Publications by authors named "Lynley Ward"

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Targeted sequencing of in familial Paget's disease of bone.
M A Sultana, N J Pavlos, Lynley Ward, J P Walsh, S L Rea

Bone Rep· June 2019

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How many cases of disease in a pedigree imply familial disease?
Frank Dudbridge, Suzanne J Brown, Lynley Ward, Scott G Wilson, John P Walsh

Ann Hum Genet· March 2018

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The Changing Presentation of Paget's Disease of Bone in Australia, A High Prevalence Region.
Cameron Britton, Suzanne Brown, Lynley Ward, Sarah L Rea, Thomas Ratajczak

Calcif Tissue Int· December 2017

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HABP2 germline variants are uncommon in familial nonmedullary thyroid cancer.
Alexia L Weeks, Scott G Wilson, Lynley Ward, Jack Goldblatt, Jennie Hui

BMC Med Genet· August 2016

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Common genetic variants associated with thyroid function may be risk alleles for Hashimoto's disease and Graves' disease.
Purdey Campbell, Thomas H Brix, Scott G Wilson, Lynley C Ward, Jennie Hui

Clin Endocrinol (Oxf)· February 2016

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Common susceptibility alleles and SQSTM1 mutations predict disease extent and severity in a multinational study of patients with Paget's disease.
Omar M E Albagha, Micaela Rios Visconti, Nerea Alonso, Sachin Wani, Kirsteen Goodman, Lynley Ward

J Bone Miner Res· November 2013

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Genome-wide association identifies three new susceptibility loci for Paget's disease of bone.
Omar M E Albagha, Sachin E Wani, Micaela R Visconti, Nerea Alonso, Kirsteen Goodman, Lynley C Ward

Nat Genet· May 2011

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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.
Sarah L Rea, John P Walsh, Lynley Ward, Aaron L Magno, Bryan K Ward

J Bone Miner Res· July 2009

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Small changes in thyroxine dosage do not produce measurable changes in hypothyroid symptoms, well-being, or quality of life: results of a double-blind, randomized clinical trial.
John P Walsh, Lynley C Ward, Valerie Burke, Chotoo I Bhagat, Lauren Shiels

J Clin Endocrinol Metab· July 2006

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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.
Sarah L Rea, John P Walsh, Lynley Ward, Kirk Yip, Bryan K Ward

J Bone Miner Res· July 2006

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Are Australian children iodine deficient? Results of the Australian National Iodine Nutrition Study.
Mu Li, Creswell J Eastman, Kay V Waite, Gary Ma, Margaret R Zacharin, Lynley C Ward

Med J Aust· February 2006

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Combined thyroxine/liothyronine treatment does not improve well-being, quality of life, or cognitive function compared to thyroxine alone: a randomized controlled trial in patients with primary hypothyroidism.
John P Walsh, Lauren Shiels, Ee Mun Lim, Chotoo I Bhagat, Lynley C Ward

J Clin Endocrinol Metab· October 2003

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Domain-specific mutations in sequestosome 1 (SQSTM1) cause familial and sporadic Paget's disease.
Lynne J Hocking, Gavin J A Lucas, Anna Daroszewska, Jon Mangion, Mark Olavesen, Lynley Ward

Hum Mol Genet· October 2002

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