Carolyn Tysoe

2.5k total citations
23 papers, 586 citations indexed

About

Carolyn Tysoe is a scholar working on Genetics, Molecular Biology and Physiology. According to data from OpenAlex, Carolyn Tysoe has authored 23 papers receiving a total of 586 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 8 papers in Molecular Biology and 5 papers in Physiology. Recurrent topics in Carolyn Tysoe's work include Alzheimer's disease research and treatments (5 papers), Genomic variations and chromosomal abnormalities (4 papers) and Connective tissue disorders research (3 papers). Carolyn Tysoe is often cited by papers focused on Alzheimer's disease research and treatments (5 papers), Genomic variations and chromosomal abnormalities (4 papers) and Connective tissue disorders research (3 papers). Carolyn Tysoe collaborates with scholars based in United Kingdom, United States and Belgium. Carolyn Tysoe's co-authors include David C. Rubinsztein, Felicia A. Huppert, Tom Dening, Douglas F. Easton, Carol Brayne, Daliah Galinsky, Christine Van Broeckhoven, John C. Whittaker, John H. Xuereb and Gordon Wilcock and has published in prestigious journals such as Biological Psychiatry, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

Carolyn Tysoe

23 papers receiving 571 citations

Peers

Countries citing papers authored by Carolyn Tysoe

Since Specialization

Citations

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

Fields of papers citing papers by Carolyn Tysoe

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Carolyn Tysoe

This figure shows the co-authorship network connecting the top 25 collaborators of Carolyn Tysoe. A scholar is included among the top collaborators of Carolyn Tysoe 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 Carolyn Tysoe. Carolyn Tysoe 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	Late-onset Pseudoxanthoma Elasticum Associated with a Hypomorphic ABCC6 Variant 2020 ·American Journal of Ophthalmology ·Peter Charbel Issa, Carolyn Tysoe, Richard Caswell	11
2	A prospective study of brachytelephalangic chondrodysplasia punctata: identification of arylsulfatase E mutations, functional analysis of novel missense alleles, and determination of potential phenocopies 2013 ·Genetics in Medicine ·(unknown), Graeme Nimmo, (unknown), Carolyn Tysoe, Martina Owens, Sherri J. Bale, Nancy Braverman	14
3	An isolated case of lissencephaly caused by the insertion of a mitochondrial genome-derived DNA sequence into the 5' untranslated region of the PAFAH1B1 (LIS1) gene 2010 ·Human Genomics ·David Millar, Carolyn Tysoe, L. Lazarou, Daniela T. Pilz, Shehla Mohammed, (unknown), Nadia Chuzhanova, D.N. Cooper, Rachel Butler	9
4	Semi-Automated Unidirectional Sequence Analysis for Mutation Detection in a Clinical Diagnostic Setting 2009 ·Genetic Testing and Molecular Biomarkers ·Sian Ellard, Beverley Shields, Carolyn Tysoe, (unknown), Shu Yau, (unknown), Andrew J. Wallace	20
5	Prenatal testing for a novel EBP missense mutation causing X‐linked dominant chondrodysplasia punctata 2008 ·Prenatal Diagnosis ·Carolyn Tysoe, (unknown), Richard Caswell, Peter T. Clayton, Sian Ellard	4
6	A family with a novel TSH receptor activating germline mutation (p.Ala485Val) 2008 ·European Journal of Pediatrics ·Sema Akçurin, Doğa Türkkahraman, Carolyn Tysoe, Sian Ellard, Anne De Leener, Gilbert Vassart, Sabine Costagliola	25
7	A neuropsychological investigation of male premutation carriers of fragile X syndrome 2004 ·Neuropsychologia ·C. J. Moore, Eileen Daly, Nicole Schmitz, Flora Tassone, Carolyn Tysoe, Randi J. Hagerman, Paul J. Hagerman, Robin G. Morris, Kieran C. Murphy, Declan Murphy	95
8	Sex determination by PCR analysis of DNA extracted from incinerated, deciduous teeth 2004 ·Science & Justice ·David W. Williams, Michael J. Lewis, (unknown), (unknown), (unknown), D K Whittaker, Carolyn Tysoe, Richard Butler	15
9	The effect of premutation CGG trinucleotide repeat expansion, and %FMRP(+) lymphocytes reduction, on brain anatomy 2003 ·Biological Psychiatry ·C. J. Moore, Eileen Daly, Flora Tassone, Carolyn Tysoe, Nicole Schmitz, Xavier Chitnis, Kieran C. Murphy, Declan Murphy	1
10	A glycine to aspartic acid substitution of COL2A1 in a family with the Strudwick variant of spondyloepimetaphyseal dysplasia 2003 ·QJM ·Carolyn Tysoe, (unknown), Lisa D. White, Nancy K. Hills, (unknown), Glen A. Evans, Theresa Cole, S. Chapman, (unknown)	8
11	Acrogeric Ehlers-Danlos syndrome type IV: report of a new patient with additional findings. 2003 ·PubMed ·Ahmet Rüçhan Akar, (unknown), (unknown), Padmini Sarathchandra, Carolyn Tysoe, (unknown)	7
12	Aberrant splicing in the presenilin-1 intron 4 mutation causes presenile Alzheimers disease by increased a beta 42 secretion 1999 ·The American Journal of Human Genetics ·Marc Cruts, C. De Jonghe, (unknown), Carolyn Tysoe, Andrew Singleton, Hugo Vanderstichele, Wendy S. Meschino, Bart Dermaut, (unknown), H. Backhovens, Eugeen Vanmechelen, Christopher M. Morris, John Hardy, (unknown), (unknown), Christine Van Broeckhoven	10
13	Apo E genotypes and risk of dementia in Down syndrome 1999 ·American Journal of Medical Genetics ·David C. Rubinsztein, (unknown), (unknown), Ian Pyrah, Carolyn Tysoe, Felicia A. Huppert, Douglas F. Easton, Anthony Holland	26
14	Aberrant Splicing in the Presenilin-1 Intron 4 Mutation Causes Presenile Alzheimer's Disease by Increased A 42 Secretion 1999 ·Human Molecular Genetics ·C. De Jonghe, (unknown), (unknown), Carolyn Tysoe, Andrew Singleton, Hugo Vanderstichele, Wendy S. Meschino, Bart Dermaut, (unknown), H. Backhovens, Eugeen Vanmechelen, Christopher M. Morris, John Hardy, (unknown), Peter St George‐Hyslop, Christine Van Broeckhoven	67
15	A Presenilin-1 Truncating Mutation Is Present in Two Cases with Autopsy-Confirmed Early-Onset Alzheimer Disease 1998 ·The American Journal of Human Genetics ·Carolyn Tysoe, John C. Whittaker, John H. Xuereb, Nigel J. Cairns, Marc Cruts, Christine Van Broeckhoven, Gordon Wilcock, David C. Rubinsztein	60
16	Apo E and Apo CI Loci Are Associated with Dementia in Younger But Not Older Late-Onset Cases 1998 ·Dementia and Geriatric Cognitive Disorders ·Carolyn Tysoe, Daliah Galinsky, (unknown), Carol Brayne, Felicia A. Huppert, Tom Dening, Eugene S. Paykel, Douglas F. Easton, David C. Rubinsztein	17
17	Presenilin-1 intron 8 polymorphism is not associated with autopsy-confirmed late-onset Alzheimer's disease 1997 ·Neuroscience Letters ·Carolyn Tysoe, John C. Whittaker, Nigel J. Cairns, Penny F Atkinson, Charles R. Harrington, John H. Xuereb, Gordon Wilcock, David C. Rubinsztein	31
18	Analysis of alpha-1 antichymotrypsin, presenilin-1, angiotensin-converting enzyme, and methylenetetrahydrofolate reductase loci as candidates for dementia 1997 ·American Journal of Medical Genetics ·Carolyn Tysoe, Daliah Galinsky, (unknown), Carol Brayne, Douglas F. Easton, Felicia A. Huppert, Tom Dening, Eugene S. Paykel, David C. Rubinsztein	45
19	Analysis of the apo E/apo C-I, angiotensin converting enzyme and methylenetetrahydrofolate reductase genes as candidates affecting human longevity 1997 ·Atherosclerosis ·Daliah Galinsky, Carolyn Tysoe, Carol Brayne, Douglas F. Easton, Felicia A. Huppert, Tom Dening, (unknown), David C. Rubinsztein	84
20	The tRNA(Gln) 4336 mitochondrial DNA variant is not a high penetrance mutation which predisposes to dementia before the age of 75 years. 1996 ·Journal of Medical Genetics ·Carolyn Tysoe, (unknown), Carol Brayne, Tom Dening, Eugene S. Paykel, Felicia A. Huppert, David C. Rubinsztein	24

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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