Mulley JC - Search Results

1

Investigation of the 15q13.3 CNV as a genetic modifier for familial epilepsies with variable phenotypes.

Mulley JC, Scheffer IE, Desai T, Bayly MA, Grinton BE, Vears DF, Berkovic SF, Dibbens LM. Mulley JC, et al. Epilepsia. 2011 Oct;52(10):e139-42. doi: 10.1111/j.1528-1167.2011.03188.x. Epub 2011 Jul 21. Epilepsia. 2011. PMID: 21777232 Free article.

2

Is photosensitive epilepsy less common in males due to variation in X chromosome photopigment genes?

Taylor I, Hodgson B, Scheffer IE, Mulley J, Berkovic SF, Dibbens L. Taylor I, et al. Epilepsia. 2007 Sep;48(9):1807-1809. doi: 10.1111/j.1528-1167.2007.01138.x. Epub 2007 May 23. Epilepsia. 2007. PMID: 17521342 Free article.

3

Genetic architecture of idiopathic generalized epilepsy: clinical genetic analysis of 55 multiplex families.

Marini C, Scheffer IE, Crossland KM, Grinton BE, Phillips FL, McMahon JM, Turner SJ, Dean JT, Kivity S, Mazarib A, Neufeld MY, Korczyn AD, Harkin LA, Dibbens LM, Wallace RH, Mulley JC, Berkovic SF. Marini C, et al. Among authors: mulley jc. Epilepsia. 2004 May;45(5):467-78. doi: 10.1111/j.0013-9580.2004.46803.x. Epilepsia. 2004. PMID: 15101828 Free article.

4

Genetic association studies in epilepsy: "the truth is out there".

Tan NC, Mulley JC, Berkovic SF. Tan NC, et al. Among authors: mulley jc. Epilepsia. 2004 Nov;45(11):1429-42. doi: 10.1111/j.0013-9580.2004.22904.x. Epilepsia. 2004. PMID: 15509244 Free article. Review.

5

SCN2A mutations and benign familial neonatal-infantile seizures: the phenotypic spectrum.

Herlenius E, Heron SE, Grinton BE, Keay D, Scheffer IE, Mulley JC, Berkovic SF. Herlenius E, et al. Among authors: mulley jc. Epilepsia. 2007 Jun;48(6):1138-42. doi: 10.1111/j.1528-1167.2007.01049.x. Epub 2007 Mar 26. Epilepsia. 2007. PMID: 17386050 Free article.

6

Extended spectrum of idiopathic generalized epilepsies associated with CACNA1H functional variants.

Heron SE, Khosravani H, Varela D, Bladen C, Williams TC, Newman MR, Scheffer IE, Berkovic SF, Mulley JC, Zamponi GW. Heron SE, et al. Among authors: mulley jc. Ann Neurol. 2007 Dec;62(6):560-8. doi: 10.1002/ana.21169. Ann Neurol. 2007. PMID: 17696120

7

Chipping away at the common epilepsies with complex genetics: the 15q13.3 microdeletion shows the way.

Mulley JC, Dibbens LM. Mulley JC, et al. Genome Med. 2009 Mar 25;1(3):33. doi: 10.1186/gm33. Genome Med. 2009. PMID: 19341504 Free PMC article.

8

Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritance.

Dibbens LM, Mullen S, Helbig I, Mefford HC, Bayly MA, Bellows S, Leu C, Trucks H, Obermeier T, Wittig M, Franke A, Caglayan H, Yapici Z; EPICURE Consortium; Sander T, Eichler EE, Scheffer IE, Mulley JC, Berkovic SF. Dibbens LM, et al. Among authors: mulley jc. Hum Mol Genet. 2009 Oct 1;18(19):3626-31. doi: 10.1093/hmg/ddp311. Epub 2009 Jul 10. Hum Mol Genet. 2009. PMID: 19592580 Free PMC article.

9

Familial neonatal seizures with intellectual disability caused by a microduplication of chromosome 2q24.3.

Heron SE, Scheffer IE, Grinton BE, Eyre H, Oliver KL, Bain S, Berkovic SF, Mulley JC. Heron SE, et al. Among authors: mulley jc. Epilepsia. 2010 Sep;51(9):1865-9. doi: 10.1111/j.1528-1167.2010.02558.x. Epilepsia. 2010. PMID: 20384724 Free article.

10

Proposed genetic classification of the "benign" familial neonatal and infantile epilepsies.

Mulley JC, Heron SE, Dibbens LM. Mulley JC, et al. Epilepsia. 2011 Mar;52(3):649-50. doi: 10.1111/j.1528-1167.2010.02953.x. Epilepsia. 2011. PMID: 21395569 Free article. No abstract available.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

261 results

Search Page

Filters