Erica R. Eichers

3.0k total citations
10 papers, 1.7k citations indexed

About

Erica R. Eichers is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Erica R. Eichers has authored 10 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 6 papers in Molecular Biology and 2 papers in Pathology and Forensic Medicine. Recurrent topics in Erica R. Eichers's work include Genetic and Kidney Cyst Diseases (9 papers), Genetic Syndromes and Imprinting (8 papers) and Hedgehog Signaling Pathway Studies (5 papers). Erica R. Eichers is often cited by papers focused on Genetic and Kidney Cyst Diseases (9 papers), Genetic Syndromes and Imprinting (8 papers) and Hedgehog Signaling Pathway Studies (5 papers). Erica R. Eichers collaborates with scholars based in United States, United Kingdom and Canada. Erica R. Eichers's co-authors include Nicholas Katsanis, Philip L. Beales, James R. Lupski, Bethan E. Hoskins, José L. Badano, Richard A. Lewis, Stephen J. Ansley, Carmen C. Leitch, Peter Scambler and William S. Davidson and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

Erica R. Eichers

10 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Erica R. Eichers United States	9	1.3k	1.3k	198	119	107	10	1.7k
Stephen J. Ansley United States	11	2.0k 1.6×	1.9k 1.5×	411 2.1×	148 1.2×	59 0.6×	11	2.5k
Dorien Lugtenberg Netherlands	18	920 0.7×	1.0k 0.8×	121 0.6×	72 0.6×	70 0.7×	34	1.6k
Guntram Borck Germany	27	681 0.5×	876 0.7×	205 1.0×	113 0.9×	133 1.2×	65	1.7k
Alison Ross United Kingdom	7	1.1k 0.9×	1.1k 0.9×	274 1.4×	211 1.8×	33 0.3×	10	1.6k
Diana Mitter Germany	15	390 0.3×	572 0.4×	152 0.8×	48 0.4×	138 1.3×	28	923
Ewa Obersztyn Poland	19	711 0.6×	692 0.5×	124 0.6×	84 0.7×	49 0.5×	78	1.2k
Maria A. Musarella Canada	22	434 0.3×	1.4k 1.1×	375 1.9×	52 0.4×	350 3.3×	45	1.8k
Dragana Josifova United Kingdom	14	611 0.5×	748 0.6×	162 0.8×	54 0.5×	86 0.8×	27	1.1k
Robert B. Hufnagel United States	20	247 0.2×	848 0.7×	199 1.0×	68 0.6×	135 1.3×	97	1.3k
Alice Goldenberg France	20	565 0.4×	678 0.5×	75 0.4×	100 0.8×	124 1.2×	49	1.1k

Countries citing papers authored by Erica R. Eichers

Since Specialization

Citations

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

Fields of papers citing papers by Erica R. Eichers

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Erica R. Eichers

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

All Works

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10 of 10 papers shown

Tobin, Jonathan L., Erica R. Eichers, Helen May‐Simera, et al.. (2008). Inhibition of neural crest migration underlies craniofacial dysmorphology and Hirschsprung's disease in Bardet–Biedl syndrome. Proceedings of the National Academy of Sciences. 105(18). 6714–6719. 154 indexed citations

Abd‐El‐Barr, Muhammad M., Erica R. Eichers, Mark E. Pennesi, et al.. (2007). Impaired photoreceptor protein transport and synaptic transmission in a mouse model of Bardet–Biedl syndrome. Vision Research. 47(27). 3394–3407. 85 indexed citations

Abd‐El‐Barr, Muhammad M., Erica R. Eichers, Zhuo Yang, et al.. (2006). Cone–Rod Dystrophy, Mislocalization of Visual Pigments, and Inner Retinal Changes in a Mouse Model of Bardet–Biedl Syndrome. Investigative Ophthalmology & Visual Science. 47(13). 2971–2971. 1 indexed citations

Eichers, Erica R., Muhammad M. Abd‐El‐Barr, Richard Paylor, et al.. (2006). Phenotypic characterization of Bbs4 null mice reveals age-dependent penetrance and variable expressivity. Human Genetics. 120(2). 211–226. 87 indexed citations

Eichers, Erica R., Richard A. Lewis, Nicholas Katsanis, & James R. Lupski. (2004). Triallelic inheritance: a bridge between Mendelian and multifactorial traits. Annals of Medicine. 36(4). 262–272. 35 indexed citations

Kulaga, Heather, Carmen C. Leitch, Erica R. Eichers, et al.. (2004). Loss of BBS proteins causes anosmia in humans and defects in olfactory cilia structure and function in the mouse. Nature Genetics. 36(9). 994–998. 270 indexed citations

Ansley, Stephen J., José L. Badano, Oliver E. Blacque, et al.. (2003). Basal body dysfunction is a likely cause of pleiotropic Bardet–Biedl syndrome. Nature. 425(6958). 628–633. 495 indexed citations

Eichers, Erica R., Jane S. Green, David W. Stockton, et al.. (2002). Newfoundland Rod-Cone Dystrophy, an Early-Onset Retinal Dystrophy, Is Caused by Splice-Junction Mutations in RLBP1. The American Journal of Human Genetics. 70(4). 955–964. 70 indexed citations

Katsanis, Nicholas, Erica R. Eichers, Stephen J. Ansley, et al.. (2002). BBS4 Is a Minor Contributor to Bardet-Biedl Syndrome and May Also Participate in Triallelic Inheritance. The American Journal of Human Genetics. 71(1). 22–29. 90 indexed citations

10.

Katsanis, Nicholas, Stephen J. Ansley, José L. Badano, et al.. (2001). Triallelic Inheritance in Bardet-Biedl Syndrome, a Mendelian Recessive Disorder. Science. 293(5538). 2256–2259. 438 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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