Kate Chandler

11.1k total citations
73 papers, 2.4k citations indexed

About

Kate Chandler is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Kate Chandler has authored 73 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Genetics, 27 papers in Molecular Biology and 13 papers in Surgery. Recurrent topics in Kate Chandler's work include Genomics and Rare Diseases (9 papers), Blood disorders and treatments (9 papers) and Genomic variations and chromosomal abnormalities (9 papers). Kate Chandler is often cited by papers focused on Genomics and Rare Diseases (9 papers), Blood disorders and treatments (9 papers) and Genomic variations and chromosomal abnormalities (9 papers). Kate Chandler collaborates with scholars based in United Kingdom, United States and Germany. Kate Chandler's co-authors include Holger A. Volk, Jill Clayton‐Smith, Annette Wessmann, Graeme C. Black, Clare Rusbridge, Stefan Meyer, Rodolfo Cappello, Juha Kolehmainen, Reijo Norio and Mette Warburg and has published in prestigious journals such as Nature Communications, Journal of Neuroscience and PLoS ONE.

In The Last Decade

Kate Chandler

72 papers receiving 2.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Kate Chandler United Kingdom 28 904 845 349 343 319 73 2.4k
Peter A. J. Leegwater Netherlands 30 1.0k 1.2× 2.0k 2.4× 268 0.8× 189 0.6× 127 0.4× 118 3.6k
Jacques Penderis United Kingdom 26 243 0.3× 448 0.5× 444 1.3× 413 1.2× 341 1.1× 96 2.5k
Veronika M. Stein Germany 25 262 0.3× 308 0.4× 308 0.9× 313 0.9× 258 0.8× 86 2.1k
Linda Clover United Kingdom 26 308 0.3× 564 0.7× 374 1.1× 75 0.2× 178 0.6× 43 3.0k
Sérgio Rosemberg Brazil 30 234 0.3× 948 1.1× 302 0.9× 220 0.6× 141 0.4× 129 2.7k
Margret L. Casal United States 25 716 0.8× 833 1.0× 85 0.2× 120 0.3× 128 0.4× 85 2.0k
Andrew J. Kornberg Australia 31 252 0.3× 1.3k 1.6× 818 2.3× 253 0.7× 134 0.4× 108 4.2k
Enrico Parano Italy 23 485 0.5× 592 0.7× 304 0.9× 216 0.6× 258 0.8× 91 2.1k
J Feingold France 27 866 1.0× 801 0.9× 438 1.3× 135 0.4× 192 0.6× 115 2.5k
Jean‐Marie Vanderwinden Belgium 32 681 0.8× 3.3k 3.9× 509 1.5× 904 2.6× 121 0.4× 81 5.7k

Countries citing papers authored by Kate Chandler

Since Specialization
Citations

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

Fields of papers citing papers by Kate Chandler

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kate Chandler

This figure shows the co-authorship network connecting the top 25 collaborators of Kate Chandler. A scholar is included among the top collaborators of Kate Chandler 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 Kate Chandler. Kate Chandler 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.
Chandler, Kate, Andrew Fennell, Tzung‐Chien Hsieh, et al.. (2024). Seven Novel Variants of Weiss‐Kruszka Syndrome and Phenotype Expansion. American Journal of Medical Genetics Part A. 197(2). e63856–e63856.
2.
Brasch‐Andersen, Charlotte, Niels Ove Illum, Tiffany Busa, et al.. (2021). Mono‐allelic loss of YTHDF3 and neurodevelopmental disorder: clinical features of four individuals with 8q12.3 deletions. Clinical Genetics. 101(2). 208–213. 2 indexed citations
3.
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
4.
Vasudevan, Pradeep, Kate Chandler, Deirdre E. Donnelly, et al.. (2017). De novo mutations in HNRNPU result in a neurodevelopmental syndrome. American Journal of Medical Genetics Part A. 173(11). 3003–3012. 30 indexed citations
5.
Stivaros, Stavros, Kate Chandler, Denise Bonney, et al.. (2015). Central nervous system abnormalities in Fanconi anaemia: patterns and frequency on magnetic resonance imaging. British Journal of Radiology. 88(1056). 20150088–20150088. 19 indexed citations
6.
Goede, Christian de, Wyatt W. Yue, Kate Chandler, et al.. (2015). Role of reverse phenotyping in interpretation of next generation sequencing data and a review of INPP5E related disorders. European Journal of Paediatric Neurology. 20(2). 286–295. 21 indexed citations
7.
Faúndes, Víctor, et al.. (2014). Raine syndrome: An overview. European Journal of Medical Genetics. 57(9). 536–542. 38 indexed citations
8.
Benigni, Livia, Kate Chandler, Jacqueline M. Cardwell, et al.. (2011). Distribution of syringomyelia along the entire spinal cord in clinically affected Cavalier King Charles Spaniels. The Veterinary Journal. 190(3). 359–363. 40 indexed citations
9.
Parry, A. T., A.R. Tanner, Kate Chandler, & Christopher R. Lamb. (2010). What Is Your Diagnosis?. Journal of the American Veterinary Medical Association. 237(4). 359–360. 7 indexed citations
10.
Wessmann, Annette, Holger A. Volk, Kate Chandler, Dave C. Brodbelt, & Balázs Szladovits. (2010). ORIGINAL RESEARCH: Significance of surface epithelial cells in canine cerebrospinal fluid and relationship to central nervous system disease. Veterinary Clinical Pathology. 39(3). 358–364. 3 indexed citations
11.
12.
Chang, Pishan, Kate Chandler, Robin S. B. Williams, & Matthew C. Walker. (2009). Inhibition of long‐term potentiation by valproic acid through modulation of cyclic AMP. Epilepsia. 51(8). 1533–1542. 16 indexed citations
13.
Balikova, Irina, Thomy de Ravel, Bernard Thienpont, et al.. (2009). Deletions in theVPS13B(COH1) gene as a cause of Cohen syndrome. Human Mutation. 30(9). E845–E854. 43 indexed citations
14.
Wessmann, Annette, Kate Chandler, & Laurent Garosi. (2008). Ischaemic and haemorrhagic stroke in the dog. The Veterinary Journal. 180(3). 290–303. 65 indexed citations
15.
Chandler, Kate, Karl Rakshi, Kelly Springell, et al.. (2005). Leucodysplasia, microcephaly, cerebral malformation (LMC): a novel recessive disorder linked to 2p16. Brain. 129(1). 272–277. 6 indexed citations
16.
Kolehmainen, Juha, Robert N. Wilkinson, Anna-Elina Lehesjoki, et al.. (2004). Delineation of Cohen Syndrome Following a Large-Scale Genotype-Phenotype Screen. The American Journal of Human Genetics. 75(1). 122–127. 69 indexed citations
17.
Kolehmainen, Juha, Graeme C. Black, Anne Saarinen, et al.. (2003). Cohen Syndrome Is Caused by Mutations in a Novel Gene, COH1, Encoding a Transmembrane Protein with a Presumed Role in Vesicle-Mediated Sorting and Intracellular Protein Transport. The American Journal of Human Genetics. 72(6). 1359–1369. 249 indexed citations
18.
Chandler, Kate, et al.. (2003). Diagnostic criteria, clinical characteristics, and natural history of Cohen syndrome. Journal of Medical Genetics. 40(4). 233–241. 100 indexed citations
19.
Rusbridge, Clare, J. V. DAVIES, Kate Chandler, et al.. (2000). Syringohydromyelia in Cavalier King Charles spaniels. Journal of the American Animal Hospital Association. 36(1). 34–41. 113 indexed citations
20.
Sailors, David M., et al.. (1993). Laparoscopic hernia repair: a preliminary report.. PubMed. 59(2). 85–9. 13 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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