F.F.B. Elder

5.2k total citations
76 papers, 3.9k citations indexed

About

F.F.B. Elder is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, F.F.B. Elder has authored 76 papers receiving a total of 3.9k indexed citations (citations by other indexed papers that have themselves been cited), including 46 papers in Genetics, 39 papers in Molecular Biology and 20 papers in Plant Science. Recurrent topics in F.F.B. Elder's work include Chromosomal and Genetic Variations (20 papers), Genomic variations and chromosomal abnormalities (13 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (12 papers). F.F.B. Elder is often cited by papers focused on Chromosomal and Genetic Variations (20 papers), Genomic variations and chromosomal abnormalities (13 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (12 papers). F.F.B. Elder collaborates with scholars based in United States, South Africa and United Kingdom. F.F.B. Elder's co-authors include Terence J. Robinson, Wilbur R. Harrison, Andrew R. Zinn, Paul A. Overbeek, Judith L. Ross, Frank Greenberg, Neal G. Copeland, Charles A. Montgomery, Nancy A. Jenkins and Takahiko Yokoyama and has published in prestigious journals such as Science, Nature Genetics and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

F.F.B. Elder

75 papers receiving 3.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
F.F.B. Elder United States 31 2.2k 2.1k 667 367 361 76 3.9k
J L Weber United States 21 2.0k 0.9× 2.2k 1.0× 896 1.3× 174 0.5× 245 0.7× 31 4.7k
John S. Waye Canada 37 2.5k 1.1× 2.8k 1.3× 1.7k 2.6× 674 1.8× 314 0.9× 167 6.2k
Delphine Samson France 11 1.4k 0.6× 2.0k 0.9× 505 0.8× 179 0.5× 296 0.8× 13 4.1k
Colette Dib France 11 2.5k 1.1× 3.1k 1.5× 518 0.8× 259 0.7× 409 1.1× 23 6.0k
Stephen T. Reeders United States 37 2.9k 1.3× 2.9k 1.3× 849 1.3× 412 1.1× 271 0.8× 83 5.7k
E. Viégas-Pèquignot France 33 2.0k 0.9× 4.2k 2.0× 810 1.2× 587 1.6× 225 0.6× 92 6.0k
Eva M. Eicher United States 51 4.2k 1.9× 4.7k 2.2× 581 0.9× 286 0.8× 298 0.8× 141 7.9k
Cécile Fizames France 22 2.0k 0.9× 2.9k 1.3× 1.7k 2.5× 195 0.5× 294 0.8× 37 6.0k
Marianne Frommer Australia 30 2.3k 1.0× 7.9k 3.7× 896 1.3× 507 1.4× 202 0.6× 57 9.5k
Paula E. May United States 18 1.7k 0.8× 1.7k 0.8× 575 0.9× 167 0.5× 137 0.4× 37 3.5k

Countries citing papers authored by F.F.B. Elder

Since Specialization
Citations

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

Fields of papers citing papers by F.F.B. Elder

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by F.F.B. Elder. 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 F.F.B. Elder. The network helps show where F.F.B. Elder may publish in the future.

Co-authorship network of co-authors of F.F.B. Elder

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

All Works

20 of 20 papers shown
1.
Bhoj, Elizabeth, Purita Ramos, Linda A. Baker, et al.. (2011). Human balanced translocation and mouse gene inactivation implicate Basonuclin 2 in distal urethral development. European Journal of Human Genetics. 19(5). 540–546. 19 indexed citations
2.
Zhang, Hui Ying, Xi Zhang, Xi Chen, et al.. (2008). Differences in activity and phosphorylation of MAPK enzymes in esophageal squamous cells of GERD patients with and without Barrett's esophagus. American Journal of Physiology-Gastrointestinal and Liver Physiology. 295(3). G470–G478. 38 indexed citations
3.
Crider, Bill P., et al.. (2008). Cryptic Chromosomal Abnormalities Identified in Children With Congenital Heart Disease. Pediatric Research. 64(4). 358–363. 74 indexed citations
4.
Zinn, Andrew R., David P. Roeltgen, Gerry A. Stefanatos, et al.. (2007). A Turner syndrome neurocognitive phenotype maps to Xp22.3. Behavioral and Brain Functions. 3(1). 24–24. 52 indexed citations
5.
Gilbert, Clément, Steven M. Goodman, Voahangy Soarimalala, et al.. (2007). Chromosomal evolution in tenrecs (Microgale and Oryzorictes, Tenrecidae) from the Central Highlands of Madagascar. Chromosome Research. 15(8). 1075–1091. 7 indexed citations
6.
Prieto, Juan Carlos, Nilda M. García, F.F.B. Elder, Andrew R. Zinn, & Linda A. Baker. (2007). Phenotypic expansion of the supernumerary derivative (22) chromosome syndrome: VACTERL and Hirschsprung's disease. Journal of Pediatric Surgery. 42(11). 1928–1932. 20 indexed citations
7.
Ross, Judith L., Carole Samango‐Sprouse, Najiba Lahlou, et al.. (2005). Early Androgen Deficiency in Infants and Young Boys with 47,XXY Klinefelter Syndrome. Hormone Research in Paediatrics. 64(1). 39–45. 117 indexed citations
8.
Robinson, Michael L., et al.. (2002). Genetic mapping of an insertional hydrocephalus-inducing mutation allelic to hy3. Mammalian Genome. 13(11). 625–632. 19 indexed citations
9.
Rambau, R.V., F.F.B. Elder, & Terence J. Robinson. (2001). Chromosomal evolution in the vlei rat, <i>Otomys irroratus</i> (Muridae: Otomyinae): a compound chromosomal rearrangement separates two major cytogenetic groups. Cytogenetic and Genome Research. 93(3-4). 253–257. 13 indexed citations
10.
Wei, Fanglin, F.F.B. Elder, Charles I. Scott, et al.. (2001). A man who inherited hisSRY gene and Leri-Weill dyschondrosteosis from his mother and neurofibromatosis type 1 from his father. American Journal of Medical Genetics. 102(4). 353–358. 14 indexed citations
11.
Lü, Wei, Carrie L. Phillips, Paul D. Killen, et al.. (1999). Insertional Mutation of the Collagen Genes Col4a3 and Col4a4 in a Mouse Model of Alport Syndrome. Genomics. 61(2). 113–124. 54 indexed citations
12.
Majumder, Kumud, et al.. (1998). YAC rescue of downless locus mutations in mice. Mammalian Genome. 9(11). 863–868. 21 indexed citations
13.
Rambau, R.V., Wilbur R. Harrison, F.F.B. Elder, & Terence J. Robinson. (1997). Chromosomes of Brants’ whistling rat and genome conservation in the Otomyinae revealed by G-banding and fluorescence in situ hybridization. Cytogenetic and Genome Research. 78(3-4). 216–220. 9 indexed citations
14.
Deere, Michelle, Wilbur R. Harrison, F.F.B. Elder, et al.. (1996). Characterization of Human DSPG3, a Small Dermatan Sulfate Proteoglycan. Genomics. 38(3). 399–404. 22 indexed citations
15.
Hecht, Jacqueline T., Laura D. Nelson, Yang Wang, et al.. (1995). Mutations in exon 17B of cartilage oligomeric matrix protein (COMP) cause pseudoachondroplasia. Nature Genetics. 10(3). 325–329. 304 indexed citations
16.
Grompe, Markus, Nagesh Rao, F.F.B. Elder, C. Thomas Caskey, & Frank Greenberg. (1992). 45,X/46,X, + r(X) can have a distinct phenotype different from Ullrich‐Turner syndrome. American Journal of Medical Genetics. 42(1). 39–43. 31 indexed citations
17.
Robinson, Terence J. & F.F.B. Elder. (1987). Multiple common fragile sites are expressed in the genome of the laboratory rat. Chromosoma. 96(1). 45–49. 45 indexed citations
18.
Elder, F.F.B., et al.. (1986). Chromosomal localization of human and rat Aα, Bβ, and γ fibrinogen genes by in situ hybridization. Cytogenetic and Genome Research. 42(1-2). 36–41. 34 indexed citations
19.
Robinson, Terence J., F.F.B. Elder, & John A. Chapman. (1983). Evolution of chromosomal variation in cottontails, genus <i>Sylvilagus </i>(Mammalia: Lagomorpha): <i>S</i>. <i>aquaticus, S</i>. <i>floridanus, </i>and <i>S</i>. <i>transitionalis</i>. Cytogenetic and Genome Research. 35(3). 216–222. 12 indexed citations
20.
Pathak, Sen, et al.. (1980). Asynaptic behavior of X and Y chromosomes in the Virginia opossum and the southern pygmy mouse. Cytogenetic and Genome Research. 26(2-4). 142–149. 25 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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