Lynley Ward

Lynley Ward

UNVERIFIED PROFILE

Are you Lynley Ward?   Register this Author

Register author
Lynley Ward

Lynley Ward

Publications by authors named "Lynley Ward"

Are you Lynley Ward?   Register this Author

13Publications

335Reads

43Profile Views

Targeted sequencing of in familial Paget's disease of bone.

Bone Rep 2019 Jun 21;10:100198. Epub 2019 Feb 21.

Department of Endocrinology and Diabetes, Sir Charles Gairdner Hospital, Nedlands, Western Australia, Australia.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.bonr.2019.100198DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6403439PMC
June 2019

How many cases of disease in a pedigree imply familial disease?

Ann Hum Genet 2018 03 23;82(2):109-113. Epub 2017 Oct 23.

Department of Endocrinology & Diabetes, Sir Charles Gairdner Hospital, Nedlands, Australia.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1111/ahg.12222DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5813157PMC
March 2018

The Changing Presentation of Paget's Disease of Bone in Australia, A High Prevalence Region.

Calcif Tissue Int 2017 12 7;101(6):564-569. Epub 2017 Sep 7.

Department of Endocrinology and Diabetes, Sir Charles Gairdner Hospital, Nedlands, WA, 6009, Australia.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/s00223-017-0312-1DOI Listing
December 2017

HABP2 germline variants are uncommon in familial nonmedullary thyroid cancer.

BMC Med Genet 2016 08 17;17(1):60. Epub 2016 Aug 17.

Department of Endocrinology & Diabetes, Sir Charles Gairdner Hospital, Nedlands, WA, 6009, Australia.

View Article

Download full-text PDF

Source
http://bmcmedgenet.biomedcentral.com/articles/10.1186/s12881
Publisher Site
http://dx.doi.org/10.1186/s12881-016-0323-1DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4988026PMC
August 2016

Common genetic variants associated with thyroid function may be risk alleles for Hashimoto's disease and Graves' disease.

Clin Endocrinol (Oxf) 2016 Feb 27;84(2):278-283. Epub 2015 Feb 27.

Department of Endocrinology and Diabetes, Sir Charles Gairdner Hospital, Nedlands, Australia.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1111/cen.12746DOI Listing
February 2016

Sequestosome 1 mutations in Paget's disease of bone in Australia: prevalence, genotype/phenotype correlation, and a novel non-UBA domain mutation (P364S) associated with increased NF-kappaB signaling without loss of ubiquitin binding.

J Bone Miner Res 2009 Jul;24(7):1216-23

Laboratory for Molecular Endocrinology, Western Australian Institute for Medical Research and UWA Centre for Medical Research, University of Western Australia, Nedlands, Australia.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1359/jbmr.090214DOI Listing
July 2009

A novel mutation (K378X) in the sequestosome 1 gene associated with increased NF-kappaB signaling and Paget's disease of bone with a severe phenotype.

J Bone Miner Res 2006 Jul;21(7):1136-45

Laboratory for Molecular Endocrinology, Western Australian Institute for Medical Research, University of Western Australia, Nedlands.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1359/jbmr.060405DOI Listing
July 2006

Are Australian children iodine deficient? Results of the Australian National Iodine Nutrition Study.

Med J Aust 2006 Feb;184(4):165-9

School of Public Health, University of Sydney, Edward Ford Building (A27), Sydney, NSW 2006, Australia.

View Article

Download full-text PDF

Source
February 2006