I. M. Nesbitt

549 citations

8 papers · 171 indexed · h-index 7

Co-authors: Anne Goodeve I. R. Peake F E Preston Türkiz Gursel Gerard Pals Jørgen Ingerslev Jan M. Cobben Adel Abuzenadah
Topics: Platelet Disorders and Treatments (4 papers)Blood groups and transfusion (3 papers)Hemophilia Treatment and Research (3 papers)
Cited by: Hematology Rheumatology Genetics
Journals: Blood Thrombosis and Haemostasis European Journal of Human Genetics
Partner nations: United Kingdom Netherlands Türkiye

In The Last Decade

I. M. Nesbitt

8 papers receiving 168 citations

Peers

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

#	Work	Indexed citations
1	Recurrent rhabdomyolysis caused by carnitine palmitoyltransferase II deficiency, common but under-recognised: Lessons to be learnt 2018 ·Molecular Genetics and Metabolism Reports ·Meena Balasubramanian,Thomas M. Jenkins,Richard Kirk,I. M. Nesbitt,S. E. Olpin,(unknown),Godfrey T. Gillett	11
2	Response to Finsterer: CPT-II deficiency needs to be detected in army personnel 2018 ·Molecular Genetics and Metabolism Reports ·Meena Balasubramanian,Thomas M. Jenkins,Richard Kirk,I. M. Nesbitt,S. E. Olpin,(unknown),Godfrey T. Gillett	1
3	Lethal/Severe Osteogenesis Imperfecta in a Large Family: A Novel Homozygous LEPRE1 Mutation and Bone Histological Findings 2010 ·Pediatric and Developmental Pathology ·Fleur S. van Dijk,Peter G. J. Nikkels,Nicolette S. den Hollander,I. M. Nesbitt,Rick R. van Rijn,Jan M. Cobben,Gerard Pals	16
4	CRTAP mutations in lethal and severe osteogenesis imperfecta: the importance of combining biochemical and molecular genetic analysis 2009 ·European Journal of Human Genetics ·Fleur S. van Dijk,I. M. Nesbitt,Peter G. J. Nikkels,Ann Dalton,Ernie M.H.F. Bongers,Jiddeke M. van de Kamp,Yvonne Hilhorst‐Hofstee,Nicolette S. den Hollander,Augusta M.A. Lachmeijer,Carlo Marcelis,Gita Tan-Sindhunata,Rick R. van Rijn,Hanne Meijers‐Heijboer,Jan M. Cobben,Gerard Pals	34
5	The management of von Willebrand's disease-associated gastrointestinal angiodysplasia 2001 ·Blood Coagulation & Fibrinolysis ·Edward S. Morris,K. K. Hampton,I. M. Nesbitt,F E Preston,(unknown),Μichael Μakris	24
6	Two novel type 2N von Willebrand disease–causing mutations that result in defective factor VIII binding, multimerization, and secretion of von Willebrand factor 2000 ·Blood ·Simon Allen,Adel Abuzenadah,(unknown),(unknown),I. M. Nesbitt,Anne Goodeve,Türkiz Gursel,Jørgen Ingerslev,I. R. Peake,Martina E. Daly	50
7	A Common Splice Site Mutation Is Shared by Two Families with Different Type 2N von Willebrand Disease Mutations 1999 ·Thrombosis and Haemostasis ·(unknown),F. E. Preston,(unknown),(unknown),I. M. Nesbitt	7
8	Characterisation of Type 2N von Willebrand Disease Using Phenotypic and Molecular Techniques 1996 ·Thrombosis and Haemostasis ·I. M. Nesbitt,Anne Goodeve,Andrea M. Guilliatt,Michael Makris,F E Preston,I. R. Peake	28

About I. M. Nesbitt

I. M. Nesbitt is a scholar working on Hematology, Clinical Biochemistry and Gastroenterology, having authored 8 papers that have together received 171 indexed citations. Recurring topics across this work include Platelet Disorders and Treatments (4 papers), Blood groups and transfusion (3 papers) and Hemophilia Treatment and Research (3 papers). The work is most often cited by research in Hematology (103 citations), Rheumatology (33 citations) and Genetics (61 citations). I. M. Nesbitt has collaborated with scholars based in United Kingdom, Netherlands and Türkiye. Frequent 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. Their work appears in journals such as Blood, Thrombosis and Haemostasis and European Journal of Human 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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