Carmen C. Leitch

7.7k total citations
22 papers, 2.8k citations indexed

About

Carmen C. Leitch is a scholar working on Genetics, Molecular Biology and Neurology. According to data from OpenAlex, Carmen C. Leitch has authored 22 papers receiving a total of 2.8k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Genetics, 13 papers in Molecular Biology and 3 papers in Neurology. Recurrent topics in Carmen C. Leitch's work include Genetic and Kidney Cyst Diseases (15 papers), Genetic Syndromes and Imprinting (10 papers) and Hedgehog Signaling Pathway Studies (8 papers). Carmen C. Leitch is often cited by papers focused on Genetic and Kidney Cyst Diseases (15 papers), Genetic Syndromes and Imprinting (10 papers) and Hedgehog Signaling Pathway Studies (8 papers). Carmen C. Leitch collaborates with scholars based in United States, United Kingdom and Canada. Carmen C. Leitch's co-authors include José L. Badano, Nicholas Katsanis, Philip L. Beales, Norann A. Zaghloul, Stephen J. Ansley, Richard A. Lewis, Bethan E. Hoskins, Michel R. Leroux, Jun Chul Kim and Erica R. Eichers and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of Clinical Investigation.

In The Last Decade

Carmen C. Leitch

22 papers receiving 2.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Carmen C. Leitch United States 20 2.1k 2.1k 483 179 169 22 2.8k
Petra Pennekamp Germany 22 1.1k 0.5× 1.1k 0.6× 218 0.5× 153 0.9× 110 0.7× 51 2.1k
Stephen J. Ansley United States 11 2.0k 1.0× 1.9k 0.9× 411 0.9× 194 1.1× 148 0.9× 11 2.5k
Yoshiko Maeda Japan 18 1.3k 0.6× 1.4k 0.7× 216 0.4× 586 3.3× 127 0.8× 41 2.5k
Isabelle Russell‐Eggitt United Kingdom 26 1.0k 0.5× 1.1k 0.5× 219 0.5× 100 0.6× 233 1.4× 58 2.4k
Guntram Borck Germany 27 681 0.3× 876 0.4× 205 0.4× 68 0.4× 113 0.7× 65 1.7k
Ayala Frumkin Israel 22 647 0.3× 1.1k 0.5× 284 0.6× 58 0.3× 124 0.7× 49 2.1k
Victoria Mok Siu Canada 25 868 0.4× 1.3k 0.6× 149 0.3× 80 0.4× 108 0.6× 73 1.9k
Laura K. Conlin United States 27 1.6k 0.7× 1.2k 0.6× 93 0.2× 119 0.7× 160 0.9× 73 2.5k
Renaud Touraine France 25 633 0.3× 1.1k 0.5× 194 0.4× 39 0.2× 354 2.1× 93 2.0k
Arnold Munnich France 25 580 0.3× 1.6k 0.8× 196 0.4× 50 0.3× 221 1.3× 55 2.3k

Countries citing papers authored by Carmen C. Leitch

Since Specialization
Citations

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

Fields of papers citing papers by Carmen C. Leitch

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Carmen C. Leitch. 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 Carmen C. Leitch. The network helps show where Carmen C. Leitch may publish in the future.

Co-authorship network of co-authors of Carmen C. Leitch

This figure shows the co-authorship network connecting the top 25 collaborators of Carmen C. Leitch. A scholar is included among the top collaborators of Carmen C. Leitch 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 Carmen C. Leitch. Carmen C. Leitch 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.
Leitch, Carmen C., Maggie S. Matern, Christopher J. Westlake, et al.. (2019). Genomic knockout of alms1 in zebrafish recapitulates Alström syndrome and provides insight into metabolic phenotypes. Human Molecular Genetics. 28(13). 2212–2223. 12 indexed citations
2.
Edie, Sarah, Norann A. Zaghloul, Carmen C. Leitch, et al.. (2018). Survey of Human Chromosome 21 Gene Expression Effects on Early Development in Danio rerio. G3 Genes Genomes Genetics. 8(7). 2215–2223. 29 indexed citations
3.
Khan, Shahid Y., Shivakumar Vasanth, Firoz Kabir, et al.. (2016). FOXE3 contributes to Peters anomaly through transcriptional regulation of an autophagy-associated protein termed DNAJB1. Nature Communications. 7(1). 10953–10953. 36 indexed citations
4.
O’Hare, Elizabeth A., Rongze Yang, Laura M. Yerges‐Armstrong, et al.. (2016). TM6SF2 rs58542926 impacts lipid processing in liver and small intestine. Hepatology. 65(5). 1526–1542. 72 indexed citations
5.
Leitch, Carmen C., et al.. (2015). Differential effects on β-cell mass by disruption of Bardet–Biedl syndrome or Alstrom syndrome genes. Human Molecular Genetics. 25(1). 57–68. 28 indexed citations
6.
Leitch, Carmen C. & Norann A. Zaghloul. (2014). BBS4 Is Necessary for Ciliary Localization of TrkB Receptor and Activation by BDNF. PLoS ONE. 9(5). e98687–e98687. 21 indexed citations
7.
Leitch, Carmen C., et al.. (2014). Basal body proteins regulate Notch signaling via endosomal trafficking. Journal of Cell Science. 127(Pt 11). 2407–19. 78 indexed citations
8.
Liu, Yangfan P., I-Chun Tsai, Manuela Morleo, et al.. (2014). Ciliopathy proteins regulate paracrine signaling by modulating proteasomal degradation of mediators. Journal of Clinical Investigation. 124(5). 2059–2070. 72 indexed citations
9.
Renn, Cynthia L., Carmen C. Leitch, W. Cameron McGuire, et al.. (2011). Brain‐derived neurotrophic factor modulates antiretroviral‐induced mechanical allodynia in the mouse. Journal of Neuroscience Research. 89(10). 1551–1565. 26 indexed citations
10.
Zaghloul, Norann A., Yangjian Liu, Jantje M. Gerdes, et al.. (2010). Functional analyses of variants reveal a significant role for dominant negative and common alleles in oligogenic Bardet–Biedl syndrome. Proceedings of the National Academy of Sciences. 107(23). 10602–10607. 84 indexed citations
12.
Renn, Cynthia L., Carmen C. Leitch, & Susan G. Dorsey. (2009). In Vivo Evidence that Truncated Trkb.T1 Participates in Nociception. Molecular Pain. 5. 61–61. 28 indexed citations
13.
Li, Chunmei, Peter N. Inglis, Carmen C. Leitch, et al.. (2008). An Essential Role for DYF-11/MIP-T3 in Assembling Functional Intraflagellar Transport Complexes. PLoS Genetics. 4(3). e1000044–e1000044. 46 indexed citations
14.
Leitch, Carmen C., Norann A. Zaghloul, Erica E. Davis, et al.. (2008). Hypomorphic mutations in syndromic encephalocele genes are associated with Bardet-Biedl syndrome. Nature Genetics. 40(4). 443–448. 292 indexed citations
15.
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
16.
Badano, José L., Carmen C. Leitch, Stephen J. Ansley, et al.. (2005). Dissection of epistasis in oligogenic Bardet–Biedl syndrome. Nature. 439(7074). 326–330. 187 indexed citations
17.
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
18.
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
19.
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
20.
Ansley, Stephen J., José L. Badano, Oliver E. Blacque, et al.. (2003). Basal body dysfunction is a likely cause of pleiotropic Bardet–Biedl syndrome. Nature. 425(6958). 628–633. 495 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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