney disease starting at young ages is found, and a significant association between a categorical cyst score and daytime hypertension is found.