Publications by authors named "Susan M Forrest"

Claim this Profile
E
Erratum: Preparing for genomic medicine: a real world demonstration of health system change.
Clara L Gaff, Ingrid M Winship, Susan M Forrest, David P Hansen, Julian Clark

NPJ Genom Med· October 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Preparing for genomic medicine: a real world demonstration of health system change.
Clara L Gaff, Ingrid M Winship, Susan M Forrest, David P Hansen, Julian Clark

NPJ Genom Med· May 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Genome sequence of an Australian kangaroo, Macropus eugenii, provides insight into the evolution of mammalian reproduction and development.
Marilyn B Renfree, Anthony T Papenfuss, Janine E Deakin, James Lindsay, Thomas Heider, Susan M Forrest

Genome Biol· August 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A duplication at chromosome 11q12.2-11q12.3 is associated with spinocerebellar ataxia type 20.
Melanie A Knight, Dena Hernandez, Scott J Diede, Hans G Dauwerse, Ian Rafferty, Susan M Forrest

Hum Mol Genet· December 2008

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
SNP selection for genes of iron metabolism in a study of genetic modifiers of hemochromatosis.
Clare C Constantine, Lyle C Gurrin, Christine E McLaren, Melanie Bahlo, Gregory J Anderson, Susan M Forrest

BMC Med Genet· March 2008

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
D
Deletion at ITPR1 underlies ataxia in mice and spinocerebellar ataxia 15 in humans.
Joyce van de Leemput, Jayanth Chandran, Melanie A Knight, Lynne A Holtzclaw, Sonja Scholz, Susan M Forrest

PLoS Genet· June 2007

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Array comparative genomic hybridisation analysis of boys with X-linked hypopituitarism identifies a 3.9 Mb duplicated critical region at Xq27 containing SOX3.
Nicola M Solomon, Shelley A Ross, Susan M Forrest, Paul Q Thomas, Thomas Morgan

J Med Genet· April 2007

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
W
Whole genome SNP arrays using DNA derived from formalin-fixed, paraffin-embedded ovarian tumor tissue.
Ella R Thompson, Shane C Herbert, Susan M Forrest, Ian G Campbell

Hum Mutat· October 2005

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
Spinocerebellar ataxia type 15.
R J McKinlay Gardner, Melanie A Knight, Kenju Hara, Shoji Tsuji, Susan M Forrest

Cerebellum· June 2005

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
Spinocerebellar ataxia type 20.
Elsdon Storey, Melanie A Knight, Susan M Forrest, R J McKinlay Gardner

Cerebellum· June 2005

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A gene for pili annulati maps to the telomeric region of chromosome 12q.
Jack Green, Elizabeth Fitzpatrick, David de Berker, Susan M Forrest, Rodney D Sinclair

J Invest Dermatol· December 2004

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
D
Dominantly inherited ataxia and dysphonia with dentate calcification: spinocerebellar ataxia type 20.
Melanie A Knight, R J McKinlay Gardner, Melanie Bahlo, Tohru Matsuura, Judith A Dixon, Susan M Forrest

Brain· May 2004

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Parametric and nonparametric genome scan analyses for human handedness.
Tom Van Agtmael, Susan M Forrest, Jurgen Del-Favero, Christine Van Broeckhoven, Robert Williamson

Eur J Hum Genet· October 2003

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
Spinocerebellar ataxia type 15 (sca15) maps to 3p24.2-3pter: exclusion of the ITPR1 gene, the human orthologue of an ataxic mouse mutant.
Melanie A Knight, Marina L Kennerson, Richard J Anney, Tohru Matsuura, Garth A Nicholson, Susan M Forrest

Neurobiol Dis· July 2003

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Progressive patterned scalp hypotrichosis, with wiry hair, onycholysis, and intermittently associated cleft lip and palate: clinical and genetic distinction from Marie Unna.
Jack Green, Elizabeth Fitzpatrick, David de Berker, Susan M Forrest, Rodney D Sinclair

J Investig Dermatol Symp Proc· June 2003

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Parametric and non-parametric linkage analysis of several candidate regions for genes for human handedness.
Tom Van Agtmael, Susan M Forrest, Robert Williamson

Eur J Hum Genet· October 2002

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
Structural and mutational analysis of antiquitin as a candidate gene for Menière disease.
Michael Lynch, Trevor L Cameron, Melanie Knight, Tak Yue Kwok, Paul Thomas, Susan M Forrest

Am J Med Genet· July 2002

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Increased gene dosage at Xq26-q27 is associated with X-linked hypopituitarism.
Nicola M Solomon, Sara Nouri, Garry L Warne, Maria Lagerström-Fermér, Susan M Forrest

Genomics· April 2002

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Conservation of CNS1 and exclusion of its role in atopic eczema susceptibility.
Kate S Elliott, Richard J l Anney, Elizabeth B Fitzpatrick, Robert Williamson, Susan M Forrest

J Allergy Clin Immunol· January 2002

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis