Andrew Green

ALG6-CDG: a recognizable phenotype with epilepsy, proximal muscle weakness, ataxia and behavioral and limb anomalies

G. Matthijs, R. Wevers, C. Thiel, 2016, Journal of Inherited Metabolic Disease.

The impact of the metabotropic glutamate receptor and other gene family interaction networks on autism

Thomas Bourgeron, Ellen M. Wijsman, Gillian Baird, 2014, Nature Communications.

Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders

Stephen J. Guter, Emily L. Crawford, D. Pinto, 2014, American journal of human genetics.

Germline de novo mutations in families with Mendelian cancer syndromes caused by defects in DNA repair

A. Campbell, J. Sampson, Lynn Martin, 2023, Nature communications.

Phenotypic analysis of familial breast cancer: comparison of BRCAx tumors with BRCA1-, BRCA2-carriers and non-familial breast cancer.

A. Green, J. Geraghty, A. O'Doherty, 2015, European journal of surgical oncology : the journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology.

Nicolaides–Baraitser syndrome in a patient with hypertrophic cardiomyopathy and SMARCA2 gene deletion

C. McMahon, D. Betts, Sophie Duignan, 2021, Cardiology in the Young.