Lindsey Kent

11.3k total citations
68 papers, 3.5k citations indexed

About

Lindsey Kent is a scholar working on Psychiatry and Mental health, Cognitive Neuroscience and Genetics. According to data from OpenAlex, Lindsey Kent has authored 68 papers receiving a total of 3.5k indexed citations (citations by other indexed papers that have themselves been cited), including 39 papers in Psychiatry and Mental health, 24 papers in Cognitive Neuroscience and 18 papers in Genetics. Recurrent topics in Lindsey Kent's work include Attention Deficit Hyperactivity Disorder (37 papers), Autism Spectrum Disorder Research (18 papers) and Genetics and Neurodevelopmental Disorders (14 papers). Lindsey Kent is often cited by papers focused on Attention Deficit Hyperactivity Disorder (37 papers), Autism Spectrum Disorder Research (18 papers) and Genetics and Neurodevelopmental Disorders (14 papers). Lindsey Kent collaborates with scholars based in United Kingdom, Ireland and United States. Lindsey Kent's co-authors include Michael Gill, Ziarih Hawi, Simon Baron‐Cohen, Nick Craddock, Anita Thapar, C. J. Feehan, Panos Vostanis, Frank Dudbridge, Michael O’Donovan and Bhismadev Chakrabarti and has published in prestigious journals such as PLoS ONE, American Journal of Psychiatry and Biological Psychiatry.

In The Last Decade

Lindsey Kent

68 papers receiving 3.4k citations

Peers

Lindsey Kent

PMH

GENET

CMN

Renato Borgatti Italy

Rosalind J. Neuman United States

Randal G. Ross United States

Umberto Balottin Italy

Richard Anney United Kingdom

Katja Becker Germany

Yuji Okazaki Japan

Sylvie Tordjman France

Konasale M. Prasad United States

Raun D. Melmed United States

Renato Borgatti Italy

Lindsey Kent

993 ×0.6

PMH

1.0k ×0.7

978 ×1.2

GENET

826 ×1.3

487 ×0.9

CMN

Citations per year, relative to Lindsey Kent Lindsey Kent (= 1×) peers Renato Borgatti

Countries citing papers authored by Lindsey Kent

Since Specialization

Citations

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

Fields of papers citing papers by Lindsey Kent

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lindsey Kent

This figure shows the co-authorship network connecting the top 25 collaborators of Lindsey Kent. A scholar is included among the top collaborators of Lindsey Kent 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 Lindsey Kent. Lindsey Kent 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:

20 of 20 papers shown

Kent, Lindsey, Kingshuk Roy Choudhury, Stephanie Melching‐Kollmuss, et al.. (2024). P02-30 Generation and evaluation of a historical control database for the creation of assay acceptance criteria for a comparative in vitro hepatic enzyme assay. Toxicology Letters. 399. S116–S116. 1 indexed citations

Hawi, Ziarih, Aurina Arnatkevičiūtė, Beth P. Johnson, et al.. (2018). A case–control genome-wide association study of ADHD discovers a novel association with the tenascin R (TNR) gene. Translational Psychiatry. 8(1). 284–284. 12 indexed citations

Hawi, Ziarih, Tarrant D.R. Cummins, Janette Tong, et al.. (2016). Rare DNA variants in the brain-derived neurotrophic factor gene increase risk for attention-deficit hyperactivity disorder: a next-generation sequencing study. Molecular Psychiatry. 22(4). 580–584. 21 indexed citations

Martin, Joanna, Miriam Cooper, Marian L. Hamshere, et al.. (2014). Biological Overlap of Attention-Deficit/Hyperactivity Disorder and Autism Spectrum Disorder: Evidence From Copy Number Variants. Journal of the American Academy of Child & Adolescent Psychiatry. 53(7). 761–770.e26. 80 indexed citations

Stergiakouli, Evie, Marian L. Hamshere, Peter Holmans, et al.. (2011). Investigating the Contribution of Common Genetic Variants to the Risk and Pathogenesis of ADHD. American Journal of Psychiatry. 169(2). 186–194. 144 indexed citations

Brookes, Keeley J., et al.. (2010). Polymorphisms of the steroid sulfatase (STS) gene are associated with attention deficit hyperactivity disorder and influence brain tissue mRNA expression. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 153B(8). 1417–1424. 26 indexed citations

Tansey, Katherine E., Keeley J. Brookes, Matthew Hill, et al.. (2010). Oxytocin receptor (OXTR) does not play a major role in the aetiology of autism: Genetic and molecular studies. Neuroscience Letters. 474(3). 163–167. 78 indexed citations

Hawi, Ziarih, Lindsey Kent, Matthew Hill, et al.. (2009). ADHD and DAT1: Further evidence of paternal over‐transmission of risk alleles and haplotype. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 153B(1). 97–102. 30 indexed citations

Kent, Lindsey, Emma Weisblatt, Greg Pasco, et al.. (2008). X-linked ichthyosis (steroid sulfatase deficiency) is associated with increased risk of attention deficit hyperactivity disorder, autism and social communication deficits. Journal of Medical Genetics. 45(8). 519–524. 108 indexed citations

10.

DeVito, Elise E., Andrew D. Blackwell, Lindsey Kent, et al.. (2008). The Effects of Methylphenidate on Decision Making in Attention-Deficit/Hyperactivity Disorder. Biological Psychiatry. 64(7). 636–639. 108 indexed citations

11.

Kent, Lindsey, Sarah Bowdin, Gail Kirby, Wendy N. Cooper, & Eamonn R. Maher. (2008). Beckwith Weidemann syndrome: A behavioral phenotype–genotype study. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 147B(7). 1295–1297. 53 indexed citations

12.

Kent, Lindsey. (2004). Recent advances in the genetics of attention deficit hyperactivity disorder. Current Psychiatry Reports. 6(2). 143–148. 14 indexed citations

13.

Humphreys, Glyn W., et al.. (2004). Visual search, singleton capture, and the control of attentional set in ADHD. Cognitive Neuropsychology. 21(6). 661–687. 29 indexed citations

14.

Kent, Lindsey. (2003). Is there a relationship between attention deficit hyperactivity disorder and bipolar disorder?. Journal of Affective Disorders. 73(3). 211–221. 90 indexed citations

15.

Mill, Jonathan, Sarah Curran, Lindsey Kent, et al.. (2002). Association study of a SNAP‐25 microsatellite and attention deficit hyperactivity disorder. American Journal of Medical Genetics. 114(3). 269–271. 74 indexed citations

16.

Holmes, Jane, Antony Payton, Jennifer H. Barrett, et al.. (2002). Association of DRD4 in children with ADHD and comorbid conduct problems. American Journal of Medical Genetics. 114(2). 150–153. 80 indexed citations

17.

Thapar, Anita, Jane Holmes, Antony Payton, et al.. (2001). Evidence of association between DRD4 and ADHD with conduct disturbance. Behavior Genetics. 31(4). 470–471. 2 indexed citations

18.

Kent, Lindsey, Elaine Green, Jane Holmes, et al.. (2001). No association between CHRNA7 microsatellite markers and attention‐deficit hyperactivity disorder. American Journal of Medical Genetics. 105(8). 686–689. 21 indexed citations

19.

Kent, Lindsey, et al.. (1998). Eyelid myoclonia with absences: phenomenology in children. Seizure. 7(3). 193–199. 15 indexed citations

20.

Kent, Lindsey, et al.. (1995). DEMONSTRATION OF HOMOLOGY BETWEEN IS6110 OF MYCOBACTERIUM-TUBERCULOSIS AND DNAS OF OTHER MYCOBACTERIUM SPP (VOL 33, PG 2290, 1995). UCL Discovery (University College London). 5 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.

Explore authors with similar magnitude of impact