Judith Conroy

5.3k total citations
31 papers, 1.0k citations indexed

About

Judith Conroy is a scholar working on Molecular Biology, Genetics and Cognitive Neuroscience. According to data from OpenAlex, Judith Conroy has authored 31 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 15 papers in Genetics and 5 papers in Cognitive Neuroscience. Recurrent topics in Judith Conroy's work include Genomics and Rare Diseases (8 papers), Genetics and Neurodevelopmental Disorders (7 papers) and Genomic variations and chromosomal abnormalities (5 papers). Judith Conroy is often cited by papers focused on Genomics and Rare Diseases (8 papers), Genetics and Neurodevelopmental Disorders (7 papers) and Genomic variations and chromosomal abnormalities (5 papers). Judith Conroy collaborates with scholars based in Ireland, United States and Italy. Judith Conroy's co-authors include Sean Ennis, Sally Ann Lynch, Mary D. King, Ricardo Segurado, Michael Gill, Nicholas M. Allen, Michael Fitzgerald, Bryan Lynch, Amre Shahwan and Louise Gallagher and has published in prestigious journals such as Nature Genetics, PLoS ONE and American Journal of Psychiatry.

In The Last Decade

Judith Conroy

31 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Judith Conroy Ireland 16 473 404 251 160 149 31 1.0k
Andreea Nissenkorn Israel 25 729 1.5× 314 0.8× 281 1.1× 294 1.8× 220 1.5× 59 1.5k
Vincenzo Salpietro Italy 22 481 1.0× 387 1.0× 150 0.6× 199 1.2× 57 0.4× 89 1.2k
Fanglin Guan China 23 544 1.2× 246 0.6× 65 0.3× 125 0.8× 70 0.5× 47 1.2k
Dorothée Ville France 20 355 0.8× 559 1.4× 367 1.5× 172 1.1× 99 0.7× 56 1.2k
Lili Long China 18 336 0.7× 147 0.4× 245 1.0× 182 1.1× 78 0.5× 78 829
Roser Pons Greece 21 644 1.4× 273 0.7× 155 0.6× 322 2.0× 100 0.7× 58 1.6k
Rita Cittadella Italy 18 274 0.6× 141 0.3× 187 0.7× 237 1.5× 64 0.4× 36 1.0k
Saadet Mercimek‐Mahmutoglu Canada 22 720 1.5× 377 0.9× 207 0.8× 183 1.1× 26 0.2× 51 1.7k
Venkateswaran Ramesh United Kingdom 13 427 0.9× 146 0.4× 230 0.9× 251 1.6× 31 0.2× 20 846
Birgit Assmann Germany 23 870 1.8× 299 0.7× 70 0.3× 304 1.9× 29 0.2× 51 1.7k

Countries citing papers authored by Judith Conroy

Since Specialization
Citations

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

Fields of papers citing papers by Judith Conroy

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Judith Conroy

This figure shows the co-authorship network connecting the top 25 collaborators of Judith Conroy. A scholar is included among the top collaborators of Judith Conroy 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 Judith Conroy. Judith Conroy 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
1.
Pratt, Jedd, Anthony W. Ryan, Thorhildur Juliusdottir, et al.. (2023). Genes encoding agrin (AGRN) and neurotrypsin (PRSS12) are associated with muscle mass, strength and plasma C-terminal agrin fragment concentration. GeroScience. 45(3). 1289–1302. 9 indexed citations
2.
Pratt, Jedd, Giuseppe De Vito, Marco Narici, et al.. (2021). Grip strength performance from 9431 participants of the GenoFit study: normative data and associated factors. GeroScience. 43(5). 2533–2546. 38 indexed citations
3.
Pratt, Jedd, Giuseppe De Vito, Marco Narici, et al.. (2021). Plasma C-Terminal Agrin Fragment as an Early Biomarker for Sarcopenia: Results From the GenoFit Study. The Journals of Gerontology Series A. 76(12). 2090–2096. 34 indexed citations
4.
Gorman, Kathleen M., et al.. (2017). Symmetrical thalamic calcification: A trio whole exome sequencing negative series. Brain and Development. 39(5). 426–430. 1 indexed citations
5.
Conroy, Judith, Nicholas M. Allen, Kathleen M. Gorman, et al.. (2016). Novel European SLC1A4 variant: infantile spasms and population ancestry analysis. Journal of Human Genetics. 61(8). 761–764. 15 indexed citations
6.
Allen, Nicholas M., Judith Conroy, Thierry Deonna, et al.. (2016). Atypical benign partial epilepsy of childhood with acquired neurocognitive, lexical semantic, and autistic spectrum disorder. Epilepsy & Behavior Case Reports. 6. 42–48. 8 indexed citations
7.
Quinn, Emma M., Anthony W. Ryan, Judith Conroy, et al.. (2015). Common polygenic variation in coeliac disease and confirmation of ZNF335 and NIFA as disease susceptibility loci. European Journal of Human Genetics. 24(2). 291–297. 27 indexed citations
8.
Gómez-Herreros, Fernando, Janneke Schuurs-Hoeijmakers, Mark McCormack, et al.. (2014). TDP2 protects transcription from abortive topoisomerase activity and is required for normal neural function. Nature Genetics. 46(5). 516–521. 115 indexed citations
9.
Allen, Nicholas M., Judith Conroy, Amre Shahwan, et al.. (2014). Excellent outcome with de novo 15q13.3 microdeletion causing infantile spasms—A further patient. American Journal of Medical Genetics Part A. 164(7). 1863–1866. 3 indexed citations
10.
Lynn, Miriam A., Naisha Shah, Judith Conroy, et al.. (2014). A Study of Alveolar Rhabdomyosarcoma Copy Number Alterations by Single Nucleotide Polymorphism Analysis. Applied immunohistochemistry & molecular morphology. 22(3). 213–221. 12 indexed citations
11.
Lynn, Miriam A., Yuexiang Wang, Naisha Shah, et al.. (2013). High-resolution Genome-wide Copy-number Analyses Identify Localized Copy-number Alterations in Ewing Sarcoma. Diagnostic Molecular Pathology. 22(2). 76–84. 14 indexed citations
12.
Conroy, Judith, Paul McGettigan, Raymond P. Murphy, et al.. (2013). A novel locus for episodic ataxia:UBR4 the likely candidate. European Journal of Human Genetics. 22(4). 505–510. 56 indexed citations
13.
Casey, Jillian P., Paul McGettigan, Niamh Lynam‐Lennon, et al.. (2012). Identification of a mutation in LARS as a novel cause of infantile hepatopathy. Molecular Genetics and Metabolism. 106(3). 351–358. 68 indexed citations
14.
Casey, Jillian P., Riki Kawaguchi, Hui Sun, et al.. (2011). First implication ofSTRA6mutations in isolated anophthalmia, microphthalmia, and coloboma: A new dimension to theSTRA6phenotype. Human Mutation. 32(12). 1417–1426. 64 indexed citations
15.
Conroy, Judith, Veronica Donoghue, M. Mullarkey, et al.. (2010). Agenesis of the corpus callosum with midline lipoma associated with an Xp22.31–Xp22.12 deletion. Clinical Dysmorphology. 20(1). 21–25. 2 indexed citations
16.
Correia, Catarina, Joana Almeida, Teresa S. Miguel, et al.. (2009). Association of the α4 integrin subunit gene (ITGA4) with autism. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 150B(8). 1147–1151. 17 indexed citations
17.
Conroy, Judith, Lynne Cochrane, Richard Anney, et al.. (2008). Fine mapping and association studies in a candidate region for autism on chromosome 2q31–q32. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 150B(4). 535–544. 9 indexed citations
18.
Yang, Mao, Lynne Cochrane, Judith Conroy, et al.. (2006). Protein kinase C-beta 1 gene variants are not associated with autism in the Irish population. Psychiatric Genetics. 17(1). 39–41. 5 indexed citations
19.
Domschke, Katharina, Karen Sheehan, Naomi Lowe, et al.. (2005). Association analysis of the monoamine oxidase A and B genes with attention deficit hyperactivity disorder (ADHD) in an Irish sample: Preferential transmission of the MAO‐A 941G allele to affected children. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 134B(1). 110–114. 63 indexed citations
20.
Segurado, Ricardo, et al.. (2005). Confirmation of Association Between Autism and the Mitochondrial Aspartate/Glutamate Carrier SLC25A12 Gene on Chromosome 2q31. American Journal of Psychiatry. 162(11). 2182–2184. 75 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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