Alison Colley

1.7k total citations
15 papers, 350 citations indexed

About

Alison Colley is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Alison Colley has authored 15 papers receiving a total of 350 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 7 papers in Genetics and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Alison Colley's work include Prenatal Screening and Diagnostics (4 papers), Congenital heart defects research (4 papers) and Genetic Syndromes and Imprinting (3 papers). Alison Colley is often cited by papers focused on Prenatal Screening and Diagnostics (4 papers), Congenital heart defects research (4 papers) and Genetic Syndromes and Imprinting (3 papers). Alison Colley collaborates with scholars based in Australia, United States and United Kingdom. Alison Colley's co-authors include Meredith Wilson, Mark J. Cowley, Sulekha Rajagopalan, Leon R. McQuade, John Christodoulou, Marcia L. Budarf, Rani Sachdev, Marcel E. Dinger, Jodie Ingles and Richard D. Bagnall and has published in prestigious journals such as Journal of the American College of Cardiology, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

Alison Colley

15 papers receiving 336 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Alison Colley Australia 9 229 129 93 44 39 15 350
Heide Seidel Germany 14 182 0.8× 192 1.5× 48 0.5× 42 1.0× 36 0.9× 24 337
Natália D. Linhares Brazil 10 168 0.7× 102 0.8× 27 0.3× 89 2.0× 26 0.7× 21 350
Clara S. Moore United States 12 209 0.9× 219 1.7× 47 0.5× 16 0.4× 23 0.6× 13 407
David S. Wargowski United States 9 112 0.5× 136 1.1× 32 0.3× 54 1.2× 22 0.6× 15 336
Cassandra R. Farthing United Kingdom 6 497 2.2× 118 0.9× 45 0.5× 13 0.3× 78 2.0× 7 571
Donna K. Mahnke United States 11 300 1.3× 70 0.5× 62 0.7× 15 0.3× 129 3.3× 14 392
V Davis United States 4 165 0.7× 37 0.3× 21 0.2× 117 2.7× 36 0.9× 8 368
Stefano Giuseppe Caraffi Italy 11 130 0.6× 112 0.9× 12 0.1× 90 2.0× 35 0.9× 41 307
Andreas Würch Germany 7 220 1.0× 56 0.4× 50 0.5× 158 3.6× 30 0.8× 9 409
Shigetatsu Shiokawa Japan 13 120 0.5× 56 0.4× 46 0.5× 217 4.9× 8 0.2× 18 468

Countries citing papers authored by Alison Colley

Since Specialization
Citations

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

Fields of papers citing papers by Alison Colley

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alison Colley

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

All Works

15 of 15 papers shown
1.
Fois, Alessandro F., Hugo Morales‐Briceño, Michael Fong, et al.. (2019). Deep Brain Stimulation as Management of Generalized Dystonia in the 18p Deletion Syndrome. Movement Disorders Clinical Practice. 6(3). 263–264. 1 indexed citations
2.
Ewans, Lisa, Alison Colley, Carles Gaston‐Massuet, et al.. (2019). Pathogenic variants in PLOD3 result in a Stickler syndrome-like connective tissue disorder with vascular complications. Journal of Medical Genetics. 56(9). 629–638. 24 indexed citations
3.
Barlow‐Stewart, Kristine, Arthavan Selvanathan, Tony Roscioli, et al.. (2018). User Acceptability of Whole Exome Reproductive Carrier Testing for Consanguineous Couples in Australia. Journal of Genetic Counseling. 28(2). 240–250. 6 indexed citations
4.
LeBlanc, Shannon, Dávid Dávid, Alison Colley, et al.. (2018). Atypical Skin Manifestations in <b><i>FGFR2</i></b>-Related Craniosynostosis Syndromes Broaden the Phenotypic Spectrum. Molecular Syndromology. 9(3). 149–153. 1 indexed citations
5.
Bagnall, Richard D., Jodie Ingles, Marcel E. Dinger, et al.. (2018). Whole Genome Sequencing Improves Outcomes of Genetic Testing in Patients With Hypertrophic Cardiomyopathy. Journal of the American College of Cardiology. 72(4). 419–429. 112 indexed citations
6.
Kirk, Edwin P., Kristine Barlow‐Stewart, Arthavan Selvanathan, et al.. (2018). Beyond the panel: preconception screening in consanguineous couples using the TruSight One “clinical exome”. Genetics in Medicine. 21(3). 608–612. 16 indexed citations
7.
Beygo, Jasmin, Benjamin Kamien, Jill Clayton‐Smith, et al.. (2017). Atypical Angelman syndrome due to a mosaic imprinting defect: Case reports and review of the literature. American Journal of Medical Genetics Part A. 173(3). 753–757. 18 indexed citations
8.
Chaoui, Asma, Viviane Baral, Yuli Watanabe, et al.. (2015). Subnuclear re-localization of SOX10 and p54NRB correlates with a unique neurological phenotype associated with SOX10 missense mutations. Human Molecular Genetics. 24(17). 4933–4947. 11 indexed citations
9.
Trent, Ronald J., Donald K. Bowden, P. Joy Ho, et al.. (2006). Complex phenotypes in the haemoglobinopathies: recommendations on screening and DNA testing. Pathology. 38(6). 507–519. 6 indexed citations
10.
11.
McQuade, Leon R., John Christodoulou, Marcia L. Budarf, et al.. (1999). Patient with a 22q11.2 deletion with no overlap of the minimal DiGeorge syndrome critical region (MDGCR). American Journal of Medical Genetics. 86(1). 27–33. 5 indexed citations
12.
McQuade, Leon R., John Christodoulou, Marcia L. Budarf, et al.. (1999). Patient with a 22q11.2 deletion with no overlap of the minimal DiGeorge syndrome critical region (MDGCR). American Journal of Medical Genetics. 86(1). 27–33. 55 indexed citations
13.
Mulley, John C., Kathrin Saar, Franz Rüschendorf, et al.. (1998). Gene Localization for an Autosomal Dominant Familial Periodic Fever to 12p13. The American Journal of Human Genetics. 62(4). 884–889. 63 indexed citations
14.
Donnelly, Andrew J., Alison Colley, Denis Crimmins, & John C. Mulley. (1996). A novel mutation in exon 6 (F236S) of the proteolipid protein gene is associated with spastic paraplegia. Human Mutation. 8(4). 384–385. 4 indexed citations
15.
Lipson, Anthony, et al.. (1996). Velo-cardio-facial and partial DiGeorge phenotype in a child with interstitial deletion at 10p13—implications for cytogenetics and molecular biology. American Journal of Medical Genetics. 65(4). 304–308. 20 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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