David St Clair

14.4k total citations · 1 hit paper
114 papers, 4.6k citations indexed

About

David St Clair is a scholar working on Molecular Biology, Physiology and Genetics. According to data from OpenAlex, David St Clair has authored 114 papers receiving a total of 4.6k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Molecular Biology, 26 papers in Physiology and 22 papers in Genetics. Recurrent topics in David St Clair's work include Alzheimer's disease research and treatments (21 papers), Genetics and Neurodevelopmental Disorders (10 papers) and Birth, Development, and Health (8 papers). David St Clair is often cited by papers focused on Alzheimer's disease research and treatments (21 papers), Genetics and Neurodevelopmental Disorders (10 papers) and Birth, Development, and Health (8 papers). David St Clair collaborates with scholars based in United Kingdom, China and United States. David St Clair's co-authors include Myles Genest, Gerome Breen, Phil Benson, Douglas Blackwood, Ezra Susser, Anthony J. Brookes, Mandy Johnstone, David Collier, Lin He and Guo-Yin Feng and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of the American Chemical Society and JAMA.

In The Last Decade

David St Clair

111 papers receiving 4.5k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Rates of Adult Schizophrenia Following Prenatal Exposure to the Chinese Famine of 1959-1961

2005 536 citations David St Clair profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
David St Clair United Kingdom	40	1.6k	1.0k	751	738	728	114	4.6k
Marco Aurélio Romano‐Silva Brazil	38	1.9k 1.2×	971 1.0×	1.3k 1.7×	664 0.9×	828 1.1×	270	5.5k
Dimitrios Avramopoulos United States	37	1.5k 0.9×	1.5k 1.5×	502 0.7×	476 0.6×	1.0k 1.4×	114	4.1k
Katsuaki Suzuki Japan	35	1.4k 0.9×	1.1k 1.1×	1.3k 1.8×	461 0.6×	852 1.2×	160	5.4k
Hideo Matsuzaki Japan	34	2.4k 1.6×	1.1k 1.1×	1.0k 1.4×	363 0.5×	472 0.6×	125	5.3k
Margaret M. Ryan Australia	30	1.9k 1.2×	651 0.6×	656 0.9×	489 0.7×	524 0.7×	62	4.4k
Daniël van den Hove Netherlands	45	2.1k 1.3×	652 0.6×	923 1.2×	856 1.2×	404 0.6×	138	5.9k
Panos Roussos United States	44	2.4k 1.6×	1.2k 1.2×	822 1.1×	626 0.8×	696 1.0×	140	5.0k
Shinichiro Nanko Japan	34	1.1k 0.7×	955 0.9×	1.0k 1.4×	418 0.6×	974 1.3×	98	3.5k
Bru Cormand Spain	36	1.9k 1.2×	896 0.9×	824 1.1×	687 0.9×	1.5k 2.1×	147	4.7k
Ira T. Lott United States	48	2.6k 1.7×	1.4k 1.4×	739 1.0×	1.9k 2.6×	1.2k 1.7×	148	8.0k

Countries citing papers authored by David St Clair

Since Specialization

Citations

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

Fields of papers citing papers by David St Clair

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by David St Clair. 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 David St Clair. The network helps show where David St Clair may publish in the future.

Co-authorship network of co-authors of David St Clair

This figure shows the co-authorship network connecting the top 25 collaborators of David St Clair. A scholar is included among the top collaborators of David St Clair 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 David St Clair. David St Clair 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

Lyu, Hailong, David St Clair, Renrong Wu, et al.. (2023). Eye Movement Abnormalities Can Distinguish First-Episode Schizophrenia, Chronic Schizophrenia, and Prodromal Patients From Healthy Controls. Schizophrenia Bulletin Open. 4(1). sgac076–sgac076. 7 indexed citations

MacBeth, Angus, Paula McSkimming, Siladitya Bhattacharya, et al.. (2022). General and age-specific fertility rates in non-affective psychosis: population-based analysis of Scottish women. Social Psychiatry and Psychiatric Epidemiology. 58(1). 105–112.

Gunasekara, Chathura, Eilís Hannon, Harry A. Mackay, et al.. (2021). A machine learning case–control classifier for schizophrenia based on DNA methylation in blood. Translational Psychiatry. 11(1). 412–412. 14 indexed citations

Clair, David St, et al.. (2016). A study of type-1 diabetes associated autoantibodies in schizophrenia. Schizophrenia Research. 176(2-3). 186–190. 16 indexed citations

Nicodemus, Kristin K., Joseph H. Callicott, Augustin Luna, et al.. (2010). Evidence of statistical epistasis between DISC1, CIT and NDEL1 impacting risk for schizophrenia: biological validation with functional neuroimaging. Human Genetics. 127(4). 441–452. 85 indexed citations

Neves-Pereira, Maria, Berndt Müller, Justin H. G. Williams, et al.. (2009). Deregulation of EIF4E: a novel mechanism for autism. Journal of Medical Genetics. 46(11). 759–765. 112 indexed citations

Knight, Helen Miranda, Ben Pickard, Alan Maclean, et al.. (2009). A Cytogenetic Abnormality and Rare Coding Variants Identify ABCA13 as a Candidate Gene in Schizophrenia, Bipolar Disorder, and Depression. The American Journal of Human Genetics. 85(6). 833–846. 88 indexed citations

Datta, Susmita, Andrew McQuillin, Mie Rizig, et al.. (2008). A threonine to isoleucine missense mutation in the pericentriolar material 1 gene is strongly associated with schizophrenia. Molecular Psychiatry. 15(6). 615–628. 45 indexed citations

Bestelmeyer, Patricia E.G., Benjamin W. Tatler, Louise H. Phillips, et al.. (2006). Global visual scanning abnormalities in schizophrenia and bipolar disorder. Schizophrenia Research. 87(1-3). 212–222. 70 indexed citations

10.

Clair, David St, Peng Wang, Yaqin Yu, et al.. (2005). Rates of Adult Schizophrenia Following Prenatal Exposure to the Chinese Famine of 1959???1961. Obstetrical & Gynecological Survey. 61(1). 2–3. 11 indexed citations

11.

Nishiguchi, Naoki, Gerome Breen, Carsten Russ, David St Clair, & David Collier. (2005). Association analysis of the glycogen synthase kinase-3β gene in bipolar disorder. Neuroscience Letters. 394(3). 243–245. 25 indexed citations

12.

Chen, Qi, Guang He, Wei Qin, et al.. (2004). Family-Based Association Study of Synapsin II and Schizophrenia. The American Journal of Human Genetics. 75(5). 873–877. 41 indexed citations

13.

Gao, Jianjun, Fuchang Zhang, Tingwei Guo, et al.. (2004). Distribution of apolipoprotein E allele frequencies of the Han Chinese in an iodine-deficient mountainous area. Annals of Human Biology. 31(5). 578–585. 3 indexed citations

14.

Zhang, Yong, Antonia L. Pritchard, Sayeed Haque, et al.. (2004). Interleukin-6 promoter polymorphism: risk and pathology of Alzheimer's disease. Neuroscience Letters. 362(2). 99–102. 29 indexed citations

15.

Fox, Helen, et al.. (2003). Degradation of specific polyunsaturated fatty acids in red blood cells stored at −20°C proceeds faster in patients with schizophrenia when compared with healthy controls. Prostaglandins Leukotrienes and Essential Fatty Acids. 69(5). 291–297. 22 indexed citations

16.

Venneri, Annalena, et al.. (2002). Memory and dating of past events in schizophrenia. Journal of the International Neuropsychological Society. 8(6). 861–866. 6 indexed citations

17.

Thomas, Naomi, Christopher M. Morris, Francesco Scaravilli, et al.. (2000). Hereditary Vascular Dementia Linked to Notch 3 Mutations: CADASIL in British Families. Annals of the New York Academy of Sciences. 903(1). 293–298. 30 indexed citations

18.

Breen, Gerome, John Brown, Helen Fox, et al.. (1999). ?141 C Del/Ins polymorphism of the dopamine receptor 2 gene is associated with schizophrenia in a British population. American Journal of Medical Genetics. 88(4). 407–410. 52 indexed citations

19.

Price, Stacey, Henrik Fox, David St Clair, & Duncan J. Shaw. (1997). Lack of association between schizophrenia and a polymorphism close to the cytosolic phospholipase A2 gene. Psychiatric Genetics. 7(3). 111–114. 27 indexed citations

20.

Shibasaki, Yoshiro, et al.. (1995). High-resolution mapping of SNCA encoding α-synuclein, the non-Aβ component of Alzheimer’s disease amyloid precursor, to human chromosome 4q21.3→q22 by fluorescence in situ hybridization. Cytogenetic and Genome Research. 71(1). 54–55. 48 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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