Works by Bennetts, Bruce H.

Results: 9

An investigation of NOS2A promoter polymorphisms in Australian multiple sclerosis patients.

Published in:

European Journal of Human Genetics, 2005, v. 13, n. 7, p. 815, doi. 10.1038/sj.ejhg.5201422

By:

Bugeja, Matthew J.;
Booth, David R.;
Bennetts, Bruce H.;
Heard, Robert N. S.;
Burgner, David;
Stewart, Graeme J.

Publication type:

Article

Gene-gene interaction between the monoamine oxidase A gene and solute carrier family 6 (neurotransmitter transporter, noradrenalin) member 2 gene in anorexia nervosa (restrictive subtype).

Published in:

European Journal of Human Genetics, 2003, v. 11, n. 12, p. 945, doi. 10.1038/sj.ejhg.5201077

By:

Urwin, Ruth E.;
Bennetts, Bruce H.;
Wilcken, Bridget;
Lampropoulos, Basiliki;
Beumont, Peter J. V.;
Russell, Janice D.;
Tanner, Sue L.;
Nunn, Kenneth P.

Publication type:

Article

Identification of 11 novel and common single nucleotide polymorphisms in the interleukin-7 receptor-a gene and their associations with multiple sclerosis.

Published in:

European Journal of Human Genetics, 2003, v. 11, n. 7, p. 509, doi. 10.1038/sj.ejhg.5200994

By:

Teutsch, Suzy M;
Booth, David R;
Bennetts, Bruce H;
Heard, Robert N S;
Stewart, Graeme J

Publication type:

Article

STRUCTURE OF HUMAN RENIN AND EXPRESSION OF THE RENIN GENE.

Published in:

Clinical & Experimental Pharmacology & Physiology, 1984, v. 11, n. 4, p. 369, doi. 10.1111/j.1440-1681.1984.tb00281.x

By:

Morris, Brian J.;
Catanzaro, Daniel F.;
Hardman, Judy;
Mesterovic, Nikola;
Tellam, Judy;
Hort, Yvonne;
Bennetts, Bruce H.;
Shine, John

Publication type:

Article

Paternal retraction of a fragile X allele to normal size, showing normal function over two generations.

Published in:

American Journal of Medical Genetics. Part A, 2022, v. 188, n. 1, p. 304, doi. 10.1002/ajmg.a.62500

By:

Bartlett, Essra;
Archibald, Alison D.;
Francis, David;
Ling, Ling;
Thomas, Rob;
Chandler, Gabrielle;
Ward, Lisa;
O'Farrell, Gemma;
Pandelache, Alison;
Delatycki, Martin B.;
Bennetts, Bruce H.;
Ho, Gladys;
Fisk, Katrina;
Baker, Emma K.;
Amor, David J.;
Godler, David E.

Publication type:

Article

Investigation of Epistasis Between the Serotonin Transporter and Norepinephrine Transporter Genes in Anorexia Nervosa.

Published in:

Neuropsychopharmacology, 2003, v. 28, n. 7, p. 1351, doi. 10.1038/sj.npp.1300204

By:

Urwin, Ruth E.;
Bennetts, Bruce H.;
Wilcken, Bridget;
Beumont, Pierre J. V.;
Russell, Janice D.;
P. Nunn, Kenneth

Publication type:

Article

The Australian Reproductive Genetic Carrier Screening Project (Mackenzie's Mission): Design and Implementation.

Published in:

Journal of Personalized Medicine, 2022, v. 12, n. 11, p. 1781, doi. 10.3390/jpm12111781

By:

Archibald, Alison D.;
McClaren, Belinda J.;
Caruana, Jade;
Tutty, Erin;
King, Emily A.;
Halliday, Jane L.;
Best, Stephanie;
Kanga-Parabia, Anaita;
Bennetts, Bruce H.;
Cliffe, Corrina C.;
Madelli, Evanthia O.;
Ho, Gladys;
Liebelt, Jan;
Long, Janet C.;
Braithwaite, Jeffrey;
Kennedy, Jillian;
Massie, John;
Emery, Jon D.;
McGaughran, Julie;
Marum, Justine E.

Publication type:

Article

Fatal late-onset ornithine transcarbamylase deficiency after coronary artery bypass surgery.

Published in:

2007

By:

Chiong, Mary Anne;
Bennetts, Bruce H;
Strasser, Simone I;
Wilcken, Bridget

Publication type:

journal article

Fracture during Intravenous Bisphosphonate Treatment in a Child with Osteogenesis Imperfecta: An Argument for a More Frequent, Low-Dose Treatment Regimen.

Published in:

Hormone Research in Paediatrics, 2014, v. 81, n. 3, p. 204, doi. 10.1159/000355111

By:

Biggin, andrew;
Briody, Julie N.;
Ormshaw, Elizabeth;
Wong, Karen K.Y.;
Bennetts, Bruce H.;
Munns, Craig F.

Publication type:

Article