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论文共 99 篇作者统计合作学者相似作者

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Haemolytic Uremic Syndrome As a Cause of Chronic Kidney Disease Stage 5 in Children is in Retreat: Results from the Polish Registry of Kidney Replacement Therapy in Children (2000–2023)
Ilona Zagożdżon, Maria Szczepańska,Jacek Rubik,Katarzyna Zachwieja, Anna Musielak, Monika Bratkowska,Irena Makulska, Katarzyna Niwińska,Beata Leszczyńska, Beata Bieniaś, Katarzyna Taranta-Janusz, Hanna Adamczyk-Kipigroch, Aleksandra Żurowska
Pediatric nephrology (Berlin, Germany) (2024)
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Exome-wide Analysis of Congenital Kidney Anomalies Reveals New Genes and Shared Architecture with Developmental Disorders
Hila Milo Rasouly, Sarath Babu Krishna Murthy,Natalie Vena, Gundula Povysil,Andrew Beenken,Miguel Verbitsky,Shirlee Shril, Iris Lekkerkerker, Atlas Khan, David Fasel, Janewit Wongboonsin,Jeremiah Martino, Juntao Ke, Naama Elefant, Nikita Tomar, Ofek Harnof, Sandy Yang, Sergey Kisselev, Shiraz Bheda, Sivan Reytan-Miron, Tze Y Lim, Anna Jamry-Dziurla,Francesca Lugani, Jun Y Zhang,Maddalena Marasa, Victoria Kolupaeva, Emily E. Groopman, Gina Jin, Iman Ghavami, Kelsey O. Stevens, Arielle C. Coughlin,Byum Hee Kil, Debanjana Chatterjee, Drew Bradbury, Jason Zheng,Karla Mehl, Maria Morban,Rachel Reingold, Stacy Piva, Xueru Mu, Adele Mittrori, Agnieszka Szmigielska,Aleksandra Gliwińska, Andrea Ranghino, Andrew S Bomback,Andrzej Badenski, Anna Latos-Bielenska, Anna Materna-Kiryluk, Antonio Amoroso, Claudia Izzi,Claudio La Scola, David Jonathan Cohen,Domenico Santoro, Dorota Drozdz, Enrico Fiaccadori, Fangming Lin,Francesco Scolari,Francesco Tondolo, Gaetano La Manna, Gerald B Appel,Gian Marco Ghiggeri, Gianluigi Zaza, Giovanni Montini,Giuseppe Masnata, Grazyna z,Isabella Pisani, Jai Radhakrishnan,Katarzyna Zachwieja, Lauren Monaco, Loreto Gesualdo, Luigi Biancone, Luisa Murer, Malgorzata Mizerska-Wasiak,Marcin Tkaczyk, Marcin Zaniew, Maria K. Borszewska-Kornacka, Maria Szczepanska,Marijan Saraga, Maya K Rao, Monica Bodria, Monika Miklaszewska, Natalie S Uy, Olga Baraldi, Omar Bjanid, Pasquale Esposito,Pasquale Zamboli, Pierluigi Marzuillo, Pietro A Canetta, Przemyslaw Sikora,Rik Westland, Russell J Crew, Shumyle Alam, Stefano Guarino, Susanna Negrisolo, Thomas Hays, Valeria Grandinetti, Velibor Tasic, Vladimir J. Lozanovski, Yasar Caliskan,David Goldstein, Richard P Lifton,Iuliana Ionita-Laza, Krzysztof Kiryluk, Albertien van Eerde,Friedhelm Hildebrandt, Simone Sanna-Cherchi, Ali G Gharavi
medrxiv（2024）
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MIP Assay-Based Targeted Gene Resequencing Identifies 22 Novel and Extremely Rare Variants in Known and Putative New Candidate Genes in Lower Urinary Tract Obstruction
Markus Hartmut Zeilmann, Arif Ekici, Clara Vidic, Wolfgang Krebs, Marcin Zaniew, Agnieszka Szmigielska, Monika Miklaszewska, Maria Szczepanska, Katarzyna Taranta-Janusz, Przemyslaw Sikora,Katarzyna Zachwieja,Friedhelm Hildebrandt,Alina Hilger
Journal of the American Society of Nephrologyno. 10S (2024)
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Case Report of Twins with Bardet-Biedl Syndrome Exhibiting a Rare Mutation in the TTC8 Gene
Agnieszka Murawska, Kamil Możdżeń, Grzegorz Horosin, Edward Pędziwiatr, Joanna Makowska, Jakub Pośpiech, Konrad Kaleta, Dorota Drożdż,Katarzyna Zachwieja
Pediatria Polska (2024)
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作者统计

#Papers: 97

#Citation: 1152

H-Index: 23

G-Index: 31

Sociability: 6

Diversity: 0

Activity: 1

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