Suchergebnisse - "Myers, Richard"

PubPharm (1.155)

51

Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer's disease

enthalten in: Nature genetics | 2022

von Holstege, H. | Hulsman, M. | Charbonnier, C. | +98

CommentIn: Nat Rev Neurol. 2023 Jan;19(1):3. - PMID 36477429

52

An integrated analysis of contact tracing and genomics to assess the efficacy of travel restrictions on SARS-CoV-2 introduction and transmission in England from June to September, 2020

enthalten in: bioRxiv.org | 2022

von Aggarwal, D. | Page, A. | Schaefer, U. | +17

53

Dissecting the shared genetic architecture of suicide attempt, psychiatric disorders and known risk factors

enthalten in: bioRxiv.org | 2022

von Mullins, N. | Kang, J. | Campos, A. | +258

54

Predicting future from past: The genomic basis of recurrent and rapid stickleback evolution

enthalten in: bioRxiv.org | 2022

von Roberts Kingman, G. | Vyas, D. | Jones, F. | +16

55

Genetic Associations with Age at Dementia Onset in thePSEN1 E280AColombian Kindred

enthalten in: bioRxiv.org | 2022

von Cochran, J. | Acosta-Uribe, J. | Esposito, B. | +26

56

M. tuberculosis microvariation is common and is associated with transmission: analysis of three years prospective universal sequencing in England

enthalten in: bioRxiv.org | 2022

von Wyllie, D. | Do, T. | Myers, R. | +7

57

The origins and molecular evolution of SARS-CoV-2 lineage B.1.1.7 in the UK

enthalten in: bioRxiv.org | 2022

von Hill, V. | Du Plessis, L. | Peacock, T. | +26

58

Context-specific emergence and growth of the SARS-CoV-2 Delta variant

enthalten in: Nature | 2022

von McCrone, J. | Hill, V. | Bajaj, S. | +38

UpdateOf: Res Sq. 2021 Dec 20;:. - PMID 34981043

59

Overexpression of Cancer- and Neurotransmitter-Associated Genes in the Nucleus Accumbens of Smokers

enthalten in: bioRxiv.org | 2022

von Stein, R. | Mamdani, F. | Bunney, B. | +10

60

Deleterious, protein-altering variants in the X-linked transcriptional coregulator ZMYM3 in 22 individuals with a neurodevelopmental delay phenotype

enthalten in: bioRxiv.org | 2022

von Hiatt, S. | Trajkova, S. | Sebastiano, M. | +72