Human Genome Epidemiology Literature Finder
Records 1 - 6 (of 6 Records) |
Query Trace: Disease Progression and HTT[original query] |
---|
CNR1 variation is associated with the age at onset in Huntington disease. European journal of medical genetics 2013 Aug 56 (8): 416-9. Kloster Eugen, Saft Carsten, Epplen Jörg T, Arning Laris |
Body weight is a robust predictor of clinical progression in Huntington disease. Annals of neurology 2017 Aug . van der Burg Jorien M M, Gardiner Sarah L, Ludolph Albert C, Landwehrmeyer G Bernhard, Roos Raymund A C, Aziz N Ahm |
Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study.
The Lancet. Neurology 2017 Jun . Moss Davina J Hensman, Pardiñas Antonio F, Langbehn Douglas, Lo Kitty, Leavitt Blair R, Roos Raymund, Durr Alexandra, Mead Simon, , , Holmans Peter, Jones Lesley, Tabrizi Sarah |
Genetics Modulate Gray Matter Variation Beyond Disease Burden in Prodromal Huntington's Disease. Frontiers in neurology 2018 4 9 190. Liu Jingyu, Ciarochi Jennifer, Calhoun Vince D, Paulsen Jane S, Bockholt H Jeremy, Johnson Hans J, Long Jeffrey D, Lin Dongdong, Espinoza Flor A, Misiura Maria B, Caprihan Arvind, Turner Jessica A, |
Clinical manifestations of homozygote allele carriers in Huntington disease. Neurology 2019 3 92 (18): e2101-e2108. Cubo Esther, Martinez-Horta Saul-Indra, Santalo Frederic Sampedro, Descalls Asunción Martínez, Calvo Sara, Gil-Polo Cecilia, Muñoz Ignacio, Llano Katia, Mariscal Natividad, Diaz Dolores, Gutierrez Aranzazu, Aguado Laura, Ramos-Arroyo María A, |
Relationship between gene-environment interaction and obsessive-compulsive disorder: A systematic review. Journal of psychiatric research 2023 6 164 281-290. Lina Wang, Yu Chen, Miao Wang, Chaoben Zhao, Dongdong Qi |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
- Content source: