Michael Bulman

2.2k total citations
21 papers, 1.6k citations indexed

About

Michael Bulman is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Michael Bulman has authored 21 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 13 papers in Genetics and 10 papers in Surgery. Recurrent topics in Michael Bulman's work include Pancreatic function and diabetes (9 papers), BRCA gene mutations in cancer (5 papers) and Renal and related cancers (4 papers). Michael Bulman is often cited by papers focused on Pancreatic function and diabetes (9 papers), BRCA gene mutations in cancer (5 papers) and Renal and related cancers (4 papers). Michael Bulman collaborates with scholars based in United Kingdom, United States and Germany. Michael Bulman's co-authors include Andrew T. Hattersley, Sian Ellard, Timothy M. Frayling, Lisa I.S. Allen, Coralie Bingham, Christine Garrett, Peter D. Turnpenny, Adrian S. Woolf, Eric S. Lander and C McKeown and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Investigation and Nature Genetics.

In The Last Decade

Michael Bulman

21 papers receiving 1.5k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Michael Bulman United Kingdom 15 921 805 804 229 143 21 1.6k
Véronique Gaston France 14 681 0.7× 616 0.8× 487 0.6× 252 1.1× 450 3.1× 22 1.4k
Jan Osinga Netherlands 23 754 0.8× 365 0.5× 384 0.5× 100 0.4× 44 0.3× 34 1.5k
Farzad Esni United States 21 871 0.9× 491 0.6× 1.2k 1.5× 297 1.3× 31 0.2× 38 1.8k
Ryuji Fukuzawa Japan 22 870 0.9× 276 0.3× 181 0.2× 50 0.2× 163 1.1× 68 1.2k
R Wadey United Kingdom 9 943 1.0× 417 0.5× 163 0.2× 123 0.5× 93 0.7× 14 1.1k
Johanna Sandgren Sweden 12 425 0.5× 335 0.4× 145 0.2× 63 0.3× 54 0.4× 21 818
Adriano Angioni Italy 21 739 0.8× 435 0.5× 176 0.2× 22 0.1× 95 0.7× 56 1.3k
Dalia L. Batista United States 14 732 0.8× 126 0.2× 371 0.5× 719 3.1× 37 0.3× 18 1.6k
Sabine Cordi Belgium 14 585 0.6× 264 0.3× 919 1.1× 58 0.3× 27 0.2× 23 1.5k
Florence Dastot France 16 385 0.4× 487 0.6× 129 0.2× 764 3.3× 54 0.4× 19 1.0k

Countries citing papers authored by Michael Bulman

Since Specialization
Citations

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

Fields of papers citing papers by Michael Bulman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Michael Bulman

This figure shows the co-authorship network connecting the top 25 collaborators of Michael Bulman. A scholar is included among the top collaborators of Michael Bulman 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 Michael Bulman. Michael Bulman 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
1.
Morgan, Robert D., George J. Burghel, Michael Bulman, et al.. (2023). Is Reflex Germline BRCA1/2 Testing Necessary in Women Diagnosed with Non-Mucinous High-Grade Epithelial Ovarian Cancer Aged 80 Years or Older?. Cancers. 15(3). 730–730. 2 indexed citations
2.
Morgan, Robert D., George J. Burghel, Michael Bulman, et al.. (2022). Predicting the likelihood of a BRCA1/2 pathogenic variant being somatic by testing only tumour DNA in non-mucinous high-grade epithelial ovarian cancer. Journal of Clinical Pathology. 76(10). 684–689. 3 indexed citations
3.
Woodward, Emma R., Kate Green, George J. Burghel, et al.. (2021). 30 year experience of index case identification and outcomes of cascade testing in high-risk breast and colorectal cancer predisposition genes. European Journal of Human Genetics. 30(4). 413–419. 18 indexed citations
4.
Morgan, Robert D., George J. Burghel, Michael Bulman, et al.. (2019). Prevalence of germline pathogenic BRCA1/2 variants in sequential epithelial ovarian cancer cases. Journal of Medical Genetics. 56(5). 301–307. 19 indexed citations
5.
Smith, Miriam J., Naomi L. Bowers, Michael Bulman, et al.. (2016). Revisiting neurofibromatosis type 2 diagnostic criteria to exclude LZTR1 -related schwannomatosis. Neurology. 88(1). 87–92. 92 indexed citations
6.
Smith, Miriam J., Soomin Ahn, Jung‐Il Lee, et al.. (2016). SMARCE1 mutation screening in classification of clear cell meningiomas. Histopathology. 70(5). 814–820. 22 indexed citations
7.
Smith, Miriam J., Jill Urquhart, Elaine F. Harkness, et al.. (2015). The Contribution of Whole Gene Deletions and Large Rearrangements to the Mutation Spectrum in Inherited Tumor Predisposing Syndromes. Human Mutation. 37(3). 250–256. 48 indexed citations
8.
Malone, Geraldine, Helen Alexandra Shaw, Liviuţa Budişan, et al.. (2008). The study of cystic fibrosis transmembrane conductance regulator gene mutations in a group of patients from Romania. Journal of Cystic Fibrosis. 7(5). 423–428. 4 indexed citations
9.
Bingham, Coralie, Michael Bulman, Sian Ellard, et al.. (2001). Mutations in the Hepatocyte Nuclear Factor-1β Gene Are Associated with Familial Hypoplastic Glomerulocystic Kidney Disease. The American Journal of Human Genetics. 68(1). 219–224. 204 indexed citations
10.
Kolatsi‐Joannou, Maria, Coralie Bingham, Sian Ellard, et al.. (2001). Hepatocyte Nuclear Factor-1β. Journal of the American Society of Nephrology. 12(10). 2175–2180. 92 indexed citations
11.
Bulman, Michael, Kenro Kusumi, Timothy M. Frayling, et al.. (2000). Mutations in the human Delta homologue, DLL3, cause axial skeletal defects in spondylocostal dysostosis. Nature Genetics. 24(4). 438–441. 297 indexed citations
12.
Bingham, Coralie, Sian Ellard, Lisa I.S. Allen, et al.. (2000). Abnormal nephron development associated with a frameshift mutation in the transcription factor hepatocyte nuclear factor-1β1. Kidney International. 57(3). 898–907. 139 indexed citations
13.
Ellard, Sian, Michael Bulman, Timothy M. Frayling, Maggie Shepherd, & Andrew T. Hattersley. (2000). Proposed mechanism for a novel insertion/deletion frameshift mutation (I414G415ATCG?CCA) in the hepatocyte nuclear factor 1 alpha (HNF-1?) gene which causes maturity-onset diabetes of the young (MODY). Human Mutation. 16(3). 273–273. 8 indexed citations
14.
Strandmann, Elke Pogge von, Sabine Senkel, Michael Bulman, et al.. (2000). The mutated human gene encoding hepatocyte nuclear factor 1β inhibits kidney formation in developing Xenopus embryos. Proceedings of the National Academy of Sciences. 97(9). 4695–4700. 62 indexed citations
15.
Turnpenny, Peter D., Michael Bulman, Timothy M. Frayling, et al.. (1999). A Gene for Autosomal Recessive Spondylocostal Dysostosis Maps to 19q13.1-q13.3. The American Journal of Human Genetics. 65(1). 175–182. 57 indexed citations
16.
Macfarlane, Wendy M., Timothy M. Frayling, Sian Ellard, et al.. (1999). Missense mutations in the insulin promoter factor-1 gene predispose to type 2 diabetes. Journal of Clinical Investigation. 104(9). R33–R39. 201 indexed citations
17.
Lemm, Ira, Elke Pogge von Strandmann, Christiane Zoidl, et al.. (1999). Loss of HNF1? function in human renal cell carcinoma: Frequent mutations in theVHL gene but not theHNF1? gene. Molecular Carcinogenesis. 24(4). 305–314. 13 indexed citations
18.
19.
Frayling, Timothy M., Michael Bulman, Sian Ellard, et al.. (1997). Mutations in the Hepatocyte Nuclear Factor–1α Gene Are a Common Cause of Maturity-Onset Diabetes of the Young in the U.K.. Diabetes. 46(4). 720–725. 192 indexed citations
20.
Williams, Jacqueline, Michael Bulman, Alison K. Huttly, Andrew L. Phillips, & Steven J. Neill. (1994). Characterization of a cDNA from Arabidopsis thaliana encoding a potential thiol protease whose expression is induced independently by wilting and abscisic acid. Plant Molecular Biology. 25(2). 259–270. 54 indexed citations

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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