Miguel L. Concha

5.9k total citations · 1 hit paper
72 papers, 4.4k citations indexed

About

Miguel L. Concha is a scholar working on Molecular Biology, Cell Biology and Cognitive Neuroscience. According to data from OpenAlex, Miguel L. Concha has authored 72 papers receiving a total of 4.4k indexed citations (citations by other indexed papers that have themselves been cited), including 38 papers in Molecular Biology, 22 papers in Cell Biology and 17 papers in Cognitive Neuroscience. Recurrent topics in Miguel L. Concha's work include Developmental Biology and Gene Regulation (23 papers), Hemispheric Asymmetry in Neuroscience (15 papers) and Zebrafish Biomedical Research Applications (12 papers). Miguel L. Concha is often cited by papers focused on Developmental Biology and Gene Regulation (23 papers), Hemispheric Asymmetry in Neuroscience (15 papers) and Zebrafish Biomedical Research Applications (12 papers). Miguel L. Concha collaborates with scholars based in Chile, United Kingdom and Germany. Miguel L. Concha's co-authors include Stephen W. Wilson, Masazumi Tada, Carl‐Philipp Heisenberg, Robert Geisler, Derek L. Stemple, Richard J. Adams, Gerd-Jörg Rauch, Leonor Saúde, James C. Smith and Claire Russell and has published in prestigious journals such as Nature, Nature Communications and Neuron.

In The Last Decade

Miguel L. Concha

67 papers receiving 4.3k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Silberblick/Wnt11 mediates convergent extension movements during zebrafish gastrulation

2000 839 citations Masazumi Tada, Miguel L. Concha et al. profile →

Peers

Miguel L. Concha

MB

CB

CN

CMN

GENET

Marnie E. Halpern United States

Jonathan D. W. Clarke United Kingdom

Teresa Nicolson United States

Rebecca D. Burdine United States

Patrick Blader France

Shigenori Nonaka Japan

Ramón Anadón Spain

Filippo M. Rijli France

Enrique Amaya United Kingdom

Isaac H. Bianco United Kingdom

Marnie E. Halpern United States

Miguel L. Concha

5.5k ×1.8

MB

2.4k ×1.7

CB

657 ×0.9

CN

998 ×1.4

CMN

1.3k ×2.7

GENET

Citations per year, relative to Miguel L. Concha Miguel L. Concha (= 1×) peers Marnie E. Halpern

Countries citing papers authored by Miguel L. Concha

Since Specialization

Citations

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

Fields of papers citing papers by Miguel L. Concha

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Miguel L. Concha

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

1.

Navarro, Carlos, Germán Reig, Eduardo Pulgar, et al.. (2023). VolumePeeler: a novel FIJI plugin for geometric tissue peeling to improve visualization and quantification of 3D image stacks. BMC Bioinformatics. 24(1). 283–283. 1 indexed citations

2.

Medinas, Danilo B., et al.. (2023). Immunohistochemical characterisation of the adult Nothobranchius furzeri intestine. Cell and Tissue Research. 395(1). 21–38. 2 indexed citations

3.

Henny, Pablo, et al.. (2021). Organization of the Catecholaminergic System in the Short-Lived Fish Nothobranchius furzeri. Frontiers in Neuroanatomy. 15. 728720–728720. 8 indexed citations

4.

Concha, Miguel L.. (2020). A tale of turns and cycles guiding to neural crest migration - an interview with Roberto Mayor. The International Journal of Developmental Biology. 65(1-2-3). 123–129.

5.

Concha, Miguel L., et al.. (2020). Developmental Biology in Chile: historical perspectives and future challenges. The International Journal of Developmental Biology. 65(1-2-3). 29–47. 1 indexed citations

6.

Stanic, Karen, Germán Reig, Juan C. Opazo, et al.. (2019). The Reprimo gene family member, reprimo-like (rprml), is required for blood development in embryonic zebrafish. Scientific Reports. 9(1). 7131–7131. 4 indexed citations

7.

Reig, Germán, Mauricio Cerda, Néstor Sepúlveda, et al.. (2017). Extra-embryonic tissue spreading directs early embryo morphogenesis in killifish. Nature Communications. 8(1). 15431–15431. 31 indexed citations

8.

Concha, Miguel L.. (2016). An evolutionary perspective on habenular asymmetry in humans. 1(8). 44–50. 4 indexed citations

9.

Guerrero, Néstor, et al.. (2016). Changes in neural circuitry associated with depression at pre-clinical, pre-motor and early motor phases of Parkinson's disease. Parkinsonism & Related Disorders. 35. 17–24. 47 indexed citations

10.

Dı́az, Eugenia, et al.. (2011). Morphologic and immunohistochemical organization of the human habenular complex. The Journal of Comparative Neurology. 519(18). 3727–3747. 34 indexed citations

11.

Regan, Jennifer C., Miguel L. Concha, Myriam Roussigné, Claire Russell, & Stephen W. Wilson. (2009). An Fgf8-Dependent Bistable Cell Migratory Event Establishes CNS Asymmetry. Neuron. 61(1). 27–34. 70 indexed citations

12.

Härtel, Steffen, et al.. (2006). 3D morpho-topological analysis of asymmetric neuronal morphogenesis in developing zebrafish. 215–220. 11 indexed citations

13.

Dagnino‐Subiabre, Alexies, Juan Orellana, Carlos Carmona‐Fontaine, et al.. (2006). Chronic stress decreases the expression of sympathetic markers in the pineal gland and increases plasma melatonin concentration in rats. Journal of Neurochemistry. 97(5). 1279–1287. 34 indexed citations

14.

Aizawa, Hidenori, Isaac H. Bianco, Toshio Miyashita, et al.. (2005). Laterotopic Representation of Left-Right Information onto the Dorso-Ventral Axis of a Zebrafish Midbrain Target Nucleus. Current Biology. 15(3). 238–243. 174 indexed citations

15.

Teraoka, Hiroki, Claire Russell, Jennifer C. Regan, et al.. (2004). Hedgehog and Fgf signaling pathways regulate the development of tphR‐expressing serotonergic raphe neurons in zebrafish embryos. Journal of Neurobiology. 60(3). 275–288. 68 indexed citations

16.

Concha, Miguel L.. (2004). The dorsal diencephalic conduction system of zebrafish as a model of vertebrate brain lateralisation. Neuroreport. 15(12). 1843–1846. 20 indexed citations

17.

Concha, Miguel L. & Stephen W. Wilson. (2001). Asymmetry in the epithalamus of vertebrates. Journal of Anatomy. 199(1-2). 63–84. 215 indexed citations

18.

Tada, Masazumi & Miguel L. Concha. (2001). Vertebrate gastrulation: Calcium waves orchestrate cell movements. Current Biology. 11(12). R470–R472. 22 indexed citations

19.

Röhr, Klaus & Miguel L. Concha. (2000). Expression of nk2.1a during early development of the thyroid gland in zebrafish. Mechanisms of Development. 95(1-2). 267–270. 77 indexed citations

20.

Mpodozis, Jorge, Juan‐Carlos Letelier, Miguel L. Concha, & Humberto R. Maturana. (1995). Conduction velocity groups in the retino-tectal and retino-thalamic visual pathways of the pigeon (Columba Livia). International Journal of Neuroscience. 81(3-4). 123–136. 24 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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