S. Melville

Multiple loci influencing hippocampal degeneration identified by genome scan

K. Lunetta, C. DeCarli, Li Shen, 2012, Annals of neurology.

Identification of a common variant in the TFR2 gene implicated in the physiological regulation of serum iron levels.

Toshiko Tanaka, S. Bandinelli, D. Hernandez, 2011, Human molecular genetics.

Genome-wide association study identifies 48 common genetic variants associated with handedness

Cameron D. Palmer, David M. Evans, N. Eriksson, 2019, bioRxiv.

A KATP channel gene effect on sleep duration: from genome-wide association studies to function in Drosophila

T. Meitinger, H. Wichmann, B. Penninx, 2011, Molecular Psychiatry.

Genetic variants in RBFOX3 are associated with sleep latency

A. Hofman, A. Uitterlinden, E. Mihailov, 2016, European Journal of Human Genetics.

A meta-analysis of genome-wide data from five European isolates reveals an association of COL22A1, SYT1, and GABRR2 with serum creatinine level

Thomas Meitinger, Michael Krawczak, Igor Rudan, 2010, BMC Medical Genetics.

Genome-wide association analysis and fine mapping of NT-proBNP level provide novel insight into the role of the MTHFR-CLCN6-NPPA-NPPB gene cluster

A. Peters, H. Wichmann, I. Heid, 2011, Human molecular genetics.

Genome-wide association study identifies 48 common genetic variants associated with handedness

Cameron D. Palmer, David M. Evans, N. Eriksson, 2020, Nature Human Behaviour.