Anne Ronan

2.1k total citations
35 papers, 881 citations indexed

About

Anne Ronan is a scholar working on Genetics, Molecular Biology and Endocrinology, Diabetes and Metabolism. According to data from OpenAlex, Anne Ronan has authored 35 papers receiving a total of 881 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 12 papers in Molecular Biology and 5 papers in Endocrinology, Diabetes and Metabolism. Recurrent topics in Anne Ronan's work include Congenital heart defects research (4 papers), Hormonal and reproductive studies (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Anne Ronan is often cited by papers focused on Congenital heart defects research (4 papers), Hormonal and reproductive studies (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Anne Ronan collaborates with scholars based in Australia, United States and France. Anne Ronan's co-authors include Anthony R. Tagliaferro, Henry J. Thompson, Michael L. Bennish, Geoffrey G Hogg, Geoffrey L. Klug, Victoria J. Vieira‐Potter, L. David Meeker, Mohammed Hanif, Md. Anisur Rahman and Christopher Semsarian and has published in prestigious journals such as The Lancet, Journal of the American College of Cardiology and American Journal of Clinical Nutrition.

In The Last Decade

Anne Ronan

33 papers receiving 855 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Anne Ronan Australia 16 285 206 128 115 113 35 881
Dewi K. Rowlands Hong Kong 19 543 1.9× 72 0.3× 155 1.2× 269 2.3× 115 1.0× 50 1.6k
M. Elizabeth Tejero Mexico 16 189 0.7× 142 0.7× 104 0.8× 53 0.5× 225 2.0× 50 849
Xiaoguang Xu China 17 430 1.5× 119 0.6× 43 0.3× 114 1.0× 83 0.7× 52 1.0k
Maria Paola Grimaldi Italy 16 286 1.0× 93 0.5× 46 0.4× 51 0.4× 265 2.3× 23 1.0k
Geli Liu China 20 422 1.5× 152 0.7× 153 1.2× 47 0.4× 80 0.7× 63 1.1k
Yuan Lv China 21 512 1.8× 54 0.3× 158 1.2× 60 0.5× 76 0.7× 61 1.2k
Razvan Arsenescu United States 21 342 1.2× 260 1.3× 104 0.8× 59 0.5× 272 2.4× 39 1.5k
M. Mochizuki Japan 19 554 1.9× 236 1.1× 72 0.6× 40 0.3× 189 1.7× 61 1.4k
Shinichiro Saito Japan 20 468 1.6× 141 0.7× 83 0.6× 35 0.3× 251 2.2× 70 1.3k
David Cruz‐Robles Mexico 17 280 1.0× 51 0.2× 82 0.6× 160 1.4× 190 1.7× 50 1.3k

Countries citing papers authored by Anne Ronan

Since Specialization
Citations

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

Fields of papers citing papers by Anne Ronan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anne Ronan

This figure shows the co-authorship network connecting the top 25 collaborators of Anne Ronan. A scholar is included among the top collaborators of Anne Ronan 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 Anne Ronan. Anne Ronan 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.
Bagnall, Richard D., Emma S. Singer, Julie Wacker, et al.. (2022). Genetic Basis of Childhood Cardiomyopathy. Circulation Genomic and Precision Medicine. 15(6). e003686–e003686. 18 indexed citations
2.
Bagnall, Richard D., Jodie Ingles, Marcel E. Dinger, et al.. (2018). Whole Genome Sequencing Improves Outcomes of Genetic Testing in Patients With Hypertrophic Cardiomyopathy. Journal of the American College of Cardiology. 72(4). 419–429. 112 indexed citations
3.
Kamien, Benjamin, Anne Ronan, Gemma Poke, et al.. (2018). A Clinical Review of Generalized Overgrowth Syndromes in the Era of Massively Parallel Sequencing. Molecular Syndromology. 9(2). 70–82. 32 indexed citations
4.
Ronan, Anne, et al.. (2017). Recurrent ATP2A2 p.(Pro602Leu) mutation differentiates Acrokeratosis verruciformis of Hopf from the allelic condition Darier disease. American Journal of Medical Genetics Part A. 173(7). 1975–1978. 1 indexed citations
5.
Olivier, Damien, et al.. (2016). Nonunion of the Posteromedial Tubercle of the Talus: Interest of SPECT/CT. Journal of Nuclear Medicine & Radiation Therapy. 7(5). 1 indexed citations
6.
Saha, Debasish, Anne Ronan, Wasif Ali Khan, & Mohammed Abdus Salam. (2014). Diagnosis of pneumonia in children with dehydrating diarrhoea.. PubMed. 32(1). 14–8. 6 indexed citations
7.
Hoischen, Alexander, Anne Badel, Anne Ronan, et al.. (2012). BDNF and DYRK1A Are Variable and Inversely Correlated in Lymphoblastoid Cell Lines from Down Syndrome Patients. Molecular Neurobiology. 46(2). 297–303. 17 indexed citations
8.
Bachmann‐Gagescu, Ruxandra, Gisele E. Ishak, Jennifer C. Dempsey, et al.. (2012). Genotype–phenotype correlation in CC2D2A-related Joubert syndrome reveals an association with ventriculomegaly and seizures. Journal of Medical Genetics. 49(2). 126–137. 50 indexed citations
9.
Schönewolf‐Greulich, Bitten, Anne Ronan, Marianne Lodahl, et al.. (2011). Two new cases with microdeletion of 17q23.2 suggest presence of a candidate gene for sensorineural hearing loss within this region. American Journal of Medical Genetics Part A. 155(12). 2964–2969. 5 indexed citations
10.
Maupetit‐Mehouas, Stéphanie, Virginie Mariot, Christelle Reynès, et al.. (2010). Quantification of the methylation at the GNAS locus identifies subtypes of sporadic pseudohypoparathyroidism type Ib. Journal of Medical Genetics. 48(1). 55–63. 45 indexed citations
11.
Ronan, Anne, et al.. (2009). Familial 4.3 Mb duplication of 21q22 sheds new light on the Down syndrome critical region. BMJ Case Reports. 2009. bcr0520091914–bcr0520091914. 14 indexed citations
12.
Vieira‐Potter, Victoria J., et al.. (2005). Elevated atopy in healthy obese women. American Journal of Clinical Nutrition. 82(3). 504–509. 51 indexed citations
13.
Morrell, Jesse Stabile, et al.. (2002). Effects of ketamine-xylazine and isoflurane on insulin sensitivity in dehydroepiandrosterone sulfate-treated minipigs (Sus scrofa domestica).. PubMed. 52(3). 233–7. 9 indexed citations
14.
Ronan, Anne, Abul Kalam Azad, Omar Rahman, Rodney E. Phillips, & Michael L. Bennish. (1997). Hyperglycemia during childhood diarrhea. The Journal of Pediatrics. 130(1). 45–51. 15 indexed citations
15.
Tagliaferro, Anthony R., et al.. (1996). Cyclic Food Restriction Alters Substrate Utilization and Abolishes Protection from Mammary Carcinogenesis in Female Rats1,2. Journal of Nutrition. 126(5). 1398–1405. 32 indexed citations
16.
Bennish, Michael L., et al.. (1996). Randomised controlled comparison of single-dose ciprofloxacin and doxycycline for cholera caused by Vibrio cholerae O1 or O139. The Lancet. 348(9023). 296–300. 53 indexed citations
17.
Ronan, Anne, Geoffrey G Hogg, & Geoffrey L. Klug. (1995). Cerebrospinal fluid shunt infections in children. The Pediatric Infectious Disease Journal. 14(9). 782–786. 76 indexed citations
18.
Hanif, Mohammed, et al.. (1995). Fatal renal failure caused by diethylene glycol in paracetamol elixir: the Bangladesh epidemic. BMJ. 311(6997). 88–91. 113 indexed citations
19.
Tagliaferro, Anthony R., Bill D. Roebuck, Anne Ronan, & L. David Meeker. (1992). Enhancement of Pancreatic Carcinogenesis by Dehydroepiandrosterone. Advances in experimental medicine and biology. 322. 119–129. 3 indexed citations
20.

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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Dewi K. Rowlands Breakdown of academic impact, for papers by M. Elizabeth Tejero Breakdown of academic impact, for papers by Xiaoguang Xu Breakdown of academic impact, for papers by Maria Paola Grimaldi Breakdown of academic impact, for papers by Geli Liu Breakdown of academic impact, for papers by Yuan Lv Breakdown of academic impact, for papers by Razvan Arsenescu Breakdown of academic impact, for papers by M. Mochizuki Breakdown of academic impact, for papers by Shinichiro Saito Breakdown of academic impact, for papers by David Cruz‐Robles
Rankless by CCL
2026