Cecilie F. Rustad

1.6k total citations
18 papers, 491 citations indexed

About

Cecilie F. Rustad is a scholar working on Molecular Biology, Genetics and Rheumatology. According to data from OpenAlex, Cecilie F. Rustad has authored 18 papers receiving a total of 491 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 6 papers in Genetics and 4 papers in Rheumatology. Recurrent topics in Cecilie F. Rustad's work include Genetic Syndromes and Imprinting (3 papers), Neurofibromatosis and Schwannoma Cases (3 papers) and Hedgehog Signaling Pathway Studies (2 papers). Cecilie F. Rustad is often cited by papers focused on Genetic Syndromes and Imprinting (3 papers), Neurofibromatosis and Schwannoma Cases (3 papers) and Hedgehog Signaling Pathway Studies (2 papers). Cecilie F. Rustad collaborates with scholars based in Norway, United Kingdom and United States. Cecilie F. Rustad's co-authors include Miriam J. Smith, D. Gareth Evans, Ketil Heimdal, Naomi L. Bowers, Andrew J. Wallace, Charlotte von der Lippe, Guy Leschziner, Olaug K. Rødningen, Rosalie E. Ferner and Susan Holder and has published in prestigious journals such as Neurology, BMJ Open and European Journal of Human Genetics.

In The Last Decade

Cecilie F. Rustad

17 papers receiving 485 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Cecilie F. Rustad Norway 11 210 170 116 111 84 18 491
Fatih Bayraklı Türkiye 15 115 0.5× 231 1.4× 83 0.7× 146 1.3× 75 0.9× 41 544
Audrey Briand‐Suleau France 11 168 0.8× 151 0.9× 122 1.1× 41 0.4× 46 0.5× 16 437
Philippe Petiot France 13 159 0.8× 408 2.4× 31 0.3× 78 0.7× 55 0.7× 26 681
Wolfram Henn Germany 12 190 0.9× 89 0.5× 145 1.3× 117 1.1× 80 1.0× 27 540
Ruth A. Heim United States 13 155 0.7× 111 0.7× 117 1.0× 57 0.5× 50 0.6× 21 643
Junmei Zhang China 11 446 2.1× 83 0.5× 143 1.2× 41 0.4× 34 0.4× 25 791
Peter Jun United States 15 301 1.4× 207 1.2× 81 0.7× 144 1.3× 28 0.3× 20 741
Philippe Kerschen France 7 133 0.6× 175 1.0× 49 0.4× 25 0.2× 73 0.9× 12 407
Constance K. Stein United States 10 380 1.8× 117 0.7× 346 3.0× 33 0.3× 41 0.5× 17 666
James Miller United Kingdom 13 239 1.1× 126 0.7× 36 0.3× 237 2.1× 100 1.2× 28 573

Countries citing papers authored by Cecilie F. Rustad

Since Specialization
Citations

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

Fields of papers citing papers by Cecilie F. Rustad

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Cecilie F. Rustad. 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 Cecilie F. Rustad. The network helps show where Cecilie F. Rustad may publish in the future.

Co-authorship network of co-authors of Cecilie F. Rustad

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

All Works

18 of 18 papers shown
1.
Rustad, Cecilie F., Ragnheiður Bragadóttir, Kristian Tveten, et al.. (2025). Clinical and genetic aspects of Bardet–Biedl syndrome in adults in Norway. Orphanet Journal of Rare Diseases. 20(1). 127–127. 3 indexed citations
2.
Rustad, Cecilie F., Ragnheiður Bragadóttir, Hilde Nordgarden, et al.. (2025). Healthcare needs, care use and health status outcomes in adults with Bardet-Biedl syndrome: a cross-sectional study in Norway. BMJ Open. 15(4). e095986–e095986. 1 indexed citations
3.
Rustad, Cecilie F., Paul Hoff Backe, Chunsheng Jin, et al.. (2024). A monoallelic UXS1 variant associated with short‐limbed short stature. Molecular Genetics & Genomic Medicine. 12(6). e2472–e2472.
4.
Jacob, Prince, Cecilie F. Rustad, V. Reid Sutton, et al.. (2023). Clinical, genetic and structural delineation of RPL13-related spondyloepimetaphyseal dysplasia suggest extra-ribosomal functions of eL13. npj Genomic Medicine. 8(1). 39–39. 1 indexed citations
5.
Rustad, Cecilie F., Kristian Tveten, Geir J. Braathen, et al.. (2022). A woman in her fifties with chronic muscle weakness. Tidsskrift for Den norske legeforening. 142(1). 1 indexed citations
6.
Berland, Siren, Cecilie F. Rustad, G Turowski, et al.. (2021). Double paternal uniparental isodisomy 7 and 15 presenting with Beckwith–Wiedemann spectrum features. Molecular Case Studies. 7(6). a006113–a006113. 5 indexed citations
7.
Fredwall, Svein O., Cecilie F. Rustad, Heidi B. Eggesbø, et al.. (2020). High prevalence of symptomatic spinal stenosis in Norwegian adults with achondroplasia: a population-based study. Orphanet Journal of Rare Diseases. 15(1). 123–123. 33 indexed citations
8.
Prescott, Trine, et al.. (2020). Genpaneltesting. Tidsskrift for Den norske legeforening. 140(3). 2 indexed citations
9.
Baliakas, Panagiotis, Bianca Tesi, Ulla Wartiovaara‐Kautto, et al.. (2019). Nordic Guidelines for Germline Predisposition to Myeloid Neoplasms in Adults: Recommendations for Genetic Diagnosis, Clinical Management and Follow-up. HemaSphere. 3(6). e321–e321. 53 indexed citations
10.
Dyment, David A., Pauline Terhal, Cecilie F. Rustad, et al.. (2019). De novo substitutions of TRPM3 cause intellectual disability and epilepsy. European Journal of Human Genetics. 27(10). 1611–1618. 44 indexed citations
11.
Smith, Miriam J., Christian Beetz, Simon G. Williams, et al.. (2014). Mutations in LZTR1 add to the complex heterogeneity of schwannomatosis. Neurology. 84(2). 141–147. 78 indexed citations
12.
Prescott, Trine, Cecilie F. Rustad, Kristin Eiklid, et al.. (2013). Characterization of a Norwegian cherubism cohort; molecular genetic findings, oral manifestations and quality of life. European Journal of Medical Genetics. 56(3). 131–137. 21 indexed citations
13.
Corsten‐Janssen, Nicole, Wilhelmina S. Kerstjens‐Frederikse, Gideon J. du Marchie Sarvaas, et al.. (2013). The Cardiac Phenotype in Patients With a CHD7 Mutation. Circulation Cardiovascular Genetics. 6(3). 248–254. 52 indexed citations
14.
Smith, Miriam J., Andrew J. Wallace, Naomi L. Bowers, et al.. (2012). Frequency of SMARCB1 mutations in familial and sporadic schwannomatosis. Neurogenetics. 13(2). 141–145. 75 indexed citations
15.
Bober, Michael B., Tim Niiler, Angela L. Duker, et al.. (2012). Growth in individuals with Majewski osteodysplastic primordial dwarfism type II caused by pericentrin mutations. American Journal of Medical Genetics Part A. 158A(11). 2719–2725. 33 indexed citations
16.
Smith, Miriam J., Cecilie F. Rustad, Naomi L. Bowers, et al.. (2011). Vestibular schwannomas occur in schwannomatosis and should not be considered an exclusion criterion for clinical diagnosis. American Journal of Medical Genetics Part A. 158A(1). 215–219. 41 indexed citations
17.
Lippe, Charlotte von der, Cecilie F. Rustad, Ketil Heimdal, & Olaug K. Rødningen. (2010). 15q11.2 microdeletion – Seven new patients with delayed development and/or behavioural problems. European Journal of Medical Genetics. 54(3). 357–360. 36 indexed citations
18.
Rustad, Cecilie F., Merete Bjørnslett, Ketil Heimdal, et al.. (2006). Germline PTEN mutations are rare and highly penetrant. Hereditary Cancer in Clinical Practice. 4(4). 177–177. 12 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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