Carol Hardy

900 total citations
11 papers, 500 citations indexed

About

Carol Hardy is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Carol Hardy has authored 11 papers receiving a total of 500 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 5 papers in Genetics and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Carol Hardy's work include Genetic Syndromes and Imprinting (4 papers), Epigenetics and DNA Methylation (3 papers) and Neurological diseases and metabolism (2 papers). Carol Hardy is often cited by papers focused on Genetic Syndromes and Imprinting (4 papers), Epigenetics and DNA Methylation (3 papers) and Neurological diseases and metabolism (2 papers). Carol Hardy collaborates with scholars based in United Kingdom, United States and France. Carol Hardy's co-authors include John A. Corbett, M W Kilpatrick, Sarah Bundey, Timothy Barrett, Fiona MacDonald, Eamonn R. Maher, Gail Kirby, Farida Latif, Joanna Poulton and Jeremy Kirk and has published in prestigious journals such as The American Journal of Human Genetics, Genomics and Developmental Medicine & Child Neurology.

In The Last Decade

Carol Hardy

10 papers receiving 474 citations

Peers

Countries citing papers authored by Carol Hardy

Since Specialization

Citations

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

Fields of papers citing papers by Carol Hardy

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Carol Hardy

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

All Works

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11 of 11 papers shown

#	Work	Indexed citations
1	Pathogen delivery route impacts disease severity in experimental Mycoplasma ovipneumoniae infection of domestic lambs 2025 ·Veterinary Research ·(unknown), (unknown), (unknown), (unknown), Carol Hardy, (unknown), (unknown), (unknown), (unknown), (unknown), Stephen W. Smith, Lizabeth Bowen, Diane Bimczok	0
2	Methylation analysis and diagnostics of Beckwith-Wiedemann syndrome in 1,000 subjects 2014 ·Clinical Epigenetics ·Abdulla Ibrahim, Gail Kirby, Carol Hardy, Renuka Dias, Louise Tee, Derek Lim, Jonathan Berg, Fiona MacDonald, Peter Nightingale, Eamonn R. Maher	87
3	Modification of severe insulin resistant diabetes in response to lifestyle changes in Alström syndrome 2014 ·European Journal of Medical Genetics ·Richard Paisey, (unknown), Michael Waterson, Robert Cramb, Richard P. Steeds, Kathleen A. Williams, Alison White, Carol Hardy	16
4	Epimutation profiling in Beckwith-Wiedemann syndrome: relationship with assisted reproductive technology 2013 ·Clinical Epigenetics ·Louise Tee, Derek Lim, Renuka Dias, Marie-Odile Baudement, (unknown), Gail Kirby, (unknown), Helen Stewart, Carol Hardy, Fiona MacDonald, Eamonn R. Maher	31
5	Infantile neuroaxonal dystrophy caused by uniparental disomy 2013 ·Developmental Medicine & Child Neurology ·Joyce Solomons, (unknown), Carol Hardy, Manju A. Kurian, Sandeep Jayawant, Sarah Hughes, Pieter Pretorius, Andrea H. Németh	11
6	Comparison of the clinical scoring systems in Silver–Russell syndrome and development of modified diagnostic criteria to guide molecular genetic testing 2013 ·Journal of Medical Genetics ·Renuka Dias, Peter Nightingale, Carol Hardy, Gail Kirby, Louise Tee, Susan Price, Fiona MacDonald, Timothy Barrett, Eamonn R. Maher	20
7	Multiplex ligation-dependent probe amplification (MLPA) analysis is an effective tool for the detection of novel intragenic PLA2G6 mutations: Implications for molecular diagnosis 2010 ·Molecular Genetics and Metabolism ·(unknown), (unknown), Lesley MacPherson, Katharine Foster, Peter Lunt, Imelda Hughes, Angela F. Brady, Michael Pike, (unknown), Neil V. Morgan, Carol Hardy, (unknown), Fiona MacDonald, Eamonn R. Maher, Manju A. Kurian	27
8	The Protein Truncation Test 2003 ·Humana Press eBooks ·Carol Hardy	1
9	Clinical and Molecular Genetic Analysis of 19 Wolfram Syndrome Kindreds Demonstrating a Wide Spectrum of Mutations in WFS1 1999 ·The American Journal of Human Genetics ·Carol Hardy, Farhat L. Khanim, Rosarelis Torres, Martin Scott-Brown, A Seller, Joanna Poulton, David Collier, Jeremy Kirk, Mihael H. Polymeropoulos, Farida Latif, Timothy Barrett	159
10	Duplication of the 15q11‐13 Region in a Patient with Autism, Epilepsy and Ataxia 1994 ·Developmental Medicine & Child Neurology ·Sarah Bundey, Carol Hardy, (unknown), M W Kilpatrick, John A. Corbett	122
11	Analysis of 133 Meioses Places the Genes for Nevoid Basal Cell Carcinoma (Gorlin) Syndrome and Fanconi Anemia Group C in a 2.6-cM Interval and Contributes to the Fine Map of 9q22.3 1994 ·Genomics ·Peter Farndon, Deborah Morris, Carol Hardy, Carmel McConville, Jean Weissenbach, Michael W. Kilpatrick, André Reis	26

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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