M. Neil Macintyre

413 citations
17 papers · 338 indexed · h-index 12
Topics
Prenatal Screening and Diagnostics (5 papers)Genomic variations and chromosomal abnormalities (5 papers)Chromosomal and Genetic Variations (2 papers)

In The Last Decade

M. Neil Macintyre

17 papers receiving 275 citations

Peers

M. Neil Macintyre
Comparison fields: 5 of 69
  • Genetics 179
  • Pediatrics, Perinatology and Child Health 103
  • Molecular Biology 89
  • Plant Science 55
  • Public Health, Environmental and Occupational Health 36
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Citations per field
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Citations per year

Countries citing papers authored by M. Neil Macintyre

Since Specialization
Citations

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

Fields of papers citing papers by M. Neil Macintyre

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of M. Neil Macintyre

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

All Works

17 of 17 papers shown
#WorkIndexed citations
1 26
2 28
3 7
4 7
5
Tertiary trisomy in a human kindred containing an E/G translocation.
12
6
Chromosomal problems of intrauterine diagnosis.
9
7 19
8 5
9 62
10 39
11 14
12 18
13 22
14 2
15
The effects of acute infection and acute starvation on skeletal development; a study of young rats.
12
16 16
17 40

About M. Neil Macintyre

M. Neil Macintyre is a scholar working on Developmental Biology, Pediatrics, Perinatology and Child Health and Genetics, having authored 17 papers that have together received 338 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (5 papers), Genomic variations and chromosomal abnormalities (5 papers) and Chromosomal and Genetic Variations (2 papers). The work is most often cited by research in Developmental Biology (20 citations), Genetics (179 citations) and Pediatrics, Perinatology and Child Health (103 citations). M. Neil Macintyre has collaborated with scholars based in United States, Ireland and Canada. Frequent co-authors include J. de Grouchy, J Lejeune, J German, R. M. Acheson, BROWN M. DOBYNS, Sharon E. Mace, Nathalie T. Khalil, James E. Hunter, John Patterson and D. B. Walden. Their work appears in journals such as The Lancet, The Journal of Clinical Endocrinology & Metabolism and The Journal of Pediatrics.

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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