H. Davidson

Abnormalities of glucocorticoid metabolism and the renin-angiotensin system: a four-corners approach to the identification of genetic determinants of blood pressure.

G. Watt, S. Harrap, R. Fraser, 1992, Journal of hypertension.

A human BRCA1 gene knockout

R. McFarlane, D. Black, H. Davidson, 1995, Nature.

Molecular analysis of pheochromocytoma after maternal transmission of SDHD mutation elucidates mechanism of parent-of-origin effect.

E. Tobias, R. Lindsay, N. Bradshaw, 2011, The Journal of clinical endocrinology and metabolism.

Recurrent dominant mutations affecting two adjacent residues in the motor domain of the monomeric kinesin KIF22 result in skeletal dysplasia and joint laxity.

G. Mortier, A. Mégarbané, R. Scott, 2011, American journal of human genetics.

Biallelic deleterious BRCA1 mutations in a woman with early-onset ovarian cancer.

F. Couch, W. Foulkes, R. Greenberg, 2013, Cancer discovery.

Mutations in TFAP2B cause Char syndrome, a familial form of patent ductus arteriosus

B. Gelb, J. Goodship, J. Burn, 2000, Nature Genetics.

A child with bisatellited, dicentric chromosome 15 arising from a maternal paracentric inversion of chromosome 15q

M. Whiteford, S. Kinmond, H. Davidson, 2000, Journal of medical genetics.

The angiotensin I converting enzyme gene and predisposition to high blood pressure.

G. Watt, S. Harrap, F. Soubrier, 1993, Hypertension.

The prenatal exclusion test for Huntington's disease: experience in the west of Scotland, 1986-1993.

J. Tolmie, J. Paterson, J. Tolmie, 1995, Journal of medical genetics.