Jenny Morton

4.2k total citations
13 papers, 716 citations indexed

About

Jenny Morton is a scholar working on Genetics, Molecular Biology and Cell Biology. According to data from OpenAlex, Jenny Morton has authored 13 papers receiving a total of 716 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 6 papers in Molecular Biology and 3 papers in Cell Biology. Recurrent topics in Jenny Morton's work include Genetics and Neurodevelopmental Disorders (4 papers), Genomics and Rare Diseases (3 papers) and Cleft Lip and Palate Research (3 papers). Jenny Morton is often cited by papers focused on Genetics and Neurodevelopmental Disorders (4 papers), Genomics and Rare Diseases (3 papers) and Cleft Lip and Palate Research (3 papers). Jenny Morton collaborates with scholars based in United Kingdom, Australia and Belgium. Jenny Morton's co-authors include J. Curtis Nickel, Laura R. Iwasaki, Joan C. Han, James J. Cox, Julia M. Keogh, Giles S.H. Yeo, Anna Adlam, John R. Hodges, Y. C. Loraine Tung and I. Sadaf Farooqi and has published in prestigious journals such as Diabetes, British Journal of Dermatology and American Journal of Orthodontics and Dentofacial Orthopedics.

In The Last Decade

Jenny Morton

12 papers receiving 681 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jenny Morton United Kingdom 9 260 227 141 138 122 13 716
Tamara N. Kolli United States 16 67 0.3× 316 1.4× 25 0.2× 47 0.3× 292 2.4× 25 888
Cristiane Mota Leite Brazil 16 79 0.3× 148 0.7× 147 1.0× 89 0.6× 61 0.5× 40 752
Mitsuhiko Matsumoto Japan 13 33 0.1× 164 0.7× 29 0.2× 134 1.0× 175 1.4× 53 569
B Miśkowiak Poland 14 33 0.1× 135 0.6× 54 0.4× 63 0.5× 132 1.1× 62 513
Heming Wang United States 17 97 0.4× 275 1.2× 124 0.9× 126 0.9× 109 0.9× 68 828
Cláudio Aparecido Casatti Brazil 14 17 0.1× 107 0.5× 75 0.5× 103 0.7× 118 1.0× 31 539
Haydeé Rosas‐Vargas Mexico 17 321 1.2× 432 1.9× 34 0.2× 190 1.4× 114 0.9× 44 946
Masato Mitome Japan 13 29 0.1× 132 0.6× 191 1.4× 90 0.7× 117 1.0× 21 523
B. Fricke Germany 15 26 0.1× 181 0.8× 50 0.4× 197 1.4× 71 0.6× 30 576
Masakazu Tazaki Japan 19 10 0.0× 473 2.1× 86 0.6× 284 2.1× 210 1.7× 60 972

Countries citing papers authored by Jenny Morton

Since Specialization
Citations

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

Fields of papers citing papers by Jenny Morton

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jenny Morton

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

All Works

13 of 13 papers shown
1.
Ochoa, Eguzkine, Magdalena Badura‐Stronka, Deirdre Donnelly, et al.. (2023). Germline pathogenic variants in HNRNPU are associated with alterations in blood methylome. European Journal of Human Genetics. 31(9). 1040–1047. 5 indexed citations
2.
Morton, Jenny, et al.. (2019). The Influence of Epigenetic Factors in Four Pairs of Twins With Non-Syndromic Craniosynostosis. Journal of Craniofacial Surgery. 31(1). 283–285. 6 indexed citations
3.
Cox, Helen, Julie Vogt, Jenny Morton, et al.. (2019). Deep phenotyping of 14 new patients with IQSEC2 variants, including monozygotic twins of discordant phenotype. Clinical Genetics. 95(4). 496–506. 21 indexed citations
4.
Pagnamenta, Alistair T., Yoshiko Murakami, Consuelo Anzilotti, et al.. (2018). A homozygous variant disrupting the PIGH start-codon is associated with developmental delay, epilepsy, and microcephaly. Human Mutation. 39(6). 822–826. 17 indexed citations
5.
Suri, Mohnish, Roman A. Laskowski, Kate Baker, et al.. (2017). Protein structure and phenotypic analysis of pathogenic and population missense variants inSTXBP1. Molecular Genetics & Genomic Medicine. 5(5). 495–507. 20 indexed citations
6.
Brueton, Louise, Jenny Morton, Dominic McMullan, et al.. (2015). Xp11.2 microduplications including IQSEC2, TSPYL2 and KDM5C genes in patients with neurodevelopmental disorders. European Journal of Human Genetics. 24(3). 373–380. 48 indexed citations
7.
Syx, Delfien, Tim Van Damme, Sofie Symoens, et al.. (2015). Genetic Heterogeneity and Clinical Variability in Musculocontractural Ehlers-Danlos Syndrome Caused by Impaired Dermatan Sulfate Biosynthesis. Human Mutation. 36(5). 535–547. 63 indexed citations
8.
Wertheim‐Tysarowska, Katarzyna, Danielle Greenblatt, David Baty, et al.. (2014). Under‐recognition of acral peeling skin syndrome: 59 new cases with 15 novel mutations. British Journal of Dermatology. 171(5). 1206–1210. 13 indexed citations
9.
Fullston, Tod, Louise Brueton, Tracey Willis, et al.. (2009). Ohtahara syndrome in a family with an ARX protein truncation mutation (c.81C>G/p.Y27X). European Journal of Human Genetics. 18(2). 157–162. 26 indexed citations
10.
Slator, Rona, et al.. (2009). Understanding cleft lip and palate. 1: an overview.. PubMed. 19(3). 101–3. 6 indexed citations
11.
Slator, Rona, et al.. (2009). Understanding cleft lip and palate. 2: The first five years.. PubMed. 19(4). 122–5.
12.
Yeo, Giles S.H., James J. Cox, Jenny Morton, et al.. (2006). Hyperphagia, Severe Obesity, Impaired Cognitive Function, and Hyperactivity Associated With Functional Loss of One Copy of the Brain-Derived Neurotrophic Factor (BDNF) Gene. Diabetes. 55(12). 3366–3371. 379 indexed citations
13.
Iwasaki, Laura R., et al.. (2000). Human tooth movement in response to continuous stress of low magnitude. American Journal of Orthodontics and Dentofacial Orthopedics. 117(2). 175–183. 112 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 Tamara N. Kolli Breakdown of academic impact, for papers by Cristiane Mota Leite Breakdown of academic impact, for papers by Mitsuhiko Matsumoto Breakdown of academic impact, for papers by B Miśkowiak Breakdown of academic impact, for papers by Heming Wang Breakdown of academic impact, for papers by Cláudio Aparecido Casatti Breakdown of academic impact, for papers by Haydeé Rosas‐Vargas Breakdown of academic impact, for papers by Masato Mitome Breakdown of academic impact, for papers by B. Fricke Breakdown of academic impact, for papers by Masakazu Tazaki
Rankless by CCL
2026