Kerry Fagan

444 total citations
10 papers, 248 citations indexed

About

Kerry Fagan is a scholar working on Genetics, Plant Science and Molecular Biology. According to data from OpenAlex, Kerry Fagan has authored 10 papers receiving a total of 248 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 5 papers in Plant Science and 4 papers in Molecular Biology. Recurrent topics in Kerry Fagan's work include Chromosomal and Genetic Variations (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genetics and Neurodevelopmental Disorders (3 papers). Kerry Fagan is often cited by papers focused on Chromosomal and Genetic Variations (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genetics and Neurodevelopmental Disorders (3 papers). Kerry Fagan collaborates with scholars based in Australia, United States and Italy. Kerry Fagan's co-authors include P. B. Harrison, S Hyde, Ian B. Wilkinson, Michael Allen, Denise Horn, Omar Abdul‐Rahman, Jozef Gécz, Christopher W. Carr, Marie Shaw and Matthew F. Hunter and has published in prestigious journals such as Journal of Medical Genetics, Human Genetics and European Journal of Human Genetics.

In The Last Decade

Kerry Fagan

10 papers receiving 227 citations

Peers

Countries citing papers authored by Kerry Fagan

Since Specialization

Citations

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

Fields of papers citing papers by Kerry Fagan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kerry Fagan

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

All Works

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10 of 10 papers shown

#	Work	Indexed citations
1	FOXP1 mutations cause intellectual disability and a recognizable phenotype 2013 ·American Journal of Medical Genetics Part A ·(unknown), (unknown), (unknown), Denise Horn, Christopher W. Carr, Omar Abdul‐Rahman, (unknown), Trent Burgess, Marie Shaw, Jozef Gécz, (unknown), Kerry Fagan, Matthew F. Hunter	67
2	14q12 microdeletions excluding FOXG1 give rise to a congenital variant Rett syndrome-like phenotype 2012 ·European Journal of Human Genetics ·Carolyn Ellaway, Gladys Ho, Elisa Bettella, (unknown), Felicity Collins, Anna Hackett, F. Ellis McKenzie, Artur Darmanian, Gregory B. Peters, Kerry Fagan, John Christodoulou	44
3	Paternal uniparental isodisomy for chromosome 14 with mosaicism for a supernumerary marker chromosome 14 2007 ·American Journal of Medical Genetics Part A ·Joërg Mattes, Bruce Whitehead, Thomas Liehr, Ian B. Wilkinson, J. C. Bear, Kerry Fagan, P. D. Craven, Bruce Bennetts, Matthew Edwards	20
4	Supernumerary ring chromosome 17 identified by fluorescent in situ hybridization 1997 ·American Journal of Medical Genetics ·Kerry Fagan, Matthew Edwards	3
5	Velo-cardio-facial and partial DiGeorge phenotype in a child with interstitial deletion at 10p13—implications for cytogenetics and molecular biology 1996 ·American Journal of Medical Genetics ·Anthony Lipson, Kerry Fagan, Alison Colley, (unknown), Gary F. Sholler, (unknown), R. Kim Oates	20
6	Translocation (8;13) and T-cell lymphoma 1993 ·Cancer Genetics and Cytogenetics ·Kerry Fagan, S Hyde, P. B. Harrison	39
7	Del(4)(q33----qter): another case report of a child with mild dysmorphism. 1989 ·Journal of Medical Genetics ·Kerry Fagan, (unknown)	14
8	The coagulation factor VII regulator is located on 8p23.1 1988 ·Human Genetics ·Kerry Fagan, Ian B. Wilkinson, Michael Allen, (unknown)	22
9	The effect of the phenoxyacetic acid herbicides 2,4,5-trichlorophenoxyacetic acid and 2,4-dichlorophenoxyacetic acid as ascertained by direct experimentation 1984 ·PubMed ·Kerry Fagan, J.K. Pollak	5
10	A deletion of heterochromatin only of the Y chromosome in an azoospermic male 1983 ·Human Genetics ·(unknown), (unknown), (unknown), Kerry Fagan, H. S. Grunstein	14

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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