Jenny E.V. Morton

3.3k total citations
11 papers, 574 citations indexed

About

Jenny E.V. Morton is a scholar working on Genetics, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Jenny E.V. Morton has authored 11 papers receiving a total of 574 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 6 papers in Molecular Biology and 2 papers in Cellular and Molecular Neuroscience. Recurrent topics in Jenny E.V. Morton's work include Craniofacial Disorders and Treatments (5 papers), Connective tissue disorders research (2 papers) and Neonatal and fetal brain pathology (1 paper). Jenny E.V. Morton is often cited by papers focused on Craniofacial Disorders and Treatments (5 papers), Connective tissue disorders research (2 papers) and Neonatal and fetal brain pathology (1 paper). Jenny E.V. Morton collaborates with scholars based in United Kingdom, United States and France. Jenny E.V. Morton's co-authors include Neil V. Morgan, Andrew O.M. Wilkie, Irene M.J. Mathijssen, Steven A. Wall, Rajat Das Gupta, Paul Gissen, Deirdre Peake, Elisabeth Rosser, Lesley MacPherson and Christian J. Hendriksz and has published in prestigious journals such as Neurology, Ophthalmology and The American Journal of Human Genetics.

In The Last Decade

Jenny E.V. Morton

11 papers receiving 564 citations

Peers

Countries citing papers authored by Jenny E.V. Morton

Since Specialization

Citations

This map shows the geographic impact of Jenny E.V. 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 E.V. 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 E.V. Morton more than expected).

Fields of papers citing papers by Jenny E.V. Morton

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jenny E.V. Morton

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

All Works

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11 of 11 papers shown

#	Work	Indexed citations
1	Reassessing the association: Evaluation of a polyalanine deletion variant of RUNX2 in non‐syndromic sagittal and metopic craniosynostosis 2024 ·Journal of Anatomy ·(unknown), Emma McCann, Astrid Weber, Jenny E.V. Morton, Peter Noons, Louise C. Wilson, (unknown), Deirdre Cilliers, D. Gale Johnson, Julie Phipps, Deborah Shears, Gregory P.L. Thomas, Steven A. Wall, Stephen R.F. Twigg, Andrew O.M. Wilkie	2
2	Dissection of contiguous gene effects for deletions around ERF on chromosome 19 2021 ·Human Mutation ·Eduardo Calpena, Simon J. McGowan, Fiona Blanco‐Kelly, (unknown), Anne Dieux‐Coëslier, Rachel Harrison, Diana Johnson, Katherine Lachlan, Jenny E.V. Morton, Helen Stewart, Pradeep Vasudevan, Stephen R.F. Twigg, Andrew O.M. Wilkie	2
3	Unexpected role of SIX1 variants in craniosynostosis: expanding the phenotype of SIX1-related disorders 2021 ·Journal of Medical Genetics ·Eduardo Calpena, Maud Wurmser, Simon J. McGowan, (unknown), Débora Romeo Bertola, Michael L. Cunningham, (unknown), David Johnson, Jenny E.V. Morton, Maria Rita Passos‐Bueno, Andrew T. Timberlake, Richard P. Lifton, Steven A. Wall, Stephen R.F. Twigg, Pascal Maire, Andrew O.M. Wilkie	5
4	Biallelic mutations in CYP26B1: A differential diagnosis for Pfeiffer and Antley–Bixler syndromes 2016 ·American Journal of Medical Genetics Part A ·Jenny E.V. Morton, (unknown), Tim Morgan, Andrew J. Sutherland‐Smith, Stephen P. Robertson	17
5	Phenotypic spectrum of neurodegeneration associated with mutations in the PLA2G6 gene (PLAN) 2008 ·Neurology ·Manju A. Kurian, Neil V. Morgan, Lesley MacPherson, Katharine Foster, Deirdre Peake, Rajat Das Gupta, (unknown), Christian J. Hendriksz, Jenny E.V. Morton, Helen Kingston, Elisabeth Rosser, Evangeline Wassmer, Paul Gissen, E.R. Maher	168
6	RAB23 Mutations in Carpenter Syndrome Imply an Unexpected Role for Hedgehog Signaling in Cranial-Suture Development and Obesity 2007 ·The American Journal of Human Genetics ·Dagan Jenkins, Dominik Seelow, Fernanda Sarquis Jehee, Chad A. Perlyn, Luís Garcia Alonso, Daniela Franco Bueno, Dian Donnai, (unknown), Irene M.J. Mathijssen, Jenny E.V. Morton, Karen Helene Ørstavik, Elizabeth Sweeney, Steven A. Wall, Jeffrey L. Marsh, Peter Nürnberg, Maria Rita Passos‐Bueno, Andrew O.M. Wilkie	175
7	The Origin of EFNB1 Mutations in Craniofrontonasal Syndrome: Frequent Somatic Mosaicism and Explanation of the Paucity of Carrier Males 2006 ·The American Journal of Human Genetics ·Stephen R.F. Twigg, Kazuya Matsumoto, Alexa Kidd, Anne Goriely, Indira B. Taylor, Richard B. Fisher, A. Jeannette M. Hoogeboom, Irene M.J. Mathijssen, Maria Teresa Cruz Lourenço, Jenny E.V. Morton, Elizabeth Sweeney, Louise C. Wilson, Han G. Brunner, John B. Mulliken, Steven A. Wall, Andrew O.M. Wilkie	73
8	Mutations in the Embryonal Subunit of the Acetylcholine Receptor (CHRNG) Cause Lethal and Escobar Variants of Multiple Pterygium Syndrome 2006 ·The American Journal of Human Genetics ·Neil V. Morgan, Louise Brueton, P. Cox, Marie T. Greally, John Tolmie, Shanaz Pasha, Irene A. Aligianis, Hans van Bokhoven, Tamás Marton, Lihadh Al‐Gazali, Jenny E.V. Morton, Christine Oley, Colin A. Johnson, Richard C. Trembath, Han G. Brunner, Eamonn R. Maher	98
9	Familial Dandy–Walker syndrome: a case report supporting an autosomal inheritance 2005 ·Child s Nervous System ·(unknown), Edward J. St. George, (unknown), Anthony D. Hockley, Jenny E.V. Morton	5
10	Micro syndrome in Muslim Pakistan children11The authors have no proprietary interests in relation to this article and its content. 2001 ·Ophthalmology ·John R. Ainsworth, Jenny E.V. Morton, Peter Good, (unknown), N D George, Julian Hamilton‐Shield, John Bradbury, (unknown), (unknown)	21
11	Craniofacial dyssynostosis: A further case report 1998 ·American Journal of Medical Genetics ·Jenny E.V. Morton	8

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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