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 — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Esther Kinning United Kingdom 13 321 256 110 94 68 28 556
Soo‐Mi Park United Kingdom 15 464 1.4× 258 1.0× 74 0.7× 79 0.8× 147 2.2× 39 794
Sahar Mansour United Kingdom 11 575 1.8× 288 1.1× 81 0.7× 47 0.5× 39 0.6× 15 854
Mark J. McCabe United Kingdom 16 331 1.0× 259 1.0× 82 0.7× 100 1.1× 234 3.4× 22 707
Ruen Yao China 15 385 1.2× 334 1.3× 44 0.4× 61 0.6× 55 0.8× 64 657
Meena Balasubramanian United Kingdom 18 310 1.0× 555 2.2× 79 0.7× 50 0.5× 45 0.7× 74 802
Jesse J. Savage United States 12 301 0.9× 213 0.8× 82 0.7× 52 0.6× 281 4.1× 23 658
Marta Albajar Spain 11 481 1.5× 110 0.4× 106 1.0× 84 0.9× 43 0.6× 22 698
A Munnich France 14 685 2.1× 347 1.4× 254 2.3× 41 0.4× 38 0.6× 37 1.1k
Tawfeg Ben‐Omran Qatar 11 353 1.1× 225 0.9× 43 0.4× 47 0.5× 19 0.3× 24 584
Grzegorz Burzynski United States 13 275 0.9× 154 0.6× 257 2.3× 32 0.3× 65 1.0× 16 680

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

20 of 20 papers shown
1.
Albaba, Shadi, Glenda Sobey, Jessica Bowen, et al.. (2025). Vascular Ehlers Danlos Syndrome and Chromosome 2q32 Microdeletion Syndrome. European Journal of Human Genetics. 33(10). 1309–1315.
2.
Allen, Stephanie, Natalie Chandler, Esther Kinning, et al.. (2023). Diagnosis of inborn errors of metabolism through prenatal exome sequencing with targeted analysis for fetal structural anomalies. Prenatal Diagnosis. 44(4). 432–442. 3 indexed citations
3.
Kinning, Esther, et al.. (2023). Fetal hydrops caused by a novel pathogenic MECOM variant. Prenatal Diagnosis. 43(6). 717–720. 2 indexed citations
4.
Lucas-Herald, Angela, Paula Beattie, Helen McDevitt, et al.. (2023). Progressive osseous heteroplasia: A case report with an unexpected trigger. Bone Reports. 18. 101665–101665. 3 indexed citations
5.
6.
Kinning, Esther, et al.. (2022). First case of desmosterolosis diagnosed by prenatal whole exome sequencing. American Journal of Medical Genetics Part A. 191(3). 859–863. 1 indexed citations
7.
Karolak, Justyna A., Przemysław Szafrański, Chirag Patel, et al.. (2019). Heterozygous CTNNB1 and TBX4 variants in a patient with abnormal lung growth, pulmonary hypertension, microcephaly, and spasticity. Clinical Genetics. 96(4). 366–370. 12 indexed citations
8.
Lucas-Herald, Angela, Petra Zürbig, Avril Mason, et al.. (2018). Proteomic Evidence of Biological Aging in a Child with a Compound Heterozygous ZMPSTE24 Mutation. PROTEOMICS - CLINICAL APPLICATIONS. 13(2). e1800135–e1800135. 5 indexed citations
9.
Laskowski, Roman A., Nidhi Tyagi, Diana Johnson, et al.. (2016). Integrating population variation and protein structural analysis to improve clinical interpretation of missense variation: application to the WD40 domain. Human Molecular Genetics. 25(5). 927–935. 19 indexed citations
10.
Kharbanda, Mira, Daniela T. Pilz, Susan Tomkins, et al.. (2016). Clinical features associated with CTNNB1 de novo loss of function mutations in ten individuals. European Journal of Medical Genetics. 60(2). 130–135. 46 indexed citations
11.
Lucas-Herald, Angela, Esther Kinning, Aritoshi Iida, et al.. (2015). A Case of Functional Growth Hormone Deficiency and Early Growth Retardation in a Child With IFT172 Mutations. The Journal of Clinical Endocrinology & Metabolism. 100(4). 1221–1224. 23 indexed citations
12.
Clark, Graeme R., Marco Sciacovelli, Edoardo Gaude, et al.. (2014). Germline FH Mutations Presenting With Pheochromocytoma. The Journal of Clinical Endocrinology & Metabolism. 99(10). E2046–E2050. 135 indexed citations
13.
Michot, Caroline, Carine Le Goff, Alice Goldenberg, et al.. (2012). Exome Sequencing Identifies PDE4D Mutations as Another Cause of Acrodysostosis. The American Journal of Human Genetics. 90(4). 740–745. 84 indexed citations
14.
Kinning, Esther, et al.. (2011). A multidisciplinary approach to understanding skeletal dysplasias. Expert Review of Endocrinology & Metabolism. 6(5). 731–743. 1 indexed citations
15.
McGowan, Ruth, et al.. (2010). Novel features in auriculo-condylar syndrome. Clinical Dysmorphology. 20(1). 1–10. 6 indexed citations
16.
Southgate, Laura, Dimitra Dafou, Jacqueline Hoyle, et al.. (2010). Novel SPG11 mutations in Asian kindreds and disruption of spatacsin function in the zebrafish. Neurogenetics. 11(4). 379–389. 25 indexed citations
17.
Navti, Osric, Esther Kinning, Pradeep Vasudevan, et al.. (2009). Review of perinatal management of arthrogryposis at a large UK teaching hospital serving a multiethnic population. Prenatal Diagnosis. 30(1). 49–56. 14 indexed citations
18.
Kinning, Esther & Margaret Barrow. (2008). Arthrogryposis in association with Peters' anomaly. Clinical Dysmorphology. 17(3). 177–179.
19.
Barber, John, Viv Maloney, Shuwen Huang, et al.. (2007). 8p23.1 duplication syndrome; a novel genomic condition with unexpected complexity revealed by array CGH. European Journal of Human Genetics. 16(1). 18–27. 67 indexed citations
20.
Kinning, Esther. (2005). Genomic duplication in Dyggve Melchior Clausen syndrome, a novel mutation mechanism in an autosomal recessive disorder. Journal of Medical Genetics. 42(12). e70–e70. 18 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.

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