Suchergebnisse - "Graff, Misa"

PubPharm (50)

1

Dietary and supplemental intake of vitamins C and E is associated with altered DNA methylation in an epigenome-wide association study meta-analysis

enthalten in: Epigenetics | 2023

von Keshawarz, A. | Joehanes, R. | Ma, J. | +31

2

Genetic Examination of Hematological Parameters in SARS-CoV-2 Infection and COVID-19

enthalten in: bioRxiv.org | 2023

von Rowland, B. | Sun, Q. | Wang, W. | +11

3

Genetic examination of hematological parameters in SARS-CoV-2 infection and COVID-19

enthalten in: Blood cells, molecules & diseases | 2023

von Sun, Q. | Rowland, B. | Wang, W. | +11

UpdateOf: medRxiv. 2022 Feb 28;:. - PMID 35262092

4

Epigenome-wide methylation and progression to high-grade cervical intraepithelial neoplasia (CIN2+) : a prospective cohort study in the United States

enthalten in: BMC cancer | 2023

von Bukowski, A. | Hoyo, C. | Vielot, N. | +9

5

Epigenome-wide methylation and progression to high-grade cervical intraepithelial neoplasia (CIN2+): a prospective cohort study in the United States

enthalten in: BMC cancer | 2023

von Bukowski, A. | Hoyo, C. | Vielot, N. | +9

6

Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variants

enthalten in: HGG advances | 2023

von Young, K. | Fisher, V. | Deng, X. | +59

7

Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations

enthalten in: bioRxiv.org | 2022

von Kowalski, M. | Qian, H. | Hou, Z. | +75

8

Enrichment analyses identify shared associations for 25 quantitative traits in over 600,000 individuals from seven diverse ancestries

enthalten in: bioRxiv.org | 2022

von Smith, S. | Shahamatdar, S. | Cheng, W. | +12

9

Enrichment analyses identify shared associations for 25 quantitative traits in over 600,000 individuals from seven diverse ancestries

enthalten in: American journal of human genetics | 2022

von Smith, S. | Shahamatdar, S. | Cheng, W. | +12

10

Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data

enthalten in: Nature genetics | 2022

von Wainschtein, P. | Jain, D. | Zheng, Z. | +149

CommentIn: Nat Genet. 2022 Mar;54(3):224-226. - PMID 35273401

1
2
3
4
5
Nächster »
[5]