Inmaculada Canal

1.6k total citations · 1 hit paper
18 papers, 1.3k citations indexed

About

Inmaculada Canal is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Inmaculada Canal has authored 18 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 10 papers in Cellular and Molecular Neuroscience and 5 papers in Genetics. Recurrent topics in Inmaculada Canal's work include Neurobiology and Insect Physiology Research (9 papers), Developmental Biology and Gene Regulation (5 papers) and Genetics, Aging, and Longevity in Model Organisms (3 papers). Inmaculada Canal is often cited by papers focused on Neurobiology and Insect Physiology Research (9 papers), Developmental Biology and Gene Regulation (5 papers) and Genetics, Aging, and Longevity in Model Organisms (3 papers). Inmaculada Canal collaborates with scholars based in Spain, United States and Germany. Inmaculada Canal's co-authors include Enrique Turiégano, Juan Botas, Olaf Pongs, Laura Torroja, Huda Y. Zoghbi, Pamela J. Skinner, Francisco J. Tejedor, Pedro Martı́nez, Xin‐Ran Zhu and Arnd Baumann and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Neuron.

In The Last Decade

Inmaculada Canal

18 papers receiving 1.3k citations

Hit Papers

Identification of genes that modify ataxin-1-induced neur... 2000 2026 2008 2017 2000 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Inmaculada Canal Spain 14 901 554 258 180 170 18 1.3k
Xin‐Ran Zhu Germany 17 862 1.0× 748 1.4× 198 0.8× 279 1.6× 165 1.0× 27 1.6k
Changan Jiang China 14 1.1k 1.2× 759 1.4× 195 0.8× 200 1.1× 62 0.4× 21 1.7k
Kuchuan Chen United States 10 668 0.7× 417 0.8× 130 0.5× 250 1.4× 32 0.2× 10 1.1k
Ann Becker United States 10 756 0.8× 604 1.1× 105 0.4× 260 1.4× 62 0.4× 18 1.2k
Amanda Charlesworth United States 22 898 1.0× 188 0.3× 83 0.3× 103 0.6× 173 1.0× 33 1.4k
David Kapfhamer United States 18 575 0.6× 299 0.5× 178 0.7× 324 1.8× 30 0.2× 23 1.1k
Benjamin A. Eaton United States 18 769 0.9× 457 0.8× 94 0.4× 399 2.2× 56 0.3× 29 1.3k
Michel Villaz France 27 1.2k 1.3× 581 1.0× 71 0.3× 157 0.9× 221 1.3× 43 1.8k
Dorota Skowronska‐Krawczyk United States 22 1.1k 1.2× 225 0.4× 196 0.8× 172 1.0× 36 0.2× 58 1.5k
M. E. Greenberg United States 9 1.7k 1.9× 624 1.1× 272 1.1× 141 0.8× 22 0.1× 9 2.2k

Countries citing papers authored by Inmaculada Canal

Since Specialization
Citations

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

Fields of papers citing papers by Inmaculada Canal

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Inmaculada Canal

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

All Works

18 of 18 papers shown
1.
Turiégano, Enrique, et al.. (2017). Presynaptic Aβ40 prevents synapse addition in the adult Drosophila neuromuscular junction. PLoS ONE. 12(5). e0177541–e0177541. 5 indexed citations
2.
Andrés, Marta, Enrique Turiégano, Martin C. Göpfert, Inmaculada Canal, & Laura Torroja. (2014). The Extracellular Matrix Protein Artichoke Is Required for Integrity of Ciliated Mechanosensory and Chemosensory Organs inDrosophilaEmbryos. Genetics. 196(4). 1091–1102. 15 indexed citations
3.
Turiégano, Enrique, et al.. (2012). Ih Current Is Necessary to Maintain Normal Dopamine Fluctuations and Sleep Consolidation in Drosophila. PLoS ONE. 7(5). e36477–e36477. 19 indexed citations
4.
Turiégano, Enrique, Ignacio Cobeta, Miguel Pita, Laura Torroja, & Inmaculada Canal. (2012). Effect of Drosophila melanogaster Female Size on Male Mating Success. Journal of Insect Behavior. 26(1). 89–100. 12 indexed citations
5.
Losada‐Pérez, María, et al.. (2011). A targeted genetic screen identifies crucial players in the specification of the Drosophila abdominal Capaergic neurons. Mechanisms of Development. 128(3-4). 208–221. 13 indexed citations
6.
Ruiz, Mario, Diego Sánchez, Inmaculada Canal, Ángel Acebes, & Marı́a D. Ganfornina. (2011). Sex-dependent modulation of longevity by two Drosophila homologues of human Apolipoprotein D, GLaz and NLaz. Experimental Gerontology. 46(7). 579–589. 30 indexed citations
7.
Herrero, Pilar, Marta Magariños, Isabel Molina, et al.. (2007). Squeeze involvement in the specification of Drosophila leucokinergic neurons: Different regulatory mechanisms endow the same neuropeptide selection. Mechanisms of Development. 124(6). 427–440. 12 indexed citations
8.
Sánchez, Diego, Laura Torroja, Inmaculada Canal, et al.. (2006). Loss of Glial Lazarillo, a Homolog of Apolipoprotein D, Reduces Lifespan and Stress Resistance in Drosophila. Current Biology. 16(7). 680–686. 115 indexed citations
9.
Herrero, Pilar, Marta Magariños, Laura Torroja, & Inmaculada Canal. (2003). Neurosecretory identity conferred by the apterous gene: Lateral horn leucokinin neurons in Drosophila. The Journal of Comparative Neurology. 457(2). 123–132. 28 indexed citations
10.
Naïmi, Benyoussef, Andrew Harrison, Upendra Nongthomba, et al.. (2001). A Tropomyosin-2 Mutation Suppresses a Troponin I Myopathy inDrosophila. Molecular Biology of the Cell. 12(5). 1529–1539. 31 indexed citations
11.
Fernández-Fúnez, Pedro, Béatrice Gouyon, Pedro Martı́nez, et al.. (2000). Identification of genes that modify ataxin-1-induced neurodegeneration. Nature. 408(6808). 101–106. 510 indexed citations breakdown →
12.
Canal, Inmaculada, et al.. (1999). The Haplolethal Region at the 16F Gene Cluster of Drosophila melanogaster: Structure and Function. Genetics. 151(1). 163–175. 19 indexed citations
13.
Rincón-Limas, Diego E., Inmaculada Canal, Manuel Calleja, et al.. (1999). Conservation of the expression and function of apterous orthologs in Drosophila and mammals. Proceedings of the National Academy of Sciences. 96(5). 2165–2170. 72 indexed citations
14.
Canal, Inmaculada, Ángel Acebes, & Alberto Ferrús. (1998). Single Neuron Mosaics of theDrosophila gigasMutant Project beyond Normal Targets and Modify Behavior. Journal of Neuroscience. 18(3). 999–1008. 27 indexed citations
15.
Canal, Inmaculada, et al.. (1995). Functional recovery of troponin I in a Drosophila heldup mutant after a second site mutation.. Molecular Biology of the Cell. 6(11). 1433–1441. 17 indexed citations
16.
Tejedor, Francisco J., Xin‐Ran Zhu, A. Ackermann, et al.. (1995). minibrain: A new protein kinase family involved in postembryonic neurogenesis in Drosophila. Neuron. 14(2). 287–301. 310 indexed citations
17.
Canal, Inmaculada, et al.. (1994). The behaving brain of a fly. Trends in Neurosciences. 17(11). 479–486. 8 indexed citations
18.
Barbas, Julio A., Joan Galcerán, José Luís de la Pompa, et al.. (1991). Troponin I is encoded in the haplolethal region of the Shaker gene complex of Drosophila.. Genes & Development. 5(1). 132–140. 51 indexed citations

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