Malcolm Parslow

533 total citations
24 papers, 374 citations indexed

About

Malcolm Parslow is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Malcolm Parslow has authored 24 papers receiving a total of 374 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Genetics, 13 papers in Molecular Biology and 7 papers in Plant Science. Recurrent topics in Malcolm Parslow's work include Genomic variations and chromosomal abnormalities (13 papers), Chromosomal and Genetic Variations (6 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers). Malcolm Parslow is often cited by papers focused on Genomic variations and chromosomal abnormalities (13 papers), Chromosomal and Genetic Variations (6 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers). Malcolm Parslow collaborates with scholars based in New Zealand, Canada and Germany. Malcolm Parslow's co-authors include Elizabeth Baker, G.R. Sutherland, A. M. O. Veale, Joe J. Hoo, Patrick MacLeod, R. J. M. Gardner, George J. Allen, Lynnette R. Ferguson, Margherita Silengo and Willard R. Centerwall and has published in prestigious journals such as Journal of Medical Genetics, Human Genetics and Acta Paediatrica.

In The Last Decade

Malcolm Parslow

23 papers receiving 332 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Malcolm Parslow New Zealand 12 286 146 132 96 25 24 374
J. M. J. C. Scheres Netherlands 14 305 1.1× 215 1.5× 147 1.1× 122 1.3× 10 0.4× 28 457
Milly Andrle Austria 7 239 0.8× 191 1.3× 195 1.5× 72 0.8× 11 0.4× 11 358
B Quack France 13 396 1.4× 250 1.7× 195 1.5× 128 1.3× 6 0.2× 23 513
Anna Frackiewicz United Kingdom 9 390 1.4× 200 1.4× 209 1.6× 185 1.9× 14 0.6× 9 532
Peter M. Kroisel Austria 14 381 1.3× 231 1.6× 59 0.4× 248 2.6× 17 0.7× 18 500
B. Biederman Canada 11 256 0.9× 132 0.9× 139 1.1× 56 0.6× 5 0.2× 18 292
H.E. Wyandt United States 9 239 0.8× 258 1.8× 222 1.7× 114 1.2× 17 0.7× 14 446
F H Allen United States 6 142 0.5× 250 1.7× 243 1.8× 44 0.5× 7 0.3× 6 510
C.-L. Richer Canada 12 176 0.6× 173 1.2× 114 0.9× 50 0.5× 36 1.4× 28 361
Geneviève Lefort France 13 262 0.9× 148 1.0× 105 0.8× 160 1.7× 6 0.2× 29 375

Countries citing papers authored by Malcolm Parslow

Since Specialization
Citations

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

Fields of papers citing papers by Malcolm Parslow

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Malcolm Parslow

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

All Works

20 of 20 papers shown
1.
Tyson, Christine, Angelika J. Dawson, Todd J. Anderson, et al.. (2009). Molecular cytogenetic investigation of two patients with Y chromosome rearrangements and intellectual disability. American Journal of Medical Genetics Part A. 149A(3). 490–495. 14 indexed citations
2.
Wang, Jia‐Chi, Bradley P. Coe, Brenda Lomax, et al.. (2008). Inverted duplication with terminal deletion of 5p and no cat‐like cry. American Journal of Medical Genetics Part A. 146A(9). 1173–1179. 14 indexed citations
3.
Boycott, Kym M., et al.. (2003). A familial contiguous gene deletion syndrome at Xp22.3 characterized by severe learning disabilities and ADHD. American Journal of Medical Genetics Part A. 122A(2). 139–147. 32 indexed citations
4.
Parslow, Malcolm, et al.. (1991). Genetic stability of the D1Z2 region: implications for DNA genotyping and paternity testing. Genome. 34(5). 733–738. 1 indexed citations
5.
Romain, D R, et al.. (1990). Three cases of partial trisomy 7q owing to rare structural rearrangements of chromosome 7.. Journal of Medical Genetics. 27(2). 109–113. 26 indexed citations
6.
Gardner, R J, Nick Monk, George J. Allen, & Malcolm Parslow. (1986). A three way translocation in mother and daughter.. Journal of Medical Genetics. 23(1). 90.1–90. 24 indexed citations
7.
Ferguson, Lynnette R., et al.. (1986). Chromosome damage by dothistromin in human peripheral blood lymphocyte cultures: a comparison with aflatoxin B1. Mutation Research/Genetic Toxicology. 170(1-2). 47–53. 19 indexed citations
8.
Sutherland, G.R., Malcolm Parslow, & Elizabeth Baker. (1985). New classes of common fragile sites induced by 5-azacytidine and bromodeoxyuridine. Human Genetics. 69(3). 233–237. 79 indexed citations
9.
Crawford, Allan M., et al.. (1983). Changes in the karyotype of the cell line, DSIR‐HA‐1179, and a comparison with that of its parent insect, Heteronychus arator (F.) (Coleoptera: Scarabaeidae). New Zealand Journal of Zoology. 10(4). 405–407. 3 indexed citations
10.
Silengo, Margherita, et al.. (1981). Interstitial deletion of the long arm of chromosome no. 5 in two unrelated children with congenital anomalies and mental retardation. Clinical Genetics. 19(3). 174–180. 31 indexed citations
11.
Baker, Allan J., Malcolm Parslow, & David Chambers. (1981). KARYOLOGICAL STUDIES OF A FEMALE VARIABLE OYSTERCATCHER (HAEMATOPUS UNICOLOR). Canadian Journal of Genetics and Cytology. 23(4). 611–619. 1 indexed citations
12.
Hoo, Joe J., et al.. (1980). The ring nature of a tiny supernumerary chromosome fragment. American Journal of Medical Genetics. 5(4). 331–337. 9 indexed citations
13.
Gardner, R. J McKinlay, et al.. (1980). Studies on an XX male. Pathology. 12(1). 142–142. 1 indexed citations
14.
Parslow, Malcolm, et al.. (1979). Combination of differential sister chromatid staining, G-banding pattern, and X-inactivation pattern. Human Genetics. 47(3). 291–295. 7 indexed citations
15.
Parslow, Malcolm, et al.. (1979). Two cases of trisomy 12p due to rcpt(12;21)(p11;p11) inherited through three generations. Human Genetics. 47(3). 253–260. 25 indexed citations
16.
Parslow, Malcolm, et al.. (1979). Complex de novo rearrangement of chromosome 9 with clinical features of monosomy 9p syndrome. Clinical Genetics. 16(3). 151–155. 5 indexed citations
17.
Parslow, Malcolm, et al.. (1977). Down's syndrome and deletion of short arms of a G chromosome.. Journal of Medical Genetics. 14(2). 147–150. 4 indexed citations
18.
Gardner, R. J. M., et al.. (1974). Are 1q+ chromosomes harmless?. Clinical Genetics. 6(5). 383–393. 27 indexed citations
19.
Parslow, Malcolm, R. J McKinlay Gardner, & A. M. O. Veale. (1973). Giemsa banding in the t(13q13q) carrier mother of a translocation trisomy 13 abortus. Human Genetics. 18(2). 183–184. 6 indexed citations
20.
Parslow, Malcolm, et al.. (1972). THE CAT‐EYE SYNDROME REVIEW AND TWO FURTHER CASES OCCURRING IN FEMALE SIBLINGS WITH NORMAL CHROMOSOMES. Acta Paediatrica. 61(5). 581–586. 14 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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