M. Mullan

Confirmation of the localization of the human GABAA receptor alpha 1-subunit gene (GABRA1) to distal 5q by linkage analysis.

A A Hicks, T. Sander, B. Riley, 1992, Genomics.

The role of genetic factors in the etiology of the affective disorders

H. Gurling, M. Mullan, S. Hodgkinson, 1990, Behavior genetics.

The Impact of Molecular Genetics on Our Understanding of the Psychoses

R. Murray, M. Mullan, Michael J. Mullan, 1989, British Journal of Psychiatry.

Chromosomal assignment of the second locus for autosomal dominant cerebellar ataxia (SCA2) to chromosome 12q23–24.1

J. Weber, J. Beckmann, M. Farrall, 1993, Nature Genetics.

Newly described form of X-linked arthrogryposis maps to the long arm of the human X chromosome.

H. Houlden, M. Wallace, R. Zori, 1998, American journal of medical genetics.

Genetic Characterization of a Novel Familial Dementia

J. Hardy, A. Goate, A. Brun, 1991, Annals of the New York Academy of Sciences.

Prion dementia without characteristic pathology

T. Crow, J. Hardy, P. Lantos, 1990, The Lancet.

Genetic linkage studies suggest that Alzheimer's disease is not a single homogeneous disorder

I. Rainero, J. L. Haines, J. A. Hardy, 1990, Nature.