Sara Rollinson
University of Michigan(US)
Publications by Year
Research Areas
Amyotrophic Lateral Sclerosis Research, Alzheimer's disease research and treatments, Neurological diseases and metabolism, Parkinson's Disease Mechanisms and Treatments, Neurogenetic and Muscular Disorders Research
Most-Cited Works
- → A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD(2011)4,423 cited
- → Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17(2006)2,083 cited
- → Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study(2012)1,213 cited
- → Polymorphisms in the methylenetetrahydrofolate reductase gene are associated with susceptibility to acute leukemia in adults(1999)530 cited
- → Genetic variation in TNF and IL10 and risk of non-Hodgkin lymphoma: a report from the InterLymph Consortium(2005)376 cited
- → Frequency and clinical characteristics of progranulin mutation carriers in the Manchester frontotemporal lobar degeneration cohort: comparison with patients with MAPT and no known mutations(2008)195 cited
- → Dipeptide repeat proteins are present in the p62 positive inclusions in patients with frontotemporal lobar degeneration and motor neurone disease associated with expansions in C9ORF72(2013)181 cited
- → A complex population of RNAs exists in human ejaculate spermatozoa: implications for understanding molecular aspects of spermiogenesis(1999)162 cited
- → The most common type of FTLD-FUS (aFTLD-U) is associated with a distinct clinical form of frontotemporal dementia but is not related to mutations in the FUS gene(2011)134 cited
- → Genome-wide analyses as part of the international FTLD-TDP whole-genome sequencing consortium reveals novel disease risk factors and increases support for immune dysfunction in FTLD(2019)128 cited