Caoimhe McKenna - Concepedia

Author

Caoimhe McKenna

Also Known As

B. Coad, C McKenna, C. McKenna, Caoimhe McKenna, Caoimhe S McKenna, Caoimhe S. McKenna, Claire McKenna, Gabriela M. Repetto, McKenna, Christopher

Publications

619

Citations

H-Index

Concepts

All Affiliations

University College London Inserm Great Ormond Street Hospital Royal Devon & Exeter NHS Foundation Trust Murdoch Children's Research Institute

About

Caoimhe McKenna is an author at University College London specializing in medicine, genetics, and clinical genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	3	3	212
2	Education	1	1	78
3	Nursing	1	1	78
4	Biology	1	1	99
5	Molecular Genetics	1	1	99

Caoimhe McKenna

Publications

587

Citations

H-Index

Page 1

	Year	Citations
Paroxysmal kinesigenic dyskinesia and infantile convulsions Kathryn J. Swoboda, Bing‐Wen Soong, Caoimhe McKenna, Neurology	2000	127
Inheritance patterns and phenotypic features of myofibrillar myopathy associated with a BAG3 mutation Zagaa Odgerel, Anna Sárközy, Hee-Suk Lee, Neuromuscular Disorders BiologyMendelian DisorderGenetic DisorderGeneticsBag3 Mutation	2010	99
Self-assessment in medical practice A. Evans, Caoimhe McKenna, Martin Oliver Journal of the Royal Society of Medicine NursingSelf-assessment SkillsPrimary CarePerformance StudiesSelf-management	2002	78
Heterozygous lamin B1 and lamin B2 variants cause primary microcephaly and define a novel laminopathy David Parry, Carol-Anne Martin, Philip Greene, Genetics in Medicine	2020	52
Leaving foster or residential care: a participatory study of care leavers' experiences of health and social care transitions Kristin Liabo, Caoimhe McKenna, Anne Ingold, Child Care Health and Development	2016	45
Trainees' perspectives on the assessment and self‐assessment of surgical skills A. Evans, Caoimhe McKenna, Martin Oliver Assessment & Evaluation in Higher Education	2004	42
Variants in GNAI1 cause a syndrome associated with variable features including developmental delay, seizures, and hypotonia Alison M. Muir, Jennifer F. Gardner, Richard H. van Jaarsveld, Genetics in Medicine Developmental AnomalyDevelopmental BiologyMendelian DisorderGenetic DisorderGenetics	2021	35
Functional and clinical studies reveal pathophysiological complexity of CLCN4-related neurodevelopmental condition Elizabeth E. Palmer, Michael Pusch, Alessandra Picollo, Molecular Psychiatry	2022	32
Presentation and Investigation of Pediatric Bone and Joint Infections in the Pediatric Emergency Department Olugbenga Akinkugbe, Charles Stewart, Caoimhe McKenna Pediatric Emergency Care	2018	21
Quantifying prediction of pathogenicity for within-codon concordance (PM5) using 7541 functional classifications of BRCA1 and MSH2 missense variants Lucy Loong, Cankut Çubuk, Subin Choi, Genetics in Medicine	2021	16

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