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On the origin of the maternal age effect in trisomy 21 Down syndrome: the Oocyte Mosaicism Selection model

Reproduction (Cambridge, England), 2010-01, Vol.139 (1), p.1-9

2010

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On the origin of crossover interference: A chromosome oscillatory movement (COM) model

Molecular cytogenetics, 2011-04, Vol.4 (1), p.10-10

Hulten, MA

2011

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On the origin of trisomy 21 Down syndrome

Molecular cytogenetics, 2008-09, Vol.1 (1), p.21-21

2008

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Maternal Germinal Trisomy 21 in Down Syndrome

Journal of clinical medicine, 2014-01, Vol.3 (1), p.167-175

2014

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Candidate epigenetic biomarkers for non-invasive prenatal diagnosis of Down syndrome

Reproductive biomedicine online, 2007, Vol.15 (2), p.227-235

2007

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Patterns of Meiotic Recombination in Human Fetal Oocytes

American journal of human genetics, 2002-06, Vol.70 (6), p.1469-1479

2002

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On the paternal origin of trisomy 21 Down syndrome

Molecular cytogenetics, 2010-02, Vol.3 (1), p.4-4

2010

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Mammalian meiotic telomeres: protein composition and redistribution in relation to nuclear pores

Molecular biology of the cell, 2000-12, Vol.11 (12), p.4189-4203

2000

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Cohesin component dynamics during meiotic prophase I in mammalian oocytes

Chromosome research, 2004-01, Vol.12 (3), p.197-213

2004

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Differential DNA Methylation as a Tool for Noninvasive Prenatal Diagnosis (NIPD) of X Chromosome Aneuploidies

The Journal of molecular diagnostics : JMD, 2010-11, Vol.12 (6), p.797-807

2010

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Germinal and Somatic Trisomy 21 Mosaicism: How Common is it, What are the Implications for Individual Carriers and How Does it Come About?

Current genomics, 2010-09, Vol.11 (6), p.409-419

2010

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Women's Experiences and Preferences for Service Delivery of Non-Invasive Prenatal Testing for Aneuploidy in a Public Health Setting: A Mixed Methods Study

PloS one, 2016-04, Vol.11 (4), p.e0153147-e0153147

2016

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Radiation-Induced Chromosomal Breaks may be DNA Repair Fragile Sites with Larger-scale Correlations to Eight Double-Strand-Break Related Data Sets over the Human Genome

Radiation research, 2019-11, Vol.192 (5), p.562

2019

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Workshop report on the extraction of foetal DNA from maternal plasma

Prenatal diagnosis, 2007-09, Vol.27 (9), p.824-829

2007

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Disomy 21 in spermatozoa and the paternal origin of trisomy 21 Down syndrome

Molecular cytogenetics, 2015-08, Vol.8 (1), p.67-67, Article 67

2015

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Distribution of the Rad51 recombinase in human and mouse spermatocytes

The EMBO journal, 1997-09, Vol.16 (17), p.5207-5215

1997

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Ricardo Benavente and Jean-Nicolas Volff: Meiosis: Karger, 2009, HB, 159 pages, 191.50€, ISBN 978-3-8055-8967-3

Human genetics, 2009-09, Vol.126 (3), p.479-479

Hultén, Maj

2009

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Ricardo Benavente and Jean-Nicolas Volff: Meiosis

Human genetics, 2009-09, Vol.126 (3), p.479

Hultén, Maj

2009

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Quantification of cell-free DNA in normal and complicated pregnancies: overcoming biological and technical issues

PloS one, 2014-07, Vol.9 (7), p.e101500-e101500

2014

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An Optimized Method for Accurate Fetal Sex Prediction and Sex Chromosome Aneuploidy Detection in Non-Invasive Prenatal Testing

PloS one, 2016-07, Vol.11 (7), p.e0159648-e0159648

2016

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Pregnancy Outcome following Prenatal Diagnosis of Chromosomal Anomaly: A Record Linkage Study of 26,261 Pregnancies

PloS one, 2016-12, Vol.11 (12), p.e0166909-e0166909

2016

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An Advanced Model to Precisely Estimate the Cell-Free Fetal DNA Concentration in Maternal Plasma

PloS one, 2016-09, Vol.11 (9), p.e0161928-e0161928

2016

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High Levels of Sample-to-Sample Variation Confound Data Analysis for Non-Invasive Prenatal Screening of Fetal Microdeletions

PloS one, 2016-06, Vol.11 (6), p.e0153182-e0153182

2016

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Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase gene

Nature (London), 1999-11, Vol.402 (6758), p.187-191

1999

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Nuclear Weapons Tests and Human Germline Mutation Rate

Science (American Association for the Advancement of Science), 2002-02, Vol.295 (5557), p.1037-1037

2002

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On the origin of the maternal age effect in trisomy 21 Down syndrome: the Oocyte Mosaicism Selection model

On the origin of crossover interference: A chromosome oscillatory movement (COM) model

On the origin of trisomy 21 Down syndrome

Maternal Germinal Trisomy 21 in Down Syndrome

Candidate epigenetic biomarkers for non-invasive prenatal diagnosis of Down syndrome

Patterns of Meiotic Recombination in Human Fetal Oocytes

On the paternal origin of trisomy 21 Down syndrome

Mammalian meiotic telomeres: protein composition and redistribution in relation to nuclear pores

Cohesin component dynamics during meiotic prophase I in mammalian oocytes

Differential DNA Methylation as a Tool for Noninvasive Prenatal Diagnosis (NIPD) of X Chromosome Aneuploidies

Germinal and Somatic Trisomy 21 Mosaicism: How Common is it, What are the Implications for Individual Carriers and How Does it Come About?

Women's Experiences and Preferences for Service Delivery of Non-Invasive Prenatal Testing for Aneuploidy in a Public Health Setting: A Mixed Methods Study

Radiation-Induced Chromosomal Breaks may be DNA Repair Fragile Sites with Larger-scale Correlations to Eight Double-Strand-Break Related Data Sets over the Human Genome

Workshop report on the extraction of foetal DNA from maternal plasma

Disomy 21 in spermatozoa and the paternal origin of trisomy 21 Down syndrome

Distribution of the Rad51 recombinase in human and mouse spermatocytes

Ricardo Benavente and Jean-Nicolas Volff: Meiosis: Karger, 2009, HB, 159 pages, 191.50€, ISBN 978-3-8055-8967-3

Ricardo Benavente and Jean-Nicolas Volff: Meiosis

Quantification of cell-free DNA in normal and complicated pregnancies: overcoming biological and technical issues

An Optimized Method for Accurate Fetal Sex Prediction and Sex Chromosome Aneuploidy Detection in Non-Invasive Prenatal Testing

Pregnancy Outcome following Prenatal Diagnosis of Chromosomal Anomaly: A Record Linkage Study of 26,261 Pregnancies

An Advanced Model to Precisely Estimate the Cell-Free Fetal DNA Concentration in Maternal Plasma

High Levels of Sample-to-Sample Variation Confound Data Analysis for Non-Invasive Prenatal Screening of Fetal Microdeletions

Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase gene

Nuclear Weapons Tests and Human Germline Mutation Rate

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