Ian Berry

2.4k total citations
24 papers, 370 citations indexed

About

Ian Berry is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Ian Berry has authored 24 papers receiving a total of 370 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 11 papers in Molecular Biology and 4 papers in Pathology and Forensic Medicine. Recurrent topics in Ian Berry's work include Genetic factors in colorectal cancer (4 papers), Genetic and Kidney Cyst Diseases (4 papers) and Cancer Genomics and Diagnostics (4 papers). Ian Berry is often cited by papers focused on Genetic factors in colorectal cancer (4 papers), Genetic and Kidney Cyst Diseases (4 papers) and Cancer Genomics and Diagnostics (4 papers). Ian Berry collaborates with scholars based in United Kingdom, United States and Belgium. Ian Berry's co-authors include David T. Bonthron, Ian Carr, Ruth Charlton, Angus Dobbie, Laura A. Crinnion, Christopher M. Watson, Agne Antanaviciute, Sally M. Harrison, Marc Tischkowitz and Helen Hanson and has published in prestigious journals such as Nature Medicine, SHILAP Revista de lepidopterología and The American Journal of Human Genetics.

In The Last Decade

Ian Berry

24 papers receiving 367 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ian Berry United Kingdom 11 226 192 53 48 27 24 370
Eva Barroso Spain 11 245 1.1× 289 1.5× 25 0.5× 66 1.4× 13 0.5× 23 437
Shinsuke Ninomiya Japan 14 268 1.2× 210 1.1× 48 0.9× 21 0.4× 39 1.4× 31 444
Natalie Canham United Kingdom 10 158 0.7× 198 1.0× 77 1.5× 31 0.6× 20 0.7× 20 388
Lilia Romdhane Tunisia 12 150 0.7× 189 1.0× 40 0.8× 23 0.5× 14 0.5× 29 394
Yu Gyoung Tak United States 6 378 1.7× 151 0.8× 95 1.8× 32 0.7× 16 0.6× 6 509
Jennifer L. Asimit United Kingdom 11 206 0.9× 397 2.1× 54 1.0× 17 0.4× 24 0.9× 22 501
Katharina Steinmann Germany 9 180 0.8× 111 0.6× 13 0.2× 30 0.6× 42 1.6× 9 350
Sonia Nizard France 10 131 0.6× 227 1.2× 36 0.7× 21 0.4× 21 0.8× 12 357
Adam C. Gunning United Kingdom 7 179 0.8× 151 0.8× 36 0.7× 27 0.6× 9 0.3× 12 291
Jan Fröhlich Czechia 13 196 0.9× 116 0.6× 28 0.5× 18 0.4× 104 3.9× 31 377

Countries citing papers authored by Ian Berry

Since Specialization
Citations

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

Fields of papers citing papers by Ian Berry

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ian Berry

This figure shows the co-authorship network connecting the top 25 collaborators of Ian Berry. A scholar is included among the top collaborators of Ian Berry 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 Ian Berry. Ian Berry 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.
Berry, Ian, et al.. (2025). SparcleQC: Automated Input File Creation for QM/MM Studies of Protein:Ligand Complexes. Journal of Chemical Information and Modeling. 65(13). 6433–6440. 1 indexed citations
2.
Greene, Daniel, Chantal Thys, Ian Berry, et al.. (2024). Mutations in the U4 snRNA gene RNU4-2 cause one of the most prevalent monogenic neurodevelopmental disorders. Nature Medicine. 30(8). 2165–2169. 27 indexed citations
3.
Bowman, Pamela, Anthony R. Dallosso, Ian Berry, et al.. (2024). Whole genome sequencing for copy number variant detection to improve diagnosis and management of rare diseases. Developmental Medicine & Child Neurology. 67(1). 126–131. 3 indexed citations
4.
Ingoe, Lorna, Dermot Neely, A. Joy Allen, et al.. (2021). Improving the identification of patients with a genetic diagnosis of familial hypercholesterolaemia in primary care: A strategy to achieve the NHS long term plan. Atherosclerosis. 325. 38–45. 5 indexed citations
5.
Çubuk, Cankut, Alice Garrett, Laura King, et al.. (2021). Clinical likelihood ratios and balanced accuracy for 44 in silico tools against multiple large-scale functional assays of cancer susceptibility genes. Genetics in Medicine. 23(11). 2096–2104. 42 indexed citations
6.
Smith, Claire E. L., James A. Poulter, Sandra Silva, et al.. (2021). Spectrum of pathogenic variants and founder effects in amelogenesis imperfecta associated with MMP20. Human Mutation. 42(5). 567–576. 5 indexed citations
7.
Garrett, Alice, Miranda Durkie, Alison Callaway, et al.. (2020). Combining evidence for and against pathogenicity for variants in cancer susceptibility genes: CanVIG-UK consensus recommendations. Journal of Medical Genetics. 58(5). 297–304. 36 indexed citations
8.
Metcalfe, Kay, et al.. (2019). DSE associated musculocontractural EDS, a milder phenotype or phenotypic variability. European Journal of Medical Genetics. 63(4). 103798–103798. 17 indexed citations
9.
Boudin, Eveline, Timothy C. R. Prickett, Bruno Lapauw, et al.. (2018). Bi-allelic Loss-of-Function Mutations in the NPR-C Receptor Result in Enhanced Growth and Connective Tissue Abnormalities. The American Journal of Human Genetics. 103(2). 288–295. 25 indexed citations
10.
Johnson, Kathryn, et al.. (2018). Genetic disorder plus prematurity: a diagnostic challenge. Archives of Disease in Childhood Education & Practice. 104(5). 252–253. 2 indexed citations
11.
Salomé, Jenny von, Tao Liu, Elke Holinski‐Feder, et al.. (2017). Haplotype analysis suggest that the MLH1 c.2059C > T mutation is a Swedish founder mutation. Familial Cancer. 17(4). 531–537. 4 indexed citations
12.
Watson, Christopher M., Laura A. Crinnion, Ian Berry, et al.. (2016). Enhanced diagnostic yield in Meckel-Gruber and Joubert syndrome through exome sequencing supplemented with split-read mapping. BMC Medical Genetics. 17(1). 1–1. 59 indexed citations
13.
Singh, Rahul, John H. Livingston, Ming Lim, Ian Berry, & Ata Siddiqui. (2016). An unusual neuroimaging finding and response to immunotherapy in a child with genetically confirmed vanishing white matter disease. European Journal of Paediatric Neurology. 21(2). 410–413. 5 indexed citations
14.
Awaad, Yasser M., Ian Berry, Solaf M. Elsayed, & Hoda Tomoum. (2015). A Novel Frameshift Mutation in SLC2A1 Associated with a Mild form of Glucose Transporter Type 1-Related Movement Disorder. Journal of Pediatric Neurology. 13(2). 88–91. 1 indexed citations
15.
Szymańska, Katarzyna, Ian Berry, Clare V. Logan, et al.. (2012). Founder mutations and genotype-phenotype correlations in Meckel-Gruber syndrome and associated ciliopathies. SHILAP Revista de lepidopterología. 1(1). 18–18. 37 indexed citations
16.
Farrell, Michael, David J. Hughes, Ian Berry, et al.. (2012). Clinical correlation and molecular evaluation confirm that the MLH1 p.Arg182Gly (c.544A>G) mutation is pathogenic and causes Lynch syndrome. Familial Cancer. 11(3). 509–518. 3 indexed citations
17.
Ken, S., et al.. (2012). Evaluation of Lactate as a Predictive Marker of Survival and Local Response to Radiation Therapy in Patients With GBM. International Journal of Radiation Oncology*Biology*Physics. 84(3). S271–S272. 2 indexed citations
18.
Tiu, Sau Cheung, Ckf Lee, Ian Berry, et al.. (2011). Molecular analysis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency in Hong Kong Chinese patients. Steroids. 76(10-11). 1057–1062. 18 indexed citations
19.
Berry, Ian, Carol A. Delaney, & Graham R. Taylor. (2007). Detecting Ligated Fragments on Oligonucleotide Microarrays. PubMed. 381. 247–265. 3 indexed citations
20.
Chevreau, Elisabeth, et al.. (2007). FEASIBILITY OF ALTERNATIVE SELECTION METHODS FOR TRANSGENIC APPLE AND PEAR USING THE DETOXIFICATION GENE VR-ERE. Acta Horticulturae. 277–281. 5 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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