A. Haworth

884 total citations
15 papers, 542 citations indexed

About

A. Haworth is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, A. Haworth has authored 15 papers receiving a total of 542 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 7 papers in Cellular and Molecular Neuroscience and 5 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in A. Haworth's work include Ion channel regulation and function (6 papers), Genetic Neurodegenerative Diseases (6 papers) and Cardiac electrophysiology and arrhythmias (4 papers). A. Haworth is often cited by papers focused on Ion channel regulation and function (6 papers), Genetic Neurodegenerative Diseases (6 papers) and Cardiac electrophysiology and arrhythmias (4 papers). A. Haworth collaborates with scholars based in United Kingdom, Italy and Netherlands. A. Haworth's co-authors include Mary B. Davis, Richa Sud, Michael G. Hanna, Emma Matthews, Stéphanie Schorge, Dimitri M. Kullmann, Doreen Fialho, Robyn Labrum, Patrick F. Chinnery and G. Meola and has published in prestigious journals such as The Journal of Immunology, Brain and Neurology.

In The Last Decade

A. Haworth

15 papers receiving 526 citations

Peers

Countries citing papers authored by A. Haworth

Since Specialization

Citations

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

Fields of papers citing papers by A. Haworth

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of A. Haworth

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

All Works

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15 of 15 papers shown

#	Work	Indexed citations
1	A report on the impact of rapid prenatal exome sequencing on the clinical management of 52 ongoing pregnancies: a retrospective review 2020 ·BJOG An International Journal of Obstetrics & Gynaecology ·(unknown), A. Haworth, (unknown), (unknown), (unknown), Eva Serra, Janna Kenny, Frances Elmslie, Elena Greco, B. Thilaganathan, Sahar Mansour, Tessa Homfray, Suzanne Drury	29
2	K11 C9orf72 Expansions Are The Most Common Genetic Cause Of Huntington's Disease Phenocopy Presentations In A Uk Cohort 2014 ·Journal of Neurology Neurosurgery & Psychiatry ·(unknown), Mark Poulter, Jon Beck, (unknown), Tracy Campbell, G Adamson, Jason Hehir, Ese Mudanohwo, Peter McColgan, Edward J. Wild, A. Haworth, Mary G. Sweeney, Henry Houlden, Simon Mead, Sarah J. Tabrizi	2
3	1154 Skeletal muscle chloride channel gene (CLCN1) copy number variation can cause myotonia congenita 2012 ·Journal of Neurology Neurosurgery & Psychiatry ·(unknown), A. Haworth, Richa Sud, Emma Matthews, Doreen Fialho, J. Burge, Simona Portaro, António Toscano, Mary Dabney Davis, Michael G. Hanna	1
4	A new explanation for recessive myotonia congenita 2012 ·Neurology ·D.L. Raja Rayan, A. Haworth, Richa Sud, Emma Matthews, Doreen Fialho, J. Burge, Simona Portaro, Stéphanie Schorge, (unknown), Peter Lunt, Meriel McEntagart, António Toscano, Mary B. Davis, Michael G. Hanna	27
5	P39 Prevalence study of skeletal muscle channelopathies in England 2012 ·Neuromuscular Disorders ·Alejandro Horga, D.L. Raja Rayan, A. Haworth, Emma Matthews, Doreen Fialho, Richa Sud, Simona Portaro, J. Burge, Mary B. Davis, Michael G. Hanna	1
6	Acetazolamide efficacy in hypokalemic periodic paralysis and the predictive role of genotype 2011 ·Neurology ·Emma Matthews, Simona Portaro, Ke Qian, Richa Sud, A. Haworth, Mary B. Davis, Robert C. Griggs, Michael G. Hanna	72
7	Genetic heterogeneity and mechanisms of phenotypic variability in human skeletal muscle channelopathies 2011 ·(unknown), Emma Matthews, (unknown), Richa Sud, James M. Polke, A. Haworth, JL Holton, (unknown), Michael G. Hanna	1
8	Voltage sensor charge loss accounts for most cases of hypokalemic periodic paralysis 2008 ·Neurology ·Emma Matthews, Robyn Labrum, Mary G. Sweeney, Richa Sud, A. Haworth, Patrick F. Chinnery, G. Meola, Stéphanie Schorge, Dimitri M. Kullmann, Mary B. Davis, Michael G. Hanna	144
9	What causes paramyotonia in the United Kingdom? 2007 ·Neurology ·Emma Matthews, S. Veronica Tan, Doreen Fialho, M G Sweeney, Richa Sud, A. Haworth, Edouard G. Stanley, Gabriel Cea, Mary B. Davis, Michael G. Hanna	49
10	Chloride channel myotonia: exon 8 hot-spot for dominant-negative interactions 2007 ·Brain ·Doreen Fialho, Stéphanie Schorge, (unknown), Nigel P. Davies, (unknown), A. Haworth, Edouard G. Stanley, Richa Sud, (unknown), Mary B. Davis, Dimitri M. Kullmann, Michael G. Hanna	90
11	The mutation status of PAX3 and p53 genes in medulloblastoma. 1998 ·PubMed ·Weiguang Wang, Santhosh Kumar Pasupuleti, (unknown), Justin P. Whalley, Mikael Schwarz, Geraldine Malone, A. Haworth, Santosh Kumar	9
12	Cystic fibrosis mutations in Romania 1997 ·European Journal of Pediatrics ·Mircea Ioan Popa, (unknown), (unknown), Martin Schwarz, G. Hambleton, Geraldine Malone, A. Haworth, M Super	6
13	Active cascade testing for carriers of cystic fibrosis gene 1994 ·BMJ ·M Super, Martin Schwarz, Geraldine Malone, (unknown), A. Haworth, Gordana Dermody	66
14	Differential expression of the HLA class I multigene family by human embryonal carcinoma and choriocarcinoma cell lines. 1990 ·The Journal of Immunology ·(unknown), Sandra A. Vloemans, Peter J. van den Elsen, A. Haworth, Peter L. Stern	36
15	NOVEL HUMAN MHC CLASS I GENES ARE EXPRESSED BY TUMOUR CELL LINES REPRESENTING EMBRYONIC AND EXTRAEMBRYONIC TISSUES 1989 ·International Journal of Immunogenetics ·(unknown), (unknown), Peter J. van den Elsen, (unknown), Robynne Sutcliffe, (unknown), A. Haworth, Peter L. Stern	9

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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