Nancy Govea

2.2k total citations · 1 hit paper
14 papers, 1.5k citations indexed

About

Nancy Govea is a scholar working on Molecular Biology, Sensory Systems and Otorhinolaryngology. According to data from OpenAlex, Nancy Govea has authored 14 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 7 papers in Sensory Systems and 3 papers in Otorhinolaryngology. Recurrent topics in Nancy Govea's work include Hearing, Cochlea, Tinnitus, Genetics (7 papers), Ear Surgery and Otitis Media (3 papers) and Cardiomyopathy and Myosin Studies (3 papers). Nancy Govea is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (7 papers), Ear Surgery and Otitis Media (3 papers) and Cardiomyopathy and Myosin Studies (3 papers). Nancy Govea collaborates with scholars based in Spain, Italy and United States. Nancy Govea's co-authors include Xavier Estivill, Paolo Gasparini, Montserrat Milà, Leopoldo Zelante, Paolo Fortina, Saul Surrey, Salvatore Melchionda, Raquel Rabionet, Elaine Mansfield and Rosaria Scozzari and has published in prestigious journals such as The Lancet, The American Journal of Human Genetics and Human Mutation.

In The Last Decade

Nancy Govea

14 papers receiving 1.5k citations

Hit Papers

Connexin-26 mutations in sporadic and inherited sensorine... 1998 2026 2007 2016 1998 100 200 300 400 500
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.

  1. Connexin-26 mutations in sporadic and inherited sensorineural deafness
    1998 523 citations Xavier Estivill, Paolo Fortina et al. The Lancet profile →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Nancy Govea Spain 13 1000 988 340 271 239 14 1.5k
L. Van Laer Belgium 11 304 0.3× 629 0.6× 260 0.8× 316 1.2× 64 0.3× 17 811
Masatsugu Masuda Japan 11 220 0.2× 664 0.7× 392 1.2× 185 0.7× 38 0.2× 32 939
A Guilhaume France 14 86 0.1× 426 0.4× 275 0.8× 184 0.7× 57 0.2× 33 636
Lisa Schweizer United States 16 227 0.2× 390 0.4× 242 0.7× 218 0.8× 69 0.3× 41 1.0k
M Pierson United States 16 215 0.2× 275 0.3× 67 0.2× 184 0.7× 25 0.1× 73 773
Adam Sheppard United States 15 188 0.2× 321 0.3× 140 0.4× 329 1.2× 13 0.1× 29 810
Kurt Stephan Austria 10 479 0.5× 366 0.4× 115 0.3× 199 0.7× 20 0.1× 17 949
Naomi Katayama Japan 18 84 0.1× 686 0.7× 953 2.8× 56 0.2× 85 0.4× 77 1.4k
S. K. Bosher United Kingdom 13 270 0.3× 863 0.9× 364 1.1× 301 1.1× 56 0.2× 15 1.1k
Montserrat Rodríguez-Ballesteros Spain 9 118 0.1× 242 0.2× 127 0.4× 121 0.4× 14 0.1× 11 370

Countries citing papers authored by Nancy Govea

Since Specialization
Citations

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

Fields of papers citing papers by Nancy Govea

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nancy Govea

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

All Works

14 of 14 papers shown
1.
Ripoll‐Vera, Tomás, et al.. (2015). Clinical and Prognostic Profiles of Cardiomyopathies Caused by Mutations in the Troponin T Gene. Revista Española de Cardiología (English Edition). 69(2). 149–158. 19 indexed citations
2.
Ripoll‐Vera, Tomás, et al.. (2015). Patrón fenotípico de las miocardiopatías por mutaciones en el gen de la desmina. Estudio clínico y genético en dos unidades de cardiopatías familiares. Revista Española de Cardiología. 68(11). 1027–1029. 8 indexed citations
3.
Ripoll‐Vera, Tomás, et al.. (2015). Perfil clínico y pronóstico de las miocardiopatías causadas por mutaciones en el gen de la troponina T. Revista Española de Cardiología. 69(2). 149–158. 12 indexed citations
4.
Ballana, Ester, Nancy Govea, Rafael de Cid, et al.. (2007). Detection of unrecognized low-level mtDNA heteroplasmy may explain the variable phenotypic expressivity of apparently homoplasmic mtDNA mutations. Human Mutation. 29(2). 248–257. 46 indexed citations
5.
Rosell, Jordi, Montse Morlá, Daniel Bachiller, et al.. (2007). Mutations in TBX1 genocopy the 22q11.2 deletion and duplication syndromes: a new susceptibility factor for mental retardation. European Journal of Human Genetics. 15(6). 658–663. 51 indexed citations
6.
Heine‐Suñer, Damián, Montse Morlá, Xavier Busquets, et al.. (2003). Fragile‐X syndrome and skewed X‐chromosome inactivation within a family: A female member with complete inactivation of the functional X chromosome. American Journal of Medical Genetics Part A. 122A(2). 108–114. 37 indexed citations
7.
López-Bigas, Núria, Salvatore Melchionda, Rafael de Cid, et al.. (2001). Identification of five new mutations of PDS/SLC26A4 in Mediterranean families with hearing impairment. Human Mutation. 18(6). 548–548. 23 indexed citations
8.
Torroni, Antonio, Fulvio Cruciani, Chiara Rengo, et al.. (1999). The A1555G Mutation in the 12S rRNA Gene of Human mtDNA: Recurrent Origins and Founder Events in Families Affected by Sensorineural Deafness. The American Journal of Human Genetics. 65(5). 1349–1358. 91 indexed citations
9.
López-Bigas, Núria, Raquel Rabionet, Rafael de Cid, et al.. (1999). Splice-site mutation in thePDS gene may result in intrafamilial variability for deafness in Pendred syndrome. Human Mutation. 14(6). 520–526. 34 indexed citations
10.
Estivill, Xavier, Paolo Fortina, Saul Surrey, et al.. (1998). Connexin-26 mutations in sporadic and inherited sensorineural deafness. The Lancet. 351(9100). 394–398. 523 indexed citations breakdown →
11.
Estivill, Xavier, Nancy Govea, Anna Barceló, et al.. (1998). Familial Progressive Sensorineural Deafness Is Mainly Due to the mtDNA A1555G Mutation and Is Enhanced by Treatment with Aminoglycosides. The American Journal of Human Genetics. 62(1). 27–35. 417 indexed citations
12.
Gasparini, Paolo, Xavier Estivill, Antonio Totaro, et al.. (1997). Linkage of DFNB1 to non-syndromic neurosensory autosomal-recessive deafness in Mediterranean families.. PubMed. 5(2). 83–8. 98 indexed citations
13.
Govea, Nancy, Montserrat Milà, Matteo Della Monica, et al.. (1997). Linkage of DFNB1 to Non-Syndromic Neurosensory Autosomal-Recessive Deafness in Mediterranean Families. European Journal of Human Genetics. 5(2). 83–88. 93 indexed citations
14.
Zelante, L., Paolo Gasparini, Xavier Estivill, et al.. (1997). CONNEXIN 26 MUTATIONS ASSOCIATED WITH THE MOST COMMON FORM OF NON SYNDROMIC NEUROSENSORY AUTOSOMAL RECESSIVE DEAFNESS (DFNB1) IN MEDITERRANEANS. ArTS Archivio della ricerca di Trieste (University of Trieste https://www.units.it/). 6(9). 1605–1609. 65 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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