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Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease.
Published in:
Nature Genetics, 2014, v. 46, n. 9, p. 989, doi. 10.1038/ng.3043
By:
- Nalls, Mike A;
- Pankratz, Nathan;
- Lill, Christina M;
- Do, Chuong B;
- Hernandez, Dena G;
- Saad, Mohamad;
- DeStefano, Anita L;
- Kara, Eleanna;
- Bras, Jose;
- Sharma, Manu;
- Schulte, Claudia;
- Keller, Margaux F;
- Arepalli, Sampath;
- Letson, Christopher;
- Edsall, Connor;
- Stefansson, Hreinn;
- Liu, Xinmin;
- Pliner, Hannah;
- Lee, Joseph H;
- Cheng, Rong
Publication type:
Article
Genome-Wide Identification and Expression of Xenopus F-Box Family of Proteins.
Published in:
PLoS ONE, 2015, v. 10, n. 9, p. 1, doi. 10.1371/journal.pone.0136929
By:
- Saritas-Yildirim, Banu;
- Pliner, Hannah A.;
- Ochoa, Angelica;
- Silva, Elena M.
Publication type:
Article
A Genome-Wide Association Study of Myasthenia Gravis.
Published in:
JAMA Neurology, 2015, v. 72, n. 4, p. 396, doi. 10.1001/jamaneurol.2014.4103
By:
- Renton, Alan E.;
- Pliner, Hannah A.;
- Provenzano, Carlo;
- Evoli, Amelia;
- Ricciardi, Roberta;
- Nalls, Michael A.;
- Marangi, Giuseppe;
- Abramzon, Yevgeniya;
- Arepalli, Sampath;
- Sean Chong;
- Hernandez, Dena G.;
- Johnson, Janel O.;
- Bartoccioni, Emanuela;
- Scuderi, Flavia;
- Maestri, Michelangelo;
- Gibbs, J. Raphael;
- Errichiello, Edoardo;
- Chiò, Adriano;
- Restagno, Gabriella;
- Sabatelli, Mario
Publication type:
Article
C9ORF72 hexanucleotide repeat exerts toxicity in a stable, inducible motor neuronal cell model, which is rescued by partial depletion of Pten.
Published in:
Human Molecular Genetics, 2017, v. 26, n. 6, p. 1133, doi. 10.1093/hmg/ddx022
By:
- Stopford, Matthew J.;
- Higginbottom, Adrian;
- Hautbergue, Guillaume M.;
- Cooper-Knock, Johnathan;
- Mulcahy, Padraig J.;
- De Vos, Kurt J.;
- Renton, Alan E.;
- Pliner, Hannah;
- Calvo, Andrea;
- Chio, Adriano;
- Traynor, Bryan J.;
- Azzouz, Mimoun;
- Heath, Paul R.;
- Kirby, Janine;
- Shaw, Pamela J.
Publication type:
Article
Searching for Grendel: origin and global spread of the C9ORF72 repeat expansion.
Published in:
Acta Neuropathologica, 2014, v. 127, n. 3, p. 391, doi. 10.1007/s00401-014-1250-x
By:
- Pliner, Hannah;
- Mann, David;
- Traynor, Bryan
Publication type:
Article
Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis.
Published in:
Nature Neuroscience, 2014, v. 17, n. 5, p. 664, doi. 10.1038/nn.3688
By:
- Johnson, Janel O;
- Pioro, Erik P;
- Boehringer, Ashley;
- Chia, Ruth;
- Feit, Howard;
- Renton, Alan E;
- Pliner, Hannah A;
- Abramzon, Yevgeniya;
- Marangi, Giuseppe;
- Winborn, Brett J;
- Gibbs, J Raphael;
- Nalls, Michael A;
- Morgan, Sarah;
- Shoai, Maryam;
- Hardy, John;
- Pittman, Alan;
- Orrell, Richard W;
- Malaspina, Andrea;
- Sidle, Katie C;
- Fratta, Pietro
Publication type:
Article

Found: 6

Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease.

Genome-Wide Identification and Expression of Xenopus F-Box Family of Proteins.

A Genome-Wide Association Study of Myasthenia Gravis.

C9ORF72 hexanucleotide repeat exerts toxicity in a stable, inducible motor neuronal cell model, which is rescued by partial depletion of Pten.

Searching for Grendel: origin and global spread of the C9ORF72 repeat expansion.

Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis.