R Wadey
Overview
Explore the profile of R Wadey including associated specialties, affiliations and a list of published articles.
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Articles
16
Citations
558
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Recent Articles
1.
Wadey R, Podlog L, Galli N, Mellalieu S
Scand J Med Sci Sports
. 2015 Nov;
26(10):1132-9.
PMID: 26589377
This study explored the applicability of organismic valuing theory (OVT) to stress-related growth (SRG) following sport injury. Specifically, the direct and indirect relationships between need satisfaction (i.e., autonomy, competence, and...
2.
Wadey R, McKie J, Papapetrou C, Sutherland H, Lohman F, Osinga J, et al.
Am J Hum Genet
. 1999 Jun;
65(1):247-9.
PMID: 10364538
No abstract available.
3.
Ross A, Wang Y, Hagan D, Scherer S, Lynch S, Lindsay S, et al.
Nat Genet
. 1998 Dec;
20(4):358-61.
PMID: 9843207
Partial absence of the sacrum is a rare congenital defect which also occurs as an autosomal dominant trait; association with anterior meningocoele, presacral teratoma and anorectal abnormalities constitutes the Currarino...
4.
Carlson C, Sirotkin H, Pandita R, Goldberg R, McKie J, Wadey R, et al.
Am J Hum Genet
. 1997 Oct;
61(3):620-9.
PMID: 9326327
Velo-cardio-facial syndrome (VCFS) is a relatively common developmental disorder characterized by craniofacial anomalies and conotruncal heart defects. Many VCFS patients have hemizygous deletions for a part of 22q11, suggesting that...
5.
Taylor C, Wadey R, ODonnell H, Roberts C, Mattei M, Kimber W, et al.
Mamm Genome
. 1997 May;
8(5):371-5.
PMID: 9107688
No abstract available.
6.
Sutherland H, Wadey R, McKie J, Taylor C, Atif U, Johnstone K, et al.
Am J Hum Genet
. 1996 Jul;
59(1):23-31.
PMID: 8659529
Most cases of DiGeorge syndrome (DGS) and related abnormalities are associated with deletions within 22q11. Shortest region of deletion overlap (SRO) mapping previously identified a critical region (the DGCR) of...
7.
Wadey R, Daw S, Taylor C, Atif U, Kamath S, Halford S, et al.
Hum Mol Genet
. 1995 Jun;
4(6):1027-33.
PMID: 7655455
Deletions within 22q11 have been associated with a wide variety of birth defects embraced by the acronym CATCH22 and including the DiGeorge syndrome, Shprintzen syndrome (velocardiofacial syndrome) and congenital heart...
8.
Halford S, Wadey R, Roberts C, Daw S, WHITING J, ODonnell H, et al.
Hum Mol Genet
. 1993 Dec;
2(12):2099-107.
PMID: 8111380
A wide spectrum of birth defects are caused by deletions of the DiGeorge syndrome critical region (DGCR) at human chromosome 22q11. Over one hundred such deletions have now been examined...
9.
Halford S, Wilson D, Daw S, Roberts C, Wadey R, Kamath S, et al.
Hum Mol Genet
. 1993 Oct;
2(10):1577-82.
PMID: 8268909
DiGeorge syndrome (DGS) is one of several syndromes associated with deletions within the proximal long-arm of chromosome 22. The region of chromosome 22q11 responsible for the haploinsufficiency syndromes (the DiGeorge...
10.
Burn J, TAKAO A, Wilson D, Cross I, Momma K, Wadey R, et al.
J Med Genet
. 1993 Oct;
30(10):822-4.
PMID: 8230157
The conotruncal anomaly face syndrome was described in a Japanese publication in 1976 and comprises dysmorphic facial appearance and outflow tract defects of the heart. The authors subsequently noted similarities...