B. Carritt

2.4k total citations
64 papers, 1.9k citations indexed

About

B. Carritt is a scholar working on Molecular Biology, Genetics and Hematology. According to data from OpenAlex, B. Carritt has authored 64 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 42 papers in Molecular Biology, 18 papers in Genetics and 13 papers in Hematology. Recurrent topics in B. Carritt's work include Blood groups and transfusion (12 papers), RNA modifications and cancer (8 papers) and Molecular Biology Techniques and Applications (7 papers). B. Carritt is often cited by papers focused on Blood groups and transfusion (12 papers), RNA modifications and cancer (8 papers) and Molecular Biology Techniques and Applications (7 papers). B. Carritt collaborates with scholars based in United Kingdom, United States and Netherlands. B. Carritt's co-authors include Mark Poulter, Tim J. Kemp, Klaas Kok, Charles H.C.M. Buys, E. Solomon, Sue Povey, Hazel Welch, Jan Osinga, Pieter E. Postmus and Annemarie H. van der Hout and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

B. Carritt

63 papers receiving 1.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
B. Carritt United Kingdom 24 1.0k 504 449 331 312 64 1.9k
C. Jones United States 30 1.3k 1.3× 586 1.2× 247 0.6× 300 0.9× 169 0.5× 66 2.3k
Christine J. Farr United Kingdom 29 2.0k 2.0× 604 1.2× 364 0.8× 375 1.1× 169 0.5× 60 2.8k
N Odartchenko Switzerland 23 721 0.7× 226 0.4× 416 0.9× 383 1.2× 136 0.4× 53 1.7k
Carol A. Westbrook United States 28 1.1k 1.1× 354 0.7× 677 1.5× 509 1.5× 117 0.4× 75 2.3k
Michael J. Getz United States 31 1.8k 1.8× 409 0.8× 153 0.3× 348 1.1× 81 0.3× 55 2.5k
Olivier Brison France 35 2.5k 2.4× 1.0k 2.0× 377 0.8× 627 1.9× 102 0.3× 80 3.4k
Ian B. Pragnell United Kingdom 25 936 0.9× 405 0.8× 467 1.0× 785 2.4× 129 0.4× 62 2.2k
P E Barker United States 22 1.0k 1.0× 399 0.8× 205 0.5× 301 0.9× 65 0.2× 32 1.8k
M Pettersson Sweden 21 1.3k 1.3× 279 0.6× 319 0.7× 424 1.3× 54 0.2× 25 1.8k
Eric H. Westin United States 28 2.2k 2.2× 631 1.3× 462 1.0× 819 2.5× 136 0.4× 66 3.6k

Countries citing papers authored by B. Carritt

Since Specialization
Citations

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

Fields of papers citing papers by B. Carritt

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of B. Carritt

This figure shows the co-authorship network connecting the top 25 collaborators of B. Carritt. A scholar is included among the top collaborators of B. Carritt 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 B. Carritt. B. Carritt 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.
Kemp, Tim J., Mark Poulter, & B. Carritt. (1999). Microsatellite Variation within the Human RHCE Gene. Vox Sanguinis. 77(3). 159–163. 7 indexed citations
3.
Carritt, B., Tim J. Kemp, & Mark Poulter. (1997). Evolution of the Human RH (Rhesus) Blood Group Genes: A 50 Year Old Prediction (Partially) Fulfilled. Human Molecular Genetics. 6(6). 843–850. 78 indexed citations
4.
Wallace, Maura, et al.. (1996). Denaturing gradient gel electrophoresis: a novel method for determining Rh phenotype from genomic DNA. British Journal of Haematology. 94(2). 417–421. 16 indexed citations
5.
Poulter, Mark, Tim J. Kemp, & B. Carritt. (1996). DNA‐Based Rhesus Typing: Simultaneous Determination of RHC and RHD Status Using the Polymerase Chain Reaction. Vox Sanguinis. 70(3). 164–168. 49 indexed citations
6.
Blunt, T, Geoff Daniels, & B. Carritt. (1994). Serotype Switching in a Partially Deleted RHD Gene. Vox Sanguinis. 67(4). 397–401. 46 indexed citations
7.
Khan, Ilyas M., Rory A. Fisher, Keith Johnson, et al.. (1994). The SON gene encodes a conserved DNA binding protein mapping to human chromosome 21. Annals of Human Genetics. 58(1). 25–34. 22 indexed citations
8.
Kok, Klaas, Anke van den Berg, Dorothy L. Buchhagen, B. Carritt, & Charles H.C.M. Buys. (1993). A PCR-Aided Transcript Titration Assay Revealing Very Low Expression of a Gene at Band 3p21 in 33 Cell Lines Derived from all Types of Lung Cancer. European Journal of Human Genetics. 1(2). 156–163. 8 indexed citations
9.
Kok, Klaas, Robert M.W. Hofstra, Alison Pilz, et al.. (1993). A gene in the chromosomal region 3p21 with greatly reduced expression in lung cancer is similar to the gene for ubiquitin-activating enzyme.. Proceedings of the National Academy of Sciences. 90(13). 6071–6075. 83 indexed citations
10.
MacGeoch, C., B. Carritt, Neil D. Avent, et al.. (1992). Assignment of the chromosomal locus of the human 30-kDal Rh (Rhesus) blood group-antigen-related protein (Rh30A) to chromosome region 1p36.13→p34. Cytogenetic and Genome Research. 59(4). 261–263. 22 indexed citations
11.
Coucke, Paul, Kathelijne Mangelschots, Frank Speleman, et al.. (1991). Assignment of the fucosidase pseudogene FUCA1P to chromosome region 2q31→q32. Cytogenetic and Genome Research. 57(2-3). 120–122. 1 indexed citations
12.
Abbott, Catherine M., Ian J. Jackson, B. Carritt, & Sue Povey. (1991). The human homolog of the mouse brown gene maps to the short arm of chromosome 9 and extends the known region of homology with mouse chromosome 4. Genomics. 11(2). 471–473. 32 indexed citations
13.
Mao, Fan, et al.. (1991). A new RFLP identified at the D3S48 locus. Nucleic Acids Research. 19(17). 4797–4797. 11 indexed citations
14.
Daly, Maria C., Jenny Douglas, N M Bleehen, et al.. (1991). An unusually proximal deletion on the short arm of chromosome 3 in a patient with small cell lung cancer. Genomics. 9(1). 113–119. 33 indexed citations
15.
Saha, N., J.S.H. Tay, & B. Carritt. (1990). Restriction Fragment Length Polymorphism (RFLP) at the DNF15S2 Locus in Three Ethnic Groups of Singapore. Human Heredity. 40(4). 250–252. 1 indexed citations
16.
Hout, Annemarie H. van der, Klaas Kok, Anke van den Berg, et al.. (1988). Direct molecular analysis of a deletion of 3p in tumors from patients with sporadic renal cell carcinoma. Cancer Genetics and Cytogenetics. 32(2). 281–285. 33 indexed citations
17.
Jeremiah, S.J., L. F. WEST, Michael G. Davis, et al.. (1988). The assignment of the human gene coding for complement C5 to chromosome 9q22‐9q33.. Annals of Human Genetics. 52(2). 111–116. 8 indexed citations
18.
Kok, Klaas, Jan Osinga, B. Carritt, et al.. (1987). Deletion of a DNA sequence at the chromosomal region 3p21 in all major types of lung cancer. Nature. 330(6148). 578–581. 351 indexed citations
19.
Povey, S., S.J. Jeremiah, Richard F. Barker, et al.. (1980). Assignment of the human locus determining phosphoglycolate phosphatase (PGP) to chromosome 16. Annals of Human Genetics. 43(3). 241–248. 59 indexed citations
20.
Povey, Sue, Yvonne Boyd, M.E. Duncan, S.J. Jeremiah, & B. Carritt. (1978). Factors affecting the expression of genes on chromosome 9. Cytogenetic and Genome Research. 22(1-6). 461–464. 2 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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