Daly, Mark J.
Broad Institute · University of Helsinki · Harvard University · Massachusetts General Hospital · Institute for Molecular Medicine Finland · Stanley Center for Psychiatric Research
170 papers on CoChatORCID 0000-0002-0949-8752
Most cited papers
- Verified
The female protective effect against autism spectrum disorder
Wigdor, E. M., Weiner, D. J., Grove, J., Fu, J. M., Thompson, W. K., Carey, C. E., Baya, N., van der Merwe, C., Walters, R. K., Satterstrom, F. K., et al. (2021) · Cell Genomics
Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders
Cited by 124
- Verified
The female protective effect against autism spectrum disorder
Wigdor, E. M., Weiner, D. J., Grove, J., Fu, J. M., Thompson, W. K., Carey, C. E., Baya, N., van der Merwe, C., Walters, R. K., Satterstrom, F. K., et al. (2022) · Cell Genomics
Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders
Cited by 124
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Geographic variation and bias in polygenic scores of complex diseases and traits in Finland
Kerminen, S., Martin, A. R., Koskela, J., Ruotsalainen, S. E., Havulinna, A. S., Surakka, I., Palotie, A., Perola, M., Salomaa, V., Daly, M. J., et al. (2018) · The American Journal of Human Genetics
Genetic Associations and EpidemiologyGenetic and phenotypic traits in livestock
Cited by 115
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Quantifying the impact of rare and ultra-rare coding variation across the phenotypic spectrum
Ganna, A., Satterstrom, F. K., Zekavat, S. M., Das, I., Kurki, M. I., Churchhouse, C., Alfoldi, J., Martin, A. R., Havulinna, A. S., Byrnes, A., et al. (2018) · The American Journal of Human Genetics
Genomics and Rare DiseasesGenetic Associations and Epidemiology
Cited by 110
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Fine mapping in 94 inbred mouse strains using a high-density haplotype resource
Kirby, A., Kang, H. M., Wade, C. M., Cotsapas, C., Kostem, E., Han, B., Furlotte, N., Kang, E. Y., Rivas, M., Bogue, M. A., et al. (2010) · Genetics
Genetic Mapping and Diversity in Plants and AnimalsGenetic Associations and Epidemiology
Cited by 102
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Fine-mapping across diverse ancestries drives the discovery of putative causal variants underlying human complex traits and diseases
Yuan, K., Longchamps, R. J., Pardiñas, A. F., Yu, M., Chen, T.-T., Lin, S.-C., Chen, Y., Lam, M., Liu, R., Xia, Y., et al. (2023) · Nature Genetics
Genetic Associations and EpidemiologyGenetic Mapping and Diversity in Plants and Animals
Cited by 94
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Common risk variants identified in autism spectrum disorder
Grove, J., Ripke, S., Als, T. D., Mattheisen, M., Walters, R., Won, H., Pallesen, J., Agerbo, E., Andreassen, O. A., Anney, R., et al. (2017) · bioRxiv (Cold Spring Harbor Laboratory)
Autism Spectrum Disorder ResearchGenetic Associations and Epidemiology
Cited by 89
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Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population
Rivas, M. A., Avila, B. E., Koskela, J., Huang, H., Stevens, C., Pirinen, M., Haritunians, T., Neale, B. M., Kurki, M., Ganna, A., et al. (2018) · PLoS Genetics
Genomics and Rare DiseasesGenetic Associations and Epidemiology
Cited by 87
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Comparing strategies to fine-map the association of common SNPs at chromosome 9p21 with type 2 diabetes and myocardial infarction
The Myocardial Infarction Genetics Consortium, Shea, J., Agarwala, V., Philippakis, A. A., Maguire, J., Banks, E., DePristo, M., Thomson, B., Guiducci, C., Onofrio, R. C., et al. (2011) · Nature Genetics
Genetic Associations and EpidemiologyGenetic Mapping and Diversity in Plants and Animals
Cited by 87
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The association between lower educational attainment and depression owing to shared genetic effects? Results in ~25 000 subjects
Peyrot, W. J., Lee, S. H., Milaneschi, Y., Abdellaoui, A., Byrne, E. M., Esko, T., de Geus, E. J. C., Hemani, G., Hottenga, J. J., Kloiber, S., et al. (2015) · Molecular Psychiatry
Genetic Associations and EpidemiologyNeurotransmitter Receptor Influence on Behavior
Cited by 84
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ARMS2/HTRA1 locus can confer differential susceptibility to the advanced subtypes of age-related macular degeneration
Sobrin, L., Reynolds, R., Yu, Y., Fagerness, J., Leveziel, N., Bernstein, P. S., Souied, E. H., Daly, M. J., & Seddon, J. M. (2011) · American Journal of Ophthalmology
Retinal Diseases and TreatmentsRetinal Imaging and Analysis
Cited by 78
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The Critical Needs and Challenges for Genetic Architecture Studies in Africa
Martin, A. R., Teferra, S., Möller, M., Hoal, E. G., & Daly, M. J. (2018) · Current Opinion in Genetics & Development
Genetic Associations and EpidemiologyRace, Genetics, and Society
Cited by 76
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Annotation of loci from genome-wide association studies using tissue-specific quantitative interaction proteomics
The QT Interval International GWAS Consortium (QT-IGC), Lundby, A., Rossin, E. J., Steffensen, A. B., Acha, M. R., Newton-Cheh, C., Pfeufer, A., Lynch, S. N., Olesen, S.-P., Brunak, S., et al. (2014) · Nature Methods
Genetic Associations and EpidemiologyBioinformatics and Genomic Networks
Cited by 71
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Inflammation status modulates the effect of host genetic variation on intestinal gene expression in inflammatory bowel disease
Hu, S., Uniken Venema, W. T., Westra, H.-J., Vich Vila, A., Barbieri, R., Voskuil, M. D., Blokzijl, T., Jansen, B. H., Li, Y., Daly, M. J., et al. (2021) · Nature Communications
Inflammatory Bowel DiseaseGenetic Associations and Epidemiology
Cited by 59
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The 22q11.2 region regulates presynaptic gene-products linked to schizophrenia
Nehme, R., Pietiläinen, O., Artomov, M., Tegtmeyer, M., Valakh, V., Lehtonen, L., Bell, C., Singh, T., Trehan, A., Sherwood, J., et al. (2022) · Nature Communications
Genomic variations and chromosomal abnormalitiesSchizophrenia research and treatment
Cited by 58
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Phenotypic extremes in rare variant study designs
Peloso, G. M., Rader, D. J., Gabriel, S., Kathiresan, S., Daly, M. J., & Neale, B. M. (2016) · European Journal of Human Genetics
Genetic Associations and EpidemiologyGenomics and Rare Diseases
Cited by 58
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Mapping the dynamic genetic regulatory architecture of HLA genes at single-cell resolution
Kang, J. B., Shen, A. Z., Gurajala, S., Nathan, A., Rumker, L., Aguiar, V. R. C., Valencia, C., Lagattuta, K. A., Zhang, F., Jonsson, A. H., et al. (2023) · Nature Genetics
Genetic Associations and EpidemiologySingle-cell and spatial transcriptomics
Cited by 49
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Distribution and Medical Impact of Loss-of-Function Variants in the Finnish Founder Population
Lim, E. T., Würtz, P., Havulinna, A. S., Palta, P., Tukiainen, T., Rehnström, K., Esko, T., Mägi, R., Inouye, M., Lappalainen, T., et al. (2014) · PLoS Genetics
Genetic Associations and EpidemiologyGenomics and Rare Diseases
Cited by 49
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Meta-Analysis of Genome-Wide Association Studies
de Bakker, P. I. W., Neale, B. M., & Daly, M. J. (2010) · Cold Spring Harbor Protocols
Genetic Associations and EpidemiologyGenetic Mapping and Diversity in Plants and Animals
Cited by 48
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ANGPTL8 protein-truncating variant associated with lower serum triglycerides and risk of coronary disease
Helkkula, P., Kiiskinen, T., Havulinna, A. S., Karjalainen, J., Koskinen, S., Salomaa, V., Daly, M. J., Palotie, A., Surakka, I., Ripatti, S., et al. (2021) · PLOS Genetics
Lipid metabolism and disordersGenetic Associations and Epidemiology
Cited by 47
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Multi-Ancestry Meta-Analysis yields novel genetic discoveries and ancestry-specific associations
Turley, P., Martin, A. R., Goldman, G., Li, H., Kanai, M., Walters, R. K., Jala, J. B., Lin, K., Millwood, I. Y., Carey, C. E., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory)
Genetic Associations and EpidemiologyForensic and Genetic Research
Cited by 35
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Genetic profile for five common variants associated with age-related macular degeneration in densely affected families: a novel analytic approach
Sobrin, L., Maller, J. B., Neale, B. M., Reynolds, R. C., Fagerness, J. A., Daly, M. J., & Seddon, J. M. (2010) · European Journal of Human Genetics
Retinal Diseases and TreatmentsGenetic Associations and Epidemiology
Cited by 31
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Integrated analyses of growth differentiation factor-15 concentration and cardiometabolic diseases in humans
Lemmelä, S., Wigmore, E. M., Benner, C., Havulinna, A. S., Ong, R. M., Kempf, T., Wollert, K. C., Blankenberg, S., Zeller, T., Peters, J. E., et al. (2022) · eLife
GDF15 and Related BiomarkersGenetic Associations and Epidemiology
Cited by 28
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Rare genetic variants confer a high risk of ADHD and implicate neuronal biology
Demontis, D., Duan, J., Hsu, Y.-H. H., Pintacuda, G., Grove, J., Nielsen, T. T., Thirstrup, J., Martorana, M., Botts, T., Satterstrom, F. K., et al. (2026) · Nature
Attention Deficit Hyperactivity DisorderGenetics and Neurodevelopmental Disorders
Cited by 17
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