Sutherland GR - Search Results

1

Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel beta1 subunit gene SCN1B.

Wallace RH, Wang DW, Singh R, Scheffer IE, George AL Jr, Phillips HA, Saar K, Reis A, Johnson EW, Sutherland GR, Berkovic SF, Mulley JC. Wallace RH, et al. Among authors: sutherland gr. Nat Genet. 1998 Aug;19(4):366-70. doi: 10.1038/1252. Nat Genet. 1998. PMID: 9697698

2

A missense mutation in the neuronal nicotinic acetylcholine receptor alpha 4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy.

Steinlein OK, Mulley JC, Propping P, Wallace RH, Phillips HA, Sutherland GR, Scheffer IE, Berkovic SF. Steinlein OK, et al. Among authors: sutherland gr. Nat Genet. 1995 Oct;11(2):201-3. doi: 10.1038/ng1095-201. Nat Genet. 1995. PMID: 7550350

3

Localization of a gene for autosomal dominant nocturnal frontal lobe epilepsy to chromosome 20q 13.2.

Phillips HA, Scheffer IE, Berkovic SF, Hollway GE, Sutherland GR, Mulley JC. Phillips HA, et al. Among authors: sutherland gr. Nat Genet. 1995 May;10(1):117-8. doi: 10.1038/ng0595-117. Nat Genet. 1995. PMID: 7647781

4

A microsatellite marker within the duplicated D16S79 locus has a null allele; significance for linkage mapping.

Phillips HA, Thompson AD, Kozman HM, Sutherland GR, Mulley JC. Phillips HA, et al. Among authors: sutherland gr. Cytogenet Cell Genet. 1993;64(2):131-2. doi: 10.1159/000133570. Cytogenet Cell Genet. 1993. PMID: 8334897

5

Integrating maps of chromosome 16.

Mulley JC, Sutherland GR. Mulley JC, et al. Among authors: sutherland gr. Curr Opin Genet Dev. 1993 Jun;3(3):425-31. doi: 10.1016/0959-437x(93)90116-7. Curr Opin Genet Dev. 1993. PMID: 8353417 Review.

6

Identification of the gene FMR2, associated with FRAXE mental retardation.

Gecz J, Gedeon AK, Sutherland GR, Mulley JC. Gecz J, et al. Among authors: sutherland gr. Nat Genet. 1996 May;13(1):105-8. doi: 10.1038/ng0596-105. Nat Genet. 1996. PMID: 8673085

7

Suggestion of a major gene for familial febrile convulsions mapping to 8q13-21.

Wallace RH, Berkovic SF, Howell RA, Sutherland GR, Mulley JC. Wallace RH, et al. Among authors: sutherland gr. J Med Genet. 1996 Apr;33(4):308-12. doi: 10.1136/jmg.33.4.308. J Med Genet. 1996. PMID: 8730286 Free PMC article.

8

A de novo mutation in sporadic nocturnal frontal lobe epilepsy.

Phillips HA, Marini C, Scheffer IE, Sutherland GR, Mulley JC, Berkovic SF. Phillips HA, et al. Among authors: sutherland gr. Ann Neurol. 2000 Aug;48(2):264-7. Ann Neurol. 2000. PMID: 10939581

9

CHRNB2 is the second acetylcholine receptor subunit associated with autosomal dominant nocturnal frontal lobe epilepsy.

Phillips HA, Favre I, Kirkpatrick M, Zuberi SM, Goudie D, Heron SE, Scheffer IE, Sutherland GR, Berkovic SF, Bertrand D, Mulley JC. Phillips HA, et al. Among authors: sutherland gr. Am J Hum Genet. 2001 Jan;68(1):225-31. doi: 10.1086/316946. Epub 2000 Dec 5. Am J Hum Genet. 2001. PMID: 11104662 Free PMC article.

10

Neuronal sodium-channel alpha1-subunit mutations in generalized epilepsy with febrile seizures plus.

Wallace RH, Scheffer IE, Barnett S, Richards M, Dibbens L, Desai RR, Lerman-Sagie T, Lev D, Mazarib A, Brand N, Ben-Zeev B, Goikhman I, Singh R, Kremmidiotis G, Gardner A, Sutherland GR, George AL Jr, Mulley JC, Berkovic SF. Wallace RH, et al. Among authors: sutherland gr. Am J Hum Genet. 2001 Apr;68(4):859-65. doi: 10.1086/319516. Epub 2001 Mar 13. Am J Hum Genet. 2001. PMID: 11254444 Free PMC article.

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