Matthew Bracher‐Smith

1.3k citations

23 papers · 667 indexed · h-index 13

Co-authors: Valentina Escott‐Price Karen Crawford James Walters Michael O’Donovan George Kirov Elliott Rees Kimberley Kendall Michael J. Owen
Topics: Genetic Associations and Epidemiology (11 papers)Genomics and Rare Diseases (8 papers)Genomic variations and chromosomal abnormalities (6 papers)
Cited by: Genetics Biological Psychiatry Health Informatics
Journals: PLoS ONE Scientific Reports Human Molecular Genetics
Partner nations: United Kingdom Australia Netherlands

In The Last Decade

Matthew Bracher‐Smith

22 papers receiving 657 citations

Peers

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

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	Decoding the genomic symphony: unravelling brain disorders through data integration and machine learning 2025 ·Molecular Psychiatry ·Matthew Bracher‐Smith,Valentina Escott‐Price	0
2	Complementary MR measures of white matter and their relation to cardiovascular health and cognition 2025 ·Scientific Reports ·(unknown),Marta Correia,Kamen A. Tsvetanov,Rafael Neto Henriques,(unknown),Matthew Bracher‐Smith,Valentina Escott‐Price,Yordan P. Raykov,Richard N. Henson	1
3	Transcriptomics and weighted protein network analyses of the LRRK2 protein interactome reveal distinct molecular signatures for sporadic and LRRK2 Parkinson’s Disease 2024 ·npj Parkinson s Disease ·(unknown),Matthew Bracher‐Smith,Yuelin Li,Kirsten Harvey,Valentina Escott‐Price,Patrick A. Lewis,Claudia Manzoni	3
4	Identifying the neurodevelopmental and psychiatric signatures of genomic disorders associated with intellectual disability: a machine learning approach 2023 ·Molecular Autism ·(unknown),Adam Cunningham,Sergio Marco Salas,Matthew Bracher‐Smith,Samuel J. R. A. Chawner,Jan Štochl,Tamsin Ford,F. Lucy Raymond,Valentina Escott‐Price,Marianne van den Bree	8
5	Pathway-specific polygenic scores for Alzheimer’s disease are associated with changes in brain structure in younger and older adults 2023 ·Brain Communications ·J. Harrison,Sonya Foley,Emily Baker,Matthew Bracher‐Smith,Peter Holmans,Evie Stergiakouli,David E.J. Linden,Xavier Caseras,Derek K. Jones,Valentina Escott‐Price	3
6	Menopause age, reproductive span and hormone therapy duration predict the volume of medial temporal lobe brain structures in postmenopausal women 2023 ·Psychoneuroendocrinology ·Jessica J. Steventon,T. Lancaster,(unknown),Matthew Bracher‐Smith,Valentina Escott‐Price,Katherine S. Ruth,William Davies,Xavier Caseras,Kevin Murphy	6
7	Whole genome analysis in APOE4 homozygotes identifies the DAB1-RELN pathway in Alzheimer's disease pathogenesis 2022 ·Neurobiology of Aging ·Matthew Bracher‐Smith,Ganna Leonenko,Emily Baker,Karen Crawford,Andrew Graham,Derviş A. Salih,Brian W. Howell,John Hardy,Valentina Escott‐Price	17
8	Copy Number Variants Increasing Risk for Schizophrenia: Shared and Distinct Effects on Brain Morphometry and Cognitive Performance 2022 ·Biological Psychiatry Global Open Science ·Xavier Caseras,Sophie E. Legge,Matthew Bracher‐Smith,Richard Anney,Michael J. Owen,Valentina Escott‐Price,George Kirov	1
9	Machine learning for prediction of schizophrenia using genetic and demographic factors in the UK biobank 2022 ·Schizophrenia Research ·Matthew Bracher‐Smith,Elliott Rees,Georgina Menzies,James Walters,Michael O’Donovan,Michael J. Owen,George Kirov,Valentina Escott‐Price	11
10	Association of genetic liability for psychiatric disorders with accelerometer-assessed physical activity in the UK Biobank 2021 ·PLoS ONE ·Charlotte Dennison,Sophie E. Legge,Matthew Bracher‐Smith,Georgina Menzies,Valentina Escott‐Price,Daniel J. Smıth,Aiden Doherty,Michael J. Owen,Michael O’Donovan,James Walters	21
11	Polygenic risk for schizophrenia and subcortical brain anatomy in the UK Biobank cohort 2020 ·Translational Psychiatry ·(unknown),(unknown),(unknown),Antonio F. Pardiñas,Sophie E. Legge,Matthew Bracher‐Smith,Georgina Menzies,Lynsey S. Hall,Andrew Pocklington,Richard Anney,Nicholas J. Bray,Valentina Escott‐Price,Xavier Caseras	18
12	Age-dependent effect of APOE and polygenic component on Alzheimer's disease 2020 ·Neurobiology of Aging ·Eftychia Bellou,Emily Baker,Ganna Leonenko,Matthew Bracher‐Smith,(unknown),Georgina Menzies,Julie Williams,Valentina Escott‐Price	31
13	Machine learning for genetic prediction of psychiatric disorders: a systematic review 2020 ·Molecular Psychiatry ·Matthew Bracher‐Smith,Karen Crawford,Valentina Escott‐Price	93
14	Effects of genomic copy number variants penetrant for schizophrenia on cortical thickness and surface area in healthy individuals: analysis of the UK Biobank 2020 ·The British Journal of Psychiatry ·Xavier Caseras,George Kirov,Kimberley Kendall,Elliott Rees,Sophie E. Legge,Matthew Bracher‐Smith,Valentina Escott‐Price,Kevin Murphy	9
15	Cognitive performance and functional outcomes of carriers of pathogenic copy number variants: analysis of the UK Biobank 2019 ·The British Journal of Psychiatry ·Kimberley Kendall,Matthew Bracher‐Smith,(unknown),Amy Lynham,Elliott Rees,Valentina Escott‐Price,Michael J. Owen,Michael O’Donovan,James Walters,George Kirov	94
16	Association of Genetic Liability to Psychotic Experiences With Neuropsychotic Disorders and Traits 2019 ·JAMA Psychiatry ·Sophie E. Legge,Hannah Jones,Kimberley Kendall,Antonio F. Pardiñas,Georgina Menzies,Matthew Bracher‐Smith,Valentina Escott‐Price,Elliott Rees,Katrina A. S. Davis,Matthew Hotopf,Jeanne E. Savage,Daniëlle Posthuma,Peter Holmans,George Kirov,Michael J. Owen,Michael O’Donovan,Stanley Zammit,James Walters	104
17	Association of Rare Copy Number Variants With Risk of Depression 2019 ·JAMA Psychiatry ·Kimberley Kendall,Elliott Rees,Matthew Bracher‐Smith,Sophie E. Legge,Lucy Riglin,Stanley Zammit,Michael O’Donovan,Michael John Owen,Ian Jones,George Kirov,James Walters	69
18	Medical consequences of pathogenic CNVs in adults: analysis of the UK Biobank 2018 ·Journal of Medical Genetics ·Karen Crawford,Matthew Bracher‐Smith,David Owen,Kimberley Kendall,Elliott Rees,Antonio F. Pardiñas,Mark Einon,Valentina Escott‐Price,James Walters,Michael O’Donovan,Michael J. Owen,George Kirov	88
19	Fractional anisotropy of the uncinate fasciculus and cingulum in bipolar disorder type I, type II, unaffected siblings and healthy controls 2018 ·The British Journal of Psychiatry ·Sonya Foley,Matthew Bracher‐Smith,Katherine E. Tansey,J. Harrison,Greg D. Parker,Xavier Caseras	27
20	Predictive modeling of schizophrenia from genomic data: Comparison of polygenic risk score with kernel support vector machines approach 2018 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·(unknown),Emily Baker,Karl Michael Schmidt,Matthew Bracher‐Smith,James Walters,Andreas Artemiou,Peter Holmans,Michael O’Donovan,Michael J. Owen,Andrew Pocklington,Valentina Escott‐Price	23

About Matthew Bracher‐Smith

Matthew Bracher‐Smith is a scholar working on Genetics, Biological Psychiatry and Health, Toxicology and Mutagenesis, having authored 23 papers that have together received 667 indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (11 papers), Genomics and Rare Diseases (8 papers) and Genomic variations and chromosomal abnormalities (6 papers). The work is most often cited by research in Genetics (346 citations), Biological Psychiatry (29 citations) and Health Informatics (15 citations). Matthew Bracher‐Smith has collaborated with scholars based in United Kingdom, Australia and Netherlands. Frequent 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. Their work appears in journals such as PLoS ONE, Scientific Reports and Human Molecular Genetics.

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