Shane McKee

7.5k total citations
44 papers, 1.1k citations indexed

About

Shane McKee is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Shane McKee has authored 44 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 21 papers in Genetics and 8 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Shane McKee's work include Genomic variations and chromosomal abnormalities (11 papers), Genomics and Rare Diseases (6 papers) and Prenatal Screening and Diagnostics (6 papers). Shane McKee is often cited by papers focused on Genomic variations and chromosomal abnormalities (11 papers), Genomics and Rare Diseases (6 papers) and Prenatal Screening and Diagnostics (6 papers). Shane McKee collaborates with scholars based in United Kingdom, United States and Netherlands. Shane McKee's co-authors include Eamonn R. Maher, Janusz Jankowski, Frances M. Richards, M. Helen Rajpar, C. McKeown, D. Gareth Evans, D. S. A. Sanders, Trevor Cole, David Fitzpatrick and Nicholas Nelson and has published in prestigious journals such as The American Journal of Human Genetics, Human Molecular Genetics and Epilepsia.

In The Last Decade

Shane McKee

43 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Shane McKee United Kingdom	17	561	467	171	144	112	44	1.1k
Janita Thusberg Finland	11	846 1.5×	685 1.5×	106 0.6×	78 0.5×	158 1.4×	14	1.4k
Bernt Popp Germany	17	589 1.0×	413 0.9×	89 0.5×	71 0.5×	66 0.6×	45	903
Shaun S. Abeysinghe United Kingdom	8	1.4k 2.5×	845 1.8×	101 0.6×	109 0.8×	186 1.7×	8	2.1k
Baoshan Gu United States	2	1.1k 2.0×	780 1.7×	113 0.7×	82 0.6×	289 2.6×	4	1.7k
Małgorzata Wiench Poland	17	889 1.6×	287 0.6×	93 0.5×	74 0.5×	192 1.7×	38	1.6k
Shanmuga Chitipiralla United States	2	1.1k 2.0×	787 1.7×	113 0.7×	82 0.6×	289 2.6×	4	1.7k
Delphine Bacq France	10	522 0.9×	304 0.7×	71 0.4×	47 0.3×	151 1.3×	12	888
P. Pearson Netherlands	21	879 1.6×	710 1.5×	88 0.5×	70 0.5×	109 1.0×	50	1.6k
Efraim H. Rosenberg Netherlands	15	413 0.7×	130 0.3×	96 0.6×	214 1.5×	163 1.5×	27	1.1k

Countries citing papers authored by Shane McKee

Since Specialization

Citations

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

Fields of papers citing papers by Shane McKee

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Shane McKee

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

Eberl, Daniel F., Güney Bademci, Stephanie Bivona, et al.. (2025). De novo variants in CDKL1 and CDKL2 are associated with neurodevelopmental symptoms. The American Journal of Human Genetics. 112(4). 846–862. 1 indexed citations

McKenna, Caoimhe, et al.. (2023). Prenatal genomic testing for ultrasound‐detected fetal structural anomalies. The Obstetrician & Gynaecologist. 25(2). 121–130.

McKee, Shane, Paolo Prontera, Francesca Faravelli, et al.. (2022). SPECC1L Mutations Are Not Common in Sporadic Cases of Opitz G/BBB Syndrome. Genes. 13(2). 252–252. 1 indexed citations

Lim, Derek, Shane McKee, Meriel McEntagart, et al.. (2021). Whole-genome analysis as a diagnostic tool for patients referred for diagnosis of Silver-Russell syndrome: a real-world study. Journal of Medical Genetics. 59(6). 613–622. 13 indexed citations

McAneney, Helen, et al.. (2020). A scoping review and proposed workflow for multi-omic rare disease research. Orphanet Journal of Rare Diseases. 15(1). 107–107. 32 indexed citations

Douzgou, Sofia, Hui Liang, Kay Metcalfe, et al.. (2019). The clinical presentation caused by truncating CHD8 variants. Clinical Genetics. 96(1). 72–84. 26 indexed citations

Rea, Gillian, Tessa Homfray, Jan Till, et al.. (2016). Histiocytoid cardiomyopathy and microphthalmia with linear skin defects syndrome: phenotypes linked by truncating variants in NDUFB11. Molecular Case Studies. 3(1). a001271–a001271. 11 indexed citations

Parker, Michael, Alan Fryer, Deborah Shears, et al.. (2015). De novo, heterozygous, loss‐of‐function mutations in SYNGAP1 cause a syndromic form of intellectual disability. American Journal of Medical Genetics Part A. 167(10). 2231–2237. 79 indexed citations

Banka, Siddharth, Damien Lederer, Valérie Benoît, et al.. (2014). Novel KDM6A (UTX) mutations and a clinical and molecular review of the X‐linked Kabuki syndrome (KS2). Clinical Genetics. 87(3). 252–258. 91 indexed citations

10.

Hammond, Peter, Shane McKee, Michael Suttie, et al.. (2014). Opposite effects on facial morphology due to gene dosage sensitivity. Human Genetics. 133(9). 1117–1125. 11 indexed citations

11.

White, Susan M., Elizabeth Fitzpatrick, Gabrielle R. Wilson, et al.. (2014). Expanding the phenotypic spectrum of ARID1B-mediated disorders and identification of altered cell-cycle dynamics due to ARID1B haploinsufficiency. Orphanet Journal of Rare Diseases. 9(1). 43–43. 15 indexed citations

12.

Oehl‐Jaschkowitz, Barbara, Olivier Vanakker, Anne De Paepe, et al.. (2013). Deletions in 14q24.1q24.3 are associated with congenital heart defects, brachydactyly, and mild intellectual disability. American Journal of Medical Genetics Part A. 164(3). 620–626. 17 indexed citations

13.

McKee, Shane, et al.. (2012). Shwachman-Diamond syndrome: a complex case demonstrating the potential for misdiagnosis as asphyxiating thoracic dystrophy (Jeune syndrome). BMC Pediatrics. 12(1). 48–48. 14 indexed citations

14.

Dixit, Abhijit, Shane McKee, Sahar Mansour, et al.. (2012). 7q11.23 Microduplication: a recognizable phenotype. Clinical Genetics. 83(2). 155–161. 37 indexed citations

15.

Suri, Mohnish, Susan M. White, Nicole de Leeuw, et al.. (2011). Pierpont syndrome: A collaborative study. American Journal of Medical Genetics Part A. 155(9). 2203–2211. 13 indexed citations

16.

Dunlop, Elaine A., Stephen C. Land, Helen M. Stuart, et al.. (2011). Determining the pathogenicity of patient-derived TSC2 mutations by functional characterization and clinical evidence. European Journal of Human Genetics. 19(7). 789–795. 9 indexed citations

17.

Donnelly, Deirdre E., et al.. (2011). Growth retardation, developmental delay and dysmorphic features in a girl with a partial duplication of Xq. Clinical Dysmorphology. 20(2). 82–85. 2 indexed citations

18.

Day, Richard O., Dian Donnai, Alan Fryer, et al.. (2008). A clinical and genetic study of the Say/Barber/Biesecker/Young‐Simpson type of Ohdo syndrome. Clinical Genetics. 74(5). 434–444. 17 indexed citations

19.

McKee, Shane, et al.. (2001). Joint and skin laxity with Dandy-Walker malformation and contractures: a distinct recessive syndrome?. Clinical Dysmorphology. 10(3). 177–180. 4 indexed citations

20.

Richards, Frances M., Shane McKee, M. Helen Rajpar, et al.. (1999). Germline E-cadherin Gene (CDH1) Mutations Predispose to Familial Gastric Cancer and Colorectal Cancer. Human Molecular Genetics. 8(4). 607–610. 251 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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