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List of works by Susan Forrest

A duplication at chromosome 11q12.2-11q12.3 is associated with spinocerebellar ataxia type 20

scientific article published on 18 September 2008

A gene for pili annulati maps to the telomeric region of chromosome 12q.

scientific article published in December 2004

Array comparative genomic hybridisation analysis of boys with X-linked hypopituitarism identifies a 3.9 Mb duplicated critical region at Xq27 containing SOX3.

scientific article published in April 2007

Association between dependent smoking and a polymorphism in the tyrosine hydroxylase gene in a prospective population-based study of adolescent health

scientific article

Clinical features of a large Australian pedigree with episodic ataxia type 1 ⬇️

scientific article published on 01 September 2001

Conservation of CNS1 and exclusion of its role in atopic eczema susceptibility

scientific article published on 01 January 2002

Deletion at ITPR1 underlies ataxia in mice and humans (SCA15)

Deletion at ITPR1 underlies ataxia in mice and spinocerebellar ataxia 15 in humans

scientific article published in June 2007

Dominantly inherited ataxia and dysphonia with dentate calcification: spinocerebellar ataxia type 20.

scientific article published on 3 March 2004

Duchenne and Becker muscular dystrophy mutations: analysis using 2.6 kb of muscle cDNA from the 5' end of the gene.

scientific article

Effective strategy for prenatal prediction of Duchenne and Becker muscular dystrophy

scientific article published on 01 December 1987

Erratum: Preparing for genomic medicine: a real world demonstration of health system change

scientific article published on 5 October 2017

Further studies of gene deletions that cause Duchenne and Becker muscular dystrophies

scientific article published on 01 February 1988

Genome sequence of an Australian kangaroo, Macropus eugenii, provides insight into the evolution of mammalian reproduction and development

scientific article

Genome sequence of an Australian kangaroo, Macropus eugenii, provides insight into the evolution of mammalian reproduction and development

article

Identification of a novel missense mutation L329I in the episodic ataxia type 1 gene KCNA1--a challenging problem

scientific article (publication date: October 2000)

Increased gene dosage at Xq26-q27 is associated with X-linked hypopituitarism

scientific article published on 01 April 2002

Molecular analysis and diagnosis of Duchenne muscular dystrophy.

scientific article published on April 1988

Molecular analysis of human X-linked diseases

scientific article published on 01 January 1986

Molecular analysis of muscular dystrophy.

scientific article published on February 1988

Parametric and non-parametric linkage analysis of several candidate regions for genes for human handedness.

scientific article

Parametric and nonparametric genome scan analyses for human handedness

scientific article published on 01 October 2003

Patterns of exon deletions in Duchenne and Becker muscular dystrophy

scientific article published on 01 October 1988

Preparing for genomic medicine: a real world demonstration of health system change

scientific article published in May 2017

Profuse familial adenomatous polyposis with an adenomatous polyposis coli exon 3 mutation

scientific article published on January 1, 2001

Progressive patterned scalp hypotrichosis, with wiry hair, onycholysis, and intermittently associated cleft lip and palate: clinical and genetic distinction from Marie Unna

scientific article published on 01 June 2003

Spinocerebellar ataxia type 15 (sca15) maps to 3p24.2-3pter: exclusion of the ITPR1 gene, the human orthologue of an ataxic mouse mutant

scientific article

Spinocerebellar ataxia type 15.

scientific article

Spinocerebellar ataxia type 20.

scientific article published in January 2005

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