Suchergebnisse - "Perret, Claire"

PubPharm (89)

1

DNA-pools targeted-sequencing as a robust cost-effective method to detect rare variants : Application to dilated cardiomyopathy genetic diagnosis

enthalten in: Clinical genetics | 2024

von Perret, C. | Proust, C. | Esslinger, U. | +9

2

DNA‐pools targeted‐sequencing as a robust cost‐effective method to detect rare variants : Application to dilated cardiomyopathy genetic diagnosis

enthalten in: Clinical Genetics | 2024

von Perret, C. | Proust, C. | Esslinger, U. | +9

3

DNA-pools targeted-sequencing as a robust cost-effective method to detect rare variants : application to dilated cardiomyopathy genetic diagnosis

enthalten in: Clinical genetics | 30 October 2023

Online version of record before inclusion in an issue

von Perret, C. | Proust, C. | Esslinger, U. | +9

4

Changes in circulating miRNA19a-3p precede insulin resistance programmed by intra-uterine growth retardation in mice

enthalten in: Molecular metabolism | 2020

von Saget, S. | Cong, R. | Decourtye, L. | +16

5

OPTIMIR, a novel algorithm for integrating available genome-wide genotype data into miRNA sequence alignment analysis

enthalten in: bioRxiv.org | 2020

von Thibord, F. | Perret, C. | Roux, M. | +5

6

Anti-integrin αv therapy improves cardiac fibrosis after myocardial infarction by blunting cardiac PW1+ stromal cells

enthalten in: Scientific reports | 2020

von Bouvet, M. | Claude, O. | Roux, M. | +16

7

Bayesian network analysis of plasma microRNA sequencing data in patients with venous thrombosis

enthalten in: European heart journal supplements : journal of the European Society of Cardiology | 2020

von Thibord, F. | Munsch, G. | Perret, C. | +7

8

Correction : Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathy

enthalten in: PloS one | 2020

von Esslinger, U. | Garnier, S. | Korniat, A. | +32

ErratumFor: PLoS One. 2017 Mar 15;12(3):e0172995. - PMID 28296976

9

Whole blood levels of S1PR4 mRNA associated with cerebral vasospasm after aneurysmal subarachnoid hemorrhage

enthalten in: Journal of neurosurgery | 2019

von Pulcrano-Nicolas, A. | Jacquens, A. | Proust, C. | +8

10

FLNC pathogenic variants in patients with cardiomyopathies : Prevalence and genotype-phenotype correlations

enthalten in: Clinical genetics | 2019

von Ader, F. | De Groote, P. | Réant, P. | +16

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