Esther Geán

839 total citations
20 papers, 434 citations indexed

About

Esther Geán is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Esther Geán has authored 20 papers receiving a total of 434 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 11 papers in Genetics and 3 papers in Cellular and Molecular Neuroscience. Recurrent topics in Esther Geán's work include Hedgehog Signaling Pathway Studies (4 papers), Epigenetics and DNA Methylation (4 papers) and Photoreceptor and optogenetics research (3 papers). Esther Geán is often cited by papers focused on Hedgehog Signaling Pathway Studies (4 papers), Epigenetics and DNA Methylation (4 papers) and Photoreceptor and optogenetics research (3 papers). Esther Geán collaborates with scholars based in Spain, United Kingdom and Argentina. Esther Geán's co-authors include Pablo Lapunzina, Miguel Carballo, Valeria Romanelli, Loreto Martorell, María Pacheco, José A. Caparrós‐Martín, Víctor L. Ruiz‐Pérez, Antonio Pérez Aytés, Judith A. Goodship and Eulalia Valencia and has published in prestigious journals such as Scientific Reports, Human Molecular Genetics and Developmental Medicine & Child Neurology.

In The Last Decade

Esther Geán

20 papers receiving 408 citations

Peers

Esther Geán

GENET

PPCH

OPHTH

SURGE

C. Pressman United States

Fernando Santos‐Simarro Spain

Maria Luigia Cavaliere Italy

Francesco Benedicenti Italy

V Der Kaloustian United States

Elizabeth Wohler United States

Rebecca C. Tyler United States

Chad Haldeman‐Englert United States

Satoru Sakazume Japan

Oscar F. Chacón‐Camacho Mexico

C. Pressman United States

Esther Geán

533 ×1.8

196 ×0.8

GENET

20 ×0.3

PPCH

54 ×1.3

OPHTH

40 ×1.0

SURGE

Citations per year, relative to Esther Geán Esther Geán (= 1×) peers C. Pressman

Countries citing papers authored by Esther Geán

Since Specialization

Citations

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

Fields of papers citing papers by Esther Geán

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Esther Geán

This figure shows the co-authorship network connecting the top 25 collaborators of Esther Geán. A scholar is included among the top collaborators of Esther Geán 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 Esther Geán. Esther Geán 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

Vidal, Francesca, et al.. (2017). An exploratory study of predisposing genetic factors for DiGeorge/velocardiofacial syndrome. Scientific Reports. 7(1). 40031–40031. 9 indexed citations

Geán, Esther, Àngela Deyà‐Martínez, Ana Esteve‐Solé, et al.. (2016). Humoral deficiency in three paediatric patients with genetic diseases. Allergologia et Immunopathologia. 44(3). 257–262. 4 indexed citations

Molina, Òscar, et al.. (2014). Deletions and duplications of the 22q11.2 region in spermatozoa from DiGeorge/velocardiofacial fathers. Molecular Cytogenetics. 7(1). 86–86. 18 indexed citations

Caparrós‐Martín, José A., Eulalia Valencia, María Pacheco, et al.. (2012). The ciliary Evc/Evc2 complex interacts with Smo and controls Hedgehog pathway activity in chondrocytes by regulating Sufu/Gli3 dissociation and Gli3 trafficking in primary cilia. Human Molecular Genetics. 22(1). 124–139. 84 indexed citations

Romanelli, Valeria, Víctor Martínez‐Glez, Mario F. Fraga, et al.. (2011). Beckwith–Wiedemann syndrome and uniparental disomy 11p: fine mapping of the recombination breakpoints and evaluation of several techniques. European Journal of Human Genetics. 19(4). 416–421. 36 indexed citations

Lapunzina, Pablo, Jennifer Gentile, Nina Tolkoff‐Rubin, et al.. (2011). Adults with Sotos syndrome: Review of 21 adults with molecularly confirmed NSD1 alterations, including a detailed case report of the oldest person. American Journal of Medical Genetics Part A. 155(9). 2105–2111. 23 indexed citations

Martínez‐Glez, Víctor, Valeria Romanelli, María Ángeles Mori, et al.. (2010). Macrocephaly–capillary malformation: Analysis of 13 patients and review of the diagnostic criteria. American Journal of Medical Genetics Part A. 152A(12). 3101–3106. 38 indexed citations

Mora, Jaume, María del Mar Pérez Gómez, Esther Geán, et al.. (2009). Axenfeld–Rieger ocular anomaly and retinoblastoma caused by constitutional chromosome 13q deletion. Pediatric Blood & Cancer. 54(3). 480–482. 5 indexed citations

Vicente, Asunción, et al.. (2009). Phylloid Hypomelanosis and Mosaic Partial Trisomy 13. Archives of Dermatology. 145(5). 576–8. 22 indexed citations

10.

Krauel, Lucas, et al.. (2008). Van der Woude Syndrome and Lower Lip Pits Treatment. Journal of Oral and Maxillofacial Surgery. 66(3). 589–592. 15 indexed citations

11.

García‐Cazorla, Àngels, et al.. (2004). White matter alterations associated with chromosomal disorders. Developmental Medicine & Child Neurology. 46(3). 148–53. 20 indexed citations

12.

García‐Cazorla, Àngels, et al.. (2004). White matter alterations associated with chromosomal disorders. Developmental Medicine & Child Neurology. 46(3). 148–153. 17 indexed citations

13.

Geán, Esther, et al.. (2004). Oral manifestations in Ellis-van Creveld syndrome: report of five cases.. PubMed. 26(3). 277–82. 48 indexed citations

14.

Armstrong, Judith, M. Pineda, Esther Geán, et al.. (2002). Prenatal Diagnosis in Rett Syndrome. Fetal Diagnosis and Therapy. 17(4). 200–204. 2 indexed citations

15.

Geán, Esther, et al.. (1999). [The Ellis-van Creveld syndrome (chondroectodermal dysplasia). Apropos a clinical case].. PubMed. 50(1). 74–6. 5 indexed citations

16.

Geán, Esther, et al.. (1996). [Identification of Arg-135-Leu mutation in the rhodopsin gene in a family with autosomal dominant retinitis pigmentosa].. PubMed. 106(6). 219–21. 1 indexed citations

17.

Póo, Pilar, et al.. (1996). [Ataxia telangiectasia: review of 13 new cases].. PubMed. 24(125). 77–80. 6 indexed citations

18.

Serra, Alicia, et al.. (1995). A point mutation in the RDS-peripherin gene in a Spanish family with central areolar choroidal dystrophy. Ophthalmic Genetics. 16(2). 39–44. 47 indexed citations

19.

Geán, Esther, et al.. (1994). A missense mutation (211His-Arg) and a silent (160Thr) mutation within the rhodopsin gene in a Spanish autosomal dominant retinitis pigmentosa family. Human Molecular Genetics. 3(1). 195–196. 20 indexed citations

20.

Geán, Esther, et al.. (1994). Identification of a novel rhodopsin mutation (Met-44-Thr) in a simplex case of retinitis pigmentosa. Human Genetics. 94(3). 283–6. 14 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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