Judith L. Leatherman

1.9k total citations
21 papers, 1.3k citations indexed

About

Judith L. Leatherman is a scholar working on Molecular Biology, Genetics and Rheumatology. According to data from OpenAlex, Judith L. Leatherman has authored 21 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 7 papers in Genetics and 4 papers in Rheumatology. Recurrent topics in Judith L. Leatherman's work include Developmental Biology and Gene Regulation (9 papers), Osteoarthritis Treatment and Mechanisms (4 papers) and Pluripotent Stem Cells Research (3 papers). Judith L. Leatherman is often cited by papers focused on Developmental Biology and Gene Regulation (9 papers), Osteoarthritis Treatment and Mechanisms (4 papers) and Pluripotent Stem Cells Research (3 papers). Judith L. Leatherman collaborates with scholars based in United States and Japan. Judith L. Leatherman's co-authors include Stephen DiNardo, Thomas A. Jongens, Maurizio Pacifici, Alvin J. Chin, Eric S. Weinberg, Christina Kelly, Eiki Koyama, Eleanor B. Golden, Atsushi Shimazu and Hyun‐Duck Nah and has published in prestigious journals such as Nature Cell Biology, Development and Current Biology.

In The Last Decade

Judith L. Leatherman

21 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Judith L. Leatherman United States 16 981 334 235 174 140 21 1.3k
Lilach Gilboa Israel 17 1.0k 1.1× 287 0.9× 183 0.8× 179 1.0× 55 0.4× 23 1.3k
Ira L. Blitz United States 29 2.3k 2.3× 500 1.5× 337 1.4× 91 0.5× 95 0.7× 47 2.7k
Cornel Popovici France 23 1.1k 1.1× 331 1.0× 161 0.7× 150 0.9× 357 2.5× 51 1.8k
Alison Miyamoto United States 14 1.7k 1.7× 193 0.6× 292 1.2× 156 0.9× 51 0.4× 17 2.1k
Brian Biehs United States 22 1.8k 1.8× 540 1.6× 409 1.7× 184 1.1× 78 0.6× 27 2.6k
Alan Rawls United States 25 2.1k 2.1× 400 1.2× 279 1.2× 108 0.6× 56 0.4× 47 2.7k
Inge The United States 13 1.1k 1.1× 267 0.8× 488 2.1× 57 0.3× 116 0.8× 17 1.7k
Vincenzo Zappavigna Italy 31 2.4k 2.5× 706 2.1× 181 0.8× 182 1.0× 52 0.4× 49 2.8k
Hiroshi Akimaru Japan 20 1.8k 1.8× 412 1.2× 157 0.7× 157 0.9× 39 0.3× 31 2.2k
Deborah A. Hursh United States 16 1.5k 1.6× 264 0.8× 236 1.0× 155 0.9× 25 0.2× 29 1.8k

Countries citing papers authored by Judith L. Leatherman

Since Specialization
Citations

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

Fields of papers citing papers by Judith L. Leatherman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Judith L. Leatherman

This figure shows the co-authorship network connecting the top 25 collaborators of Judith L. Leatherman. A scholar is included among the top collaborators of Judith L. Leatherman 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 Judith L. Leatherman. Judith L. Leatherman 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.
Leatherman, Judith L., et al.. (2022). Pvr regulates cyst stem cell division in the Drosophila testis niche, and has functions distinct from Egfr. PubMed. 173. 203822–203822. 1 indexed citations
2.
Johnson, Bryan W. & Judith L. Leatherman. (2021). Merlin and expanded integrate cell signaling that regulates cyst stem cell proliferation in the Drosophila testis niche. Developmental Biology. 477. 133–144. 2 indexed citations
3.
4.
Elgin, Sarah C. R., et al.. (2016). The GEP: Crowd-Sourcing Big Data Analysis with Undergraduates. Trends in Genetics. 33(2). 81–85. 20 indexed citations
5.
Leatherman, Judith L.. (2013). Stem cells supporting other stem cells. Frontiers in Genetics. 4. 257–257. 28 indexed citations
6.
Leatherman, Judith L. & Stephen DiNardo. (2010). Germline self-renewal requires cyst stem cells and stat regulates niche adhesion in Drosophila testes. Nature Cell Biology. 12(8). 806–811. 194 indexed citations
7.
Leatherman, Judith L. & Stephen DiNardo. (2008). Zfh-1 controls somatic stem cell self-renewal in the Drosophila testis, and non-autonomously influences germline stem cell self-renewal. Developmental Biology. 319(2). 548–548. 9 indexed citations
8.
Leatherman, Judith L. & Stephen DiNardo. (2008). Zfh-1 Controls Somatic Stem Cell Self-Renewal in the Drosophila Testis and Nonautonomously Influences Germline Stem Cell Self-Renewal. Cell stem cell. 3(1). 44–54. 243 indexed citations
9.
Leatherman, Judith L. & Thomas A. Jongens. (2003). Transcriptional silencing and translational control: key features of early germline development. BioEssays. 25(4). 326–335. 76 indexed citations
10.
Leatherman, Judith L., et al.. (2002). germ cell-less Acts to Repress Transcription during the Establishment of the Drosophila Germ Cell Lineage. Current Biology. 12(19). 1681–1685. 70 indexed citations
11.
Leatherman, Judith L., Klaus H. Kaestner, & Thomas A. Jongens. (2000). Identification of a mouse germ cell-less homologue with conserved activity in Drosophila. Mechanisms of Development. 92(2). 145–153. 29 indexed citations
12.
Kelly, Christina, et al.. (2000). Maternally controlled β-catenin-mediated signaling is required for organizer formation in the zebrafish. Development. 127(18). 3899–3911. 181 indexed citations
13.
14.
Koyama, Eiki, Atsushi Shimazu, Judith L. Leatherman, et al.. (1996). Expression of syndecan‐3 and tenascin‐C: Possible involvement in periosteum development. Journal of Orthopaedic Research®. 14(3). 403–412. 47 indexed citations
15.
Koyama, Eiki, Judith L. Leatherman, Sumihare Noji, & Maurizio Pacifici. (1996). Early chick limb cartilaginous elements possess polarizing activity and expresshedgehog-related morphogenetic factors. Developmental Dynamics. 207(3). 344–364. 46 indexed citations
16.
Shimazu, Atsushi, Hyun-Duck Nah, Thorsten Kirsch, et al.. (1996). Syndecan-3 and the Control of Chondrocyte Proliferation during Endochondral Ossification. Experimental Cell Research. 229(1). 126–136. 48 indexed citations
17.
Koyama, Eiki, Judith L. Leatherman, Sumihare Noji, & Maurizio Pacifici. (1996). Polarizing Activity in Early Limb Cartilaginous Condensations. Annals of the New York Academy of Sciences. 785(1). 281–283. 2 indexed citations
18.
Koyama, Eiki, Tomoichiro Yamaai, Sachiko Iseki, et al.. (1996). Polarizing activity, Sonic hedgehog , and tooth development in embryonic and postnatal mouse. Developmental Dynamics. 206(1). 59–72. 62 indexed citations
19.
Koyama, Eiki, Judith L. Leatherman, Atsushi Shimazu, Hyun‐Duck Nah, & Maurizio Pacifici. (1995). Syndecan‐3, tenascin‐C, and the development of cartilaginous skeletal elements and joints in chick limbs. Developmental Dynamics. 203(2). 152–162. 67 indexed citations
20.
Pacifici, Maurizio, et al.. (1993). Tenascin is associated with articular cartilage development. Developmental Dynamics. 198(2). 123–134. 72 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.

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