Emer O’Connor

1.3k total citations
17 papers, 404 citations indexed

About

Emer O’Connor is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Psychiatry and Mental health. According to data from OpenAlex, Emer O’Connor has authored 17 papers receiving a total of 404 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 8 papers in Cellular and Molecular Neuroscience and 6 papers in Psychiatry and Mental health. Recurrent topics in Emer O’Connor's work include Migraine and Headache Studies (6 papers), Genetic Neurodegenerative Diseases (6 papers) and Mitochondrial Function and Pathology (5 papers). Emer O’Connor is often cited by papers focused on Migraine and Headache Studies (6 papers), Genetic Neurodegenerative Diseases (6 papers) and Mitochondrial Function and Pathology (5 papers). Emer O’Connor collaborates with scholars based in United Kingdom, France and Ireland. Emer O’Connor's co-authors include Henry Houlden, Roisin Sullivan, Wai Yan Yau, David P. Finn, Catherine Diskin, Michelle Roche, Manjit Matharu, Jana Vandrovcová, Lou Grangeon and Benjamin S. Simpson and has published in prestigious journals such as Brain, Neurology and Journal of Neurology Neurosurgery & Psychiatry.

In The Last Decade

Emer O’Connor

17 papers receiving 397 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Emer O’Connor United Kingdom	8	256	193	108	57	55	17	404
Adriana Moro Brazil	14	265 1.0×	243 1.3×	339 3.1×	35 0.6×	32 0.6×	38	589
Alessandra Cifra Italy	10	142 0.6×	109 0.6×	60 0.6×	35 0.6×	19 0.3×	10	312
Katherine Halievski Canada	12	255 1.0×	172 0.9×	52 0.5×	27 0.5×	22 0.4×	19	472
Roberto Di Fabio Italy	13	208 0.8×	127 0.7×	93 0.9×	99 1.7×	10 0.2×	28	405
Jianning Lu Germany	8	137 0.5×	129 0.7×	47 0.4×	27 0.5×	29 0.5×	10	374
J. Veyssière France	10	143 0.6×	156 0.8×	52 0.5×	21 0.4×	34 0.6×	10	392
Allyson Alexander United States	11	268 1.0×	93 0.5×	114 1.1×	152 2.7×	68 1.2×	28	562
Stefania Sellitti Italy	7	286 1.1×	223 1.2×	41 0.4×	25 0.4×	13 0.2×	10	426
Yueh‐Jan Wang Taiwan	14	221 0.9×	98 0.5×	104 1.0×	17 0.3×	12 0.2×	28	485

Countries citing papers authored by Emer O’Connor

Since Specialization

Citations

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

Fields of papers citing papers by Emer O’Connor

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Emer O’Connor. 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 Emer O’Connor. The network helps show where Emer O’Connor may publish in the future.

Co-authorship network of co-authors of Emer O’Connor

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

All Works

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17 of 17 papers shown

Yau, Wai Yan, Roisin Sullivan, Emer O’Connor, et al.. (2025). Diagnostic yield and limitations of whole-genome sequencing for hereditary cerebellar ataxia. Brain Communications. 7(3). fcaf188–fcaf188. 1 indexed citations

O’Connor, Emer, et al.. (2022). The clinical characteristics of familial cluster headache. Cephalalgia. 42(8). 715–721. 2 indexed citations

Stubberud, Anker, Emer O’Connor, Erling Tronvik, Henry Houlden, & Manjit Matharu. (2021). R1352Q <b><i>CACNA1A</i></b> Variant in a Patient with Sporadic Hemiplegic Migraine, Ataxia, Seizures and Cerebral Oedema: A Case Report. Case Reports in Neurology. 13(1). 123–130. 6 indexed citations

Grangeon, Lou, Emer O’Connor, Daisuke Danno, et al.. (2021). Is pituitary MRI screening necessary in cluster headache?. Cephalalgia. 41(7). 779–788. 8 indexed citations

Grangeon, Lou, et al.. (2020). New insights in post-traumatic headache with cluster headache phenotype: a cohort study. Journal of Neurology Neurosurgery & Psychiatry. 91(6). 572–579. 14 indexed citations

O’Connor, Emer, Benjamin S. Simpson, Henry Houlden, Jana Vandrovcová, & Manjit Matharu. (2020). Prevalence of familial cluster headache: a systematic review and meta-analysis. The Journal of Headache and Pain. 21(1). 37–37. 20 indexed citations

Gang, Qiang, Conceição Bettencourt, Janice L. Holton, et al.. (2020). A novel frameshift deletion in autosomal recessive SBF1-related syndromic neuropathy with necklace fibres. Journal of Neurology. 267(9). 2705–2712. 5 indexed citations

Lambru, Giorgio, Khadija Rantell, Emer O’Connor, et al.. (2020). Trigeminal neurovascular contact in SUNCT and SUNA: a cross-sectional magnetic resonance study. Brain. 143(12). 3619–3628. 14 indexed citations

Hostettler, Isabel C., Benjamin O’Callaghan, Enrico Bugiardini, et al.. (2020). ANGPTL6 Genetic Variants Are an Underlying Cause of Familial Intracranial Aneurysms. Neurology. 96(6). e947–e955. 7 indexed citations

10.

Sullivan, Roisin, Wai Yan Yau, Emer O’Connor, & Henry Houlden. (2018). Spinocerebellar ataxia: an update. Journal of Neurology. 266(2). 533–544. 200 indexed citations

11.

Yau, Wai Yan, et al.. (2018). DNA repair in trinucleotide repeat ataxias. FEBS Journal. 285(19). 3669–3682. 10 indexed citations

12.

Doherty, Mark, Emer O’Connor, David W. Hannon, et al.. (2018). Absence of thyroid transcription factor-1 expression is associated with poor survival in patients with advanced pulmonary adenocarcinoma treated with pemetrexed-based chemotherapy. Irish Journal of Medical Science (1971 -). 188(1). 69–74. 6 indexed citations

13.

Chelban, Viorica, Sarah Wiethoff, Nourelhoda A. Haridy, et al.. (2018). Genotype‐phenotype correlations, dystonia and disease progression in spinocerebellar ataxia type 14. Movement Disorders. 33(7). 1119–1129. 25 indexed citations

14.

O’Connor, Emer, Laura Williams, John S. Butler, et al.. (2017). Menstrual cycle and the temporal discrimination threshold. Physiological Measurement. 38(2). N65–N72. 3 indexed citations

15.

Chelban, Viorica, Andreea Manole, Lasse Pihlstrøm, et al.. (2016). Analysis of the prion protein gene in multiple system atrophy. Neurobiology of Aging. 49. 216.e15–216.e18. 7 indexed citations

16.

Roche, Michelle, Emer O’Connor, Catherine Diskin, & David P. Finn. (2007). The effect of CB₁ receptor antagonism in the right basolateral amygdala on conditioned fear and associated analgesia in rats. European Journal of Neuroscience. 26(9). 2643–2653. 74 indexed citations

17.

Taylor, Mélissa, et al.. (1981). Kawasaki disease in Ireland.. PubMed. 74(3). 85–6. 2 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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