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The Lancet. Neurology|July 22, 2006
Clinical factors and ABCB1 polymorphisms in prediction of antiepileptic drug response: a prospective cohort studyGuy Leschziner, Andrea L Jorgensen, Toby Andrew, et al.
Human Molecular Genetics|June 19, 2013
Genetic screening for Niemann-Pick disease type C in adults with neurological and psychiatric symptoms: findings from the ZOOM studyPeter Bauer, David J Balding, Hans H Klünemann, et al.
American Journal of Human Genetics|October 26, 2022
A founder event causing a dominant childhood epilepsy survives 800 years through weak selective pressureBronwyn E Grinton, Erandee Robertson, Liam G Fearnley, et al.
Thorax|March 12, 2014
Interaction between gas cooking and GSTM1 null genotype in bronchial responsiveness: results from the European Community Respiratory Health SurveyAndré F S Amaral, Adaikalavan Ramasamy, Francesc Castro-Giner, et al.
Human Molecular Genetics|January 3, 2012
Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNPSimon Mead, James Uphill, John Beck, et al.
Forensic Science International|November 8, 2016
A comment on the PCAST report: Skip the "match"/"non-match" stageGeoffrey Stewart Morrison, David H Kaye, David J Balding, et al.
The New England Journal of Medicine|January 7, 2011
AIP mutation in pituitary adenomas in the 18th century and todayHarvinder S Chahal, Karen Stals, Martina Unterländer, et al.
Nature|February 13, 2007
A genome-wide association study identifies novel risk loci for type 2 diabetesRobert Sladek, Ghislain Rocheleau, Johan Rung, et al.
International Journal of Epidemiology|September 28, 2007
Assessment of cumulative evidence on genetic associations: interim guidelinesJohn P A Ioannidis, Paolo Boffetta, Julian Little, et al.
The Journal of Allergy and Clinical Immunology|November 1, 2011
A genome-wide meta-analysis of genetic variants associated with allergic rhinitis and grass sensitization and their interaction with birth orderAdaikalavan Ramasamy, Ivan Curjuric, Lachlan J Coin, et al.
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