Suchergebnisse - "Niewisch, Marena R"

PubPharm (12)

1

Research on Rare Diseases in Germany - The cancer predisposition syndrome registry

enthalten in: Journal of health monitoring | 2023

von Dutzmann, C. | Palmaers, N. | Müntnich, L. | +9

2

Clinical manifestations of telomere biology disorders in adults

enthalten in: Hematology. American Society of Hematology. Education Program | 2023

von Niewisch, M. | Beier, F. | Savage, S.

3

The distribution and accumulation of the shortest telomeres in telomere biology disorders

enthalten in: British journal of haematology | 2023

von Raj, H. | Lai, T. | Niewisch, M. | +6

4

Progression of liver disease and portal hypertension in dyskeratosis congenita and related telomere biology disorders

enthalten in: Hepatology (Baltimore, Md.) | 2023

von Vittal, A. | Niewisch, M. | Bhala, S. | +8

5

Differential diagnosis of bone marrow failure syndromes guided by machine learning

enthalten in: Blood | 2023

von Gutierrez-Rodrigues, F. | Munger, E. | Ma, X. | +35

CommentIn: Blood. 2023 Apr 27;141(17):2040-2042. - PMID 37103950

6

Next-generation sequencing errors due to genetic variation in WRAP53 encoding TCAB1 on chromosome 17

enthalten in: Human mutation | 2022

von Savage, S. | Jones, K. | Teshome, K. | +3

7

Disease progression and clinical outcomes in telomere biology disorders

enthalten in: Blood | 2022

von Niewisch, M. | Giri, N. | McReynolds, L. | +4

CommentIn: Blood. 2022 Mar 24;139(12):1776-1777. - PMID 35323880

8

Next‐generation sequencing errors due to genetic variation in WRAP53 encoding TCAB1 on chromosome 17

enthalten in: Human mutation | 2022

von Savage, S. | Jones, K. | Teshome, K. | +3

9

Publisher Correction : Clinical evolution, genetic landscape and trajectories of clonal hematopoiesis in SAMD9/SAMD9L syndromes

enthalten in: Nature medicine | 2021

von Sahoo, S. | Pastor, V. | Goodings, C. | +94

ErratumFor: Nat Med. 2021 Oct;27(10):1806-1817. - PMID 34621053

10

Clinical evolution, genetic landscape and trajectories of clonal hematopoiesis in SAMD9/SAMD9L syndromes

enthalten in: Nature medicine | 2021

von Sahoo, S. | Pastor, V. | Goodings, C. | +94

ErratumIn: Nat Med. 2021 Dec;27(12):2248. - PMID 34799732