Dr Christine Patch’s publications (since 2008)
Middleton A, Patch C, Wiggins J, Barnes K, Crawford G, Benjamin C, Bruce
A Position statement on opportunistic genomic screening from the
Association of Genetic Nurses and Counsellors (UK and Ireland) (2014)
European Journal of Human Genetics, doi: 10.1038/ejhg.2013.301
Jacobs C, Patch C Identifying individuals who might benefit from genetic
services and information Nurs Stand. 2013 Oct 30;28(9):37-42.
Skirton H Patch C Factors affecting the clinical use of non-invasive prenatal
testing: a mixed methods systematic review 2013 Prenatal Diagnosis 2013
April 2013 Doi: 10.1002/pd.4094 [Epub ahead of print]
Skirton H, Barnoy S, Ingvoldstad C, van Kessel I, Patch C, O'Connor A,
Serra-Juhe C, Stayner B, Voelckel MA. A Delphi study to determine the
European core curriculum for Master programmes in genetic counselling. Eur
J Hum Genet. 2013 Jan 23. doi: 10.1038/ejhg.2012.302. [Epub ahead of
print].
Skirton H, Kerzin Storrar L, Barnes C, Hall G, Longmuir M, Patch C, Scott G,
Walford-Moore J. Building the Genetic Counsellor Profession in the United
Kingdom: Two Decades of Growth and Development. J Genet Counsel 2013
2013 Jan 22. [Epub ahead of print] DOI 10.1007/s10897-012-9560-4
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. Developing a policy for paediatric biobanks: principles for good
practice. Eur J Hum Genet. 2013 21(1) 2-7.
Patch C, Charlton J, Roderick P, Gulliford M, Use of Antihypertensive
Medications and Mortality of Patients With Autosomal Dominant Polycystic
Kidney Disease: A Population-Based Study. American Journal of Kidney
Disease (2011) 57(6):856-862.
Becker F, van El C, Ibarreta D, Zika E, Hogarth S, Borry P, CambonThomsen A, Cassiman JJ, Evers-Kiebooms G, Hodgson S, Janssens AC,
Kaariainen H, Krawczak M, Kristoffersson U, Lubinski J, Patch C,
Penchaszadeh V, Read A, Rogowski W, Sequeiros J, Tranebjaerg L, van
Langen I, Wallace H, Zimmern R, Schmidtke J, Cornel MC. Genetic testing
and common disorders in a public health framework: how to assess relevance
and
Possibilities Background Document to the ESHG recommendations on
genetic testing and common disorders
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European Journal of Human Genetics (2011) 19, S6–S44;
doi:10.1038/ejhg.2010.249
Skirton H, Patch C, Voelckel MA Using a Community of Practice to develop
standards of practice and education for genetic counsellors in Europe J
Community Genetics 2010 1:169-173.
Vassos E, Collier D, Holden S, Patch C, Rujescu D, St Clair D, Lewis C.
Penetrance for copy number variants associated with schizophrenia. Human
Molecular Genetics, 2010;19(17):3477-81.
Collier D, Vassos E, Holden S, Patch C, McGuire P, Lewis C Advances in the
genetics of schizophrenia: will high-risk copy number variants be useful in
clinical genetics or diagnostics?F1000 Medicine Reports 2009, 1:61 (doi:
10.3410/M1-61)
Bryant J, Cooper K, Picot J, Clegg A, Roderick P, Rosenberg W, Patch C.
Diagnostic Strategies using DNA testing for hereditary haemochromatosis in
at-risk populations: a systematic review and economic evaluation. Health
Technology Assessment (2009) 13 (23) Doi 10.3310/hta13230
Genetic testing in asymptomatic minors: background considerations towards
ESHG Recommendations.
Borry P, Evers-Kiebooms G, Cornel MC, Clarke A, Dierickx K; Public and
Professional Policy Committee (PPPC) of the European Society of Human
Genetics (ESHG). Eur J Hum Genet. 2009 Jun;17(6):711-9. Epub 2009 Mar
11. PMID: 19277061
Genetic testing in asymptomatic minors: Recommendations of the European
Society of Human Genetics.
European Society of Human Genetics. Eur J Hum Genet. 2009
Jun;17(6):720-1. Epub 2009 Mar 11. No abstract available. PMID: 19277059
Patch C, Sequeiros J, Cornel MC. Direct to consumer genetic tests.
European Journal of Human Genetics advance online publication 29 April
2009; doi:10.1038/ejhg.2009.66
Patch C, Sequeiros J, Cornel MC. Genetic horoscopes: is it all in the genes?
Points for regulatory control of direct-to-consumer genetic testing. European
Journal of Human Genetics advance online publication 4 March 2009; doi:
10.1038/ejhg.2008.246
Picot J, Bryant J, Cooper K, Clegg A, Roderick P, Rosenberg W, Patch C
(2009)
Psychosocial Aspects of DNA Testing for Hereditary Hemochromatosis in AtRisk Individuals: A Systematic Review
Genetic Testing and Molecular Biomarkers. 2009; 13(1): 7-14
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Cooper K, Bryant J, Picot J, Clegg A, Roderick PR, Rosenberg WM, Patch C
(2008) A decision analysis model for diagnostic strategies using DNA testing
for hereditary haemochromatosis in at risk populations. Qjm, (2008); 101
(80): 631-641. doi: 10.1093/qjmed/hcn070
Ayme S, Matthijs G & Soini S, on behalf of the ESHG Working Party on
Patenting and Licensing, members were, Ayme S, Matthijs G, Anastasiadou
V, Atalar F, Braga S, Burn J, Cassiman JJ, Cornel M, Coviello D, EversKiebooms G, Gorry P, Hodgson S, Kaariainen H, Kosztolanyi G,
Kristoffersson U, Macek M, Patch C, Schmidtke J, Sequeiros J, StoppaLyonnet D, Tranebjaerg L, van Heyningen V & van Ommen GJ (2008)
Patenting and licensing in genetic testing: Recommendations of the
European Society of Human Genetics. Eur J Hum Genet, 16 (4) 405-411.
(Reprinted Eur J Hum Genet, 16 (Suppl) S3-S9.)
doi: 10.1038/sj.ejhg.5201929
Bryant J, Cooper K, Picot J, Clegg A, Roderick P, Rosenberg W & Patch C.
(2008) A systematic review of the clinical validity and clinical utility of DNA
testing for hereditary haemochromatosis in at-risk populations. J Med Genet,
45 (8) 513-518. doi: 10.1136/jmg.2007.055806
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