N.J. Barton

545 total citations
10 papers, 453 citations indexed

About

N.J. Barton is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, N.J. Barton has authored 10 papers receiving a total of 453 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 8 papers in Molecular Biology and 1 paper in Genetics. Recurrent topics in N.J. Barton's work include Genetic and Kidney Cyst Diseases (7 papers), Renal and related cancers (5 papers) and Genetic Syndromes and Imprinting (3 papers). N.J. Barton is often cited by papers focused on Genetic and Kidney Cyst Diseases (7 papers), Renal and related cancers (5 papers) and Genetic Syndromes and Imprinting (3 papers). N.J. Barton collaborates with scholars based in United Kingdom, United States and Azerbaijan. N.J. Barton's co-authors include Stephen T. Reeders, Peter C. Harris, Andrew O.M. Wilkie, Janette Lamb, Douglas R. Higgs, Veronica J. Buckle, R H Lindenbaum, Gregory G. Germino, Debra Weinstat‐Saslow and Michael Schneider and has published in prestigious journals such as The Lancet, Genomics and Cytogenetic and Genome Research.

In The Last Decade

N.J. Barton

8 papers receiving 436 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
N.J. Barton United Kingdom	7	303	264	77	59	53	10	453
Hideaki Chiyo Japan	14	196 0.6×	216 0.8×	69 0.9×	78 1.3×	26 0.5×	24	430
R.N. Simmers Australia	9	158 0.5×	205 0.8×	31 0.4×	9 0.2×	24 0.5×	10	389
C. Becker Germany	9	276 0.9×	334 1.3×	22 0.3×	28 0.5×	32 0.6×	9	484
G. Bourrouillou France	14	398 1.3×	279 1.1×	95 1.2×	23 0.4×	41 0.8×	40	587
ShunJiang Yu Canada	15	97 0.3×	270 1.0×	13 0.2×	23 0.4×	43 0.8×	18	492
Н. П. Кулешов Russia	10	129 0.4×	133 0.5×	61 0.8×	10 0.2×	46 0.9×	17	337
Franca Bernardi Italy	10	246 0.8×	116 0.4×	128 1.7×	19 0.3×	30 0.6×	13	367
Steven Schonberg United States	13	147 0.5×	247 0.9×	39 0.5×	80 1.4×	14 0.3×	19	422
D Liu United States	10	141 0.5×	197 0.7×	8 0.1×	92 1.6×	29 0.5×	11	416
G. R. Stalder Switzerland	12	256 0.8×	146 0.6×	87 1.1×	14 0.2×	53 1.0×	21	387

Countries citing papers authored by N.J. Barton

Since Specialization

Citations

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

Fields of papers citing papers by N.J. Barton

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of N.J. Barton

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

All Works

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10 of 10 papers shown

Somlo, Stefan, Gregory G. Germino, Brunhilde Wirth, et al.. (2015). The Molecular Genetics of Autosomal-Dominant Polycystic Kidney Disease of the PKD1 Type. Contributions to nephrology. 97. 101–109.

Lisowsky, Thomas, Debra Weinstat‐Saslow, N.J. Barton, Stephen T. Reeders, & Michael Schneider. (1995). A New Human Gene Located in thePKD1Region of Chromosome 16 Is a Functional Homologue toERV1of Yeast. Genomics. 29(3). 690–697. 48 indexed citations

Thomas, Spencer A., Michael Schneider, N.J. Barton, et al.. (1994). Linkage disequilibrium in the region of the autosomal dominant polycystic kidney disease gene (PKD1).. PubMed. 55(2). 365–71. 49 indexed citations

Germino, Gregory G., Debra Weinstat‐Saslow, Heinz Himmelbauer, et al.. (1992). The gene for autosomal dominant polycystic kidney disease lies in a 750-kb CpG-rich region. Genomics. 13(1). 144–151. 65 indexed citations

Mulley, J.C., N.J. Barton, & David F. Callen. (1990). Localisation of human PGP and HAGH genes to 16p13.3. Cytogenetic and Genome Research. 53(2-3). 175–176. 5 indexed citations

Germino, Gregory G., N.J. Barton, Janette Lamb, et al.. (1990). Identification of a locus which shows no genetic recombination with the autosomal dominant polycystic kidney disease gene on chromosome 16.. PubMed. 46(5). 925–33. 61 indexed citations

Harris, Peter C., N.J. Barton, Douglas R. Higgs, Stephen T. Reeders, & Andrew O.M. Wilkie. (1990). A long-range restriction map between the α-globin complex and a marker closely linked to the polycystic kidney disease 1 (PKD1) locus. Genomics. 7(2). 195–206. 43 indexed citations

Wilkie, Andrew O.M., Veronica J. Buckle, Peter C. Harris, et al.. (1990). Clinical features and molecular analysis of the alpha thalassemia/mental retardation syndromes. I. Cases due to deletions involving chromosome band 16p13.3.. PubMed. 46(6). 1112–26. 110 indexed citations

Lamb, Janette, R H Lindenbaum, Stephen T. Reeders, et al.. (1989). DETECTION OF BREAKPOINTS IN SUBMICROSCOPIC CHROMOSOMAL TRANSLOCATION, ILLUSTRATING AN IMPORTANT MECHANISM FOR GENETIC DISEASE. The Lancet. 334(8667). 819–824. 71 indexed citations

10.

Keith, Tim P., et al.. (1987). Linkage studies of autosomal dominant polycystic kidney disease pkd1 and a genetic map of chromosome 16 based on 40 rflp markers. 172. 1 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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