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Contingency and entrenchment in protein evolution under purifying selection

Proceedings of the National Academy of Sciences - PNAS, 2015-06, Vol.112 (25), p.E3226-E3235

2015

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Rate-Limiting Steps in Yeast Protein Translation

Cell, 2013-06, Vol.153 (7), p.1589-1601

2013

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A tRNA modification balances carbon and nitrogen metabolism by regulating phosphate homeostasis

eLife, 2019-07, Vol.8

2019

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Neurodevelopmental disorders and neurodiversity: definition of terms from Scotland's National Autism Implementation Team

British journal of psychiatry, 2022-09, Vol.221 (3), p.577-579

2022

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Explaining complex codon usage patterns with selection for translational efficiency, mutation bias, and genetic drift

Proceedings of the National Academy of Sciences - PNAS, 2011-06, Vol.108 (25), p.10231-10236

2011

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Non-optimal codon usage is a mechanism to achieve circadian clock conditionality

Nature (London), 2013-03, Vol.495 (7439), p.116-120

2013

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The landscape of transcriptional and translational changes over 22 years of bacterial adaptation

eLife, 2022-10, Vol.11

2022

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Intragenomic variation in non-adaptive nucleotide biases causes underestimation of selection on synonymous codon usage

PLoS genetics, 2022-06, Vol.18 (6), p.e1010256

2022

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Linking genotypic and phenotypic changes in the E. coli long-term evolution experiment using metabolomics

eLife, 2023-11, Vol.12

2023

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The medical model is dead – long live the medical model

British journal of psychiatry, 2007-11, Vol.191 (5), p.375-377

2007

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The hypoxia response pathway promotes PEP carboxykinase and gluconeogenesis in C. elegans

Nature communications, 2022-10, Vol.13 (1), p.6168-6168, Article 6168

2022

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riboviz: analysis and visualization of ribosome profiling datasets

BMC bioinformatics, 2017-10, Vol.18 (1), p.461-461, Article 461

2017

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XACT-Seq Comprehensively Defines the Promoter-Position and Promoter-Sequence Determinants for Initial-Transcription Pausing

Molecular cell, 2020-09, Vol.79 (5), p.797-811.e8

2020

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EVIDENCE FOR REPEATED LOSS OF SELECTIVE CONSTRAINT IN RHODOPSIN OF AMBLYOPSID CAVEFISHES (TELEOSTEI: AMBLYOPSIDAE)

Evolution, 2013-03, Vol.67 (3), p.732-748

2013

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Effect of correlated tRNA abundances on translation errors and evolution of codon usage bias

PLoS genetics, 2010-09, Vol.6 (9), p.e1001128-e1001128

2010

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Reply to: Potential contribution of PEP carboxykinase-dependent malate dismutation to the hypoxia response in C. elegans

Nature communications, 2023-07, Vol.14 (1), p.3937-3937, Article 3937

2023

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Celf4 controls mRNA translation underlying synaptic development in the prenatal mammalian neocortex

Nature communications, 2023-09, Vol.14 (1), p.6025-6025, Article 6025

2023

Volltextzugriff (PDF)

Implementation of Nanopore sequencing as a pragmatic workflow for copy number variant confirmation in the clinic

Journal of translational medicine, 2023-06, Vol.21 (1), p.378-378, Article 378

2023

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NADcapPro and circNC: methods for accurate profiling of NAD and non-canonical RNA caps in eukaryotes

Communications biology, 2023-04, Vol.6 (1), p.406-14, Article 406

2023

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P646: Development of an affordable rapid human genome sequencing assay using long read PromethiON 2

Genetics in Medicine Open, 2024, Vol.2, p.101552, Article 101552

2024

Volltextzugriff (PDF)

Adults with attention-deficit hyperactivity disorder – diagnosis or normality?

British journal of psychiatry, 2013-11, Vol.203 (5), p.317-319

2013

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Simultaneous Ribosome Profiling of Human Host Cells Infected with Toxoplasma gondii

mSphere, 2019-06, Vol.4 (3)

2019

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Posttranscriptional regulation of colonic epithelial repair by RNA binding protein IMP1/IGF2BP1

EMBO reports, 2021-08, Vol.22 (8), p.e47074-n/a

2021

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P659: Whole-genome sequencing as a first assay has the potential to shorten diagnosis time for neurodevelopmental disorders

Genetics in Medicine Open, 2023, Vol.1 (1), p.100724, Article 100724

2023

Volltextzugriff (PDF)

P498: Development and validation of a clinical nanopore sequencing assay to confirm microdeletions and microduplications

Genetics in Medicine Open, 2023, Vol.1 (1), p.100545, Article 100545

2023

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Contingency and entrenchment in protein evolution under purifying selection

Rate-Limiting Steps in Yeast Protein Translation

A tRNA modification balances carbon and nitrogen metabolism by regulating phosphate homeostasis

Neurodevelopmental disorders and neurodiversity: definition of terms from Scotland's National Autism Implementation Team

Explaining complex codon usage patterns with selection for translational efficiency, mutation bias, and genetic drift

Non-optimal codon usage is a mechanism to achieve circadian clock conditionality

The landscape of transcriptional and translational changes over 22 years of bacterial adaptation

Intragenomic variation in non-adaptive nucleotide biases causes underestimation of selection on synonymous codon usage

Linking genotypic and phenotypic changes in the E. coli long-term evolution experiment using metabolomics

The medical model is dead – long live the medical model

The hypoxia response pathway promotes PEP carboxykinase and gluconeogenesis in C. elegans

riboviz: analysis and visualization of ribosome profiling datasets

XACT-Seq Comprehensively Defines the Promoter-Position and Promoter-Sequence Determinants for Initial-Transcription Pausing

EVIDENCE FOR REPEATED LOSS OF SELECTIVE CONSTRAINT IN RHODOPSIN OF AMBLYOPSID CAVEFISHES (TELEOSTEI: AMBLYOPSIDAE)

Effect of correlated tRNA abundances on translation errors and evolution of codon usage bias

Reply to: Potential contribution of PEP carboxykinase-dependent malate dismutation to the hypoxia response in C. elegans

Celf4 controls mRNA translation underlying synaptic development in the prenatal mammalian neocortex

Implementation of Nanopore sequencing as a pragmatic workflow for copy number variant confirmation in the clinic

NADcapPro and circNC: methods for accurate profiling of NAD and non-canonical RNA caps in eukaryotes

P646: Development of an affordable rapid human genome sequencing assay using long read PromethiON 2

Adults with attention-deficit hyperactivity disorder – diagnosis or normality?

Simultaneous Ribosome Profiling of Human Host Cells Infected with Toxoplasma gondii

Posttranscriptional regulation of colonic epithelial repair by RNA binding protein IMP1/IGF2BP1

P659: Whole-genome sequencing as a first assay has the potential to shorten diagnosis time for neurodevelopmental disorders

P498: Development and validation of a clinical nanopore sequencing assay to confirm microdeletions and microduplications

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