Deirdre Cilliers

4.7k total citations
11 papers, 181 citations indexed

About

Deirdre Cilliers is a scholar working on Genetics, Molecular Biology and Cell Biology. According to data from OpenAlex, Deirdre Cilliers has authored 11 papers receiving a total of 181 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 6 papers in Molecular Biology and 2 papers in Cell Biology. Recurrent topics in Deirdre Cilliers's work include Craniofacial Disorders and Treatments (3 papers), Dermatological and Skeletal Disorders (2 papers) and Genomics and Rare Diseases (2 papers). Deirdre Cilliers is often cited by papers focused on Craniofacial Disorders and Treatments (3 papers), Dermatological and Skeletal Disorders (2 papers) and Genomics and Rare Diseases (2 papers). Deirdre Cilliers collaborates with scholars based in United Kingdom, Canada and United States. Deirdre Cilliers's co-authors include Evan Reid, Mohsin Malik, Katrina Tatton‐Brown, Nazneen Rahman, Valérie Cormier‐Daire, Karen Barker, John Burn, Jenny Douglas, Didier Lacombe and Dragana Josifova and has published in prestigious journals such as Nature Genetics, Genetics in Medicine and Journal of Anatomy.

In The Last Decade

Deirdre Cilliers

11 papers receiving 179 citations

Peers

Deirdre Cilliers

GENET

PPCH

NEURO

PRM

Juliane Eckhold Germany

Siddaramappa J. Patil India

María Gabriela Obregón Argentina

Julien Tarabeux France

Marie‐Louise Bondeson Sweden

Daoqin Zhang China

B. Petrák Czechia

Mamiko Yamada Japan

Bianca Russell United States

David Tegay United States

Juliane Eckhold Germany

Deirdre Cilliers

66 ×0.5

GENET

116 ×1.3

22 ×1.0

PPCH

16 ×0.8

NEURO

8 ×0.4

PRM

Citations per year, relative to Deirdre Cilliers Deirdre Cilliers (= 1×) peers Juliane Eckhold

Countries citing papers authored by Deirdre Cilliers

Since Specialization

Citations

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

Fields of papers citing papers by Deirdre Cilliers

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Deirdre Cilliers

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

All Works

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11 of 11 papers shown

McCann, Emma, Astrid Weber, Jenny E.V. Morton, et al.. (2024). Reassessing the association: Evaluation of a polyalanine deletion variant of RUNX2 in non‐syndromic sagittal and metopic craniosynostosis. Journal of Anatomy. 245(6). 874–878. 2 indexed citations

Allen, Stephanie, Natalie Chandler, Esther Kinning, et al.. (2023). Diagnosis of inborn errors of metabolism through prenatal exome sequencing with targeted analysis for fetal structural anomalies. Prenatal Diagnosis. 44(4). 432–442. 3 indexed citations

Wellesley, Diana, et al.. (2021). Prenatal chromosome microarray: ‘The UK experience’. A survey of reporting practices in UK genetic services (2012–2019). Prenatal Diagnosis. 41(6). 661–667. 8 indexed citations

Ghali, Neeti, Duncan Baker, Angela F. Brady, et al.. (2019). Atypical COL3A1 variants (glutamic acid to lysine) cause vascular Ehlers–Danlos syndrome with a consistent phenotype of tissue fragility and skin hyperextensibility. Genetics in Medicine. 21(9). 2081–2091. 14 indexed citations

Burca, Anna de, C. Ioannou, Anthony Vandersteen, F. Michael Pope, & Deirdre Cilliers. (2018). Intrafamilial variability of clinical features in distal arthrogryposis type 2B. Clinical Dysmorphology. 28(1). 35–37. 2 indexed citations

Eley, Karen A., Gregory P.L. Thomas, Fintan Sheerin, et al.. (2016). The Significance of Squamosal Suture Synostosis. Journal of Craniofacial Surgery. 27(6). 1543–1549. 19 indexed citations

Solomons, Joyce, Paul Coucke, Sofie Symoens, et al.. (2013). Dermatosparaxis (Ehlers–Danlos Type VIIC): Prenatal Diagnosis Following a Previous Pregnancy With Unexpected Skull Fractures at Delivery. American Journal of Medical Genetics Part A. 161(5). 1122–1125. 17 indexed citations

Rosenfeld, Jill A., John A. Crolla, Susan Tomkins, et al.. (2010). Refinement of causative genes in monosomy 1p36 through clinical and molecular cytogenetic characterization of small interstitial deletions. American Journal of Medical Genetics Part A. 152A(8). 1951–1959. 37 indexed citations

Cilliers, Deirdre, Peter Clayton, S A Cairns, et al.. (2007). A new X-linked mental retardation (XLMR) syndrome with late-onset primary testicular failure, short stature and microcephaly maps to Xq25–q26. European Journal of Medical Genetics. 50(3). 216–223. 2 indexed citations

10.

Cilliers, Deirdre, Yasemin Alanay, Koray Boduroğlu, et al.. (2007). Cerebro-facio-thoracic dysplasia: expanding the phenotype. Clinical Dysmorphology. 16(2). 121–125. 7 indexed citations

11.

Douglas, Jenny, Deirdre Cilliers, Kim Coleman, et al.. (2007). Mutations in RNF135, a gene within the NF1 microdeletion region, cause phenotypic abnormalities including overgrowth. Nature Genetics. 39(8). 963–965. 70 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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