Fiona MacDonald

7.3k total citations
129 papers, 3.7k citations indexed

About

Fiona MacDonald is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Fiona MacDonald has authored 129 papers receiving a total of 3.7k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Molecular Biology, 25 papers in Genetics and 21 papers in Oncology. Recurrent topics in Fiona MacDonald's work include Genetic factors in colorectal cancer (15 papers), Prenatal Screening and Diagnostics (12 papers) and Substance Abuse Treatment and Outcomes (12 papers). Fiona MacDonald is often cited by papers focused on Genetic factors in colorectal cancer (15 papers), Prenatal Screening and Diagnostics (12 papers) and Substance Abuse Treatment and Outcomes (12 papers). Fiona MacDonald collaborates with scholars based in United Kingdom, Australia and United States. Fiona MacDonald's co-authors include Frank C. Odds, Eamonn R. Maher, Dion Morton, Neil McKeganey, Yvonne Wallis, Emma R. Woodward, C. McKeown, Alastair D. Sutherland, James McIntosh and Wendy N. Cooper and has published in prestigious journals such as Nature, The Lancet and JAMA.

In The Last Decade

Fiona MacDonald

124 papers receiving 3.5k citations

Peers

Countries citing papers authored by Fiona MacDonald

Since Specialization

Citations

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

Fields of papers citing papers by Fiona MacDonald

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Fiona MacDonald

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Agents of change in bushfire recovery: Young people's acts of citizenship in a youth-focused, animal-welfare and environmental program 2023 ·International Journal of Disaster Risk Reduction ·Fiona MacDonald, (unknown), (unknown), (unknown), (unknown), (unknown)	4
2	Non-invasive prenatal diagnosis of spinal muscular atrophy by relative haplotype dosage 2017 ·European Journal of Human Genetics ·Michael Parks, (unknown), (unknown), Siobhán Cleary, Samuel Clokie, (unknown), Denise Williams, Trevor Cole, Fiona MacDonald, Mike Griffiths, Stephanie Allen	74
3	Genotype-phenotype correlation in 153 adult patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency - analysis of the United Kingdom Congenital adrenal Hyperplasia Adult Study Executive (CaHASE) cohort 2012 ·UCL Discovery (University College London) ·Nils Krone, I.C. Rose, Debbie Willis, Sarah H. Wild, James Hodson, (unknown), Stefanie Hahner, Silvia Parajes, Roland H. Stimson, (unknown), Paul Carroll, Gerard S. Conway, Brian R. Walker, Fiona MacDonald, Richard Ross, Wiebke Arlt	1
4	Clinical correlation and molecular evaluation confirm that the MLH1 p.Arg182Gly (c.544A>G) mutation is pathogenic and causes Lynch syndrome 2012 ·Familial Cancer ·Michael Farrell, David J. Hughes, Ian Berry, David Gallagher, Emily Glogowski, Stewart J. Payne, Michael J. Kennedy, (unknown), Susan A. White, Cian Muldoon, Fiona MacDonald, (unknown), (unknown), Solvig Roring, (unknown), Trudi McDevitt, David Barton, Shirley V. Hodgson, Andrew Green, Peter A. Daly	3
5	Neuropathy in a Human Without the PMP22 Gene 2011 ·Archives of Neurology ·Mario Saporta, István Katona, Xuebao Zhang, Helen Roper, (unknown), Fiona MacDonald, Louise Brueton, Julian Blake, Ueli Suter, Mary M. Reilly, Michael E. Shy, Jun Li	20
6	Epigenotype–phenotype correlations in Silver–Russell syndrome 2010 ·Journal of Medical Genetics ·Emma Wakeling, (unknown), Mariëlle Alders, Jet Bliek, Elizabeth Forsythe, Sudhesh Kumar, Derek Lim, Fiona MacDonald, Deborah Mackay, Eamonn R. Maher, Gudrun E. Moore, (unknown), (unknown), Trine Tangeraas, (unknown), Mieke M. van Haelst, (unknown), I. Karen Temple, J. M. Cobben	120
7	A new locus-specific database (LSDB) for mutations in the folliculin (FLCN) gene 2009 ·Human Mutation ·(unknown), (unknown), Michael S. Nahorski, Fiona MacDonald, Tijs Claessens, Michel van Geel, Lieke Gijezen, Gilles Thomas, Sophie Giraud, Richard J. Kahnoski, Maurice A. M. Van Steensel, Fred H. Menko, Eamonn R. Maher	81
8	Microarray based analysis of 3p25‐p26 deletions (3p‐ syndrome) 2009 ·American Journal of Medical Genetics Part A ·Salwati Shuib, Dominic McMullan, Eleanor Rattenberry, (unknown), Fatimah Rahman, Malgorzata Zatyka, Cyril Chapman, Fiona MacDonald, Farida Latif, Val Davison, Eamonn R. Maher	76
9	Current management, morbidity and genotypephenotype correlation in adults with congenital adrenal hyperplasia – analysis of the United Kingdom congenital adrenal hyperplasia adult study executive (CaHASE) cohort [Abstract] 2009 ·ORCA Online Research @Cardiff ·Nils Krone, Debbie Willis, Ian T. Rose, Andrew H. Crosby, Sarah H. Wild, (unknown), Stefanie Hahner, Thang S. Han, Roland H. Stimson, Paul Carroll, (unknown), Aled Rees, Brian R. Walker, Fiona MacDonald, Richard Ross, Wiebke Arlt	1
10	Clinical and molecular genetic features of Beckwith-Wiedemann syndrome associated with assisted reproductive technologies 2008 ·Human Reproduction ·(unknown), Sarah Bowdin, Louise Tee, Gail Kirby, Edward Blair, Anthony A. Fryer, Wayne Lam, Christine Oley, Tim Cole, L A Brueton, Wolf Reik, Fiona MacDonald, Eamonn R. Maher	160
11	Mitotic recombination and uniparental disomy in Beckwith–Wiedemann syndrome 2007 ·Genomics ·Wendy N. Cooper, (unknown), Fiona MacDonald, Eamonn R. Maher	34
12	Preteens and illegal drugs: Use, offers, exposure and prevention 2005 ·Drugs ·Neil McKeganey, J. McIntosh, Fiona MacDonald, Éilish Gilvarry, (unknown), (unknown), Martin Hill	3
13	Application of multiplex ligation-dependent probe analysis to define a small deletion encompassing PMP22 exons 4 and 5 in hereditary neuropathy with liability to pressure palsies 2004 ·Neuromuscular Disorders ·Ian Sutton, (unknown), (unknown), (unknown), (unknown), J. Winer, Fiona MacDonald	5
14	Improving general practitioners’ assessment and management of suicide risk 2001 ·International Journal of Health Care Quality Assurance ·Roger Paxton, Fiona MacDonald, (unknown), (unknown), (unknown), Margaret Smith	3
15	Dictionary of pharmacological agents 1997 ·Chapman & Hall eBooks ·Fiona MacDonald	49
16	An unusually severe phenotype for familial adenomatous polyposis 1997 ·Archives of Disease in Childhood ·Diana Eccles, Peter Lunt, Yvonne Wallis, (unknown), Bhupinder Sandhu, (unknown), Dion Morton, (unknown), Fiona MacDonald	34
17	The genetics of inherited colon cancer 1996 ·Molecular Pathology ·Yvonne Wallis, Fiona MacDonald	2
18	Effect of heat treatment on Listeria monocytogenes and Gram‐negative bacteria in sheep, cow and goat milks 1993 ·Journal of Applied Bacteriology ·Fiona MacDonald, A.D. Sutherland	26
19	Regulation of intracellular cyclic AMP concentrations in hepatocytes involves the integrated activation and desensitization of adenylyl cyclase coupled with the action and activation of specific isoforms of cyclic AMP phosphodiesterase 1992 ·Biochemical Society Transactions ·Miles D. Houslay, Susanne L. Griffiths, (unknown), Callum Livingstone, Margaret D. Lobban, Fiona MacDonald, Nicholas J. Morris, James G. Pryde, Grant Scotland, Yasmin Shakur, Gary Sweeney, Eric Tang	14
20	Immunoadsorbent Purification of Carcinoembryonic Antigen using a Monoclonal Antibody: A Direct Comparison with a Conventional Method 1987 ·Tumor Biology ·C. H. J. Ford, Fiona MacDonald, J A Griffin, Paul Life, Stephen Bartlett	4

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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