Robert A. Cucci

763 total citations
8 papers, 591 citations indexed

About

Robert A. Cucci is a scholar working on Sensory Systems, Molecular Biology and Endocrine and Autonomic Systems. According to data from OpenAlex, Robert A. Cucci has authored 8 papers receiving a total of 591 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Sensory Systems, 4 papers in Molecular Biology and 4 papers in Endocrine and Autonomic Systems. Recurrent topics in Robert A. Cucci's work include Hearing, Cochlea, Tinnitus, Genetics (6 papers), Neuroscience of respiration and sleep (4 papers) and Connexins and lens biology (3 papers). Robert A. Cucci is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (6 papers), Neuroscience of respiration and sleep (4 papers) and Connexins and lens biology (3 papers). Robert A. Cucci collaborates with scholars based in United States, Belgium and Canada. Robert A. Cucci's co-authors include Richard J. Smith, Sai Prasad, Glenn E. Green, Colleen A. Campbell, Lawrence P. Karniski, Val C. Sheffield, Maithilee Menezes, Virginie Vervoort, Charles E. Schwartz and Eugene H. Chang and has published in prestigious journals such as Human Mutation, American Journal of Medical Genetics Part A and Advances in oto-rhino-laryngology.

In The Last Decade

Robert A. Cucci

8 papers receiving 578 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Robert A. Cucci United States	6	404	258	196	137	120	8	591
Faiad Adawi Israel	2	523 1.3×	416 1.6×	282 1.4×	210 1.5×	51 0.4×	2	920
C. W. R. J. Cremers Netherlands	8	227 0.6×	67 0.3×	124 0.6×	185 1.4×	73 0.6×	11	373
PJ Willems Greece	5	271 0.7×	356 1.4×	124 0.6×	47 0.3×	27 0.2×	8	590
Elona Cama Italy	11	288 0.7×	158 0.6×	125 0.6×	52 0.4×	32 0.3×	18	404
Kyu Yup Lee South Korea	8	270 0.7×	135 0.5×	138 0.7×	56 0.4×	23 0.2×	16	362
Nathalie Pallarès-Ruiz France	8	262 0.6×	279 1.1×	81 0.4×	22 0.2×	23 0.2×	13	440
Nancy Smythe United States	12	313 0.8×	122 0.5×	150 0.8×	37 0.3×	20 0.2×	17	489
Daisuke Yamauchi Japan	9	170 0.4×	147 0.6×	203 1.0×	68 0.5×	66 0.6×	24	457
Aki Oshima Japan	8	187 0.5×	149 0.6×	91 0.5×	42 0.3×	28 0.2×	12	306
Constantinos Economou Greece	10	122 0.3×	226 0.9×	173 0.9×	56 0.4×	60 0.5×	22	540

Countries citing papers authored by Robert A. Cucci

Since Specialization

Citations

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

Fields of papers citing papers by Robert A. Cucci

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Robert A. Cucci. 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 Robert A. Cucci. The network helps show where Robert A. Cucci may publish in the future.

Co-authorship network of co-authors of Robert A. Cucci

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

All Works

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8 of 8 papers shown

Chang, Eugene H., Maithilee Menezes, Nicole C. Meyer, et al.. (2004). Branchio-oto-renal syndrome: The mutation spectrum inEYA1and its phenotypic consequences. Human Mutation. 23(6). 582–589. 159 indexed citations

Prasad, Sai, et al.. (2003). Pendred syndrome and DFNB4‐mutation screening of SLC26A4 by denaturing high‐performance liquid chromatography and the identification of eleven novel mutations. American Journal of Medical Genetics Part A. 124A(1). 1–9. 53 indexed citations

McGuirt, Wyman T., Sudhakar Prasad, Robert A. Cucci, Glenn E. Green, & Richard J. Smith. (2002). Clinical Presentation of DFNB1. Advances in oto-rhino-laryngology. 61. 113–119. 2 indexed citations

Najmabadi, Hossein, Robert A. Cucci, Solmaz Sahebjam, et al.. (2002). GJB2 mutations in Iranians with autosomal recessive non-syndromic sensorineural hearing loss. Human Mutation. 19(5). 572–572. 44 indexed citations

Vescan, Allan, et al.. (2002). Cochlear Implantation and Pendred's Syndrome Mutation in Monozygotic Twins with Large Vestibular Aqueduct Syndrome. The Journal of Otolaryngology. 31(1). 54–54. 3 indexed citations

Campbell, Colleen A., Robert A. Cucci, Sai Prasad, et al.. (2001). Pendred syndrome, DFNB4, andPDS/SLC26A4 identification of eight novel mutations and possible genotype-phenotype correlations. Human Mutation. 17(5). 403–411. 223 indexed citations

Cucci, Robert A., Sai Prasad, Philip M. Kelley, et al.. (2000). The M34T Allele Variant of Connexin 26. Genetic Testing. 4(4). 335–344. 43 indexed citations

Prasad, Sai, Robert A. Cucci, Glenn E. Green, & Richard J. Smith. (2000). Genetic testing for hereditary hearing loss: Connexin 26 (GJB2) allele variants and two novel deafness-causing mutations (R32C and 645-648delTAGA). Human Mutation. 16(6). 502–508. 64 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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