Lucy Jenkins - Concepedia

Author

Lucy Jenkins

Also Known As

Diana Johnson, Jane Hurst, Joanna Jarvis, L Jenkins, L. Jenkins, LUCY JENKINS, Lucy A Jenkins, Lucy A. Jenkins, Lucy Harrison, Lucy Jenkins

Publications

7.8K

Citations

H-Index

Concepts

All Affiliations

University College London Great Ormond Street Hospital for Children NHS Foundation Trust Great Ormond Street Hospital University of Oxford University of Manchester

About

Lucy Jenkins is an author at University College London specializing in medicine, genetics, and pediatrics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	12	12	811
2	Education	2	2	73
3	Arts	1	1	551
4	Engineering	1	1	105
5	Natural Sciences	1	1	131

Lucy Jenkins

Publications

5.2K

Citations

H-Index

Page 1

	Year	Citations
Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study Jenny Lord, Dominic McMullan, Ruth Y. Eberhardt, The Lancet	2019	694
GJB2 Mutations and Degree of Hearing Loss: A Multicenter Study Rikkert L. Snoeckx, P.L.M. Huygen, Delphine Feldmann, The American Journal of Human Genetics Genetic DisorderGeneticsAudiologyGenetic EpidemiologyGjb2 Mutations	2005	551
Child–Parent Familial Hypercholesterolemia Screening in Primary Care David S Wald, Jonathan P. Bestwick, Joan K. Morris, New England Journal of Medicine	2016	305
Multi‐method Psycho‐educational Intervention for Preschool Children with Disruptive Behavior: Preliminary Results at Post‐treatment Russell A. Barkley, Terri L. Shelton, Cheryl Crosswait, Journal of Child Psychology and Psychiatry	2000	293
Long-term benefits and adverse effects of intermittent versus daily glucocorticoids in boys with Duchenne muscular dystrophy Valeria Ricotti, Deborah Ridout, E. Scott, Journal of Neurology Neurosurgery & Psychiatry	2012	255
Non‐invasive prenatal diagnosis of achondroplasia and thanatophoric dysplasia: next‐generation sequencing allows for a safer, more accurate, and comprehensive approach Lyn S. Chitty, Sarah Mason, Angela N. Barrett, Prenatal Diagnosis	2015	213
Improving diagnosis and broadening the phenotypes in early-onset seizure and severe developmental delay disorders through gene panel analysis Natalie Trump, Amy McTague, Helen Brittain, Journal of Medical Genetics	2016	206
X-linked primary ciliary dyskinesia due to mutations in the cytoplasmic axonemal dynein assembly factor PIH1D3 Chiara Olcese, Mitali Patel, Amelia Shoemark, Nature Communications	2017	150
Uptake, outcomes, and costs of implementing non-invasive prenatal testing for Down’s syndrome into NHS maternity care: prospective cohort study in eight diverse maternity units Lyn S. Chitty, D. Wright, Melissa Hill, BMJ	2016	147
Mutations in Outer Dynein Arm Heavy Chain DNAH9 Cause Motile Cilia Defects and Situs Inversus Mahmoud R. Fassad, Amelia Shoemark, Marie Legendre, The American Journal of Human Genetics ChromatinGenome InstabilityChromosome DynamicsDevelopmental BiologyCytogenetics	2018	131

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