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Oncogene|October 7, 2008
APC and the three-hit hypothesisS Segditsas, A J Rowan, K Howarth, et al.
Neurology|June 16, 2005
New onset geriatric epilepsy: a randomized study of gabapentin, lamotrigine, and carbamazepineA J Rowan, R E Ramsay, J F Collins, et al.
The New England Journal of Medicine|September 17, 1998
A comparison of four treatments for generalized convulsive status epilepticus. Veterans Affairs Status Epilepticus Cooperative Study GroupD M Treiman, P D Meyers, N Y Walton, et al.
Journal of Autism and Developmental Disorders|January 19, 2000
The screening and diagnosis of autistic spectrum disordersP A Filipek, P J Accardo, G T Baranek, et al.
Neurology|August 23, 2000
Practice parameter: screening and diagnosis of autism: report of the Quality Standards Subcommittee of the American Academy of Neurology and the Child Neurology Society [RETIRED]P A Filipek, P J Accardo, S Ashwal, et al.
Gut|February 8, 2006
Disease severity and genetic pathways in attenuated familial adenomatous polyposis vary greatly but depend on the site of the germline mutationO M Sieber, S Segditsas, A L Knudsen, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 28, 2002
Whole-gene APC deletions cause classical familial adenomatous polyposis, but not attenuated polyposis or "multiple" colorectal adenomasO M Sieber, H Lamlum, M D Crabtree, et al.
American Journal of Human Genetics|April 16, 2003
An ancestral Ashkenazi haplotype at the HMPS/CRAC1 locus on 15q13-q14 is associated with hereditary mixed polyposis syndromeE E M Jaeger, K L Woodford-Richens, M Lockett, et al.
Oncogene|March 3, 2015
SETD2 loss-of-function promotes renal cancer branched evolution through replication stress and impaired DNA repairN Kanu, E Grönroos, P Martinez, et al.
Human Molecular Genetics|May 23, 2003
Genetic and functional analyses of FH mutations in multiple cutaneous and uterine leiomyomatosis, hereditary leiomyomatosis and renal cancer, and fumarate hydratase deficiencyN A Alam, A J Rowan, N C Wortham, et al.
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