Ibis Menéndez

1.4k total citations
20 papers, 776 citations indexed

About

Ibis Menéndez is a scholar working on Molecular Biology, Sensory Systems and Ophthalmology. According to data from OpenAlex, Ibis Menéndez has authored 20 papers receiving a total of 776 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 6 papers in Sensory Systems and 5 papers in Ophthalmology. Recurrent topics in Ibis Menéndez's work include Hearing, Cochlea, Tinnitus, Genetics (6 papers), Cancer-related Molecular Pathways (5 papers) and Ocular Oncology and Treatments (5 papers). Ibis Menéndez is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (6 papers), Cancer-related Molecular Pathways (5 papers) and Ocular Oncology and Treatments (5 papers). Ibis Menéndez collaborates with scholars based in United States, Cuba and Spain. Ibis Menéndez's co-authors include Manuela Villamar, Felipe Moreno, Ignacio del Castillo, Araceli Álvarez, Dolores Tellerı́a, Miguel A. Moreno‐Pelayo, Francisco Castillo, Mustafa Tekin, Joseph Foster and Filiz Başak Cengiz and has published in prestigious journals such as New England Journal of Medicine, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Ibis Menéndez

18 papers receiving 766 citations

Peers

Countries citing papers authored by Ibis Menéndez

Since Specialization

Citations

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

Fields of papers citing papers by Ibis Menéndez

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ibis Menéndez

This figure shows the co-authorship network connecting the top 25 collaborators of Ibis Menéndez. A scholar is included among the top collaborators of Ibis Menéndez 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 Ibis Menéndez. Ibis Menéndez 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	Novel EYA1 variants causing Branchio-oto-renal syndrome 2017 ·International Journal of Pediatric Otorhinolaryngology ·(unknown), (unknown), Selçuk Arslan, (unknown), Hakan Gürkan, Selma Demır, Reza Maroofian, (unknown), (unknown), (unknown), Nursel Elçioğlu, Ibis Menéndez, Mahdiyeh Behnam, Joseph Foster, Shengru Guo, (unknown), Filiz Başak Cengiz, Duygu Duman, Güney Bademci, Mustafa Tekin	15
2	Dominant deafness–onychodystrophy syndrome caused by an ATP6V1B2 mutation 2017 ·Clinical Case Reports ·Ibis Menéndez, (unknown), (unknown), (unknown), Joseph Foster, Filiz Başak Cengiz, Güney Bademci, Mustafa Tekin	22
3	Targeted Resequencing of Deafness Genes Reveals a FounderMYO15AVariant in Northeastern Brazil 2016 ·Annals of Human Genetics ·(unknown), Güney Bademci, Angelina Xavier Acosta, Têmis Maria Félix, Filiz Başak Cengiz, Joseph Foster, (unknown), Ibis Menéndez, (unknown), Demet Tekin, Susan H. Blanton, Kiyoko Abe‐Sandes, Xue Zhong Liu, Mustafa Tekin	14
4	Novel domain-specific POU3F4 mutations are associated with X-linked deafness: examples from different populations 2015 ·BMC Medical Genetics ·Güney Bademci, Akeem O. Lasisi, Kemal O. Yariz, Paola Montenegro, Ibis Menéndez, (unknown), (unknown), (unknown), (unknown), Susan H. Blanton, Suat Fítöz, Armağan İncesulu, Levent Sennaroğlu, Mustafa Tekin	19
5	A Mayan founder mutation is a common cause of deafness in Guatemala 2015 ·Clinical Genetics ·(unknown), Ibis Menéndez, Mariana Herrera Piñero, (unknown), (unknown), Fausto Maldonado, Laura Rosales, (unknown), (unknown), D. Alvarez, Joseph Foster, Shengru Guo, Susan H. Blanton, Güney Bademci, Mustafa Tekin	18
6	An Amino Acid Deletion in SZT2 in a Family with Non-Syndromic Intellectual Disability 2013 ·PLoS ONE ·(unknown), Kemal O. Yariz, David Ross, Joseph Foster, Ibis Menéndez, Mustafa Tekin	25
7	Correction: Whole-Exome Sequencing Efficiently Detects Rare Mutations in Autosomal Recessive Nonsyndromic Hearing Loss 2013 ·PLoS ONE ·Oscar Diaz‐Horta, Duygu Duman, Joseph Foster, (unknown), Michael Gonzalez, Nejat Mahdieh, (unknown), Mortaza Bonyadi, (unknown), Ibis Menéndez, (unknown), Yvonne J. K. Edwards, (unknown), Susan H. Blanton, Mustafa Tekin	7
8	Whole-Exome Sequencing Efficiently Detects Rare Mutations in Autosomal Recessive Nonsyndromic Hearing Loss 2012 ·PLoS ONE ·Oscar Diaz‐Horta, Duygu Duman, Joseph Foster, Aslı Sırmacı, Michael Gonzalez, Nejat Mahdieh, (unknown), Mortaza Bonyadi, Filiz Başak Cengiz, Ibis Menéndez, (unknown), Yvonne J. K. Edwards, Stephan Züchner, Susan H. Blanton, Mustafa Tekin	127
9	Unique spectrum of GJB2 mutations in Mexico 2012 ·International Journal of Pediatric Otorhinolaryngology ·María de la Luz Arenas‐Sordo, Ibis Menéndez, Edgar Hernández‐Zamora, Aslı Sırmacı, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Mustafa Tekin	16
10	Pathogenic validation of unique germline intronic variants ofRB1 in retinoblastoma patients using minigenes 2007 ·Human Mutation ·Angelo Gámez‐Pozo, Itziar Palacios, Milica Kontić, Ibis Menéndez, (unknown), Purificación García‐Miguel, (unknown), Ángel Pestaña, Javier Alonso	11
11	Diagnóstico molecular del retinoblastoma: epidemiología molecular y consejo genético 2006 ·Medicina Clínica ·Javier Alonso, Itziar Palacios, Angelo Gámez‐Pozo, (unknown), Helena Frayle, Ibis Menéndez, Milica Kontić, Purificación García‐Miguel, Ana Méndez‐Echevarría, (unknown), (unknown), Constantino Sábado, Aurora Navajas, (unknown), (unknown), (unknown), Jordi Rosell, Ángel Pestaña	3
12	Two independent RB1‐inactivating mutations in peripheral blood DNA of a hereditary retinoblastoma patient 2004 ·Genes Chromosomes and Cancer ·Javier Alonso, Ibis Menéndez, Andrés López, Helena Frayle, (unknown), Ángel Pestaña	0
13	Identification of 26 new constitutionalRB1gene mutations in Spanish, Colombian, and Cuban retinoblastoma patients 2004 ·Human Mutation ·Javier Alonso, Helena Frayle, Ibis Menéndez, Andrés López, Purificación García‐Miguel, (unknown), (unknown), M. Vendrell, Aurora Navajas, (unknown), (unknown), (unknown), (unknown), Itziar Palacios, Ángel Pestaña	25
14	El Retinoblastoma: paradigma del cáncer hereditario 2002 ·SHILAP Revista de lepidopterología ·Ibis Menéndez, Marta Puig, (unknown)	1
15	A Deletion Involving the Connexin 30 Gene in Nonsyndromic Hearing Impairment 2002 ·New England Journal of Medicine ·Ignacio del Castillo, Manuela Villamar, Miguel A. Moreno‐Pelayo, Francisco Castillo, Araceli Álvarez, Dolores Tellerı́a, Ibis Menéndez, Felipe Moreno	459
16	Mutaciones del gen de la conexina 26 (GJB2) en familias cubanas con sorderas no sindrómicas autosómicas recesivas 2001 ·SHILAP Revista de lepidopterología ·Ibis Menéndez, Ignacio del Castillo, (unknown), Manuela Villamar, (unknown), (unknown), Felipe Moreno	6
17	Alternativas preventivas en cáncer de mama 2000 ·(unknown), (unknown), Ibis Menéndez, (unknown)	3
18	Sorderas neurosensoriales no sindrómicas: Análisis de la herencia en 10 familias 1998 ·SHILAP Revista de lepidopterología ·Ibis Menéndez, (unknown), (unknown), (unknown)	3
19	[11q distal trisomy due to a familial 11;18 translocation]. 1990 ·PubMed ·Ibis Menéndez, Humberto Cantú Rivera, (unknown), (unknown), Manuel Jiménez‐Estrada	2
20	Dermatoglyphics in Saethre-Chotzen syndrome: a family study. 1983 ·PubMed ·(unknown), Ibis Menéndez	0

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