J. Dreesen

发表

Präimplantationsdiagnostik in den Niederlanden

A. Paulussen, J. Geraedts, Edith Coonen, 2016, medizinische genetik.

Validation of preimplantation genetic diagnosis by PCR analysis: genotype comparison of the blastomere and corresponding embryo, implications for clinical practice.

J. Dreesen, C. D. de Die-Smulders, M. Drüsedau, 2008, Molecular human reproduction.

Hereditary breast and ovarian cancer and reproduction: an observational study on the suitability of preimplantation genetic diagnosis for both asymptomatic carriers and breast cancer survivors

A. Paulussen, H. Tournaye, J. Dreesen, 2014, Breast Cancer Research and Treatment.

Preimplantation Genetic Testing for Monogenic Kidney Disease.

A. Paulussen, N. Knoers, J. Dreesen, 2020, Clinical journal of the American Society of Nephrology : CJASN.

Preimplantation genetic diagnosis in mitochondrial DNA disorders: challenge and success

I. D. de Coo, H. Smeets, J. Dreesen, 2013, Journal of Medical Genetics.

Mutation-specific effects in germline transmission of pathogenic mtDNA variants

H. Smeets, M. Herbert, A. Paulussen, 2018, Human reproduction.

PGD for the m.14487 T>C mitochondrial DNA mutation resulted in the birth of a healthy boy

H. Smeets, M. Zeviani, A. Paulussen, 2017, Human reproduction.

Molecular cloning and restriction endonuclease mapping of the rat cytomegalovirus genome.

C. V. van Boven, J. Dreesen, H. Meijer, 1986, The Journal of general virology.

Mutations in the vasopressin type 2 receptor gene (AVPR2) associated with nephrogenic diabetes insipidus

M. Rocchi, A. Ouweland, N. Knoers, 1992, Nature Genetics.

Nephrogenic diabetes insipidus: identification of the genetic defect

A. Ouweland, N. Knoers, J. Dreesen, 1993, Pediatric Nephrology.

Allelic dropout caused by allele-specific amplification failure in single-cell PCR of the cystic fibrosis ΔF508 deletion

J. Dreesen, E. Coonen, J. Dumoulin, 1996, Journal of Assisted Reproduction and Genetics.

Perinatal follow-up of children born after preimplantation genetic diagnosis between 1995 and 2014

A. Paulussen, N. Muntjewerff, F. Broekmans, 2018, Journal of assisted reproduction and genetics.

Evaluation of PCR-based preimplantation genetic diagnosis applied to monogenic diseases: a collaborative ESHRE PGD consortium study

S. Dhanjal, C. Moutou, J. Dreesen, 2013, European Journal of Human Genetics.

Preimplantation genetic diagnosis for mitochondrial DNA mutations: analysis of one blastomere suffices

H. Smeets, A. Paulussen, J. Dreesen, 2017, Journal of Medical Genetics.

First trimester prenatal diagnosis of haemophilia A: Two years' experience

P. Pearson, J. Dreesen, H. Kanhai, 1988, Prenatal diagnosis.

SNP array-based copy number and genotype analyses for preimplantation genetic diagnosis of human unbalanced translocations

H. Smeets, J. Dreesen, M. Drüsedau, 2012, European Journal of Human Genetics.

ESHRE PGT Consortium good practice recommendations for the detection of monogenic disorders

C. Moutou, V. Goossens, J. Dreesen, 2020, Human reproduction open.

Preventing the transmission of mitochondrial DNA disorders using prenatal or preimplantation genetic diagnosis

H. Smeets, J. Dreesen, S. Sallevelt, 2015, Annals of the New York Academy of Sciences.

Selecting the Right Embryo in Mitochondrial Disorders

H. Smeets, J. Dreesen, S. Sallevelt, 2015 .

Genome-wide karyomapping accurately identifies the inheritance of single-gene defects in human preimplantation embryos in vitro

Alex J. Bladon, A. Paulussen, J. Dreesen, 2014, Genetics in Medicine.

[Results from 10 years of preimplantation-genetic diagnostics in The Netherlands].

J. Dreesen, C. D. de Die-Smulders, E. Coonen, 2004, Nederlands tijdschrift voor geneeskunde.

Multipoint linkage analysis of DXS369 and DXS304 in fragile X families.

B. V. van Oost, A. Smits, D. Smeets, 1991, American journal of medical genetics.

PGD for hereditary breast and ovarian cancer: the route to universal tests for BRCA1 and BRCA2 mutation carriers

H. Smeets, A. Paulussen, M. Blok, 2013, European Journal of Human Genetics.

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

Joris Robert Vermeesch, Joke Allemeersch, Heleen Masset, 2019, Human reproduction.

Somatic origin of inherited haemophilia A

P. Reitsma, P. Pearson, J. Dreesen, 1990, Human Genetics.

Genotype Assignment of Haemophilia A by Use of Intragenic and Extragenic Restriction Fragment Length Polymorphisms

P. Pearson, J. Dreesen, R. Quadt, 1987, Thrombosis and Haemostasis.

[Genetic diagnosis of IVF embryos: preliminary results from 'preimplantation genetic diagnoses' in the Netherlands].

J. Dreesen, C. D. de Die-Smulders, E. Coonen, 1998, Nederlandsch tijdschrift voor geneeskunde.

RS46(DXS548) genotyping of reproductive cells: approaching preimplantation testing of the fragile-X syndrome

J. Dreesen, J. Dumoulin, J. Geraedts, 1995, Human Genetics.

Recombination of DXS548 (RS46) with the FRAXA locus.

B. V. van Oost, A. Smits, J. Dreesen, 1994, American journal of medical genetics.

Validation of linkage-based DNA-diagnosis of fragile X gene carriers with the CGG repeat probe.

B. V. van Oost, A. V. D. van den Ouweland, A. Smits, 1992, American journal of medical genetics.

High prevalence of the fra(X) syndrome cannot be explained by a high mutation rate.

B. V. van Oost, A. Smits, D. Smeets, 1992, American journal of medical genetics.

Clinical application of FISH for sex determination of embryos in preimplantation diagnosis of X-linked diseases

J. Dreesen, E. Coonen, J. Dumoulin, 1996, Journal of Assisted Reproduction and Genetics.

Session 42: Preimplantation Genetic Diagnosis

H. Smeets, A. Mercader, C. Rubio, 2010 .

Parental origin of the fra(X) gene is a major determinant of the cytogenetic expression and the CGG repeat length in female carriers.

B. V. van Oost, A. Smits, D. Smeets, 1992, American journal of medical genetics.

Preimplantation genetic diagnosis of spinocerebellar ataxia 3 by (CAG)(n) repeat detection.

J. Dreesen, C. D. de Die-Smulders, M. Drüsedau, 2004, Molecular human reproduction.

Preimplantation genetic testing for more than one genetic condition: clinical and ethical considerations and dilemmas.

A. Paulussen, J. Dreesen, E. Coonen, 2019, Human reproduction.

Prediction of mental status in carriers of the fragile X mutation using CGG repeat length.

B. V. van Oost, A. Smits, D. Smeets, 1994, American journal of medical genetics.

The fragile X syndrome: no evidence for any recent mutations.

S. Warren, B. V. van Oost, A. Smits, 1993, Journal of medical genetics.

Diagnosing and preventing inherited disease: Multiplex polymerase chain reaction for sex determination of single mouse blastomeres

J. Dreesen, J. Dumoulin, J. Geraedts, 1995 .

Preimplantation genetic testing for Neurofibromatosis type 1: more than 20 years of clinical experience

A. Paulussen, C. Stumpel, J. Dreesen, 2023, European Journal of Human Genetics.

Effect of Ca2+/Mg2+-free medium on the biopsy procedure for preimplantation genetic diagnosis and further development of human embryos.

J. Dreesen, E. Coonen, J. Dumoulin, 1998, Human reproduction.

Preimplantation genetic diagnosis (PGD) for Huntington's disease: the experience of three European centres

C. Moutou, S. Viville, I. Liebaers, 2011, European Journal of Human Genetics.

Multiplex PCR of polymorphic markers flanking the CFTR gene; a general approach for preimplantation genetic diagnosis of cystic fibrosis.

J. Dreesen, H. Smeets, J. Dumoulin, 2000, Molecular human reproduction.

DXS539, a polymorphic DNA marker proximal of the fragile-X gene

A. Smits, J. Dreesen, B. Oost, 1993, Human Genetics.

O-075. Multiplex PCR of polymorphic markers flanking the CFTR gene: a general approach for pre-implantation genetic diagnosis of cystic fibrosis

J. Dreesen, H. Smeets, J. Dumoulin, 1999 .