Bridget O’Connor

550 total citations
20 papers, 214 citations indexed

About

Bridget O’Connor is a scholar working on Clinical Psychology, Pediatrics, Perinatology and Child Health and Genetics. According to data from OpenAlex, Bridget O’Connor has authored 20 papers receiving a total of 214 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Clinical Psychology, 6 papers in Pediatrics, Perinatology and Child Health and 6 papers in Genetics. Recurrent topics in Bridget O’Connor's work include Family and Disability Support Research (8 papers), Genomics and Rare Diseases (5 papers) and Infant Development and Preterm Care (4 papers). Bridget O’Connor is often cited by papers focused on Family and Disability Support Research (8 papers), Genomics and Rare Diseases (5 papers) and Infant Development and Preterm Care (4 papers). Bridget O’Connor collaborates with scholars based in United States, Australia and United Kingdom. Bridget O’Connor's co-authors include Christine Imms, Claire Kerr, Nora Shields, Catherine E. Keegan, Pesi Katrak, Beverly M. Yashar, Shane C. Quinonez, Christopher N. Vlangos, Ayesha Ahmad and Mark Hannibal and has published in prestigious journals such as PLoS ONE, Scientific Reports and Developmental Biology.

In The Last Decade

Bridget O’Connor

18 papers receiving 208 citations

Peers

Bridget O’Connor
Ambreen Asim India
Sarita Agarwal India
Sarah Helen Evans United States
Srinivasan Muthuswamy India
Shin Young Kim South Korea
Tarek Omar Egypt
Carlos Augusto Bastos de Souza Brazil
Maina Kava Australia
Anneliese Schwenkhagen Germany
Andrew Evans Australia
Ambreen Asim India
Bridget O’Connor
Citations per year, relative to Bridget O’Connor Bridget O’Connor (= 1×) peers Ambreen Asim

Countries citing papers authored by Bridget O’Connor

Since Specialization
Citations

This map shows the geographic impact of Bridget 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 Bridget 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 Bridget O’Connor more than expected).

Fields of papers citing papers by Bridget O’Connor

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

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

This figure shows the co-authorship network connecting the top 25 collaborators of Bridget O’Connor. A scholar is included among the top collaborators of Bridget 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 Bridget O’Connor. Bridget O’Connor 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
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O’Connor, Bridget, et al.. (2024). Exploring the impact of professional development about family-centred service for health professionals working in paediatric disability: a scoping review. Disability and Rehabilitation. 47(16). 4063–4078. 2 indexed citations
5.
Miller, Laura, Christine Imms, Andrea Cross, et al.. (2022). Impact of “early intervention” parent workshops on outcomes for caregivers of children with neurodisabilities: a mixed-methods study. Disability and Rehabilitation. 45(23). 3900–3911. 12 indexed citations
6.
Appelbaum, Paul S., Karolynn Siegel, Julia Wynn, et al.. (2022). Challenges of variant reinterpretation: Opinions of stakeholders and need for guidelines. Genetics in Medicine. 24(9). 1878–1887. 19 indexed citations
7.
Cross, Andrea, et al.. (2022). Co‐development of the ENVISAGE‐Families programme for parents of children with disabilities: Reflections on a parent–researcher partnership. Australian Occupational Therapy Journal. 69(6). 653–661. 13 indexed citations
8.
Quinonez, Shane C., et al.. (2021). The introduction of genetic counseling in Ethiopia: Results of a training workshop and lessons learned. PLoS ONE. 16(7). e0255278–e0255278. 11 indexed citations
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Jacobs, Michelle F., et al.. (2020). Knowledge and attitudes about genetic counseling in patients at a major hospital in Addis Ababa, Ethiopia. Journal of Genetic Counseling. 30(2). 544–552. 5 indexed citations
10.
Zaghi, Soroush, et al.. (2020). Assessment of Nasal Breathing Using Lip Taping: A Simple and Effective Screening Tool. 6(1). 10–10. 6 indexed citations
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Ziats, Mark N., Ayesha Ahmad, John Bernat, et al.. (2019). Genotype–phenotype analysis of 523 patients by genetics evaluation and clinical exome sequencing. Pediatric Research. 87(4). 735–739. 25 indexed citations
12.
Uehara, Tomoko, Hidenori Suzuki, Nobuhiko Okamoto, et al.. (2019). Pathogenetic basis of Takenouchi-Kosaki syndrome: Electron microscopy study using platelets in patients and functional studies in a Caenorhabditis elegans model. Scientific Reports. 9(1). 4418–4418. 13 indexed citations
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O’Connor, Bridget, et al.. (2019). Primary care physicians’ understanding and utilization of pediatric exome sequencing results. Journal of Genetic Counseling. 28(6). 1130–1138. 6 indexed citations
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O’Connor, Bridget, Claire Kerr, Nora Shields, Brooke Adair, & Christine Imms. (2019). Steering towards collaborative assessment: a qualitative study of parents’ experiences of evidence-based assessment practices for their child with cerebral palsy. Disability and Rehabilitation. 43(4). 458–467. 11 indexed citations
15.
O’Connor, Bridget, Claire Kerr, Nora Shields, & Christine Imms. (2017). Understanding allied health practitioners’ use of evidence-based assessments for children with cerebral palsy: a mixed methods study. Disability and Rehabilitation. 41(1). 53–65. 12 indexed citations
16.
Beck, David B., Megan T. Cho, Francisca Millan, et al.. (2016). A recurrent de novo CTBP1 mutation is associated with developmental delay, hypotonia, ataxia, and tooth enamel defects. Neurogenetics. 17(3). 173–178. 25 indexed citations
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O’Connor, Bridget, Claire Kerr, Nora Shields, & Christine Imms. (2015). A systematic review of evidence‐based assessment practices by allied health practitioners for children with cerebral palsy. Developmental Medicine & Child Neurology. 58(4). 332–347. 18 indexed citations
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O’Connor, Bridget, Erica L. Macke, & Catherine E. Keegan. (2011). Additive effect of TAp63 deficiency on the adrenocortical dysplasia (acd) phenotype. Mammalian Genome. 22(11-12). 714–721. 1 indexed citations
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Vlangos, Christopher N., et al.. (2009). Caudal regression in adrenocortical dysplasia (acd) mice is caused by telomere dysfunction with subsequent p53-dependent apoptosis. Developmental Biology. 334(2). 418–428. 20 indexed citations
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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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