I. M. Nesbitt

549 total citations
8 papers, 171 citations indexed

About

I. M. Nesbitt is a scholar working on Hematology, Genetics and Molecular Biology. According to data from OpenAlex, I. M. Nesbitt has authored 8 papers receiving a total of 171 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Hematology, 3 papers in Genetics and 2 papers in Molecular Biology. Recurrent topics in I. M. Nesbitt's work include Platelet Disorders and Treatments (4 papers), Blood groups and transfusion (3 papers) and Hemophilia Treatment and Research (3 papers). I. M. Nesbitt is often cited by papers focused on Platelet Disorders and Treatments (4 papers), Blood groups and transfusion (3 papers) and Hemophilia Treatment and Research (3 papers). I. M. Nesbitt collaborates with scholars based in United Kingdom, Netherlands and Türkiye. I. M. Nesbitt's co-authors include Anne Goodeve, I. R. Peake, F E Preston, Türkiz Gursel, Gerard Pals, Jørgen Ingerslev, Jan M. Cobben, Adel Abuzenadah, Nicolette S. den Hollander and Martina E. Daly and has published in prestigious journals such as Blood, Thrombosis and Haemostasis and European Journal of Human Genetics.

In The Last Decade

I. M. Nesbitt

8 papers receiving 168 citations

Peers

I. M. Nesbitt

HEMAT

GENET

SURGE

RHEUM

MB

Agustín Rodríguez‐Alén Spain

Ángela Rodríguez-Trillo Spain

Hironobu Mukaiyama Japan

Daniela Bartoletti Italy

Mathieu Platteel Netherlands

Hélène Antoine‐Poirel Belgium

Andrés Moret Spain

Sigrún Reykdal Iceland

Elisa Civaschi Italy

Dom McMullan United Kingdom

Agustín Rodríguez‐Alén Spain

I. M. Nesbitt

84 ×0.8

HEMAT

31 ×0.5

GENET

11 ×0.3

SURGE

19 ×0.6

RHEUM

18 ×0.7

MB

Citations per year, relative to I. M. Nesbitt I. M. Nesbitt (= 1×) peers Agustín Rodríguez‐Alén

Countries citing papers authored by I. M. Nesbitt

Since Specialization

Citations

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

Fields of papers citing papers by I. M. Nesbitt

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of I. M. Nesbitt

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

All Works

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8 of 8 papers shown

1.

Balasubramanian, Meena, Thomas M. Jenkins, Richard Kirk, et al.. (2018). Recurrent rhabdomyolysis caused by carnitine palmitoyltransferase II deficiency, common but under-recognised: Lessons to be learnt. Molecular Genetics and Metabolism Reports. 15. 69–70. 11 indexed citations

2.

Balasubramanian, Meena, Thomas M. Jenkins, Richard Kirk, et al.. (2018). Response to Finsterer: CPT-II deficiency needs to be detected in army personnel. Molecular Genetics and Metabolism Reports. 16. 12–12. 1 indexed citations

3.

Dijk, Fleur S. van, Peter G. J. Nikkels, Nicolette S. den Hollander, et al.. (2010). Lethal/Severe Osteogenesis Imperfecta in a Large Family: A Novel Homozygous LEPRE1 Mutation and Bone Histological Findings. Pediatric and Developmental Pathology. 14(3). 228–234. 16 indexed citations

4.

Dijk, Fleur S. van, I. M. Nesbitt, Peter G. J. Nikkels, et al.. (2009). CRTAP mutations in lethal and severe osteogenesis imperfecta: the importance of combining biochemical and molecular genetic analysis. European Journal of Human Genetics. 17(12). 1560–1569. 34 indexed citations

5.

Morris, Edward S., et al.. (2001). The management of von Willebrand's disease-associated gastrointestinal angiodysplasia. Blood Coagulation & Fibrinolysis. 12(2). 143–148. 24 indexed citations

6.

Allen, Simon, Adel Abuzenadah, I. M. Nesbitt, et al.. (2000). Two novel type 2N von Willebrand disease–causing mutations that result in defective factor VIII binding, multimerization, and secretion of von Willebrand factor. Blood. 95(6). 2000–2007. 50 indexed citations

7.

Preston, F. E., et al.. (1999). A Common Splice Site Mutation Is Shared by Two Families with Different Type 2N von Willebrand Disease Mutations. Thrombosis and Haemostasis. 82(9). 1061–1064. 7 indexed citations

8.

Nesbitt, I. M., Anne Goodeve, Andrea M. Guilliatt, et al.. (1996). Characterisation of Type 2N von Willebrand Disease Using Phenotypic and Molecular Techniques. Thrombosis and Haemostasis. 75(6). 959–964. 28 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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