Esther Kinning

3.7k total citations
28 papers, 556 citations indexed

About

Esther Kinning is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Esther Kinning has authored 28 papers receiving a total of 556 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Genetics, 12 papers in Molecular Biology and 6 papers in Surgery. Recurrent topics in Esther Kinning's work include Genetic Syndromes and Imprinting (5 papers), Renal and related cancers (5 papers) and Connective tissue disorders research (5 papers). Esther Kinning is often cited by papers focused on Genetic Syndromes and Imprinting (5 papers), Renal and related cancers (5 papers) and Connective tissue disorders research (5 papers). Esther Kinning collaborates with scholars based in United Kingdom, Australia and United States. Esther Kinning's co-authors include Richard C. Trembath, Eamonn R. Maher, Marco Sciacovelli, Gail Kirby, Edoardo Gaude, Jonathan Berg, Graeme R. Clark, Michael A. Simpson, Christian Frezza and Patrick J. Morrison and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

Esther Kinning

24 papers receiving 550 citations

Peers

Countries citing papers authored by Esther Kinning

Since Specialization

Citations

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

Fields of papers citing papers by Esther Kinning

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Esther Kinning

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

#	Work	Indexed citations
1	Vascular Ehlers Danlos Syndrome and Chromosome 2q32 Microdeletion Syndrome 2025 ·European Journal of Human Genetics ·(unknown), Shadi Albaba, Glenda Sobey, Jessica Bowen, Deirdre E. Donnelly, Marina Colombi, Marco Ritelli, (unknown), Neeti Ghali, Fleur S. van Dijk, Emma Hobson, (unknown), Esther Kinning, Abhijit Dixit, (unknown), Duncan Baker, Diana Johnson	0
2	Diagnosis of inborn errors of metabolism through prenatal exome sequencing with targeted analysis for fetal structural anomalies 2023 ·Prenatal Diagnosis ·Stephanie Allen, Natalie Chandler, Esther Kinning, Victoria Harrison, (unknown), Suresh Vijay, James Castleman, Deirdre Cilliers	3
3	Fetal hydrops caused by a novel pathogenic MECOM variant 2023 ·Prenatal Diagnosis ·(unknown), (unknown), Esther Kinning, Tamás Marton	2
4	Progressive osseous heteroplasia: A case report with an unexpected trigger 2023 ·Bone Reports ·(unknown), Angela Lucas-Herald, Paula Beattie, Helen McDevitt, Lorenzo Iughetti, (unknown), Esther Kinning, S. Faisal Ahmed, Avril Mason	3
5	Next Generation Sequencing after Invasive Prenatal Testing in Fetuses with Congenital Malformations: Prenatal or Neonatal Investigation 2022 ·Genes ·(unknown), James Castleman, Stephanie Allen, Denise Williams, Esther Kinning, Mark D. Kilby	12
6	First case of desmosterolosis diagnosed by prenatal whole exome sequencing 2022 ·American Journal of Medical Genetics Part A ·(unknown), (unknown), (unknown), Esther Kinning, Suresh Vijay, (unknown)	1
7	Heterozygous CTNNB1 and TBX4 variants in a patient with abnormal lung growth, pulmonary hypertension, microcephaly, and spasticity 2019 ·Clinical Genetics ·Justyna A. Karolak, Przemysław Szafrański, (unknown), Chirag Patel, (unknown), Esther Kinning, Kate Chandler, Shalini N. Jhangiani, Zeynep H. Coban Akdemir, James R. Lupski, Edwina J. Popek, Paweł Stankiewicz	12
8	Proteomic Evidence of Biological Aging in a Child with a Compound Heterozygous ZMPSTE24 Mutation 2018 ·PROTEOMICS - CLINICAL APPLICATIONS ·Angela Lucas-Herald, Petra Zürbig, Avril Mason, Esther Kinning, (unknown), (unknown), William Mullen, S. Faisal Ahmed, Christian Delles	5
9	Integrating population variation and protein structural analysis to improve clinical interpretation of missense variation: application to the WD40 domain 2016 ·Human Molecular Genetics ·Roman A. Laskowski, Nidhi Tyagi, Diana Johnson, Shelagh Joss, Esther Kinning, Catherine McWilliam, Miranda Splitt, Janet M. Thornton, Helen V. Firth, (unknown), (unknown)	19
10	Clinical features associated with CTNNB1 de novo loss of function mutations in ten individuals 2016 ·European Journal of Medical Genetics ·Mira Kharbanda, Daniela T. Pilz, Susan Tomkins, Kate Chandler, (unknown), Alan Fryer, Victoria McKay, Pedro Louro, Jill Smith, John Burn, Usha Kini, Anna de Burca, David Fitzpatrick, Esther Kinning	46
11	A Case of Functional Growth Hormone Deficiency and Early Growth Retardation in a Child With IFT172 Mutations 2015 ·The Journal of Clinical Endocrinology & Metabolism ·Angela Lucas-Herald, Esther Kinning, Aritoshi Iida, Zheng Wang, Noriko Miyake, Shiro Ikegawa, Jane McNeilly, S. Faisal Ahmed	23
12	Germline FH Mutations Presenting With Pheochromocytoma 2014 ·The Journal of Clinical Endocrinology & Metabolism ·Graeme R. Clark, Marco Sciacovelli, Edoardo Gaude, (unknown), Gail Kirby, Michael A. Simpson, Richard C. Trembath, Jonathan Berg, Emma R. Woodward, Esther Kinning, Patrick J. Morrison, Christian Frezza, Eamonn R. Maher	135
13	Exome Sequencing Identifies PDE4D Mutations as Another Cause of Acrodysostosis 2012 ·The American Journal of Human Genetics ·Caroline Michot, Carine Le Goff, Alice Goldenberg, Avinash Abhyankar, Céline Klein, Esther Kinning, Anne‐Marie Guerrot, (unknown), (unknown), Geneviève Baujat, Stanislas Lyonnet, Caroline Thalassinos, Patrick Nitschké, Jean‐Laurent Casanova, Martine Le Merrer, Arnold Münnich, Valérie Cormier‐Daire	84
14	A multidisciplinary approach to understanding skeletal dysplasias 2011 ·Expert Review of Endocrinology & Metabolism ·Esther Kinning, Helen McDevitt, (unknown), S. Faisal Ahmed	1
15	Novel features in auriculo-condylar syndrome 2010 ·Clinical Dysmorphology ·Ruth McGowan, Victoria Murday, Esther Kinning, (unknown), David Koppel, Margo Whiteford	6
16	Novel SPG11 mutations in Asian kindreds and disruption of spatacsin function in the zebrafish 2010 ·Neurogenetics ·Laura Southgate, Dimitra Dafou, Jacqueline Hoyle, Nan Li, Esther Kinning, Peter Critchley, Andrea H. Németh, Kevin Talbot, Parayil Sankaran Bindu, Sanjib Sinha, Arun B. Taly, (unknown), Ferenc Müller, Eamonn R. Maher, Richard C. Trembath	25
17	Review of perinatal management of arthrogryposis at a large UK teaching hospital serving a multiethnic population 2009 ·Prenatal Diagnosis ·Osric Navti, Esther Kinning, Pradeep Vasudevan, Margaret Barrow, Helen Porter, E. S. Howarth, Justin C. Konje, M. Khare	14
18	Arthrogryposis in association with Peters' anomaly 2008 ·Clinical Dysmorphology ·Esther Kinning, Margaret Barrow	0
19	8p23.1 duplication syndrome; a novel genomic condition with unexpected complexity revealed by array CGH 2007 ·European Journal of Human Genetics ·John Barber, Viv Maloney, Shuwen Huang, David J. Bunyan, Lara Cresswell, Esther Kinning, (unknown), Tim Cheetham, (unknown), Sally Ann Lynch, (unknown), Laura Prescott, Yanick J. Crow, (unknown), Emma Hobson	67
20	Genomic duplication in Dyggve Melchior Clausen syndrome, a novel mutation mechanism in an autosomal recessive disorder 2005 ·Journal of Medical Genetics ·Esther Kinning	18

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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