M. Bulman

777 citations
17 papers · 576 · h-index 12

Impact in

  • Genetics top 5%
    • Diabetes and associated disorders
    • BRCA gene mutations in cancer
    • Genetics and Neurodevelopmental Disorders
    • Genomic variations and chromosomal abnormalities
  • Surgery top 10%
    • Pancreatic function and diabetes

Papers in

    • BRCA gene mutations in cancer 8
    • Diabetes and associated disorders 4
    • Genomic variations and chromosomal abnormalities 3
    • Pancreatic function and diabetes 6

M. Bulman

17 papers receiving 560 citations

Peers

M. Bulman
Comparison fields: 5 of 55
  • Genetics 327
  • Surgery 301
  • Endocrinology, Diabetes and Metabolism 85
  • Reproductive Medicine 27
  • Molecular Biology 188
Replace Antti Kyrönlahti with:
Antti Kyrönlahti Finland
Laurence Michel‐Calemard France
Stacey C. Chapman United States
C. Diatloff‐Zito France
Greg Landes United States
Stanisław Zajączek Poland
M. A. Timmerman Netherlands
J. Szpirer Belgium
Erina Inoue Japan
M. Bulman relative to Antti Kyrönlahti Finland Antti Kyrönlahti's profile →
Citations per field
00.5×3.1×
Antti Kyrönlahti · 1×
Citations per year

Countries citing papers authored by M. Bulman

Since Specialization
Citations

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

Fields of papers citing papers by M. Bulman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

17 of 17 papers shown
#Work
1 2001203
2 200683
3 199740
4 199840
5 201536
6 199929
7 199428
8 200226
9 200825
10 200221
11 200414
12 200113
13 200311
14 20074
15 20181
16 20191
17 20231

About M. Bulman

M. Bulman is a scholar working on Genetics, Surgery, Molecular Biology, Reproductive Medicine and Cancer Research, having authored 17 papers that have together received 576 indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (8 papers), Pancreatic function and diabetes (6 papers), Diabetes and associated disorders (4 papers), Cancer Genomics and Diagnostics (3 papers), Ovarian cancer diagnosis and treatment (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Metabolism, Diabetes, and Cancer (2 papers) and Sarcoma Diagnosis and Treatment (1 paper). The work is most often cited by research in Genetics (327 citations), Surgery (301 citations), Endocrinology, Diabetes and Metabolism (85 citations), Reproductive Medicine (27 citations) and Molecular Biology (188 citations). M. Bulman has collaborated with scholars based in United Kingdom, United States and Denmark. Frequent co-authors include Andrew T. Hattersley, Sian Ellard, Timothy M. Frayling, Lisa I.S. Allen, D. Gareth Evans, Fiona Lalloo, Maggie Shepherd, Michael Hannemann, Coralie Bingham and Julie Evans. Their work appears in journals such as Journal of Medical Genetics, Diabetes, Familial Cancer, Diabetologia and Clinical Genetics.

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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