A. Curtis

Association of less cornmon cystic fibrosis mutations with a mild phenotypec

S. Bhattacharya, M. Porteous, J. Burn, 2022 .

Association of NOD2 with Crohn's Disease in a homogenous Irish population

C. O'Morain, M. Gardner, F. Shanahan, 2003, European Journal of Human Genetics.

Absence of a genetic association between IL-1RN and IL-1B gene polymorphisms in ulcerative colitis and Crohn disease in multiple populations from northeast England.

J. Mansfield, P. Donaldson, M. Hudson, 2001, Scandinavian journal of gastroenterology.

Mutation screening in exons 3 and 4 of alpha-synuclein in sporadic Parkinson's and sporadic and familial dementia with Lewy bodies cases.

E. Jaros, D. Middleton, R. Perry, 1998, Neuroreport.

Phenotypic characterization of individuals with 30-40 CAG repeats in the Huntington disease (HD) gene reveals HD cases with 36 repeats and apparently normal elderly individuals with 36-39 repeats.

P S Harper, D Curtis, S. Folstein, 1996, American journal of human genetics.

Metastatic disease to the chest in patients with extrathoracic malignancy

L. Coppage, A. Curtis, C. Shaw, 1987, Journal of thoracic imaging.

A novel tissue inhibitor of metalloproteinases-3 mutation reveals a common molecular phenotype in Sorsby's fundus dystrophy.

J. Goodship, M. Barker, M. Clarke, 2000, The Journal of biological chemistry.