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Pavlína Plevová

ResearcherPublications, citations & collaboration network

Pavlína Plevová is a researcher indexed in ScholarIQ from OpenAlex & ORCID.

How many works does Pavlína Plevová have?

ScholarIQindexed works

Pavlína Plevová has 59 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.

How many citations does Pavlína Plevová have?

ScholarIQcitation count

Pavlína Plevová has 963 citations in the OpenAlex counts ScholarIQ stores.

What is the h-index of Pavlína Plevová?

ScholarIQh-index

Pavlína Plevová has an h-index of 13 in OpenAlex.

What is the i10-index of Pavlína Plevová?

ScholarIQi10-index

Pavlína Plevová has an i10-index of 19 in OpenAlex.

What is the ORCID of Pavlína Plevová?

ScholarIQorcid

The ORCID for Pavlína Plevová is on the source record.

What is the OpenAlex record for Pavlína Plevová?

ScholarIQopenalex

The OpenAlex for Pavlína Plevová is on the source record.

What are the most-cited papers on Pavlína Plevová?

ScholarIQmost cited works
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
Utrecht University Repository (Utrecht University). 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
Human Molecular Genetics. 201567 CitationsOPEN ACCESS

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