Ann Curtis

2.3k total citations
53 papers, 1.6k citations indexed

About

Ann Curtis is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Ann Curtis has authored 53 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 12 papers in Cellular and Molecular Neuroscience and 9 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Ann Curtis's work include Genetic Neurodegenerative Diseases (11 papers), Cystic Fibrosis Research Advances (7 papers) and Genetic factors in colorectal cancer (5 papers). Ann Curtis is often cited by papers focused on Genetic Neurodegenerative Diseases (11 papers), Cystic Fibrosis Research Advances (7 papers) and Genetic factors in colorectal cancer (5 papers). Ann Curtis collaborates with scholars based in United Kingdom, United States and Belgium. Ann Curtis's co-authors include John Burn, Paul G. Ince, Patrick F. Chinnery, George Fink, Andrew R.J. Curtis, David Bates, Christopher M. Morris, Alan Coulthard, Margaret Jackson and Laurence A. Bindoff and has published in prestigious journals such as The Lancet, Nature Genetics and Annals of Neurology.

In The Last Decade

Ann Curtis

52 papers receiving 1.6k citations

Peers

Countries citing papers authored by Ann Curtis

Since Specialization

Citations

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

Fields of papers citing papers by Ann Curtis

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ann Curtis

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Allelic mRNA expression imbalance in C-type lectins reveals a frequent regulatory SNP in the human surfactant protein A (SP-A) gene 2013 ·Genes and Immunity ·Abul Kalam Azad, Ann Curtis, A C Papp, Amy Webb, Daren L. Knoell, Wolfgang Sadée, Larry S. Schlesinger	6
2	MLH1 Differential Allelic Expression in Mutation Carriers and Controls 2010 ·Annals of Human Genetics ·Mauro Santibáñez Koref, Valerie Wilson, (unknown), Michael S. Cunnington, John C. Mathers, D. Timothy Bishop, Ann Curtis, Malcolm G. Dunlop, John Burn	12
3	Molecular epidemiology of spinocerebellar ataxia type 6 2004 ·Annals of Neurology ·Kate Craig, Sharon Keers, (unknown), Ann Curtis, Patrick F. Chinnery	35
4	Neuroferritinopathy: A Window on the Role of Iron in Neurodegeneration 2002 ·Blood Cells Molecules and Diseases ·Douglas E. Crompton, Patrick F. Chinnery, (unknown), Andrew R.J. Curtis, Christopher M. Morris, (unknown), Alastair D. Burt, (unknown), Alan Coulthard, Ann Curtis, Paul G. Ince, David Bates, Margaret Jackson, John Burn	55
5	Late‐onset axial jerky dystonia due to the DYT1 deletion 2002 ·Movement Disorders ·Patrick F. Chinnery, Paul Reading, (unknown), Ann Curtis, David J. Burn	16
6	Donor-Acquired Small Cell Lung Cancer Following Pulmonary Transplantation 2001 ·CHEST Journal ·Anthony De Soyza, John H. Dark, Dinah V. Parums, Ann Curtis, Paul A. Corris	36
7	Mutation in the gene encoding ferritin light polypeptide causes dominant adult-onset basal ganglia disease 2001 ·Nature Genetics ·Andrew R.J. Curtis, (unknown), Christopher M. Morris, Laurence A. Bindoff, Paul G. Ince, Patrick F. Chinnery, Alan Coulthard, Margaret Jackson, Andrew P. Jackson, Duncan P. McHale, (unknown), William Barker, Alex Markham, David Bates, Ann Curtis, John Burn	386
8	Detection of mutations in mismatch repair genes in Portuguese families with hereditary non-polyposis colorectal cancer (HNPCC) by a multi-method approach 2000 ·European Journal of Human Genetics ·Paulo Fidalgo, Maria Rosário Almeida, Sarah L. West, Cláudia Gaspar, (unknown), Juul Wijnen, Cristina Albuquerque, Ann Curtis, Marília Cravo, Riccardo Fodde, C. Nobre Leitão, John Burn	28
9	Comparative Evaluation of Three Continuous Speech Recognition Software Packages in the Generation of Medical Reports 2000 ·Journal of the American Medical Informatics Association ·Eric Devine, Stephan A. Gaehde, Ann Curtis	68
10	Delayed engraftment and mixed chimerism after HLA-identical sibling donor BMT in Fanconi anaemia 1999 ·Bone Marrow Transplantation ·(unknown), Ann Curtis, V. Spencer, D Barge, Roderick Skinner	6
11	Novel insertion in the KSP region of the neurofilament heavy gene in amyotrophic lateral sclerosis (ALS) 1998 ·Neuroreport ·Janine Tomkins, (unknown), Janet Y. Slade, Paul G. Ince, Ann Curtis, K. Bushby, Pamela J. Shaw	123
12	Mutation detection in exons 1–14 of the adenomatous polyposis coli gene: identification of an alternatively spliced transcript 1996 ·Molecular and Cellular Probes ·(unknown), Sarah P. West, (unknown), John Burn, Ann Curtis	1
13	Absence of cystic fibrosis mutations in a large Asian population sample and occurrence of a homozygous S549N mutation in an inbred Pakistani family. 1993 ·Journal of Medical Genetics ·Ann Curtis, Rebecca J. Richardson, (unknown), Adam Jackson, Roger Nelson, S.S. Bhattacharya	24
14	Molecular genetics of inherited retinal degenerations 1992 ·Current Opinion in Genetics & Development ·Susan Lindsay, C.F. Inglehearn, Ann Curtis, Shomi S. Bhattacharya	11
15	Association of less common cystic fibrosis mutations with a mild phenotype. 1991 ·Journal of Medical Genetics ·Ann Curtis, Roger Nelson, Mary Porteous, John Burn, Siladitya Bhattacharya	17
16	The haplotype distribution of the ΔF508 mutation in cystic fibrosis families in Scotland 1990 ·Human Genetics ·Iain McIntosh, Ann Curtis, (unknown), M Keston, (unknown), (unknown), D. J. H. Brock	9
17	Genetic linkage between Huntington's disease and D4S10(G8) in Scottish families 1989 ·Clinical Genetics ·Susan Holloway, (unknown), Ann Curtis, Moira Mennie, D. J. H. Brock	1
18	Use of linkage disequilibrium data in prenatal diagnosis of cystic fibrosis 1988 ·Human Genetics ·Lisa Strain, Ann Curtis, Moira Mennie, Susan Holloway, D. J. H. Brock	14
19	First‐trimester prenatal diagnosis of cystic fibrosis using fibroblasts from a deceased index child to establish haplotypes 1988 ·Prenatal Diagnosis ·Ann Curtis, Lisa Strain, Moira Mennie, Susan Holloway, J. A. Raeburn, G. T. N. Besley, D. J. H. Brock	2
20	Genotyping of cystic fibrosis families with linked DNA probes 1988 ·Clinical Genetics ·Ann Curtis, Lisa Strain, D. J. H. Brock	3

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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