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Hilary C. Martin

Wellcome Sanger Institute · GB
Area of research
Genetics · Cognitive Neuroscience
Research interest
Research interests include Genetic Associations and Epidemiology, Genomics and Rare Diseases, Genomic variations and chromosomal abnormalities, and Genetics and Neurodevelopmental Disorders.
h-index
46
citations
12,662
works
155
NIH funding
primary concept
Medicine
email

Recent publications

Genome-wide association study meta-analysis provides insights into the etiology of heart failure and its subtypes
Nature Genetics 2025cited by 35position: middledoi
Somatic mutation and selection at population scale
Nature 2025cited by 27position: middledoi
Multi-ancestry genome-wide association study of major depression aids locus discovery, fine mapping, gene prioritization and causal inference
Nature Genetics 2024cited by 165position: middledoi
Examining the role of common variants in rare neurodevelopmental conditions
Nature 2024cited by 50position: lastdoi
Genetic basis of early onset and progression of type 2 diabetes in South Asians
Nature Medicine 2024cited by 34position: middledoi
The importance of family-based sampling for biobanks
Nature 2024cited by 23position: middledoi
Genetic architecture of routinely acquired blood tests in a British South Asian cohort
Nature Communications 2024cited by 21position: middledoi
Using Organoids to Model Sex Differences in the Human Brain
Biological Psychiatry Global Open Science 2024cited by 18position: middledoi
Polygenic prediction of preeclampsia and gestational hypertension
Nature Medicine 2023cited by 117position: middledoi
Genetic insights into human cortical organization and development through genome-wide analyses of 2,347 neuroimaging phenotypes
Nature Genetics 2023cited by 79position: middledoi
Influence of autozygosity on common disease risk across the phenotypic spectrum
Cell 2023cited by 37position: lastdoi
Author Correction: The power of genetic diversity in genome-wide association studies of lipids
Nature 2023cited by 14position: middledoi
Additional file 21 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
UWA Profiles and Research Repository (UWA) 2023cited by 0position: middledoi
Additional file 5 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
UWA Profiles and Research Repository (UWA) 2023cited by 0position: middledoi
Additional file 22 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
UWA Profiles and Research Repository (UWA) 2023cited by 0position: middledoi
Additional file 23 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
UWA Profiles and Research Repository (University of Western Australia) 2023cited by 0position: middledoi
Additional file 1 of Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
UWA Profiles and Research Repository (University of Western Australia) 2023cited by 0position: middledoi
Recommendations for clinical interpretation of variants found in non-coding regions of the genome
Genome Medicine 2022cited by 252position: middledoi
Genetic correlates of phenotypic heterogeneity in autism
Nature Genetics 2022cited by 144position: middledoi
Transferability of genetic loci and polygenic scores for cardiometabolic traits in British Pakistani and Bangladeshi individuals
Nature Communications 2022cited by 77position: middledoi
Integrating polygenic risk scores in the prediction of type 2 diabetes risk and subtypes in British Pakistanis and Bangladeshis: A population-based cohort study
PLoS Medicine 2022cited by 70position: middledoi
A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids
The American Journal of Human Genetics 2022cited by 63position: middledoi
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
Genome biology 2022cited by 62position: middledoi
The power of genetic diversity in genome-wide association studies of lipids
Nature 2021cited by 1,033position: middledoi
MC3R links nutritional state to childhood growth and the timing of puberty
Nature 2021cited by 136position: middledoi
The contribution of X-linked coding variation to severe developmental disorders
Nature Communications 2021cited by 65position: firstdoi
Fine-scale population structure and demographic history of British Pakistanis
Nature Communications 2021cited by 43position: lastdoi
Implicating genes, pleiotropy and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
medRxiv 2021cited by 9position: middledoi
A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids
bioRxiv (Cold Spring Harbor Laboratory) 2021cited by 4position: middledoi
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations
Cell 2020cited by 726position: middledoi

Grants

No grants ingested yet.

Frequent collaborators

David A. van Heel · Harvard University5 papers (2019–2023) · 5 papers (2021–2024)John Wright · Society for the Investigation of Early Pregnancy4 papers (2019–2022)Chris Griffiths · Queen Mary University of London4 papers (2019–2023) · 4 papers (2019–2023)Karen A. Hunt · Icahn School of Medicine at Mount Sinai3 papers (2019–2022) · 3 papers (2021–2024)Richard C. Trembath · King's College London3 papers (2019–2022)William G. Newman · University of Manchester2 papers (2022–2023)R Thomas Lumbers · Health Data Research UK2 papers (2022–2022) · 2 papers (2019–2023)Bhavi Trivedi · Queen Mary University of London2 papers (2019–2022) · 2 papers (2023–2024)Karoline Kuchenbaecker · Universitäres Kinderwunschzentrum Lübeck2 papers (2022–2022)Rohini Mathur · Science Oxford2 papers (2022–2023) · 2 papers (2021–2022)Emilie M. Wigdor · Wellcome Sanger Institute2 papers (2023–2024)Neneh Sallah · London School of Hygiene & Tropical Medicine2 papers (2022–2022)Sam Hodgson · University of Southampton2 papers (2022–2022)Eamonn Sheridan · University of Leeds2 papers (2021–2024)