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How has Pavlína Plevová's publication output changed over time?
ScholarIQpublication output · 1999–2021
Output grew100% over the shown period — from 1 works in 1999 to 2 in 2021.
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1
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2
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2
1999200420052015201720192021
What are the most-cited papers on Pavlína Plevová?
ScholarIQmost cited works
Prevention and treatment of chemotherapy- and radiotherapy-induced oral mucositis: a review
Pavlína Plevová
S102916872. 1999135 Citations
Consensus statement on standards and guidelines for the molecular diagnostics of Alport syndrome: refining the ACMG criteria
Judy Savige, Helen Storey, E. Watson, Jens Michael Hertz, Constantinos Deltas, Alessandra Renieri, Francesca Mari, Pascale Hilbert, Pavlína Plevová, Peter H. Byers, Agnė Čerkauskaitė, Martin C. Gregory, Rimantė Čerkauskienė, Danica Galešić Ljubanović, Francesca Becherucci, Carmela Errichiello, Laura Massella, Valeria Aiello, Rachel Lennon, Louise Hopkinson, Ania Koziell, Adrian Lungu, H. Rothe, Julia Hoefele, Miriam Zacchia, Tamara Nikuševa Martić, Asheeta Gupta, Albertien M. van Eerde, Susie Gear, Samuela Landini, Viviana Palazzo, Laith Al‐Rabadi, Kathleen Claes, Anniek Corveleyn, Evelien Van Hoof, Micheel van Geel, Maggie Williams, Emma Ashton, Hendica Belge, Elisabet Ars, Agnieszka Bierżyńska, Concetta Gangemi, Beata S. Lipska‐Ziętkiewicz
European Journal of Human Genetics. 2021129 CitationsOPEN ACCESS
Guidelines for Genetic Testing and Management of Alport Syndrome
Judy Savige, Beata S. Lipska‐Ziętkiewicz, E. Watson, Jens Michael Hertz, Constantinos Deltas, Francesca Mari, Pascale Hilbert, Pavlína Plevová, Peter H. Byers, Agnė Čerkauskaitė, Martin C. Gregory, Rimantė Čerkauskienė, Danica Galešić Ljubanović, Francesca Becherucci, Carmela Errichiello, Laura Massella, Valeria Aiello, Rachel Lennon, Louise Hopkinson, Ania Koziell, Adrian Lungu, H. Rothe, Julia Hoefele, Miriam Zacchia, Tamara Nikuševa Martić, Asheeta Gupta, Albertien M. van Eerde, Susie Gear, Samuela Landini, Viviana Palazzo, Laith Al‐Rabadi, Kathleen Claes, Anniek Corveleyn, Elke Van Hoof, Micheel van Geel, Maggie Williams, Emma Ashton, Hendica Belge, Elisabet Ars, Agnieszka Bierżyńska, Concetta Gangemi, Alessandra Renieri, Helen Storey, Frances Flinter, Judy Savige, Beata S. Lipska‐Ziętkiewicz, E. Watson, Jens Michael Hertz, Constantinos Deltas, Francesca Mari, Pascale Hilbert, Pavlína Plevová, Peter H. Byers, Agnė Čerkauskaitė, Martin C. Gregory, Rimantė Čerkauskienė, Danica Galešić Ljubanović, Francesca Becherucci, Carmela Errichiello, Laura Massella, Valeria Aiello, Rachel Lennon, Louise Hopkinson, Ania Koziell, Adrian Lungu, H. Rothe, Julia Hoefele, Miriam Zacchia, Tamara Nikuševa Martić, Asheeta Gupta, Albertien M. van Eerde, Susie Gear, Samuela Landini, Viviana Palazzo, Laith Al‐Rabadi, Kathleen Claes, Anniek Corveleyn, Elke Van Hoof, Micheel van Geel, Maggie Williams, Emma Ashton, Hendica Belge, Elisabet Ars, Agnieszka Bierżyńska, Concetta Gangemi, Alessandra Renieri, Helen Storey, Frances Flinter
S4306401649. 2021115 CitationsOPEN ACCESS
Identification of five new families strengthens the link between childhood choroid plexus carcinoma and germline TP53 mutations
Vera Krutilkova, Marie Trková, Julie Fleitz, Vladimír Gregor, Kamila Novotna, Anna Křepelová, David Sumerauer, Roman Kodet, Simona Širůčková, Pavlína Plevová, Šárka Bendová, Petra Hedvičáková, Nicholas K. Foreman, Zdeněk Sedláček
European Journal of Cancer. 200598 Citations
HCFC1 loss-of-function mutations disrupt neuronal and neural progenitor cells of the developing brain
Lachlan A. Jolly, Lam Son Nguyen, Deepti Domingo, Yongsheng Sun, Simon C. Barry, Miroslava Hančárová, Pavlína Plevová, Markéta Vlčková, Markéta Havlovičová, Vera M. Kalscheuer, Claudio Graziano, Tommaso Pippucci, Elena Bonora, Zdeněk Sedláček, Jozef Gécz
S166515463. 201567 CitationsOPEN ACCESS
Related on ScholarIQ
University Hospital Ostrava
Institution
Prevention and treatment of chemotherapy- and radiotherapy-induced oral mucositis: a review
Paper
Consensus statement on standards and guidelines for the molecular diagnostics of Alport syndrome: refining the ACMG criteria
Paper
Guidelines for Genetic Testing and Management of Alport Syndrome
Paper
Identification of five new families strengthens the link between childhood choroid plexus carcinoma and germline TP53 mutations
Paper
HCFC1 loss-of-function mutations disrupt neuronal and neural progenitor cells of the developing brain
Paper