Sutherland GR - Search Results

1

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

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

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

4

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.

5

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

6

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.

7

Integration of the cytogenetic and genetic linkage maps of human chromosome 16 using 50 physical intervals and 50 polymorphic loci.

Kozman HM, Phillips HA, Callen DF, Sutherland GR, Mulley JC. Kozman HM, et al. Among authors: sutherland gr. Cytogenet Cell Genet. 1993;62(4):194-8. doi: 10.1159/000133474. Cytogenet Cell Genet. 1993. PMID: 8440136

8

Incidence and origin of "null" alleles in the (AC)n microsatellite markers.

Callen DF, Thompson AD, Shen Y, Phillips HA, Richards RI, Mulley JC, Sutherland GR. Callen DF, et al. Among authors: sutherland gr. Am J Hum Genet. 1993 May;52(5):922-7. Am J Hum Genet. 1993. PMID: 8488841 Free PMC article.

9

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

10

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.

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