Angus Dobbie

3.7k total citations
20 papers, 675 citations indexed

About

Angus Dobbie is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Angus Dobbie has authored 20 papers receiving a total of 675 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 9 papers in Molecular Biology and 3 papers in Surgery. Recurrent topics in Angus Dobbie's work include Genomic variations and chromosomal abnormalities (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Genetic Syndromes and Imprinting (2 papers). Angus Dobbie is often cited by papers focused on Genomic variations and chromosomal abnormalities (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Genetic Syndromes and Imprinting (2 papers). Angus Dobbie collaborates with scholars based in United Kingdom, Australia and Netherlands. Angus Dobbie's co-authors include Elizabeth Baker, David F. Callen, Sian Ellard, Meryl Altree, Eric Haan, Erica Woollatt, Elizabeth Thompson, Peter Thompson, Helen J. Eyre and Grant R. Sutherland and has published in prestigious journals such as Journal of Biological Chemistry, PLoS ONE and The Journal of Physiology.

In The Last Decade

Angus Dobbie

19 papers receiving 661 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Angus Dobbie United Kingdom 12 402 284 108 67 65 20 675
Soo‐Mi Park United Kingdom 15 464 1.2× 258 0.9× 74 0.7× 51 0.8× 26 0.4× 39 794
Maria Descartes United States 16 399 1.0× 431 1.5× 72 0.7× 40 0.6× 60 0.9× 34 720
A. Jeannette M. Hoogeboom Netherlands 18 562 1.4× 617 2.2× 133 1.2× 41 0.6× 28 0.4× 36 1.0k
Sahar Mansour United Kingdom 11 575 1.4× 288 1.0× 81 0.8× 37 0.6× 18 0.3× 15 854
Nisha Patel Saudi Arabia 17 428 1.1× 267 0.9× 53 0.5× 18 0.3× 28 0.4× 39 727
Marion Gérard France 14 436 1.1× 386 1.4× 107 1.0× 94 1.4× 19 0.3× 29 837
Tadeusz Mazurczak Poland 17 299 0.7× 444 1.6× 86 0.8× 15 0.2× 116 1.8× 57 763
Sabine Uhrig Germany 16 376 0.9× 430 1.5× 104 1.0× 22 0.3× 206 3.2× 23 823
Julie S. Fryburg United States 12 341 0.8× 412 1.5× 59 0.5× 110 1.6× 21 0.3× 25 790
Boris Keren France 21 649 1.6× 515 1.8× 44 0.4× 49 0.7× 27 0.4× 70 1.1k

Countries citing papers authored by Angus Dobbie

Since Specialization
Citations

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

Fields of papers citing papers by Angus Dobbie

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Angus Dobbie

This figure shows the co-authorship network connecting the top 25 collaborators of Angus Dobbie. A scholar is included among the top collaborators of Angus Dobbie 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 Angus Dobbie. Angus Dobbie 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.
Boudin, Eveline, Timothy C. R. Prickett, Bruno Lapauw, et al.. (2018). Bi-allelic Loss-of-Function Mutations in the NPR-C Receptor Result in Enhanced Growth and Connective Tissue Abnormalities. The American Journal of Human Genetics. 103(2). 288–295. 25 indexed citations
2.
Watson, Christopher M., Laura A. Crinnion, Ian Berry, et al.. (2016). Enhanced diagnostic yield in Meckel-Gruber and Joubert syndrome through exome sequencing supplemented with split-read mapping. BMC Medical Genetics. 17(1). 1–1. 59 indexed citations
3.
4.
Hartill, Verity, Carolyn Tysoe, N. J. Manning, et al.. (2014). An unusual phenotype of X‐linked developmental delay and extreme behavioral difficulties associated with a mutation in the EBP gene. American Journal of Medical Genetics Part A. 164(4). 907–914. 8 indexed citations
5.
Wedatilake, Yehani, Ruth M. Brown, Robert McFarland, et al.. (2013). SURF1 deficiency: a multi-centre natural history study. Orphanet Journal of Rare Diseases. 8(1). 96–96. 91 indexed citations
6.
Parry, David, Clare V. Logan, Alexander P.A. Stegmann, et al.. (2013). SAMS, a Syndrome of Short Stature, Auditory-Canal Atresia, Mandibular Hypoplasia, and Skeletal Abnormalities Is a Unique Neurocristopathy Caused by Mutations in Goosecoid. The American Journal of Human Genetics. 93(6). 1135–1142. 27 indexed citations
7.
Olsen, Rikke Katrine Jentoft, Rugivan Sabaratnam, Thomas Koed Doktor, et al.. (2013). TheETFDHc.158A>G Variation Disrupts the Balanced Interplay of ESE- and ESS-Binding Proteins thereby Causing Missplicing and Multiple Acyl-CoA Dehydrogenation Deficiency. Human Mutation. 35(1). 86–95. 24 indexed citations
8.
Carr, Ian, Christine P. Diggle, Kamron N. Khan, et al.. (2012). Rapid Visualisation of Microarray Copy Number Data for the Detection of Structural Variations Linked to a Disease Phenotype. PLoS ONE. 7(8). e43466–e43466. 1 indexed citations
9.
Thompson, Dorothy, Sally Feather, Horia Stanescu, et al.. (2011). Altered electroretinograms in patients with KCNJ10 mutations and EAST syndrome. The Journal of Physiology. 589(7). 1681–1689. 61 indexed citations
10.
Spiegel, Ronen, Angus Dobbie, Corina Hartman, et al.. (2011). Clinical characterization of a newly described neonatal diabetes syndrome caused by RFX6 mutations. American Journal of Medical Genetics Part A. 155(11). 2821–2825. 33 indexed citations
11.
Kleta, Robert, et al.. (2009). EAST SYNDROME (EPILEPSY, ATAXIA, SENSORINEURAL DEAFNESS AND TUBULOPATHY) IS CAUSED BY MUTATIONS IN KCNJ10. Pediatric Nephrology. 1 indexed citations
12.
Gorman, Shaun, et al.. (2008). A further example of a distinctive autosomal recessive syndrome comprising neonatal diabetes mellitus, intestinal atresias and gall bladder agenesis. American Journal of Medical Genetics Part A. 146A(13). 1713–1717. 33 indexed citations
13.
Sprigg, Alan, et al.. (2005). Brachydactyly with extrahepatic biliary atresia, patent ductus arteriosus and seizures ??? a new syndrome?. Clinical Dysmorphology. 14(3). 117–121. 2 indexed citations
14.
Nesbit, M. Andrew, Michael R. Bowl, Brian Harding, et al.. (2004). Characterization of GATA3 Mutations in the Hypoparathyroidism, Deafness, and Renal Dysplasia (HDR) Syndrome. Journal of Biological Chemistry. 279(21). 22624–22634. 122 indexed citations
15.
Janssens, Katrien, Elizabeth D. Thompson, Filip Vanhoenacker, et al.. (2003). Macrocephaly and sclerosis of the tubular bones in an isolated patient: a mild case of craniodiaphyseal dysplasia?. Clinical Dysmorphology. 12(4). 245–250. 2 indexed citations
16.
Baker, Elizabeth, et al.. (2002). A familial cryptic subtelomeric deletion 12p with variable phenotypic effect. Clinical Genetics. 61(3). 198–201. 29 indexed citations
17.
Baker, Elizabeth, David F. Callen, Meryl Altree, et al.. (2001). Study of 250 children with idiopathic mental retardation reveals nine cryptic and diverse subtelomeric chromosome anomalies. American Journal of Medical Genetics. 107(4). 285–293. 102 indexed citations
18.
Comenius, Johann Amos & Angus Dobbie. (1993). Panorthosia or Universal Reform. 3 indexed citations
19.
Dobbie, Angus, et al.. (1989). Panglottia, or, Universal Language Being Part Five of His Universal Deliberation on the Reform of Human Affairs. 1 indexed citations
20.
Dobbie, Angus, et al.. (1988). Comenius's Pampaedia. British Journal of Educational Studies. 36(1). 83–83. 1 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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