Sebastian May-Wilson

ORCID: 0000-0003-2668-5717
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About
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Research Areas
  • Genetic Associations and Epidemiology
  • Cancer-related molecular mechanisms research
  • Colorectal Cancer Treatments and Studies
  • Epigenetics and DNA Methylation
  • PI3K/AKT/mTOR signaling in cancer
  • Chronic Obstructive Pulmonary Disease (COPD) Research
  • Synthesis and Biological Activity
  • Adipose Tissue and Metabolism
  • Sensory Analysis and Statistical Methods
  • Obesity, Physical Activity, Diet
  • Asthma and respiratory diseases
  • Cancer, Lipids, and Metabolism
  • Peroxisome Proliferator-Activated Receptors
  • Regulation of Appetite and Obesity
  • Biochemical Analysis and Sensing Techniques
  • Bioinformatics and Genomic Networks
  • Gene expression and cancer classification
  • Genetics and Neurodevelopmental Disorders
  • Protein Kinase Regulation and GTPase Signaling
  • Genetic Mapping and Diversity in Plants and Animals
  • Neonatal Respiratory Health Research
  • Lipid metabolism and disorders
  • Nutrition, Genetics, and Disease
  • Olfactory and Sensory Function Studies

University of Edinburgh
2019-2024

Cancer Research UK Scotland Institute
2020-2023

Centre for Global Health Research
2019-2022

Institute of Cancer Research
2017

Abstract We present the results of a GWAS food liking conducted on 161,625 participants from UK-Biobank. Liking was assessed over 139 specific foods using 9-point scale. Genetic correlations coupled with structural equation modelling identified multi-level hierarchical map food-liking three main dimensions: “Highly-palatable”, “Acquired” and “Low-caloric”. The Highly-palatable dimension is genetically uncorrelated other two, suggesting that independent processes underlie high reward foods....

10.1038/s41467-022-30187-w article EN cc-by Nature Communications 2022-05-18

Abstract KRAS-mutant colorectal cancers are resistant to therapeutics, presenting a significant problem for ∼40% of cases. Rapalogs, which inhibit mTORC1 and thus protein synthesis, significantly less potent in cancer. Using Kras-mutant mouse models mouse- patient-derived organoids, we demonstrate that KRAS with G12D mutation fundamentally rewires translation increase both bulk mRNA-specific initiation. This occurs via the MNK/eIF4E pathway culminating sustained expression c-MYC. By genetic...

10.1158/2159-8290.cd-20-0652 article EN Cancer Discovery 2020-12-16

Background: Lung function is highly heritable and differs between the sexes throughout life. However, little known about sex-differential genetic effects on lung function. We aimed to conduct first genome-wide genotype-by-sex interaction study identify that differ males females. Methods: tested for interactions 7,745,864 variants sex spirometry-based measures of in UK Biobank (N=303,612), sought replication 75,696 independent individuals from SpiroMeta consortium. Results: Five...

10.12688/wellcomeopenres.15846.1 preprint EN cc-by Wellcome Open Research 2020-06-01

Abstract Genetically predicted levels of multi-omic traits can uncover the molecular underpinnings common phenotypes in a highly efficient manner. Here, we utilised large cohort (INTERVAL; N=50,000 participants) with extensive data for plasma proteomics (SomaScan, N=3,175; Olink, N=4,822), metabolomics (Metabolon HD4, N=8,153), serum (Nightingale, N=37,359), and whole blood Illumina RNA sequencing (N=4,136). We used machine learning to train genetic scores 17,227 traits, including 10,521...

10.1101/2022.04.17.488593 preprint EN cc-by bioRxiv (Cold Spring Harbor Laboratory) 2022-04-17
Nick Shrine Abril G. Izquierdo Jing Chen Richard Packer Robert J. Hall and 95 more Anna L. Guyatt Chiara Batini Rebecca Thompson Chandan Pavuluri Vidhi Malik Brian D. Hobbs Matthew Moll Wonji Kim Ruth Tal‐Singer Per Bakke Katherine A. Fawcett Catherine John Kayesha Coley Noemi Nicole Piga Alfred Pozarickij Kuang Lin Iona Y. Millwood Zhengming Chen Liming Li Sara RA Wielscher Lies Lahousse Guy Brusselle André G. Uitterlinden Ani Manichaikul Elizabeth C. Oelsner Stephen S. Rich R. Graham Barr Shona M. Kerr Véronique Vitart Michael R. Brown Matthias Wielscher Medea Imboden Ayoung Jeong Traci M. Bartz Sina A. Gharib Claudia Flexeder Stefan Karrasch Christian Gieger Annette Peters Beate Stubbe Xiaowei Hu Victor E. Ortega Deborah A. Meyers Eugene R. Bleecker Stacey Gabriel Namrata Gupta Albert V. Smith Jian’an Luan Jinghua Zhao Ailin Falkmo Hansen Arnulf Langhammer Cristen J. Willer Laxmi Bhatta David J. Porteous Blair H. Smith Archie Campbell Tamar Sofer Jiwon Lee Martha L. Daviglus Bing Yu Elise Lim Hanfei Xu George O'connor Gaurav Thareja Omar M E. Hamdi Mbarek Karsten Suhre Raquel Granell Tariq Faquih Pieter S. Hiemstra Annelies M. Slats Benjamin H. Mullin Jennie Hui Anthony James John Beilby Karina Patasova Pirro G. Hysi Jukka Koskela Annah B. Wyss Jianping Jin Sinjini Sikdar Mi Kyeong Lee Sebastian May-Wilson Nicola Pirastu Katherine A. Kentistou Peter K. Joshi Paul R. H. J. Timmers Alexander T. Williams Robert C. Free Xueyang Wang John L. Morrison Frank D. Gilliland Zhanghua Chen Carol A. Wang Rachel E. Foong

Abstract Lung function impairment underlies chronic obstructive pulmonary disease (COPD) and predicts mortality. In the largest multi-ancestry GWAS meta-analysis of lung to date, comprising 580,869 participants, 1020 independent association signals identified 559 genes supported by ≥2 criteria from a systematic variant-to-gene mapping framework. These were enriched in 29 pathways. Individual variants showed heterogeneity across ancestries, age smoking groups, collectively as genetic risk...

10.1101/2022.05.11.22274314 preprint EN cc-by medRxiv (Cold Spring Harbor Laboratory) 2022-05-14

Abstract Variable preferences for different foods are among the main determinants of their intake and influenced by many factors, including genetics. Despite considerable twins’ heritability, studies aimed at uncovering food-liking genetics have focused mostly on taste receptors. Here, we present first results a large-scale genome-wide association study food liking conducted 161,625 participants from UK Biobank. Liking was assessed over 139 specific using 9-point hedonic scale. After...

10.1101/2021.07.28.454120 preprint EN bioRxiv (Cold Spring Harbor Laboratory) 2021-07-28

<ns4:p><ns4:bold>Background: </ns4:bold>Lung function is highly heritable and differs between the sexes throughout life. However, little known about sex-differential genetic effects on lung function. We aimed to conduct first genome-wide genotype-by-sex interaction study identify that differ males females.</ns4:p><ns4:p> <ns4:bold>Methods:</ns4:bold> tested for interactions 7,745,864 variants sex spirometry-based measures of in UK Biobank (N=303,612), sought replication 75,696 independent...

10.12688/wellcomeopenres.15846.2 preprint EN cc-by Wellcome Open Research 2021-05-24

A lack of physical activity (PA) is one the most pressing health issues today. Our individual propensity for PA influenced by genetic factors. Stated liking different types may help capture additional and informative dimensions behavior genetics.In over 157,000 individuals from UK Biobank, we performed genome-wide association studies five items assessing types, plus an derived trait overall PA-liking. We attempted to replicate significant associations in Netherlands Twin Register (NTR)...

10.1249/mss.0000000000002907 article EN Medicine & Science in Sports & Exercise 2022-03-11

Understanding the genetic basis of neuro-related proteins is essential for dissecting disease etiology neuropsychiatric disorders and other complex traits diseases. Here, SCALLOP Consortium conducted a genome-wide association meta-analysis over 12,500 individuals 184 in human plasma. The analysis identified 117 cis-regulatory protein quantitative trait loci (cis-pQTL) 166 trans-pQTL. mapped pQTL capture on average 50% each protein’s heritability. Mendelian randomization analyses revealed...

10.1101/2023.02.10.23285650 preprint EN cc-by-nc-nd medRxiv (Cold Spring Harbor Laboratory) 2023-02-14

<title>Abstract</title> Understanding the genetic basis of neuro-related proteins is essential for dissecting molecular human behavioral traits and disease etiology neuropsychiatric disorders. Here, SCALLOP Consortium conducted a genome-wide association meta-analysis over 12,500 individuals 184 in plasma. The analysis identified 117 cis-regulatory protein quantitative trait loci (cis-pQTL) 166 trans-pQTL. mapped pQTL capture on average 50% each protein's heritability. Mendelian randomization...

10.21203/rs.3.rs-2720355/v1 preprint EN cc-by Research Square (Research Square) 2023-03-31

&lt;div&gt;Abstract&lt;p&gt;&lt;i&gt;KRAS&lt;/i&gt;-mutant colorectal cancers are resistant to therapeutics, presenting a significant problem for ∼40% of cases. Rapalogs, which inhibit mTORC1 and thus protein synthesis, significantly less potent in &lt;i&gt;KRAS&lt;/i&gt;-mutant cancer. Using &lt;i&gt;Kras&lt;/i&gt;-mutant mouse models mouse- patient-derived organoids, we demonstrate that KRAS with G12D mutation fundamentally rewires translation increase both bulk mRNA-specific initiation....

10.1158/2159-8290.c.6549409.v1 preprint EN 2023-04-03

&lt;div&gt;Abstract&lt;p&gt;&lt;i&gt;KRAS&lt;/i&gt;-mutant colorectal cancers are resistant to therapeutics, presenting a significant problem for ∼40% of cases. Rapalogs, which inhibit mTORC1 and thus protein synthesis, significantly less potent in &lt;i&gt;KRAS&lt;/i&gt;-mutant cancer. Using &lt;i&gt;Kras&lt;/i&gt;-mutant mouse models mouse- patient-derived organoids, we demonstrate that KRAS with G12D mutation fundamentally rewires translation increase both bulk mRNA-specific initiation....

10.1158/2159-8290.c.6549409 preprint EN 2023-04-03

Abstract Adult lung function is highly heritable and 279 genetic loci were recently reported as associated with spirometry-based measures of function. Though development differ between males females throughout life, there has been no genome-wide study to identify variants differential effects on in females. Here, we present the first genotype-by-sex interaction four traits 303,612 participants from UK Biobank. We detected five SNPs showing significant (P&lt;5 × 10 −8 ) interactions sex...

10.1101/594457 preprint EN bioRxiv (Cold Spring Harbor Laboratory) 2019-03-31

ABSTRACT A lack of physical activity (PA) is one the most pressing health issues facing society today. Our individual propensity for PA partly influenced by genetic factors. Stated liking various behaviors may capture additional dimensions behavior that are not captured other measures, and contribute to our understanding genetics behavior. Here, in over 157,000 individuals from UK Biobank, we sought complement extend previous findings on performing genome-wide association studies...

10.1101/2021.10.13.21264969 preprint EN cc-by-nc-nd medRxiv (Cold Spring Harbor Laboratory) 2021-10-14
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