Publications by authors named "Michelle Jennens"

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α-thalassemia trait caused by frameshift mutations in exon 2 of the α2-globin gene: HBA2:c.131delT and HBA2:c.143delA.
Jill Finlayson, Reza Ghassemifar, Paula Holmes, Dianne Grey, Christopher Newbound, Michelle Jennens

Hemoglobin· January 2013

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A molecular tool to assess the pathological relevance of alpha-globin DNA variants.
Talal Qadah, Jill Finlayson, Christopher Newbound, Nicole Pell, Michelle Jennens

Pathology· June 2012

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Hb Lynwood [α107(G14) (-T) (α2) HBA2:c.323delT)] in conjunction with the α(3.7) deletion produces a moderately severe α-thalassemia phenotype.
Jill Finlayson, Reza Ghassemifar, Paula Holmes, Dianne Grey, Christopher Newbound, Michelle Jennens

Hemoglobin· August 2011

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Hb East Timor [β80(EF4)Asn→His, AAC>CAC (HBB c.241A>C)], a variant hemoglobin associated with normal hematology.
Jill Finlayson, Reza Ghassemifar, Paula Holmes, Dianne Grey, Lisa Figliomeni, Michelle Jennens

Hemoglobin· April 2011

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Association of Interleukin-1 gene polymorphisms with central obesity and metabolic syndrome in a coronary heart disease population.
Kim W Carter, Joseph Hung, Brenda L Powell, Steven Wiltshire, Brendan T X Foo, Michelle Jennens

Hum Genet· October 2008

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The apolipoprotein AII rs5082 variant is associated with reduced risk of coronary artery disease in an Australian male population.
Jing Xiao, Fan Zhang, Steven Wiltshire, Joseph Hung, Michelle Jennens

Atherosclerosis· August 2008

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Investigating the association between K198N coding polymorphism in EDN1 and hypertension, lipoprotein levels, the metabolic syndrome and cardiovascular disease.
Steven Wiltshire, Brenda L Powell, Michelle Jennens, Pamela A McCaskie, Kim W Carter

Hum Genet· April 2008

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IL18 haplotypes are associated with serum IL-18 concentrations in a population-based study and a cohort of individuals with premature coronary heart disease.
Simon R Thompson, Pamela A McCaskie, John P Beilby, Joseph Hung, Michelle Jennens

Clin Chem· December 2007

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