G K Suthers
Overview
Explore the profile of G K Suthers including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
37
Citations
654
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Worthley D, Phillips K, Wayte N, Schrader K, Healey S, Kaurah P, et al.
Gut
. 2011 Aug;
61(5):774-9.
PMID: 21813476
Objective: The purpose of this study was the clinical and pathological characterisation of a new autosomal dominant gastric polyposis syndrome, gastric adenocarcinoma and proximal polyposis of the stomach (GAPPS). Methods:...
2.
ODoherty K, Suthers G
J Genet Couns
. 2007 May;
16(4):409-17.
PMID: 17473963
A genetic counselor is often faced with the difficult task of conveying a set of complex and highly abstract factors associated with the client's risk of developing a familial disorder....
3.
Suthers G, Armstrong J, McCormack J, Trott D
J Med Genet
. 2005 Dec;
43(8):665-70.
PMID: 16371501
Objective: To increase the awareness among at risk relatives of the availability of genetic testing for a familial disorder while respecting their autonomy and privacy. Methods: This was a comparison...
4.
Turnbull M, Humeniuk V, Stein B, Suthers G
J Med Genet
. 2005 Aug;
42(8):e50.
PMID: 16061556
Cowden syndrome (OMIM No 158350) is a pleomorphic, autosomal dominant syndrome characterised by hamartomas in tissues derived from the endoderm, mesoderm, and ectoderm. It is caused by germline mutations in...
5.
Lobb E, Butow P, Meiser B, Barratt A, Gaff C, Young M, et al.
Br J Cancer
. 2002 Aug;
87(5):502-8.
PMID: 12189544
This multicentre study examined the influence of patient demographic, disease status and psychological variables on clinical geneticists/genetic counsellors (consultants) behaviours in initial consultations with women from high-risk breast cancer families....
6.
Gardner R, Savarirayan R, Dunne K, McLellan J, Coleman L, Suthers G
Clin Dysmorphol
. 2001 Jul;
10(3):203-8.
PMID: 11446415
We describe two children with a brain defect similar to that described as 'microlissencephaly', as defined in Barkovich et aL [(1998) Neuroped 29: 113-119]. Concomitant malformations (cardiac, spinal, urogenital) may...
7.
Cox T, Allen L, Cox L, Hopwood B, Goodwin B, Haan E, et al.
Hum Mol Genet
. 2000 Oct;
9(17):2553-62.
PMID: 11030761
Opitz syndrome (OS) is a genetically heterogeneous malformation disorder. Patients with OS may present with a variable array of malformations that are indicative of a disturbance of the primary midline...
8.
Hollway G, Suthers G, Battese K, Turner A, David D, Mulley J
Lancet
. 1998 Apr;
351(9106):877-8.
PMID: 9525367
No abstract available.
9.
Hollway G, Suthers G, Haan E, Thompson E, David D, Gecz J, et al.
Hum Genet
. 1997 Feb;
99(2):251-5.
PMID: 9048930
Five autosomal dominant craniosynostosis syndromes (Apert, Crouzon, Pfeiffer, Jackson-Weiss and Crouzon syndrome with acanthosis nigricans) result from mutations in FGFR genes. Fourteen unrelated patients with FGFR2-related craniosynostosis syndromes were screened...
10.
Suthers G, Earley A, Huson S
Clin Dysmorphol
. 1993 Oct;
2(4):342-5.
PMID: 7508318
A boy with brachycephaly without craniosynostosis, raised intracranial pressure, deafness, cataracts, and global developmental delay is described.