Joanne Doherty

1.7k total citations
17 papers, 569 citations indexed

About

Joanne Doherty is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Joanne Doherty has authored 17 papers receiving a total of 569 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 8 papers in Molecular Biology and 6 papers in Cognitive Neuroscience. Recurrent topics in Joanne Doherty's work include Congenital heart defects research (8 papers), Genomic variations and chromosomal abnormalities (6 papers) and Genetics and Neurodevelopmental Disorders (5 papers). Joanne Doherty is often cited by papers focused on Congenital heart defects research (8 papers), Genomic variations and chromosomal abnormalities (6 papers) and Genetics and Neurodevelopmental Disorders (5 papers). Joanne Doherty collaborates with scholars based in United Kingdom, United States and Netherlands. Joanne Doherty's co-authors include Michael J. Owen, Marianne van den Bree, Anthony James, Mojtaba Zarei, Samuel J. R. A. Chawner, Louise Winmill, Isobel Heyman, David Mataix‐Cols, Paul M. Matthews and M. Hough and has published in prestigious journals such as Biological Psychiatry, The British Journal of Psychiatry and Neuropsychopharmacology.

In The Last Decade

Joanne Doherty

16 papers receiving 560 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Joanne Doherty United Kingdom	10	214	207	187	122	110	17	569
Jishui Zhang China	17	178 0.8×	420 2.0×	171 0.9×	182 1.5×	137 1.2×	53	856
William J. Cutter United Kingdom	12	305 1.4×	276 1.3×	212 1.1×	71 0.6×	86 0.8×	16	659
Kimon Runge Germany	16	66 0.3×	153 0.7×	132 0.7×	132 1.1×	92 0.8×	55	708
Marie-Christine Ottet Switzerland	10	95 0.4×	329 1.6×	206 1.1×	60 0.5×	95 0.9×	11	544
Marieke Klein Netherlands	17	231 1.1×	491 2.4×	156 0.8×	87 0.7×	427 3.9×	36	920
Kamran Razi United States	12	246 1.1×	205 1.0×	167 0.9×	55 0.5×	239 2.2×	15	639
Weiqiu Cheng Norway	13	192 0.9×	87 0.4×	126 0.7×	56 0.5×	101 0.9×	29	452
Birgit Ekholm Sweden	9	182 0.9×	120 0.6×	213 1.1×	88 0.7×	215 2.0×	10	666
Oswald Bloemen Netherlands	16	144 0.7×	380 1.8×	215 1.1×	73 0.6×	315 2.9×	29	797
Rikke Hilker Denmark	9	176 0.8×	98 0.5×	122 0.7×	65 0.5×	175 1.6×	18	478

Countries citing papers authored by Joanne Doherty

Since Specialization

Citations

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

Fields of papers citing papers by Joanne Doherty

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Joanne Doherty

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

All Works

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17 of 17 papers shown

Doherty, Joanne, Adam Cunningham, Samuel J. R. A. Chawner, et al.. (2023). Atypical cortical networks in children at high-genetic risk of psychiatric and neurodevelopmental disorders. Neuropsychopharmacology. 49(2). 368–376. 2 indexed citations

Kendall, Kimberley, et al.. (2023). The translation of psychiatric genetic findings to the clinic. Schizophrenia Research. 267. 470–472. 1 indexed citations

Raven, Erika P., Jelle Veraart, Rogier Kievit, et al.. (2023). In vivo evidence of microstructural hypo-connectivity of brain white matter in 22q11.2 deletion syndrome. Molecular Psychiatry. 28(10). 4342–4352. 9 indexed citations

Raven, Erika P., Jelle Veraart, Rogier Kievit, et al.. (2022). P417. In Vivo Evidence of Microstructural Hypo-Connectivity of Brain White Matter in 22q11.2 Deletion Syndrome. Biological Psychiatry. 91(9). S256–S256. 1 indexed citations

Chamberland, Maxime, Sila Genc, Chantal M. W. Tax, et al.. (2021). Detecting microstructural deviations in individuals with deep diffusion MRI tractometry. Nature Computational Science. 1(9). 598–606. 34 indexed citations

Chamberland, Maxime, Sila Genc, Erika P. Raven, et al.. (2020). Tractometry-based anomaly detection for single-subject white matter analysis. ORCA Online Research @Cardiff.

Dima, Diana C., Stefanie C. Linden, Jacqueline Smith, et al.. (2020). Electrophysiological network alterations in adults with copy number variants associated with high neurodevelopmental risk. Translational Psychiatry. 10(1). 324–324. 9 indexed citations

Niarchou, Maria, Samuel J. R. A. Chawner, Joanne Doherty, et al.. (2019). Psychiatric disorders in children with 16p11.2 deletion and duplication. Translational Psychiatry. 9(1). 8–8. 93 indexed citations

Chawner, Samuel J. R. A., Joanne Doherty, Hayley Moss, et al.. (2019). A GENETIC FIRST APPROACH TO DISSECTING THE HETEROGENEITY OF AUTISM: PHENOTYPIC COMPARISON OF AUTISM RISK COPY NUMBER VARIANTS. European Neuropsychopharmacology. 29. S783–S784. 5 indexed citations

10.

Chawner, Samuel J. R. A., Maria Niarchou, Joanne Doherty, et al.. (2018). The emergence of psychotic experiences in the early adolescence of 22q11.2 Deletion Syndrome. Journal of Psychiatric Research. 109. 10–17. 17 indexed citations

11.

Doherty, Joanne, et al.. (2018). Genomic and Imaging Biomarkers in Schizophrenia. Current topics in behavioral neurosciences. 40. 325–352. 8 indexed citations

12.

Doherty, Joanne, Miriam Cooper, & Anita Thapar. (2018). Advances in our understanding of the genetics of childhood neurodevelopmental disorders. Evidence-Based Mental Health. 21(4). 171–172. 5 indexed citations

13.

Chawner, Samuel J. R. A., Joanne Doherty, Hayley Moss, et al.. (2017). Childhood cognitive development in 22q11.2 deletion syndrome: Case–control study. The British Journal of Psychiatry. 211(4). 223–230. 27 indexed citations

14.

Doherty, Joanne & Michael J. Owen. (2014). Genomic insights into the overlap between psychiatric disorders: implications for research and clinical practice. Genome Medicine. 6(4). 29–29. 149 indexed citations

15.

Yip, Sarah W., Joanne Doherty, Judi Wakeley, et al.. (2012). Reduced Subjective Response to Acute Ethanol Administration Among Young Men with a Broad Bipolar Phenotype. Neuropsychopharmacology. 37(8). 1808–1815. 22 indexed citations

16.

Zarei, Mojtaba, David Mataix‐Cols, Isobel Heyman, et al.. (2011). Changes in Gray Matter Volume and White Matter Microstructure in Adolescents with Obsessive-Compulsive Disorder. Biological Psychiatry. 70(11). 1083–1090. 129 indexed citations

17.

Doherty, Joanne, et al.. (2011). Recent genomic advances in schizophrenia. Clinical Genetics. 81(2). 103–109. 58 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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