M. W. Partington

6.8k total citations
110 papers, 3.5k citations indexed

About

M. W. Partington is a scholar working on Genetics, Molecular Biology and Clinical Biochemistry. According to data from OpenAlex, M. W. Partington has authored 110 papers receiving a total of 3.5k indexed citations (citations by other indexed papers that have themselves been cited), including 53 papers in Genetics, 35 papers in Molecular Biology and 21 papers in Clinical Biochemistry. Recurrent topics in M. W. Partington's work include Genetics and Neurodevelopmental Disorders (36 papers), Metabolism and Genetic Disorders (21 papers) and Genomic variations and chromosomal abnormalities (12 papers). M. W. Partington is often cited by papers focused on Genetics and Neurodevelopmental Disorders (36 papers), Metabolism and Genetic Disorders (21 papers) and Genomic variations and chromosomal abnormalities (12 papers). M. W. Partington collaborates with scholars based in Canada, Australia and United Kingdom. M. W. Partington's co-authors include Gillian Turner, John C. Mulley, Jozef Gécz, Ági K. Gedeon, A. Hunter, H. Ghadimi, Shubha Bagrodia, Richard A. Cerione, John MacMillan and Christopher A. Walsh and has published in prestigious journals such as Nature, New England Journal of Medicine and The Lancet.

In The Last Decade

M. W. Partington

106 papers receiving 3.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
M. W. Partington Canada 33 2.0k 1.8k 506 314 309 110 3.5k
Dawna Armstrong United States 20 2.1k 1.0× 3.0k 1.7× 793 1.6× 360 1.1× 863 2.8× 33 4.2k
Petter Strømme Norway 28 1.1k 0.6× 1.2k 0.7× 311 0.6× 296 0.9× 296 1.0× 76 2.7k
J Boué France 22 1.5k 0.8× 1.4k 0.8× 583 1.2× 377 1.2× 224 0.7× 82 2.6k
Helger G. Yntema Netherlands 35 2.6k 1.3× 2.7k 1.5× 401 0.8× 357 1.1× 372 1.2× 100 4.9k
Generoso G. Gascon Saudi Arabia 33 538 0.3× 1.3k 0.7× 419 0.8× 378 1.2× 368 1.2× 92 3.5k
Patrick MacLeod Canada 29 910 0.5× 1.3k 0.8× 184 0.4× 403 1.3× 644 2.1× 74 3.1k
Marlène Rio France 33 1.7k 0.8× 2.2k 1.2× 197 0.4× 263 0.8× 237 0.8× 112 3.5k
David Schlessinger United States 31 2.2k 1.1× 2.4k 1.3× 577 1.1× 185 0.6× 413 1.3× 61 3.8k
Mårten Kyllerman Sweden 34 759 0.4× 1.2k 0.7× 291 0.6× 1.0k 3.2× 350 1.1× 88 3.1k
Luba Kalaydjieva Australia 34 1.4k 0.7× 1.5k 0.9× 221 0.4× 99 0.3× 669 2.2× 95 3.5k

Countries citing papers authored by M. W. Partington

Since Specialization
Citations

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

Fields of papers citing papers by M. W. Partington

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by M. W. Partington. 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 M. W. Partington. The network helps show where M. W. Partington may publish in the future.

Co-authorship network of co-authors of M. W. Partington

This figure shows the co-authorship network connecting the top 25 collaborators of M. W. Partington. A scholar is included among the top collaborators of M. W. Partington 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 M. W. Partington. M. W. Partington 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.
Ropers, Hans‐Hilger, Maria Hoeltzenbein, Vera M. Kalscheuer, et al.. (2003). Nonsyndromic X-linked mental retardation: where are the missing mutations?. Trends in Genetics. 19(6). 316–320. 46 indexed citations
2.
Shoichet, Sarah A., Kirsten Hoffmann, Corinna Menzel, et al.. (2003). Mutations in the ZNF41 Gene Are Associated with Cognitive Deficits: Identification of a New Candidate for X-Linked Mental Retardation. The American Journal of Human Genetics. 73(6). 1341–1354. 65 indexed citations
3.
Turner, Gillian, Ági K. Gedeon, Bronwyn Kerr, et al.. (2002). Syndromic form of X‐linked mental retardation with marked hypotonia in early life, severe mental handicap, and difficult adult behavior maps to Xp22. American Journal of Medical Genetics Part A. 117A(3). 245–250. 14 indexed citations
4.
Partington, M. W., David Mowat, Stewart Einfeld, Bruce J. Tonge, & Gillian Turner. (2000). Genes on the X chromosome are important in undiagnosed mental retardation. American Journal of Medical Genetics. 92(1). 57–61. 26 indexed citations
5.
Partington, M. W., et al.. (1999). Marketing in 3-D. The McKinsey Quarterly. 6. 6 indexed citations
6.
Donnelly, Andrew J., et al.. (1996). Regional localization of two non-specific X-linked mental retardation genes (MRX30 andMRX31). American Journal of Medical Genetics. 64(1). 113–120. 24 indexed citations
7.
Partington, M. W., et al.. (1996). Confirmation of early menopause in fragile X carriers. American Journal of Medical Genetics. 64(2). 370–372. 52 indexed citations
8.
Biancalana, Valérie, Elisabeth Trivier, C. R. Weber, et al.. (1994). Construction of a High-Resolution Linkage Map for Xp22.1-p22.2 and Refinement of the Genetic Localization of the Coffin-Lowry Syndrome Gene. Genomics. 22(3). 617–625. 32 indexed citations
9.
Gedeon, Ági K., Emma K. Baker, Harriet L. Robinson, et al.. (1992). Fragile X syndrome without CCG amplification has an FMR1 deletion. Nature Genetics. 1(5). 341–344. 167 indexed citations
10.
Laing, Susan T., et al.. (1988). Is there a fragile(X) negative Martin‐Bell syndrome?. American Journal of Medical Genetics. 30(1-2). 459–471. 4 indexed citations
11.
Partington, M. W., John M. Opitz, & James F. Reynolds. (1986). Female relatives in families with the fragile X syndrome. American Journal of Medical Genetics. 23(1-2). 111–126. 7 indexed citations
12.
Partington, M. W., et al.. (1981). Familial cutaneous amyloidosis with systemic manifestations in males. American Journal of Medical Genetics. 10(1). 65–75. 34 indexed citations
13.
Partington, M. W. & Alexander C. Ferguson. (1977). Serotonin metabolism in cystic fibrosis.. Archives of Disease in Childhood. 52(5). 386–390. 4 indexed citations
14.
Partington, M. W. & Nicola Roberts. (1969). The heights and weights of Indian and Eskimo school children on James Bay and Hudson Bay.. PubMed Central. 100(11). 502–9. 15 indexed citations
15.
Hanley, Will, et al.. (1969). The newborn phenylketonuria screening program in Ontario.. PubMed. 101(4). 185–90. 3 indexed citations
16.
Partington, M. W.. (1967). Phenylketonuria and diet.. PubMed. 97(17). 1033–4. 4 indexed citations
17.
Partington, M. W.. (1964). WAARDENBURG'S SYNDROME AND HETEROCHROMIA IRIDUM IN A DEAF SCHOOL POPULATION.. PubMed. 90. 1008–17. 48 indexed citations
18.
Partington, M. W., et al.. (1964). CASE-FINDING IN PHENYLKETONURIA. I. REPORT OF A SURVEY BY THE COLLEGE OF GENERAL PRACTICE OF CANADA.. PubMed. 90. 1312–4. 4 indexed citations
19.
Partington, M. W., et al.. (1964). CASE FINDING IN PHENYLKETONURIA. II. THE GUTHRIE TEST.. PubMed. 91. 105–14. 12 indexed citations
20.
Partington, M. W. & Elizabeth Lewis. (1963). Variations with age in plasma phenylalanine and tyrosine levels in phenylketonuria. The Journal of Pediatrics. 62(3). 348–357. 27 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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