José L. Badano

8.3k total citations · 1 hit paper
43 papers, 5.9k citations indexed

About

José L. Badano is a scholar working on Genetics, Molecular Biology and Cell Biology. According to data from OpenAlex, José L. Badano has authored 43 papers receiving a total of 5.9k indexed citations (citations by other indexed papers that have themselves been cited), including 38 papers in Genetics, 36 papers in Molecular Biology and 6 papers in Cell Biology. Recurrent topics in José L. Badano's work include Genetic and Kidney Cyst Diseases (34 papers), Hedgehog Signaling Pathway Studies (23 papers) and Genetic Syndromes and Imprinting (21 papers). José L. Badano is often cited by papers focused on Genetic and Kidney Cyst Diseases (34 papers), Hedgehog Signaling Pathway Studies (23 papers) and Genetic Syndromes and Imprinting (21 papers). José L. Badano collaborates with scholars based in United States, Uruguay and United Kingdom. José L. Badano's co-authors include Nicholas Katsanis, Philip L. Beales, Phil Beales, Norimasa Mitsuma, Carmen C. Leitch, Stephen J. Ansley, Richard A. Lewis, Bethan E. Hoskins, James R. Lupski and Erica R. Eichers and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

José L. Badano

42 papers receiving 5.8k citations

Hit Papers

The Ciliopathies: An Emerging Class of Human Genetic Diso... 2006 2026 2012 2019 2006 250 500 750

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
José L. Badano United States 30 4.7k 4.5k 1.0k 444 353 43 5.9k
Philip L. Beales United Kingdom 51 7.5k 1.6× 6.9k 1.5× 1.4k 1.3× 724 1.6× 633 1.8× 101 9.5k
Diane C. Slusarski United States 35 2.9k 0.6× 6.0k 1.3× 1.6k 1.6× 165 0.4× 282 0.8× 60 7.1k
Oliver E. Blacque Ireland 32 3.6k 0.8× 3.4k 0.8× 1.4k 1.4× 273 0.6× 313 0.9× 62 4.5k
Edgar A. Otto United States 42 3.5k 0.7× 4.8k 1.1× 514 0.5× 996 2.2× 796 2.3× 106 6.3k
Hilde Van Esch Belgium 40 3.5k 0.7× 3.5k 0.8× 352 0.3× 629 1.4× 91 0.3× 148 5.6k
Charles Searby United States 42 2.8k 0.6× 3.9k 0.9× 934 0.9× 208 0.5× 263 0.7× 86 5.8k
Carmen C. Leitch United States 20 2.1k 0.4× 2.1k 0.5× 483 0.5× 156 0.4× 179 0.5× 22 2.8k
Tom Glaser United States 31 1.8k 0.4× 5.9k 1.3× 637 0.6× 672 1.5× 231 0.7× 51 7.7k
Kerstin Kutsche Germany 32 1.3k 0.3× 2.3k 0.5× 685 0.7× 198 0.4× 112 0.3× 118 3.6k
Saikat Mukhopadhyay United States 25 2.1k 0.5× 2.3k 0.5× 667 0.6× 209 0.5× 178 0.5× 60 3.1k

Countries citing papers authored by José L. Badano

Since Specialization
Citations

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

Fields of papers citing papers by José L. Badano

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by José L. Badano. 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 José L. Badano. The network helps show where José L. Badano may publish in the future.

Co-authorship network of co-authors of José L. Badano

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

All Works

20 of 20 papers shown
1.
Cárdenas-Rodríguez, Magdalena, Mariana Bresque, Martina Crispo, et al.. (2022). Generation and characterization of Ccdc28b mutant mice links the Bardet-Biedl associated gene with mild social behavioral phenotypes. PLoS Genetics. 18(6). e1009896–e1009896. 3 indexed citations
2.
Koziol, Uriel, et al.. (2021). Insights into in vivo adipocyte differentiation through cell-specific labeling in zebrafish. Biology Open. 10(9). 2 indexed citations
3.
Badano, José L., et al.. (2020). Photoreceptor progenitor dynamics in the zebrafish embryo retina and its modulation by primary cilia and N-cadherin. The International Journal of Developmental Biology. 65(4-5-6). 439–455. 3 indexed citations
4.
Colman, Laura, Paola Contreras, Claudia C.S. Chini, et al.. (2019). A novel form of Deleted in breast cancer 1 (DBC1) lacking the N-terminal domain does not bind SIRT1 and is dynamically regulated in vivo. Scientific Reports. 9(1). 14381–14381. 8 indexed citations
5.
Suárez‐Bregua, Paula, et al.. (2019). Functional analysis of new human Bardet-Biedl syndrome loci specific variants in the zebrafish model. Scientific Reports. 9(1). 12936–12936. 6 indexed citations
7.
Cárdenas-Rodríguez, Magdalena, Florencia Irigoı́n, Daniel P. S. Osborn, et al.. (2013). The Bardet–Biedl syndrome-related protein CCDC28B modulates mTORC2 function and interacts with SIN1 to control cilia length independently of the mTOR complex. Human Molecular Genetics. 22(20). 4031–4042. 29 indexed citations
8.
Cárdenas-Rodríguez, Magdalena, Daniel P. S. Osborn, Florencia Irigoı́n, et al.. (2012). Characterization of CCDC28B reveals its role in ciliogenesis and provides insight to understand its modifier effect on Bardet–Biedl syndrome. Human Genetics. 132(1). 91–105. 30 indexed citations
9.
Irigoı́n, Florencia & José L. Badano. (2011). Keeping the Balance Between Proliferation and Differentiation:The Primary Cilium. Current Genomics. 12(4). 285–297. 57 indexed citations
10.
Gerdes, Jantje M., Yangfan Liu, Norann A. Zaghloul, et al.. (2007). Disruption of the basal body compromises proteasomal function and perturbs intracellular Wnt response. Nature Genetics. 39(11). 1350–1360. 331 indexed citations
11.
Badano, José L., Norimasa Mitsuma, Phil Beales, & Nicholas Katsanis. (2006). The Ciliopathies: An Emerging Class of Human Genetic Disorders. Annual Review of Genomics and Human Genetics. 7(1). 125–148. 884 indexed citations breakdown →
12.
Badano, José L., Tanya M. Teslovich, & Nicholas Katsanis. (2005). The centrosome in human genetic disease. Nature Reviews Genetics. 6(3). 194–205. 194 indexed citations
13.
Kim, Jun Chul, José L. Badano, Muneer A. Esmail, et al.. (2004). The Bardet-Biedl protein BBS4 targets cargo to the pericentriolar region and is required for microtubule anchoring and cell cycle progression. Nature Genetics. 36(5). 462–470. 329 indexed citations
14.
Kulaga, Heather, Carmen C. Leitch, Erica R. Eichers, et al.. (2004). Loss of BBS proteins causes anosmia in humans and defects in olfactory cilia structure and function in the mouse. Nature Genetics. 36(9). 994–998. 270 indexed citations
15.
Beales, Philip L., José L. Badano, Alison Ross, et al.. (2003). Genetic Interaction of BBS1 Mutations with Alleles at Other BBS Loci Can Result in Non-Mendelian Bardet-Biedl Syndrome. The American Journal of Human Genetics. 72(5). 1187–1199. 182 indexed citations
16.
Badano, José L.. (2003). Heterozygous mutations in BBS1, BBS2 and BBS6 have a potential epistatic effect on Bardet-Biedl patients with two mutations at a second BBS locus. Human Molecular Genetics. 12(14). 1651–1659. 148 indexed citations
17.
Badano, José L., Stephen J. Ansley, Carmen C. Leitch, et al.. (2003). Identification of a Novel Bardet-Biedl Syndrome Protein, BBS7, That Shares Structural Features with BBS1 and BBS2. The American Journal of Human Genetics. 72(3). 650–658. 161 indexed citations
18.
Katsanis, Nicholas, Stephen J. Ansley, José L. Badano, et al.. (2001). Triallelic Inheritance in Bardet-Biedl Syndrome, a Mendelian Recessive Disorder. Science. 293(5538). 2256–2259. 438 indexed citations
19.
Wu, Yuanqing, José L. Badano, Christopher McCaskill, et al.. (2000). Haploinsufficiency of ALX4 as a Potential Cause of Parietal Foramina in the 11p11.2 Contiguous Gene–Deletion Syndrome. The American Journal of Human Genetics. 67(5). 1327–1332. 65 indexed citations
20.
Wu, Yuanqing, José L. Badano, Christopher McCaskill, et al.. (2000). Haploinsufficiency ofALX4as a Potential Cause of Parietal Foramina in the 11p11.2 Contiguous Gene–Deletion Syndrome. The American Journal of Human Genetics. 67(5). 1327–1332. 22 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