David Goudie

10.0k total citations · 1 hit paper
69 papers, 2.6k citations indexed

About

David Goudie is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, David Goudie has authored 69 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Molecular Biology, 31 papers in Genetics and 13 papers in Oncology. Recurrent topics in David Goudie's work include BRCA gene mutations in cancer (9 papers), Skin and Cellular Biology Research (6 papers) and Connective tissue disorders research (6 papers). David Goudie is often cited by papers focused on BRCA gene mutations in cancer (9 papers), Skin and Cellular Biology Research (6 papers) and Connective tissue disorders research (6 papers). David Goudie collaborates with scholars based in United Kingdom, United States and France. David Goudie's co-authors include Haihui Liao, Frances J.D. Smith, W.H. Irwin McLean, Alan D. Irvine, M.A. Ferguson‐Smith, Ana Terron-Kwiatkowski, Aileen Sandilands, Yiwei Zhao, Gráinne M. O’Regan and Nabeel A. Affara and has published in prestigious journals such as The Lancet, Nucleic Acids Research and Nature Genetics.

In The Last Decade

David Goudie

68 papers receiving 2.5k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Loss-of-function mutations in the gene encoding filaggrin cause ichthyosis vulgaris

2006 681 citations Frances J.D. Smith, Alan D. Irvine et al. Nature Genetics profile →

Peers

Countries citing papers authored by David Goudie

Since Specialization

Citations

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

Fields of papers citing papers by David Goudie

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of David Goudie

This figure shows the co-authorship network connecting the top 25 collaborators of David Goudie. A scholar is included among the top collaborators of David Goudie 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 David Goudie. David Goudie 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	Faecal haemoglobin can define risk of colorectal neoplasia at surveillance colonoscopy in patients at increased risk of colorectal cancer 2020 ·United European Gastroenterology Journal ·Jayne Digby, (unknown), (unknown), Pooja Datt, David Goudie, R. Steele, Judith A Strachan, Adam Humphries, Callum G. Fraser, Craig Mowat	16
2	P6505Urinary desmosine, an elastin-specific degradation product is associated with maximum aortic root size and aortic z-scores in patients with bicuspid aortic valve 2019 ·European Heart Journal ·(unknown), Jeffrey Huang, Ify Mordi, (unknown), Calvin Chin, David Goudie, Catherine McWilliam, (unknown), (unknown), Chim C. Lang, Anna Maria Choy	1
3	Why do women not return family history forms when referred to breast cancer genetics services? A mixed‐method study 2014 ·Health Expectations ·(unknown), Michael Steel, David Goudie, (unknown), (unknown), (unknown), Frank Sullivan, Jonathan Berg, Gerry Humphris, Gözde Özakinci	1
4	Digenic/multilocus aetiology of multiple self-healing squamous epithelioma (Ferguson-Smith disease): TGFBR1 and a second linked locus 2014 ·The International Journal of Biochemistry & Cell Biology ·M.A. Ferguson‐Smith, David Goudie	7
5	Lifestyle Changes in Women at Genetic Risk of Breast Cancer: an Observational Study 2012 ·International Journal of Behavioral Medicine ·(unknown), (unknown), (unknown), David Goudie, Jonathan Berg, Michelle Harvie, (unknown), (unknown), C. M. Steel	8
6	Biological Therapy for Paediatric Inflammatory Bowel Disease: The Scottish Nationwide 'Real Life' Experience 2009 ·Scottish Medical Journal ·(unknown), (unknown), Michelle Wilson, Gamal Mahdi, David Goudie, Richard K. Russell, David C. Wilson	1
7	Unusual presentation of Lynch Syndrome 2009 ·Hereditary Cancer in Clinical Practice ·Veronica Yu, Marco Novelli, Stewart J. Payne, (unknown), Rebecca A. Barnetson, Ian M. Frayling, Ann Barrett, David Goudie, Audrey Ardern‐Jones, Rosalind A. Eeles, Susan Shanley	13
8	Mutations in the chromatin-associated protein ATRX 2008 ·Human Mutation ·Richard J. Gibbons, Takahito Wada, Christopher A. Fisher, N Malik, (unknown), David P. Steensma, Alan Fryer, David Goudie, Ian D. Krantz, Joanne Traeger‐Synodinos	125
9	Prevalent and Rare Mutations in the Gene Encoding Filaggrin Cause Ichthyosis Vulgaris and Predispose Individuals to Atopic Dermatitis 2006 ·Journal of Investigative Dermatology ·Aileen Sandilands, Gráinne M. O’Regan, Haihui Liao, Yiwei Zhao, Ana Terron-Kwiatkowski, Rosemarie M. Watson, Andrew Cassidy, David Goudie, Frances J.D. Smith, W.H. Irwin McLean, Alan D. Irvine	169
10	Loss-of-function mutations in the gene encoding filaggrin cause ichthyosis vulgaris breakdown → 2006 ·Nature Genetics ·Frances J.D. Smith, Alan D. Irvine, Ana Terron-Kwiatkowski, Aileen Sandilands, Linda Campbell, Yiwei Zhao, Haihui Liao, Alan Evans, David Goudie, Sue Lewis‐Jones, Gehan Arseculeratne, Colin S. Munro, Ann Sergeant, Gráinne M. O’Regan, Sherri J. Bale, John G. Compton, John J. DiGiovanna, Richard B. Presland, Philip Fleckman, W.H. Irwin McLean	681
11	Analysis of referrals to a multi-disciplinary breast cancer genetics clinic: practical and economic considerations 2006 ·Familial Cancer ·(unknown), Dorothy C. Young, (unknown), David Goudie, Alan Cook, Frank Sullivan, (unknown), Alison Fordyce, Roger J. Black, Manouche Tavakoli, Michael Steel	8
12	Biotinidase deficiency: Novel mutations and their biochemical and clinical correlates 2005 ·Human Mutation ·Barry Wolf, Kevin P. Jensen, Bruce A. Barshop, Miriam G. Blitzer, Martha Carlson, David Goudie, Gülden Gökçay, Mübeccel Demirkol, T. Baykal, Ferhat Demir, (unknown), (unknown), Hélio Pedro, (unknown), Alfred E. Slonim	30
13	Phenotypic Comparison of Two Scottish Families with Mutations in Different Genes Causing Autosomal Dominant Nocturnal Frontal Lobe Epilepsy 2003 ·Epilepsia ·Ailsa McLellan, Hilary A. Phillips, Christopher Rittey, Martin Kirkpatrick, John C. Mulley, David Goudie, John B.P. Stephenson, John Tolmie, Ingrid E. Scheffer, Samuel F. Berkovic, Sameer M. Zuberi	51
14	Survival in prospectively ascertained familial breast cancer: Analysis of a series stratified by tumour characteristics, BRCA mutations and oophorectomy 2002 ·International Journal of Cancer ·Pål Møller, Åke Borg, D. Gareth Evans, Neva E. Haites, (unknown), Hans F. A. Vasen, Elaine Anderson, C. M. Steel, Jaran Apold, David Goudie, Anthony Howell, Fiona Lalloo, Lovise Mæhle, Helen Gregory, Ketil Heimdal	88
15	CHRNB2 Is the Second Acetylcholine Receptor Subunit Associated with Autosomal Dominant Nocturnal Frontal Lobe Epilepsy* 2001 ·The American Journal of Human Genetics ·Hilary A. Phillips, Isabelle Favre, Martin Kirkpatrick, Sameer M. Zuberi, David Goudie, Sarah E. Heron, Ingrid E. Scheffer, Grant R. Sutherland, Samuel F. Berkovic, Daniel Bertrand, John C. Mulley	239
16	An investigation of the Peutz-Jeghers gene (LKB1) in sporadic breast and colon cancers 2000 ·Journal of Clinical Pathology ·Lucy Forster, Sylviane Defres, David Goudie, David Baty, F. A. CAREY	25
17	Multiple self–healing squamous epitheliomata (ESS1) mapped to chromosome 9q22–q31 in families with common ancestry 1993 ·Nature Genetics ·David Goudie, Martin Yuille, Margaret Leversha, Robert A. Furlong, Nigel P. Carter, Michael Lush, Nabeel A. Affara, M.A. Ferguson‐Smith	68
18	A dinucleotide repeat polymorphism at the D9S127 locus 1992 ·Nucleic Acids Research ·(unknown), R. A. Furlong, Martin Yuille, David Goudie, M. Leversha, Nabeel A. Affara, M.A. Ferguson‐Smith	20
19	The gene for aarskog syndrome is located between DXS255 and DXS566 (Xp11.2–Xq13) 1992 ·Genomics ·Mary Porteous, A Curtis, Susan Lindsay, Owen Williams, David Goudie, Smaragda Kamakari, Siladitya Bhattacharya	19
20	Aarskog syndrome. 1991 ·Journal of Medical Genetics ·Mary Porteous, David Goudie	24

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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