Aimée L Fenwick

1.5k total citations
11 papers, 286 citations indexed

About

Aimée L Fenwick is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Aimée L Fenwick has authored 11 papers receiving a total of 286 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 6 papers in Molecular Biology and 3 papers in Surgery. Recurrent topics in Aimée L Fenwick's work include Craniofacial Disorders and Treatments (8 papers), Cleft Lip and Palate Research (6 papers) and Connective tissue disorders research (3 papers). Aimée L Fenwick is often cited by papers focused on Craniofacial Disorders and Treatments (8 papers), Cleft Lip and Palate Research (6 papers) and Connective tissue disorders research (3 papers). Aimée L Fenwick collaborates with scholars based in United Kingdom, Netherlands and United States. Aimée L Fenwick's co-authors include Andrew O.M. Wilkie, Steven A. Wall, Peter J. van der Spek, Louise M. Judd, Marja L. Mikkola, Louise Brueton, Irene M. J. Mathijssen, Sven Kreiborg, Neil V. Morgan and Irma Thesleff and has published in prestigious journals such as International Journal of Molecular Sciences, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

Aimée L Fenwick

11 papers receiving 284 citations

Peers

Countries citing papers authored by Aimée L Fenwick

Since Specialization

Citations

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

Fields of papers citing papers by Aimée L Fenwick

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Aimée L Fenwick. 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 Aimée L Fenwick. The network helps show where Aimée L Fenwick may publish in the future.

Co-authorship network of co-authors of Aimée L Fenwick

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

All Works

Sort: Min cites: Since: Top N: Style:

11 of 11 papers shown

#	Work	Indexed citations
1	Development of Erf-Mediated Craniosynostosis and Pharmacological Amelioration 2023 ·International Journal of Molecular Sciences ·(unknown), Kleoniki Keklikoglou, (unknown), (unknown), Athanasios Zacharopoulos, (unknown), (unknown), (unknown), (unknown), Melodie Richardson, Aimée L Fenwick, (unknown), Christos Arvanitidis, Jeremy Robertson, John Parthenios, Giannis Zacharakis, Stephen R.F. Twigg, Andrew O.M. Wilkie, George Mavrothalassitis	2
2	Disruption ofTWIST1translation by 5′ UTR variants in Saethre-Chotzen syndrome 2018 ·Human Mutation ·Yan Zhou, Nils Koelling, Aimée L Fenwick, Simon J. McGowan, Eduardo Calpena, Steven A. Wall, Sarah Smithson, Andrew O.M. Wilkie, Stephen R.F. Twigg	13
3	Localized TWIST1 and TWIST2 basic domain substitutions cause four distinct human diseases that can be modeled in Caenorhabditis elegans 2017 ·Human Molecular Genetics ·Sharon Kim, Stephen R.F. Twigg, (unknown), Aditi Chandra, Tyler Hansen, (unknown), Aimée L Fenwick, Simon J. McGowan, Helen Lord, Tracy Lester, Elizabeth Sweeney, Astrid Weber, Helen Cox, Andrew O.M. Wilkie, Andy Golden, Ann K. Corsi	18
4	Identification of Intragenic Exon Deletions and Duplication ofTCF12by Whole Genome or Targeted Sequencing as a Cause ofTCF12-Related Craniosynostosis 2016 ·Human Mutation ·Jacqueline A.C. Goos, Aimée L Fenwick, Sigrid M. A. Swagemakers, Simon J. McGowan, Samantha J.L. Knight, Stephen R.F. Twigg, A. Jeannette M. Hoogeboom, Marieke F. van Dooren, (unknown), Steven A. Wall, Irene M.J. Mathijssen, Andrew O.M. Wilkie, Peter J. van der Spek, Ans M.W. van den Ouweland	17
5	TCF12 microdeletion in a 72‐year‐old woman with intellectual disability 2015 ·American Journal of Medical Genetics Part A ·Juliette Piard, (unknown), A Czorny, Marion Lenoir, Mylène Valduga, Aimée L Fenwick, Andrew O.M. Wilkie, Lionel Van Maldergem	11
6	Apparently synonymous substitutions in FGFR2affect splicing and result in mild Crouzon syndrome 2014 ·BMC Medical Genetics ·Aimée L Fenwick, Jacqueline A.C. Goos, Julia Rankin, Helen Lord, Tracy Lester, A. Jeannette M. Hoogeboom, Ans MW van den Ouweland, Steven A. Wall, (unknown), Andrew O.M. Wilkie	12
7	Frank-ter Haar syndrome associated with sagittal craniosynostosis and raised intracranial pressure 2012 ·BMC Medical Genetics ·Charlotte L. Bendon, Aimée L Fenwick, Jane A. Hurst, Gudrun Nürnberg, Peter Nürnberg, Steven A. Wall, Andrew O.M. Wilkie, David Johnson	21
8	Homozygous SALL1 Mutation Causes a Novel Multiple Congenital Anomaly—Mental Retardation Syndrome 2012 ·The Journal of Pediatrics ·Julia Vodopiutz, Heinz Zoller, Aimée L Fenwick, (unknown), Max Schmid, Daniela Prayer, Thomas Müller, Andreas Repa, Arnold Pollak, Christoph Aufricht, Andrew O.M. Wilkie, Andreas Janecke	22
9	A deletion of FGFR2 creating a chimeric IIIb/IIIc exon in a child with Apert syndrome 2011 ·BMC Medical Genetics ·Aimée L Fenwick, Sarah Bowdin, (unknown), Andrew O.M. Wilkie	14
10	Inactivation of IL11 Signaling Causes Craniosynostosis, Delayed Tooth Eruption, and Supernumerary Teeth 2011 ·The American Journal of Human Genetics ·Pekka Nieminen, Neil V. Morgan, Aimée L Fenwick, (unknown), (unknown), Marja L. Mikkola, Peter J. van der Spek, Andrew S. Giraud, Louise M. Judd, Sirpa Arte, Louise Brueton, Steven A. Wall, Irene M. J. Mathijssen, Eamonn R. Maher, Andrew O.M. Wilkie, Sven Kreiborg, Irma Thesleff	135
11	Novel Mutations in GJA1 Cause Oculodentodigital syndrome 2008 ·Journal of Dental Research ·Aimée L Fenwick, Rebecca J. Richardson, (unknown), Martin Barron, Michael J. Dixon	21

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