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Transforming machine translation: a deep learning system reaches news translation quality comparable to human professionals

Nature communications, 2020-09, Vol.11 (1), p.4381-4381, Article 4381

2020

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Bisulfite-free direct detection of 5-methylcytosine and 5-hydroxymethylcytosine at base resolution

Nature biotechnology, 2019-04, Vol.37 (4), p.424-429

2019

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Mutational signature distribution varies with DNA replication timing and strand asymmetry

Genome Biology, 2018-09, Vol.19 (1), p.129-12, Article 129

2018

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DNA Modifications: Naturally More Error Prone?

Trends in genetics, 2018-08, Vol.34 (8), p.627-638

2018

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5-hydroxymethylcytosine marks regions with reduced mutation frequency in human DNA

eLife, 2016-05, Vol.5

2016

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NT‐proBNP predicts mortality in adults with transposition of the great arteries late after Mustard or Senning correction

Congenital heart disease, 2017-07, Vol.12 (4), p.448-457

2017

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Determinants of heritable gene silencing for KRAB-dCas9 + DNMT3 and Ezh2-dCas9 + DNMT3 hit-and-run epigenome editing

Nucleic acids research, 2022-04, Vol.50 (6), p.3239

2022

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Expression of Idh1(R132H) in the Murine Subventricular Zone Stem Cell Niche Recapitulates Features of Early Gliomagenesis

Cancer cell, 2016-10, Vol.30 (4), p.578

2016

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DNA Replication and associated repair pathways are involved in the mutagenesis of methylated cytosine

DNA repair, 2018-02, Vol.62, p.1-7

2018

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Dr.Nod: computational framework for discovery of regulatory non-coding drivers in tissue-matched distal regulatory elements

Nucleic acids research, 2023-02, Vol.51 (4), p.e23

2023

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DNA damage remodels the MITF interactome to increase melanoma genomic instability

Genes & development, 2024-01, Vol.38 (1-2), p.70

2024

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Abstract 825: TAPS: A bisulfite-free, base-resolution and quantitative sequencing method for cytosine modifications

Cancer research (Chicago, Ill.), 2019-07, Vol.79 (13_Supplement), p.825-825

2019

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Erratum to “DNA Replication and associated repair pathways are involved in the mutagenesis of methylated cytosine”[DNA Repair, 62 (2018) 1–7]

DNA repair, 2018-05, Vol.65, p.79-79

2018

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Tumor monocyte content predicts immunochemotherapy outcomes in esophageal adenocarcinoma

Cancer cell, 2023-07, Vol.41 (7), p.1222-1241.e7

2023

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Abstract 4661: Deciphering the causes of the COSMIC mutational signature 17 by combining pan-cancer data with experimental mouse models

Cancer research (Chicago, Ill.), 2019-07, Vol.79 (13_Supplement), p.4661-4661

2019

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The polymorphic variant rs1800734 influences methylation acquisition and allele-specific TFAP4 binding in the MLH1 promoter leading to differential mRNA expression

Scientific reports, 2019-09, Vol.9 (1), p.13463-10, Article 13463

2019

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The relationship between dna modifications and mutations in cancer

Tomkova, Marketa

2017

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ProQuest

Modulation of Cardiac Alternans by Altered Sarcoplasmic Reticulum Calcium Release: A Simulation Study

Frontiers in physiology, 2018-09, Vol.9, p.1306-1306

2018

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Usefulness of N -Terminal Pro-Brain Natriuretic Peptide to Predict Mortality in Adults With Congenital Heart Disease

The American journal of cardiology, 2015-11, Vol.116 (9), p.1425-1430

2015

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Characterization of the genetic determinants of context-specific DNA methylation in primary monocytes

Cell genomics, 2024-05, Vol.4 (5), p.100541-100541, Article 100541

2024

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β-Adrenergic Receptor Stimulation and Alternans in the Border Zone of a Healed Infarct: An ex vivo Study and Computational Investigation of Arrhythmogenesis

Frontiers in physiology, 2019-03, Vol.10, p.350-350

2019

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Long-Term Survival of Adult Patients With Atrial Septal Defect With Regards to Defect Closure and Pulmonary Hypertension

Frontiers in cardiovascular medicine, 2022-04, Vol.9, p.867012

2022

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Normalization of Four Different Types of Pulmonary Hypertension After Atrial Septal Defect Closure

Frontiers in cardiovascular medicine, 2022-06, Vol.9, p.876755-876755

2022

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Transforming machine translation: a deep learning system reaches news translation quality comparable to human professionals

Bisulfite-free direct detection of 5-methylcytosine and 5-hydroxymethylcytosine at base resolution

Mutational signature distribution varies with DNA replication timing and strand asymmetry

DNA Modifications: Naturally More Error Prone?

5-hydroxymethylcytosine marks regions with reduced mutation frequency in human DNA

Expression of Idh1R132H in the Murine Subventricular Zone Stem Cell Niche Recapitulates Features of Early Gliomagenesis

NT‐proBNP predicts mortality in adults with transposition of the great arteries late after Mustard or Senning correction

Determinants of heritable gene silencing for KRAB-dCas9 + DNMT3 and Ezh2-dCas9 + DNMT3 hit-and-run epigenome editing

Expression of Idh1(R132H) in the Murine Subventricular Zone Stem Cell Niche Recapitulates Features of Early Gliomagenesis

DNA Replication and associated repair pathways are involved in the mutagenesis of methylated cytosine

Dr.Nod: computational framework for discovery of regulatory non-coding drivers in tissue-matched distal regulatory elements

DNA damage remodels the MITF interactome to increase melanoma genomic instability

Abstract 825: TAPS: A bisulfite-free, base-resolution and quantitative sequencing method for cytosine modifications

Erratum to “DNA Replication and associated repair pathways are involved in the mutagenesis of methylated cytosine”[DNA Repair, 62 (2018) 1–7]

Tumor monocyte content predicts immunochemotherapy outcomes in esophageal adenocarcinoma

Abstract 4661: Deciphering the causes of the COSMIC mutational signature 17 by combining pan-cancer data with experimental mouse models

The polymorphic variant rs1800734 influences methylation acquisition and allele-specific TFAP4 binding in the MLH1 promoter leading to differential mRNA expression

The relationship between dna modifications and mutations in cancer

Modulation of Cardiac Alternans by Altered Sarcoplasmic Reticulum Calcium Release: A Simulation Study

Usefulness of N -Terminal Pro-Brain Natriuretic Peptide to Predict Mortality in Adults With Congenital Heart Disease

Characterization of the genetic determinants of context-specific DNA methylation in primary monocytes

β-Adrenergic Receptor Stimulation and Alternans in the Border Zone of a Healed Infarct: An ex vivo Study and Computational Investigation of Arrhythmogenesis

Long-Term Survival of Adult Patients With Atrial Septal Defect With Regards to Defect Closure and Pulmonary Hypertension

Expression of Idh1 R132H in the Murine Subventricular Zone Stem Cell Niche Recapitulates Features of Early Gliomagenesis

Normalization of Four Different Types of Pulmonary Hypertension After Atrial Septal Defect Closure

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