Eric D. Lynch

4.4k total citations
35 papers, 3.4k citations indexed

About

Eric D. Lynch is a scholar working on Molecular Biology, Sensory Systems and Genetics. According to data from OpenAlex, Eric D. Lynch has authored 35 papers receiving a total of 3.4k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 14 papers in Sensory Systems and 11 papers in Genetics. Recurrent topics in Eric D. Lynch's work include Hearing, Cochlea, Tinnitus, Genetics (12 papers), Genomic variations and chromosomal abnormalities (4 papers) and Vestibular and auditory disorders (4 papers). Eric D. Lynch is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (12 papers), Genomic variations and chromosomal abnormalities (4 papers) and Vestibular and auditory disorders (4 papers). Eric D. Lynch collaborates with scholars based in United States, United Kingdom and Israel. Eric D. Lynch's co-authors include Mary‐Claire King, Jonathan Kil, Ming K. Lee, Lori S. Friedman, Elizabeth Ostermeyer, Carol Pierce, Rende Gu, S E Rowell, Patrick J. Dowd and Csilla I. Szabo and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and The Lancet.

In The Last Decade

Eric D. Lynch

34 papers receiving 3.3k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Eric D. Lynch United States	24	1.8k	1.1k	796	450	340	35	3.4k
Heon Yung Gee South Korea	31	1.5k 0.8×	261 0.2×	691 0.9×	133 0.3×	366 1.1×	108	3.0k
Tatsiana Pakladok Germany	18	2.0k 1.1×	327 0.3×	339 0.4×	82 0.2×	113 0.3×	35	3.8k
Edna Ben‐Asher Israel	27	1.5k 0.9×	401 0.4×	482 0.6×	67 0.1×	49 0.1×	46	2.8k
Evelyn Fein Germany	9	1.7k 0.9×	278 0.3×	273 0.3×	77 0.2×	108 0.3×	10	3.6k
Nili Avidan Israel	25	1.4k 0.8×	404 0.4×	367 0.5×	71 0.2×	57 0.2×	40	2.9k
Rainer Waldmann France	35	5.3k 3.0×	1.7k 1.5×	263 0.3×	61 0.1×	197 0.6×	48	6.8k
Wolfgang Jagla Germany	20	908 0.5×	151 0.1×	220 0.3×	195 0.4×	116 0.3×	30	2.6k
Giuseppe Borsani Italy	37	3.1k 1.7×	226 0.2×	1.2k 1.5×	180 0.4×	25 0.1×	90	4.7k
Lijuan Zhou China	30	2.0k 1.1×	382 0.3×	145 0.2×	93 0.2×	85 0.3×	124	3.9k
Steven U. Walkley United States	44	2.0k 1.1×	164 0.1×	357 0.4×	308 0.7×	86 0.3×	109	6.3k

Countries citing papers authored by Eric D. Lynch

Since Specialization

Citations

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

Fields of papers citing papers by Eric D. Lynch

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Eric D. Lynch. 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 Eric D. Lynch. The network helps show where Eric D. Lynch may publish in the future.

Co-authorship network of co-authors of Eric D. Lynch

This figure shows the co-authorship network connecting the top 25 collaborators of Eric D. Lynch. A scholar is included among the top collaborators of Eric D. Lynch 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 Eric D. Lynch. Eric D. Lynch 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

Shahin, Hashem, Tom Walsh, Tama Sobe, et al.. (2005). Mutations in a Novel Isoform of TRIOBP That Encodes a Filamentous-Actin Binding Protein Are Responsible for DFNB28 Recessive Nonsyndromic Hearing Loss. The American Journal of Human Genetics. 78(1). 144–152. 85 indexed citations

Lynch, Eric D. & Jonathan Kil. (2005). Compounds for the prevention and treatment of noise-induced hearing loss. Drug Discovery Today. 10(19). 1291–1298. 123 indexed citations

Lynch, Eric D., Rende Gu, Carol Pierce, & Jonathan Kil. (2005). Combined oral delivery of ebselen and allopurinol reduces multiple cisplatin toxicities in rat breast and ovarian cancer models while enhancing anti-tumor activity. Anti-Cancer Drugs. 16(5). 569–579. 53 indexed citations

Zheng, Joanna J., Eric D. Lynch, & Steve E. Unger. (2002). Comparison of SPE and fast LC to eliminate mass spectrometric matrix effects from microsomal incubation products. Journal of Pharmaceutical and Biomedical Analysis. 28(2). 279–285. 21 indexed citations

Shahin, Hashem, Tom Walsh, Tama Sobe, et al.. (2002). Genetics of congenital deafness in the Palestinian population: multiple connexin 26 alleles with shared origins in the Middle East. Human Genetics. 110(3). 284–289. 105 indexed citations

MacDonald, Nicola, Andy Ryan, Ian Jacobs, et al.. (2000). PTEN methylation is associated with advanced stage and microsatellite instability in endometrial carcinoma. International Journal of Cancer. 91(1). 22–26. 245 indexed citations

McGuirt, Wyman T., Sai Prasad, Andrew J. Griffith, et al.. (1999). Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13). Nature Genetics. 23(4). 413–419. 193 indexed citations

Lee, Ming K., Eric D. Lynch, & Mary‐Claire King. (1998). SeqHelp: A Program to Analyze Molecular Sequences Utilizing Common Computational Resources. Genome Research. 8(3). 306–312. 26 indexed citations

Lalwani, Anil K., Robert K. Jackler, Robert W. Sweetow, et al.. (1998). Further Characterization of the DFNA1 Audiovestibular Phenotype. Archives of Otolaryngology - Head and Neck Surgery. 124(6). 699–699. 35 indexed citations

10.

Robertson, Nahid G., Yi Yin, Stanislawa Weremowicz, et al.. (1997). An Ancient Conserved Gene Expressed in the Human Inner Ear: Identification, Expression Analysis, and Chromosomal Mapping of Human and Mouse Antiquitin (ATQ1). Genomics. 46(2). 191–199. 34 indexed citations

11.

Friedman, Lori S., Elizabeth Ostermeyer, Eric D. Lynch, et al.. (1995). 22 genes from chromosome 17q21: cloning, sequencing, and characterization of mutations in breast cancer families and tumors. Genomics. 25(1). 256–263. 41 indexed citations

12.

Friedman, Lori S., Elizabeth Ostermeyer, Csilla I. Szabo, et al.. (1994). Confirmation of BRCA1 by analysis of germline mutations linked to breast and ovarian cancer in ten families. Nature Genetics. 8(4). 399–404. 494 indexed citations

13.

Friedman, Lori S., Eric D. Lynch, & Mary‐Claire King. (1993). Two independent polymorphisms at the 17β-hydroxysteroid dehydrogenase (EDH17B) gene (17q21). Human Molecular Genetics. 2(6). 821–821. 11 indexed citations

14.

Lebo, Roger V., Lúcia Martelli, Ying Su, et al.. (1993). Prenatal diagnosis of Charcot‐Marie‐Tooth disease type 1a by multicolor in situ hybridization. American Journal of Medical Genetics. 47(3). 441–450. 18 indexed citations

15.

Anderson, Lee, Lori S. Friedman, Sherri Osborne‐Lawrence, et al.. (1993). High-Density Genetic Map of the BRCA1 Region of Chromosome 17q12-q21. Genomics. 17(3). 618–623. 76 indexed citations

16.

Lebo, Roger V., Eric D. Lynch, Mitchell S. Golbus, et al.. (1993). Prenatal in situ hybridization test for deleted steroid sulfatase gene. American Journal of Medical Genetics. 46(6). 652–658. 10 indexed citations

17.

Flejter, Wendy L., Eric D. Lynch, Michael Boehnke, et al.. (1993). Multicolor FISH Mapping with Alu-PCR-Amplified YAC Clone DNA Determines the Order of Markers in the BRCA1 Region on Chromosome 17q12-q21. Genomics. 17(3). 624–631. 18 indexed citations

18.

Lebo, Roger V., et al.. (1992). Prenatal diagnosis with repetitive in situ hybridization probes. American Journal of Medical Genetics. 43(5). 848–854. 47 indexed citations

19.

Bonifas, Jeannette M., John W. Bare, Eric D. Lynch, Roger V. Lebo, & Ervin H. Epstein. (1992). Regional assignment of the human keratin 5 (KRT5) gene to chromosome 12q near D12S14 by PCR analysis of somatic cell hybrids and multicolor in situ hybridization. Genomics. 13(2). 452–454. 10 indexed citations

20.

Lebo, R V, et al.. (1990). Rare McArdle disease locus polymorphic site on 11q13 contains CpG sequence. Human Genetics. 86(1). 17–24. 21 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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