Matthew Bracher‐Smith

1.3k total citations
23 papers, 667 citations indexed

About

Matthew Bracher‐Smith is a scholar working on Genetics, Molecular Biology and Physiology. According to data from OpenAlex, Matthew Bracher‐Smith has authored 23 papers receiving a total of 667 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Genetics, 7 papers in Molecular Biology and 3 papers in Physiology. Recurrent topics in Matthew Bracher‐Smith's work include Genetic Associations and Epidemiology (11 papers), Genomics and Rare Diseases (8 papers) and Genomic variations and chromosomal abnormalities (6 papers). Matthew Bracher‐Smith is often cited by papers focused on Genetic Associations and Epidemiology (11 papers), Genomics and Rare Diseases (8 papers) and Genomic variations and chromosomal abnormalities (6 papers). Matthew Bracher‐Smith collaborates with scholars based in United Kingdom, Australia and Netherlands. Matthew Bracher‐Smith's co-authors include Valentina Escott‐Price, Karen Crawford, James Walters, Michael O’Donovan, George Kirov, Elliott Rees, Kimberley Kendall, Michael J. Owen, Sophie E. Legge and Antonio F. Pardiñas and has published in prestigious journals such as PLoS ONE, Scientific Reports and Human Molecular Genetics.

In The Last Decade

Matthew Bracher‐Smith

22 papers receiving 657 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Matthew Bracher‐Smith United Kingdom	13	346	190	139	122	57	23	667
Zachary F. Gerring Australia	14	175 0.5×	186 1.0×	110 0.8×	106 0.9×	44 0.8×	27	537
D. C. Rao United States	15	242 0.7×	119 0.6×	187 1.3×	81 0.7×	44 0.8×	29	751
Thomas Werge Denmark	7	439 1.3×	225 1.2×	160 1.2×	68 0.6×	36 0.6×	11	741
Hamel Patel United Kingdom	13	218 0.6×	193 1.0×	77 0.6×	39 0.3×	78 1.4×	27	623
Bram P. Prins United Kingdom	13	222 0.6×	197 1.0×	68 0.5×	38 0.3×	48 0.8×	20	699
Ofélia P. Carvalho United Kingdom	9	197 0.6×	363 1.9×	99 0.7×	128 1.0×	27 0.5×	9	858
Michael W. Nagle United States	9	316 0.9×	329 1.7×	85 0.6×	43 0.4×	72 1.3×	13	951
Patrick Sleiman United States	10	80 0.2×	157 0.8×	148 1.1×	314 2.6×	112 2.0×	16	719
L. Giuffra United States	12	393 1.1×	201 1.1×	149 1.1×	110 0.9×	43 0.8×	23	797
Berit Kerner United States	17	194 0.6×	175 0.9×	244 1.8×	42 0.3×	22 0.4×	35	646

Countries citing papers authored by Matthew Bracher‐Smith

Since Specialization

Citations

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

Fields of papers citing papers by Matthew Bracher‐Smith

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Matthew Bracher‐Smith. 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 Matthew Bracher‐Smith. The network helps show where Matthew Bracher‐Smith may publish in the future.

Co-authorship network of co-authors of Matthew Bracher‐Smith

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

All Works

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20 of 20 papers shown

Bracher‐Smith, Matthew & Valentina Escott‐Price. (2025). Decoding the genomic symphony: unravelling brain disorders through data integration and machine learning. Molecular Psychiatry. 30(12). 5914–5925.

Correia, Marta, Kamen A. Tsvetanov, Rafael Neto Henriques, et al.. (2025). Complementary MR measures of white matter and their relation to cardiovascular health and cognition. Scientific Reports. 15(1). 28890–28890. 1 indexed citations

Bracher‐Smith, Matthew, Yuelin Li, Kirsten Harvey, et al.. (2024). Transcriptomics and weighted protein network analyses of the LRRK2 protein interactome reveal distinct molecular signatures for sporadic and LRRK2 Parkinson’s Disease. npj Parkinson s Disease. 10(1). 144–144. 3 indexed citations

Cunningham, Adam, Sergio Marco Salas, Matthew Bracher‐Smith, et al.. (2023). Identifying the neurodevelopmental and psychiatric signatures of genomic disorders associated with intellectual disability: a machine learning approach. Molecular Autism. 14(1). 19–19. 8 indexed citations

Harrison, J., Sonya Foley, Emily Baker, et al.. (2023). Pathway-specific polygenic scores for Alzheimer’s disease are associated with changes in brain structure in younger and older adults. Brain Communications. 5(5). fcad229–fcad229. 3 indexed citations

Steventon, Jessica J., T. Lancaster, Matthew Bracher‐Smith, et al.. (2023). Menopause age, reproductive span and hormone therapy duration predict the volume of medial temporal lobe brain structures in postmenopausal women. Psychoneuroendocrinology. 158. 106393–106393. 6 indexed citations

Bracher‐Smith, Matthew, Ganna Leonenko, Emily Baker, et al.. (2022). Whole genome analysis in APOE4 homozygotes identifies the DAB1-RELN pathway in Alzheimer's disease pathogenesis. Neurobiology of Aging. 119. 67–76. 17 indexed citations

Caseras, Xavier, Sophie E. Legge, Matthew Bracher‐Smith, et al.. (2022). Copy Number Variants Increasing Risk for Schizophrenia: Shared and Distinct Effects on Brain Morphometry and Cognitive Performance. Biological Psychiatry Global Open Science. 3(4). 902–911. 1 indexed citations

Bracher‐Smith, Matthew, Elliott Rees, Georgina Menzies, et al.. (2022). Machine learning for prediction of schizophrenia using genetic and demographic factors in the UK biobank. Schizophrenia Research. 246. 156–164. 11 indexed citations

10.

Dennison, Charlotte, Sophie E. Legge, Matthew Bracher‐Smith, et al.. (2021). Association of genetic liability for psychiatric disorders with accelerometer-assessed physical activity in the UK Biobank. PLoS ONE. 16(3). e0249189–e0249189. 21 indexed citations

11.

Pardiñas, Antonio F., Sophie E. Legge, Matthew Bracher‐Smith, et al.. (2020). Polygenic risk for schizophrenia and subcortical brain anatomy in the UK Biobank cohort. Translational Psychiatry. 10(1). 309–309. 18 indexed citations

12.

Bellou, Eftychia, Emily Baker, Ganna Leonenko, et al.. (2020). Age-dependent effect of APOE and polygenic component on Alzheimer's disease. Neurobiology of Aging. 93. 69–77. 31 indexed citations

13.

Bracher‐Smith, Matthew, Karen Crawford, & Valentina Escott‐Price. (2020). Machine learning for genetic prediction of psychiatric disorders: a systematic review. Molecular Psychiatry. 26(1). 70–79. 93 indexed citations

14.

Caseras, Xavier, George Kirov, Kimberley Kendall, et al.. (2020). Effects of genomic copy number variants penetrant for schizophrenia on cortical thickness and surface area in healthy individuals: analysis of the UK Biobank. The British Journal of Psychiatry. 218(2). 104–111. 9 indexed citations

15.

Kendall, Kimberley, Matthew Bracher‐Smith, Amy Lynham, et al.. (2019). Cognitive performance and functional outcomes of carriers of pathogenic copy number variants: analysis of the UK Biobank. The British Journal of Psychiatry. 214(5). 297–304. 94 indexed citations

16.

Legge, Sophie E., Hannah Jones, Kimberley Kendall, et al.. (2019). Association of Genetic Liability to Psychotic Experiences With Neuropsychotic Disorders and Traits. JAMA Psychiatry. 76(12). 1256–1256. 104 indexed citations

17.

Kendall, Kimberley, Elliott Rees, Matthew Bracher‐Smith, et al.. (2019). Association of Rare Copy Number Variants With Risk of Depression. JAMA Psychiatry. 76(8). 818–818. 69 indexed citations

18.

Crawford, Karen, Matthew Bracher‐Smith, David Owen, et al.. (2018). Medical consequences of pathogenic CNVs in adults: analysis of the UK Biobank. Journal of Medical Genetics. 56(3). 131–138. 88 indexed citations

19.

Foley, Sonya, Matthew Bracher‐Smith, Katherine E. Tansey, et al.. (2018). Fractional anisotropy of the uncinate fasciculus and cingulum in bipolar disorder type I, type II, unaffected siblings and healthy controls. The British Journal of Psychiatry. 213(3). 548–554. 27 indexed citations

20.

Baker, Emily, Karl Michael Schmidt, Matthew Bracher‐Smith, et al.. (2018). Predictive modeling of schizophrenia from genomic data: Comparison of polygenic risk score with kernel support vector machines approach. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 180(1). 80–85. 23 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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