Search details
1.
NIPA1 polyalanine repeat expansions are associated with amyotrophic lateral sclerosis.
Hum Mol Genet
; 21(11): 2497-502, 2012 Jun 01.
Article
in English
| MEDLINE | ID: mdl-22378146
2.
A large genome scan for rare CNVs in amyotrophic lateral sclerosis.
Hum Mol Genet
; 19(20): 4091-9, 2010 Oct 15.
Article
in English
| MEDLINE | ID: mdl-20685689
3.
Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis.
Ann Neurol
; 70(6): 964-73, 2011 Dec.
Article
in English
| MEDLINE | ID: mdl-22190368
4.
Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis.
Proc Natl Acad Sci U S A
; 106(22): 9004-9, 2009 Jun 02.
Article
in English
| MEDLINE | ID: mdl-19451621
5.
Variants of the elongator protein 3 (ELP3) gene are associated with motor neuron degeneration.
Hum Mol Genet
; 18(3): 472-81, 2009 Feb 01.
Article
in English
| MEDLINE | ID: mdl-18996918
6.
Multifocal motor neuropathy is not associated with genetic variation in PTPN22, BANK1, Blk, FCGR2B, CD1A/E, and TAG-1 genes.
J Peripher Nerv Syst
; 16(3): 175-9, 2011 Sep.
Article
in English
| MEDLINE | ID: mdl-22003931
7.
SMN1 Duplications Are Associated With Progressive Muscular Atrophy, but Not With Multifocal Motor Neuropathy and Primary Lateral Sclerosis.
Neurol Genet
; 7(4): e598, 2021 Aug.
Article
in English
| MEDLINE | ID: mdl-34169148
8.
Weighted gene co-expression network analysis of the peripheral blood from Amyotrophic Lateral Sclerosis patients.
BMC Genomics
; 10: 405, 2009 Aug 27.
Article
in English
| MEDLINE | ID: mdl-19712483
9.
Analysis of FGGY as a risk factor for sporadic amyotrophic lateral sclerosis.
Amyotroph Lateral Scler
; 10(5-6): 441-7, 2009.
Article
in English
| MEDLINE | ID: mdl-19922138
10.
P413L CHGB is not associated with ALS susceptibility or age at onset in a Dutch population.
Proc Natl Acad Sci U S A
; 107(19): E77; author reply E78, 2010 May 11.
Article
in English
| MEDLINE | ID: mdl-20431044
11.
Whole blood transcriptome analysis in amyotrophic lateral sclerosis: A biomarker study.
PLoS One
; 13(6): e0198874, 2018.
Article
in English
| MEDLINE | ID: mdl-29939990
12.
The association between H63D mutations in HFE and amyotrophic lateral sclerosis in a Dutch population.
Arch Neurol
; 64(1): 63-7, 2007 Jan.
Article
in English
| MEDLINE | ID: mdl-17210810
13.
Ciliary neurotrophic factor null alleles are not a risk factor for Charcot-Marie-Tooth disease, hereditary neuropathy with pressure palsies and amyotrophic lateral sclerosis.
Neuromuscul Disord
; 17(11-12): 964-7, 2007 Dec.
Article
in English
| MEDLINE | ID: mdl-17651970
14.
Analysis of the KIFAP3 gene in amyotrophic lateral sclerosis: a multicenter survival study.
Neurobiol Aging
; 35(10): 2420.e13-4, 2014 Oct.
Article
in English
| MEDLINE | ID: mdl-24838185
15.
Gene expression profile of SOD1-G93A mouse spinal cord, blood and muscle.
Amyotroph Lateral Scler Frontotemporal Degener
; 14(3): 190-8, 2013 Apr.
Article
in English
| MEDLINE | ID: mdl-23298163
16.
Screening for rare variants in the coding region of ALS-associated genes at 9p21.2 and 19p13.3.
Neurobiol Aging
; 34(5): 1518.e5-7, 2013 May.
Article
in English
| MEDLINE | ID: mdl-23141412
17.
H63D polymorphism in HFE is not associated with amyotrophic lateral sclerosis.
Neurobiol Aging
; 34(5): 1517.e5-7, 2013 May.
Article
in English
| MEDLINE | ID: mdl-23063643
18.
Rare and common paraoxonase gene variants in amyotrophic lateral sclerosis patients.
Neurobiol Aging
; 33(8): 1845.e1-3, 2012 Aug.
Article
in English
| MEDLINE | ID: mdl-22330174
19.
Novel optineurin mutations in sporadic amyotrophic lateral sclerosis patients.
Neurobiol Aging
; 33(5): 1016.e1-7, 2012 May.
Article
in English
| MEDLINE | ID: mdl-21802176
20.
UNC13A is a modifier of survival in amyotrophic lateral sclerosis.
Neurobiol Aging
; 33(3): 630.e3-8, 2012 Mar.
Article
in English
| MEDLINE | ID: mdl-22118904