Patch C - Search Results

1

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.

2

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

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

Comparison of genotypic and phenotypic strategies for population screening in hemochromatosis: assessment of anxiety, depression, and perception of health.

Patch C, Roderick P, Rosenberg W. Patch C, et al. Genet Med. 2005 Oct;7(8):550-6. doi: 10.1097/01.gim.0000182466.87113.ce. Genet Med. 2005. PMID: 16247293 Free article.

5

Developing a policy for paediatric biobanks: principles for good practice.

Hens K, Van El CE, Borry P, Cambon-Thomsen A, Cornel MC, Forzano F, Lucassen A, Patch C, Tranebjaerg L, Vermeulen E, Salvaterra E, Tibben A, Dierickx K; PPPC of the European Society of Human Genetics. Hens K, et al. Among authors: patch c. Eur J Hum Genet. 2013 Jan;21(1):2-7. doi: 10.1038/ejhg.2012.99. Epub 2012 Jun 20. Eur J Hum Genet. 2013. PMID: 22713814 Free PMC article.

6

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

7

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.

8

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.

9

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.

10

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

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