John MacPherson

541 total citations
13 papers, 405 citations indexed

About

John MacPherson is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, John MacPherson has authored 13 papers receiving a total of 405 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 5 papers in Molecular Biology and 5 papers in Cognitive Neuroscience. Recurrent topics in John MacPherson's work include Genetics and Neurodevelopmental Disorders (10 papers), Genomic variations and chromosomal abnormalities (6 papers) and Autism Spectrum Disorder Research (5 papers). John MacPherson is often cited by papers focused on Genetics and Neurodevelopmental Disorders (10 papers), Genomic variations and chromosomal abnormalities (6 papers) and Autism Spectrum Disorder Research (5 papers). John MacPherson collaborates with scholars based in United Kingdom, United States and India. John MacPherson's co-authors include Newton E. Morton, Anna Murray, P. A. Jacobs, N R Dennis, C.E. Bennett, Gerard Conway, David L. Nelson, Mark C. Hirst, Kay E. Davies and Veronica J. Buckle and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Human Molecular Genetics and Human Reproduction.

In The Last Decade

John MacPherson

13 papers receiving 394 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
John MacPherson United Kingdom	10	347	219	183	64	20	13	405
Marja‐Leena Väisänen Finland	8	336 1.0×	200 0.9×	203 1.1×	37 0.6×	20 1.0×	11	447
Joana Cobilanschi Germany	6	251 0.7×	234 1.1×	133 0.7×	118 1.8×	12 0.6×	7	420
Stela Filipovic-Sadic United States	7	511 1.5×	304 1.4×	358 2.0×	40 0.6×	12 0.6×	7	553
Joana Almeida Portugal	8	184 0.5×	123 0.6×	189 1.0×	25 0.4×	10 0.5×	13	309
James Macpherson United Kingdom	11	570 1.6×	303 1.4×	328 1.8×	71 1.1×	26 1.3×	17	677
Bert Ba de Vries Netherlands	5	270 0.8×	169 0.8×	121 0.7×	18 0.3×	10 0.5×	7	305
Mar Xunclà Spain	8	297 0.9×	220 1.0×	164 0.9×	51 0.8×	5 0.3×	13	355
Kathleen Rao United States	7	156 0.4×	203 0.9×	65 0.4×	24 0.4×	16 0.8×	9	312
Isabel Tejada Spain	6	359 1.0×	248 1.1×	223 1.2×	47 0.7×	12 0.6×	9	414

Countries citing papers authored by John MacPherson

Since Specialization

Citations

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

Fields of papers citing papers by John MacPherson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of John MacPherson

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

All Works

Sort: Min cites: Since: Top N: Style:

13 of 13 papers shown

Bennett, C.E., Gerard Conway, John MacPherson, P. A. Jacobs, & Anna Murray. (2010). Intermediate sized CGG repeats are not a common cause of idiopathic premature ovarian failure. Human Reproduction. 25(5). 1335–1338. 60 indexed citations

MacPherson, John. (2009). The Eucalyptus in the Daily Life and Medical Practice of the Australian Aborigines.. Mankind. 2(6). 175–180. 1 indexed citations

Ennis, Sarah, Andrew Collins, William Tapper, et al.. (2001). Allelic association discriminates draft orders. Annals of Human Genetics. 65(5). 503–504. 4 indexed citations

Ennis, Sarah, Andrew Collins, Anna Murray, John MacPherson, & Newton E. Morton. (2000). Allelic association in the FRAX region. Annals of Human Genetics. 64(6). 513–518. 1 indexed citations

Gunter, Chris, William Paradee, Dana C. Crawford, et al.. (1998). Re-examination of factors associated with expansion of CGG repeats using a single nucleotide polymorphism in FMR1. Human Molecular Genetics. 7(12). 1935–1946. 59 indexed citations

Teague, J., Newton E. Morton, N R Dennis, et al.. (1998). FRAXA and FRAXE: Evidence against segregation distortion and for an effect of intermediate alleles on learning disability. Proceedings of the National Academy of Sciences. 95(2). 719–724. 14 indexed citations

Murray, Anna, John MacPherson, Sheila Youings, et al.. (1997). The Role of Size, Sequence and Haplotype in the Stability of FRAXA and FRAXE Alleles during Transmission. Human Molecular Genetics. 6(2). 173–184. 62 indexed citations

Dennis, N R, et al.. (1996). Molecular re-investigation of patients with Huntington's disease in Wessex reveals a family with dentatorubral and pallidoluysian atrophy. Human Genetics. 97(1). 76–8. 19 indexed citations

MacPherson, John, John A. Crolla, N R Dennis, et al.. (1995). Unusual (CGG)n expansion and recombination in a family with fragile X and DiGeorge syndrome.. Journal of Medical Genetics. 32(3). 236–239. 21 indexed citations

10.

Morris, Adam P., Newton E. Morton, Andrew Collins, Sandra Lawrence, & John MacPherson. (1995). Evolutionary dynamics of the FMR1 locus. Annals of Human Genetics. 59(3). 283–289. 9 indexed citations

11.

Flynn, Geraldine, Mark C. Hirst, Samantha J.L. Knight, et al.. (1993). Identification of the FRAXE fragile site in two families ascertained for X linked mental retardation.. Journal of Medical Genetics. 30(2). 97–100. 52 indexed citations

12.

MacPherson, John, David L. Nelson, & P. A. Jacobs. (1992). Frequent small amplifications in the FMR-1 gene in fra(X) families: limits to the diagnosis of 'premutations'.. Journal of Medical Genetics. 29(11). 802–806. 17 indexed citations

13.

Morton, Newton E. & John MacPherson. (1992). Population genetics of the fragile-X syndrome: multiallelic model for the FMR1 locus.. Proceedings of the National Academy of Sciences. 89(9). 4215–4217. 86 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.

Explore authors with similar magnitude of impact