P.F.R. Little

777 total citations
13 papers, 638 citations indexed

About

P.F.R. Little is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, P.F.R. Little has authored 13 papers receiving a total of 638 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 5 papers in Genetics and 3 papers in Genetics. Recurrent topics in P.F.R. Little's work include DNA and Nucleic Acid Chemistry (7 papers), DNA Repair Mechanisms (5 papers) and Hemoglobinopathies and Related Disorders (5 papers). P.F.R. Little is often cited by papers focused on DNA and Nucleic Acid Chemistry (7 papers), DNA Repair Mechanisms (5 papers) and Hemoglobinopathies and Related Disorders (5 papers). P.F.R. Little collaborates with scholars based in United Kingdom, Netherlands and United States. P.F.R. Little's co-authors include R. Williamson, J.M. Kooter, Richard A. Flavell, Ernie de Boer, R. A. Flavell, S. M. Darling, B. Modell, René Bernards, S Malcolm and David Westaway and has published in prestigious journals such as Nature, Cell and Nucleic Acids Research.

In The Last Decade

P.F.R. Little

13 papers receiving 561 citations

Peers

P.F.R. Little
T. Nakatsuji United States
Peter M. Green United Kingdom
Beatriz Nuez Spain
Anoop K. Sendamarai United States
Joëlle Starck France
Hamza Celik United States
Fiorella Shabtai Israel
N Blais Canada
Keqin Zheng Canada
Scott C. Crable United States
T. Nakatsuji United States
P.F.R. Little
Citations per year, relative to P.F.R. Little P.F.R. Little (= 1×) peers T. Nakatsuji

Countries citing papers authored by P.F.R. Little

Since Specialization
Citations

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

Fields of papers citing papers by P.F.R. Little

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by P.F.R. Little. 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 P.F.R. Little. The network helps show where P.F.R. Little may publish in the future.

Co-authorship network of co-authors of P.F.R. Little

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

All Works

13 of 13 papers shown
1.
Alders, Mariëlle, Andy Ryan, Matt Hodges, et al.. (2000). Disruption of a Novel Imprinted Zinc-Finger Gene, ZNF215, in Beckwith-Wiedemann Syndrome. The American Journal of Human Genetics. 66(5). 1473–1484. 40 indexed citations
2.
Hadjantonakis, Anna‐Katerina, et al.. (1996). Human MASH2 (HASH2) maps to chromosome 11p15 and is expressed in extravillus trophoblast. Placenta. 17(5-6). A15–A15. 3 indexed citations
3.
Mathew, Christopher G., Elizabeth W. Jones, Douglas F. Easton, et al.. (1990). Regional localization of polymorphic markers on chromosome 10 by physical and genetic mapping. Annals of Human Genetics. 54(2). 121–129. 26 indexed citations
4.
John, Rosalind M., et al.. (1989). A cosmid clone map derived from a small region of human chromosome 11. Genomics. 5(3). 501–509. 14 indexed citations
5.
Little, P.F.R.. (1984). Sequencing techniques: A close look at the genome. Nature. 310(5976). 369–369. 1 indexed citations
6.
Little, P.F.R.. (1984). RNA probes prepared in vitro. Nature. 309(5964). 191–191. 2 indexed citations
7.
Little, P.F.R., Emma Whitelaw, R. Williamson, et al.. (1980). The detection and use of hemoglobin mutants in the direct analysis of human globin genes. Blood. 55(6). 1060–1062. 12 indexed citations
8.
Little, P.F.R., et al.. (1980). Model for antenatal diagnosis of β-thalassaemia and other monogenic disorders by molecular analysis of linked DNA polymorphisms. Nature. 285(5761). 144–147. 104 indexed citations
9.
Little, P.F.R., et al.. (1979). Structure of the human fetal globin gene locus. Nature. 278(5701). 227–231. 95 indexed citations
10.
Flavell, Richard A., René Bernards, J.M. Kooter, et al.. (1979). The structure of the human β-globin gene in β-thalassaemia. Nucleic Acids Research. 6(8). 2749–2760. 61 indexed citations
11.
Senno, Laura del, F. Conconi, P.F.R. Little, & R. Williamson. (1979). Restriction enzyme analysis of the β-globin gene in DNA from β°-thalassaemic subjects from Ferrara. Biochemical and Biophysical Research Communications. 91(2). 548–553. 6 indexed citations
12.
Flavell, Richard A., J.M. Kooter, Ernie de Boer, P.F.R. Little, & R. Williamson. (1978). Analysis of the β-δ-globin gene loci in normal and hb lepore DNA: Direct determination of gene linkage and intergene distance. Cell. 15(1). 25–41. 216 indexed citations
13.
Little, P.F.R., Peter J. Curtis, Johan Berg, et al.. (1978). Isolation and partial sequence of recombinant plasmids containing human α-, β- and γ-globin cDNA fragments. Nature. 273(5664). 640–643. 58 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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