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Postovulatory aging affects dynamics of mRNA, expression and localization of maternal effect proteins, spindle integrity and pericentromeric proteins in mouse oocytes

Human reproduction (Oxford), 2016-01, Vol.31 (1), p.133-149

2016

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Idiopathic male infertility is strongly associated with aberrant methylation of MEST and IGF2/H19 ICR1

International journal of andrology, 2010-08, Vol.33 (4), p.642-649

2010

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Biallelic loss of function of the promyelocytic leukaemia zinc finger (PLZF) gene causes severe skeletal defects and genital hypoplasia

Journal of medical genetics, 2008-11, Vol.45 (11), p.731-737

2008

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The spectrum of RB1 germ-line mutations in hereditary retinoblastoma

American journal of human genetics, 1996-05, Vol.58 (5), p.940-949

1996

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A 5-kb imprinting center deletion in a family with Angelman syndrome reduces the shortest region of deletion overlap to 880 bp

Human genetics, 1999-12, Vol.105 (6), p.665-666

1999

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Parental-origin-determination fluorescence in situ hybridization distinguishes homologous human chromosomes on a single-cell level

International journal of molecular medicine, 2008-02, Vol.21 (2), p.189-200

2008

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P–529 Whole-genome methylation analysis of testicular germ cells from cryptozoospermic men points to recurrent and functionally relevant DNA methylation changes

Human reproduction (Oxford), 2021-08, Vol.36 (Supplement_1)

2021

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Impact of geometry and viewing angle on classification accuracy of 2D based analysis of dysmorphic faces

European journal of medical genetics, 2008-01, Vol.51 (1), p.44-53

2008

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Incorrect use of the term synteny

Nature genetics, 1999-12, Vol.23 (4), p.387-387

1999

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Uwe Claussen (1945–2008)

Medizinische Genetik, 2008-09, Vol.20 (3), p.332-333

Horsthemke, B.

2008

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Imprinting mutations suggested by abnormal DNA methylation patterns in familial Angelman and Prader-Willi syndromes

American journal of human genetics, 1994-05, Vol.54 (5), p.741-747

1994

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The European Prader-Willi Syndrome Clinical Research Database: an aid in the investigation of a rare genetically determined neurodevelopmental disorder

Journal of intellectual disability research, 2009-06, Vol.53 (6), p.538-547

2009

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Marked differences in unilateral isolated retinoblastomas from young and older children studied by comparative genomic hybridization

Human genetics, 2001-02, Vol.108 (2), p.98-104

2001

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Premature ovarian failure associated with a small terminal Xq deletion: narrowing the POF1 region down to Xq27.2/Xq27.3-qter

Clinical genetics, 2005-05, Vol.67 (5), p.434-437

2005

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Imprinting und assistierte Reproduktion

Gynäkologische Endokrinologie, 2007-02, Vol.5 (1), p.33-38

Horsthemke, B.

2007

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Epimutations in Prader-Willi and Angelman Syndromes: A Molecular Study of 136 Patients with an Imprinting Defect

American journal of human genetics, 2003-03, Vol.72 (3), p.571-577

2003

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Maternal Meiosis I Non-Disjunction of Chromosome 15: Dependence of the Maternal Age Effect on Level of Recombination

Human molecular genetics, 1998-06, Vol.7 (6), p.1011-1019

1998

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Identification of Brain-Specific and Imprinted Small Nucleolar RNA Genes Exhibiting an Unusual Genomic Organization

Proceedings of the National Academy of Sciences - PNAS, 2000-12, Vol.97 (26), p.14311-14316

2000

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The IC-SNURF-SNRPN transcript serves as a host for multiple small nucleolar RNA species and as an antisense RNA for UBE3A

Human molecular genetics, 2001-11, Vol.10 (23), p.2687-2700

2001

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Tumor classification based on gene expression profiling shows that uveal melanomas with and without monosomy 3 represent two distinct entities

Cancer research (Chicago, Ill.), 2003-05, Vol.63 (10), p.2578-2584

2003

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Genomisches Imprinting und Imprintingfehler

Medizinische Genetik, 2010-12, Vol.22 (4), p.385-391

Horsthemke, B.

2010

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A PCR test for the detection of hypermethylated alleles at the retinoblastoma locus

Journal of medical genetics, 1999-10, Vol.36 (10), p.793-794

1999

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CD36 expression and its relationship with obesity in blood cells from people with and without Prader-Willi syndrome

Clinical genetics, 2006-01, Vol.69 (1), p.26-32

2006

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Molecular dissection of a contiguous gene syndrome: localization of the genes involved in the Langer—Giedion syndrome

Human molecular genetics, 1995-01, Vol.4 (1), p.31-36

1995

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Imprinting of RB1 (the new kid on the block)

Briefings in functional genomics, 2010-07, Vol.9 (4), p.347-353

2010

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Postovulatory aging affects dynamics of mRNA, expression and localization of maternal effect proteins, spindle integrity and pericentromeric proteins in mouse oocytes

Idiopathic male infertility is strongly associated with aberrant methylation of MEST and IGF2/H19 ICR1

Biallelic loss of function of the promyelocytic leukaemia zinc finger (PLZF) gene causes severe skeletal defects and genital hypoplasia

The spectrum of RB1 germ-line mutations in hereditary retinoblastoma

A 5-kb imprinting center deletion in a family with Angelman syndrome reduces the shortest region of deletion overlap to 880 bp

Parental-origin-determination fluorescence in situ hybridization distinguishes homologous human chromosomes on a single-cell level

P–529 Whole-genome methylation analysis of testicular germ cells from cryptozoospermic men points to recurrent and functionally relevant DNA methylation changes

Impact of geometry and viewing angle on classification accuracy of 2D based analysis of dysmorphic faces

Incorrect use of the term synteny

Uwe Claussen (1945–2008)

Imprinting mutations suggested by abnormal DNA methylation patterns in familial Angelman and Prader-Willi syndromes

The European Prader-Willi Syndrome Clinical Research Database: an aid in the investigation of a rare genetically determined neurodevelopmental disorder

Marked differences in unilateral isolated retinoblastomas from young and older children studied by comparative genomic hybridization

Premature ovarian failure associated with a small terminal Xq deletion: narrowing the POF1 region down to Xq27.2/Xq27.3-qter

Imprinting und assistierte Reproduktion

Epimutations in Prader-Willi and Angelman Syndromes: A Molecular Study of 136 Patients with an Imprinting Defect

Maternal Meiosis I Non-Disjunction of Chromosome 15: Dependence of the Maternal Age Effect on Level of Recombination

Identification of Brain-Specific and Imprinted Small Nucleolar RNA Genes Exhibiting an Unusual Genomic Organization

The IC-SNURF-SNRPN transcript serves as a host for multiple small nucleolar RNA species and as an antisense RNA for UBE3A

Tumor classification based on gene expression profiling shows that uveal melanomas with and without monosomy 3 represent two distinct entities

Genomisches Imprinting und Imprintingfehler

A PCR test for the detection of hypermethylated alleles at the retinoblastoma locus

CD36 expression and its relationship with obesity in blood cells from people with and without Prader-Willi syndrome

Molecular dissection of a contiguous gene syndrome: localization of the genes involved in the Langer—Giedion syndrome

Imprinting of RB1 (the new kid on the block)

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