D. Pearson

Non-penetrance in a MODY 3 family with a mutation in the hepatic nuclear factor 1α gene: implications for predictive testing

S. Ellard, Z. Miedzybrodzka, N. Haites, 1999, European Journal of Human Genetics.

The risk of Parkinson’s disease in type 1 Gaucher disease

P. Mistry, G. Pastores, M. Boxer, 2010, Journal of Inherited Metabolic Disease.

Epilepsy Risk Prediction Model for Patients With Tuberous Sclerosis Complex.

G. Cutter, B. Scherrer, Melissa A. Richard, 2020, Pediatric neurology.

Tuberous Sclerosis Complex Genotypes and Developmental Phenotype.

B. Scherrer, D. Pearson, S. Roberds, 2019, Pediatric neurology.

A Genome-Wide Association Search for Type 2 Diabetes Genes in African Americans

Simon C. Potter, Nicholette D. Palmer, Joshua P. Lewis, 2012, PLoS ONE.

Novel Loci for Adiponectin Levels and Their Influence on Type 2 Diabetes and Metabolic Traits: A Multi-Ethnic Meta-Analysis of 45,891 Individuals

Karen L. Mohlke, Luigi Ferrucci, Florian Kronenberg, 2012, PLoS genetics.

Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge

Alex Doney, Beverley Balkau, Meena Kumari, 2010, Nature Genetics.

New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk (vol 42, pg 105, 2010)

Simon C. Potter, Albert R. Singleton, Jarvelin, 2010 .