Anwar Alhaq

454 total citations
19 papers, 345 citations indexed

About

Anwar Alhaq is a scholar working on Genetics, Hematology and Immunology. According to data from OpenAlex, Anwar Alhaq has authored 19 papers receiving a total of 345 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 12 papers in Hematology and 7 papers in Immunology. Recurrent topics in Anwar Alhaq's work include Coagulation, Bradykinin, Polyphosphates, and Angioedema (12 papers), Blood Coagulation and Thrombosis Mechanisms (8 papers) and Mast cells and histamine (5 papers). Anwar Alhaq is often cited by papers focused on Coagulation, Bradykinin, Polyphosphates, and Angioedema (12 papers), Blood Coagulation and Thrombosis Mechanisms (8 papers) and Mast cells and histamine (5 papers). Anwar Alhaq collaborates with scholars based in United Kingdom, France and United States. Anwar Alhaq's co-authors include Geoffrey F. Savidge, Michael Mitchell, Mark P. Smith, Diego Vergani, Letian Dai, Lutz-Peter Berg, D.N. Cooper, Katherine Spence, Simon Brown and Paula Bolton‐Maggs and has published in prestigious journals such as Blood, Human Molecular Genetics and British Journal of Haematology.

In The Last Decade

Anwar Alhaq

19 papers receiving 341 citations

Peers

Countries citing papers authored by Anwar Alhaq

Since Specialization

Citations

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

Fields of papers citing papers by Anwar Alhaq

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anwar Alhaq

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

All Works

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19 of 19 papers shown

#	Work	Indexed citations
1	Characterisation of five factor XI mutations 2007 ·Thrombosis and Haemostasis ·Letian Dai, John Clarke, Paula Bolton‐Maggs, Geoffrey F. Savidge, Anwar Alhaq, Michael Mitchell	6
2	Spectrum of factor XI (F11) mutations in the UK population – 116 index cases and 140 mutations 2006 ·Human Mutation ·Michael Mitchell, Roger Mountford, Rachel Butler, Anwar Alhaq, Letian Dai, Geoffrey F. Savidge, Paula Bolton‐Maggs	33
3	A G>A Transition in the Non-Coding Exon 1 of the Factor XI Gene as the Cause of Factor XI Deficiency in Three Afro-Caribbean Patients. 2005 ·Blood ·Michael Mitchell, Letian Dai, Anwar Alhaq, Geoffrey F. Savidge	1
4	The profibrinolytic effect of plasma thrombomodulin in factor XI deficiency and its implications in hemostasis 2004 ·Journal of Thrombosis and Haemostasis ·Lei Dai, Michael Mitchell, (unknown), Anwar Alhaq	11
5	Validation of a quantitative SPR assay for recombinant FVIII 2004 ·Clinical & Laboratory Haematology ·(unknown), (unknown), Geoffrey F. Savidge, Anwar Alhaq	6
6	Real‐Time quantitative PCR analysis of factor XI mRNA variants in human platelets 2004 ·Journal of Thrombosis and Haemostasis ·(unknown), Mark P. Smith, Geoffrey F. Savidge, Anwar Alhaq	18
7	An Alu-mediated 31.5-kb deletion as the cause of factor XI deficiency in 2 unrelated patients 2004 ·Blood ·Michael Mitchell, Letian Dai, Geoffrey F. Savidge, Anwar Alhaq	11
8	Anti-Von Willebrand Factor Antibody Is Responsible for Lower Levels of Plasma vWF in Blood Group O Individuals. 2004 ·Blood ·Letian Dai, (unknown), (unknown), Geoffrey F. Savidge, Anwar Alhaq	1
9	Eighteen unrelated patients with factor XI deficiency, four novel mutations and a 100% detection rate by denaturing high‐performance liquid chromatography 2003 ·British Journal of Haematology ·Michael Mitchell, (unknown), (unknown), Savita Rangarajan, Geoffrey F. Savidge, Anwar Alhaq	23
10	Evaluation of an automated screening assay for von Willebrand Disease Type 2N 2002 ·Clinical & Laboratory Haematology ·Steve L. Taylor, (unknown), Geoffrey F. Savidge, Anwar Alhaq	6
11	Novel mutations in heterozygous factor XI deficiency and hemorrhagic tendency 2000 ·Blood ·Anwar Alhaq, M. Leach, Dominique J. Pepper, (unknown), Geoffrey F. Savidge	3
12	Identification of an intronic regulatory element in the human protein C ( PROC) gene 2000 ·Human Genetics ·(unknown), Nadia Chuzhanova, Brad A. Friedman, (unknown), Anwar Alhaq, Sarah E. Millar, D.N. Cooper, Lutz-Peter Berg	19
13	Identification of a novel mutation in a non‐Jewish factor XI deficient kindred 1999 ·British Journal of Haematology ·Anwar Alhaq, Michael Mitchell, (unknown), Salman Rahman, Geraldine Flynn, (unknown), (unknown), Mark P. Smith, Geoffrey F. Savidge	24
14	Heterozygous factor XI deficiency associated with three novel mutations 1999 ·British Journal of Haematology ·Michael Mitchell, (unknown), Simon R. Thompson, Gary Moore, (unknown), Mark P. Smith, Geoffrey F. Savidge, Anwar Alhaq	28
15	Immune Tolerance Therapy for Haemophilia A Patients with Acquired Factor VIII Alloantibodies: Comprehensive Analysis of Experience at a Single Institution 1999 ·Thrombosis and Haemostasis ·Katherine Spence, (unknown), (unknown), Michael Mitchell, Jerry M. Cuttler, Anwar Alhaq, Simon Brown, Geoffrey F. Savidge, Mark P. Smith	53
16	Disruption of a binding site for hepatocyte nuclear factor 1 in the protein C gene promoter is associated with hereditary thrombophilia 1994 ·Human Molecular Genetics ·Lutz-Peter Berg, (unknown), Anwar Alhaq, Vijay V. Kakkar, D.N. Cooper	21
17	Clinical application of new technique that measures C4d for assessment of activation of classical complement pathway. 1988 ·Journal of Clinical Pathology ·Edward T. Davies, (unknown), Anwar Alhaq, Giorgio Senaldi, Diego Vergani	17
18	Activation of the alternative complement pathway: clinical application of a new technique to measure fragment Ba. 1987 ·Journal of Clinical Pathology ·Giorgio Senaldi, Mark Peakman, Anwar Alhaq, (unknown), D E Tee, Diego Vergani	14
19	Pathways to complement activation during cardiopulmonary bypass. 1984 ·BMJ ·(unknown), Anwar Alhaq, (unknown), (unknown), R.J. Ware, N J Dodd, (unknown), J Ponte, Diego Vergani	50

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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