Elizabeth Young

959 total citations
15 papers, 486 citations indexed

About

Elizabeth Young is a scholar working on Pediatrics, Perinatology and Child Health, Molecular Biology and Genetics. According to data from OpenAlex, Elizabeth Young has authored 15 papers receiving a total of 486 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Pediatrics, Perinatology and Child Health, 5 papers in Molecular Biology and 5 papers in Genetics. Recurrent topics in Elizabeth Young's work include Prenatal Screening and Diagnostics (5 papers), Fetal and Pediatric Neurological Disorders (4 papers) and Neurogenetic and Muscular Disorders Research (3 papers). Elizabeth Young is often cited by papers focused on Prenatal Screening and Diagnostics (5 papers), Fetal and Pediatric Neurological Disorders (4 papers) and Neurogenetic and Muscular Disorders Research (3 papers). Elizabeth Young collaborates with scholars based in United Kingdom, United States and Türkiye. Elizabeth Young's co-authors include John H. Paul, Lauren D. McDaniel, Jennifer Delaney, Kim B. Ritchie, Stephanie Allen, Sian Ellard, Peter D. Turnpenny, John B. Emans, Simón Carlo and Karen Staehling-Hampton and has published in prestigious journals such as Science, PLoS ONE and Biochemical and Biophysical Research Communications.

In The Last Decade

Elizabeth Young

15 papers receiving 471 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Elizabeth Young United Kingdom	9	264	202	149	56	52	15	486
Céline Lucchetti-Miganeh France	8	471 1.8×	81 0.4×	129 0.9×	15 0.3×	12 0.2×	11	593
Georg Hemmrich‐Stanisak Germany	12	297 1.1×	31 0.2×	105 0.7×	15 0.3×	21 0.4×	18	542
Irina Korschineck Austria	13	264 1.0×	39 0.2×	110 0.7×	11 0.2×	31 0.6×	19	484
Timothy J. C. Bruxner Australia	11	449 1.7×	52 0.3×	207 1.4×	30 0.5×	11 0.2×	11	637
Valeria Merico Italy	20	568 2.2×	41 0.2×	210 1.4×	75 1.3×	55 1.1×	47	1.0k
Biaobang Chen China	19	762 2.9×	59 0.3×	360 2.4×	397 7.1×	27 0.5×	47	1.4k
Laurentijn Tilleman Belgium	14	291 1.1×	32 0.2×	53 0.4×	30 0.5×	23 0.4×	32	541
Aaron Buechlein United States	13	329 1.2×	83 0.4×	62 0.4×	3 0.1×	11 0.2×	31	564
Queenie Wing-Lei Wong Hong Kong	13	223 0.8×	26 0.1×	99 0.7×	4 0.1×	26 0.5×	21	500
Adam Harvey United States	10	250 0.9×	35 0.2×	78 0.5×	9 0.2×	25 0.5×	23	528

Countries citing papers authored by Elizabeth Young

Since Specialization

Citations

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

Fields of papers citing papers by Elizabeth Young

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elizabeth Young

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

All Works

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15 of 15 papers shown

Hanson, Britt, Joseph Shaw, Elizabeth Young, et al.. (2024). Expanding Access to Noninvasive Prenatal Diagnosis for Monogenic Conditions to Consanguineous Families. Clinical Chemistry. 70(5). 727–736. 1 indexed citations

Young, Elizabeth, Amy Gerrish, Michael Parks, et al.. (2020). Clinical Service Delivery of Noninvasive Prenatal Diagnosis by Relative Haplotype Dosage for Single-Gene Disorders. Journal of Molecular Diagnostics. 22(9). 1151–1161. 18 indexed citations

Gerrish, Amy, Elizabeth Young, Simon Ramsden, et al.. (2020). Non-Invasive Prenatal Diagnosis of Retinoblastoma Inheritance by Combined Targeted Sequencing Strategies. Journal of Clinical Medicine. 9(11). 3517–3517. 11 indexed citations

Togneri, Fiona S., Mark D. Kilby, Elizabeth Young, et al.. (2019). Implementation of cell-free DNA-based non-invasive prenatal testing in a National Health Service Regional Genetics Laboratory. Genetics Research. 101. e11–e11. 6 indexed citations

Allen, Stephanie, et al.. (2017). Noninvasive prenatal diagnosis for single gene disorders. Current Opinion in Obstetrics & Gynecology. 29(2). 73–79. 23 indexed citations

Young, Elizabeth, et al.. (2016). Time From Uterine Incision-to-Delivery in Cesarean Deliveries and Associated Neonatal Outcomes [22I]. Obstetrics and Gynecology. 127(Supplement 1). 79S–79S. 1 indexed citations

Young, Elizabeth, et al.. (2015). The utility of clinical findings to predict laboratory values in hypertensive disorders of pregnancy. Journal of Perinatal Medicine. 44(3). 277–81. 1 indexed citations

McDaniel, Lauren D., et al.. (2012). Environmental Factors Influencing Gene Transfer Agent (GTA) Mediated Transduction in the Subtropical Ocean. PLoS ONE. 7(8). e43506–e43506. 23 indexed citations

Şıklar, Zeynep, Sian Ellard, Emel Okulu, et al.. (2011). Transient neonatal diabetes with two novel mutations in the KCNJ11 gene and response to sulfonylurea treatment in a preterm infant. Journal of Pediatric Endocrinology and Metabolism. 24(11-12). 1077–80. 16 indexed citations

10.

Gucev, Zoran, Velibor Tasić, Nada Pop‐Jordanova, et al.. (2010). Autosomal dominant spondylocostal dysostosis in three generations of a Macedonian family: Negative mutation analysis of DLL3, MESP2, HES7, and LFNG. American Journal of Medical Genetics Part A. 152A(6). 1378–1382. 18 indexed citations

11.

McDaniel, Lauren D., et al.. (2010). High Frequency of Horizontal Gene Transfer in the Oceans. Science. 330(6000). 50–50. 264 indexed citations

12.

Cornier, Alberto S., Karen Staehling-Hampton, Kym Delventhal, et al.. (2008). Mutations in the MESP2 Gene Cause Spondylothoracic Dysostosis/Jarcho-Levin Syndrome. The American Journal of Human Genetics. 82(6). 1334–1341. 55 indexed citations

13.

Lorson, Monique A., Alexa Dickson, Adrian G. Todd, et al.. (2008). Identification and characterisation of a nuclear localisation signal in the SMN associated protein, Gemin4. Biochemical and Biophysical Research Communications. 375(1). 33–37. 7 indexed citations

14.

Young, Philip J., et al.. (2008). Valproate and spinal muscular atrophy (Review). Molecular Medicine Reports. 1(2). 161–5. 4 indexed citations

15.

Andrews, Caroline, Douglas R. Fredrick, Linlea Armstrong, et al.. (2007). Three novel mutations in KIF21A highlight the importance of the third coiled-coil stalk domain in the etiology of CFEOM1. BMC Genetics. 8(1). 26–26. 38 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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