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Browse > Neurological Disorders > Neurogenetics
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Recommended
F1000 Factor 3.0

Confirmation
New Finding
 SLC6A4 variation and citalopram response.
Mrazek DA, Rush AJ, …, Black JL, Weinshilboum RM
Am J Med Genet B Neuropsychiatr Genet 2008 Jul 10 [abstract on PubMed] [related articles] [full text]
Selected by | Alan Apter with Sefi Kronenberg
Evaluated 1 Dec 2008

Exceptional
F1000 Factor 9.0

Confirmation
New Finding
 Dok-7 myasthenia: phenotypic and molecular genetic studies in 16 patients.
Selcen D, Milone M, …, Wieben ED, Engel AG
Ann Neurol 2008 Jul 64(1):71-87 [abstract on PubMed] [related articles] [full text] [order article]
Selected by | Richard Lewis
Evaluated 27 Nov 2008

Must Read
F1000 Factor 6.0

Confirmation
 GAB2 alleles modify Alzheimer's risk in APOE epsilon4 carriers.
Reiman EM, Webster JA, …, Papassotiropoulos A, Stephan DA
Neuron 2007 Jun 7 54(5):713-20 [abstract on PubMed] [related articles] [full text] [order article]
Selected by | Jean-Charles Lambert with Julien Chapuis
Evaluated 26 Nov 2008

Must Read
F1000 Factor 6.0

New Finding
 Altered Expression of Genes Involved in GABAergic Transmission and Neuromodulation of Granule Cell Activity in the Cerebellum of Schizophrenia Patients.
Bullock WM, Cardon K, …, Roberts RC, Perrone-Bizzozero NI
Am J Psychiatry 2008 Oct 15 [abstract on PubMed] [related articles] [full text]
Selected by | Francine Benes with Guoqing Sheng
Evaluated 26 Nov 2008

Recommended
F1000 Factor 3.0

Confirmation
 The role of autophagy-lysosome pathway in neurodegeneration associated with Parkinson's disease.
Pan T, Kondo S, Le W, Jankovic J
Brain 2008 Aug 131(Pt 8):1969-78 [abstract on PubMed] [related articles] [full text] [order article]
Selected by | Alfredo Berardelli with Antonio Suppa
Evaluated 26 Nov 2008

Recommended
F1000 Factor 3.0

Confirmation
 Detection of Huntington's disease decades before diagnosis: the Predict-HD study.
Paulsen JS, Langbehn DR, …, Hayden M, Predict-HD Investigators and Coordinators of the Huntington Study Group
J Neurol Neurosurg Psychiatry 2008 Aug 79(8):874-80 [abstract on PubMed] [related articles] [FREE full text]
Selected by | Stefano Di Donato
Evaluated 20 Nov 2008

Must Read
F1000 Factor 4.8

New Finding
 TMEM70 mutations cause isolated ATP synthase deficiency and neonatal mitochondrial encephalocardiomyopathy.
Cízková A, Stránecký V, …, Houstek J, Kmoch S
Nat Genet 2008 Nov 40(11):1288-90 [abstract on PubMed] [related articles] [full text] [order article]
Selected by | Salvatore Di Mauro / Nereo Bresolin with Dario Ronchi
First evaluation 11 Nov 2008 | Latest evaluation 17 Nov 2008

Recommended
F1000 Factor 3.0

New Finding
 Parkin deficiency increases vulnerability to inflammation-related nigral degeneration.
Frank-Cannon TC, Tran T, …, Goldberg MS, Tansey MG
J Neurosci 2008 Oct 22 28(43):10825-34 [abstract on PubMed] [related articles] [full text] [order article]
Selected by | X.William Yang with Xiao-Hong Lu
Evaluated 31 Oct 2008

Must Read
F1000 Factor 4.8

New Finding
 Relation between obesity and blunted striatal response to food is moderated by TaqIA A1 allele.
Stice E, Spoor S, Bohon C, Small DM
Science 2008 Oct 17 322(5900):449-52 [abstract on PubMed] [related articles] [full text] [order article]
Selected by | Cynthia Bulik with Jocilyn Dellava / Martien Kas with Marek Brandys
First evaluation 29 Oct 2008 | Latest evaluation 6 Nov 2008

Recommended
F1000 Factor 3.0

New Finding
 Mannosidase I inhibition rescues the human alpha-sarcoglycan R77C recurrent mutation.
Bartoli M, Gicquel E, …, Danos O, Richard I
Hum Mol Genet 2008 May 1 17(9):1214-21 [abstract on PubMed] [related articles] [full text] [order article]
Selected by | Nigel Laing with Gianina Ravenscroft
Evaluated 27 Oct 2008


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