Gillian A. Wallis

5.1k total citations
62 papers, 2.7k citations indexed

About

Gillian A. Wallis is a scholar working on Rheumatology, Genetics and Molecular Biology. According to data from OpenAlex, Gillian A. Wallis has authored 62 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Rheumatology, 30 papers in Genetics and 27 papers in Molecular Biology. Recurrent topics in Gillian A. Wallis's work include Connective tissue disorders research (24 papers), Osteoarthritis Treatment and Mechanisms (16 papers) and Bone and Dental Protein Studies (12 papers). Gillian A. Wallis is often cited by papers focused on Connective tissue disorders research (24 papers), Osteoarthritis Treatment and Mechanisms (16 papers) and Bone and Dental Protein Studies (12 papers). Gillian A. Wallis collaborates with scholars based in United Kingdom, United States and South Africa. Gillian A. Wallis's co-authors include Peter H. Byers, Ray Boot-Handford, Marcia Willing, Peter Beighton, Christopher G. Mathew, Michael E. Grant, Claudia Lindner, T.F. Cootes, J. Mark Wilkinson and Shankar Thiagarajah and has published in prestigious journals such as Journal of Biological Chemistry, The Journal of Cell Biology and The EMBO Journal.

In The Last Decade

Gillian A. Wallis

62 papers receiving 2.6k citations

Peers

Gillian A. Wallis
Michael D. Briggs United Kingdom
Jaspal S. Khillan United States
Rosa Serra United States
Marion C. Dickson United Kingdom
Gillian A. Wallis
Citations per year, relative to Gillian A. Wallis Gillian A. Wallis (= 1×) peers Antonio Rossi

Countries citing papers authored by Gillian A. Wallis

Since Specialization
Citations

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

Fields of papers citing papers by Gillian A. Wallis

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Gillian A. Wallis. 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 Gillian A. Wallis. The network helps show where Gillian A. Wallis may publish in the future.

Co-authorship network of co-authors of Gillian A. Wallis

This figure shows the co-authorship network connecting the top 25 collaborators of Gillian A. Wallis. A scholar is included among the top collaborators of Gillian A. Wallis 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 Gillian A. Wallis. Gillian A. Wallis 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.
Howard, Mark, Rocky S. Tuan, & Gillian A. Wallis. (2015). The function and interrelationship between GDF5 and ERG-010 during chondrogenesis in vitro. In Vitro Cellular & Developmental Biology - Animal. 52(2). 182–192. 3 indexed citations
2.
Lindner, Claudia, Shankar Thiagarajah, J. Mark Wilkinson, et al.. (2015). Investigation of Association Between Hip Osteoarthritis Susceptibility Loci and Radiographic Proximal Femur Shape. Arthritis & Rheumatology. 67(8). 2076–2084. 25 indexed citations
3.
Lindner, Claudia, Shankar Thiagarajah, J. Mark Wilkinson, Gillian A. Wallis, & T.F. Cootes. (2013). Development of a fully automatic shape model matching (FASMM) system to derive statistical shape models from radiographs: application to the accurate capture and global representation of proximal femur shape. Osteoarthritis and Cartilage. 21(10). 1537–1544. 29 indexed citations
4.
Lindner, Claudia, et al.. (2012). Accurate Fully Automatic Femur Segmentation in Pelvic Radiographs Using Regression Voting. Lecture notes in computer science. 15(Pt 3). 353–360. 23 indexed citations
5.
Scott, John L., Rose K. Davidson, T.E. Swingler, et al.. (2010). Superoxide dismutase downregulation in osteoarthritis progression and end-stage disease. Annals of the Rheumatic Diseases. 69(8). 1502–1510. 210 indexed citations
6.
Hyde, Gareth, et al.. (2007). Lineage tracing using matrilin-1 gene expression reveals that articular chondrocytes exist as the joint interzone forms. Developmental Biology. 304(2). 825–833. 82 indexed citations
7.
Greig, Carolyn, Richard Aspinwall, Mark Grant, et al.. (2006). Linkage to nodal osteoarthritis: quantitative and qualitative analyses of data from a whole-genome screen identify trait-dependent susceptibility loci. Annals of the Rheumatic Diseases. 65(9). 1131–1138. 14 indexed citations
8.
Ramesar, Raj, et al.. (2005). A Mutation in the Variable Repeat Region of the Aggrecan Gene (AGC1) Causes a Form of Spondyloepiphyseal Dysplasia Associated with Severe, Premature Osteoarthritis. The American Journal of Human Genetics. 77(3). 484–490. 115 indexed citations
9.
Wallis, Gillian A., et al.. (2001). Endochondral ossification: A delicate balance between growth and mineralisation. Current Biology. 11(15). R589–R591. 29 indexed citations
10.
Marks, Debora S., Carl A. Gregory, Gillian A. Wallis, et al.. (1999). Metaphyseal Chondrodysplasia Type Schmid Mutations Are Predicted to Occur in Two Distinct Three-dimensional Clusters within Type X Collagen NC1 Domains That Retain the Ability to Trimerize. Journal of Biological Chemistry. 274(6). 3632–3641. 31 indexed citations
11.
Wallis, Gillian A.. (1996). Bone growth: Coordinating chondrocyte differentiation. Current Biology. 6(12). 1577–1580. 57 indexed citations
12.
Hillarby, M Chantal, et al.. (1996). Localization of Gene Expression during Endochondral Ossification. Annals of the New York Academy of Sciences. 785(1). 263–266. 8 indexed citations
13.
Culbert, Ainsley A., Gillian A. Wallis, & Karl E. Kadler. (1996). Tracing the pathway between mutation and phenotype in osteogenesis imperfecta: Isolation of mineralization-specific genes. American Journal of Medical Genetics. 63(1). 167–174. 12 indexed citations
14.
Rash, Brian G., Bryan Sykes, Taylor Thomas, et al.. (1994). Seven polymorphisms at the COL10A1 locus. Human Molecular Genetics. 3(6). 1032–1032. 2 indexed citations
15.
Byers, Peter H., Gillian A. Wallis, & Marcia Willing. (1991). Osteogenesis imperfecta: translation of mutation to phenotype.. Journal of Medical Genetics. 28(7). 433–442. 238 indexed citations
16.
Pruchno, Charles J., Daniel H. Cohn, Gillian A. Wallis, et al.. (1991). Osteogenesis imperfecta due to recurrent point mutations at CpG dinucleotides in the COL1A1 gene of type I collagen. Human Genetics. 87(1). 33–40. 29 indexed citations
17.
Goldblatt, Jack, et al.. (1989). Emery‐Dreifuss syndrome and X‐linked muscular dystrophy with contractures: evidence for homogeneity. Clinical Genetics. 35(1). 1–4. 14 indexed citations
18.
Beighton, Peter, et al.. (1988). Osteogenesis Imperfecta in Southern Africa Diagnostic Categorisation and Biomolecular Findingsa. Annals of the New York Academy of Sciences. 543(1). 40–46. 4 indexed citations
19.
Goldblatt, Jack, et al.. (1987). Duchenne muscular dystrophy in South Africa. Prevention by molecular techniques.. PubMed. 72(12). 835–7. 2 indexed citations
20.
Wallis, Gillian A., Peter Beighton, C. D. Boyd, & Christopher G. Mathew. (1986). Mutations linked to the pro alpha 2(I) collagen gene are responsible for several cases of osteogenesis imperfecta type I.. Journal of Medical Genetics. 23(5). 411–416. 20 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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