Rosa Rademakers

Molecular Biology · 2006–2022

A researcher in the Science corpus: 13 papers; trusts 1 researcher and is trusted by 2 researchers here, as inferred from the citation graph.

Subfields

• Molecular Biology — 58 citations into it

Whom Rosa Rademakers trusts overall

Their strongest outbound trust, strongest first, inferred from their citations.

1. Heng Li
2. Wouter De Coster
3. James K. Bonfield

Who trusts Rosa Rademakers overall

1. D. Cleveland
2. M. Polymenidou

Papers from Rosa Rademakers's perspective

Ordered by how strongly the researchers Rosa Rademakers trusts endorse each paper. Same corpus, a different order for every researcher.

1. Ubiquitinated TDP-43 in Frontotemporal Lobar Degeneration and Amyotrophic Lateral Sclerosis (Science)
2. Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method. (Methods)
3. Molecular biology of amyotrophic lateral sclerosis: insights from genetics (Nature Reviews Neuroscience)
4. Mutations in the FUS/TLS Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis (Science)
5. A genome-wide association study of global gene expression (Nature Genetics)
6. Rethinking ALS: the FUS about TDP-43. (Cell)
7. Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21 (Nature)
8. Stages of the Pathologic Process in Alzheimer Disease: Age Categories From 1 to 100 Years (Journal of Neuropathology and Experimental Neurology)
9. Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17 (Nature)
10. Minimap2: pairwise alignment for nucleotide sequences (Bioinform.)

Their papers

• Detection of long repeat expansions from PCR-free whole-genome sequence data (2016) — 348 citations
• NanoPack2: population-scale evaluation of long-read sequencing data (2022) — 630 citations
• Limbic-predominant age-related TDP-43 encephalopathy (LATE): consensus working group report (2019) — 1,263 citations
• Progranulin Deficiency Promotes Circuit-Specific Synaptic Pruning by Microglia via Complement Activation (2016) — 659 citations
• Unconventional translation of C9ORF72 GGGGCC expansion generates insoluble polypeptides specific to c9FTD/ALS. (2013) — 1,092 citations
• TREM2 Variants in Alzheimer's Disease (2012) — 2,718 citations
• Expanded GGGGCC hexanucleotide repeat in non-coding region of C9ORF72 causes chromosome 9p-linked frontotemporal dementia and amyotrophic lateral sclerosis (2011) — 4,680 citations
• TDP-43 and FUS in amyotrophic lateral sclerosis and frontotemporal dementia. (2010) — 987 citations
• Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions (2010) — 595 citations
• A new subtype of frontotemporal lobar degeneration with FUS pathology. (2009) — 727 citations
• TDP‐43 A315T mutation in familial motor neuron disease (2008) — 639 citations
• Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17 (2006) — 2,004 citations
• Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21 (2006) — 1,503 citations