Edward Blair

10.6k total citations · 1 hit paper
47 papers, 3.5k citations indexed

About

Edward Blair is a scholar working on Genetics, Molecular Biology and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Edward Blair has authored 47 papers receiving a total of 3.5k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Genetics, 20 papers in Molecular Biology and 15 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Edward Blair's work include Cardiomyopathy and Myosin Studies (12 papers), Genomic variations and chromosomal abnormalities (9 papers) and Genomics and Rare Diseases (7 papers). Edward Blair is often cited by papers focused on Cardiomyopathy and Myosin Studies (12 papers), Genomic variations and chromosomal abnormalities (9 papers) and Genomics and Rare Diseases (7 papers). Edward Blair collaborates with scholars based in United Kingdom, United States and Germany. Edward Blair's co-authors include Hugh Watkins, Charles Redwood, Houman Ashrafian, Jenny C. Taylor, Ingegerd Östman‐Smith, Kate Thomson, Andrew M. Blamire, B. Rajagopalan, Kieran Clarke and Ernest Boehm and has published in prestigious journals such as Circulation, Journal of Clinical Investigation and Nature Genetics.

In The Last Decade

Edward Blair

47 papers receiving 3.4k 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.

Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples

2016 451 citations Roddy Walsh, Kate Thomson et al. Genetics in Medicine profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Edward Blair United Kingdom	27	1.6k	1.4k	1.2k	348	259	47	3.5k
Mariëlle Alders Netherlands	36	2.1k 1.3×	1.6k 1.1×	1.2k 1.0×	364 1.0×	494 1.9×	114	4.0k
Weizhen Ji United States	14	1.9k 1.1×	257 0.2×	1.1k 0.9×	571 1.6×	119 0.5×	47	3.3k
Matthew S. Lebo United States	27	973 0.6×	453 0.3×	1.5k 1.3×	172 0.5×	213 0.8×	74	2.9k
Hennie Bikker Netherlands	28	1.4k 0.9×	1.3k 0.9×	353 0.3×	171 0.5×	194 0.7×	70	3.0k
Mary B. Davis United Kingdom	39	2.3k 1.4×	439 0.3×	461 0.4×	187 0.5×	90 0.3×	111	4.3k
Ute I. Scholl Germany	29	2.0k 1.2×	525 0.4×	733 0.6×	1.4k 3.9×	78 0.3×	55	4.1k
Manuela C. Koch Germany	32	2.8k 1.7×	1.1k 0.7×	321 0.3×	228 0.7×	196 0.8×	67	3.7k
Steven M. Harrison United States	22	1.5k 0.9×	264 0.2×	1.7k 1.4×	186 0.5×	285 1.1×	52	3.2k
Sebastian Preißl United States	27	2.9k 1.7×	227 0.2×	599 0.5×	393 1.1×	149 0.6×	44	3.8k
Sami A. Sanjad Lebanon	16	2.6k 1.6×	242 0.2×	704 0.6×	262 0.8×	239 0.9×	46	3.8k

Countries citing papers authored by Edward Blair

Since Specialization

Citations

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

Fields of papers citing papers by Edward Blair

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Edward Blair

This figure shows the co-authorship network connecting the top 25 collaborators of Edward Blair. A scholar is included among the top collaborators of Edward Blair 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 Edward Blair. Edward Blair 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

Gold, Nina B., Dong Li, Anna Chassevent, et al.. (2020). Heterozygous de novo variants in CSNK1G1 are associated with syndromic developmental delay and autism spectrum disorder. Clinical Genetics. 98(6). 571–576. 10 indexed citations

Buchanan, James, Edward Blair, Kate Thomson, et al.. (2019). Do health professionals value genomic testing? A discrete choice experiment in inherited cardiovascular disease. European Journal of Human Genetics. 27(11). 1639–1648. 11 indexed citations

Mackley, Michael P., Edward Blair, Michael Parker, et al.. (2018). Views of rare disease participants in a UK whole-genome sequencing study towards secondary findings: a qualitative study. European Journal of Human Genetics. 26(5). 652–659. 25 indexed citations

Hastings, Robert, Charlotte Hooper, Elizabeth Ormondroyd, et al.. (2016). Combination of Whole Genome Sequencing, Linkage, and Functional Studies Implicates a Missense Mutation in Titin as a Cause of Autosomal Dominant Cardiomyopathy With Features of Left Ventricular Noncompaction. Circulation Cardiovascular Genetics. 9(5). 426–435. 43 indexed citations

Walsh, Roddy, Kate Thomson, James S. Ware, et al.. (2016). Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples. Genetics in Medicine. 19(2). 192–203. 451 indexed citations breakdown →

Bailey, Claire, Edward Blair, Clifford J. Garratt, & William G. Newman. (2015). Effective cascade screening through identification of a mutation in RYR2 in a large family with a history of sudden death. Journal of Cardiology Cases. 13(1). 9–13. 1 indexed citations

Kienzler, Anne‐Kathrin, Pauline A. van Schouwenburg, John Taylor, et al.. (2015). Hypomorphic function and somatic reversion of DOCK8 cause combined immunodeficiency without hyper-IgE. Clinical Immunology. 163. 17–21. 12 indexed citations

Ormondroyd, Elizabeth, et al.. (2013). Pre-symptomatic genetic testing for inherited cardiac conditions: a qualitative exploration of psychosocial and ethical implications. European Journal of Human Genetics. 22(1). 88–93. 54 indexed citations

Kohler, Malcolm, Alex Pitcher, Edward Blair, et al.. (2012). The Impact of Obstructive Sleep Apnea on Aortic Disease in Marfan's Syndrome. Respiration. 86(1). 39–44. 37 indexed citations

10.

Vogel, Maartje J., Louise Brueton, P. Cox, et al.. (2012). Mutations in GRIP1 cause Fraser syndrome. Journal of Medical Genetics. 49(5). 303–306. 58 indexed citations

11.

Chehadeh-Djebbar, Salima El, Edward Blair, Muriel Holder‐Espinasse, et al.. (2012). Changing facial phenotype in Cohen syndrome: towards clues for an earlier diagnosis. European Journal of Human Genetics. 21(7). 736–742. 22 indexed citations

12.

Adams, Matthew, Roslyn Simms, Zakia Abdelhamed, et al.. (2011). A meckelin–filamin A interaction mediates ciliogenesis. Human Molecular Genetics. 21(6). 1272–1286. 85 indexed citations

13.

Anand, Geetha, Tariq Ali, Jeremy Hull, et al.. (2011). Early use of high‐dose riboflavin in a case of Brown–Vialetto–Van Laere syndrome. Developmental Medicine & Child Neurology. 54(2). 187–189. 54 indexed citations

14.

Blair, Edward, et al.. (2009). Ulnar mammary syndrome and TBX3: Expanding the phenotype. American Journal of Medical Genetics Part A. 149A(12). 2809–2812. 48 indexed citations

15.

Bowdin, Sarah, Louise Tee, Gail Kirby, et al.. (2008). Clinical and molecular genetic features of Beckwith-Wiedemann syndrome associated with assisted reproductive technologies. Human Reproduction. 24(3). 741–747. 160 indexed citations

16.

Wordsworth, Sarah, James Buchanan, Regina Regan, et al.. (2007). Diagnosing idiopathic learning disability: a cost-effectiveness analysis of microarray technology in the National Health Service of the United Kingdom. PubMed. 1(1-2). 35–45. 27 indexed citations

17.

Sharp, Andrew J., Rebecca R. Selzer, Ze Cheng, et al.. (2006). Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome. Nature Genetics. 38(9). 1038–1042. 429 indexed citations

18.

Crilley, Jenifer, Ernest Boehm, Edward Blair, et al.. (2003). Hypertrophic cardiomyopathy due to sarcomeric gene mutations is characterized by impaired energy metabolism irrespective of the degree of hypertrophy. Journal of the American College of Cardiology. 41(10). 1776–1782. 329 indexed citations

19.

Oliveira, María José, Javed Ehtisham, Charles Redwood, et al.. (2002). Mutation analysis of genes encoding Subunits of AMP-activated protein kinase (AMPK) in inherited cardiomyopathies. Circulation. 106. 140–140. 3 indexed citations

20.

Blair, Edward, Charles Redwood, Houman Ashrafian, et al.. (2001). Mutations in the gamma2 subunit of AMP-activated protein kinase cause familial hypertrophic cardiomyopathy: evidence for the central role of energy compromise in disease pathogenesis.. Journal of Medical Genetics. 38. 115 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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