Edward R. Wilcox

6.2k total citations
49 papers, 3.4k citations indexed

About

Edward R. Wilcox is a scholar working on Molecular Biology, Sensory Systems and Neurology. According to data from OpenAlex, Edward R. Wilcox has authored 49 papers receiving a total of 3.4k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Molecular Biology, 28 papers in Sensory Systems and 8 papers in Neurology. Recurrent topics in Edward R. Wilcox's work include Hearing, Cochlea, Tinnitus, Genetics (28 papers), RNA regulation and disease (11 papers) and RNA and protein synthesis mechanisms (10 papers). Edward R. Wilcox is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (28 papers), RNA regulation and disease (11 papers) and RNA and protein synthesis mechanisms (10 papers). Edward R. Wilcox collaborates with scholars based in United States, Pakistan and India. Edward R. Wilcox's co-authors include Thomas B. Friedman, Andrew J. Griffith, Sheikh Riazuddin, Robert J. Morell, Zubair M. Ahmed, Saima Riazuddin, Tenesha N. Smith, Sadaf Naz, Inna A. Belyantseva and Shaheen Khan and has published in prestigious journals such as Science, Cell and Nucleic Acids Research.

In The Last Decade

Edward R. Wilcox

49 papers receiving 3.3k citations

Peers

Countries citing papers authored by Edward R. Wilcox

Since Specialization

Citations

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

Fields of papers citing papers by Edward R. Wilcox

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Edward R. Wilcox. 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 Edward R. Wilcox. The network helps show where Edward R. Wilcox may publish in the future.

Co-authorship network of co-authors of Edward R. Wilcox

This figure shows the co-authorship network connecting the top 25 collaborators of Edward R. Wilcox. A scholar is included among the top collaborators of Edward R. Wilcox 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 Edward R. Wilcox. Edward R. Wilcox 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	Highly accurate long reads are crucial for realizing the potential of biodiversity genomics 2023 ·BMC Genomics ·Scott Hotaling, Edward R. Wilcox, Jacqueline Heckenhauer, Russell J. Stewart, Paul B. Frandsen	19
2	Modifier variant of METTL13 suppresses human GAB1–associated profound deafness 2018 ·Journal of Clinical Investigation ·Rizwan Yousaf, Zubair M. Ahmed, Arnaud P. J. Giese, Robert J. Morell, Ayala Lagziel, Alain Dabdoub, Edward R. Wilcox, Sheikh Riazuddin, Thomas B. Friedman, Saima Riazuddin	29
3	Profound, prelingual nonsyndromic deafness maps to chromosome 10q21 and is caused by a novel missense mutation in the Usher syndrome type IF gene PCDH15 2008 ·European Journal of Human Genetics ·Lance P. Doucette, Nancy D. Merner, (unknown), Elizabeth Ives, (unknown), (unknown), Tom Walsh, (unknown), (unknown), Bridget A. Fernandez, Jane S. Green, Edward R. Wilcox, (unknown), (unknown), Ming Lee, Mary‐Claire King, Terry‐Lynn Young	30
4	The Tip-Link Antigen, a Protein Associated with the Transduction Complex of Sensory Hair Cells, Is Protocadherin-15 2006 ·Journal of Neuroscience ·Zubair M. Ahmed, Richard J. Goodyear, Saima Riazuddin, Ayala Lagziel, P. Kevin Legan, Martine Behra, Shawn M. Burgess, Kathryn S. Lilley, Edward R. Wilcox, Sheikh Riazuddin, Andrew J. Griffith, Gregory I. Frolenkov, Inna A. Belyantseva, Guy P. Richardson, Thomas B. Friedman	219
5	Mutations in TRIOBP, Which Encodes a Putative Cytoskeletal-Organizing Protein, Are Associated with Nonsyndromic Recessive Deafness 2005 ·The American Journal of Human Genetics ·Saima Riazuddin, Shaheen N. Khan, Zubair M. Ahmed, Manju Ghosh, Kyle Caution, (unknown), Madhulika Kabra, Ahmad Usman Zafar, Kevin Chen, Sadaf Naz, Anthony Antonellis, William J. Pavan, Eric D. Green, Edward R. Wilcox, Penelope L. Friedman, Robert J. Morell, Sheikh Riazuddin, Thomas B. Friedman	76
6	A new locus for nonsyndromic deafness DFNB49 maps to chromosome 5q12.3-q14.1 2004 ·Human Genetics ·Khushnooda Ramzan, Rehan Sadiq Shaikh, (unknown), Shaheen N. Khan, Saima Riazuddin, Zubair M. Ahmed, Thomas B. Friedman, Edward R. Wilcox, Sheikh Riazuddin	21
7	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
8	Mutations in the Gene Encoding Tight Junction Claudin-14 Cause Autosomal Recessive Deafness DFNB29 2001 ·Cell ·Edward R. Wilcox, (unknown), Sadaf Naz, Saima Riazuddin, Tenesha N. Smith, Barbara Ploplis, Inna A. Belyantseva, Tamar Ben‐Yosef, (unknown), Robert J. Morell, Bechara Kachar, Doris K. Wu, Andrew J. Griffith, Sheikh Riazuddin, Thomas B. Friedman	344
9	Novel mutations of MYO15A associated with profound deafness in consanguineous families and moderately severe hearing loss in a patient with Smith-Magenis syndrome 2001 ·Human Genetics ·(unknown), Manju Ghosh, Saima Riazuddin, Sadaf Naz, Shaheen Khan, Zubair M. Ahmed, Sheikh Riazuddin, Yong Liang, P.S.N. Menon, Tenesha N. Smith, Ann C. M. Smith, Ken‐Shiung Chen, James R. Lupski, Edward R. Wilcox, Lorraine Potocki, Thomas B. Friedman	94
10	OTOF Encodes Multiple Long and Short Isoforms: Genetic Evidence That the Long Ones Underlie Recessive Deafness DFNB9 2000 ·The American Journal of Human Genetics ·Shin’ichiro Yasunaga, M’hamed Grati, Sébastien Chardenoux, Tenesha N. Smith, Thomas B. Friedman, Anil K. Lalwani, Edward R. Wilcox, Christine Petit	150
11	Dominant modifier DFNM1 suppresses recessive deafness DFNB26 2000 ·Nature Genetics ·Saima Riazuddin, (unknown), Zubair M. Ahmed, Anil K. Lalwani, M Mastroianni, Sadaf Naz, Tenesha N. Smith, (unknown), (unknown), Andrew J. Griffith, Sheikh Riazuddin, Edward R. Wilcox	104
12	A PAX3 polymorphism (T315K) in a family exhibiting Waardenburg Syndrome Type 2 (WS2) 1998 ·Molecular and Cellular Probes ·Cynthia Wang, Eugene S. Kim, (unknown), Tenesha N. Smith, Edward R. Wilcox, Anil K. Lalwani	6
13	A Gene for Recessive Nonsyndromic Sensorineural Deafness (DFNB18) Maps to the Chromosomal Region 11p14–p15.1 Containing the Usher Syndrome Type 1C Gene 1998 ·Genomics ·Pawan Kumar Jain, Anil K. Lalwani, (unknown), (unknown), Tenesha N. Smith, Achih Chen, Dilip Deshmukh, Ishwar C. Verma, Richard J. Smith, Edward R. Wilcox	34
14	A Five-Generation Family with Late-Onset Progressive Hereditary Hearing Impairment Due to Cochleosaccular Degeneration 1997 ·Audiology and Neurotology ·Anil K. Lalwani, Fred H. Linthicum, Edward R. Wilcox, Jean K. Moore, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), William M. Luxford	30
15	A novel zinc finger gene preferentially expressed in the retina and the organ of Corti localizes to human chromosome 12q24.3 1996 ·Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression ·Marcelo N. Rivolta, (unknown), Edward R. Wilcox	6
16	A novel and simple methodology to generate subtracted cDNA libraries 1995 ·Nucleic Acids Research ·Marcelo N. Rivolta, Edward R. Wilcox	8
17	Construction of a cDNA library from microdissected guinea pig crista ampullaris 1994 ·Hearing Research ·Edward R. Wilcox, Jörgen Fex	4
18	Construction of a cDNA library from microdissected guinea pig organ of Corti 1992 ·Hearing Research ·Edward R. Wilcox, Jörgen Fex	31
19	The PAX3 gene is mapped to human chromosome 2 together with a highly informative CA dinucleotide repeat 1992 ·Human Molecular Genetics ·Edward R. Wilcox, Marcelo N. Rivolta, Barbara Ploplis, S. Brian Potterf, Jörgen Fex	21
20	Chromogenic Immuno detection of Human Serum Albumin and α- l -Fucosidase Clones in a Human Hepatoma cDNA Expression Library 1984 ·DNA ·Jeffrey R. de Wet, (unknown), Nazneen N. Dewji, Edward R. Wilcox, John S. O’Brien, Donald R. Helinski	68

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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