Emma Wakeling

9.8k total citations
69 papers, 1.4k citations indexed

About

Emma Wakeling is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Emma Wakeling has authored 69 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 47 papers in Genetics, 40 papers in Molecular Biology and 15 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Emma Wakeling's work include Genetic Syndromes and Imprinting (22 papers), Prenatal Screening and Diagnostics (15 papers) and Epigenetics and DNA Methylation (14 papers). Emma Wakeling is often cited by papers focused on Genetic Syndromes and Imprinting (22 papers), Prenatal Screening and Diagnostics (15 papers) and Epigenetics and DNA Methylation (14 papers). Emma Wakeling collaborates with scholars based in United Kingdom, United States and Netherlands. Emma Wakeling's co-authors include Gudrun E. Moore, Philip Stanier, Sayeda Abu‐Amero, Deborah Mackay, Michael A. Preece, I. Karen Temple, Susan Holder, Megan P. Hitchins, David Monk and Margaret Lever and has published in prestigious journals such as Nature Genetics, SHILAP Revista de lepidopterología and Brain.

In The Last Decade

Emma Wakeling

66 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Emma Wakeling United Kingdom 19 903 887 543 135 125 69 1.4k
Beate Albrecht Germany 23 1.0k 1.2× 862 1.0× 264 0.5× 214 1.6× 114 0.9× 45 1.7k
Christèle Dubourg France 28 1.1k 1.3× 1.5k 1.7× 442 0.8× 135 1.0× 87 0.7× 67 1.9k
Ann Haskins Olney United States 19 716 0.8× 842 0.9× 214 0.4× 169 1.3× 142 1.1× 43 1.4k
H. Enders Germany 18 933 1.0× 899 1.0× 313 0.6× 100 0.7× 43 0.3× 40 1.5k
Melita Irving United Kingdom 20 1.2k 1.3× 977 1.1× 178 0.3× 264 2.0× 184 1.5× 80 1.8k
Udo Trautmann Germany 23 1.1k 1.2× 930 1.0× 328 0.6× 132 1.0× 111 0.9× 65 1.7k
Jacques C. Giltay Netherlands 23 760 0.8× 665 0.7× 306 0.6× 97 0.7× 70 0.6× 65 1.3k
M.H. Breuning Netherlands 16 1.7k 1.9× 1.4k 1.6× 207 0.4× 123 0.9× 118 0.9× 26 2.1k
L A Brueton United Kingdom 19 693 0.8× 728 0.8× 410 0.8× 154 1.1× 34 0.3× 25 1.3k
Jennifer M. Kalish United States 22 804 0.9× 976 1.1× 463 0.9× 131 1.0× 86 0.7× 82 1.4k

Countries citing papers authored by Emma Wakeling

Since Specialization
Citations

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

Fields of papers citing papers by Emma Wakeling

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Emma Wakeling

This figure shows the co-authorship network connecting the top 25 collaborators of Emma Wakeling. A scholar is included among the top collaborators of Emma Wakeling 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 Wakeling. Emma Wakeling 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.
Morton, Sarah U., Gregory Costain, Courtney E. French, et al.. (2024). Exome and Genome Sequencing to Diagnose the Genetic Basis of Neonatal Hypotonia. Neurology. 104(1). e210106–e210106.
2.
Al‐Balool, Haya H., Alice Gardham, Emma Wakeling, et al.. (2023). Expanding the allelic spectrum of ELOVL4‐related autosomal recessive neuro‐ichthyosis. Molecular Genetics & Genomic Medicine. 11(12). e2256–e2256. 4 indexed citations
3.
Wakeling, Emma, Kimberly Gilmour, Mark M. Davis, et al.. (2023). Combined novel homozygous variants in both SGPL1 and STAT1 presenting with severe combined immune deficiency: case report and literature review. Frontiers in Immunology. 14. 1186575–1186575. 2 indexed citations
4.
Calpena, Eduardo, et al.. (2022). Craniosynostosis, inner ear, and renal anomalies in a child with complete loss of SPRY1 (sprouty homolog 1) function. Journal of Medical Genetics. 60(7). 712–716. 2 indexed citations
5.
Sabanathan, Saraswathy, Kshitij Mankad, James Davison, et al.. (2022). Expanding the phenotype of children presenting with hypoventilation with biallelic TBCK pathogenic variants and literature review. Neuromuscular Disorders. 33(1). 50–57. 3 indexed citations
6.
Wakeling, Emma, Meriel McEntagart, Charles Shaw‐Smith, et al.. (2020). Missense substitutions at a conserved 14-3-3 binding site in HDAC4 cause a novel intellectual disability syndrome. SHILAP Revista de lepidopterología. 2(1). 100015–100015. 11 indexed citations
7.
Hietamäki, Johanna, Louise Gregory, Kirsi Vaaralahti, et al.. (2020). Loss-of-Function Variants in TBC1D32 Underlie Syndromic Hypopituitarism. The Journal of Clinical Endocrinology & Metabolism. 105(6). 1748–1758. 18 indexed citations
8.
Ansari, Morad, Hemant Bengani, Graeme R. Grimes, et al.. (2018). BRD4 interacts with NIPBL and BRD4 is mutated in a Cornelia de Lange–like syndrome. Nature Genetics. 50(3). 329–332. 89 indexed citations
9.
Musso, Camila Manso, Lucas Alvizi, Luciano Abreu Brito, et al.. (2018). Complexity of the 5′ Untranslated Region of EIF4A3, a Critical Factor for Craniofacial and Neural Development. Frontiers in Genetics. 9. 149–149. 6 indexed citations
10.
Gardham, Alice, et al.. (2013). Froster syndrome. Clinical Dysmorphology. 22(2). 84–86. 1 indexed citations
11.
Chen, Huijia, et al.. (2011). Exacerbation of X-linked ichthyosis phenotype in a female by inheritance of filaggrin and steroid sulfatase mutations. Journal of Dermatological Science. 64(3). 159–162. 15 indexed citations
12.
Parker, Lee D., Jitendra Mangwani, Emma Wakeling, & Dishan Singh. (2011). Hallux valgus interphalangeus and a novel mutation in HOXA13. Part of the broadening spectrum of Hand-Foot-Genital syndrome. Foot and Ankle Surgery. 17(2). e28–e30. 14 indexed citations
13.
Wakeling, Emma, Mariëlle Alders, Jet Bliek, et al.. (2010). Epigenotype–phenotype correlations in Silver–Russell syndrome. Journal of Medical Genetics. 47(11). 760–768. 120 indexed citations
14.
Turner, Claire, Deborah Mackay, Jonathan L A Callaway, et al.. (2010). Methylation analysis of 79 patients with growth restriction reveals novel patterns of methylation change at imprinted loci. European Journal of Human Genetics. 18(6). 648–655. 73 indexed citations
15.
Wakeling, Emma, et al.. (2008). Congenital microgastria in association with Pierre–Robin sequence. Clinical Dysmorphology. 17(2). 143–144. 8 indexed citations
16.
Lonie, Lorne, Daniel Porter, Maria Fraser, et al.. (2006). Determination of the mutation spectrum of theEXT1/EXT2genes in British Caucasian patients with multiple osteochondromas, and exclusion of six candidate genes inEXTnegative cases. Human Mutation. 27(11). 1160–1160. 45 indexed citations
17.
Noone, Peadar G., Zhaoqing Zhou, Emma Wakeling, et al.. (2000). Lung Disease Associated with the IVS8 5T Allele of the CFTR Gene. American Journal of Respiratory and Critical Care Medicine. 162(5). 1919–1924. 76 indexed citations
18.
Monk, David, Emma Wakeling, Virginia K. Proud, et al.. (2000). Duplication of 7p11.2-p13, Including GRB10, in Silver-Russell Syndrome. The American Journal of Human Genetics. 66(1). 36–46. 107 indexed citations
19.
Wakeling, Emma, et al.. (1998). Human EGFR, a candidate gene for the Silver-Russell syndrome, is biallelically expressed in a wide range of fetal tissues. European Journal of Human Genetics. 6(2). 158–164. 20 indexed citations
20.
Abu‐Amero, Sayeda, Michael Preece, Emma Wakeling, Gudrun E. Moore, & Philip Stanier. (1997). A common polymorphism in exon 16 of the human insulin-like growth factor-1 receptor gene (IGF1R). Molecular and Cellular Probes. 11(5). 381–383. 3 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Beate Albrecht Breakdown of academic impact, for papers by Christèle Dubourg Breakdown of academic impact, for papers by Ann Haskins Olney Breakdown of academic impact, for papers by H. Enders Breakdown of academic impact, for papers by Melita Irving Breakdown of academic impact, for papers by Udo Trautmann Breakdown of academic impact, for papers by Jacques C. Giltay Breakdown of academic impact, for papers by M.H. Breuning Breakdown of academic impact, for papers by L A Brueton Breakdown of academic impact, for papers by Jennifer M. Kalish
Rankless by CCL
2026