Andrew J. Griffith

11.6k total citations
117 papers, 6.8k citations indexed

About

Andrew J. Griffith is a scholar working on Sensory Systems, Molecular Biology and Neurology. According to data from OpenAlex, Andrew J. Griffith has authored 117 papers receiving a total of 6.8k indexed citations (citations by other indexed papers that have themselves been cited), including 85 papers in Sensory Systems, 54 papers in Molecular Biology and 39 papers in Neurology. Recurrent topics in Andrew J. Griffith's work include Hearing, Cochlea, Tinnitus, Genetics (85 papers), Vestibular and auditory disorders (38 papers) and Ear Surgery and Otitis Media (23 papers). Andrew J. Griffith is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (85 papers), Vestibular and auditory disorders (38 papers) and Ear Surgery and Otitis Media (23 papers). Andrew J. Griffith collaborates with scholars based in United States, Japan and Pakistan. Andrew J. Griffith's co-authors include Thomas B. Friedman, Kiyoto Kurima, Inna A. Belyantseva, Zubair M. Ahmed, Edward R. Wilcox, Sheikh Riazuddin, Gregory I. Frolenkov, Robert J. Morell, Saima Riazuddin and Yoshiyuki Kawashima and has published in prestigious journals such as New England Journal of Medicine, Cell and Journal of Biological Chemistry.

In The Last Decade

Andrew J. Griffith

116 papers receiving 6.7k citations

Peers

Countries citing papers authored by Andrew J. Griffith

Since Specialization

Citations

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

Fields of papers citing papers by Andrew J. Griffith

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Andrew J. Griffith

This figure shows the co-authorship network connecting the top 25 collaborators of Andrew J. Griffith. A scholar is included among the top collaborators of Andrew J. 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 Andrew J. Griffith. Andrew J. 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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20 of 20 papers shown

#	Work	Indexed citations
1	Transgenic Tg(Kcnj10-ZsGreen) fluorescent reporter mice allow visualization of intermediate cells in the stria vascularis 2024 ·Scientific Reports ·(unknown), Rafal T. Olszewski, (unknown), Soumya Korrapati, Samuel Mawuli Adadey, Andrew J. Griffith, Yijun Su, Jiamin Liu, Harshad D. Vishwasrao, Shoujun Gu, Thomas L. Saunders, Isabelle Roux, Michael Hoa	4
2	Small Molecule MIF Modulation Enhances Ferroptosis by Impairing DNA Repair Mechanisms 2024 ·Advanced Science ·Deng Chen, Chunlong Zhao, Jianqiu Zhang, (unknown), (unknown), (unknown), (unknown), Zhangping Xiao, (unknown), Andrew J. Griffith, (unknown), (unknown), Robert P. Coppes, Amalia M. Dolga, Hidde J. Haisma, Frank J. Dekker	7
3	CHD7 variants associated with hearing loss and enlargement of the vestibular aqueduct 2023 ·Human Genetics ·Isabelle Roux, Cristina Fenollar‐Ferrer, (unknown), Parna Chattaraj, Iván A. López, Kyungreem Han, Keiji Honda, Carmen C. Brewer, John A. Butman, Robert J. Morell, Donna M. Martin, Andrew J. Griffith	8
4	Vaccination with human alphapapillomavirus-derived L2 multimer protects against human betapapillomavirus challenge, including in epidermodysplasia verruciformis model mice 2022 ·Virology ·(unknown), Margaret Wong, Hua‐Ling Tsai, Hao Wang, Reinhard Kirnbauer, Andrew J. Griffith, Paul F. Lambert, Richard B.S. Roden	3
5	Vestibular phenotype‐genotype correlation in a cohort of 90 patients with Usher syndrome 2020 ·Clinical Genetics ·(unknown), Rabia Faridi, Kelly King, Christopher Zalewski, Rizwan Yousaf, Julie M. Schultz, Robert J. Morell, Julie Muskett, Amy Turriff, Ekaterini Tsilou, Andrew J. Griffith, Thomas B. Friedman, Wadih M. Zein, Carmen C. Brewer	24
6	Genetic Hearing Loss Associated With Autoinflammation 2020 ·Frontiers in Neurology ·Hiroshi Nakanishi, (unknown), Taku Ito, (unknown), Carmen C. Brewer, (unknown), Isabelle Roux, Seiji Hosokawa, Andrew J. Griffith	34
7	Transmembrane channel-like (TMC) genes are required for auditory and vestibular mechanosensation 2014 ·Pflügers Archiv - European Journal of Physiology ·Yoshiyuki Kawashima, Kiyoto Kurima, Bifeng Pan, Andrew J. Griffith, Jeffrey R. Holt	65
8	Slc26a4-insufficiency causes fluctuating hearing loss and stria vascularis dysfunction 2014 ·Neurobiology of Disease ·Taku Ito, Xiangming Li, Kiyoto Kurima, Byung Yoon Choi, Philine Wangemann, Andrew J. Griffith	36
9	SLC26A4 Targeted to the Endolymphatic Sac Rescues Hearing and Balance in Slc26a4 Mutant Mice 2013 ·PLoS Genetics ·Xiangming Li, Joel D. Sanneman, Donald G. Harbidge, Fei Zhou, Taku Ito, Raoul D. Nelson, Nicolas Picard, Régine Chambrey, Dominique Eladari, (unknown), Andrew J. Griffith, Daniel C. Marcus, Philine Wangemann	48
10	TMC1 and TMC2 Are Components of the Mechanotransduction Channel in Hair Cells of the Mammalian Inner Ear 2013 ·Neuron ·Bifeng Pan, Gwenaëlle S. G. Géléoc, Yukako Asai, (unknown), Kiyoto Kurima, Kotaro Ishikawa, Yoshiyuki Kawashima, Andrew J. Griffith, Jeffrey R. Holt	306
11	Hereditary Hearing Loss with Thyroid Abnormalities 2011 ·Advances in oto-rhino-laryngology ·Byung Yoon Choi, Julie Muskett, Kelly King, Christopher Zalewski, Thomas H. Shawker, James C. Reynolds, John A. Butman, Carmen C. Brewer, Andrew K. Stewart, Seth L. Alper, Andrew J. Griffith	10
12	Cell Type–Specific Transcriptome Analysis Reveals a Major Role for Zeb1 and miR-200b in Mouse Inner Ear Morphogenesis 2011 ·PLoS Genetics ·Ronna Hertzano, Ran Elkon, Kiyoto Kurima, (unknown), (unknown), Michelle A. Sallin, (unknown), Douglas S. Darling, Andrew J. Griffith, David J. Eisenman, Scott E. Strome	67
13	Evidence for a founder mutation causing DFNA5 hearing loss in East Asians 2009 ·Journal of Human Genetics ·Hong-Joon Park, Hyun-Ju Cho, Jeong‐In Baek, Tamar Ben‐Yosef, Tae-Jun Kwon, Andrew J. Griffith, Un‐Kyung Kim	44
14	Amino acid 572 in TMC1: hot spot or critical functional residue for dominant mutations causing hearing impairment 2009 ·Journal of Human Genetics ·Nele Hilgert, (unknown), Kiyoto Kurima, (unknown), Rick A. Friedman, Andrew J. Griffith, Guy Van Camp	12
15	Evaluation of the Thyroid in Patients With Hearing Loss and Enlarged Vestibular Aqueducts 2009 ·Archives of Otolaryngology - Head and Neck Surgery ·Anne C. Madeo, Ani Manichaikul, James C. Reynolds, Nicholas J. Sarlis, Shannon Pryor, Thomas H. Shawker, Andrew J. Griffith	21
16	Stickler syndrome: Clinical characteristics and diagnostic criteria 2005 ·American Journal of Medical Genetics Part A ·Peter S. Rose, Howard P. Levy, Ruth M. Liberfarb, Joie Davis, (unknown), Benjamin I. Rubin, Ekaterini Tsilou, Andrew J. Griffith, Clair A. Francomano	103
17	Genetic insights into the morphogenesis of inner ear hair cells 2004 ·Nature Reviews Genetics ·Gregory I. Frolenkov, Inna A. Belyantseva, Thomas B. Friedman, Andrew J. Griffith	165
18	Mutations of MYO6 Are Associated with Recessive Deafness, DFNB37 2003 ·The American Journal of Human Genetics ·Zubair M. Ahmed, Robert J. Morell, Saima Riazuddin, Andrea Gropman, Shahzad Shaukat, (unknown), Saidi Mohiddin, Lameh Fananapazir, Rafael C. Caruso, Tayyab Husnaın, Shaheen N. Khan, Sheikh Riazuddin, Andrew J. Griffith, Thomas B. Friedman, Edward R. Wilcox	151
19	Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13) 1999 ·Nature Genetics ·Wyman T. McGuirt, Sai Prasad, Andrew J. Griffith, Henricus P. M. Kunst, Glenn E. Green, Karl B. Shpargel, Christina L. Runge, (unknown), Robert F. Mueller, Eric D. Lynch, Mary‐Claire King, Han G. Brunner, Cor W. R. J. Cremers, Masamine Takanosu, Shiwu Li, Machiko Arita, Richard Mayne, Darwin J. Prockop, Guy Van Camp, Richard J. Smith	193
20	Molecular characterization of the ku autoantigen 1988 ·Clinical research ·Andrew J. Griffith, Tatsuyuki Mimori, Joseph Craft, Nicholas Birchall, Thomas S. Kupper, N Hama, (unknown), (unknown), M. Homma, John Hardin	3

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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