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Thibaud Boutin

NHS Tayside ·
Area of research
Genetics · Endocrinology, Diabetes and Metabolism
Research interest
Research interests include Genetic Associations and Epidemiology, Thyroid Disorders and Treatments, Birth, Development, and Health, and Epigenetics and DNA Methylation.
h-index
31
citations
8,725
works
106
NIH funding
primary concept
email

Recent publications

Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits
Nature Genetics 2024cited by 176position: middledoi
A genome-wide association analysis reveals new pathogenic pathways in gout
Nature Genetics 2024cited by 79position: middledoi
Multi-trait analysis characterizes the genetics of thyroid function and identifies causal associations with clinical implications
Nature Communications 2024cited by 72position: middledoi
X-chromosome and kidney function: evidence from a multi-trait genetic analysis of 908,697 individuals reveals sex-specific and sex-differential findings in genes regulated by androgen response elements
Nature Communications 2024cited by 12position: middledoi
The trans-ancestral genomic architecture of glycemic traits
Nature Genetics 2021cited by 878position: middledoi
Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals
Nature Metabolism 2020cited by 766position: middledoi
Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction
Nature Communications 2020cited by 109position: middledoi
A catalog of genetic loci associated with kidney function from analyses of a million individuals
Nature Genetics 2019cited by 911position: middledoi
Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels
Nature Genetics 2019cited by 426position: middledoi
Author Correction: Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases
Nature Communications 2019cited by 2position: middledoi
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits
Nature Genetics 2018cited by 1,486position: middledoi
Trans-ethnic association study of blood pressure determinants in over 750,000 individuals
Nature Genetics 2018cited by 496position: middledoi
Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases
Nature Communications 2018cited by 97position: middledoi
Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits
Nature Genetics 2018cited by 38position: middledoi
Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk
Nature Genetics 2017cited by 639position: middledoi
Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity
Nature Communications 2017cited by 176position: middledoi
New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics.
Human Molecular Genetics 2016cited by 188position: middledoi
When do myopia genes have their effect? Comparison of genetic risks between children and adults
Genetic Epidemiology 2016cited by 50position: middledoi
Genome-wide Regional Heritability Mapping Identifies a Locus Within the TOX2 Gene Associated With Major Depressive Disorder
Biological Psychiatry 2016cited by 34position: middledoi
Genomic analyses for age at menarche identify 389 independent signals and indicate BMI-independent effects of puberty timing on cancer susceptibility
bioRxiv (Cold Spring Harbor Laboratory) 2016cited by 3position: middledoi
Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair
Nature Genetics 2015cited by 449position: middledoi

Grants

No grants ingested yet.

Frequent collaborators

René Höhn · University of Freiburg1 papers (2016–2016)Yi Lu · The University of Sydney1 papers (2016–2016)Vincent W. V. Jaddoe · Erasmus MC - Sophia Children’s Hospital1 papers (2016–2016)Cathy Williams · University Hospitals Bristol NHS Foundation Trust1 papers (2016–2016)Mingguang He · Tianjin Medical University1 papers (2016–2016)Caroline C. W. Klaver · Erasmus MC1 papers (2016–2016)Stuart MacGregor · The University of Queensland1 papers (2016–2016)Jeremy A. Guggenheim · Australian National University1 papers (2016–2016)Qiao Fan · National University of Singapore1 papers (2016–2016)David A. Mackey · Ericsson (Ireland)1 papers (2016–2016)Tanja Zeller · Friedrich Schiller University Jena1 papers (2016–2016) · 1 papers (2016–2016) · 1 papers (2016–2016)Stefan Nickels · Johannes Gutenberg University Mainz1 papers (2016–2016)Jan Roelof Polling · Utrecht University1 papers (2016–2016)Anthony P. Khawaja · Moorfields Eye Hospital NHS Foundation Trust1 papers (2016–2016)Paul J. Foster · SingHealth1 papers (2016–2016)Seang‐Mei Saw · National University of Singapore1 papers (2016–2016) · 1 papers (2016–2016)Véronique Vitart · UK Biobank1 papers (2016–2016)