B. Carritt

2.4k citations

64 papers · 1.9k indexed · h-index 24

Impact in

Hematology top 2%
- Blood groups and transfusion
- Chronic Myeloid Leukemia Treatments
Genetics top 5%
- Genomic variations and chromosomal abnormalities

Papers in ⓘ

Molecular Biology 42
- RNA modifications and cancer 8
- Molecular Biology Techniques and Applications 7
- RNA and protein synthesis mechanisms 5
- Genomics and Chromatin Dynamics 4
Genetics 18
- Genomic variations and chromosomal abnormalities 7

Co-authors: Mark Poulter (6 shared papers)Tim J. Kemp (6 shared papers)Klaas Kok (7 shared papers)Charles H.C.M. Buys (7 shared papers)E. Solomon (4 shared papers)Sue Povey (6 shared papers)Hazel Welch (5 shared papers)Annemarie H. van der Hout (3 shared papers)
Journals: Annals of Human Genetics (9 papers)Cytogenetic and Genome Research (9 papers)Vox Sanguinis (6 papers)Nature (4 papers)Experimental Cell Research (4 papers)
Partner nations: United Kingdom United States Netherlands

In The Last Decade

B. Carritt

63 papers receiving 1.8k citations

Peers

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-authors

The 25 scholars most cited alongside B. Carritt, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with B. Carritt Line = papers co-authored together B. Carritt links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 64 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Deletion of a DNA sequence at the chromosomal region 3p21 in all major types of lung cancer Nature ·Klaas Kok, Jan Osinga, B. Carritt, Mary B. Davis, Annemarie H. van der Hout, Anneke Y. van der Veen, Rudy M. Landsvater, Lou F. M. H. de Leij, Henk H. Berendsen, Pieter E. Postmus, Sibrand Poppema, Charles H.C.M. Buys	1987	351
2	Chromosomal localization of human cellular homologues of two viral oncogenes Nature ·Nora Heisterkamp, John Groffen, John Stephenson, Nigel K. Spurr, Peter N. Goodfellow, E. Solomon, B. Carritt, Walter F. Bodmer	1982	256
3	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 ·Klaas Kok, Robert M.W. Hofstra, Alison Pilz, Anke van den Berg, P. Terpstra, C.H.C.M. Buys, B. Carritt	1993	83
4	Evolution of the Human RH (Rhesus) Blood Group Genes: A 50 Year Old Prediction (Partially) Fulfilled Human Molecular Genetics ·B. Carritt, Tim J. Kemp, Mark Poulter	1997	78
5	Assignment of the human locus determining phosphoglycolate phosphatase (PGP) to chromosome 16 Annals of Human Genetics ·S. Povey, S.J. Jeremiah, Richard F. Barker, D. A. HOPKINSON, E.B. Robson, P.J.L. Cook, E. Solomon, Martin Bobrow, B. Carritt, K.E. Buckton	1980	59
6	cDNA cloning, sequencing and chromosome mapping of a non-erythroid spectrin, human α-fodrin Differentiation ·Andrew P. McMahon, Dawn H. Giebelhaus, Janet E. Champion, Juliet A. Bailes, Simon F. Lacey, B. Carritt, Susan K. Henchman, Randall T. Moon	1987	55
7	Sequences homologous to the human D1S1 locus present on human chromosome 3. PubMed ·B. Carritt, Hazel Welch, Nilima Parry‐Jones	1986	55
8	Regional assignments of the loci <i>AK</i><sub>3</sub>, <i>ACO</i><i>N</i><sub>s</sub>, and <i>ASS</i> on human chromosome 9 Cytogenetic and Genome Research ·B. Carritt, Sue Povey	1979	53
9	DNA‐Based Rhesus Typing: Simultaneous Determination of RHC and RHD Status Using the Polymerase Chain Reaction Vox Sanguinis ·Mark Poulter, Tim J. Kemp, B. Carritt	1996	49
10	A recombination hot spot in the Rh genes revealed by analysis of unrelated donors with the rare D-- phenotype. PubMed ·Tim J. Kemp, Mark Poulter, B. Carritt	1996	48
11	Serotype Switching in a Partially Deleted RHD Gene Vox Sanguinis ·T Blunt, Geoff Daniels, B. Carritt	1994	46
12	Assignment of the DIA₁ locus to chromosome 22 Annals of Human Genetics ·Rosemary A. Fisher, S. Povey, Martin Bobrow, E. Solomon, Yvonne Boyd, B. Carritt	1977	46
13	Report of the committee on the genetic constitution of chromosomes 20 and 21 Cytogenetic and Genome Research ·B. Carritt, M. Litt	1988	45
14	Chromosome assignment of a human gene for argininosuccinate synthetase expression in Chinese hamster X human somatic cell hybrids Experimental Cell Research ·B. Carritt, Peter S. Goldfarb, M.L. Hooper, C. Slack	1977	43
15	Isolation and characterisation of Chinese hamster cells resistant to 5-fluorodeoxyuridine Experimental Cell Research ·C. Slack, Robert Morgan, B. Carritt, Peter S. Goldfarb, M HOOPER	1976	40
16	Adenosine 3′,5′ cyclic monophosphate in Life Sciences ·James J. Keirns, B. Carritt, Jenny Freeman, Jerome M. Eisenstadt, Mark W. Bitensky	1973	37
17	A gene from human chromosome region 3p21 with reduced expression in small cell lung cancer Lung Cancer ·B. Carritt, Klaas Kok, Anke van den Berg, J. Osinga, Alison Pilz, Robert M.W. Hofstra, M B Davis, A Y van der Veen, P.H. Rabbitts, K. Gulati	1993	36
18	Direct molecular analysis of a deletion of 3p in tumors from patients with sporadic renal cell carcinoma Cancer Genetics and Cytogenetics ·Annemarie H. van der Hout, Klaas Kok, Anke van den Berg, J. Wolter Oosterhuis, B. Carritt, Charles H.C.M. Buys	1988	33
19	An unusually proximal deletion on the short arm of chromosome 3 in a patient with small cell lung cancer Genomics ·Maria C. Daly, Jenny Douglas, N M Bleehen, P. Hastleton, P R Twentyman, V. Sundaresan, B. Carritt, Jonas Bergh, Pamela Rabbitts	1991	33
20	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 ·Catherine M. Abbott, Ian J. Jackson, B. Carritt, Sue Povey	1991	32

About B. Carritt

B. Carritt is a scholar working on Molecular Biology, Genetics, Hematology, Physiology and Epidemiology, having authored 64 papers that have together received 1.9k indexed citations. Recurring topics across this work include Blood groups and transfusion (12 papers), RNA modifications and cancer (8 papers), Genomic variations and chromosomal abnormalities (7 papers), Molecular Biology Techniques and Applications (7 papers), Erythrocyte Function and Pathophysiology (6 papers), Chromosomal and Genetic Variations (5 papers), RNA and protein synthesis mechanisms (5 papers) and Genomics and Chromatin Dynamics (4 papers). The work is most often cited by research in Hematology (449 citations), Genetics (504 citations), Cancer Research (259 citations), Genetics (180 citations) and Molecular Biology (1.0k citations). B. Carritt has collaborated with scholars based in United Kingdom, United States and Netherlands. Frequent co-authors include Mark Poulter, Tim J. Kemp, Klaas Kok, Charles H.C.M. Buys, E. Solomon, Sue Povey, Hazel Welch, Annemarie H. van der Hout, Pieter E. Postmus and Jan Osinga. Their work appears in journals such as Annals of Human Genetics, Cytogenetic and Genome Research, Vox Sanguinis, Nature and Experimental Cell Research.

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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