Laura Russell

2.3k total citations
36 papers, 1.3k citations indexed

About

Laura Russell is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Laura Russell has authored 36 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 12 papers in Genetics and 6 papers in Surgery. Recurrent topics in Laura Russell's work include Cold Atom Physics and Bose-Einstein Condensates (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Craniofacial Disorders and Treatments (4 papers). Laura Russell is often cited by papers focused on Cold Atom Physics and Bose-Einstein Condensates (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Craniofacial Disorders and Treatments (4 papers). Laura Russell collaborates with scholars based in United States, Canada and Ireland. Laura Russell's co-authors include Sherri J. Bale, John J. DiGiovanna, John G. Compton, Nemat Hashem, David D. Weaver, Marilyn J. Bull, Peter M. Steinert, Geraldine R. Rogers, Gabriele Richard and Ethylin Wang Jabs and has published in prestigious journals such as Nature Genetics, Blood and PEDIATRICS.

In The Last Decade

Laura Russell

36 papers receiving 1.2k citations

Peers

Laura Russell

GENET

SURGE

Mohnish Suri United Kingdom

Chi-Ming Hai United States

Sylvie Marchand France

Linda S. Musil United States

Tsuyoshi Hirashima Japan

Wadih M. Zein United States

Jennifer M. Martin United States

Johan Zwaan United States

J. François Belgium

W E Nance United States

Mohnish Suri United Kingdom

Laura Russell

1.2k ×2.2

260 ×0.6

736 ×2.7

GENET

158 ×1.1

200 ×1.4

SURGE

Citations per year, relative to Laura Russell Laura Russell (= 1×) peers Mohnish Suri

Countries citing papers authored by Laura Russell

Since Specialization

Citations

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

Fields of papers citing papers by Laura Russell

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Laura Russell

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Heathers, Laura, et al.. (2025). Optimizing wrist-worn wearable compliance with insights from two Parkinson’s disease cohort studies. npj Parkinson s Disease. 11(1). 152–152. 1 indexed citations

Stanton, Julie V., et al.. (2024). Integrated lymphoedema and tissue viability service: improving patient and wound outcomes. British Journal of Community Nursing. 29(Sup4). S19–S26. 1 indexed citations

Darwich, Rami, et al.. (2021). Isolated bilateral congenital lacrimal gland agenesis—a case series. Journal of American Association for Pediatric Ophthalmology and Strabismus. 25(2). 109–112.e1. 2 indexed citations

Gallagher, J., et al.. (2019). PCN25 IMPACT OF GEMTUZUMAB OZOGAMICIN ON THE IRISH HEALTHCARE SYSTEM. Value in Health. 22. S439–S440. 1 indexed citations

Accogli, Andrea, Laura Russell, Guillaume Sébire, et al.. (2019). Pathogenic variants in AIMP1 cause pontocerebellar hypoplasia. Neurogenetics. 20(2). 103–108. 13 indexed citations

Accogli, Andrea, et al.. (2018). Diagnostic Yield of Intellectual Disability Gene Panels. Pediatric Neurology. 92. 32–36. 22 indexed citations

Mackey, Jason, Jeffrey J. Wing, Gina Norato, et al.. (2015). High Rate of Microbleed Formation following Primary Intracerebral Hemorrhage. International Journal of Stroke. 10(8). 1187–1191. 8 indexed citations

Russell, Laura, et al.. (2014). Investigation of a⁸⁵Rb dark magneto-optical trap using an optical nanofibre. Measurement Science and Technology. 25(5). 55203–55203. 3 indexed citations

Revençu, Nicole, Laurence M. Boon, A. Dompmartin, et al.. (2013). Germline Mutations in RASA1 Are Not Found in Patients with Klippel-Trenaunay Syndrome or Capillary Malformation with Limb Overgrowth. Molecular Syndromology. 4(4). 173–178. 29 indexed citations

10.

Russell, Laura, et al.. (2011). Sub-Doppler temperature measurements of laser-cooled atoms using optical nanofibres. Measurement Science and Technology. 23(1). 15201–15201. 16 indexed citations

11.

Kaloustian, Vazken M. Der, Laura Russell, Swaroop Aradhya, et al.. (2011). A de novo 2.1‐Mb deletion of 13q12.11 in a child with developmental delay and minor dysmorphic features. American Journal of Medical Genetics Part A. 155(10). 2538–2542. 6 indexed citations

12.

Griffith, Andrew J., Yandan Yang, Shannon Pryor, et al.. (2006). Cochleosaccular Dysplasia Associated With a Connexin 26 Mutation in Keratitis–Ichthyosis–Deafness Syndrome. The Laryngoscope. 116(8). 1404–1408. 40 indexed citations

13.

Richard, Gabriele, Fatima Rouan, Colin E. Willoughby, et al.. (2002). Missense Mutations in GJB2 Encoding Connexin-26 Cause the Ectodermal Dysplasia Keratitis-Ichthyosis-Deafness Syndrome. The American Journal of Human Genetics. 70(5). 1341–1348. 264 indexed citations

14.

Russell, Laura, et al.. (2002). Auditory Manifestations of Keratitis‐Ichthyosis‐Deafness (KID) Syndrome. The Laryngoscope. 112(2). 272–280. 32 indexed citations

15.

Beiraghi, Soraya, William J. Kimberling, Laura Russell, et al.. (1999). Confirmation of linkage of Van der Woude syndrome to chromosome 1q32: evidence of association with STR alleles suggests possible unique origin of the disease mutation.. PubMed. 19(3). 128–34. 6 indexed citations

16.

Bale, Sherri J., Laura Russell, Minjoo Larry Lee, John G. Compton, & John J. DiGiovanna. (1996). Congenital Recessive Ichthyosis Unlinked to Loci for Epidermal Transglutaminases. Journal of Investigative Dermatology. 107(6). 808–811. 25 indexed citations

17.

Russell, Laura, John J. DiGiovanna, Geraldine R. Rogers, et al.. (1995). Mutations in the gene for transglutaminase 1 in autosomal recessive lamellar ichthyosis. Nature Genetics. 9(3). 279–283. 298 indexed citations

18.

Russell, Laura, John J. DiGiovanna, Nemat Hashem, John G. Compton, & Sherri J. Bale. (1994). Linkage of autosomal recessive lamellar ichthyosis to chromosome 14q.. PubMed. 55(6). 1146–52. 80 indexed citations

19.

Verdi, Gerald D., Joseph H. Hersh, & Laura Russell. (1991). Partial Duplication of the Face. Plastic & Reconstructive Surgery. 87(4). 759–762. 22 indexed citations

20.

Schiffman, Mark, Ana L. Viciana, Catherine Schairer, et al.. (1988). Fecapentaenes and their precursors throughout the bowel — Results of an autopsy study. Mutation Research Letters. 208(1). 9–15. 11 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