Lucy Jenkins

7.9k total citations
43 papers, 2.1k citations indexed

About

Lucy Jenkins is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Lucy Jenkins has authored 43 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 16 papers in Pediatrics, Perinatology and Child Health and 12 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Lucy Jenkins's work include Prenatal Screening and Diagnostics (13 papers), Child and Adolescent Psychosocial and Emotional Development (6 papers) and Cystic Fibrosis Research Advances (6 papers). Lucy Jenkins is often cited by papers focused on Prenatal Screening and Diagnostics (13 papers), Child and Adolescent Psychosocial and Emotional Development (6 papers) and Cystic Fibrosis Research Advances (6 papers). Lucy Jenkins collaborates with scholars based in United Kingdom, United States and India. Lucy Jenkins's co-authors include Lyn S. Chitty, Terri L. Shelton, Russell A. Barkley, Kenneth E. Fletcher, Lori Metevia, Susan Barrett, Fiona McKay, Melissa Hill, Sarah Mason and Nicholas Lench and has published in prestigious journals such as New England Journal of Medicine, PLoS ONE and Annals of the New York Academy of Sciences.

In The Last Decade

Lucy Jenkins

41 papers receiving 2.0k citations

Peers

Lucy Jenkins
Michael J. Noetzel United States
Simona Orcesi Italy
Brian Hon‐Yin Chung Hong Kong
Emily G. Allen United States
Arthur R. Van Gool Netherlands
John B. Moeschler United States
Décio Brunoni Brazil
Howard M. Saal United States
Avinoam Shuper Israel
Bradley S. Miller United States
Michael J. Noetzel United States
Lucy Jenkins
Citations per year, relative to Lucy Jenkins Lucy Jenkins (= 1×) peers Michael J. Noetzel

Countries citing papers authored by Lucy Jenkins

Since Specialization
Citations

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

Fields of papers citing papers by Lucy Jenkins

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lucy Jenkins

This figure shows the co-authorship network connecting the top 25 collaborators of Lucy Jenkins. A scholar is included among the top collaborators of Lucy Jenkins 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 Lucy Jenkins. Lucy Jenkins 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
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Fassad, Mahmoud R., Heba Morsy, Mitali Patel, et al.. (2019). Clinical and genetic spectrum in 33 Egyptian families with suspected primary ciliary dyskinesia. Clinical Genetics. 97(3). 509–515. 15 indexed citations
4.
Mestek, Lamia, Emma Clement, Wendy D. Jones, et al.. (2018). Rapid Paediatric Sequencing (RaPS): comprehensive real-life workflow for rapid diagnosis of critically ill children. Journal of Medical Genetics. 55(11). 721–728. 89 indexed citations
5.
Ashton, Emma, Anne Debost‐Legrand, Valérie Benoît, et al.. (2018). Simultaneous sequencing of 37 genes identified causative mutations in the majority of children with renal tubulopathies. Kidney International. 93(4). 961–967. 67 indexed citations
6.
Fassad, Mahmoud R., Amelia Shoemark, Pierrick Le Borgne, et al.. (2018). C11orf70 Mutations Disrupting the Intraflagellar Transport-Dependent Assembly of Multiple Axonemal Dyneins Cause Primary Ciliary Dyskinesia. The American Journal of Human Genetics. 102(5). 956–972. 48 indexed citations
7.
Walsh, Patrick R., Yincent Tse, Emma Ashton, et al.. (2017). Clinical and diagnostic features of Bartter and Gitelman syndromes. Clinical Kidney Journal. 11(3). 302–309. 42 indexed citations
8.
Jenkins, Lucy, Zandra C. Deans, Celine Lewis, & Stephanie Allen. (2017). Delivering an accredited non‐invasive prenatal diagnosis service for monogenic disorders and recommendations for best practice. Prenatal Diagnosis. 38(1). 44–51. 59 indexed citations
9.
Chitty, Lyn S., D. Wright, Melissa Hill, et al.. (2016). Uptake, Outcomes, and Costs of Implementing Non-invasive Prenatal Testing for Down Syndrome Into NHS Maternity Care: Prospective Cohort Study in Eight Diverse Maternity Units. Obstetrical & Gynecological Survey. 71(11). 637–639. 5 indexed citations
10.
Engelhardt, Karin R., Yaobo Xu, Angela Grainger, et al.. (2016). Identification of Heterozygous Single- and Multi-exon Deletions in IL7R by Whole Exome Sequencing. Journal of Clinical Immunology. 37(1). 42–50. 14 indexed citations
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Trump, Natalie, Amy McTague, Helen Brittain, et al.. (2016). Improving diagnosis and broadening the phenotypes in early-onset seizure and severe developmental delay disorders through gene panel analysis. Journal of Medical Genetics. 53(5). 310–317. 147 indexed citations
13.
Chitty, Lyn S., Sarah Mason, Angela N. Barrett, et al.. (2015). Non‐invasive prenatal diagnosis of achondroplasia and thanatophoric dysplasia: next‐generation sequencing allows for a safer, more accurate, and comprehensive approach. Prenatal Diagnosis. 35(7). 656–662. 112 indexed citations
14.
Hill, Melissa, Philip Twiss, Talitha I. Verhoef, et al.. (2015). Non‐invasive prenatal diagnosis for cystic fibrosis: detection of paternal mutations, exploration of patient preferences and cost analysis. Prenatal Diagnosis. 35(10). 950–958. 61 indexed citations
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Scott, Richard H., Cathy Meaney, Lucy Jenkins, Alistair Calder, & Jane A. Hurst. (2013). The postnatal features of bent bone dysplasia-FGFR2 type. Clinical Dysmorphology. 23(1). 8–11. 5 indexed citations
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Ashton, Emma, et al.. (2013). Genetic testing in children with surfactant dysfunction. Archives of Disease in Childhood. 98(7). 490–495. 42 indexed citations
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Hill, Melissa, Celine Lewis, Lucy Jenkins, et al.. (2012). Implementing noninvasive prenatal fetal sex determination using cell-free fetal DNA in the United Kingdom. Expert Opinion on Biological Therapy. 12(sup1). S119–S126. 30 indexed citations
18.
Bitner‐Glindzicz, Maria, Tony Sirimanna, David C. Webb, et al.. (2010). Aminoglycoside-induced deafness during treatment of acute leukaemia. Archives of Disease in Childhood. 95(2). 153–155. 4 indexed citations
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Common, John, Maria Bitner‐Glindzicz, Edel A. O’Toole, et al.. (2005). Specific loss of connexin 26 expression in ductal sweat gland epithelium associated with the deletion mutation del(GJB6-D13S1830). Clinical and Experimental Dermatology. 30(6). 688–693. 27 indexed citations
20.
Barkley, Russell A., Terri L. Shelton, Kenneth E. Fletcher, et al.. (2002). Preschool children with disruptive behavior: Three-year outcome as a function of adaptivedisability. Development and Psychopathology. 14(1). 45–67. 42 indexed citations

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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