R S James

2.0k total citations · 1 hit paper
16 papers, 1.3k citations indexed

About

R S James is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Surgery. According to data from OpenAlex, R S James has authored 16 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 7 papers in Pediatrics, Perinatology and Child Health and 2 papers in Surgery. Recurrent topics in R S James's work include Prenatal Screening and Diagnostics (7 papers), Genomic variations and chromosomal abnormalities (7 papers) and Genetic Syndromes and Imprinting (6 papers). R S James is often cited by papers focused on Prenatal Screening and Diagnostics (7 papers), Genomic variations and chromosomal abnormalities (7 papers) and Genetic Syndromes and Imprinting (6 papers). R S James collaborates with scholars based in United Kingdom, United States and Greece. R S James's co-authors include P. A. Jacobs, Pamela Dalton, Brian Coppin, Dorothy Bishop, Cathy Creswell, Rhona McGurk, David Skuse, M.M. Power, D Skuse and D Robinson and has published in prestigious journals such as Nature, The American Journal of Human Genetics and Journal of Medical Genetics.

In The Last Decade

R S James

16 papers receiving 1.2k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive function

1997 522 citations David Skuse, R S James et al. Nature profile →

Peers

R S James

GENET

MB

PPCH

PS

CN

Walter Vegetti Italy

Akira Morishima United States

Susan Howell United States

Karen Kowal United States

Sheila Youings United Kingdom

Nicholas R. Dennis United Kingdom

Ichiko Nishijima Japan

Allison M. Cotton Canada

Chao Tian United States

Brian Coppin United Kingdom

Walter Vegetti Italy

R S James

696 ×0.7

GENET

352 ×0.7

MB

508 ×2.1

PPCH

106 ×0.6

PS

141 ×0.8

CN

Citations per year, relative to R S James R S James (= 1×) peers Walter Vegetti

Countries citing papers authored by R S James

Since Specialization

Citations

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

Fields of papers citing papers by R S James

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by R S James. 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 R S James. The network helps show where R S James may publish in the future.

Co-authorship network of co-authors of R S James

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

All Works

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16 of 16 papers shown

1.

Bowen, Wayne P., J.E. Carey, Atiqa Miah, et al.. (2000). Measurement of Cytochrome P450 Gene Induction in Human Hepatocytes using Quantitative Real-Time Reverse Transcriptase-Polymerase Chain Reaction. Drug Metabolism and Disposition. 28(7). 781–788. 92 indexed citations

2.

Dalton, Pamela, Brian Coppin, R S James, D Skuse, & P. A. Jacobs. (1998). Three patients with a 45,X/46,X,psu dic(Xp) karyotype.. Journal of Medical Genetics. 35(6). 519–524. 10 indexed citations

3.

Skuse, David, R S James, Dorothy Bishop, et al.. (1997). Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive function. Nature. 387(6634). 705–708. 522 indexed citations breakdown →

4.

James, R S, et al.. (1997). Molecular characterization of isochromosomes of Xq. Annals of Human Genetics. 61(6). 485–490. 23 indexed citations

5.

Jacobs, P. A., Pamela Dalton, R S James, et al.. (1997). Turner syndrome: a cytogenetic and molecular study. Annals of Human Genetics. 61(6). 471–483. 171 indexed citations

6.

Gardner, R J, Emma Wadsworth, Margo L. Whiteford, et al.. (1997). Aetiopathology and genetic basis of neonatal diabetes: Table 1. Archives of Disease in Childhood Fetal & Neonatal. 76(1). F39–F42. 103 indexed citations

7.

Power, M.M., R S James, John Barber, et al.. (1997). RDCI, the vasoactive intestinal peptide receptor: a candidate gene for the features of Albright hereditary osteodystrophy associated with deletion of 2q37.. Journal of Medical Genetics. 34(4). 287–290. 20 indexed citations

8.

Jacobs, P. A., Pamela Dalton, R S James, et al.. (1997). Turner syndrome: a cytogenetic and molecular study. Annals of Human Genetics. 61(6). 471–483. 132 indexed citations

9.

James, R S, Andrew J. Sharp, Annette E. Cockwell, Brian Coppin, & P. A. Jacobs. (1997). Evidence for a cryptic 46,XX cell line in a 45,X/46,X,psu idic(Xq) patient with normal reproduction.. Journal of Medical Genetics. 34(12). 1030–1032. 5 indexed citations

10.

Cockwell, Annette E., R S James, Isabella Moore, Eli Hatchwell, & John A. Crolla. (1996). Clinical outcomes of adjacent 1 segregation in a familial translocation t(8;18)(p21.3;p11.23).. Journal of Medical Genetics. 33(6). 515–517. 13 indexed citations

11.

James, R S, I. Karen Temple, N R Dennis, & John A. Crolla. (1995). A Search for Uniparental Disomyin Carriers of SupernumeraryMarker Chromosomes. European Journal of Human Genetics. 3(1). 21–26. 58 indexed citations

12.

Stallard, Richard E., et al.. (1995). Uniparental isodisomy 13 in a normal female due to transmission of a maternal t(13q13q). American Journal of Medical Genetics. 57(1). 14–18. 46 indexed citations

13.

James, R S, et al.. (1994). Paternal isodisomy of chromosome 6 in association with a maternal supernumerary marker chromosome (6). The American Journal of Human Genetics. 55(7). 469–70. 2 indexed citations

14.

James, R S, I. Karen Temple, Christine Patch, et al.. (1994). A Systematic Search forUniparental Disomy in Carriers ofChromosome Translocations. European Journal of Human Genetics. 2(2). 83–95. 29 indexed citations

15.

Houlston, Richard S., et al.. (1994). Duplication of 16q22-->qter confirmed by fluorescence in situ hybridisation and molecular analysis.. Journal of Medical Genetics. 31(11). 884–887. 22 indexed citations

16.

Temple, I. Karen, John Barber, R S James, & D.M. Burge. (1994). Diaphragmatic herniae and translocations involving 8q22 in two patients.. Journal of Medical Genetics. 31(9). 735–737. 22 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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