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LINE-1 activation after fertilization regulates global chromatin accessibility in the early mouse embryo

Nature genetics, 2017-10, Vol.49 (10), p.1502-1510

2017

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Differences between germline genomes of monozygotic twins

Nature genetics, 2021-01, Vol.53 (1), p.27-34

2021

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Dynamics of DNA hydroxymethylation and methylation during mouse embryonic and germline development

Nature genetics, 2023-01, Vol.55 (1), p.130-143

2023

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A single-cell transcriptome atlas of human euploid and aneuploid blastocysts

Nature genetics, 2024-07, Vol.56 (7), p.1468-1481

2024

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Dosage compensation of the active X chromosome in mammals

Nature genetics, 2006-01, Vol.38 (1), p.47-53

2006

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Ras-MAPK signaling promotes trophectoderm formation from embryonic stem cells and mouse embryos

Nature genetics, 2008-07, Vol.40 (7), p.921-926

2008

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The pre-implantation ontogeny of the H19 methylation imprint

Nature genetics, 1997-11, Vol.17 (3), p.275-276

1997

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Mater , a maternal effect gene required for early embryonic development in mice

Nature genetics, 2000-11, Vol.26 (3), p.267-268

2000

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Pten is essential for embryonic development and tumour suppression

Nature genetics, 1998-08, Vol.19 (4), p.348-355

1998

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Gata3 loss leads to embryonic lethality due to noradrenaline deficiency of the sympathetic nervous system

Nature genetics, 2000-06, Vol.25 (2), p.209-212

2000

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Efficient generation and mapping of recessive developmental mutations using ENU mutagenesis

Nature genetics, 2002-02, Vol.30 (2), p.185-189

2002

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Tumorigenesis and a DNA repair defect in mice with a truncating Brca2 mutation

Nature genetics, 1997-12, Vol.17 (4), p.423-430

1997

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Mutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouse

Nature genetics, 1998-06, Vol.19 (2), p.125-133

1998

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Mice lacking the folic acid-binding protein Folbp1 are defective in early embryonic development

Nature genetics, 1999-10, Vol.23 (2), p.228-232

1999

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Esx1 is an X-chromosome-imprinted regulator of placental development and fetal growth

Nature genetics, 1998-11, Vol.20 (3), p.309-311

1998

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Heterozygosity with respect to Zfp148 causes complete loss of fetal germ cells during mouse embryogenesis

Nature genetics, 2003-02, Vol.33 (2), p.172-176

2003

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Genetic and epigenetic incompatibilities underlie hybrid dysgenesis in Peromyscus

Nature genetics, 2000-05, Vol.25 (1), p.120-124

2000

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The Sry -related gene Sox9 is expressed during chondrogenesis in mouse embryos

Nature genetics, 1995-01, Vol.9 (1), p.15-20

1995

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Delayed early embryonic lethality following disruption of the murine cyclin A2 gene

Nature genetics, 1997-01, Vol.15 (1), p.83-86

1997

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Loss of imprinting of IGF2 is linked to reduced expression and abnormal methylation of H19 in Wilms' tumour

Nature genetics, 1994-07, Vol.7 (3), p.433-439

1994

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Ryk-deficient mice exhibit craniofacial defects associated with perturbed Eph receptor crosstalk

Nature genetics, 2000-08, Vol.25 (4), p.414-418

2000

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A paternal-specific methylation imprint marks the alleles of the mouse H19 gene

Nature genetics, 1995-04, Vol.9 (4), p.407-413

1995

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Peg1/Mest imprinted gene on chromosome 6 identified by cDNA subtraction hybridization

Nature genetics, 1995-09, Vol.11 (1), p.52-59

1995

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Control of neurulation by the nucleosome assembly protein-1-like 2

Nature genetics, 2000-08, Vol.25 (4), p.431-435

2000

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Placental alpha(2)-adrenoceptors control vascular development at the interface between mother and embryo

Nature genetics, 2002-07, Vol.31 (3), p.311-315

2002

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LINE-1 activation after fertilization regulates global chromatin accessibility in the early mouse embryo

Differences between germline genomes of monozygotic twins

Dynamics of DNA hydroxymethylation and methylation during mouse embryonic and germline development

A single-cell transcriptome atlas of human euploid and aneuploid blastocysts

Dosage compensation of the active X chromosome in mammals

Ras-MAPK signaling promotes trophectoderm formation from embryonic stem cells and mouse embryos

The pre-implantation ontogeny of the H19 methylation imprint

Mater , a maternal effect gene required for early embryonic development in mice

Pten is essential for embryonic development and tumour suppression

Gata3 loss leads to embryonic lethality due to noradrenaline deficiency of the sympathetic nervous system

Efficient generation and mapping of recessive developmental mutations using ENU mutagenesis

Tumorigenesis and a DNA repair defect in mice with a truncating Brca2 mutation

Mutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouse

Mice lacking the folic acid-binding protein Folbp1 are defective in early embryonic development

Esx1 is an X-chromosome-imprinted regulator of placental development and fetal growth

Heterozygosity with respect to Zfp148 causes complete loss of fetal germ cells during mouse embryogenesis

Genetic and epigenetic incompatibilities underlie hybrid dysgenesis in Peromyscus

The Sry -related gene Sox9 is expressed during chondrogenesis in mouse embryos

Delayed early embryonic lethality following disruption of the murine cyclin A2 gene

Loss of imprinting of IGF2 is linked to reduced expression and abnormal methylation of H19 in Wilms' tumour

Ryk-deficient mice exhibit craniofacial defects associated with perturbed Eph receptor crosstalk

A paternal-specific methylation imprint marks the alleles of the mouse H19 gene

Peg1/Mest imprinted gene on chromosome 6 identified by cDNA subtraction hybridization

Control of neurulation by the nucleosome assembly protein-1-like 2

Placental alpha(2)-adrenoceptors control vascular development at the interface between mother and embryo

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