Ciara Fahey

2.5k total citations
25 papers, 1.2k citations indexed

About

Ciara Fahey is a scholar working on Genetics, Cognitive Neuroscience and Molecular Biology. According to data from OpenAlex, Ciara Fahey has authored 25 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 7 papers in Cognitive Neuroscience and 5 papers in Molecular Biology. Recurrent topics in Ciara Fahey's work include Genetic Associations and Epidemiology (5 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Functional Brain Connectivity Studies (5 papers). Ciara Fahey is often cited by papers focused on Genetic Associations and Epidemiology (5 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Functional Brain Connectivity Studies (5 papers). Ciara Fahey collaborates with scholars based in Ireland, United States and Canada. Ciara Fahey's co-authors include Derek W. Morris, Michael Gill, Thomas Frodl, Angela Carballedo, James F. Meaney, Gary Donohoe, Elaine Kenny, Paul Cormican, Aiden Corvin and Ivan N. Shatsky and has published in prestigious journals such as PLoS ONE, NeuroImage and Biological Psychiatry.

In The Last Decade

Ciara Fahey

25 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ciara Fahey Ireland	19	572	286	254	152	136	25	1.2k
Janice M. Fullerton Australia	25	533 0.9×	665 2.3×	269 1.1×	221 1.5×	215 1.6×	65	1.9k
Gianluca Ursini United States	20	320 0.6×	242 0.8×	339 1.3×	116 0.8×	278 2.0×	38	1.1k
Julien Bryois United States	17	797 1.4×	735 2.6×	186 0.7×	162 1.1×	150 1.1×	27	1.7k
Franziska Degenhardt Germany	20	321 0.6×	291 1.0×	148 0.6×	69 0.5×	136 1.0×	59	838
Guiqing Cai United States	22	717 1.3×	747 2.6×	504 2.0×	264 1.7×	214 1.6×	37	1.9k
Aaron J. Towers United States	10	516 0.9×	328 1.1×	265 1.0×	102 0.7×	129 0.9×	11	1.2k
John D. H. Stead Canada	19	455 0.8×	244 0.9×	100 0.4×	122 0.8×	274 2.0×	25	1.3k
Andreas G. Chiocchetti Germany	17	474 0.8×	335 1.2×	284 1.1×	125 0.8×	77 0.6×	50	983
Mihovil Pletikos United States	18	680 1.2×	358 1.3×	458 1.8×	126 0.8×	297 2.2×	21	1.8k
Valeria Latorre Italy	19	364 0.6×	229 0.8×	897 3.5×	108 0.7×	269 2.0×	28	1.8k

Countries citing papers authored by Ciara Fahey

Since Specialization

Citations

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

Fields of papers citing papers by Ciara Fahey

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ciara Fahey

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

All Works

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20 of 20 papers shown

Moran, Bruce, Ciara Fahey, Tatjana Vlajnic, et al.. (2020). Evaluating liquid biopsies for methylomic profiling of prostate cancer. Epigenetics. 15(6-7). 715–727. 17 indexed citations

Booij, Linda, Moshe Szyf, Angela Carballedo, et al.. (2015). DNA Methylation of the Serotonin Transporter Gene in Peripheral Cells and Stress-Related Changes in Hippocampal Volume: A Study in Depressed Patients and Healthy Controls. PLoS ONE. 10(3). e0119061–e0119061. 112 indexed citations

Tozzi, Leonardo, Angela Carballedo, Friedrich Wetterling, et al.. (2015). Single-Nucleotide Polymorphism of the FKBP5 Gene and Childhood Maltreatment as Predictors of Structural Changes in Brain Areas Involved in Emotional Processing in Depression. Neuropsychopharmacology. 41(2). 487–497. 62 indexed citations

Andreev, Dmitry E., Patrick B. F. O’Connor, Ciara Fahey, et al.. (2015). Translation of 5′ leaders is pervasive in genes resistant to eIF2 repression. eLife. 4. e03971–e03971. 265 indexed citations

Morris, Derek W., Ciara Fahey, Andréia da Silva Costa, et al.. (2014). Effects of ZNF804A on auditory P300 response in schizophrenia. Translational Psychiatry. 4(1). e345–e345. 17 indexed citations

Kelly, Sinéad, Derek W. Morris, Omar Mothersill, et al.. (2014). Genome-wide schizophrenia variant at MIR137 does not impact white matter microstructure in healthy participants. Neuroscience Letters. 574. 6–10. 12 indexed citations

Fahey, Ciara, Susan Byrne, Russell L. McLaughlin, et al.. (2013). Analysis of the hexanucleotide repeat expansion and founder haplotype at C9ORF72 in an Irish psychosis case-control sample. Neurobiology of Aging. 35(6). 1510.e1–1510.e5. 27 indexed citations

Mothersill, Omar, Derek W. Morris, Sinéad Kelly, et al.. (2013). Effects of MIR137 on fronto-amygdala functional connectivity. NeuroImage. 90. 189–195. 39 indexed citations

Carballedo, Angela, Derek W. Morris, Peter Zill, et al.. (2013). Brain‐derived neurotrophic factor Val66Met polymorphism and early life adversity affect hippocampal volume. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 162(2). 183–190. 60 indexed citations

10.

Kenny, Elaine, Paul Cormican, Sarah Furlong, et al.. (2013). Excess of rare novel loss-of-function variants in synaptic genes in schizophrenia and autism spectrum disorders. Molecular Psychiatry. 19(8). 872–879. 131 indexed citations

11.

Rose, Emma J., April Hargreaves, Derek W. Morris, et al.. (2013). Effects of a novel schizophrenia risk variant rs7914558 atCNNM2on brain structure and attributional style. The British Journal of Psychiatry. 204(2). 115–121. 25 indexed citations

12.

Rose, Emma J., Derek W. Morris, April Hargreaves, et al.. (2013). Neural effects of the CSMD1 genome‐wide associated schizophrenia risk variant rs10503253. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 162(6). 530–537. 27 indexed citations

13.

Carballedo, Angela, Francesco Amico, Andrew Fagan, et al.. (2012). Reduced fractional anisotropy in the uncinate fasciculus in patients with major depression carrying the met‐allele of the Val66Met brain‐derived neurotrophic factor genotype. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 159B(5). 537–548. 75 indexed citations

14.

Carballedo, Angela, Danuta Lisiecka, Andrew Fagan, et al.. (2012). Effect of Genetic Variant in BICC1 on Functional and Structural Brain Changes in Depression. Neuropsychopharmacology. 37(13). 2855–2862. 19 indexed citations

15.

Murphy, Melissa, Angela Carballedo, Andrew Fagan, et al.. (2012). Neurotrophic Tyrosine Kinase Polymorphism Impacts White Matter Connections in Patients with Major Depressive Disorder. Biological Psychiatry. 72(8). 663–670. 50 indexed citations

16.

Rose, Emma J., Derek W. Morris, Ciara Fahey, et al.. (2012). The Effect of the Neurogranin Schizophrenia Risk Variant rs12807809 on Brain Structure and Function. Twin Research and Human Genetics. 15(3). 296–303. 20 indexed citations

17.

Morris, Derek W., Ciara Fahey, Andréia da Silva Costa, et al.. (2011). A NOS1 variant implicated in cognitive performance influences evoked neural responses during a high density EEG study of early visual perception. Human Brain Mapping. 33(5). 1202–1211. 18 indexed citations

18.

He, Ya‐Wen, Christian R. Marshall, Raymond Wong, et al.. (2011). Euchromatic 9q13-q21 duplication variants are tandem segmental amplifications of sequence reciprocal to 9q13-q21 deletions. Journal of Medical Genetics. 48(5). 317–322. 9 indexed citations

19.

Rose, Emma J., Ciara M. Greene, Sinéad Kelly, et al.. (2011). The NOS1 variant rs6490121 is associated with variation in prefrontal function and grey matter density in healthy individuals. NeuroImage. 60(1). 614–622. 21 indexed citations

20.

Johnson, Nancy, Ciara Fahey, Brian Chicoine, George Chong, & Darren R. Gitelman. (2003). Effects of Donepezil on Cognitive Functioning in Down Syndrome. American Journal on Mental Retardation. 108(6). 367–367. 42 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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