Isabel Martínez‐Garay

1.6k total citations
26 papers, 1.0k citations indexed

About

Isabel Martínez‐Garay is a scholar working on Molecular Biology, Genetics and Developmental Neuroscience. According to data from OpenAlex, Isabel Martínez‐Garay has authored 26 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 13 papers in Genetics and 10 papers in Developmental Neuroscience. Recurrent topics in Isabel Martínez‐Garay's work include Genetics and Neurodevelopmental Disorders (8 papers), Neurogenesis and neuroplasticity mechanisms (8 papers) and Axon Guidance and Neuronal Signaling (6 papers). Isabel Martínez‐Garay is often cited by papers focused on Genetics and Neurodevelopmental Disorders (8 papers), Neurogenesis and neuroplasticity mechanisms (8 papers) and Axon Guidance and Neuronal Signaling (6 papers). Isabel Martínez‐Garay collaborates with scholars based in United Kingdom, Spain and United States. Isabel Martínez‐Garay's co-authors include Santos J. Franco, Cristina Gil‐Sanz, Ulrich Müller, Sarah Harkins‐Perry, Ana Espinosa, Cynthia De la Garza‐Ramos, Kerstin Kutsche, Hans‐Hermann Gerdes, Amin Rustom and Zoltán Molnár and has published in prestigious journals such as Science, Neuron and PLoS ONE.

In The Last Decade

Isabel Martínez‐Garay

25 papers receiving 1.0k citations

Peers

Countries citing papers authored by Isabel Martínez‐Garay

Since Specialization

Citations

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

Fields of papers citing papers by Isabel Martínez‐Garay

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Isabel Martínez‐Garay. 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 Isabel Martínez‐Garay. The network helps show where Isabel Martínez‐Garay may publish in the future.

Co-authorship network of co-authors of Isabel Martínez‐Garay

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Proteomic analysis of the developing mammalian brain links PCDH19 to the Wnt/β-catenin signalling pathway 2024 ·Molecular Psychiatry ·(unknown), Alison Gardner, Clare L. van Eyk, (unknown), Paul Q. Thomas, (unknown), Lachlan A. Jolly, Isabel Martínez‐Garay, (unknown), Karthik Shantharam Kamath, Raman Kumar, Jozef Gécz	4
2	Transcriptional control of embryonic and adult neural progenitor activity 2023 ·Frontiers in Neuroscience ·Niharika Singh, Florian A. Siebzehnrübl, Isabel Martínez‐Garay	0
3	The placenta protects the fetal circulation from anxiety-driven elevations in maternal serum levels of brain-derived neurotrophic factor 2021 ·Translational Psychiatry ·Hayley Dingsdale, Xinsheng Nan, (unknown), Annett Mueller, (unknown), Pedro Chacón, Isabel Martínez‐Garay, Cédric Ghevaert, Yves‐Alain Barde, Rosalind M. John	14
4	Neuregulin-4 Is Required for Maintaining Soma Size of Pyramidal Neurons in the Motor Cortex 2021 ·eNeuro ·(unknown), (unknown), Stéphane J. Baudouin, Isabel Martínez‐Garay, Alun M. Davies	6
5	Molecular Mechanisms of Cadherin Function During Cortical Migration 2020 ·Frontiers in Cell and Developmental Biology ·Isabel Martínez‐Garay	18
6	Dbx1-Derived Pyramidal Neurons Are Generated Locally in the Developing Murine Neocortex 2018 ·Frontiers in Neuroscience ·(unknown), Isabel Martínez‐Garay, Juan Manuel Encinas, Zoltán Molnár, Fernando García‐Moreno	14
7	A tubulin alpha 8 mouse knockout model indicates a likely role in spermatogenesis but not in brain development 2017 ·PLoS ONE ·Christine P. Diggle, Isabel Martínez‐Garay, Zoltán Molnár, Martin H. Brinkworth, Ed White, Ewan D. Fowler, Ruth Hughes, Bruce E. Hayward, Ian Carr, Christopher M. Watson, Laura A. Crinnion, Aruna Asipu, Ben Woodman, P. Louise Coletta, Alexander F. Markham, T. Neil Dear, David T. Bonthron, Michelle Peckham, Ewan E. Morrison, Eamonn Sheridan	23
8	Normal radial migration and lamination are maintained in dyslexia-susceptibility candidate gene homolog Kiaa0319 knockout mice 2016 ·Brain Structure and Function ·Isabel Martínez‐Garay, (unknown), Zoe G. Holloway, (unknown), Daniel Lyngholm, Tomasz Schneider, Timothy Donnison, Simon J. B. Butt, Anthony P. Monaco, Zoltán Molnár, Antonio Velayos‐Baeza	13
9	Lineage Tracing Using Cux2-Cre and Cux2-CreERT2 Mice 2015 ·Neuron ·Cristina Gil‐Sanz, Ana Espinosa, (unknown), (unknown), Christopher L. Cunningham, Isabel Martínez‐Garay, Hongkui Zeng, Santos J. Franco, Ulrich Müller	62
10	Cajal-Retzius Cells Instruct Neuronal Migration by Coincidence Signaling between Secreted and Contact-Dependent Guidance Cues 2013 ·Neuron ·Cristina Gil‐Sanz, Santos J. Franco, Isabel Martínez‐Garay, Ana Espinosa, Sarah Harkins‐Perry, Ulrich Müller	115
11	Fate-Restricted Neural Progenitors in the Mammalian Cerebral Cortex 2012 ·Science ·Santos J. Franco, Cristina Gil‐Sanz, Isabel Martínez‐Garay, Ana Espinosa, Sarah Harkins‐Perry, Cynthia De la Garza‐Ramos, Ulrich Müller	231
12	Reelin Regulates Cadherin Function via Dab1/Rap1 to Control Neuronal Migration and Lamination in the Neocortex 2011 ·Neuron ·Santos J. Franco, Isabel Martínez‐Garay, Cristina Gil‐Sanz, Sarah Harkins‐Perry, Ulrich Müller	263
13	Duplication of the Williams–Beuren critical region: case report and further delineation of the phenotypic spectrum 2009 ·BMJ Case Reports ·Carmen Orellana, (unknown), Sandra Monfort, Marion Rosello, Silvestre Oltra, Irene Ferrer, (unknown), Isabel Martínez‐Garay, Francisco Martı́nez	1
14	Duplication of the Williams–Beuren critical region: case report and further delineation of the phenotypic spectrum 2009 ·BMJ Case Reports ·Carmen Orellana, (unknown), Sandra Monfort, Mónica Rosello, Silvestre Oltra, Irene Ferrer, (unknown), Isabel Martínez‐Garay, Francisco Martı́nez	2
15	Gypsy endogenous retrovirus maintains potential infectivity in several species of Drosophilids 2008 ·BMC Evolutionary Biology ·José Vicente Llorens, Jonathan B. Clark, Isabel Martínez‐Garay, Sirena Soriano, Rosa de Llanos, M. J. Martínez-Sebastián	16
16	Deleción subtelomérica 9qter: definición del síndrome y origen parental en 2 pacientes 2007 ·Medicina Clínica ·Mónica Rosello, Sandra Monfort, Carmen Orellana, Silvestre Oltra, Isabel Martínez‐Garay, Francisco Martı́nez	4
17	A two base pair deletion in the PQBP1 gene is associated with microphthalmia, microcephaly, and mental retardation 2006 ·European Journal of Human Genetics ·Isabel Martínez‐Garay, Miguel Tomás Vila, Silvestre Oltra, Juliane Ramser, María Dolores Moltó, Félix Prieto, Alfons Meindl, Kerstin Kutsche, Francisco Martı́nez	28
18	The novel centrosomal associated protein CEP55 is present in the spindle midzone and the midbody 2006 ·Genomics ·Isabel Martínez‐Garay, Amin Rustom, Hans‐Hermann Gerdes, Kerstin Kutsche	68
19	Localization of MRX82: A new nonsyndromic X‐linked mental retardation locus to Xq24‐q25 in a Basque family 2004 ·American Journal of Medical Genetics Part A ·Francisco Martı́nez, Isabel Martínez‐Garay, Silvestre Oltra, María Dolores Moltó, Carmen Orellana, Sandra Monfort, Félix Prieto, Isabel Tejada	5
20	Intronic L1 insertion and F268S, novel mutations in RPS6KA3 (RSK2) causing Coffin–Lowry syndrome 2003 ·Clinical Genetics ·Isabel Martínez‐Garay, (unknown), Silvestre Oltra, Carmen Orellana, A. Palomeque, María Dolores Moltó, F. Prieto, Francisco Martı́nez	21

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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