Mark Kroese

999 citations
28 papers · 633 · h-index 14

Impact in

    • Prenatal Screening and Diagnostics
    • Fetal and Pediatric Neurological Disorders
  • Genetics top 10%
    • BRCA gene mutations in cancer
    • Genomics and Rare Diseases
    • Genomic variations and chromosomal abnormalities

Papers in

    • BRCA gene mutations in cancer 13
    • Genomics and Rare Diseases 10
    • Genetic Associations and Epidemiology 5
    • Nutrition, Genetics, and Disease 4

Mark Kroese

28 papers receiving 596 citations

Peers

Mark Kroese
Comparison fields: 5 of 88
  • Pediatrics, Perinatology and Child Health 203
  • Genetics 241
  • Ophthalmology 51
  • Health Informatics 6
  • Infectious Diseases 72
Replace Virginie Hivert with:
Virginie Hivert France
David Westergaard Denmark
Ghazi Omar Tadmouri Türkiye
Shawneequa Callier United States
Juan Carlos Fernández-López Mexico
Juli Bollinger United States
Shalu Jain India
Chengcheng Liu China
Anne‐Marie Laberge Canada
Katherine Kolor United States
Mark Kroese relative to Virginie Hivert France Virginie Hivert's profile →
Citations per field
00.5×6.4×
Virginie Hivert · 1×
Citations per year

Countries citing papers authored by Mark Kroese

Since Specialization
Citations

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

Fields of papers citing papers by Mark Kroese

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Mark Kroese, 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 Mark Kroese Line = papers co-authored together Mark Kroese links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 28 papers — load more, or switch the sort, to bring in the rest.

#Work
1 2016109
2 200583
3 201476
4 201461
5 200732
6 200228
7 200425
8 200724
9 200924
10 202022
11 200322
12 200720
13 200720
14 200713
15 201012
16 201512
17 20148
18 20078
19 20227
20 20026

About Mark Kroese

Mark Kroese is a scholar working on Genetics, Molecular Biology, Radiology, Nuclear Medicine and Imaging, Infectious Diseases and Pediatrics, Perinatology and Child Health, having authored 28 papers that have together received 633 indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (13 papers), Genomics and Rare Diseases (10 papers), Genetic Associations and Epidemiology (5 papers), Nutrition, Genetics, and Disease (4 papers), Prenatal Screening and Diagnostics (3 papers), Cancer Genomics and Diagnostics (3 papers), Glaucoma and retinal disorders (2 papers) and Genetic factors in colorectal cancer (2 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (203 citations), Genetics (241 citations), Ophthalmology (51 citations), Health Informatics (6 citations) and Infectious Diseases (72 citations). Mark Kroese has collaborated with scholars based in United Kingdom, United States and Estonia. Frequent co-authors include Ron Zimmern, Simon Sanderson, R.L. Zimmern, Hilary Burton, Gurdeep S. Sagoo, Alison Hall, Julian P. T. Higgins, Jon Emery, Christine Patch and Alison Stewart. Their work appears in journals such as Genetics in Medicine, Journal of the Royal Society of Medicine, British Journal of Ophthalmology, Zoonoses and Public Health and Genome Medicine.

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.

Explore authors with similar magnitude of impact