Jackson, Ian J.

Mouse genomic variation and its effect on phenotypes and gene regulation.

Keane, T. M., Goodstadt, L., Danecek, P., White, M. A., Wong, K., Yalcin, B., Heger, A., Agam, A., Slater, G., Goodson, M., et al. (2011) · Nature

Genetic Mapping and Diversity in Plants and AnimalsGenetic and phenotypic traits in livestock

Cited by 1,580

Variants of the melanocyte−stimulating hormone receptor gene are associated with red hair and fair skin in humans

Valverde, P., Healy, E., Jackson, I., Rees, J. L., & Thody, A. J. (1995) · Nature Genetics

melanin and skin pigmentationGenetic Associations and Epidemiology

Cited by 999

A comparative phenotypic and genomic analysis of C57BL/6J and C57BL/6N mouse strains

Simon, M. M., Greenaway, S., White, J. K., Fuchs, H., Gailus-Durner, V., Wells, S., Sorg, T., Wong, K., Bedu, E., Cartwright, E. J., et al. (2013) · Genome Biology

Genetic and phenotypic traits in livestockGenetic Mapping and Diversity in Plants and Animals

Cited by 507

The melanocyte lineage in development and disease

Mort, R. L., Jackson, I. J., & Patton, E. E. (2015) · Development

melanin and skin pigmentationDevelopmental Biology and Gene Regulation

Cited by 416

Evidence for Variable Selective Pressures at MC1R

Harding, R. M., Healy, E., Ray, A. J., Ellis, N. S., Flanagan, N., Todd, C., Dixon, C., Sajantila, A., Jackson, I. J., Birch-Machin, M. A., et al. (2000) · The American Journal of Human Genetics

melanin and skin pigmentationForensic and Genetic Research

Cited by 389

A Cell/Cilia Cycle Biosensor for Single-Cell Kinetics Reveals Persistence of Cilia after G1/S Transition Is a General Property in Cells and Mice

Ford, M. J., Yeyati, P. L., Mali, G. R., Keighren, M. A., Waddell, S. H., Mjoseng, H. K., Douglas, A. T., Hall, E. A., Sakaue-Sawano, A., Miyawaki, A., et al. (2018) · Developmental Cell

Genetic and Kidney Cyst DiseasesCystic Fibrosis Research Advances

Cited by 89

HEATR2 Plays a Conserved Role in Assembly of the Ciliary Motile Apparatus

Diggle, C. P., Moore, D. J., Mali, G., zur Lage, P., Ait-Lounis, A., Schmidts, M., Shoemark, A., Garcia Munoz, A., Halachev, M. R., Gautier, P., et al. (2014) · PLoS Genetics

Genetic and Kidney Cyst DiseasesCystic Fibrosis Research Advances

Cited by 67

Mouse Slc9a8 Mutants Exhibit Retinal Defects Due to Retinal Pigmented Epithelium Dysfunction

Jadeja, S., Barnard, A. R., McKie, L., Cross, S. H., White, J. K., Robertson, M., Budd, P. S., MacLaren, R. E., & Jackson, I. J. (2015) · Investigative Opthalmology & Visual Science

Retinal Development and DisordersRetinal Diseases and Treatments

Cited by 13

A custom capture sequence approach for oculocutaneous albinism identifies structural variant alleles at the OCA2 locus

Loftus, S. K., Lundh, L., Watkins‐Chow, D. E., Baxter, L. L., Pairo‐Castineira, E., Program, N. C. S., Jackson, I. J., Oetting, W. S., Pavan, W. J., & Adams, D. R. (2021) · Human Mutation

melanin and skin pigmentationGenomics and Rare Diseases

Cited by 12