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Epigenome-wide Association Study Shows Differential DNA Methylation of MDC1, KLF9, and CUTA in Autoimmune Thyroid Disease.
Published in:
Journal of Clinical Endocrinology & Metabolism, 2024, v. 109, n. 4, p. 992, doi. 10.1210/clinem/dgad659
By:
- Lafontaine, Nicole;
- Shore, Christopher J;
- Campbell, Purdey J;
- Mullin, Benjamin H;
- Brown, Suzanne J;
- Panicker, Vijay;
- Dudbridge, Frank;
- Brix, Thomas H;
- Hegedüs, Laszlo;
- Wilson, Scott G;
- Bell, Jordana T;
- Walsh, John P
Publication type:
Article
DNA Methylation in Autoimmune Thyroid Disease.
Published in:
Journal of Clinical Endocrinology & Metabolism, 2023, v. 108, n. 3, p. 604, doi. 10.1210/clinem/dgac664
By:
- Lafontaine, Nicole;
- Wilson, Scott G.;
- Walsh, John P.
Publication type:
Article
Response to Letter to the Editor: "Changes in Thyroid Function Across Adolescence: A Longitudinal Study".
Published in:
2020
By:
- Campbell, Purdey J.;
- Kendrew, Phillip;
- Lewer, Michelle;
- Ee Mun Lim;
- Wilson, Scott G.;
- Walsh, John P.;
- Lim, Ee Mun
Publication type:
Letter
Changes in Thyroid Function Across Adolescence: A Longitudinal Study.
Published in:
2020
By:
- Campbell, Purdey J;
- Brown, Suzanne J;
- Kendrew, Phillip;
- Lewer, Michelle;
- Lim, Ee Mun;
- Joseph, John;
- Cross, Simone M;
- Wright, Margaret J;
- Martin, Nicholas G;
- Wilson, Scott G;
- Walsh, John P
Publication type:
journal article
Common Sequence Variation in FLNB Regulates Bone Structure in Women in the General Population and FLNB mRNA Express in Osteoblasts In Vitro.
Published in:
Journal of Bone & Mineral Research, 2009, v. 24, n. 12, p. 1989, doi. 10.1359/JBMR.090530
By:
- Wilson, Scott G.;
- Jones, Michelle R.;
- Mullin, Ben H.;
- Dick, Ian M.;
- Richards, J. Brent;
- Pastinen, Tomi M.;
- Grundberg, Elin;
- Ljunggren, Östen;
- Surdulescu, Gabriela L.;
- Dudbridge, Frank;
- Elliott, Katherine S.;
- Cervino, Alessandra C. L.;
- Spector, Timothy D.;
- Prince, Richard L.
Publication type:
Article
HABP2 germline variants are uncommon in familial nonmedullary thyroid cancer.
Published in:
BMC Medical Genetics, 2016, v. 17, p. 1, doi. 10.1186/s12881-016-0323-1
By:
- Weeks, Alexia L.;
- Wilson, Scott G.;
- Ward, Lynley;
- Goldblatt, Jack;
- Hui, Jennie;
- Walsh, John P.
Publication type:
Article
Influence of ARHGEF3 and RHOA Knockdown on ACTA2 and Other Genes in Osteoblasts and Osteoclasts.
Published in:
PLoS ONE, 2014, v. 9, n. 5, p. 1, doi. 10.1371/journal.pone.0098116
By:
- Mullin, Benjamin H.;
- Mamotte, Cyril;
- Prince, Richard L.;
- Wilson, Scott G.
Publication type:
Article
Identification of PLCL1 Gene for Hip Bone Size Variation in Females in a Genome-Wide Association Study.
Published in:
PLoS ONE, 2008, v. 3, n. 9, p. 1, doi. 10.1371/journal.pone.0003160
By:
- Yao-Zhong Liu;
- Wilson, Scott G.;
- Liang Wang;
- Xiao-Gang Liu;
- Yan-Fang Guo;
- Jian Li;
- Han Yan;
- Deloukas, Panos;
- Soranzo, Nicole;
- Chinnapen-Horsley, Usha;
- Cervino, Alesandra;
- Williams, Frances M.;
- Dong-Hai Xiong;
- Yin-Ping Zhang;
- Tian-Bo Jin;
- Levy, Shawn;
- Papasian, Christopher J.;
- Drees, Betty M.;
- Hamilton, James J.;
- Recker, Robert R.
Publication type:
Article
Human lactation: Forearm trabecular bone loss, increased bone turnover, and renal conservation of calcium and inorganic phosphate with recovery of bone mass following weaning.
Published in:
Journal of Bone & Mineral Research, 1990, v. 5, n. 4, p. 361, doi. 10.1002/jbmr.5650050409
By:
- Kent, G. Neil;
- Price, Roger I.;
- Gutteridge, Donald H.;
- Allen, Janet R.;
- Barnes, Marion P.;
- Hickling, Caroline J.;
- Retallack, Robert W.;
- Wilson, Scott G.;
- Devlin, Rowena D.;
- Smith, Margaret;
- Bhagat, Chotoo I.;
- Davies, Charmian;
- St. Johns, Andrew
Publication type:
Article
Genetic Loci Linked to Pituitary-Thyroid Axis Set Points: A Genome-Wide Scan of a Large Twin Cohort.
Published in:
Journal of Clinical Endocrinology & Metabolism, 2008, v. 93, n. 9, p. 3519, doi. 10.1210/jc.2007-2650
By:
- Panicker, Vijay;
- Wilson, Scott G.;
- Spector, Tim D.;
- Brown, Suzanne J.;
- Kato, Bernet S.;
- Reed, Peter W.;
- Falchi, Mario;
- Richards, J. Brent;
- Surdulescu, Gabriela L.;
- Lim, Ee M.;
- Fletcher, Steven J.;
- Walsh, John P.
Publication type:
Article
Effects of calcium and vitamin D supplementation on hip bone mineral density and calcium-related analytes in elderly ambulatory Australian women: a five-year randomized controlled trial.
Published in:
2008
By:
- Zhu, Kun;
- Devine, Amanda;
- Dick, Ian M.;
- Wilson, Scott G.;
- Prince, Richard L.
Publication type:
journal article
Linkage of Genes to Total Lean Body Mass in Normal Women.
Published in:
Journal of Clinical Endocrinology & Metabolism, 2007, v. 92, n. 8, p. 3171, doi. 10.1210/jc.2007-0418
By:
- Livshits, Gregory;
- Kato, Bernet S.;
- Wilson, Scott G.;
- Spector, Tim D.
Publication type:
Article
Genome-wide association study using family-based cohorts identifies the WLS and CCDC170/ESR1 loci as associated with bone mineral density.
Published in:
BMC Genomics, 2016, v. 17, p. 1, doi. 10.1186/s12864-016-2481-0
By:
- Mullin, Benjamin H.;
- Walsh, John P.;
- Hou-Feng Zheng;
- Brown, Suzanne J.;
- Surdulescu, Gabriela L.;
- Curtis, Charles;
- Breen, Gerome;
- Dudbridge, Frank;
- Richards, J. Brent;
- Spector, Tim D.;
- Wilson, Scott G.
Publication type:
Article
Functional Assessment of Calcium-Sensing Receptor Variants Confirms Familial Hypocalciuric Hypercalcemia.
Published in:
Journal of the Endocrine Society, 2022, v. 6, n. 5, p. 1, doi. 10.1210/jendso/bvac025
By:
- Mullin, Benjamin H;
- Pavlos, Nathan J;
- Brown, Suzanne J;
- Walsh, John P;
- McKellar, Ross A;
- Wilson, Scott G;
- Ward, Bryan K
Publication type:
Article
Familial Dysalbuminemic Hyperthyroxinemia as a Cause for Discordant Thyroid Function Tests.
Published in:
Journal of the Endocrine Society, 2021, v. 5, n. 4, p. 1, doi. 10.1210/jendso/bvab012
By:
- Ting, Matthew J M;
- Zhang, Rui;
- Lim, Ee Mun;
- Ward, Bryan K;
- Wilson, Scott G;
- Walsh, John P
Publication type:
Article
SERUM FREE 1,25-DIHYDROXYVITAMIN D AND THE FREE 1,25-DIHYDROXYVITAMIN D INDEX DURING A LONGITUDINAL STUDY OF HUMAN PREGNANCY AND LACTATION.
Published in:
Clinical Endocrinology, 1990, v. 32, n. 5, p. 613, doi. 10.1111/j.1365-2265.1990.tb00905.x
By:
- WILSON, SCOTT G.;
- RETALLACK, ROBERT W.;
- KENT, JACQUELINE C.;
- WORTH, GRAEME K.;
- GUTTERIDGE, DONALD H.
Publication type:
Article
Linkage and potential association of obesity-related phenotypes with two genes on chromosome 12q24 in a female dizygous twin cohort.
Published in:
European Journal of Human Genetics, 2006, v. 14, n. 3, p. 340, doi. 10.1038/sj.ejhg.5201551
By:
- Wilson, Scott G.;
- Adam, Gail;
- Langdown, Maria;
- Reneland, Rikard;
- Braun, Andreas;
- Andrew, Toby;
- Surdulescu, Gabriela L.;
- Norberg, Maria;
- Dudbridge, Frank;
- Reed, Peter W.;
- Sambrook, Philip N.;
- Kleyn, Patrick W.;
- Spector, Tim D.
Publication type:
Article
Genetic determinants of thyroid function in children.
Published in:
European Journal of Endocrinology, 2023, v. 189, n. 2, p. 164, doi. 10.1093/ejendo/lvad086
By:
- Mulder, Tessa A.;
- Campbell, Purdey J.;
- Taylor, Peter N.;
- Peeters, Robin P.;
- Wilson, Scott G.;
- Medici, Marco;
- Dayan, Colin;
- Jaddoe, Vincent V. W.;
- Walsh, John P.;
- Martin, Nicholas G.;
- Tiemeier, Henning;
- Korevaar, Tim I. M.
Publication type:
Article
Genome-wide analysis of thyroid function in Australian adolescents highlights SERPINA7 and NCOA3.
Published in:
European Journal of Endocrinology, 2021, v. 185, n. 5, p. 743, doi. 10.1530/EJE-21-0614
By:
- Nolan, James;
- Campbell, Purdey J.;
- Brown, Suzanne J.;
- Gu Zhu;
- Gordon, Scott;
- Ee Mun Lim;
- Joseph, John;
- Cross, Simone M.;
- Panicker, Vijay;
- Medland, Sarah E.;
- Melton, Phillip E.;
- Beilin, Lawrence J.;
- Mori, Trevor A.;
- Mullin, Benjamin H.;
- Pennell, Craig E.;
- Wang, Carol A.;
- Dudbridge, Frank;
- Walsh, John P.;
- Martin, Nicholas G.;
- Wilson, Scott G.
Publication type:
Article
A Flexible Model for Association Analysis in Sibships with Missing Genotype Data.
Published in:
Annals of Human Genetics, 2011, v. 75, n. 3, p. 428, doi. 10.1111/j.1469-1809.2010.00636.x
By:
- Dudbridge, Frank;
- Holmans, Peter A.;
- Wilson, Scott G.
Publication type:
Article
Conditional testing of multiple variants associated with bone mineral density in the FLNB gene region suggests that they represent a single association signal.
Published in:
BMC Genetics, 2013, v. 14, n. 1, p. 1, doi. 10.1186/1471-2156-14-107
By:
- Mullin, Benjamin H.;
- Mamotte, Cyril;
- Prince, Richard L.;
- Spector, Tim D.;
- Dudbridge, Frank;
- Wilson, Scott G.
Publication type:
Article
Shared genetics and causal relationships between migraine and thyroid function traits.
Published in:
Cephalalgia, 2023, v. 43, n. 2, p. 1, doi. 10.1177/03331024221139253
By:
- Tasnim, Sana;
- Wilson, Scott G;
- Walsh, John P;
- Nyholt, Dale R
Publication type:
Article
How many cases of disease in a pedigree imply familial disease?
Published in:
Annals of Human Genetics, 2018, v. 82, n. 2, p. 109, doi. 10.1111/ahg.12222
By:
- Dudbridge, Frank;
- Brown, Suzanne J.;
- Ward, Lynley;
- Wilson, Scott G.;
- Walsh, John P.
Publication type:
Article
Genome-wide association study meta-analysis for quantitative ultrasound parameters of bone identifies five novel loci for broadband ultrasound attenuation.
Published in:
Human Molecular Genetics, 2017, v. 26, n. 14, p. 2791, doi. 10.1093/hmg/ddx174
By:
- Mullin, Benjamin H.;
- Jing Hua Zhao;
- Brown, Suzanne J.;
- Perry, John R. B.;
- Luan, Jian'an;
- Hou-Feng Zheng;
- Langenberg, Claudia;
- Dudbridge, Frank;
- Scott, Robert;
- Wareham, Nick J.;
- Spector, Tim D.;
- Richards, J. Brent;
- Walsh, John P.;
- Wilson, Scott G.
Publication type:
Article
Genetic determinants of heel bone properties: genome-wide association meta-analysis and replication in the GEFOS/GENOMOS consortium.
Published in:
Human Molecular Genetics, 2014, v. 23, n. 11, p. 3054, doi. 10.1093/hmg/ddt675
By:
- Moayyeri, Alireza;
- Hsu, Yi-Hsiang;
- Karasik, David;
- Estrada, Karol;
- Xiao, Su-Mei;
- Nielson, Carrie;
- Srikanth, Priya;
- Giroux, Sylvie;
- Wilson, Scott G.;
- Zheng, Hou-Feng;
- Smith, Albert V.;
- Pye, Stephen R.;
- Leo, Paul J.;
- Teumer, Alexander;
- Hwang, Joo-Yeon;
- Ohlsson, Claes;
- McGuigan, Fiona;
- Minster, Ryan L.;
- Hayward, Caroline;
- Olmos, José M.
Publication type:
Article
Quantitative Linkage Analysis for Pancreatic B-cell Function and Insulin Resistance in a Large Twin Cohort.
Published in:
Diabetes, 2008, v. 57, n. 4, p. 1120, doi. 10.2337/db07-0708
By:
- Falchi, Mario;
- Wilson, Scott G.;
- Paximadas, Dimitrios;
- Swaminathan, Ramasamyiyer;
- Spector, Tim D.
Publication type:
Article
Leveraging osteoclast genetic regulatory data to identify genes with a role in osteoarthritis.
Published in:
Genetics, 2023, v. 225, n. 2, p. 1, doi. 10.1093/genetics/iyad150
By:
- Mullin, Benjamin H.;
- Kun Zhu;
- Brown, Suzanne J.;
- Mullin, Shelby;
- Dudbridge, Frank;
- Pavlos, Nathan J.;
- Richards, J. Brent;
- Grundberg, Elin;
- Bell, Jordana T.;
- Zeggini, Eleftheria;
- Walsh, John P.;
- Jiake Xu;
- Wilson, Scott G.
Publication type:
Article
Dysregulated Antibody, Natural Killer Cell and Immune Mediator Profiles in Autoimmune Thyroid Diseases.
Published in:
Cells (2073-4409), 2020, v. 9, n. 3, p. 665, doi. 10.3390/cells9030665
By:
- Martin, Tiphaine C.;
- Ilieva, Kristina M.;
- Visconti, Alessia;
- Beaumont, Michelle;
- Kiddle, Steven J.;
- Dobson, Richard J. B.;
- Mangino, Massimo;
- Lim, Ee Mun;
- Pezer, Marija;
- Steves, Claire J.;
- Bell, Jordana T.;
- Wilson, Scott G.;
- Lauc, Gordan;
- Roederer, Mario;
- Walsh, John P.;
- Spector, Tim D.;
- Karagiannis, Sophia N.
Publication type:
Article
Age-dependent genetic regulation of osteoarthritis: independent effects of immune system genes.
Published in:
Arthritis Research & Therapy, 2023, v. 25, n. 1, p. 1, doi. 10.1186/s13075-023-03216-2
By:
- Kenny, Jacob;
- Mullin, Benjamin H.;
- Tomlinson, William;
- Robertson, Brett;
- Yuan, Jinbo;
- Chen, Weiwei;
- Zhao, Jinmin;
- Pavlos, Nathan J.;
- Walsh, John P.;
- Wilson, Scott G.;
- Tickner, Jennifer;
- Morahan, Grant;
- Xu, Jiake
Publication type:
Article
A Meta-Analysis of Thyroid-Related Traits Reveals Novel Loci and Gender-Specific Differences in the Regulation of Thyroid Function.
Published in:
PLoS Genetics, 2013, v. 9, n. 2, p. 1, doi. 10.1371/journal.pgen.1003266
By:
- Porcu, Eleonora;
- Medici, Marco;
- Pistis, Giorgio;
- Volpato, Claudia B.;
- Wilson, Scott G.;
- Cappola, Anne R.;
- Bos, Steffan D.;
- Deelen, Joris;
- den Heijer, Martin;
- Freathy, Rachel M.;
- Lahti, Jari;
- Chunyu Liu;
- Lopez, Lorna M.;
- Nolte, Ilja M.;
- O'Connell, Jeffrey R.;
- Tanaka, Toshiko;
- Trompet, Stella;
- Arnold, Alice;
- Bandinelli, Stefania;
- Beekman, Marian
Publication type:
Article
An Integration of Genome-Wide Association Study and Gene Expression Profiling to Prioritize the Discovery of Novel Susceptibility Loci for Osteoporosis-Related Traits.
Published in:
PLoS Genetics, 2010, v. 6, n. 6, p. 1, doi. 10.1371/journal.pgen.1000977
By:
- Yi-Hsiang Hsu;
- Zillikens, M. Carola;
- Wilson, Scott G.;
- Farber, Charles R.;
- Demissie, Serkalem;
- Soranzo, Nicole;
- Bianchi, Estelle N.;
- Grundberg, Elin;
- Liming Liang;
- Richards, J. Brent;
- Estrada, Karol;
- Yanhua Zhou;
- van Nas, Atila;
- Moffatt, Miriam F.;
- Guangju Zhai;
- Hofman, Albert;
- van Meurs, Joyce B.;
- Pols, Huibert A. P.;
- Price, Roger I.;
- Nilsson, Olle
Publication type:
Article
Functional Analysis of Calcium-Sensing Receptor Variants Identified in Families Provisionally Diagnosed with Familial Hypocalciuric Hypercalcaemia.
Published in:
2020
By:
- Magno, Aaron L.;
- Leatherbarrow, Kassandra M.;
- Brown, Suzanne J.;
- Wilson, Scott G.;
- Walsh, John P.;
- Ward, Bryan K.
Publication type:
journal article
Genetic regulatory mechanisms in human osteoclasts suggest a role for the STMP1 and DCSTAMP genes in Paget's disease of bone.
Published in:
Scientific Reports, 2019, v. 9, n. 1, p. 1, doi. 10.1038/s41598-018-37609-0
By:
- Mullin, Benjamin H.;
- Zhu, Kun;
- Brown, Suzanne J.;
- Mullin, Shelby;
- Tickner, Jennifer;
- Pavlos, Nathan J.;
- Dudbridge, Frank;
- Xu, Jiake;
- Walsh, John P.;
- Wilson, Scott G.
Publication type:
Article
Case Presentation: Functional Assessment of a CASR Variant Identified in a Patient with Hypercalcaemia Confirms Familial Hypocalciuric Hypercalcaemia in the Patient and a Sister Previously Misdiagnosed with Primary Hyperparathyroidism.
Published in:
2024
By:
- Ward, Bryan K.;
- Loffell, Kirsten A.;
- Walsh, John P.;
- Howe, Warwick D.;
- Brown, Suzanne J.;
- Wilson, Scott G.
Publication type:
Case Study
Metabolomic markers reveal novel pathways of ageing and early development in human populations.
Published in:
International Journal of Epidemiology, 2013, v. 42, n. 4, p. 1111, doi. 10.1093/ije/dyt094
By:
- Menni, Cristina;
- Kastenmüller, Gabriella;
- Petersen, Ann Kristin;
- Bell, Jordana T;
- Psatha, Maria;
- Tsai, Pei-Chien;
- Gieger, Christian;
- Schulz, Holger;
- Erte, Idil;
- John, Sally;
- Brosnan, M Julia;
- Wilson, Scott G;
- Tsaprouni, Loukia;
- Lim, Ee Mun;
- Stuckey, Bronwyn;
- Deloukas, Panos;
- Mohney, Robert;
- Suhre, Karsten;
- Spector, Tim D;
- Valdes, Ana M
Publication type:
Article
Digenic Congenital Hypogonadotropic Hypogonadism Due to Heterozygous GNRH1 p.R31C and AMHR2 p.G445_L453del Variants.
Published in:
Genes, 2023, v. 14, n. 6, p. 1204, doi. 10.3390/genes14061204
By:
- Stuckey, Bronwyn G. A.;
- Jones, Timothy W.;
- Ward, Bryan K.;
- Wilson, Scott G.
Publication type:
Article
Identification of Differentially Expressed Genes and Molecular Pathways Involved in Osteoclastogenesis Using RNA-seq.
Published in:
Genes, 2023, v. 14, n. 4, p. 916, doi. 10.3390/genes14040916
By:
- Rashid, Sarah;
- Wilson, Scott G.;
- Zhu, Kun;
- Walsh, John P.;
- Xu, Jiake;
- Mullin, Benjamin H.
Publication type:
Article
Cross-Trait Genetic Analyses Indicate Pleiotropy and Complex Causal Relationships between Headache and Thyroid Function Traits.
Published in:
Genes, 2023, v. 14, n. 1, p. 16, doi. 10.3390/genes14010016
By:
- Tasnim, Sana;
- Wilson, Scott G.;
- Walsh, John P.;
- Nyholt, Dale R.
Publication type:
Article
Characterisation of genetic regulatory effects for osteoporosis risk variants in human osteoclasts.
Published in:
Genome Biology, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s13059-020-01997-2
By:
- Mullin, Benjamin H.;
- Tickner, Jennifer;
- Zhu, Kun;
- Kenny, Jacob;
- Mullin, Shelby;
- Brown, Suzanne J.;
- Dudbridge, Frank;
- Pavlos, Nathan J.;
- Mocarski, Edward S.;
- Walsh, John P.;
- Xu, Jiake;
- Wilson, Scott G.
Publication type:
Article
Collaborative Meta-analysis: Associations of 150 Candidate Genes With Osteoporosis and Osteoporotic Fracture.
Published in:
Annals of Internal Medicine, 2009, v. 151, n. 8, p. 528, doi. 10.7326/0003-4819-151-8-200910200-00006
By:
- Richards, J. Brent;
- Kavvoura, Fotini K.;
- Rivadeneira, Fernando;
- Styrkársdóttir, Unnur;
- Estrada, Karol;
- Halldórsson, Bjarni V.;
- Yi-Hsiang Hsu;
- Zillikens, M. Carola;
- Wilson, Scott G.;
- Mullin, Benjamin H.;
- Amin, Najaf;
- Aulchenko, Yurii S.;
- Cupples, L. Adrienne;
- Deloukas, Panagiotis;
- Demissie, Serkalem;
- Hofman, Albert;
- Kong, Augustine;
- Karasik, David;
- van Meurs, Joyce B.;
- Oostra, Ben A.
Publication type:
Article
Identification of Novel Loci Associated With Hip Shape: A Meta‐Analysis of Genomewide Association Studies.
Published in:
Journal of Bone & Mineral Research, 2019, v. 34, n. 2, p. 241, doi. 10.1002/jbmr.3605
By:
- Baird, Denis A;
- Evans, Daniel S;
- Kamanu, Frederick K;
- Gregory, Jennifer S;
- Saunders, Fiona R;
- Giuraniuc, Claudiu V;
- Barr, Rebecca J;
- Aspden, Richard M;
- Jenkins, Deborah;
- Kiel, Douglas P;
- Orwoll, Eric S;
- Cummings, Steven R;
- Lane, Nancy E;
- Mullin, Benjamin H;
- Williams, Frances MK;
- Richards, J Brent;
- Wilson, Scott G;
- Spector, Tim D;
- Faber, Benjamin G;
- Lawlor, Deborah A
Publication type:
Article
Expression Quantitative Trait Locus Study of Bone Mineral Density GWAS Variants in Human Osteoclasts.
Published in:
Journal of Bone & Mineral Research, 2018, v. 33, n. 6, p. 1044, doi. 10.1002/jbmr.3412
By:
- Mullin, Benjamin H.;
- Zhu, Kun;
- Xu, Jiake;
- Brown, Suzanne J.;
- Mullin, Shelby;
- Tickner, Jennifer;
- Pavlos, Nathan J.;
- Dudbridge, Frank;
- Walsh, John P.;
- Wilson, Scott G.
Publication type:
Article
Common genetic variants associated with thyroid function may be risk alleles for Hashimoto's disease and Graves' disease.
Published in:
Clinical Endocrinology, 2016, v. 84, n. 2, p. 278, doi. 10.1111/cen.12746
By:
- Campbell, Purdey;
- Brix, Thomas H.;
- Wilson, Scott G.;
- Ward, Lynley C.;
- Hui, Jennie;
- Beilby, John P.;
- Hegedüs, Laszlo;
- Walsh, John P.
Publication type:
Article
A cohort study of the effects of serum osteoprotegerin and osteoprotegerin gene polymorphisms on cardiovascular mortality in elderly women.
Published in:
Clinical Endocrinology, 2009, v. 71, n. 6, p. 828, doi. 10.1111/j.1365-2265.2009.03605.x
By:
- Ueland, Thor;
- Wilson, Scott G.;
- Islam, F. M. Amirul;
- Mullin, Ben;
- Devine, Amanda;
- Bollerslev, Jens;
- Kun Zhu;
- Prince, Richard L.
Publication type:
Article
Complement C5a Induces Renal Injury in Diabetic Kidney Disease by Disrupting Mitochondrial Metabolic Agility.
Published in:
2020
By:
- Sih Min Tan;
- Ziemann, Mark;
- Thallas-Bonke, Vicki;
- Snelson, Matthew;
- Kumar, Vinod;
- Laskowski, Adrienne;
- Nguyen, Tuong-Vi;
- Huynh, Kevin;
- Clarke, Michele V.;
- Libianto, Renata;
- Baker, Scott T.;
- Skene, Alison;
- Power, David A.;
- MacIsaac, Richard J.;
- Henstridge, Darren C.;
- Wetsel, Rick A.;
- El-Osta, Assam;
- Meikle, Peter J.;
- Wilson, Scott G.;
- Forbes, Josephine M.
Publication type:
journal article
Association between a variation in the phosphodiesterase 4D gene and bone mineral density.
Published in:
BMC Medical Genetics, 2005, v. 6, p. 9, doi. 10.1186/1471-2350-6-9
By:
- Reneland, Richard H;
- Mah, Steven;
- Kammerer, Stefan;
- Hoyal, Carolyn R.;
- Marnellos, George;
- Wilson, Scott G.;
- Sambrook, Philip N.;
- Spector, Tim D.;
- Nelson, Matthew R.;
- Braun, Andreas
Publication type:
Article

Found: 46