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Patrick Morrison

Research Profile

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Procedures

Genetic Testing

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TOP 3
Ellen Mawhinney; Patrick J Morrison; Jim Morrow; Linda Parsons; Aline Russell; W Henry Smithson; John Craig; Norman Delanty; Beth Irwin; Brenda Liggan; Stephen J Hunt
Levetiracetam in pregnancy: results from the UK and Ireland epilepsy and pregnancy registers.
Ellen Campbell; Emma Devenney; Stephen Hunt; Beth Irwin; Patrick J Morrison; Jim Morrow; Linda Parsons; Iain Robertson; Aline Russell; William Henry Smithson; John Craig
Recurrence risk of congenital malformations in infants exposed to antiepileptic drugs in utero.
Patrick J Morrison
Prevalence estimates of Huntington disease in Caucasian populations are gross underestimates.

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All Publications

2013: Ellen Mawhinney; Patrick J Morrison; Jim Morrow; Linda Parsons; Aline Russell; W Henry Smithson; John Craig; Norman Delanty; Beth Irwin; Brenda Liggan; Stephen J Hunt
Levetiracetam in pregnancy: results from the UK and Ireland epilepsy and pregnancy registers.
Neurology 2013;80(4):400-5.
2013: Ellen Campbell; Emma Devenney; Stephen Hunt; Beth Irwin; Patrick J Morrison; Jim Morrow; Linda Parsons; Iain Robertson; Aline Russell; William Henry Smithson; John Craig
Recurrence risk of congenital malformations in infants exposed to antiepileptic drugs in utero.
Epilepsia 2013;54(1):165-71.
2012: Patrick J Morrison
Prevalence estimates of Huntington disease in Caucasian populations are gross underestimates.
Movement disorders : official journal of the Movement Disorder Society 2012;27(13):1707-8; author reply 1708-9.
2012: Rachel Hardy; Shane A McKee; Deirdre E Donnelly; Charles W Shepherd; Patrick J Morrison
Constellation of five facial features of tuberous sclerosis in a child with a TSC2 1808A>G mutation.
The oncologist 2012;17(7):925-6.
2012: Patrick J Morrison; Paula D Ryan
Faciocutaneous cancer syndromes: spot the diagnosis.
The oncologist 2012;17(7):886-7.
2011: R Stevenson; A Fatehullah; I Jagan; R K Deevi; V Bingham; Alexandra E Irvine; M Armstrong; Patrick J Morrison; I Dimmick; R Stewart; F C Campbell
Enhanced lymphocyte interferon (IFN)-γ responses in a PTEN mutation-negative Cowden disease kindred.
Clinical and experimental immunology 2011;164(2):202-10.
2011: Harvinder S Chahal; Karen Stals; Martina Unterländer; David J Balding; Mark Thomas; Ajith V Kumar; G Michael Besser; A Brew Atkinson; Patrick J Morrison; Trevor A Howlett; Miles J Levy; Steve M Orme; Scott A Akker; Richard L Abel; Ashley B Grossman; Joachim Burger; Sian Ellard; Marta Korbonits
AIP mutation in pituitary adenomas in the 18th century and today.
The New England journal of medicine 2011;364(1):43-50.
2011: Lisa Bradley; Patrick J Morrison
Giants of the British Isles.
The Ulster medical journal 2011;80(1):31-2.
2011: Sarinda Millar; Lisa Bradley; Dennis Carson; Deirdre E Donnelly; Patrick J Morrison
Familial pediatric endocrine tumors.
The oncologist 2011;16(10):1388-96.
2010: Patrick J Morrison
Accurate prevalence and uptake of testing for Huntington's disease.
Lancet neurology 2010;9(12):1147.
2010: Gillian Rea; Simon McCullough; Susan McNerlan; Brian Craig; Patrick J Morrison
Delineation of a recognisable phenotype of interstitial deletion 3 (q22.3q25.1) in a case with previously unreported truncus arteriosus.
European journal of medical genetics 2010;53(3):162-7.
2010: Patrick J Morrison; Deirdre E Donnelly; A Brew Atkinson; A Peter Maxwell
Advances in the genetics of familial renal cancer.
The oncologist 2010;15(6):532-8.
2009: Patrick J Morrison; A Brew Atkinson
Genetic aspects of familial thyroid cancer.
The oncologist 2009;14(6):571-7.
2009: Patrick J Morrison
Tuberous sclerosis: epidemiology, genetics and progress towards treatment.
Neuroepidemiology 2009;33(4):342-3.
2008: Lisa A Devlin; Colin A Graham; John H Price; Patrick J Morrison
Germline MSH6 mutations are more prevalent in endometrial cancer patient cohorts than hereditary non polyposis colorectal cancer cohorts.
The Ulster medical journal 2008;77(1):25-30.
2007: Seamus J Murphy; Brian P McIlhatton; W Peter Logan; Kenneth G Porter; Patrick J Morrison
A splice-site mutation in exon 4 of the APC gene in a family with attenuated familial adenomatous polyposis.
Digestive diseases and sciences 2007;52(10):2784-7.
2006: Patrick J Morrison
Paediatric and adult ataxias (update 5).
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society 2006;10(5-6):249-53.
2006: Lisa A Devlin; C H Shepherd; H Crawford; Patrick J Morrison
Tuberous sclerosis complex: clinical features, diagnosis, and prevalence within Northern Ireland.
Developmental medicine and child neurology 2006;48(6):495-9.
2006: Tabib Dabir; Steven J Hunter; Colin F J Russell; Damien McCall; Patrick J Morrison
The RET mutation E768D confers a late-onset familial medullary thyroid carcinoma -- only phenotype with incomplete penetrance: implications for screening and management of carrier status.
Familial cancer 2006;5(2):201-4.
2006: Tabib Dabir; Patrick J Morrison
Trisomy 10p with clinical features of facio-auriculo-vertebral spectrum: a case report.
Clinical dysmorphology 2006;15(1):25-7.
2005: Patrick J Morrison
Insurance, unfair discrimination, and genetic testing.
Lancet 2005;366(9489):877-80.
2005: Lisa A Devlin; J H Price; Patrick J Morrison
Hereditary non-polyposis colon cancer.
The Ulster medical journal 2005;74(1):14-21.
2005: Yansong Bian; Trinidad Caldes; Juul Wijnen; Patrick Franken; H F A Vasen; Virginia G Kaklamani; Khedoudja Nafa; Paolo Peterlongo; Nathan Ellis; John A Baron; John Burn; Gabriela Moeslein; Patrick J Morrison; Yu Chen; Habibul Ahsan; Patrice Watson; Henry T Lynch; Albert de La Chapelle; Riccardo Fodde; Boris Pasche
TGFBR1*6A may contribute to hereditary colorectal cancer.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2005;23(13):3074-8.
2004: Lisa A Devlin; Patrick J Morrison
Mosaic Down's syndrome prevalence in a complete population study.
Archives of disease in childhood 2004;89(12):1177-8.
2004: V McConnell; R Derham; D McManus; Patrick J Morrison
Mosaic monosomy 14: clinical features and recognizable facies.
Clinical dysmorphology 2004;13(3):155-60.
2004: Lisa A Devlin; Patrick J Morrison
Accuracy of the clinical diagnosis of Down syndrome.
The Ulster medical journal 2004;73(1):4-12.
2004: C Foster; D G R Evans; Rosalind Eeles; Diana Eccles; S Ashley; L Brooks; Trevor Cole; J Cook; R Davidson; Helen Gregory; James Mackay; Patrick J Morrison; M Watson
Non-uptake of predictive genetic testing for BRCA1/2 among relatives of known carriers: attributes, cancer worry, and barriers to testing in a multicenter clinical cohort.
Genetic testing 2004;8(1):23-9.
2003: V McConnell; T Brown; Patrick J Morrison
An Irish three-generation family of Cornelia de Lange syndrome displaying autosomal dominant inheritance.
Clinical dysmorphology 2003;12(4):241-4.
2003: Patrick J Morrison
Paediatric and adult movement disorders.
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society 2003;7(5):235-7.
2003: Patrick J Morrison
Paediatric and adult ataxias (update).
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society 2003;7(5):231-3.
2003: Patrick J Morrison
Hereditary ataxias and paediatric neurology: new movers and shakers enter the field.
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society 2003;7(5):217-9.
2001: J Hughes; NC Nevin; Patrick J Morrison
Familial craniosynostosis due to Pro250Arg mutation in the fibroblast growth factor receptor 3 gene.
The Ulster medical journal 2001;70(1):47-50.
2001: Patrick J Morrison
Paediatric and adult movement disorders (update).
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society 2001;5(6):265-8.
2000: M Bhat; Patrick J Morrison; A Getty; D McManus; R Tubman; NC Nevin
First clinical case of small de novo duplication of 19q (13.3-13.4) confirmed by FISH.
American journal of medical genetics 2000;91(3):201-3.
2000: Patrick J Morrison
Adult and paediatric movement disorders.
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society 2000;4(1):45-7.
2000: Patrick J Morrison
The spinocerebellar ataxias: molecular progress and newly recognized paediatric phenotypes.
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society 2000;4(1):9-15.
1999: Pål Møller; G Evans; Neva E Haites; H F A Vasen; Marta M Reis; Elaine Anderson; Jaran Apold; Shirley Hodgson; Diana Eccles; H Olsson; D Stoppa-Lyonnet; Jenny Chang-Claude; Patrick J Morrison; G Bevilacqua; Ketil Heimdal; Lovise Maehle; Fiona Lalloo; Helen Gregory; PE Preece; Ake Borg; NC Nevin; MA Caligo; C Michael Steel
Guidelines for follow-up of women at high risk for inherited breast cancer: consensus statement from the Biomed 2 Demonstration Programme on Inherited Breast Cancer.
Disease markers 1999;15(1-3):207-11.
1999: Patrick J Morrison; C Michael Steel; H F A Vasen; Diana Eccles; D G R Evans; Pål Møller; Shirley Hodgson; D Stoppa-Lyonnet; Jenny Chang-Claude; MA Caligo; Edith Olah; Neva E Haites; NC Nevin
Insurance implications for individuals with a high risk of breast and ovarian cancer in Europe.
Disease markers 1999;15(1-3):159-65.
1999: Patrick J Morrison; C E Chu; NC Nevin
A second family with probable CRAC (colorectal adenomata and carcinoma) syndrome--a new familial cancer.
Disease markers 1999;15(1-3):120-2.
1999: D Stoppa-Lyonnet; MA Caligo; Diana Eccles; D G R Evans; Neva E Haites; N S Hodgson; Pål Møller; Patrick J Morrison; C Michael Steel; H F A Vasen; Jenny Chang-Claude
Genetic testing for breast cancer predisposition in 1999: which molecular strategy and which family criteria?
Disease markers 1999;15(1-3):67-8.
1999: Patrick J Morrison; NC Nevin
Cancer genetics services in Northern Ireland.
Disease markers 1999;15(1-3):37-40.
1999: Patrick J Morrison
Adult and paediatric movement disorders.
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society 1999;3(1):39-41.
1998: Patrick J Morrison
Implications of genetic testing for insurance in the UK.
Lancet 1998;352(9141):1647-8.
1998: Patrick J Morrison
Genetic testing and insurance in the United Kingdom.
Clinical genetics 1998;54(5):375-9.
1998: Patrick J Morrison; C H Shepherd; FJ Stewart; NC Nevin
Prevalence of tuberous sclerosis in UK.
Lancet 1998;352(9124):318-9.
1998: Patrick J Morrison; FJ Stewart; A C Magee; NC Nevin
Confidential inquiry into families with two siblings with cystic fibrosis.
Archives of disease in childhood 1998;78(6):578.
1998: Patrick J Morrison; M Mirakhur; Victor Patterson
Discordant repeat size and phenotype in Kennedy syndrome.
Clinical genetics 1998;53(4):276-7.
1997: D McNally; W J Campbell; J M Sloan; Patrick J Morrison; Colin F J Russell
Thyroidectomy for medullary carcinoma in MEN 2A: positive genetic screening as the sole indicator for surgery.
The Ulster medical journal 1997;66(2):134-5.
1996: Patrick J Morrison; NC Nevin
Multiple endocrine neoplasia type 2B (mucosal neuroma syndrome, Wagenmann-Froboese syndrome).
Journal of medical genetics 1996;33(9):779-82.
1996: Patrick J Morrison
Anticipating more anticipation.
Lancet 1996;347(9009):1132.
1995: Patrick J Morrison; W P Johnston; NC Nevin
The epidemiology of Huntington's disease in Northern Ireland.
Journal of medical genetics 1995;32(7):524-30.
1994: Patrick J Morrison; NC Nevin
Serum iron, total iron binding capacity and ferritin in early Huntington disease patients.
Irish journal of medical science 1994;163(5):236-7.
1993: Patrick J Morrison; C A Graham; NC Nevin
Significant linkage disequilibrium between the Huntington's disease locus and markers at loci D4S10, D4S95, and D4S111 in Northern Ireland.
Journal of medical genetics 1993;30(12):1018-9.
1993: Patrick J Morrison; NC Nevin
Huntington disease in County Donegal: epidemiological trends over four decades.
The Ulster medical journal 1993;62(2):141-4.
1992: Patrick J Morrison; H Connor Mulholland; B G Craig; NC Nevin
Cardiovascular abnormalities in the oculo-auriculo-vertebral spectrum (Goldenhar syndrome).
American journal of medical genetics 1992;44(4):425-8.
1992: Patrick J Morrison; J Jones; NC Nevin
Interstitial deletion 8p21.3----p23.1 in a 6-year-old girl.
American journal of medical genetics 1992;42(5):678-80.
1991: Patrick J Morrison; D R Hadden; Anne E Hughes; L Kennedy; C J Russell; NC Nevin
Gene probe analysis in an informative family with multiple endocrine neoplasia syndrome type 2A (MEN 2A). Improvement in carrier risk estimation.
The Quarterly journal of medicine 1991;80(291):597-603.
1991: Patrick J Morrison; NC Nevin; R W Kendrick
Unknown syndrome: proportionate short stature, mandibular prognathism, and short femoral necks.
Journal of medical genetics 1991;28(6):422-3.
1990: NC Nevin; Patrick J Morrison; J Jones; M M Reid
Inverted tandem duplication of 8p12----p23.1 in a child with increased activity of glutathione reductase.
Journal of medical genetics 1990;27(2):135-6.
1989: A J Hill; C A Graham; E D Kelly; Patrick J Morrison; NC Nevin
Linkage disequilibrium and CF allele segregation analysis in cystic fibrosis families in Northern Ireland.
Human genetics 1989;83(4):391-4.