M. W. Partington

6.8k citations
110 papers · 3.5k indexed · h-index 33
Topics
Genetics and Neurodevelopmental Disorders (36 papers)Metabolism and Genetic Disorders (21 papers)Genomic variations and chromosomal abnormalities (12 papers)

In The Last Decade

M. W. Partington

106 papers receiving 3.2k citations

Peers

M. W. Partington
Comparison fields: 5 of 120
  • Genetics 2.0k
  • Molecular Biology 1.8k
  • Cognitive Neuroscience 506
  • Pediatrics, Perinatology and Child Health 314
  • Cellular and Molecular Neuroscience 309
Replace E. Schwinger with:
E. Schwinger Germany
Irma Järvelä Finland
Carlos A. Bacino United States
Anatole S. Dekaban United States
Helger G. Yntema Netherlands
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Citations per field
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E. Schwinger · 1×
Citations per year

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
#WorkIndexed citations
1 102
2 39
3 65
4 14
5 317
6 26
7
Marketing in 3-D
6
8 24
9 15
10 104
11 167
12 33
13 5
14 47
15
The newborn phenylketonuria screening program in Ontario.
3
16
The heights and weights of Indian and Eskimo school children on James Bay and Hudson Bay.
15
17
CASE-FINDING IN PHENYLKETONURIA. I. REPORT OF A SURVEY BY THE COLLEGE OF GENERAL PRACTICE OF CANADA.
4
18
CASE FINDING IN PHENYLKETONURIA. II. THE GUTHRIE TEST.
12
19
WAARDENBURG'S SYNDROME AND HETEROCHROMIA IRIDUM IN A DEAF SCHOOL POPULATION.
48
20 27

About M. W. Partington

M. W. Partington is a scholar working on Clinical Biochemistry, Developmental Biology and Genetics, having authored 110 papers that have together received 3.5k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (36 papers), Metabolism and Genetic Disorders (21 papers) and Genomic variations and chromosomal abnormalities (12 papers). The work is most often cited by research in Genetics (2.0k citations), Clinical Biochemistry (291 citations) and Developmental Biology (86 citations). M. W. Partington has collaborated with scholars based in Canada, Australia and United Kingdom. Frequent co-authors include Gillian Turner, John C. Mulley, Jozef Gécz, Ági K. Gedeon, A. Hunter, H. Ghadimi, Joseph G. Gleeson, Kristina M. Allen, Christopher A. Walsh and Richard A. Cerione. Their work appears in journals such as Nature, New England Journal of Medicine and The Lancet.

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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