C Grundy

1.2k total citations
12 papers, 312 citations indexed

About

C Grundy is a scholar working on Hematology, Molecular Biology and Nutrition and Dietetics. According to data from OpenAlex, C Grundy has authored 12 papers receiving a total of 312 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Hematology, 3 papers in Molecular Biology and 3 papers in Nutrition and Dietetics. Recurrent topics in C Grundy's work include Blood Coagulation and Thrombosis Mechanisms (9 papers), Hemophilia Treatment and Research (5 papers) and Vitamin K Research Studies (3 papers). C Grundy is often cited by papers focused on Blood Coagulation and Thrombosis Mechanisms (9 papers), Hemophilia Treatment and Research (5 papers) and Vitamin K Research Studies (3 papers). C Grundy collaborates with scholars based in United Kingdom, Germany and Sweden. C Grundy's co-authors include Andrew G. Tomkins, D.N. Cooper, Vijay V. Kakkar, V V Kakkar, Nicholas J. Lowe, Jenny Douglas, Anthony J. Bench, Ian Roberts, Donald Ogilvie and Jonas Bergh and has published in prestigious journals such as Nucleic Acids Research, Oncogene and Genomics.

In The Last Decade

C Grundy

12 papers receiving 300 citations

Peers

Countries citing papers authored by C Grundy

Since Specialization

Citations

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

Fields of papers citing papers by C Grundy

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of C Grundy

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

All Works

Sort: Min cites: Since: Top N: Style:

12 of 12 papers shown

#	Work	Indexed citations
1	Upper Temperature Limits of Orogenic Gold Deposit Formation: Constraints from the Granulite-Hosted Griffin's Find Deposit, Yilgarn Craton 2009 ·Economic Geology ·Andrew G. Tomkins, C Grundy	99
2	Homozygous deletions at 3p12 in breast and lung cancer 1998 ·Oncogene ·Vasi Sundaresan, Grace Chung, Amanda Heppell-Parton, (unknown), C Grundy, Ian Roberts, Louise James, Anthony Cahn, Anthony J. Bench, Jenny Douglas, John D. Minna, Yoshitaka Sekido, Michael I. Lerman, (unknown), Jonas Bergh, (unknown), Nicholas J. Lowe, Donald Ogilvie, Pamela Rabbitts	97
3	A novel nonsense mutation in the protein C (PROC) gene (Trp-29?Term) causing recurrent venous thrombosis 1993 ·Human Genetics ·(unknown), C Grundy, P Bignell, Drake C. Mitchell, (unknown), J. Paul Woods, V V Kakkar, D.N. Cooper	4
4	A Gla domain mutation (Arg 15???Trp) in the protein C (PROC) gene causing type 2 protein C deficiency and recurrent venous thrombosis 1993 ·Blood Coagulation & Fibrinolysis ·(unknown), C Grundy, P Bignell, (unknown), (unknown), V V Kakkar, D.N. Cooper	5
5	Protein C deficiency and thromboembolism: recurrent mutation at Arg 306 in the protein C gene 1992 ·Human Genetics ·C Grundy, Sam Schulman, Michael Krawczak, (unknown), V V Kakkar, D.N. Cooper	9
6	De novo splice site mutation in the antithrombin III (AT3) gene causing recurrent venous thrombosis: Demonstration of exon skipping by ectopic transcript analysis 1992 ·Genomics ·Lutz-Peter Berg, C Grundy, Frank J. Thomas, (unknown), (unknown), Ryszard Słomski, Jochen Reiss, Vijay V. Kakkar, D.N. Cooper	27
7	A novel missense mutation in the antithrombin III gene (Ser349→Pro) causing recurrent venous thrombosis 1992 ·Human Genetics ·C Grundy, (unknown), David Millar, Vijay V. Kakkar, D.N. Cooper	7
8	A single base-pair deletion in the protein C gene causing recurrent thromboembolism 1991 ·Thrombosis Research ·C Grundy, Hansjoerg Plendl, W. Grote, Barbara Zoll, V V Kakkar, D.N. Cooper	8
9	Improved carrier detection of haemophilia A using novel RFLPs at the DXS115 (767) locus 1990 ·Human Genetics ·Pavel Jedlička, Steven Greer, David Millar, C Grundy, EdmundC. Jenkins, Michael Mitchell, R.S. Mibashan, V V Kakkar, D.N. Cooper	2
10	The molecular genetic analysis of haemophilia A; characterization of six partial deletions in the factor VIII gene 1990 ·Human Genetics ·David Millar, Ricarda A. Steinbrecher, Kerstin Wieland, C Grundy, U. Martinowitz, Michael Krawczak, Barbara Zoll, D. H. Whitmore, J Stephenson, R.S. Mibashan, V V Kakkar, D.N. Cooper	34
11	Mspl RFLP in the human heparin cofactor II (HCF2) gene 1990 ·Nucleic Acids Research ·(unknown), C Grundy, Vijay V. Kakkar, D.N. Cooper	3
12	Protein C London 1: recurrent mutation at Arg 169 (CGG—TGG) in the protein C gene causing thrombosis 1989 ·Nucleic Acids Research ·C Grundy, A Chitolie, (unknown), David Bevan, Vijay V. Kakkar, D.N. Cooper	17

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