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Linn Öijerstedt

Researcher at Karolinska University Hospital

Publications -  7
Citations -  181

Linn Öijerstedt is an academic researcher from Karolinska University Hospital. The author has contributed to research in topics: Frontotemporal dementia & Genome-wide association study. The author has an hindex of 4, co-authored 7 publications receiving 104 citations. Previous affiliations of Linn Öijerstedt include Karolinska Institutet.

Papers
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Journal ArticleDOI

Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study

Cyril Pottier, +145 more
- 01 Jun 2018 - 
TL;DR: In this paper, a meta-analysis was conducted to identify potential genetic modifiers of disease onset and disease risk in frontotemporal lobar degeneration (FTLD) carriers.
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Functional network resilience to pathology in presymptomatic genetic frontotemporal dementia

Timothy Rittman, +132 more
TL;DR: It is proposed that maintaining the efficient organization of the brain's functional network supports cognitive health even as atrophy and connectivity decline presymptomatically.
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Social cognition impairment in genetic frontotemporal dementia within the GENFI cohort

Lucy L. Russell, +133 more
- 01 Dec 2020 - 
TL;DR: In this paper, facial emotion recognition (FER) and faux pas (FP) recognition tests were used to study social cognition within the Genetic Frontotemporal Dementia Initiative (GENFI), a large familial FTD cohort of C9orf72, GRN, and MAPT mutation carriers.
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Maternal Germinal Trisomy 21 in Down Syndrome.

TL;DR: Data is presented here on the incidence of trisomy 21 mosaicism in a cohort of normal fetal ovarian samples, indicating that an accumulation of tr isomy 21 germ cells does indeed take place during fetal oogenesis, and this trend continues during the third trimester of pregnancy and postnatally, up until ovulation, thereby explaining the maternal age effect in Down syndrome.
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A panel of CSF proteins separates genetic frontotemporal dementia from presymptomatic mutation carriers: a GENFI study.

Sofia Bergström, +151 more
TL;DR: In this paper, a multiplexed antibody-based suspension bead array was used to analyse levels of 111 proteins in CSF samples from 221 individuals from families with genetic frontotemporal dementia.