M. Preus

1.3k citations
44 papers · 1.1k · h-index 19

Impact in

Papers in

    • Connective tissue disorders research 6
    • Dermatoglyphics and Human Traits 5
    • Genomic variations and chromosomal abnormalities 4
    • Diabetes and associated disorders 2

M. Preus

44 papers receiving 996 citations

Peers

M. Preus
Comparison fields: 5 of 89
  • Developmental Neuroscience 152
  • Developmental Biology 78
  • Genetics 472
  • Pediatrics, Perinatology and Child Health 142
  • Genetics 74
Replace N R Dennis with:
N R Dennis United Kingdom
Peter St. J. Dignan United States
S. Stengel‐Rutkowski Germany
Ann Haskins Olney United States
Jean‐Pierre Fryns Belgium
Kay Metcalfe United Kingdom
E. Ferda Perçin Türkiye
I. T. Thomas United States
Walter Fuhrmann Germany
Riyana Babul‐Hirji Canada
M. Preus relative to N R Dennis United Kingdom N R Dennis's profile →
Citations per field
00.5×1.5×1.9×
N R Dennis · 1×
Citations per year

Countries citing papers authored by M. Preus

Since Specialization
Citations

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

Fields of papers citing papers by M. Preus

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside M. Preus, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with M. Preus Line = papers co-authored together M. Preus links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 44 papers — load more, or switch the sort, to bring in the rest.

#Work
1 1985183
2 1984126
3 197262
4 198354
5 198648
6 198445
7 197336
8 197434
9 198633
10 198229
11 197726
12 197925
13 198525
14 198424
15 197722
16 198321
17 197121
18 198520
19 197418
20 197718

About M. Preus

M. Preus is a scholar working on Genetics, Molecular Biology, Pathology and Forensic Medicine, Clinical Biochemistry and Developmental Neuroscience, having authored 44 papers that have together received 1.1k indexed citations. Recurring topics across this work include Connective tissue disorders research (6 papers), Dermatoglyphics and Human Traits (5 papers), Metabolism and Genetic Disorders (4 papers), Williams Syndrome Research (4 papers), Genomic variations and chromosomal abnormalities (4 papers), Chromosomal and Genetic Variations (4 papers), Ophthalmology and Eye Disorders (3 papers) and Diabetes and associated disorders (2 papers). The work is most often cited by research in Developmental Neuroscience (152 citations), Developmental Biology (78 citations), Genetics (472 citations), Pediatrics, Perinatology and Child Health (142 citations) and Genetics (74 citations). M. Preus has collaborated with scholars based in Canada, United States and France. Frequent co-authors include F. Clarke Fraser, James F. Reynolds, Ségolène Aymé, John M. Opitz, Judith Allanson, Judith G. Hall, Helen E. Hughes, F C Fraser, Paige Kaplan and Michel Vekemans. Their work appears in journals such as Clinical Genetics, The Journal of Pediatrics, American Journal of Medical Genetics, Clinical Endocrinology and Obstetrical & Gynecological Survey.

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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