Margo Whiteford

2.7k total citations
15 papers, 398 citations indexed

About

Margo Whiteford is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Margo Whiteford has authored 15 papers receiving a total of 398 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 7 papers in Molecular Biology and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Margo Whiteford's work include Connective tissue disorders research (6 papers), Renal and related cancers (2 papers) and Prenatal Screening and Diagnostics (2 papers). Margo Whiteford is often cited by papers focused on Connective tissue disorders research (6 papers), Renal and related cancers (2 papers) and Prenatal Screening and Diagnostics (2 papers). Margo Whiteford collaborates with scholars based in United Kingdom, United States and Switzerland. Margo Whiteford's co-authors include David Fitzpatrick, Wim Wuyts, Martin Zenker, Deborah Ruddy, Wayne Lam, Richard C. Trembath, Diana Johnson, Katie Snape, Jill Clayton‐Smith and N. C. Nevin and has published in prestigious journals such as PLoS ONE, The American Journal of Human Genetics and Journal of Bone and Mineral Research.

In The Last Decade

Margo Whiteford

15 papers receiving 386 citations

Peers

Margo Whiteford
Harinder Gill Canada
Henrik Jörnvall Sweden
Anne De Paepe Belgium
Baiba Lāce Latvia
Mariana F.A. Funari Brazil
Eusebiu Vlad Gorduza Romania
Maria Addis Italy
A. J. van Essen Netherlands
Gabrielle C. Geddes United States
Hayden-William Courtland United States
Harinder Gill Canada
Margo Whiteford
Citations per year, relative to Margo Whiteford Margo Whiteford (= 1×) peers Harinder Gill

Countries citing papers authored by Margo Whiteford

Since Specialization
Citations

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

Fields of papers citing papers by Margo Whiteford

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Margo Whiteford

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

All Works

15 of 15 papers shown
1.
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
2.
Syx, Delfien, Brecht Guillemyn, Sofie Symoens, et al.. (2015). Defective Proteolytic Processing of Fibrillar Procollagens and Prodecorin Due to Biallelic BMP1 Mutations Results in a Severe, Progressive Form of Osteogenesis Imperfecta. Journal of Bone and Mineral Research. 30(8). 1445–1456. 38 indexed citations
3.
McGowan, Ruth, P.M. McHenry, Alexander Cooke, et al.. (2011). Clinical features and respiratory complications in Myhre syndrome. European Journal of Medical Genetics. 54(6). e553–e559. 24 indexed citations
4.
Hershkovitz, Dov, et al.. (2011). Novel mutations in GALNT3 causing hyperphosphatemic familial tumoral calcinosis. Journal of Bone and Mineral Metabolism. 29(5). 621–625. 25 indexed citations
5.
Harewood, Louise, Jean W. Keeling, Alan G. Howatson, et al.. (2010). Bilateral Renal Agenesis/Hypoplasia/Dysplasia (BRAHD): Postmortem Analysis of 45 Cases with Breakpoint Mapping of Two De Novo Translocations. PLoS ONE. 5(8). e12375–e12375. 22 indexed citations
6.
McGowan, Ruth, et al.. (2010). Novel features in auriculo-condylar syndrome. Clinical Dysmorphology. 20(1). 1–10. 6 indexed citations
7.
Snape, Katie, Deborah Ruddy, Martin Zenker, et al.. (2009). The spectra of clinical phenotypes in aplasia cutis congenita and terminal transverse limb defects. American Journal of Medical Genetics Part A. 149A(8). 1860–1881. 70 indexed citations
8.
Fantes, Judith A., Jacqueline Ramsay, Dian Donnai, et al.. (2008). FISH Mapping of De Novo Apparently Balanced Chromosome Rearrangements Identifies Characteristics Associated with Phenotypic Abnormality. The American Journal of Human Genetics. 82(4). 916–926. 31 indexed citations
9.
Slavotinek, Anne, Amalia Dutra, Evgenia Pak, et al.. (2004). A female with complete lack of Müllerian fusion, postaxial polydactyly, and tetralogy of fallot: Genetic heterogeneity of McKusick–Kaufman syndrome or a unique syndrome?. American Journal of Medical Genetics Part A. 129A(1). 69–72. 10 indexed citations
10.
Little, Julian, M. Ian Gilmour, Peter Mossey, et al.. (2004). Smoking and Orofacial Clefts: A United Kingdom–Based Case-Control Study. The Cleft Palate-Craniofacial Journal. 41(4). 381–386. 83 indexed citations
11.
Longman, Cheryl, Margo Whiteford, David Koppel, et al.. (2003). Craniosynostosis associated with intracranial calcification: a novel recessive syndrome. Clinical Dysmorphology. 12(4). 215–220. 2 indexed citations
12.
Kidd, A., et al.. (2001). Breast cancer in two sisters with Friedreich's ataxia. European Journal of Surgical Oncology. 27(5). 512–514. 13 indexed citations
13.
McEntagart, Meriel, Lars Allan Larsen, Margo Whiteford, et al.. (2001). Mutational spectrum in the cardioauditory syndrome of Jervell and Lange-Nielsen. Human Genetics. 108(1). 75–75. 3 indexed citations
14.
Tranebjærg, Lisbeth, Meriel McEntagart, Lars Allan Larsen, et al.. (2000). Mutational spectrum in the cardioauditory syndrome of Jervell and Lange-Nielsen. Human Genetics. 107(5). 499–503. 54 indexed citations
15.
Stewart, Gregory D., et al.. (1997). Expect the worse or hope for the best? Prenatal diagnosis of geleophysic dysplasia. Prenatal Diagnosis. 17(11). 1067–1070. 3 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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