Matthew Bracher‐Smith

1.3k citations

23 papers · 667 indexed · h-index 13

Genetics top 5%
- Genetic Associations and Epidemiology 11
- Genomics and Rare Diseases 8
- Genomic variations and chromosomal abnormalities 6
- Genetics and Neurodevelopmental Disorders 2
Biological Psychiatry
Health Informatics top 10%
Psychiatry and Mental health top 10%
Cognitive Neuroscience top 10%
Molecular Biology
- Bioinformatics and Genomic Networks 3
- Congenital heart defects research 2
Artificial Intelligence
- Machine Learning in Healthcare 2
Physiology
- Alzheimer's disease research and treatments 2

Co-authors: Valentina Escott‐Price Karen Crawford James Walters Michael O’Donovan George Kirov Elliott Rees Kimberley Kendall Michael J. Owen
Cited by: Genetics Biological Psychiatry Health Informatics
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

The 25 scholars most cited alongside Matthew Bracher‐Smith, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Matthew Bracher‐Smith Line = papers co-authored together Matthew Bracher‐Smith links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Decoding the genomic symphony: unravelling brain disorders through data integration and machine learning Matthew Bracher‐Smith,Valentina Escott‐Price	2025	0
2	Complementary MR measures of white matter and their relation to cardiovascular health and cognition Petar Raykov,Marta Correia,Kamen A. Tsvetanov,Rafael Neto Henriques,Alberto del Cerro‐León,Matthew Bracher‐Smith,Valentina Escott‐Price,Yordan P. Raykov,Richard N. Henson	2025	1
3	Transcriptomics and weighted protein network analyses of the LRRK2 protein interactome reveal distinct molecular signatures for sporadic and LRRK2 Parkinson’s Disease Yibo Zhao,Matthew Bracher‐Smith,Yuelin Li,Kirsten Harvey,Valentina Escott‐Price,Patrick A. Lewis,Claudia Manzoni	2024	3
4	Identifying the neurodevelopmental and psychiatric signatures of genomic disorders associated with intellectual disability: a machine learning approach Nicholas A Donnelly,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	2023	8
5	Pathway-specific polygenic scores for Alzheimer’s disease are associated with changes in brain structure in younger and older adults 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	2023	3
6	Menopause age, reproductive span and hormone therapy duration predict the volume of medial temporal lobe brain structures in postmenopausal women Jessica J. Steventon,T. Lancaster,Emily Simmonds Baker,Matthew Bracher‐Smith,Valentina Escott‐Price,Katherine S. Ruth,William Davies,Xavier Caseras,Kevin Murphy	2023	6
7	Whole genome analysis in APOE4 homozygotes identifies the DAB1-RELN pathway in Alzheimer's disease pathogenesis Matthew Bracher‐Smith,Ganna Leonenko,Emily Baker,Karen Crawford,Andrew Graham,Derviş A. Salih,Brian W. Howell,John Hardy,Valentina Escott‐Price	2022	17
8	Copy Number Variants Increasing Risk for Schizophrenia: Shared and Distinct Effects on Brain Morphometry and Cognitive Performance Xavier Caseras,Sophie E. Legge,Matthew Bracher‐Smith,Richard Anney,Michael J. Owen,Valentina Escott‐Price,George Kirov	2022	1
9	Machine learning for prediction of schizophrenia using genetic and demographic factors in the UK biobank Matthew Bracher‐Smith,Elliott Rees,Georgina Menzies,James Walters,Michael O’Donovan,Michael J. Owen,George Kirov,Valentina Escott‐Price	2022	11
10	Association of genetic liability for psychiatric disorders with accelerometer-assessed physical activity in the UK Biobank 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	2021	21
11	Polygenic risk for schizophrenia and subcortical brain anatomy in the UK Biobank cohort Steluta Grama,Isabella Willcocks,John Hubert,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	2020	18
12	Age-dependent effect of APOE and polygenic component on Alzheimer's disease Eftychia Bellou,Emily Baker,Ganna Leonenko,Matthew Bracher‐Smith,Paula Daunt,Georgina Menzies,Julie Williams,Valentina Escott‐Price	2020	31
13	Machine learning for genetic prediction of psychiatric disorders: a systematic review Matthew Bracher‐Smith,Karen Crawford,Valentina Escott‐Price	2020	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 Xavier Caseras,George Kirov,Kimberley Kendall,Elliott Rees,Sophie E. Legge,Matthew Bracher‐Smith,Valentina Escott‐Price,Kevin Murphy	2020	9
15	Cognitive performance and functional outcomes of carriers of pathogenic copy number variants: analysis of the UK Biobank Kimberley Kendall,Matthew Bracher‐Smith,H Fitzpatrick,Amy Lynham,Elliott Rees,Valentina Escott‐Price,Michael J. Owen,Michael O’Donovan,James Walters,George Kirov	2019	94
16	Association of Genetic Liability to Psychotic Experiences With Neuropsychotic Disorders and Traits 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	2019	104
17	Association of Rare Copy Number Variants With Risk of Depression 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	2019	69
18	Medical consequences of pathogenic CNVs in adults: analysis of the UK Biobank 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	2018	88
19	Fractional anisotropy of the uncinate fasciculus and cingulum in bipolar disorder type I, type II, unaffected siblings and healthy controls Sonya Foley,Matthew Bracher‐Smith,Katherine E. Tansey,J. Harrison,Greg D. Parker,Xavier Caseras	2018	27
20	Predictive modeling of schizophrenia from genomic data: Comparison of polygenic risk score with kernel support vector machines approach Timothy Vivian‐Griffiths,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	2018	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), Genomic variations and chromosomal abnormalities (6 papers), Bioinformatics and Genomic Networks (3 papers), Machine Learning in Healthcare (2 papers), Alzheimer's disease research and treatments (2 papers), Congenital heart defects research (2 papers) and Genetics and Neurodevelopmental Disorders (2 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.

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