Tapio Pantzar

767 total citations
12 papers, 420 citations indexed

About

Tapio Pantzar is a scholar working on Genetics, Surgery and Molecular Biology. According to data from OpenAlex, Tapio Pantzar has authored 12 papers receiving a total of 420 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 4 papers in Surgery and 4 papers in Molecular Biology. Recurrent topics in Tapio Pantzar's work include Prenatal Screening and Diagnostics (4 papers), Genomic variations and chromosomal abnormalities (3 papers) and Genetic Syndromes and Imprinting (2 papers). Tapio Pantzar is often cited by papers focused on Prenatal Screening and Diagnostics (4 papers), Genomic variations and chromosomal abnormalities (3 papers) and Genetic Syndromes and Imprinting (2 papers). Tapio Pantzar collaborates with scholars based in Canada, United States and France. Tapio Pantzar's co-authors include Dagmar K. Kalousek, Douglas E. Horsman, Randy D. Gascoyne, Joseph M. Connors, Barbara McGillivray, Siu Li Yong, F. J. Dill, R. Douglas Wilson, Ming‐Shiun Tsai and David Chitayat and has published in prestigious journals such as Pediatric Research, Human Genetics and Genes Chromosomes and Cancer.

In The Last Decade

Tapio Pantzar

11 papers receiving 395 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Tapio Pantzar Canada 9 188 180 106 104 80 12 420
Nataline B. Kardon United States 13 281 1.5× 329 1.8× 36 0.3× 58 0.6× 66 0.8× 26 640
David Peakman United States 15 192 1.0× 278 1.5× 24 0.2× 97 0.9× 59 0.7× 30 636
Elena Kolomietz Canada 11 225 1.2× 269 1.5× 77 0.7× 132 1.3× 45 0.6× 23 734
Javier Suela Spain 13 57 0.3× 145 0.8× 79 0.7× 83 0.8× 26 0.3× 31 539
Michal Daniely Israel 12 269 1.4× 225 1.3× 15 0.1× 32 0.3× 109 1.4× 15 585
H.F.L. Mark United States 13 58 0.3× 156 0.9× 31 0.3× 30 0.3× 24 0.3× 38 375
Longina M. Gibas United States 7 81 0.4× 140 0.8× 251 2.4× 17 0.2× 98 1.2× 11 481
Renée Bernstein South Africa 13 64 0.3× 195 1.1× 33 0.3× 71 0.7× 29 0.4× 26 466
Luc Dehaspe Belgium 11 297 1.6× 191 1.1× 124 1.2× 23 0.2× 38 0.5× 21 593
Audrey Basinko France 13 72 0.4× 119 0.7× 47 0.4× 118 1.1× 19 0.2× 33 512

Countries citing papers authored by Tapio Pantzar

Since Specialization
Citations

This map shows the geographic impact of Tapio Pantzar'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 Tapio Pantzar with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Tapio Pantzar more than expected).

Fields of papers citing papers by Tapio Pantzar

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Tapio Pantzar. 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 Tapio Pantzar. The network helps show where Tapio Pantzar may publish in the future.

Co-authorship network of co-authors of Tapio Pantzar

This figure shows the co-authorship network connecting the top 25 collaborators of Tapio Pantzar. A scholar is included among the top collaborators of Tapio Pantzar 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 Tapio Pantzar. Tapio Pantzar is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

12 of 12 papers shown
1.
Schrader, Kasmintan A., Tanya N. Nelson, Deborah E. McFadden, Tapio Pantzar, & Sylvie Langlois. (2007). Renal–hepatic–pancreatic dysplasia: An autosomal recessive condition that is not linked to the PKHD1 gene on chromosome 6p21.1‐p12. American Journal of Medical Genetics Part A. 143A(15). 1806–1808. 2 indexed citations
2.
Bruyèrè, Hélène, Marsha Speevak, E.J.T. Winsor, et al.. (2006). Isodicentric Yp: prenatal diagnosis and outcome in 12 cases. Prenatal Diagnosis. 26(4). 324–329. 27 indexed citations
3.
Lin, Yulia, Hélène Bruyèrè, Douglas E. Horsman, et al.. (2006). Philadelphia-negative clonal hematopoiesis following imatinib therapy in patients with chronic myeloid leukemia: a report of nine cases and analysis of predictive factors. Cancer Genetics and Cytogenetics. 170(1). 16–23. 20 indexed citations
4.
Bruyèrè, Hélène, Evica Rajcan‐Separovic, Jason Doyle, Tapio Pantzar, & Sylvie Langlois. (2003). Familial cryptic translocation (2;17) ascertained through recurrent spontaneous abortions. American Journal of Medical Genetics Part A. 123A(3). 285–289. 11 indexed citations
5.
Horsman, Douglas E., Joseph M. Connors, Tapio Pantzar, & Randy D. Gascoyne. (2001). Analysis of secondary chromosomal alterations in 165 cases of follicular lymphoma with t(14;18). Genes Chromosomes and Cancer. 30(4). 375–382. 112 indexed citations
6.
Rajcan‐Separovic, Evica, Wendy P. Robinson, Mary D. Stephenson, et al.. (2001). Recurrent trisomy 15 in a female carrier of der(15)t(Y;15)(q12;p13). American Journal of Medical Genetics. 99(4). 320–324. 13 indexed citations
7.
Kalousek, Dagmar K., et al.. (1993). Early spontaneous abortion: morphologic and karyotypic findings in 3,912 cases.. PubMed. 29(1). 53–61. 44 indexed citations
8.
McGillivray, Barbara, et al.. (1990). Familial 5q11.2→q13.3 segmental duplication cosegregating with multiple anomalies, including schizophrenia. American Journal of Medical Genetics. 35(1). 10–13. 21 indexed citations
9.
Bamforth, J., Claire O. Leonard, Bernard N. Chodirker, et al.. (1989). Congenital diaphragmatic hernia, coarse facies, and acral hypoplasia: Fryns syndrome. American Journal of Medical Genetics. 32(1). 93–99. 53 indexed citations
10.
Kalousek, Dagmar K., Tapio Pantzar, & Randall Craver. (1988). So-Called Primitive Neuroectodermal Tumor in Aborted Previable Fetuses. Pediatric Pathology. 8(5). 503–511. 2 indexed citations
11.
Kalousek, Dagmar K., F. J. Dill, Tapio Pantzar, et al.. (1987). Confined chorionic mosaicism in prenatal diagnosis. Human Genetics. 77(2). 163–167. 115 indexed citations
12.
Pantzar, Tapio, et al.. (1987). FRYNS SYNDROME: FURTHER DELINEATION AND ANTENATAL DIAGNOSIS. Pediatric Research. 21(4). 224A–224A.

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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