Juleen A Cavanaugh
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Explore the profile of Juleen A Cavanaugh including associated specialties, affiliations and a list of published articles.
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18
Citations
445
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Recent Articles
1.
Hickman P, Koerbin G, Potter J, Glasgow N, Cavanaugh J, Abhayaratna W, et al.
Clin Chem
. 2021 Jul;
66(12):1558-1561.
PMID: 34214151
Background: Reference intervals are an important aid in medical practice as they provide clinicians a guide as to whether a patient is healthy or diseased.Outlier results in population studies are...
2.
3.
Ayoub M, Angelicheva D, Vile D, Chandler D, Morar B, Cavanaugh J, et al.
PLoS One
. 2012 Mar;
7(3):e32849.
PMID: 22448230
We analysed a phenotypically well-characterised sample of 450 schziophrenia patients and 605 controls for rare non-synonymous single nucleotide polymorphisms (nsSNPs) in the GRM1 gene, their functional effects and family segregation....
4.
Simms L, Doecke J, Roberts R, Fowler E, Zhao Z, McGuckin M, et al.
Am J Gastroenterol
. 2010 Apr;
105(10):2209-17.
PMID: 20407432
Objectives: Crohn's disease (CD; MIM 266600) is one of the most common forms of inflammatory bowel disease (IBD), and represents a significant burden to health care in developed countries. Our...
5.
Broer S, Bailey C, Kowalczuk S, Ng C, Vanslambrouck J, Rodgers H, et al.
J Clin Invest
. 2008 Nov;
118(12):3881-92.
PMID: 19033659
Iminoglycinuria (IG) is an autosomal recessive abnormality of renal transport of glycine and the imino acids proline and hydroxyproline, but the specific genetic defect(s) have not been determined. Similarly, although...
6.
Fowler E, Doecke J, Simms L, Zhao Z, Webb P, Hayward N, et al.
Am J Gastroenterol
. 2008 Aug;
103(10):2519-26.
PMID: 18671817
Objectives: Crohn's disease (CD) and ulcerative colitis (UC) are the two most common forms of inflammatory bowel disease (IBD), representing a significant health-care burden. A variant in the autophagy gene...
7.
Schmuck E, Cappello J, Coggan M, Brew J, Cavanaugh J, Blackburn A, et al.
Int J Biochem Cell Biol
. 2008 Jun;
40(11):2553-9.
PMID: 18571971
The Omega class glutathione transferase GSTO1-1 can catalyze the reduction of pentavalent methylated arsenic species and is responsible for the biotransfomation of potentially toxic alpha-haloketones. We investigated the cause of...
8.
Azmanov D, Kowalczuk S, Rodgers H, Auray-Blais C, Giguere R, Rasko J, et al.
Hum Mutat
. 2008 May;
29(10):1217-21.
PMID: 18484095
Hartnup disorder is an autosomal recessive impairment of amino acid transport in kidney and intestine. Mutations in SLC6A19 have been shown to cosegregate with the disease in the predicted recessive...
9.
Azmanov D, Rodgers H, Auray-Blais C, Giguere R, Bailey C, Broer S, et al.
Ann Hum Genet
. 2007 Jun;
71(Pt 6):755-61.
PMID: 17555458
Hartnup disorder is an aminoaciduria that results from mutations in the recently described gene SLC6A19 on chromosome 5p15.33. The disease is inherited in a simple recessive manner and ten different...
10.
Walsh A, Dixon J, Ramm G, Hewett D, Lincoln D, Anderson G, et al.
Clin Gastroenterol Hepatol
. 2006 Sep;
4(11):1403-10.
PMID: 16979952
Background & Aims: Two major mutations are defined within the hemochromatosis gene, HFE. Although the effects of the C282Y substitution have been well characterized, the clinical significance of the C282Y/H63D...