Hinds, David A.

A Genomewide Association Study of Skin Pigmentation in a South Asian Population

Stokowski, R. P., Pant, P. V. K., Dadd, T., Fereday, A., Hinds, D. A., Jarman, C., Filsell, W., Ginger, R. S., Green, M. R., van der Ouderaa, F. J., et al. (2007) · The American Journal of Human Genetics

melanin and skin pigmentationGenetic Associations and Epidemiology

Cited by 315

Germ line variants predispose to both JAK2 V617F clonal hematopoiesis and myeloproliferative neoplasms

Hinds, D. A., Barnholt, K. E., Mesa, R. A., Kiefer, A. K., Do, C. B., Eriksson, N., Mountain, J. L., Francke, U., Tung, J. Y., Nguyen, H. (., et al. (2016) · Blood

Myeloproliferative Neoplasms: Diagnosis and TreatmentGenetic Associations and Epidemiology

Cited by 267

Genetic analyses identify widespread sex-differential participation bias

Pirastu, N., Cordioli, M., Nandakumar, P., Mignogna, G., Abdellaoui, A., Hollis, B., Kanai, M., Rajagopal, V. M., Parolo, P. D. B., Baya, N., et al. (2021) · Nature Genetics

Genetic Associations and EpidemiologyGenetic Mapping and Diversity in Plants and Animals

Cited by 251

A genome-wide association meta-analysis of self-reported allergy identifies shared and allergy-specific susceptibility loci

Hinds, D. A., McMahon, G., Kiefer, A. K., Do, C. B., Eriksson, N., Evans, D. M., St Pourcain, B., Ring, S. M., Mountain, J. L., Francke, U., et al. (2013) · Nature Genetics

Genetic Associations and EpidemiologyAsthma and respiratory diseases

Cited by 246

A lattice model for protein structure prediction at low resolution.

Hinds, D. A., & Levitt, M. (1992) · Proceedings of the National Academy of Sciences

Protein Structure and DynamicsEnzyme Structure and Function

Cited by 217

Genome-wide association analysis identifies 11 risk variants associated with the asthma with hay fever phenotype

Ferreira, M. A. R., Matheson, M. C., Tang, C. S., Granell, R., Ang, W., Hui, J., Kiefer, A. K., Duffy, D. L., Baltic, S., Danoy, P., et al. (2014) · Journal of Allergy and Clinical Immunology

Asthma and respiratory diseasesGenetic Associations and Epidemiology

Cited by 216

Genetic variants associated with motion sickness point to roles for inner ear development, neurological processes and glucose homeostasis

Hromatka, B. S., Tung, J. Y., Kiefer, A. K., Do, C. B., Hinds, D. A., & Eriksson, N. (2015) · Human Molecular Genetics

Vestibular and auditory disordersNausea and vomiting management

Cited by 105

Social and non-social autism symptoms and trait domains are genetically dissociable

Warrier, V., Toro, R., Won, H., Leblond, C. S., Cliquet, F., Delorme, R., De Witte, W., Bralten, J., Chakrabarti, B., Børglum, A. D., et al. (2019) · Communications Biology

Autism Spectrum Disorder ResearchGenetic Associations and Epidemiology

Cited by 94