C Hardy

601 total citations
11 papers, 378 citations indexed

About

C Hardy is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, C Hardy has authored 11 papers receiving a total of 378 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 6 papers in Genetics and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in C Hardy's work include Genetic Syndromes and Imprinting (6 papers), Genomic variations and chromosomal abnormalities (4 papers) and Prenatal Screening and Diagnostics (3 papers). C Hardy is often cited by papers focused on Genetic Syndromes and Imprinting (6 papers), Genomic variations and chromosomal abnormalities (4 papers) and Prenatal Screening and Diagnostics (3 papers). C Hardy collaborates with scholars based in United Kingdom, Ireland and United States. C Hardy's co-authors include J. Gorham, C. N. Law, R. G. Wyn Jones, L. R. Joppa, T. Webb, Marissa King, Tim Cole, M. Dahlitz, M W Kilpatrick and Bert L. Vallée and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Theoretical and Applied Genetics and Journal of Medical Genetics.

In The Last Decade

C Hardy

11 papers receiving 333 citations

Peers

Countries citing papers authored by C Hardy

Since Specialization

Citations

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

Fields of papers citing papers by C Hardy

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of C Hardy

This figure shows the co-authorship network connecting the top 25 collaborators of C Hardy. A scholar is included among the top collaborators of C 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 C Hardy. C 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	PLA2G6-associated neurodegeneration (PLAN): Further expansion of the clinical, radiological and mutation spectrum associated with infantile and atypical childhood-onset disease 2014 ·Molecular Genetics and Metabolism ·Marjorie Illingworth, Esther Meyer, W.K. Chong, Adnan Y. Manzur, Lucinda Carr, R. T. Younis, C Hardy, Fiona McDonald, Anne Marie Childs, Bruce H. Stewart, Daniel Warren, Rachel Kneen, Marissa King, Susan J. Hayflick, Manju A. Kurian	69
2	Is PATCHED an important candidate gene for neural tube defects? Cranial and thoracic neural tube defects in a family with Gorlin syndrome: a case report 2011 ·Clinical Genetics ·(unknown), Peter Farndon, Alison D. Murray, C Hardy, Zosia Miedzybrodzka	5
3	Familial Prader‐Willi syndrome: case report and a literature review 2000 ·Clinical Genetics ·(unknown), T. Webb, C Hardy, (unknown)	12
4	A clinical, cytogenetic and molecular study of ten probands with supernumerary inv dup (15) marker chromosomes 1998 ·Clinical Genetics ·T. Webb, C Hardy, Marissa King, (unknown), (unknown), Tim Cole	40
5	A clinical, cytogenetic and molecular study of ten probands with supernumerary inv dup (15) marker chromosomes 1998 ·Clinical Genetics ·T. Webb, C Hardy, Marissa King, (unknown), (unknown), Tim Cole	11
6	A boy with developmental delay and a maternally inherited deletion in 15q11q13. 1996 ·Journal of Medical Genetics ·Marissa King, C Hardy, (unknown), M W Kilpatrick, T. Webb	1
7	A clinical, cytogenetic, and molecular study of 40 adults with the Prader-Willi syndrome. 1995 ·Journal of Medical Genetics ·T. Webb, (unknown), C Hardy, M W Kilpatrick, John A. Corbett, M. Dahlitz	21
8	A male with a de novo translocation involving loss of 15q11q13 material and Prader-Willi syndrome. 1994 ·Journal of Medical Genetics ·(unknown), M. Dahlitz, C Hardy, M W Kilpatrick, T. Webb	18
9	Response of Eragrostis tef to Salinity and Acute Water Shortage 1990 ·Journal of Plant Physiology ·J. Gorham, C Hardy	8
10	Chromosomal location of a K/Na discrimination character in the D genome of wheat 1987 ·Theoretical and Applied Genetics ·J. Gorham, C Hardy, R. G. Wyn Jones, L. R. Joppa, C. N. Law	168
11	RNA metabolism, manganese, and RNA polymerases of zinc-sufficient and zinc-deficient Euglena gracilis. 1978 ·Proceedings of the National Academy of Sciences ·Kenneth H. Falchuk, C Hardy, (unknown), Bert L. Vallée	25

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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