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Jon Mangion

Research Profile

Physiology

Disorders

Anatomy

Chromosomes, Human, Pair 7

Concepts & Ideas

Chemicals & Drugs

Occupations

Procedures

Geographic Areas

Australia

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Co-author Network

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Publications

TOP 3
Krina T Zondervan; Susan A Treloar; Jianghai Lin; Daniel E Weeks; Dale R Nyholt; Jon Mangion; Ian J Mackay; Lon R Cardon; Nicholas G Martin; Stephen Kennedy; Grant W Montgomery
Significant evidence of one or more susceptibility loci for endometriosis with near-Mendelian inheritance on chromosome 7p13-15.
Roy Pettipher; Jon Mangion; Michael G Hunter; Ian Mackay
Identification of G-protein-coupled receptors involved in inflammatory disease by genetic association studies.
Lynne J Hocking; Gavin J A Lucas; Anna Daroszewska; Jon Mangion; Mark Olavesen; Tim Cundy; Geoffrey C Nicholson; Lynley Ward; Simon T Bennett; Wim Wuyts; Wim Van Hul; Stuart H Ralston
Domain-specific mutations in sequestosome 1 (SQSTM1) cause familial and sporadic Paget's disease.

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All Publications

2007: Krina T Zondervan; Susan A Treloar; Jianghai Lin; Daniel E Weeks; Dale R Nyholt; Jon Mangion; Ian J Mackay; Lon R Cardon; Nicholas G Martin; Stephen Kennedy; Grant W Montgomery
Significant evidence of one or more susceptibility loci for endometriosis with near-Mendelian inheritance on chromosome 7p13-15.
Human reproduction (Oxford, England) 2007;22(3):717-28.
2005: Roy Pettipher; Jon Mangion; Michael G Hunter; Ian Mackay
Identification of G-protein-coupled receptors involved in inflammatory disease by genetic association studies.
Current opinion in pharmacology 2005;5(4):412-7.
2002: Lynne J Hocking; Gavin J A Lucas; Anna Daroszewska; Jon Mangion; Mark Olavesen; Tim Cundy; Geoffrey C Nicholson; Lynley Ward; Simon T Bennett; Wim Wuyts; Wim Van Hul; Stuart H Ralston
Domain-specific mutations in sequestosome 1 (SQSTM1) cause familial and sporadic Paget's disease.
Human molecular genetics 2002;11(22):2735-9.

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