Comment on "blinders, phenotype, and fashionable genetic analysis: A critical examination of the current state of epilepsy genetic studies"

Epilepsia

Volumn 52, Issue 1, 2011, Pages 190-191

  Johnson, Michael R ^a  

^a IMPERIAL COLLEGE LONDON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

SODIUM CHANNEL NAV1.1;

EPILEPSY; GENE EXPRESSION; GENE MUTATION; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENETIC VARIABILITY; HUMAN; NOTE; PHENOTYPE; PRIORITY JOURNAL; RISK FACTOR; SEIZURE;

EPILEPSY; GENOME-WIDE ASSOCIATION STUDY; HUMANS; PHENOTYPE;

EID: 78651342482     PISSN: 00139580     EISSN: 15281167     Source Type: Journal    
DOI: 10.1111/j.1528-1167.2010.02791.x     Document Type: Note

References (4)

1. Goh K, Cusick ME, Valle D, Childs B, Vidal M, Barabasi A-L,. (2007) The human disease network. Proc Natl Acad Sci U S A 104: 8685-8690.
2. Greenberg DA, Subaran R,. (2010) Blinders, phenotype, and fashionable genetic analysis: a critical examination of the current state of epilepsy genetic studies. Epilepsia 52 (1): 1-9.
3. Mefford HC, Muhle H, Ostertag P, von Spiczak S, Buysse K, Baker C, Franke A, Malafosse A, Genton P, Thomas P, Gurnett CA, Schreiber S, Bassuk AG, Guipponi M, Stephani U, Helbig I, Eichler EE,. (2010) Genome-wide copy number variation in epilepsy: novel susceptibility loci in idiopathic generalized and focal epilepsies. PLoS Genet 6: e1000962.
4. Scheffer IE, Berkovic SF,. (1997) Generalized epilepsy with febrile seizures plus. A genetic disorder with heterogeneous clinical phenotypes. Brain 120: 479-490.