Lista de obras -

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.

artículo científico publicado en 2017

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

artículo científico publicado en 2015

Aneuploidy and copy number variation in early human development

artículo científico

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

artículo científico publicado en 2011

Chromosome Instability Is Common in Human Cleavage-Stage Embryos

Chromosome instability is common in human cleavage-stage embryos

artículo científico publicado en 2009

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

artículo científico publicado en 2015

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

artículo científico publicado en 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

artículo científico publicado en 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

artículo científico publicado en 2018

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

artículo científico publicado en 2015

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

artículo científico publicado en 2013

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

artículo científico publicado en 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

artículo científico publicado en 2010

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

artículo científico publicado en 2016

Heterotypic cell-cell communication regulates glandular stem cell multipotency

artículo científico publicado en 2020

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

artículo científico publicado en 2015

Identification of region-specific astrocyte subtypes at single cell resolution

artículo científico publicado en 2020

Identification of the tumour transition states occurring during EMT.

artículo científico publicado en 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

artículo científico publicado en 2020

LifeTime and improving European healthcare through cell-based interceptive medicine

artículo científico publicado en 2020

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

artículo científico publicado en 2013

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

artículo científico publicado en 2020

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

artículo científico publicado en 2012

Microarray analysis of copy number variation in single cells.

artículo científico publicado en 2012

Mosaic copy number variation in human neurons

artículo científico publicado en 2013

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

artículo científico publicado en 2016

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

artículo científico publicado en 2019

Mutational Processes Shaping the Genome in Early Human Embryos

artículo científico publicado en 2017

New array approaches to explore single cells genomes

artículo científico publicado en 2012

Next-generation sequencing of disseminated tumor cells

artículo científico publicado en 2013

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

artículo científico publicado en 2012

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

artículo científico publicado en 2020

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

artículo científico publicado en 2015

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

artículo científico publicado el 2 de febrero de 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

artículo científico

Pluripotent state transitions coordinate morphogenesis in mouse and human embryos

artículo científico publicado en 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

artículo científico publicado en 2017

Pseudoautosomal region 1 length polymorphism in the human population

artículo científico publicado en 2014

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

artículo científico publicado en 2021

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

artículo científico publicado en 2018

SNES makes sense? Single-cell exome sequencing evolves

artículo científico publicado en 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

artículo científico publicado en 2016

Single cell analysis of cancer genomes

artículo científico

Single cell genomics: advances and future perspectives

artículo científico publicado en 2014

Single cell segmental aneuploidy detection is compromised by S phase

artículo científico publicado en 2014

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

artículo científico publicado en 2017

Single-Cell Multiomics: Multiple Measurements from Single Cells

artículo científico publicado en 2017

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

artículo científico publicado en 2016

Single-cell copy number variation detection.

artículo científico publicado en 2011

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

artículo científico publicado en 2013

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

artículo científico publicado en 2017

Somatic genomic variations in early human prenatal development

artículo científico publicado en 2010

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

artículo científico publicado en 2014

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

artículo científico publicado el 11 de octubre de 2012

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

artículo científico publicado el 9 de febrero de 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

artículo científico publicado en 2016

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

artículo científico publicado en 2019

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

artículo científico publicado en 2016

Lista de obras de

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