Emma McCann

4.6k total citations
10 papers, 315 citations indexed

About

Emma McCann is a scholar working on Genetics, Molecular Biology and Nephrology. According to data from OpenAlex, Emma McCann has authored 10 papers receiving a total of 315 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 5 papers in Molecular Biology and 2 papers in Nephrology. Recurrent topics in Emma McCann's work include Genomics and Rare Diseases (2 papers), Craniofacial Disorders and Treatments (2 papers) and Cleft Lip and Palate Research (2 papers). Emma McCann is often cited by papers focused on Genomics and Rare Diseases (2 papers), Craniofacial Disorders and Treatments (2 papers) and Cleft Lip and Palate Research (2 papers). Emma McCann collaborates with scholars based in United Kingdom, Ireland and Australia. Emma McCann's co-authors include Melissa Gladstone, Rachel Kneen, Nine V.A.M. Knoers, Paul May, Mariëlle E.M. Swinkels, Annet Simons, Bert B.A. de Vries, Rolph Pfundt, Conny M.A. van Ravenswaaij‐Arts and Lisenka E.L.M. Vissers and has published in prestigious journals such as Archives of Disease in Childhood, Genetics in Medicine and Journal of Anatomy.

In The Last Decade

Emma McCann

8 papers receiving 298 citations

Peers

Emma McCann

GENET

MB

PPCH

PS

PMH

Anna Stittrich Germany

Nicklas Heine Staunstrup Denmark

Magdalena Bartnik Poland

Katherine Christensen United States

Elena Lopez‐Rangel Canada

M. C. E. Jansweijer Netherlands

Jin Szatkiewicz United States

Aude Charollais France

Britt Marie Anderlid Sweden

Lucia Pucci Italy

Anna Stittrich Germany

Emma McCann

141 ×0.8

GENET

123 ×0.8

MB

28 ×0.3

PPCH

28 ×0.8

PS

38 ×1.5

PMH

Citations per year, relative to Emma McCann Emma McCann (= 1×) peers Anna Stittrich

Countries citing papers authored by Emma McCann

Since Specialization

Citations

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

Fields of papers citing papers by Emma McCann

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Emma McCann

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

All Works

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10 of 10 papers shown

1.

Cormican, Sarah, Omri Teltsh, Matthew D. Griffin, et al.. (2025). Characterization of Monogenic Kidney Disease in Older Patients With CKD. Kidney International Reports. 10(7). 2140–2152.

2.

McCann, Emma, Astrid Weber, Jenny E.V. Morton, et al.. (2024). Reassessing the association: Evaluation of a polyalanine deletion variant of RUNX2 in non‐syndromic sagittal and metopic craniosynostosis. Journal of Anatomy. 245(6). 874–878. 2 indexed citations

3.

Williams, Simon G., et al.. (2023). Genomic testing in patients with renal disease. British Journal of Hospital Medicine. 84(7). 1–11. 2 indexed citations

4.

Salem, Joseph A., et al.. (2023). The Role of Airway Management on Feeding Difficulties in Children With Pfeiffer Syndrome. Journal of Craniofacial Surgery. 34(7). 1985–1988.

5.

Mirza, Nasir, et al.. (2020). Is NIPA1-associated hereditary spastic paraplegia always ‘pure’? Further evidence of motor neurone disease and epilepsy as rare manifestations. Neurogenetics. 21(4). 305–308. 7 indexed citations

6.

Kneen, Rachel, et al.. (2017). Current evidence-based recommendations on investigating children with global developmental delay. Archives of Disease in Childhood. 102(11). 1071–1076. 92 indexed citations

7.

Wilson, Brian T., Zornitza Stark, Sumita Danda, et al.. (2015). The Cockayne Syndrome Natural History (CoSyNH) study: clinical findings in 102 individuals and recommendations for care. Genetics in Medicine. 18(5). 483–493. 108 indexed citations

8.

McCann, Emma, et al.. (2009). Improving service delivery by evaluation of the referral pattern and capacity in a clinical genetics setting. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 151C(3). 200–206. 6 indexed citations

9.

Swinkels, Mariëlle E.M., Annet Simons, Dominique Smeets, et al.. (2008). Clinical and cytogenetic characterization of 13 Dutch patients with deletion 9p syndrome: Delineation of the critical region for a consensus phenotype. American Journal of Medical Genetics Part A. 146A(11). 1430–1438. 89 indexed citations

10.

McCann, Emma, Alan Fryer, Ross Craigie, et al.. (2006). Genitourinary malformations as a feature of the Pallister–Hall syndrome. Clinical Dysmorphology. 15(2). 75–79. 9 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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