J. Peters

880 total citations
30 papers, 653 citations indexed

About

J. Peters is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, J. Peters has authored 30 papers receiving a total of 653 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 14 papers in Genetics and 5 papers in Surgery. Recurrent topics in J. Peters's work include Genetic Syndromes and Imprinting (5 papers), Pancreatic function and diabetes (5 papers) and Erythrocyte Function and Pathophysiology (4 papers). J. Peters is often cited by papers focused on Genetic Syndromes and Imprinting (5 papers), Pancreatic function and diabetes (5 papers) and Erythrocyte Function and Pathophysiology (4 papers). J. Peters collaborates with scholars based in United Kingdom, United States and Netherlands. J. Peters's co-authors include A.G. Searle, E.P. Evans, Mary F. Lyon, J. H. Edwards, Veronica J. Buckle, J. F. Loutit, R. J. Berry, Donald P. Doolittle, P.A. Lalley and A.L. Hillyard and has published in prestigious journals such as The Lancet, Analytical Biochemistry and Genetics.

In The Last Decade

J. Peters

30 papers receiving 612 citations

Peers

J. Peters

GENET

IMMUN

PPCH

Patrick D. Storto United States

J.B. Whitney United States

Tim L. Reudelhuber United States

P Meltzer United States

Thomas C. R. Miller United States

A C Syvänen Finland

S M Iguchi-Ariga Japan

P A Weller United Kingdom

Uwe Menzel Sweden

Patricia L. Yeyati United Kingdom

Patrick D. Storto United States

J. Peters

381 ×1.0

250 ×0.9

GENET

78 ×1.2

46 ×0.8

IMMUN

23 ×0.4

PPCH

Citations per year, relative to J. Peters J. Peters (= 1×) peers Patrick D. Storto

Countries citing papers authored by J. Peters

Since Specialization

Citations

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

Fields of papers citing papers by J. Peters

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of J. Peters

This figure shows the co-authorship network connecting the top 25 collaborators of J. Peters. A scholar is included among the top collaborators of J. Peters 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 J. Peters. J. Peters 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

Kelly, Michelle L., Lee Moir, Quentin M. Anstee, et al.. (2009). A missense mutation in the non-neural G-protein α-subunit isoforms modulates susceptibility to obesity. International Journal of Obesity. 33(5). 507–518. 22 indexed citations

Peters, J., et al.. (2006). Imprinting control within the compact <i>Gnas</i> locus. Cytogenetic and Genome Research. 113(1-4). 194–201. 18 indexed citations

Williamson, Catherine, C.V. Beechey, Simon Ball, et al.. (1998). Localisation of the imprinted gene neuronatin, <i>Nnat,</i> confirms and refines the location of a second imprinting region on mouse chromosome 2. Cytogenetic and Genome Research. 81(1). 73–78. 18 indexed citations

Evers, L. J. M., C. T. R. M. Schrander‐Stumpel, J.J.M. Engelen, et al.. (1996). Deletion of the long arm of chromosome 6: two new patients and literature review. Clinical Genetics. 50(3). 138–144. 21 indexed citations

Christner, Paul J., Linda D. Siracusa, David F. Hawkins, et al.. (1996). A high-resolution linkage map of the tight skin 2 (Tsk2) locus: A mouse model for scleroderma (SSc) and other cutaneous fibrotic diseases. Mammalian Genome. 7(8). 610–612. 19 indexed citations

Pearce, Stephen R., Michael J. Morgan, Simon Ball, J. Peters, & Pelin Faik. (1995). Sequence characterization of alleles Gpi1-s a and Gpi1-s b at the glucose phosphate isomerase structural locus. Mammalian Genome. 6(8). 537–539. 6 indexed citations

Engelen, J.J.M., et al.. (1994). Mosaic tetrasomy 8p in two patients: Clinical data and review of the literature. American Journal of Medical Genetics. 50(4). 377–380. 16 indexed citations

Tissier, Paul Le, J. Peters, & C. J. Skidmore. (1994). Development of an Assay Method for Purine Catabolic Enzymes in the Mouse and Its Adaptation for Use on an Autoanalyzer. Analytical Biochemistry. 222(1). 168–175. 10 indexed citations

Malas, Stavros, J. Peters, & Catherine M. Abbott. (1994). The genes for endothelin 3, vitamin D 24-hydroxylase, and melanocortin 3 receptor map to distal mouse Chromosome 2, in the region of conserved synteny with human Chromosome 20. Mammalian Genome. 5(9). 577–579. 7 indexed citations

10.

Peters, J. & Susan E. Lewis. (1991). Electrophoretic variation in multiple recessive tester, T, stock mice. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 249(2). 323–330. 2 indexed citations

11.

Peters, J. & Simon Ball. (1990). Parental influences on expression of glucose-6-phosphate dehydrogenase,G6pd, in the mouse; a case of imprinting. Genetics Research. 56(2-3). 245–252. 2 indexed citations

12.

Lalley, P.A., J. Peters, Donald P. Doolittle, et al.. (1990). Report of the comparative subcommittee for human and mouse homologies. Cytogenetic and Genome Research. 55(1-4). 434–456. 39 indexed citations

13.

Cattanach, B.M., J. Peters, & C. Rasberry. (1989). Induction of specific locus mutations in mouse spermatogonial stem cells by combined chemical X-ray treatments. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 212(1). 91–101. 8 indexed citations

14.

Searle, A.G., J. Peters, Mary F. Lyon, et al.. (1987). Chromosome maps of man and mouse, III. Genomics. 1(1). 3–18. 148 indexed citations

15.

Berry, R. J., Maili Jakobson, & J. Peters. (1987). Inherited differences within an island population of the House mouse (Mus domesticus). Journal of Zoology. 211(4). 605–618. 19 indexed citations

16.

Peters, J., et al.. (1986). The detection of gene mutations by electrophoresis, and their analysis.. PubMed. 209B. 367–74. 19 indexed citations

17.

Loutit, J. F., J. Peters, & A.G. Searle. (1986). Radiation and Haematopoiesis in Harwell Steel Mice. International Journal of Radiation Biology and Related Studies in Physics Chemistry and Medicine. 50(6). 1103–1116. 1 indexed citations

18.

Peters, J., et al.. (1983). Physiological variation of mouse haemoglobins. Proceedings of the Royal Society of London. Series B, Biological sciences. 218(1213). 443–453. 17 indexed citations

19.

Peters, J., et al.. (1982). Case report of mosaic partial tetrasomy 9 mimicking Klinefelter syndrome.. PubMed. 18(3B). 287–93. 10 indexed citations

20.

Peters, J.. (1962). LYMPHOEPITHELIAL STRUCTURES AND AUTOIMMUNE DISEASE. The Lancet. 280(7269). 1331–1331. 5 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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