Hartiala, Jaana

Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction

Do, R., Stitziel, N. O., Won, H.-H., Jørgensen, A. B., Duga, S., Angelica Merlini, P., Kiezun, A., Farrall, M., Goel, A., Zuk, O., et al. (2015) · Nature

Lipoproteins and Cardiovascular HealthGenetic Associations and Epidemiology

Cited by 650

Maternal periconceptional folic acid intake and risk of autism spectrum disorders and developmental delay in the CHARGE (CHildhood Autism Risks from Genetics and Environment) case-control study

Schmidt, R. J., Tancredi, D. J., Ozonoff, S., Hansen, R. L., Hartiala, J., Allayee, H., Schmidt, L. C., Tassone, F., & Hertz-Picciotto, I. (2012) · The American Journal of Clinical Nutrition

Folate and B Vitamins ResearchAutism Spectrum Disorder Research

Cited by 408

Prenatal vitamins, one-carbon metabolism gene variants, and risk for autism

Schmidt, R. J., Hansen, R. L., Hartiala, J., Allayee, H., Schmidt, L. C., Tancredi, D. J., Tassone, F., & Hertz-Picciotto, I. (2011) · Epidemiology

Autism Spectrum Disorder ResearchFolate and B Vitamins Research

Cited by 308

Genome-wide analysis highlights contribution of immune system pathways to the genetic architecture of asthma

Han, Y., Jia, Q., Jahani, P. S., Hurrell, B. P., Pan, C., Huang, P., Gukasyan, J., Woodward, N. C., Eskin, E., Gilliland, F. D., et al. (2020) · Nature Communications

Asthma and respiratory diseasesGenetic Associations and Epidemiology

Cited by 222

Genetic demography of Antioquia (Colombia) and the Central Valley of Costa Rica

Carvajal-Carmona, L. G., Ophoff, R., Service, S., Hartiala, J., Molina, J., Leon, P., Ospina, J., Bedoya, G., Freimer, N., & Ruiz-Linares, A. (2003) · Human Genetics

Forensic and Genetic ResearchGenetic diversity and population structure

Cited by 182

Comparative Genome-Wide Association Studies in Mice and Humans for Trimethylamine N -Oxide, a Proatherogenic Metabolite of Choline and l -Carnitine

Hartiala, J., Bennett, B. J., Tang, W. H. W., Wang, Z., Stewart, A. F. R., Roberts, R., McPherson, R., Lusis, A. J., Hazen, S. L., & Allayee, H. (2014) · Arteriosclerosis, Thrombosis, and Vascular Biology

Genetic Associations and EpidemiologyNutrition, Genetics, and Disease

Cited by 133

Genome-wide association study and targeted metabolomics identifies sex-specific association of CPS1 with coronary artery disease

Hartiala, J. A., Wilson Tang, W. H., Wang, Z., Crow, A. L., Stewart, A. F. R., Roberts, R., McPherson, R., Erdmann, J., Willenborg, C., Hazen, S. L., et al. (2016) · Nature Communications

Genetic Associations and EpidemiologyMetabolism and Genetic Disorders

Cited by 130

Selected vitamin D metabolic gene variants and risk for Autism Spectrum Disorder in the charge study

Schmidt, R. J., Hansen, R. L., Hartiala, J., Allayee, H., Sconberg, J. L., Schmidt, L. C., Volk, H. E., & Tassone, F. (2015) · Early Human Development

Autism Spectrum Disorder ResearchVitamin D Research Studies

Cited by 68

Exposure to Nanoscale Particulate Matter from Gestation to Adulthood Impairs Metabolic Homeostasis in Mice

Woodward, N. C., Crow, A. L., Zhang, Y., Epstein, S., Hartiala, J., Johnson, R., Kocalis, H., Saffari, A., Sankaranarayanan, I., Akbari, O., et al. (2019) · Scientific Reports

Air Quality and Health ImpactsAdipokines, Inflammation, and Metabolic Diseases

Cited by 32