Martin Pı́sačka

468 total citations
15 papers, 307 citations indexed

About

Martin Pı́sačka is a scholar working on Hematology, Physiology and Genetics. According to data from OpenAlex, Martin Pı́sačka has authored 15 papers receiving a total of 307 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Hematology, 10 papers in Physiology and 3 papers in Genetics. Recurrent topics in Martin Pı́sačka's work include Blood groups and transfusion (12 papers), Erythrocyte Function and Pathophysiology (9 papers) and Complement system in diseases (3 papers). Martin Pı́sačka is often cited by papers focused on Blood groups and transfusion (12 papers), Erythrocyte Function and Pathophysiology (9 papers) and Complement system in diseases (3 papers). Martin Pı́sačka collaborates with scholars based in Czechia, United Kingdom and Germany. Martin Pı́sačka's co-authors include Willy A. Flegel, Franz F. Wagner, Neil D. Avent, Inge von Zabern, Andrea Doescher, Wendy Liu, Zdeňka Gašová, D. Voak, Martina Novotná and J. Watt and has published in prestigious journals such as Blood, Transfusion and Parasitology.

In The Last Decade

Martin Pı́sačka

15 papers receiving 300 citations

Peers

Countries citing papers authored by Martin Pı́sačka

Since Specialization

Citations

This map shows the geographic impact of Martin Pı́sačka's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Martin Pı́sačka with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Martin Pı́sačka more than expected).

Fields of papers citing papers by Martin Pı́sačka

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Martin Pı́sačka. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Martin Pı́sačka. The network helps show where Martin Pı́sačka may publish in the future.

Co-authorship network of co-authors of Martin Pı́sačka

This figure shows the co-authorship network connecting the top 25 collaborators of Martin Pı́sačka. A scholar is included among the top collaborators of Martin Pı́sačka based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Martin Pı́sačka. Martin Pı́sačka is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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15 of 15 papers shown

#	Work	Indexed citations
1	A new missense variant in exon 7 of the ABO gene, c.662G>A, in a family with B_w phenotype 2022 ·Transfusion ·Annika K. Hult, Åsa Hellberg, Jill R. Storry, Martin Pı́sačka, Martin L. Olsson	3
2	Optimization of diagnostic strategy for non‐invasive cell‐free foetal RHD determination from maternal plasma 2021 ·Vox Sanguinis ·(unknown), (unknown), Marie Korabečná, (unknown), Martin Pı́sačka, (unknown), Pavel Calda, Aleš Hořínek	5
3	Autoimmune hemolytic anemia. 2019 ·PubMed ·Jaroslav Čermák, Martin Pı́sačka	2
4	Autoimmune hemolytic anemia 2018 ·Vnitřní lékařství ·Jaroslav Čermák, Martin Pı́sačka	2
5	FYA* silencing by the GATA‐motif variant FYA(−69C)* in a Caucasian family 2015 ·Transfusion ·Martin Pı́sačka, Iuri Marinov, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown)	4
6	D variants at the RhD vestibule in the weak D type 4 and Eurasian D clusters 2009 ·Transfusion ·Willy A. Flegel, Inge von Zabern, Andrea Doescher, Franz F. Wagner, Klaus Strathmann, Christof Geisen, Miodrag Palfi, Martin Pı́sačka, Joyce Poole, Helene Polin, Christian Gabriel, Neil D. Avent	40
7	Toxoplasmaand reaction time: role of toxoplasmosis in the origin, preservation and geographical distribution of Rh blood group polymorphism 2008 ·Parasitology ·Martina Novotná, Jan Havlı́ček, Andrew Smith, Petra Kolbeková, Anna Skallová, Jiřı́ Klose, Zdeňka Gašová, Martin Pı́sačka, (unknown), Jaroslav Flegr	63
8	DCS‐1, DCS‐2, and DFV share amino acid substitutions at the extracellular RhD protein vestibule 2007 ·Transfusion ·Willy A. Flegel, Inge von Zabern, Andrea Doescher, Franz F. Wagner, (unknown), Martin Pı́sačka	23
9	The McLeod syndrome without acanthocytes 2007 ·Parkinsonism & Related Disorders ·Jiří Klempíř, Jan Roth, Kateřina Zárubová, Martin Pı́sačka, N Spacková, Louise Tilley	9
10	Immunological Profiles of Patients with Chronic Myeloid Leukaemia. I. State before the Start of Treatment 2006 ·Folia Biologica ·(unknown), Hana Klamová, I Janatková, (unknown), I Šterzl, (unknown), Eva Hamšíková, C Haškovec, Martin Pı́sačka, Petr Cetkovský, K Michalová, (unknown), (unknown), (unknown), K Roubalová, Z. Roth, V. Vonka	15
11	Section 1B: Rh flow cytometryCoordinatorˈs report.Rhesus index and antigen density: an analysis of the reproducibility of flow cytometric determination 2002 ·Transfusion Clinique et Biologique ·Willy A. Flegel, Vladka Čurin Šerbec, M. Delamaire, (unknown), Hiroya Ikeda, Jorunn B. Jørgensen, Belinda M. Kumpel, P.Y. Le Pennec, Martin Pı́sačka, Yoshihiko Tani, Makoto Uchikawa, Silvano Wendel, Franz F. Wagner	57
12	Solid phase synthesis of glycopeptide dendrimers with Tn antigenic structure and their biological activities. Part I 1999 ·Journal of Peptide Science ·Jan Ježek, Jiřı́ Velek, (unknown), (unknown), Tomáš Trnka, (unknown), M Ledvina, Jiřı́ Vondrášek, Martin Pı́sačka	20
13	Blood group B glycosphingolipids in α-galactosidase deficiency (Fabry disease): influence of secretor status 1997 ·Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism ·J. Ledvinová, Helena Poupětová, (unknown), Martin Pı́sačka, M. Elleder	17
14	Molecular Analysis of Rh Transcripts and Polypeptides From Individuals Expressing the DVI Variant Phenotype: An RHD Gene Deletion Event Does Not Generate All DVIccEe Phenotypes 1997 ·Blood ·Neil D. Avent, Wendy Liu, J.W. Jones, Marion L. Scott, D. Voak, Martin Pı́sačka, J. Watt, Anne Fletcher	2
15	Molecular Analysis of Rh Transcripts and Polypeptides From Individuals Expressing the DVI Variant Phenotype: An RHD Gene Deletion Event Does Not Generate All DVIccEe Phenotypes 1997 ·Blood ·Neil D. Avent, Wendy Liu, J.W. Jones, Marion L. Scott, D. Voak, Martin Pı́sačka, J. Watt, Anne Fletcher	45

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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