Patch C - Search Results

1

Penetrance for copy number variants associated with schizophrenia.

Vassos E, Collier DA, Holden S, Patch C, Rujescu D, St Clair D, Lewis CM. Vassos E, et al. Among authors: patch c. Hum Mol Genet. 2010 Sep 1;19(17):3477-81. doi: 10.1093/hmg/ddq259. Epub 2010 Jun 29. Hum Mol Genet. 2010. PMID: 20587603

2

Advances in the genetics of schizophrenia: will high-risk copy number variants be useful in clinical genetics or diagnostics?

Collier DA, Vassos E, Holden S, Patch C, McGuire P, Lewis C. Collier DA, et al. Among authors: patch c. F1000 Med Rep. 2009 Aug 17;1:61. doi: 10.3410/M1-61. F1000 Med Rep. 2009. PMID: 20948719 Free PMC article.

3

Molecular re-investigation of patients with Huntington's disease in Wessex reveals a family with dentatorubral and pallidoluysian atrophy.

Connarty M, Dennis NR, Patch C, Macpherson JN, Harvey JF. Connarty M, et al. Among authors: patch c. Hum Genet. 1996 Jan;97(1):76-8. doi: 10.1007/BF00218837. Hum Genet. 1996. PMID: 8557266

4

A systematic review of the clinical validity and clinical utility of DNA testing for hereditary haemochromatosis type 1 in at-risk populations.

Bryant J, Cooper K, Picot J, Clegg A, Roderick P, Rosenberg W, Patch C. Bryant J, et al. Among authors: patch c. J Med Genet. 2008 Aug;45(8):513-8. doi: 10.1136/jmg.2007.055806. Epub 2008 Feb 29. J Med Genet. 2008. PMID: 18310265 Review.

5

A systematic search for uniparental disomy in carriers of chromosome translocations.

James RS, Temple IK, Patch C, Thompson EM, Hassold T, Jacobs PA. James RS, et al. Among authors: patch c. Eur J Hum Genet. 1994;2(2):83-95. doi: 10.1159/000472348. Eur J Hum Genet. 1994. PMID: 8044660 Review.

6

Protelomeric sequences are deleted in cases of short arm inverted duplication of chromosome 8.

Barber JC, James RS, Patch C, Temple IK. Barber JC, et al. Among authors: patch c. Am J Med Genet. 1994 Apr 15;50(3):296-9. doi: 10.1002/ajmg.1320500315. Am J Med Genet. 1994. PMID: 8042676

7

A decision analysis model for diagnostic strategies using DNA testing for hereditary haemochromatosis in at risk populations.

Cooper K, Bryant J, Picot J, Clegg A, Roderick PR, Rosenberg WM, Patch C. Cooper K, et al. Among authors: patch c. QJM. 2008 Aug;101(8):631-41. doi: 10.1093/qjmed/hcn070. Epub 2008 Jun 3. QJM. 2008. PMID: 18522976

8

Diagnostic strategies using DNA testing for hereditary haemochromatosis in at-risk populations: a systematic review and economic evaluation.

Bryant J, Cooper K, Picot J, Clegg A, Roderick P, Rosenberg W, Patch C. Bryant J, et al. Among authors: patch c. Health Technol Assess. 2009 Apr;13(23):iii, ix-xi, 1-126. doi: 10.3310/hta13230. Health Technol Assess. 2009. PMID: 19406046 Free article. Review.

9

Factors affecting the uptake of screening: a randomised controlled non-inferiority trial comparing a genotypic and a phenotypic strategy for screening for haemochromatosis.

Patch C, Roderick P, Rosenberg W. Patch C, et al. J Hepatol. 2005 Jul;43(1):149-55. doi: 10.1016/j.jhep.2005.02.018. Epub 2005 Apr 11. J Hepatol. 2005. PMID: 15876471 Clinical Trial.

10

Psychosocial aspects of DNA testing for hereditary hemochromatosis in at-risk individuals: a systematic review.

Picot J, Bryant J, Cooper K, Clegg A, Roderick P, Rosenberg W, Patch C. Picot J, et al. Among authors: patch c. Genet Test Mol Biomarkers. 2009 Feb;13(1):7-14. doi: 10.1089/gtmb.2008.0064. Genet Test Mol Biomarkers. 2009. PMID: 19309267 Review.

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