Malcolm Ferguson-Smith

796 total citations
16 papers, 548 citations indexed

About

Malcolm Ferguson-Smith is a scholar working on Genetics, Plant Science and Molecular Biology. According to data from OpenAlex, Malcolm Ferguson-Smith has authored 16 papers receiving a total of 548 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 10 papers in Plant Science and 6 papers in Molecular Biology. Recurrent topics in Malcolm Ferguson-Smith's work include Chromosomal and Genetic Variations (10 papers), Prenatal Screening and Diagnostics (6 papers) and Genomic variations and chromosomal abnormalities (6 papers). Malcolm Ferguson-Smith is often cited by papers focused on Chromosomal and Genetic Variations (10 papers), Prenatal Screening and Diagnostics (6 papers) and Genomic variations and chromosomal abnormalities (6 papers). Malcolm Ferguson-Smith collaborates with scholars based in United Kingdom, United States and Brazil. Malcolm Ferguson-Smith's co-authors include Edivaldo Herculano Corrêa de Oliveira, Rafael Kretschmer, M.A. Ferguson‐Smith, Nicholas J. Lowe, C. Tease, Helen Impey, Cordelia Langford, Nigel Carter, Amanda Heppell-Parton and Pamela Rabbitts and has published in prestigious journals such as Nucleic Acids Research, Nature Genetics and PLoS ONE.

In The Last Decade

Malcolm Ferguson-Smith

16 papers receiving 534 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Malcolm Ferguson-Smith United Kingdom	11	312	249	222	160	54	16	548
Arvind Babu United States	9	359 1.2×	268 1.1×	349 1.6×	107 0.7×	25 0.5×	26	665
J. Olert Germany	12	224 0.7×	172 0.7×	305 1.4×	97 0.6×	33 0.6×	18	648
Jutta Müller‐Navia Germany	9	227 0.7×	168 0.7×	201 0.9×	76 0.5×	22 0.4×	13	396
Kasinathan Muralidharan United States	14	190 0.6×	72 0.3×	196 0.9×	79 0.5×	37 0.7×	21	561
Chenguang Zheng China	18	133 0.4×	49 0.2×	308 1.4×	86 0.5×	46 0.9×	62	792
H. F. de France Netherlands	13	324 1.0×	129 0.5×	144 0.6×	180 1.1×	33 0.6×	24	459
Mie Naruse Japan	7	230 0.7×	113 0.5×	372 1.7×	150 0.9×	19 0.4×	15	524
G Trabuchet France	18	261 0.8×	65 0.3×	278 1.3×	90 0.6×	7 0.1×	38	897
S. McBeath United Kingdom	13	475 1.5×	254 1.0×	313 1.4×	98 0.6×	15 0.3×	17	612
T Shiroishi Japan	13	385 1.2×	68 0.3×	555 2.5×	98 0.6×	22 0.4×	18	764

Countries citing papers authored by Malcolm Ferguson-Smith

Since Specialization

Citations

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

Fields of papers citing papers by Malcolm Ferguson-Smith

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Malcolm Ferguson-Smith. 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 Malcolm Ferguson-Smith. The network helps show where Malcolm Ferguson-Smith may publish in the future.

Co-authorship network of co-authors of Malcolm Ferguson-Smith

This figure shows the co-authorship network connecting the top 25 collaborators of Malcolm Ferguson-Smith. A scholar is included among the top collaborators of Malcolm Ferguson-Smith 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 Malcolm Ferguson-Smith. Malcolm Ferguson-Smith 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

Furo, Ivanete de Oliveira, Patrícia C. M. O’Brien, Jorge C. Pereira, et al.. (2021). Comparative chromosome painting in Spizaetus tyrannus and Gallus gallus with the use of macro- and microchromosome probes. PLoS ONE. 16(11). e0259905–e0259905. 2 indexed citations

Kretschmer, Rafael, Malcolm Ferguson-Smith, & Edivaldo Herculano Corrêa de Oliveira. (2018). Karyotype Evolution in Birds: From Conventional Staining to Chromosome Painting. Genes. 9(4). 181–181. 72 indexed citations

Kretschmer, Rafael, Ricardo José Gunski, Analía Del Valle Garnero, et al.. (2017). Chromosome Painting in Tyrant Flycatchers Confirms a Set of Inversions Shared by Oscines and Suboscines (Aves, Passeriformes). Cytogenetic and Genome Research. 153(4). 205–212. 16 indexed citations

Sessions, Stanley K., et al.. (2016). Evidence for Sex Chromosome Turnover in Proteid Salamanders. Cytogenetic and Genome Research. 148(4). 305–313. 19 indexed citations

Unger, Kristian, Johannes Wienberg, Andrew Riches, et al.. (2009). Novel gene rearrangements in transformed breast cells identified by high-resolution breakpoint analysis of chromosomal aberrations. Endocrine Related Cancer. 17(1). 87–98. 29 indexed citations

Doležel, Jaroslav, et al.. (2003). Introduction. Chromosome Research. 12(1). 1–4. 8 indexed citations

Stanyon, Roscoe, Stefania Consigliere, F. Bigoni, et al.. (2001). Reciprocal chromosome painting between a New World primate, the woolly monkey, and humans. Chromosome Research. 9(2). 97–106. 51 indexed citations

Rabbitts, Pamela, Helen Impey, Amanda Heppell-Parton, et al.. (1995). Chromosome specific paints from a high resolution flow karyotype of the mouse. Nature Genetics. 9(4). 369–375. 126 indexed citations

Maniatis, George M., et al.. (1994). Prenatal detection of trisomy 21 in uncultured amniocytes by fluorescence in situ hybridization: A prospective study. Prenatal Diagnosis. 14(11). 1049–1054. 36 indexed citations

10.

Goodburn, S., James R. Yates, P R Raggatt, et al.. (1994). Second‐trimester maternal serum screening using alpha‐fetoprotein, human chorionic gonadotrophin, and unconjugated oestriol: Experience of a regional programme. Prenatal Diagnosis. 14(5). 391–402. 83 indexed citations

11.

Waters, Jonathan J., et al.. (1990). Prenatal diagnosis of a double bisatellited marker with an unusual copy number ratio. Prenatal Diagnosis. 10(10). 677–681. 3 indexed citations

12.

Carter, N. P., et al.. (1990). Study of X chromosome abnormality in XX males using bivariate flow karyotype analysis and flow sorted dot blots. Cytometry. 11(1). 202–207. 40 indexed citations

13.

Stefani, Lorraine, James R. Galt, Anne S. Palmer, et al.. (1988). Expression of chromosome 21 specific sequences in normal and Down's syndrome tissues. Nucleic Acids Research. 16(7). 2885–2896. 13 indexed citations

14.

Besley, G. T. N., et al.. (1988). First trimester diagnosis of Gaucher disease in a fetus with trisomy 21. Prenatal Diagnosis. 8(6). 471–474. 5 indexed citations

15.

Tolmie, John, et al.. (1987). Normal development in two six‐year‐old boys born after prenatal diagnosis of trisomy 20 mosaicism. Prenatal Diagnosis. 7(8). 597–601. 7 indexed citations

16.

McNay, M. B., et al.. (1984). Aneuploidy and cystic hygroma detectable by ultrasound. Prenatal Diagnosis. 4(5). 377–382. 38 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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