Vang Q. Le

Aalborg, Denmark

Last Updated: 09/26/2026

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Found 11 publications

Metabolic signature of COVID-19 progression: potential prognostic markers for severity and outcome.

Metabolic signature of COVID-19 progression: potential prognostic markers for severity and outcome.

Journal: Metabolomics : Official journal of the Metabolomic Society

Published: March 05, 2025

Metabolic fingerprint of progression of chronic hepatitis B: changes in the metabolome and novel diagnostic possibilities.

Metabolic fingerprint of progression of chronic hepatitis B: changes in the metabolome and novel diagnostic possibilities.

Journal: Metabolomics : Official journal of the Metabolomic Society

Published: August 13, 2020

Whole-exome sequencing identifies a GREB1L variant in a three-generation family with Müllerian and renal agenesis: a novel candidate gene in Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome. A case report.

Whole-exome sequencing identifies a GREB1L variant in a three-generation family with Müllerian and renal agenesis: a novel candidate gene in Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome. A case report.

Journal: Human reproduction (Oxford, England)

Published: March 26, 2019

Chromium sequencing: the doors open for genomics of obligate plant pathogens.

Chromium sequencing: the doors open for genomics of obligate plant pathogens.

Journal: BioTechniques

Published: November 06, 2018

De novo KAT6B Mutation Identified with Whole-Exome Sequencing in a Girl with Say-Barber/Biesecker/Young-Simpson Syndrome.

De novo KAT6B Mutation Identified with Whole-Exome Sequencing in a Girl with Say-Barber/Biesecker/Young-Simpson Syndrome.

Journal: Molecular syndromology

Published: September 05, 2016

In vivo gene expression in a Staphylococcus aureus prosthetic joint infection characterized by RNA sequencing and metabolomics: a pilot study.

In vivo gene expression in a Staphylococcus aureus prosthetic joint infection characterized by RNA sequencing and metabolomics: a pilot study.

Journal: BMC microbiology

Published: November 10, 2015

The PHF6 Mutation c.1A>G; pM1V Causes Börjeson-Forsman-Lehmann Syndrome in a Family with Four Affected Young Boys.

The PHF6 Mutation c.1A>G; pM1V Causes Börjeson-Forsman-Lehmann Syndrome in a Family with Four Affected Young Boys.

Journal: Molecular syndromology

Published: September 08, 2015

Nitrosospira lacus sp. nov., a psychrotolerant, ammonia-oxidizing bacterium from sandy lake sediment.

Nitrosospira lacus sp. nov., a psychrotolerant, ammonia-oxidizing bacterium from sandy lake sediment.

Journal: International journal of systematic and evolutionary microbiology

Published: October 23, 2014

ECEL1 mutation causes fetal arthrogryposis multiplex congenita.

ECEL1 mutation causes fetal arthrogryposis multiplex congenita.

Journal: American journal of medical genetics. Part A

Published: May 15, 2014

Draft Genome Sequence of Nitrosospira sp. Strain APG3, a Psychrotolerant Ammonia-Oxidizing Bacterium Isolated from Sandy Lake Sediment.

Draft Genome Sequence of Nitrosospira sp. Strain APG3, a Psychrotolerant Ammonia-Oxidizing Bacterium Isolated from Sandy Lake Sediment.

Journal: Genome announcements

Published: November 09, 2013

A metabolic model for members of the genus Tetrasphaera involved in enhanced biological phosphorus removal.

A metabolic model for members of the genus Tetrasphaera involved in enhanced biological phosphorus removal.

Journal: The ISME journal

Published: November 27, 2012

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Last Updated: 09/26/2026