List of works - Thierry Voet

A Single-Cell Transcriptome Atlas of the Aging Drosophila Brain

article by Kristofer Davie et al published 9 August 2018 in Cell

A protective mutation

journal article; published in Nature on 2012-08-01

Accurate and comprehensive analysis of single nucleotide variants and large deletions of the human mitochondrial genome in DNA and single cells.

scientific article

Analysis of the genetic phylogeny of multifocal prostate cancer identifies multiple independent clonal expansions in neoplastic and morphologically normal prostate tissue

scientific article

Aneuploidy and copy number variation in early human development

scientific article published on 21 June 2012

Breakage-fusion-bridge cycles leading to inv dup del occur in human cleavage stage embryos

scientific article published in July 2011

Chromosome Instability Is Common in Human Cleavage-Stage Embryos

Chromosome instability is common in human cleavage-stage embryos

scientific article published on 26 April 2009

Combined Single-Cell Functional and Gene Expression Analysis Resolves Heterogeneity within Stem Cell Populations

scientific article

Concurrent whole-genome haplotyping and copy-number profiling of single cells

scientific article published on 14 May 2015

Defining the Design Principles of Skin Epidermis Postnatal Growth

scientific article published on 05 April 2020

Early lineage segregation of multipotent embryonic mammary gland progenitors

scientific article published on 21 May 2018

Erratum: Corrigendum: Analysis of the genetic phylogeny of multifocal prostate cancer identifies multiple independent clonal expansions in neoplastic and morphologically normal prostate tissue

scholarly article by Colin S Cooper et al published June 2015 in Nature Genetics

Erratum: Pluripotent state transitions coordinate morphogenesis in mouse and human embryos

scientific article published in Nature

G&T-seq: parallel sequencing of single-cell genomes and transcriptomes

scientific article

Genome-wide copy number profiling of single cells in S-phase reveals DNA-replication domains

scientific article published on 7 January 2013

Genome-wide in vivo screen identifies novel host regulators of metastatic colonization

scientific article published on 4 January 2017

Genomic rearrangements of the GREM1-FMN1 locus cause oligosyndactyly, radio-ulnar synostosis, hearing loss, renal defects syndrome and Cenani--Lenz-like non-syndromic oligosyndactyly

scientific article published on 7 July 2010

Heterogeneity in Oct4 and Sox2 Targets Biases Cell Fate in 4-Cell Mouse Embryos.

scientific article

Heterotypic cell-cell communication regulates glandular stem cell multipotency

scientific article published on 26 August 2020

Homozygous missense mutation in STYXL1 associated with moderate intellectual disability, epilepsy and behavioural complexities

scientific article published on 24 February 2015

Identification of region-specific astrocyte subtypes at single cell resolution

scientific article published on 05 March 2020

Identification of the tumour transition states occurring during EMT.

scientific article published on 18 April 2018

In vitro fertilization does not increase the incidence of de novo copy number alterations in fetal and placental lineages

scientific article published on 04 November 2019

Interstitial Cell Remodeling Promotes Aberrant Adipogenesis in Dystrophic Muscles

scientific article published on 01 May 2020

LifeTime and improving European healthcare through cell-based interceptive medicine

scientific article published on 07 September 2020

Meander: visually exploring the structural variome using space-filling curves

scientific article

Mechanisms of stretch-mediated skin expansion at single-cell resolution

scientific article published on 29 July 2020

Meiotic errors followed by two parallel postzygotic trisomy rescue events are a frequent cause of constitutional segmental mosaicism

scientific article

Microarray analysis of copy number variation in single cells.

scientific article published on 19 January 2012

Mosaic copy number variation in human neurons

scientific article

Mouse model of chromosome mosaicism reveals lineage-specific depletion of aneuploid cells and normal developmental potential

scientific article

Multi-centre evaluation of a comprehensive preimplantation genetic test through haplotyping-by-sequencing

scientific article published on 01 August 2019

Mutational Processes Shaping the Genome in Early Human Embryos.

scientific article

New array approaches to explore single cells genomes

scientific article published on 27 March 2012

Next-generation sequencing of disseminated tumor cells

scientific article published on 31 December 2013

Nonallelic homologous recombination between retrotransposable elements is a driver of de novo unbalanced translocations.

scientific article

Noninvasive prenatal diagnosis by genome-wide haplotyping of cell-free plasma DNA

scientific article published on 06 February 2020

On the identification of low allele frequency mosaic mutations in the brains of Alzheimer's disease patients

scientific article

PGD for a complex chromosomal rearrangement by array comparative genomic hybridization ⬇️

scientific article published on February 2, 2011

PREIMPLANTATION GENETIC TESTING: Single-cell technologies at the forefront of PGT and embryo research

scientific article published on 01 November 2020

Parallel single-cell sequencing links transcriptional and epigenetic heterogeneity

scientific article published on 11 January 2016

Pluripotent state transitions coordinate morphogenesis in mouse and human embryos

scientific article published on 29 November 2017

Preimplantation genetic diagnosis guided by single-cell genomics

scientific article published on 19 August 2013

Principles guiding embryo selection following genome-wide haplotyping of preimplantation embryos

scientific article published on 2 February 2017

Pseudoautosomal region 1 length polymorphism in the human population

scientific article

Publisher Correction: Early lineage segregation of multipotent embryonic mammary gland progenitors

scientific article published on 01 September 2018

Publisher Correction: LifeTime and improving European healthcare through cell-based interceptive medicine

scientific article published on 17 March 2021

Publisher Correction: Self-assembly of embryonic and two extra-embryonic stem cell types into gastrulating embryo-like structures

scientific article published on 01 October 2018

SNES makes sense? Single-cell exome sequencing evolves

scientific article published on 29 April 2015

Self-assembly of embryonic and two extra-embryonic stem cell types into gastrulating embryo-like structures

scientific article published on 23 July 2018

Separation and parallel sequencing of the genomes and transcriptomes of single cells using G&T-seq

scientific article

Single cell analysis of cancer genomes

scientific article published on 26 February 2014

Single cell genomics: advances and future perspectives

scientific article

Single cell segmental aneuploidy detection is compromised by S phase

scientific article

Single-Cell (Multi)omics Technologies

scientific article published on 04 May 2018

Single-Cell Landscape of Transcriptional Heterogeneity and Cell Fate Decisions during Mouse Early Gastrulation

scientific article published on August 2017

Single-Cell Multiomics: Multiple Measurements from Single Cells

scientific article published on 12 January 2017

Single-Cell RNA-Sequencing Reveals a Continuous Spectrum of Differentiation in Hematopoietic Cells

scientific article

Single-cell copy number variation detection.

scientific article published on 29 August 2011

Single-cell paired-end genome sequencing reveals structural variation per cell cycle

scientific article

Small chromosomal regions position themselves autonomously according to their chromatin class.

scientific article published on 24 March 2017

Somatic genomic variations in early human prenatal development

scientific article

Spatial and temporal diversity in genomic instability processes defines lung cancer evolution

scientific article

Telomere length homeostasis and telomere position effect on a linear human artificial chromosome are dictated by the genetic background ⬇️

scientific article published on October 11, 2012

The Human Cleavage Stage Embryo Is a Cradle of Chromosomal Rearrangements ⬇️

scientific article published on 09 February 2011

Toward Minimal Residual Disease-Directed Therapy in Melanoma

scientific article published on 12 July 2018

Tracing the origin of disseminated tumor cells in breast cancer using single-cell sequencing

scientific article

What next for preimplantation genetic screening? High mitotic chromosome instability rate provides the biological basis for the low success rate

scientific article published on 24 July 2009

Zebrafish MITF-Low Melanoma Subtype Models Reveal Transcriptional Subclusters and MITF-Independent Residual Disease

scientific article published on 03 October 2019

Zygotes segregate entire parental genomes in distinct blastomere lineages causing cleavage-stage chimerism and mixoploidy

scientific article published on 12 April 2016

List of works by Thierry Voet

A Single-Cell Transcriptome Atlas of the Aging Drosophila Brain

A protective mutation

Accurate and comprehensive analysis of single nucleotide variants and large deletions of the human mitochondrial genome in DNA and single cells.

Analysis of the genetic phylogeny of multifocal prostate cancer identifies multiple independent clonal expansions in neoplastic and morphologically normal prostate tissue

Aneuploidy and copy number variation in early human development

Breakage-fusion-bridge cycles leading to inv dup del occur in human cleavage stage embryos

Chromosome Instability Is Common in Human Cleavage-Stage Embryos

Chromosome instability is common in human cleavage-stage embryos

Combined Single-Cell Functional and Gene Expression Analysis Resolves Heterogeneity within Stem Cell Populations

Concurrent whole-genome haplotyping and copy-number profiling of single cells

Defining the Design Principles of Skin Epidermis Postnatal Growth

Early lineage segregation of multipotent embryonic mammary gland progenitors

Erratum: Corrigendum: Analysis of the genetic phylogeny of multifocal prostate cancer identifies multiple independent clonal expansions in neoplastic and morphologically normal prostate tissue

Erratum: Pluripotent state transitions coordinate morphogenesis in mouse and human embryos

G&T-seq: parallel sequencing of single-cell genomes and transcriptomes

Genome-wide copy number profiling of single cells in S-phase reveals DNA-replication domains

Genome-wide in vivo screen identifies novel host regulators of metastatic colonization

Genomic rearrangements of the GREM1-FMN1 locus cause oligosyndactyly, radio-ulnar synostosis, hearing loss, renal defects syndrome and Cenani--Lenz-like non-syndromic oligosyndactyly

Heterogeneity in Oct4 and Sox2 Targets Biases Cell Fate in 4-Cell Mouse Embryos.

Heterotypic cell-cell communication regulates glandular stem cell multipotency

Homozygous missense mutation in STYXL1 associated with moderate intellectual disability, epilepsy and behavioural complexities

Identification of region-specific astrocyte subtypes at single cell resolution

Identification of the tumour transition states occurring during EMT.

In vitro fertilization does not increase the incidence of de novo copy number alterations in fetal and placental lineages

Interstitial Cell Remodeling Promotes Aberrant Adipogenesis in Dystrophic Muscles

LifeTime and improving European healthcare through cell-based interceptive medicine

Meander: visually exploring the structural variome using space-filling curves

Mechanisms of stretch-mediated skin expansion at single-cell resolution

Meiotic errors followed by two parallel postzygotic trisomy rescue events are a frequent cause of constitutional segmental mosaicism

Microarray analysis of copy number variation in single cells.

Mosaic copy number variation in human neurons

Mouse model of chromosome mosaicism reveals lineage-specific depletion of aneuploid cells and normal developmental potential

Multi-centre evaluation of a comprehensive preimplantation genetic test through haplotyping-by-sequencing

Mutational Processes Shaping the Genome in Early Human Embryos.

New array approaches to explore single cells genomes

Next-generation sequencing of disseminated tumor cells

Nonallelic homologous recombination between retrotransposable elements is a driver of de novo unbalanced translocations.

Noninvasive prenatal diagnosis by genome-wide haplotyping of cell-free plasma DNA

On the identification of low allele frequency mosaic mutations in the brains of Alzheimer's disease patients

PGD for a complex chromosomal rearrangement by array comparative genomic hybridization ⬇️

PREIMPLANTATION GENETIC TESTING: Single-cell technologies at the forefront of PGT and embryo research

Parallel single-cell sequencing links transcriptional and epigenetic heterogeneity

Pluripotent state transitions coordinate morphogenesis in mouse and human embryos

Preimplantation genetic diagnosis guided by single-cell genomics

Principles guiding embryo selection following genome-wide haplotyping of preimplantation embryos

Pseudoautosomal region 1 length polymorphism in the human population

Publisher Correction: Early lineage segregation of multipotent embryonic mammary gland progenitors

Publisher Correction: LifeTime and improving European healthcare through cell-based interceptive medicine

Publisher Correction: Self-assembly of embryonic and two extra-embryonic stem cell types into gastrulating embryo-like structures

SNES makes sense? Single-cell exome sequencing evolves

Self-assembly of embryonic and two extra-embryonic stem cell types into gastrulating embryo-like structures

Separation and parallel sequencing of the genomes and transcriptomes of single cells using G&T-seq

Single cell analysis of cancer genomes

Single cell genomics: advances and future perspectives

Single cell segmental aneuploidy detection is compromised by S phase

Single-Cell (Multi)omics Technologies

Single-Cell Landscape of Transcriptional Heterogeneity and Cell Fate Decisions during Mouse Early Gastrulation

Single-Cell Multiomics: Multiple Measurements from Single Cells

Single-Cell RNA-Sequencing Reveals a Continuous Spectrum of Differentiation in Hematopoietic Cells

Single-cell copy number variation detection.

Single-cell paired-end genome sequencing reveals structural variation per cell cycle

Small chromosomal regions position themselves autonomously according to their chromatin class.

Somatic genomic variations in early human prenatal development

Spatial and temporal diversity in genomic instability processes defines lung cancer evolution

Telomere length homeostasis and telomere position effect on a linear human artificial chromosome are dictated by the genetic background ⬇️

The Human Cleavage Stage Embryo Is a Cradle of Chromosomal Rearrangements ⬇️

Toward Minimal Residual Disease-Directed Therapy in Melanoma

Tracing the origin of disseminated tumor cells in breast cancer using single-cell sequencing

What next for preimplantation genetic screening? High mitotic chromosome instability rate provides the biological basis for the low success rate

Zebrafish MITF-Low Melanoma Subtype Models Reveal Transcriptional Subclusters and MITF-Independent Residual Disease

Zygotes segregate entire parental genomes in distinct blastomere lineages causing cleavage-stage chimerism and mixoploidy