M. Black

Characterization of APOE Christchurch carriers in 455,306 UK Biobank participants

S. Lovestone, Y. Zhang, Q. Li, 2022, Molecular Neurodegeneration.

Comparison of the 15q deletions in Prader-Willi and Angelman syndromes: specific regions, extent of deletions, parental origin, and clinical consequences.

J. Zonana, S. Lafranchi, R. Magenis, 1990, American journal of medical genetics.

The impact of Short Tandem Repeats on grey matter brain imaging derived phenotypes in UK Biobank

L. Winchester, N. Amin, C. V. van Duijn, 2023, medRxiv.

Clinical outcomes of four patients with microdeletion in the long arm of chromosome 2.

S. Olson, J. Reiss, R. Magenis, 1998, American journal of medical genetics.

Metabolic Syndrome is linked to Chromosome 7q21 and associated with genetic variants in CD36 and GNAT3 in Mexican Americans

L. Almasy, R. Duggirala, T. Buchanan, 2012, Obesity.