Sarah E. Sheppard

1.1k total citations
35 papers, 289 citations indexed

About

Sarah E. Sheppard is a scholar working on Surgery, Molecular Biology and Genetics. According to data from OpenAlex, Sarah E. Sheppard has authored 35 papers receiving a total of 289 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Surgery, 14 papers in Molecular Biology and 11 papers in Genetics. Recurrent topics in Sarah E. Sheppard's work include Vascular Malformations and Hemangiomas (11 papers), Lymphatic System and Diseases (3 papers) and Hedgehog Signaling Pathway Studies (3 papers). Sarah E. Sheppard is often cited by papers focused on Vascular Malformations and Hemangiomas (11 papers), Lymphatic System and Diseases (3 papers) and Hedgehog Signaling Pathway Studies (3 papers). Sarah E. Sheppard collaborates with scholars based in United States, United Kingdom and Netherlands. Sarah E. Sheppard's co-authors include Dong Li, Yoav Dori, Håkon Håkonarson, Denise M. Adams, Jessica Foster, Michael March, Nathan D. Lawson, Lihua Julie Zhu, Elaine H. Zackai and Neil Kumar and has published in prestigious journals such as Journal of Clinical Investigation, Bioinformatics and Scientific Reports.

In The Last Decade

Sarah E. Sheppard

32 papers receiving 280 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sarah E. Sheppard United States 10 120 95 73 64 34 35 289
Antonio González‐Meneses Spain 11 60 0.5× 225 2.4× 25 0.3× 106 1.7× 19 0.6× 34 393
Güven Toksoy Türkiye 12 56 0.5× 185 1.9× 39 0.5× 116 1.8× 14 0.4× 51 353
Magdalena Badura‐Stronka Poland 12 77 0.6× 183 1.9× 20 0.3× 141 2.2× 13 0.4× 32 357
Jonathan I. Lake United States 8 272 2.3× 111 1.2× 14 0.2× 48 0.8× 25 0.7× 10 457
Sylva Bartel-Friedrich Germany 7 90 0.8× 62 0.7× 32 0.4× 63 1.0× 9 0.3× 14 233
James Yan United States 8 32 0.3× 105 1.1× 25 0.3× 112 1.8× 16 0.5× 11 301
Irati Romero‐Garmendia Spain 9 49 0.4× 212 2.2× 46 0.6× 29 0.5× 21 0.6× 19 367
Amrita Ray United States 8 83 0.7× 112 1.2× 23 0.3× 20 0.3× 19 0.6× 20 311
Swei-Ming Lin Taiwan 11 187 1.6× 33 0.3× 34 0.5× 24 0.4× 108 3.2× 26 333
Angeline Lai Singapore 10 67 0.6× 152 1.6× 19 0.3× 133 2.1× 19 0.6× 31 349

Countries citing papers authored by Sarah E. Sheppard

Since Specialization
Citations

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

Fields of papers citing papers by Sarah E. Sheppard

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sarah E. Sheppard. 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 Sarah E. Sheppard. The network helps show where Sarah E. Sheppard may publish in the future.

Co-authorship network of co-authors of Sarah E. Sheppard

This figure shows the co-authorship network connecting the top 25 collaborators of Sarah E. Sheppard. A scholar is included among the top collaborators of Sarah E. Sheppard 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 Sarah E. Sheppard. Sarah E. Sheppard 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
1.
Epstein, Joshua, et al.. (2025). A Retrospective Review of Oral N‐Acetylcysteine for Habit‐Driven Cutaneous Disorders. Pediatric Dermatology. 42(3). 560–563.
2.
Sheppard, Sarah E., et al.. (2025). Unusual Presentation of Coronary Artery Fistula in Capillary Malformation Arteriovenous Malformation 2 Syndrome: A Case Report. American Journal of Medical Genetics Part A. 197(7). e64041–e64041.
3.
Ahimaz, Priyanka, Nga Nguyen, Rachel Lewis, et al.. (2024). Phenotype driven molecular genetic test recommendation for diagnosing pediatric rare disorders. npj Digital Medicine. 7(1). 333–333. 2 indexed citations
4.
Heymann, Warren R., et al.. (2023). Segmental vasoconstricted patches with a border of telangiectasia. Pediatric Dermatology. 40(3). 565–567.
5.
Surrey, Lea F., Abhay Srinivasan, Dong Li, et al.. (2023). Microcystic lymphatic malformations in Turner syndrome are due to somatic mosaicism of PIK3CA. American Journal of Medical Genetics Part A. 194(1). 64–69. 1 indexed citations
6.
Treat, James R., et al.. (2023). Mosaic pathogenic variants in AKT3 cause capillary malformation and undergrowth. American Journal of Medical Genetics Part A. 191(5). 1442–1446. 3 indexed citations
7.
Schindewolf, Erica, et al.. (2023). The importance of patient‐specific resources for families dealing with prenatal rare diseases. American Journal of Medical Genetics Part A. 194(3). e63450–e63450. 1 indexed citations
8.
Smith, Christopher L., David M. Biko, Dong Li, et al.. (2022). Genetics etiologies and genotype phenotype correlations in a cohort of individuals with central conducting lymphatic anomaly. European Journal of Human Genetics. 30(9). 1022–1028. 19 indexed citations
9.
Grand, Katheryn, et al.. (2021). Genetic skin disorders: The value of a multidisciplinary clinic. American Journal of Medical Genetics Part A. 185(4). 1159–1167. 6 indexed citations
10.
Wild, K. Taylor, Tomoki Nomakuchi, Sarah E. Sheppard, et al.. (2021). Hyperinsulinism in an individual with an EP300 variant of Rubinstein‐Taybi syndrome. American Journal of Medical Genetics Part A. 185(4). 1251–1255. 1 indexed citations
11.
Gold, Nina B., Ian M. Campbell, Sarah E. Sheppard, & Wen‐Hann Tan. (2021). Proposed criteria for nevoid basal cell carcinoma syndrome in children assessed using statistical optimization. Scientific Reports. 11(1). 19791–19791. 5 indexed citations
12.
Sheppard, Sarah E., Abhay Srinivasan, Laura S. Finn, et al.. (2021). Cerebrofacial vascular metameric syndrome is caused by somatic pathogenic variants in PIK3CA. Molecular Case Studies. 7(6). a006147–a006147. 4 indexed citations
13.
Sheppard, Sarah E., Anna Smith, Katheryn Grand, et al.. (2020). Further delineation of the phenotypic spectrum of nevus comedonicus syndrome to include congenital pulmonary airway malformation of the lung and aneurysm. American Journal of Medical Genetics Part A. 182(4). 746–754. 6 indexed citations
14.
Muir, Alison M., Jennifer L. Cohen, Sarah E. Sheppard, et al.. (2020). Bi-allelic Loss-of-Function Variants in NUP188 Cause a Recognizable Syndrome Characterized by Neurologic, Ocular, and Cardiac Abnormalities. The American Journal of Human Genetics. 106(5). 623–631. 19 indexed citations
15.
Foster, Jessica, Dong Li, Michael March, et al.. (2020). Kaposiform lymphangiomatosis effectively treated with MEK inhibition. EMBO Molecular Medicine. 12(10). e12324–e12324. 58 indexed citations
16.
Sheppard, Sarah E., et al.. (2019). Generalized, severe epidermolysis bullosa simplex caused by a Keratin 5 p.E477K mutation. Pediatric Dermatology. 36(6). 1007–1009. 1 indexed citations
17.
Sheppard, Sarah E., Emilie Lalonde, N. Scott Adzick, et al.. (2019). Androgenetic chimerism as an etiology for Beckwith–Wiedemann syndrome: diagnosis and management. Genetics in Medicine. 21(11). 2644–2649. 12 indexed citations
18.
Walzman, M, et al.. (2009). The psychological impact caused by genital warts: has the Department of Health's choice of vaccination missed the opportunity to prevent such morbidity?. International Journal of STD & AIDS. 20(10). 696–700. 10 indexed citations
19.
Kumar, Neil, et al.. (2007). Quantitative analysis of Akt phosphorylation and activity in response to EGF and insulin treatment. Biochemical and Biophysical Research Communications. 354(1). 14–20. 22 indexed citations
20.
Smithells, R. W. & Sarah E. Sheppard. (1978). Fetal malformation after Debendox treatment in early pregnancy. BMJ. 1(6119). 1055.3–1056. 8 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Antonio González‐Meneses Breakdown of academic impact, for papers by Güven Toksoy Breakdown of academic impact, for papers by Magdalena Badura‐Stronka Breakdown of academic impact, for papers by Jonathan I. Lake Breakdown of academic impact, for papers by Sylva Bartel-Friedrich Breakdown of academic impact, for papers by James Yan Breakdown of academic impact, for papers by Irati Romero‐Garmendia Breakdown of academic impact, for papers by Amrita Ray Breakdown of academic impact, for papers by Swei-Ming Lin Breakdown of academic impact, for papers by Angeline Lai
Rankless by CCL
2026