CoCites: A citation-based method for searching scientific literature

Evidence of a common founder for SCA12 in the Indian population.

S Bahl, K Virdi, U Mittal, M P Sachdeva, A K Kalla, S E Holmes, E O'Hearn, R L Margolis, S Jain, A K Srivastava, M Mukerji. Ann Hum Genet 2005
Times Cited: 43

Spinocerebellar ataxias in the Netherlands: prevalence and age at onset variance analysis.

B P C van de Warrenburg, R J Sinke, C C Verschuuren-Bemelmans, H Scheffer, E R Brunt, P F Ippel, J A Maat-Kievit, D Dooijes, N C Notermans, D Lindhout, N V A M Knoers, H P H Kremer. Neurology 2002
Times Cited: 161

List of shared articles

Times cited

Epidemiology and population genetics of degenerative ataxias.
Jorge Sequeiros, Sandra Martins, Isabel Silveira. Handb Clin Neurol 2012

Spinocerebellar ataxia type 12.
Elizabeth O'Hearn, Susan E Holmes, Russell L Margolis. Handb Clin Neurol 2012

Exploration of CAG triplet repeat in nontranslated region of SCA12 gene.
Waseem Gul Lone, Imran Ali Khan, Subhadra Poornima, Noor Ahmad Shaik, Angmuthu Kanikannan Meena, Kaipa Prabhakar Rao, Qurratulain Hasan. J Genet 2016

Autosomal dominant cerebellar ataxia type I: a review of the phenotypic and genotypic characteristics.
Nathaniel Robb Whaley, Shinsuke Fujioka, Zbigniew K Wszolek. Orphanet J Rare Dis 2011

Spinocerebellar ataxia type 12 identified in two Italian families may mimic sporadic ataxia.
Alessandro Brussino, Claudio Graziano, Dario Giobbe, Marina Ferrone, Elisa Dragone, Carlo Arduino, Raffaele Lodi, Caterina Tonon, Anna Gabellini, Rita Rinaldi,[...]. Mov Disord 2010

Role of dynamic and mitochondrial mutations in neurodegenerative diseases with ataxia: lower repeats and LNAs at multiple loci as alternative pathogenesis.
Waseem Gul Lone, Subhadra Poornima, Angmuthu Kanikannan Meena, Kaipa Prabhakar Rao, Qurratulain Hasan. J Mol Neurosci 2014

Ataxias with autosomal, X-chromosomal or maternal inheritance.
Josef Finsterer. Can J Neurol Sci 2009