Publications by authors named "Sheila Simpson"

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27 years of prenatal diagnosis for Huntington disease in the United Kingdom.
Raul E Piña-Aguilar, Sheila A Simpson, Abdulrahman Alshatti, Angus Clarke, David Craufurd

Genet Med· July 2019

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Mutations in XPR1 cause primary familial brain calcification associated with altered phosphate export.
Andrea Legati, Donatella Giovannini, Gaël Nicolas, Uriel López-Sánchez, Beatriz Quintáns, Sheila A Simpson

Nat Genet· June 2015

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Nosocomial pulmonary tuberculosis contact investigation in a neonatal intensive care unit.
Kate E Fisher, Robert Guaran, Jacqueline Stack, Sheila Simpson, William Krause

Infect Control Hosp Epidemiol· July 2013

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How do partners find out about the risk of Huntington's disease in couple relationships?
Karen Forrest Keenan, Sheila A Simpson, Zosia Miedzybrodzka, David A Alexander, June Semper

J Genet Couns· June 2013

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Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification.
Sandy Chan Hsu, Renee L Sears, Roberta R Lemos, Beatriz Quintáns, Alden Huang, Sheila A Simpson

Neurogenetics· February 2013

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Factor analysis of behavioural symptoms in Huntington's disease.
Hugh Rickards, Jenny De Souza, Marleen van Walsem, Erik van Duijn, Sheila A Simpson

J Neurol Neurosurg Psychiatry· April 2011

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Challenges assessing clinical endpoints in early Huntington disease.
Jane S Paulsen, Chiachi Wang, Kevin Duff, Roger Barker, Martha Nance, Sheila Simpson

Mov Disord· November 2010

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How young people find out about their family history of Huntington's disease.
Karen Forrest Keenan, Edwin van Teijlingen, Lorna McKee, Zosia Miedzybrodzka, Sheila A Simpson

Soc Sci Med· May 2009

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Mycophenolate mofetil embryopathy may be dose and timing dependent.
Ghee Soon Ang, Sheila A Simpson, Aravind R Reddy

Am J Med Genet A· August 2008

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Recurrence of tuberculosis at a Sydney chest clinic between 1994 and 2006: reactivation or reinfection?
Claudia C Dobler, Guy B Marks, Sheila E Simpson, A B Hamish Crawford

Med J Aust· February 2008

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Teaching children basic life support skills.
Ian Maconochie, Sheila Simpson, Bob Bingham

BMJ· June 2007

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Late stage care in Huntington's disease.
Sheila A Simpson

Brain Res Bull· April 2007

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European Resuscitation Council guidelines for resuscitation 2005. Section 6. Paediatric life support.
Dominique Biarent, Robert Bingham, Sam Richmond, Ian Maconochie, Jonathan Wyllie, Sheila Simpson

Resuscitation· December 2005

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Genetic professionals' reports of nondisclosure of genetic risk information within families.
Angus Clarke, Martin Richards, Lauren Kerzin-Storrar, Jane Halliday, Mary Anne Young, Sheila A Simpson

Eur J Hum Genet· May 2005

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Family communication about genetic risk: the little that is known.
Brenda J Wilson, Karen Forrest, Edwin R van Teijlingen, Lorna McKee, Neva Haites, Sheila A Simpson

Community Genet· February 2005

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Homozygosity for CAG mutation in Huntington disease is associated with a more severe clinical course.
Ferdinando Squitieri, Cinzia Gellera, Milena Cannella, Caterina Mariotti, Giuliana Cislaghi, Sheila A Simpson

Brain· April 2003

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Effective monosomy or trisomy of chromosome band 2q37.3 due to the unbalanced segregation of a 2;11 translocation.
Paul J Batstone, Sheila Simpson, David T Bonthron, Wee T Keng, Doreen Hamilton

Am J Med Genet A· April 2003

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Prenatal testing for Huntington's disease: a European collaborative study.
Sheila A Simpson, Moniek W Zoeteweij, Kurt Nys, Peter Harper, Alexandra Dürr

Eur J Hum Genet· November 2002

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New challenges for gamete donation programmes: changes in guidelines are needed.
Rafet Gazvani, Mark P R Hamilton, Sheila A Simpson, Allan Templeton

Hum Fertil (Camb)· November 2002

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Predictive DNA-testing for Huntington's disease and reproductive decision making: a European collaborative study.
Gerry Evers-Kiebooms, Kurt Nys, Peter Harper, Moniek Zoeteweij, Alexandra Dürr, Sheila Simpson

Eur J Hum Genet· March 2002

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