Denise Harold

27.1k total citations
49 papers, 1.6k citations indexed

About

Denise Harold is a scholar working on Genetics, Molecular Biology and Physiology. According to data from OpenAlex, Denise Harold has authored 49 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Genetics, 18 papers in Molecular Biology and 10 papers in Physiology. Recurrent topics in Denise Harold's work include Genetic Associations and Epidemiology (16 papers), Alzheimer's disease research and treatments (8 papers) and Genomics and Rare Diseases (6 papers). Denise Harold is often cited by papers focused on Genetic Associations and Epidemiology (16 papers), Alzheimer's disease research and treatments (8 papers) and Genomics and Rare Diseases (6 papers). Denise Harold collaborates with scholars based in United Kingdom, Ireland and United States. Denise Harold's co-authors include Julie Williams, Michael J. Owen, Michael O’Donovan, Lesley Jones, Valentina Moskvina, Peter Holmans, Natalie Cope, Gary Hill, Jim Stevenson and Paul Hollingworth and has published in prestigious journals such as PLoS ONE, Annals of Neurology and Biological Psychiatry.

In The Last Decade

Denise Harold

47 papers receiving 1.6k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Denise Harold United Kingdom 23 625 531 315 279 190 49 1.6k
Xinyu Wang China 19 1.6k 2.5× 468 0.9× 240 0.8× 32 0.1× 299 1.6× 86 2.4k
Angela Wilson United States 19 362 0.6× 23 0.0× 159 0.5× 166 0.6× 77 0.4× 44 1.1k
Xifeng Wang China 16 409 0.7× 216 0.4× 201 0.6× 9 0.0× 90 0.5× 50 1.4k
Sylvia Chen United States 20 873 1.4× 87 0.2× 272 0.9× 161 0.6× 510 2.7× 43 1.7k
Yoshiaki Nakajima Japan 22 757 1.2× 57 0.1× 110 0.3× 24 0.1× 767 4.0× 50 1.5k
Astrid M. Vicente Portugal 20 497 0.8× 664 1.3× 53 0.2× 10 0.0× 169 0.9× 72 1.7k
David Nicholl United Kingdom 23 435 0.7× 97 0.2× 285 0.9× 22 0.1× 624 3.3× 45 1.7k
Alexander M. Wolf Japan 19 619 1.0× 100 0.2× 390 1.2× 38 0.1× 436 2.3× 41 1.8k
Dawei Li China 23 767 1.2× 235 0.4× 110 0.3× 45 0.2× 267 1.4× 76 1.9k
Caroline Dalton United Kingdom 21 305 0.5× 156 0.3× 152 0.5× 12 0.0× 177 0.9× 71 1.4k

Countries citing papers authored by Denise Harold

Since Specialization
Citations

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

Fields of papers citing papers by Denise Harold

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Denise Harold

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

All Works

20 of 20 papers shown
1.
Bernard, David J., et al.. (2022). Mito-SiPE is a sequence-independent and PCR-free mtDNA enrichment method for accurate ultra-deep mitochondrial sequencing. Communications Biology. 5(1). 1269–1269. 10 indexed citations
2.
Harold, Denise, et al.. (2021). RNA-seq analysis of murine peyer’s patches at 6 and 18 h post infection with Fasciola hepatica metacecariae. Veterinary Parasitology. 302. 109643–109643. 1 indexed citations
3.
Harold, Denise, Aiden Corvin, Michael Gill, et al.. (2020). Effects of complement gene‐set polygenic risk score on brain volume and cortical measures in patients with psychotic disorders and healthy controls. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 183(8). 445–453. 8 indexed citations
4.
Heron, Elizabeth A., Denise Harold, James Walters, et al.. (2020). Identifying schizophrenia patients who carry pathogenic genetic copy number variants using standard clinical assessment: retrospective cohort study. The British Journal of Psychiatry. 216(5). 275–279. 8 indexed citations
5.
Hubbard, Leon, Elliott Rees, Derek W. Morris, et al.. (2020). Rare Copy Number Variants Are Associated With Poorer Cognition in Schizophrenia. Biological Psychiatry. 90(1). 28–34. 19 indexed citations
6.
Harold, Denise, Brien P. Riley, Kenneth S. Kendler, et al.. (2019). Population‐based identity‐by‐descent mapping combined with exome sequencing to detect rare risk variants for schizophrenia. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 180(3). 223–231. 2 indexed citations
7.
Mothersill, David, Denise Harold, Sinéad Kelly, et al.. (2018). Effects of MiR‐137 genetic risk score on brain volume and cortical measures in patients with schizophrenia and controls. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 177(3). 369–376. 8 indexed citations
8.
Mothersill, Omar, Kimberley Kendall, Bettina Konte, et al.. (2017). Cognitive Characterization of Schizophrenia Risk Variants Involved in Synaptic Transmission: Evidence of CACNA1C's Role in Working Memory. Neuropsychopharmacology. 42(13). 2612–2622. 29 indexed citations
9.
Chao, Michael J., Tammy Gillis, Ranjit Singh Atwal, et al.. (2017). Haplotype-based stratification of Huntington's disease. European Journal of Human Genetics. 25(11). 1202–1209. 18 indexed citations
10.
Mok, Kin Y., Emma L. Jones, Denise Harold, et al.. (2014). Polymorphisms in BACE2 may affect the age of onset Alzheimer's dementia in Down syndrome. Neurobiology of Aging. 35(6). 1513.e1–1513.e5. 30 indexed citations
11.
Hinney, Anke, Özgür Albayrak, Jochen Antel, et al.. (2014). Genetic variation at the CELF1 (CUGBP, elav‐like family member 1 gene) locus is genome‐wide associated with Alzheimer's disease and obesity. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 165(4). 283–293. 33 indexed citations
12.
Gusareva, Elena S., Minerva M. Carrasquillo, Céline Bellenguez, et al.. (2014). Genome-wide association interaction analysis for Alzheimer's disease. Neurobiology of Aging. 35(11). 2436–2443. 50 indexed citations
13.
Jones, Emma L., Kin Y. Mok, Denise Harold, et al.. (2013). Evidence that PICALM affects age at onset of Alzheimer's dementia in Down syndrome. Neurobiology of Aging. 34(10). 2441.e1–2441.e5. 37 indexed citations
14.
Lee, Sang, Denise Harold, Dale R. Nyholt, et al.. (2012). Estimation and partitioning of polygenic variation captured by common SNPs for Alzheimer's disease, multiple sclerosis and endometriosis. Human Molecular Genetics. 22(4). 832–841. 128 indexed citations
15.
Chapman, Jade, Rebecca Sims, Denise Harold, et al.. (2012). P4‐106: Alzheimer's disease with agitation: A genome‐wide association study. Alzheimer s & Dementia. 8(4S_Part_18).
16.
Jones, Lesley, Peter Holmans, Denise Harold, et al.. (2010). O2‐07‐05: Genetic evidence implicates the immune system and cholesterol metabolism in the etiology of Alzheimer's disease. Alzheimer s & Dementia. 6(4S_Part_4). 2 indexed citations
17.
Hollingworth, Paul, Denise Harold, Lesley Jones, Michael J. Owen, & Julie Williams. (2010). Alzheimer's disease genetics: current knowledge and future challenges. International Journal of Geriatric Psychiatry. 26(8). 793–802. 74 indexed citations
18.
Morgan, Angharad R., Gillian Hamilton, Dragana Turic, et al.. (2007). Association analysis of 528 intra‐genic SNPs in a region of chromosome 10 linked to late onset Alzheimer's disease. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 147B(6). 727–731. 35 indexed citations
19.
Harold, Denise, Silvia Paracchini, Thomas Scerri, et al.. (2006). Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia. Molecular Psychiatry. 11(12). 1085–1091. 127 indexed citations
20.
Harold, Denise, T Peirce, Marian L. Hamshere, et al.. (2002). No association of polymorphisms in the chat locus with late-onset Alzheimer's disease. Neurobiology of Aging. 23(1). 1 indexed citations

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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