Moira Blyth

3.9k total citations
22 papers, 379 citations indexed

About

Moira Blyth is a scholar working on Genetics, Molecular Biology and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Moira Blyth has authored 22 papers receiving a total of 379 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 7 papers in Molecular Biology and 5 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Moira Blyth's work include Congenital Heart Disease Studies (3 papers), Congenital heart defects research (3 papers) and Genetics and Neurodevelopmental Disorders (3 papers). Moira Blyth is often cited by papers focused on Congenital Heart Disease Studies (3 papers), Congenital heart defects research (3 papers) and Genetics and Neurodevelopmental Disorders (3 papers). Moira Blyth collaborates with scholars based in United Kingdom, United States and France. Moira Blyth's co-authors include Diana Wellesley, James Gnanapragasam, Danielle Howe, David J. Bunyan, Shuwen Huang, John A. Crolla, Viv Maloney, I. Karen Temple, Amber Young and Ghislaine Plessis and has published in prestigious journals such as BJOG An International Journal of Obstetrics & Gynaecology, Journal of Medical Genetics and European Journal of Human Genetics.

In The Last Decade

Moira Blyth

20 papers receiving 352 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Moira Blyth United Kingdom 12 162 139 75 68 57 22 379
Eusebiu Vlad Gorduza Romania 12 149 0.9× 161 1.2× 46 0.6× 32 0.5× 65 1.1× 49 385
Hermine E. Veenstra‐Knol Netherlands 13 220 1.4× 276 2.0× 33 0.4× 51 0.8× 37 0.6× 20 561
Diana Carli Italy 14 272 1.7× 279 2.0× 36 0.5× 90 1.3× 124 2.2× 51 599
Anna Baroncini Italy 13 256 1.6× 149 1.1× 50 0.7× 64 0.9× 61 1.1× 29 458
Sally Rosengren United States 9 207 1.3× 293 2.1× 32 0.4× 38 0.6× 52 0.9× 15 665
Goran Čuturilo Serbia 11 149 0.9× 167 1.2× 43 0.6× 47 0.7× 29 0.5× 32 323
David S. Wargowski United States 9 136 0.8× 112 0.8× 46 0.6× 22 0.3× 35 0.6× 15 336
Sophie Julia France 12 241 1.5× 163 1.2× 29 0.4× 42 0.6× 26 0.5× 27 372
Licia Turolla Italy 11 175 1.1× 95 0.7× 63 0.8× 29 0.4× 83 1.5× 23 345
Birsen Karaman Türkiye 12 157 1.0× 180 1.3× 33 0.4× 44 0.6× 64 1.1× 58 345

Countries citing papers authored by Moira Blyth

Since Specialization
Citations

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

Fields of papers citing papers by Moira Blyth

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Moira Blyth

This figure shows the co-authorship network connecting the top 25 collaborators of Moira Blyth. A scholar is included among the top collaborators of Moira Blyth 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 Moira Blyth. Moira Blyth 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.
Sharif, Saghira Malik, Moira Blyth, Mushtaq Ahmed, et al.. (2020). Enhancing inclusion of diverse populations in genomics: A competence framework. Journal of Genetic Counseling. 29(2). 282–292. 13 indexed citations
2.
Blyth, Moira, Kamran Moradkhani, Dubravka Hranilović, et al.. (2019). Variable neurodevelopmental and morphological phenotypes of carriers with 12q12 duplications. Molecular Genetics & Genomic Medicine. 8(1). e1013–e1013. 1 indexed citations
3.
Blyth, Moira, Ingrid Scurr, Peter D. Turnpenny, et al.. (2018). Extending the clinical and genetic spectrum of ARID2 related intellectual disability. A case series of 7 patients. European Journal of Medical Genetics. 62(1). 27–34. 9 indexed citations
4.
Pysden, Karen, et al.. (2017). Carbamazepine Improves Apneic Episodes in Congenital Central Hypoventilation Syndrome (CCHS) With a Novel PHOX2B Exon 1 Missense Mutation. Journal of Clinical Sleep Medicine. 13(11). 1359–1362. 7 indexed citations
5.
Hartill, Verity, Mitchell W. Dillon, Daniel Warren, & Moira Blyth. (2016). RAF1-associated Noonan syndrome presenting antenatally with an abnormality of skull shape, subdural haematoma and associated with novel cerebral malformations. Clinical Dysmorphology. 26(2). 101–106. 4 indexed citations
6.
Breckpot, Jeroen, Britt‐Marie Anderlid, Yasemin Alanay, et al.. (2015). Chromosome 22q12.1 microdeletions: confirmation of the MN1 gene as a candidate gene for cleft palate. European Journal of Human Genetics. 24(1). 51–58. 20 indexed citations
7.
Pagnamenta, Alistair T., Moira Blyth, Sahar Mansour, et al.. (2015). Deletions and de novo mutations of SOX11 are associated with a neurodevelopmental disorder with features of Coffin–Siris syndrome. Journal of Medical Genetics. 53(3). 152–162. 53 indexed citations
8.
Blyth, Moira, Viv Maloney, Sarah J. Beal, et al.. (2015). Pallister-Killian syndrome: a study of 22 British patients. Journal of Medical Genetics. 52(7). 454–464. 33 indexed citations
9.
Bunyan, David J., et al.. (2014). Homozygosity for a novel deletion downstream of the SHOX gene provides evidence for an additional long range regulatory region with a mild phenotypic effect. American Journal of Medical Genetics Part A. 164(11). 2764–2768. 16 indexed citations
10.
Petit, Florence, Ghislaine Plessis, Matthieu Décamp, et al.. (2014). 21q21 deletion involving NCAM2: Report of 3 cases with neurodevelopmental disorders. European Journal of Medical Genetics. 58(1). 44–46. 27 indexed citations
11.
Jewell, Rosalyn, et al.. (2014). Phenotypic features of diploid/triploid mosaicism in an adult. Clinical Dysmorphology. 23(2). 56–59. 5 indexed citations
12.
Blyth, Moira & A Griffiths. (2013). Chiari network in pregnancy. Journal of Obstetrics and Gynaecology. 33(3). 309–309.
13.
Blyth, Moira & Diana Baralle. (2011). Anophthalmia in fronto–facial–nasal dysplasia. Clinical Dysmorphology. 20(2). 73–74. 3 indexed citations
14.
Blyth, Moira & Katherine Lachlan. (2010). Amniotic bands in paternal half-siblings. Clinical Dysmorphology. 19(2). 62–64. 5 indexed citations
15.
Blyth, Moira, Danielle Howe, James Gnanapragasam, & Diana Wellesley. (2008). The hidden mortality of transposition of the great arteries and survival advantage provided by prenatal diagnosis. BJOG An International Journal of Obstetrics & Gynaecology. 115(9). 1096–1100. 61 indexed citations
16.
Blyth, Moira, Nicola Foulds, Claire Turner, & David J. Bunyan. (2008). Severe Marfan syndrome due to FBN1 exon deletions. American Journal of Medical Genetics Part A. 146A(10). 1320–1324. 19 indexed citations
17.
Blyth, Moira, Shuwen Huang, Viv Maloney, John A. Crolla, & I. Karen Temple. (2008). A 2.3 Mb deletion of 17q24.2–q24.3 associated with ‘Carney Complex plus’. European Journal of Medical Genetics. 51(6). 672–678. 22 indexed citations
18.
Blyth, Moira, Sarah J. Beal, Shuwen Huang, John A. Crolla, & Nicola Foulds. (2008). A novel 2.43 Mb deletion of 7q11.22–q11.23. American Journal of Medical Genetics Part A. 146A(24). 3206–3210. 4 indexed citations
19.
Blyth, Moira, et al.. (2008). The Hidden Mortality of Transposition of the Great Arteries and Survival Advantage Provided by Prenatal Diagnosis. Obstetrical & Gynecological Survey. 63(11). 694–695.
20.
Blyth, Moira, et al.. (2007). Severe staphylococcal scalded skin syndrome in children. Burns. 34(1). 98–103. 21 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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