Laszlo Furu

1.8k total citations
9 papers, 1.0k citations indexed

About

Laszlo Furu is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Laszlo Furu has authored 9 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 6 papers in Molecular Biology and 3 papers in Surgery. Recurrent topics in Laszlo Furu's work include Genetic and Kidney Cyst Diseases (7 papers), Genetic Syndromes and Imprinting (4 papers) and Renal and related cancers (2 papers). Laszlo Furu is often cited by papers focused on Genetic and Kidney Cyst Diseases (7 papers), Genetic Syndromes and Imprinting (4 papers) and Renal and related cancers (2 papers). Laszlo Furu collaborates with scholars based in United States, Brazil and Germany. Laszlo Furu's co-authors include Stefan Somlo, Gregory G. Germino, Luiz F. Onuchic, Lisa M. Guay‐Woodford, Carsten Bergmann, Klaus Zerres, Jan Senderek, Thomas Eggermann, Xiaoying Hou and Yasuyuki Nagasawa and has published in prestigious journals such as Journal of the American Society of Nephrology, The American Journal of Human Genetics and Journal of Animal Science.

In The Last Decade

Laszlo Furu

9 papers receiving 987 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Laszlo Furu United States 8 831 801 204 164 90 9 1.0k
Angela J. Stroope United States 10 536 0.6× 446 0.6× 100 0.5× 299 1.8× 31 0.3× 13 820
Intza Garin Spain 17 506 0.6× 476 0.6× 41 0.2× 91 0.6× 114 1.3× 32 638
Sachin Hajarnis United States 13 316 0.4× 531 0.7× 57 0.3× 61 0.4× 68 0.8× 15 664
L Chadwick United States 7 205 0.2× 247 0.3× 61 0.3× 24 0.1× 46 0.5× 9 362
Isabelle Guilleret Switzerland 13 156 0.2× 615 0.8× 39 0.2× 50 0.3× 32 0.4× 16 832
Noriyuki Sugiyama Japan 12 295 0.4× 531 0.7× 20 0.1× 59 0.4× 36 0.4× 16 690
Ryan J. Russo United States 10 374 0.5× 386 0.5× 104 0.5× 13 0.1× 45 0.5× 10 506
Lynelle K. Jones Australia 14 91 0.1× 199 0.2× 24 0.1× 77 0.5× 44 0.5× 19 522
P. Martin Petkovich Canada 9 91 0.1× 199 0.2× 149 0.7× 23 0.1× 24 0.3× 11 375
Esther Vamos Belgium 15 179 0.2× 286 0.4× 39 0.2× 28 0.2× 85 0.9× 21 533

Countries citing papers authored by Laszlo Furu

Since Specialization
Citations

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

Fields of papers citing papers by Laszlo Furu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Laszlo Furu

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

All Works

9 of 9 papers shown
1.
Geller, David S., Junhui Zhang, Maria‐Christina Zennaro, et al.. (2006). Autosomal Dominant Pseudohypoaldosteronism Type 1. Journal of the American Society of Nephrology. 17(5). 1429–1436. 83 indexed citations
2.
Bergmann, Carsten, Jan Senderek, Fabian Küpper, et al.. (2004). PKHD1mutations in autosomal recessive polycystic kidney disease (ARPKD). Human Mutation. 23(5). 453–463. 115 indexed citations
3.
Li, Airong, Sonia Dávila, Laszlo Furu, et al.. (2003). Mutations in PRKCSH Cause Isolated Autosomal Dominant Polycystic Liver Disease. The American Journal of Human Genetics. 72(3). 691–703. 134 indexed citations
4.
Furu, Laszlo, Luiz F. Onuchic, Ali G. Gharavi, et al.. (2003). Milder Presentation of Recessive Polycystic Kidney Disease Requires Presence of Amino Acid Substitution Mutations. Journal of the American Society of Nephrology. 14(8). 2004–2014. 90 indexed citations
5.
Bergmann, Carsten, Jan Senderek, Thomas Eggermann, et al.. (2003). Spectrum of Mutations in the Gene for Autosomal Recessive Polycystic Kidney Disease (ARPKD/PKHD1). Journal of the American Society of Nephrology. 14(1). 76–89. 146 indexed citations
6.
Onuchic, Luiz F., Laszlo Furu, Yasuyuki Nagasawa, et al.. (2002). PKHD1, the Polycystic Kidney and Hepatic Disease 1 Gene, Encodes a Novel Large Protein Containing Multiple Immunoglobulin-Like Plexin-Transcription–Factor Domains and Parallel Beta-Helix 1 Repeats. The American Journal of Human Genetics. 70(5). 1305–1317. 340 indexed citations
7.
Onuchic, Luiz F., Michal Mrug, Xiaoying Hou, et al.. (2002). Refinement of the autosomal recessive polycystic kidney disease (PKHD1) interval and exclusion of an EF hand‐containing gene as aPKHD1candidate gene. American Journal of Medical Genetics. 110(4). 346–352. 12 indexed citations
8.
Nagasawa, Yasuyuki, Sonja Matthiesen, Luiz F. Onuchic, et al.. (2002). Identification and Characterization of Pkhd1, the Mouse Orthologue of the Human ARPKD Gene. Journal of the American Society of Nephrology. 13(9). 2246–2258. 87 indexed citations
9.
Furu, Laszlo, G.W. Kazmer, Linda D. Strausbaugh, & S Zinn. (1999). Cloning and characterization of the bovine somatostatin gene.. Journal of Animal Science. 77(2). 492–492. 1 indexed citations

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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026