Suchergebnisse - "Boers, Ruben G"

PubPharm (13)

1

Distinctive cell-free DNA methylation characterizes presymptomatic genetic frontotemporal dementia

enthalten in: Annals of clinical and translational neurology | 2024

von Giannini, L. | Boers, R. | van der Ende, E. | +12

2

Distinctive cell‐free DNA methylation characterizes presymptomatic genetic frontotemporal dementia

enthalten in: Annals of Clinical and Translational Neurology | 2024

von Giannini, L. | Boers, R. | Ende, E. | +12

3

Hypermethylation of DNA Methylation Markers in Non-Cirrhotic Hepatocellular Carcinoma

enthalten in: Cancers | 2023

von Fu, S. | Deger, T. | Boers, R. | +6

4

Liquid Biopsies for Colorectal Cancer and Advanced Adenoma Screening and Surveillance : What to Measure?

enthalten in: Cancers | 2023

von Eikenboom, E. | Wilting, S. | Deger, T. | +11

5

Methylated Cell-Free DNA Sequencing (MeD-seq) of LpnPI Digested Fragments to Identify Early Progression in Metastatic Renal Cell Carcinoma Patients on Watchful Waiting

enthalten in: Cancers | 2023

von Bos, M. | Verhoeff, S. | Oosting, S. | +8

6

High throughput and affordable genome-wide methylation profiling of circulating cell-free DNA by Methylated DNA sequencing (MeD-seq) of LpnPI digested fragments

enthalten in: bioRxiv.org | 2022

von Deger, T. | Boers, R. | de Weerd, V. | +13

7

High-throughput and affordable genome-wide methylation profiling of circulating cell-free DNA by methylated DNA sequencing (MeD-seq) of LpnPI digested fragments

enthalten in: Clinical epigenetics | 2021

von Deger, T. | Boers, R. | de Weerd, V. | +13

8

High-throughput and affordable genome-wide methylation profiling of circulating cell-free DNA by methylated DNA sequencing (MeD-seq) of LpnPI digested fragments

enthalten in: Clinical epigenetics | 2021

von Deger, T. | Boers, R. | de Weerd, V. | +13

9

High-throughput and affordable genome-wide methylation profiling of circulating cell-free DNA by methylated DNA sequencing (MeD-seq) of LpnPI digested fragments

enthalten in: Clinical epigenetics | 2021

von Deger, T. | Boers, R. | de Weerd, V. | +13

10

SPEN haploinsufficiency causes a neurodevelopmental disorder overlapping proximal 1p36 deletion syndrome with an episignature of X chromosomes in females

enthalten in: American journal of human genetics | 2021

von Radio, F. | Pang, K. | Ciolfi, A. | +98