Amy Gerrish

20.8k total citations
18 papers, 289 citations indexed

About

Amy Gerrish is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Genetics. According to data from OpenAlex, Amy Gerrish has authored 18 papers receiving a total of 289 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 5 papers in Pediatrics, Perinatology and Child Health and 5 papers in Genetics. Recurrent topics in Amy Gerrish's work include Prenatal Screening and Diagnostics (4 papers), Genomic variations and chromosomal abnormalities (3 papers) and Fetal and Pediatric Neurological Disorders (3 papers). Amy Gerrish is often cited by papers focused on Prenatal Screening and Diagnostics (4 papers), Genomic variations and chromosomal abnormalities (3 papers) and Fetal and Pediatric Neurological Disorders (3 papers). Amy Gerrish collaborates with scholars based in United Kingdom, Germany and Switzerland. Amy Gerrish's co-authors include Julie Williams, Trevor Cole, Helen Jenkinson, Emma J. Kidd, Rhian S. Thomas, Lesley Jones, Samuel Clokie, Stephanie Allen, Dobril Ivanov and Michael O’Donovan and has published in prestigious journals such as Radiology, Human Molecular Genetics and Clinical Chemistry.

In The Last Decade

Amy Gerrish

17 papers receiving 289 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Amy Gerrish United Kingdom 10 112 74 64 61 54 18 289
Christian Gauthier United States 9 107 1.0× 39 0.5× 54 0.8× 12 0.2× 80 1.5× 10 313
Martin Krenn Austria 13 135 1.2× 18 0.2× 31 0.5× 60 1.0× 22 0.4× 36 394
Shorafidinkhuja Dadakhujaev South Korea 10 199 1.8× 31 0.4× 21 0.3× 21 0.3× 60 1.1× 10 379
Kevin Y. Zhang United States 7 133 1.2× 67 0.9× 101 1.6× 36 0.6× 16 0.3× 14 416
Serena Mirra Spain 11 220 2.0× 49 0.7× 34 0.5× 16 0.3× 16 0.3× 20 314
Chunyu Tian China 10 165 1.5× 77 1.0× 40 0.6× 24 0.4× 12 0.2× 17 366
Katarzyna Tońska Poland 14 400 3.6× 32 0.4× 31 0.5× 44 0.7× 9 0.2× 40 502
Banan Al‐Younes Saudi Arabia 12 222 2.0× 29 0.4× 29 0.5× 92 1.5× 7 0.1× 18 387
Vanessa M. López‐Ozuna Canada 12 192 1.7× 28 0.4× 27 0.4× 34 0.6× 118 2.2× 24 399
Sushil Devkota South Korea 11 226 2.0× 9 0.1× 69 1.1× 33 0.5× 42 0.8× 16 373

Countries citing papers authored by Amy Gerrish

Since Specialization
Citations

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

Fields of papers citing papers by Amy Gerrish

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Amy Gerrish

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

All Works

18 of 18 papers shown
1.
Hanson, Britt, Joseph Shaw, Elizabeth Young, et al.. (2024). Expanding Access to Noninvasive Prenatal Diagnosis for Monogenic Conditions to Consanguineous Families. Clinical Chemistry. 70(5). 727–736. 1 indexed citations
2.
Matet, Alexandre, Adeline Berger, Ángel M. Carcaboso, et al.. (2022). Retinoblastoma: From genes to patient care. European Journal of Medical Genetics. 66(1). 104674–104674. 11 indexed citations
3.
Gerrish, Amy, Helen Jenkinson, & Trevor Cole. (2021). The Impact of Cell-Free DNA Analysis on the Management of Retinoblastoma. Cancers. 13(7). 1570–1570. 20 indexed citations
4.
Young, Elizabeth, Amy Gerrish, Michael Parks, et al.. (2020). Clinical Service Delivery of Noninvasive Prenatal Diagnosis by Relative Haplotype Dosage for Single-Gene Disorders. Journal of Molecular Diagnostics. 22(9). 1151–1161. 18 indexed citations
5.
Gerrish, Amy, Elizabeth Young, Simon Ramsden, et al.. (2020). Non-Invasive Prenatal Diagnosis of Retinoblastoma Inheritance by Combined Targeted Sequencing Strategies. Journal of Clinical Medicine. 9(11). 3517–3517. 11 indexed citations
6.
Gerrish, Amy, E. C. Stone, Samuel Clokie, et al.. (2019). Non-invasive diagnosis of retinoblastoma using cell-free DNA from aqueous humour. British Journal of Ophthalmology. 103(5). 721–724. 48 indexed citations
7.
Pericleous, Agamemnon, et al.. (2019). Peritonsillar abscess in an infant with congenital bone marrow failure. International Journal of Pediatric Otorhinolaryngology. 124. 200–202. 2 indexed citations
8.
Gerrish, Amy, et al.. (2017). Hydrocephalus and trigeminal neuralgia: exploring the association and management options. British Journal of Neurosurgery. 31(3). 296–299. 1 indexed citations
9.
Gerrish, Amy, et al.. (2017). Case 239: Cerebrotendinous Xanthomatosis. Radiology. 282(3). 916–921. 7 indexed citations
10.
Thomas, Rhian S., et al.. (2016). Decreasing the expression of PICALM reduces endocytosis and the activity of β-secretase: implications for Alzheimer’s disease. BMC Neuroscience. 17(1). 50–50. 48 indexed citations
11.
Dunstan, Melanie, Amy Gerrish, Taniesha Morgan, et al.. (2016). P1‐145: The Role of CD2AP in APP Processing. Alzheimer s & Dementia. 12(7S_Part_9). 3 indexed citations
12.
Dunstan, Melanie, Amy Gerrish, Rhian S. Thomas, et al.. (2015). P4‐202: The effects of CD2AP expression on app processing. Alzheimer s & Dementia. 11(7S_Part_18). 1 indexed citations
13.
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
14.
Thomas, Rhian S., et al.. (2014). P1‐089: DECREASING PICALM EXPRESSION ALTERS THE AMYLOIDOGENIC PROCESSING OF AMYLOID PRECURSOR PROTEIN. Alzheimer s & Dementia. 10(4S_Part_8). 1 indexed citations
15.
Gerrish, Amy, Adam G. Thomas, & Robert A. Dineen. (2014). Brain White Matter Tracts: Functional Anatomy and Clinical Relevance. Seminars in Ultrasound CT and MRI. 35(5). 432–444. 16 indexed citations
16.
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).
17.
Chapman, Jade, Elliott Rees, Denise Harold, et al.. (2012). A genome-wide study shows a limited contribution of rare copy number variants to Alzheimer's disease risk. Human Molecular Genetics. 22(4). 816–824. 25 indexed citations
18.
Norton, Nadine, Hywel Williams, Sarah Dwyer, et al.. (2005). No evidence for association between polymorphisms in GRM3and schizophrenia. BMC Psychiatry. 5(1). 23–23. 43 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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