AJ Griffith

457 total citations
9 papers, 237 citations indexed

About

AJ Griffith is a scholar working on Sensory Systems, Neurology and Otorhinolaryngology. According to data from OpenAlex, AJ Griffith has authored 9 papers receiving a total of 237 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Sensory Systems, 5 papers in Neurology and 3 papers in Otorhinolaryngology. Recurrent topics in AJ Griffith's work include Hearing, Cochlea, Tinnitus, Genetics (7 papers), Vestibular and auditory disorders (5 papers) and Ear Surgery and Otitis Media (3 papers). AJ Griffith is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (7 papers), Vestibular and auditory disorders (5 papers) and Ear Surgery and Otitis Media (3 papers). AJ Griffith collaborates with scholars based in United States, Pakistan and Poland. AJ Griffith's co-authors include TB Friedman, Tomoko Makishima, Tayyab Husnaın, Saima Riazuddin, Mohsin Shahzad, Sheikh Riazuddin, Ryan P. McNamara, Anne C. Madeo, Tali Friedman and Robert J. Morell and has published in prestigious journals such as Clinical Genetics, Oral Diseases and Advances in oto-rhino-laryngology.

In The Last Decade

AJ Griffith

9 papers receiving 234 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
AJ Griffith United States	7	198	121	97	40	39	9	237
Dilip Deshmukh United States	5	257 1.3×	218 1.8×	83 0.9×	32 0.8×	45 1.2×	6	331
Typhaine Dupont France	6	213 1.1×	142 1.2×	59 0.6×	30 0.8×	60 1.5×	9	276
Margot Tertrais France	7	184 0.9×	149 1.2×	39 0.4×	15 0.4×	62 1.6×	7	275
Saima Anwar Pakistan	5	155 0.8×	134 1.1×	82 0.8×	52 1.3×	13 0.3×	6	236
Rasheeda Bashir Pakistan	9	98 0.5×	75 0.6×	102 1.1×	26 0.7×	13 0.3×	27	258
Charlotte Calvet France	7	173 0.9×	150 1.2×	31 0.3×	15 0.4×	55 1.4×	11	271
Jaime Gallo‐Terán Spain	7	202 1.0×	74 0.6×	108 1.1×	45 1.1×	73 1.9×	18	229
Emma L. Coghill United Kingdom	4	102 0.5×	153 1.3×	43 0.4×	29 0.7×	25 0.6×	5	241
Kayla Hill United States	10	321 1.6×	136 1.1×	118 1.2×	14 0.3×	93 2.4×	11	411

Countries citing papers authored by AJ Griffith

Since Specialization

Citations

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

Fields of papers citing papers by AJ Griffith

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of AJ Griffith

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

All Works

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9 of 9 papers shown

1.

Friedman, TB, et al.. (2016). Unresolved questions regarding human hereditary deafness. Oral Diseases. 23(5). 551–558. 21 indexed citations

2.

Riazuddin, Saima, et al.. (2009). Identities and frequencies of mutations of the otoferlin gene (OTOF) causing DFNB9 deafness in Pakistan. Clinical Genetics. 75(3). 237–243. 79 indexed citations

3.

Peters, Linda, et al.. (2008). A locus for autosomal dominant progressive non‐syndromic hearing loss, DFNA27, is on chromosome 4q12‐13.1. Clinical Genetics. 73(4). 367–372. 14 indexed citations

4.

Makishima, Tomoko, et al.. (2007). A novel mutation at the DFNA36 hearing loss locus reveals a critical function and potential genotype–phenotype correlation for amino acid‐572 of TMC1. Clinical Genetics. 71(2). 148–152. 42 indexed citations

5.

McNamara, Ryan P., Tomoko Makishima, Tayyab Husnaın, et al.. (2007). Identities, frequencies and origins of TMC1 mutations causing DFNB7/B11 deafness in Pakistan. Clinical Genetics. 72(6). 546–550. 55 indexed citations

6.

Labay, Valentina, Gema Garrido, Anne C. Madeo, et al.. (2007). Haplogroup analysis supports a pathogenic role for the 7510T>C mutation of mitochondrial tRNA^Ser(UCN) in sensorineural hearing loss. Clinical Genetics. 73(1). 50–54. 11 indexed citations

7.

Ahmed, Zubair M., et al.. (2002). Clinical Manifestations of DFNB29 Deafness. Advances in oto-rhino-laryngology. 61. 156–160. 6 indexed citations

8.

Riazuddin, Sheikh, et al.. (2002). Genetic Modifiers of Hereditary Hearing Loss. Advances in oto-rhino-laryngology. 61. 224–229. 4 indexed citations

9.

Griffith, AJ. (1992). Biological and clinical aspects of autoimmune inner ear disease.. PubMed. 65(1). 17–28. 5 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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