A citation-based method for searching scientific literature

B Kremer, P Goldberg, S E Andrew, J Theilmann, H Telenius, J Zeisler, F Squitieri, B Lin, A Bassett, E Almqvist. N Engl J Med 1994
Times Cited: 417



Fiona K Baine, Chris Kay, Maria E Ketelaar, Jennifer A Collins, Alicia Semaka, Crystal N Doty, Amanda Krause, L Jacquie Greenberg, Michael R Hayden. Eur J Hum Genet 2013
Times Cited: 35




List of shared articles



Times cited

Tracing the mutated HTT and haplotype of the African ancestor who spread Huntington disease into the Middle East.
Ferdinando Squitieri, Tommaso Mazza, Sabrina Maffi, Alessandro De Luca, Qasem AlSalmi, Salma AlHarasi, Jennifer A Collins, Chris Kay, Fiona Baine-Savanhu, Bernard G Landwhermeyer,[...]. Genet Med 2020
1



Epidemiology of Huntington disease.
Chris Kay, Michael R Hayden, Blair R Leavitt. Handb Clin Neurol 2017
17

Genetic aspects of Huntington's disease in Latin America. A systematic review.
R M Castilhos, M C Augustin, J A Santos, C Perandones, M L Saraiva-Pereira, L B Jardim. Clin Genet 2016
13

The Frequency of Huntington Disease and Huntington Disease-Like 2 in the South African Population.
Fiona K Baine, Amanda Krause, L Jacquie Greenberg. Neuroepidemiology 2016
15

Junctophilin 3 (JPH3) expansion mutations causing Huntington disease like 2 (HDL2) are common in South African patients with African ancestry and a Huntington disease phenotype.
Amanda Krause, Claire Mitchell, Fahmida Essop, Susan Tager, James Temlett, Giovanni Stevanin, Christopher Ross, Dobrila Rudnicki, Russell Margolis. Am J Med Genet B Neuropsychiatr Genet 2015
30