Eric D. Green

53.3k total citations · 1 hit paper
65 papers, 7.7k citations indexed

About

Eric D. Green is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, Eric D. Green has authored 65 papers receiving a total of 7.7k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Molecular Biology, 19 papers in Genetics and 9 papers in Plant Science. Recurrent topics in Eric D. Green's work include Chromosomal and Genetic Variations (9 papers), Genomics and Chromatin Dynamics (7 papers) and Genomic variations and chromosomal abnormalities (7 papers). Eric D. Green is often cited by papers focused on Chromosomal and Genetic Variations (9 papers), Genomics and Chromatin Dynamics (7 papers) and Genomic variations and chromosomal abnormalities (7 papers). Eric D. Green collaborates with scholars based in United States, United Kingdom and Japan. Eric D. Green's co-authors include Elizabeth A. Grice, Gerard G. Bouffard, Sean Conlan, Heidi H. Kong, Maria L. Turner, Joie Davis, Alice Young, Robert W. Blakesley, Patrick R. Murray and Clayton Deming and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Eric D. Green

65 papers receiving 7.5k citations

Hit Papers

align trajectories sort by overperformance

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Topographical and Temporal Diversity of the Human Skin Microbiome

2009 2.1k citations Elizabeth A. Grice, Heidi H. Kong et al. Science profile →

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author						Papers	Cites
Eric D. Green	3.8k	1.5k	869	563	499	65	7.7k
Thomas Scholzen	2.4k 0.6×	424 0.3×	821 0.9×	215 0.4×	586 1.2×	65	7.4k
Hendrik Nolte	3.2k 0.8×	360 0.2×	1.7k 1.9×	232 0.4×	629 1.3×	261	8.8k
Helmut Fuchs	2.8k 0.7×	912 0.6×	135 0.2×	643 1.1×	331 0.7×	185	5.4k
Thomas Boehm	4.9k 1.3×	1.5k 1.0×	267 0.3×	800 1.4×	470 0.9×	228	12.3k
Janine Altmüller	3.4k 0.9×	1.3k 0.9×	140 0.2×	570 1.0×	239 0.5×	213	6.5k
Lyn R. Griffiths	3.0k 0.8×	1.3k 0.8×	132 0.2×	136 0.2×	528 1.1×	399	8.7k
Cory Teuscher	1.9k 0.5×	1.2k 0.8×	166 0.2×	156 0.3×	464 0.9×	189	7.0k
Nikolaus Blin	4.4k 1.1×	1.2k 0.8×	191 0.2×	850 1.5×	335 0.7×	203	7.7k
Pascal Barbry	7.5k 2.0×	916 0.6×	143 0.2×	542 1.0×	849 1.7×	170	11.5k
Toshihiko Shiroishi	6.2k 1.6×	2.7k 1.7×	88 0.1×	277 0.5×	250 0.5×	192	9.1k

Countries citing papers authored by Eric D. Green

Since Specialization

Citations

This map shows the geographic impact of Eric D. Green'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. Green 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. Green more than expected).

Fields of papers citing papers by Eric D. Green

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

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

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

Oliver, Peter L., Benjamin Edwards, Amanda F. P. Cheung, et al.. (2014). Disruption ofVisc-2, a Brain-Expressed Conserved Long Noncoding RNA, Does Not Elicit an Overt Anatomical or Behavioral Phenotype. Cerebral Cortex. 25(10). 3572–3585. 28 indexed citations

Horvath, Julie E., Stephanie L. Merrett, Abdoulaye Baniré Diallo, et al.. (2011). Comparative analysis of the primate X-inactivation center region and reconstruction of the ancestral primate XIST locus. Genome Research. 21(6). 850–862. 13 indexed citations

Goodstadt, Leo, Tamara Sirey, Peter L. Oliver, et al.. (2010). Long noncoding RNA genes: conservation of sequence and brain expression among diverse amniotes. Genome biology. 11(7). R72–R72. 202 indexed citations

Grice, Elizabeth A., Heidi H. Kong, Sean Conlan, et al.. (2009). Topographical and Temporal Diversity of the Human Skin Microbiome. Science. 324(5931). 1190–1192. 2098 indexed citations breakdown →

Ziegler, Shira G., Kathleen S. Hruska, Barbara Stubblefield, et al.. (2009). In silico and functional studies of the regulation of the glucocerebrosidase gene. Molecular Genetics and Metabolism. 99(3). 275–282. 11 indexed citations

Carone, Dawn M., et al.. (2009). Distinct retroelement classes define evolutionary breakpoints demarcating sites of evolutionary novelty. BMC Genomics. 10(1). 334–334. 53 indexed citations

Rudd, M. Katharine, Cynthia Friedman, Megan Walker, et al.. (2008). Comparative sequence analysis of primate subtelomeres originating from a chromosome fission event. Genome Research. 19(1). 33–41. 16 indexed citations

Antonellis, Anthony, Rachel E. Ellsworth, Nyamkhishig Sambuughin, et al.. (2003). Glycyl tRNA Synthetase Mutations in Charcot-Marie-Tooth Disease Type 2D and Distal Spinal Muscular Atrophy Type V. The American Journal of Human Genetics. 72(5). 1293–1299. 420 indexed citations

Shugart, Yin Yao, et al.. (2003). Results of a genome‐wide linkage scan for stuttering. American Journal of Medical Genetics Part A. 124A(2). 133–135. 55 indexed citations

10.

Kratz, Christian P., Brooke M. Emerling, Jeannette M. Bonifas, et al.. (2002). Genomic structure of the PIK3CG gene on chromosome band 7q22 and evaluation as a candidate myeloid tumor suppressor. Blood. 99(1). 372–374. 27 indexed citations

11.

Lipkin, Steven M., Peter B. Møens, Victoria Wang, et al.. (2002). Meiotic arrest and aneuploidy in MLH3-deficient mice. Nature Genetics. 31(4). 385–390. 290 indexed citations

12.

Touchman, Jeffrey W., Yair Anikster, Nicole Dietrich, et al.. (2000). The Genomic Region Encompassing the Nephropathic Cystinosis Gene (CTNS): Complete Sequencing of a 200-kb Segment and Discovery of a Novel Gene within the Common Cystinosis-Causing Deletion. Genome Research. 10(2). 165–173. 101 indexed citations

13.

Lai, Cecilia, Simon E. Fisher, Jane A. Hurst, et al.. (2000). The SPCH1 Region on Human 7q31: Genomic Characterization of the Critical Interval and Localization of Translocations Associated with Speech and Language Disorder. The American Journal of Human Genetics. 67(2). 357–368. 147 indexed citations

14.

Thomas, James W., Shih-Queen Lee-Lin, Valerie V. Maduro, et al.. (2000). Comparative Genome Mapping in the Sequence-based Era: Early Experience with Human Chromosome 7. Genome Research. 10(5). 624–633. 23 indexed citations

15.

Royaux, Inès, Koichi Suzuki, Atsumi Mori, et al.. (2000). Pendrin, the Protein Encoded by the Pendred Syndrome Gene (PDS), Is an Apical Porter of Iodide in the Thyroid and Is Regulated by Thyroglobulin in FRTL-5 Cells. Endocrinology. 141(2). 839–845. 315 indexed citations

16.

DeSilva, Udaya, Hillary F. Massa, Barbara J. Trask, & Eric D. Green. (1999). Comparative Mapping of the Region of Human Chromosome 7 Deleted in Williams Syndrome. Genome Research. 9(5). 428–436. 53 indexed citations

17.

Claussen, Uwe, Eric D. Green, Bernhard Horsthemke, et al.. (1997). Isolation of DNA from the centromere of human chromosome 7 by microdissection. Chromosome Research. 5(4). 215–220. 5 indexed citations

18.

Howard, Timothy D., William A. Paznekas, Eric D. Green, et al.. (1997). Mutations in TWIST, a basic helix–loop–helix transcription factor, in Saethre-Chotzen syndrome. Nature Genetics. 15(1). 36–41. 488 indexed citations

19.

Kusaba, Hitoshi, Masaaki Nakayama, Taishi Harada, et al.. (1997). Maintenance of hypomethylation status and preferential expression of exogenous humanMDR1/PGY1 gene in mouse L cells by YAC mediated transfer. Somatic Cell and Molecular Genetics. 23(4). 259–274. 14 indexed citations

20.

Green, Eric D., Valerie V. Braden, Robert S. Fulton, et al.. (1994). Integration of physical, genetic and cytogenetic maps of human chromosome 7: isolation and analysis of yeast artificial chromosome clones for 117 mapped genetic markers. Human Molecular Genetics. 3(3). 489–501. 47 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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