Andrew Colley

1.4k total citations
26 papers, 895 citations indexed

About

Andrew Colley is a scholar working on Molecular Biology, Genetics and Neurology. According to data from OpenAlex, Andrew Colley has authored 26 papers receiving a total of 895 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 11 papers in Genetics and 6 papers in Neurology. Recurrent topics in Andrew Colley's work include Neurofibromatosis and Schwannoma Cases (4 papers), Connective tissue disorders research (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). Andrew Colley is often cited by papers focused on Neurofibromatosis and Schwannoma Cases (4 papers), Connective tissue disorders research (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). Andrew Colley collaborates with scholars based in Australia, United Kingdom and South Africa. Andrew Colley's co-authors include Dian Donnai, D. Gareth Evans, R Harris, Eric Haan, Kristin Hadfield, Andrew J. Wallace, Emily P. McCann, Naomi L. Bowers, Dorothy Trump and William G. Newman and has published in prestigious journals such as The Lancet, British Journal of Cancer and British Journal of Ophthalmology.

In The Last Decade

Andrew Colley

26 papers receiving 853 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Andrew Colley Australia 16 400 334 267 111 99 26 895
Emilia K. Bijlsma Netherlands 16 645 1.6× 696 2.1× 210 0.8× 134 1.2× 41 0.4× 25 1.2k
Maila Penttinen Finland 19 383 1.0× 173 0.5× 219 0.8× 128 1.2× 35 0.4× 31 920
D. J. J. Halley Netherlands 17 548 1.4× 555 1.7× 168 0.6× 116 1.0× 87 0.9× 38 1.3k
Julie S. Cohen United States 22 617 1.5× 578 1.7× 121 0.5× 84 0.8× 63 0.6× 44 1.4k
J P Fryns Belgium 14 506 1.3× 418 1.3× 197 0.7× 237 2.1× 32 0.3× 29 944
Helen Kingston United Kingdom 24 839 2.1× 645 1.9× 319 1.2× 137 1.2× 79 0.8× 63 1.9k
Yo Niida Japan 21 453 1.1× 334 1.0× 75 0.3× 88 0.8× 114 1.2× 93 1.6k
Mie‐Jef Descheemaeker Belgium 16 235 0.6× 337 1.0× 596 2.2× 277 2.5× 41 0.4× 20 989
Tena Rosser United States 19 233 0.6× 185 0.6× 597 2.2× 266 2.4× 87 0.9× 43 1.1k
Alessandra Murgia Italy 23 724 1.8× 638 1.9× 114 0.4× 74 0.7× 62 0.6× 76 1.6k

Countries citing papers authored by Andrew Colley

Since Specialization
Citations

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

Fields of papers citing papers by Andrew Colley

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Andrew Colley

This figure shows the co-authorship network connecting the top 25 collaborators of Andrew Colley. A scholar is included among the top collaborators of Andrew Colley 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 Andrew Colley. Andrew Colley 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.
Colley, Andrew, et al.. (2021). Enhancing Wellbeing and Independence for Young People with Profound and Multiple Learning Difficulties: Lives Lived Well. 4 indexed citations
2.
Colley, Andrew, et al.. (2017). Inclusion is Dead. 39 indexed citations
3.
Klopocki, Eva, Luitgard Graul‐Neumann, Sabine Uhrig, et al.. (2013). Novel mutations of the PRKAR1A gene in patients with acrodysostosis. Clinical Genetics. 84(6). 531–538. 21 indexed citations
4.
Hadfield, Kristin, William G. Newman, Naomi L. Bowers, et al.. (2008). Molecular characterisation of SMARCB1 and NF2 in familial and sporadic schwannomatosis. Journal of Medical Genetics. 45(6). 332–339. 135 indexed citations
5.
Featherstone, C., Andrew Colley, Kathy Tucker, Judy Kirk, & Michael Bartoň. (2007). Estimating the referral rate for cancer genetic assessment from a systematic review of the evidence. British Journal of Cancer. 96(2). 391–398. 12 indexed citations
6.
Summers, Kim, Maria Nataatmadja, Dongming Xu, et al.. (2005). Histopathology and fibrillin‐1 distribution in severe early onset Marfan syndrome. American Journal of Medical Genetics Part A. 139A(1). 2–8. 17 indexed citations
7.
Simunovic, Matthew P., et al.. (2004). How Well Does Color Perimetry Isolate Responses from Individual Cone Mechanisms?. Journal of Glaucoma. 13(1). 22–27. 5 indexed citations
8.
Friend, Kathryn, Denis Crimmins, Thanh G. Phan, et al.. (1999). Detection of a novel missense mutation and second recurrent mutation in the CACNA1A gene in individuals with EA-2 and FHM. Human Genetics. 105(3). 261–265. 56 indexed citations
9.
Colley, Andrew, Dian Donnai, & D. Gareth Evans. (1996). Neurofibromatosis/Noonan phenotype: a variable feature of type 1 neurofibromatosis. Clinical Genetics. 49(2). 59–64. 62 indexed citations
10.
Adès, Lesley C., et al.. (1996). Characterisation of four novel fibrillin-1 (FBN1) mutations in Marfan syndrome.. Journal of Medical Genetics. 33(8). 665–671. 25 indexed citations
11.
Kennedy, Catriona, et al.. (1994). An interstitial deletion of chromosome 7(q35).. Journal of Medical Genetics. 31(9). 738–739. 7 indexed citations
12.
Lloyd, I. Christopher, et al.. (1993). Dominantly inherited unilateral retinal dysplasia.. British Journal of Ophthalmology. 77(6). 378–380. 5 indexed citations
13.
Tassabehji, Mayada, T Strachan, Mike Sharland, et al.. (1993). Tandem duplication within a neurofibromatosis type 1 (NF1) gene exon in a family with features of Watson syndrome and Noonan syndrome.. PubMed. 53(1). 90–5. 65 indexed citations
14.
Benjamin, Caroline, Andrew Colley, Dian Donnai, et al.. (1993). Neurofibromatosis type 1 (NF1): knowledge, experience, and reproductive decisions of affected patients and families.. Journal of Medical Genetics. 30(7). 567–574. 74 indexed citations
15.
Colley, Andrew, et al.. (1992). Sport participation in middle childhood: association with styles of play and parental participation.. International journal of sport psychology. 23(3). 193–206. 24 indexed citations
16.
Turner, Gillian, Hazel M. Robinson, Susan T. Laing, et al.. (1992). Population screening for fragile X. The Lancet. 339(8803). 1210–1213. 62 indexed citations
17.
Colley, Andrew, et al.. (1992). Unbalanced 13;18 translocation and Williams syndrome.. Journal of Medical Genetics. 29(1). 63–65. 14 indexed citations
18.
Dixon, Michael J., Andrew Read, Dian Donnai, et al.. (1991). The gene for Treacher Collins syndrome maps to the long arm of chromosome 5.. PubMed. 49(1). 17–22. 66 indexed citations
19.
Colley, Andrew, et al.. (1991). Ectopia lentis et pupillae: the genetic aspects and differential diagnosis.. Journal of Medical Genetics. 28(11). 791–794. 20 indexed citations
20.
Colley, Andrew, M. Leversha, Lucille Voullaire, & John Rogers. (1990). Five cases demonstrating the distinctive behavioural features of chromosome deletion 17(p 11.2 p 11.2) (Smith‐Magenis syndrome). Journal of Paediatrics and Child Health. 26(1). 17–21. 47 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Emilia K. Bijlsma Breakdown of academic impact, for papers by Maila Penttinen Breakdown of academic impact, for papers by D. J. J. Halley Breakdown of academic impact, for papers by Julie S. Cohen Breakdown of academic impact, for papers by J P Fryns Breakdown of academic impact, for papers by Helen Kingston Breakdown of academic impact, for papers by Yo Niida Breakdown of academic impact, for papers by Mie‐Jef Descheemaeker Breakdown of academic impact, for papers by Tena Rosser Breakdown of academic impact, for papers by Alessandra Murgia
Rankless by CCL
2026