Current issues in medically assisted reproduction and genetics in Europe: research, clinical practice, ethics, legal issues and policy (Q56973422)

Jorge Sequeiros

12

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Martina C. Cornel

4

Martina C Cornel

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Pascal Borry

3

Pascal Borry

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Heather Skirton

H. Skirton

15

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Guido de Wert

21

Guido de Wert

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Joris R Vermeesch

19

Joris Robert Vermeesch

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Anna Veiga Lluch

18

Anna Veiga

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author name string

Joyce Harper

1

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Joep Geraedts

2

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Wybo J Dondorp

5

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Luca Gianaroli

6

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Gary Harton

7

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Tanya Milachich

8

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Helena Kääriäinen

9

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Inge Liebaers

10

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Michael Morris

11

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Karen Sermon

13

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Françoise Shenfield

14

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Sirpa Soini

16

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Claudia Spits

17

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Stéphane Viville

20

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Milan Macek

22

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J. Harper

1

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J. Geraedts

2

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P. Borry

3

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M. C. Cornel

4

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W. J. Dondorp

5

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L. Gianaroli

6

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G. Harton

7

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T. Milachich

8

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H. Kaariainen

9

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I. Liebaers

10

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M. Morris

11

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J. Sequeiros

12

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K. Sermon

13

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F. Shenfield

14

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S. Soini

16

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C. Spits

17

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A. Veiga

18

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J. R. Vermeesch

19

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S. Viville

20

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G. de Wert

21

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M. Macek

Screening ethnically diverse human embryonic stem cells identifies a chromosome 20 minimal amplicon conferring growth advantage

22

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language of work or name

English

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publication date

August 2014

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8 July 2014

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published in

Human Reproduction

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volume

29

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issue

8

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page(s)

1603-9

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1603-1609

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Direct-to-consumer genome scanning services. Also for children?

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Dealing with uncertainties: ethics of prenatal diagnosis and preimplantation genetic diagnosis to prevent mitochondrial disorders

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The clinical benefit and safety of current and future assisted reproductive technology

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Molecular pathogenesis of Kallmann's syndrome.

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Comparison of concomitant outcome achieved with fresh and cryopreserved donor oocytes vitrified by the Cryotop method

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Genetic screening of sperm and oocyte donors: ethical and policy implications

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Primary ovarian insufficiency

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Preconception care and genetic risk: ethical issues

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The 'thousand-dollar genome': an ethical exploration

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Genetic aspects of female reproduction

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Male infertility and androgen receptor gene mutations: clinical features and identification of seven novel mutations

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Maternal and child outcome after in vitro fertilization--a review of 25 years of population-based data from Sweden

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Aneuploidy in the human blastocyst

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Polar body array CGH for prediction of the status of the corresponding oocyte. Part I: clinical results

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ESHRE PGD Consortium data collection XI: cycles from January to December 2008 with pregnancy follow-up to October 2009.

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The use of arrays in preimplantation genetic diagnosis and screening

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Accreditation of the PGD laboratory

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When and how should new technology be introduced into the IVF laboratory?

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The ESHRE PGD Consortium: 10 years of data collection

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ESHRE PGD consortium best practice guidelines for organization of a PGD centre for PGD/preimplantation genetic screening.

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Dynamics and ethics of comprehensive preimplantation genetic testing: a review of the challenges

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Idiopathic recurrent miscarriage is caused mostly by aneuploid embryos

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Are the kids really all right? Direct-to-consumer genetic testing in children: are company policies clashing with professional norms?

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A genome-wide association study in Chinese men identifies three risk loci for non-obstructive azoospermia

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Androgen insensitivity syndrome

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Letting the genome out of the bottle--will we get our wish?

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A high degree of aneuploidy in frozen-thawed human preimplantation embryos

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Transgenerational Epigenetic Inheritance: Prevalence, Mechanisms, and Implications for the Study of Heredity and Evolution

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Clinical manifestations of impaired GnRH neuron development and function

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Increased frequency of the DI genotype of the angiotensin-I converting enzyme and association of the II genotype with insulin resistance in polycystic ovary syndrome.

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Genome-wide association study identifies candidate genes for male fertility traits in humans

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The genetic origin of Klinefelter syndrome and its effect on spermatogenesis

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Preimplantation genetic screening: a systematic review and meta-analysis of RCTs

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Recurrent miscarriage and thrombophilia: an update

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Increased rate of aneuploid embryos in young women with previous aneuploid conceptions

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Genetic dissection of the AZF regions of the human Y chromosome: thriller or filler for male (in)fertility?

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Blastocyst biopsy with comprehensive chromosome screening and fresh embryo transfer significantly increases in vitro fertilization implantation and delivery rates: a randomized controlled trial

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Clinical consequences of microdeletions of the Y chromosome: the extended Münster experience

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The interface between assisted reproductive technologies and genetics: technical, social, ethical and legal issues.

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Application of next generation sequencing in mammalian embryogenomics: lessons learned from endogenous betaretroviruses of sheep

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Recurrent chromosomal abnormalities in human embryonic stem cells

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Genetic evaluation of the azoospermic or severely oligozoospermic male

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Users' motivations to purchase direct-to-consumer genome-wide testing: an exploratory study of personal stories

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Oligogenic basis of isolated gonadotropin-releasing hormone deficiency.

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Diseases in a dish: modeling human genetic disorders using induced pluripotent cells

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Five mutations of mitochondrial DNA polymerase-gamma (POLG) are not a prevalent etiology for spontaneous 46,XX primary ovarian insufficiency

21 January 2018

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Gene polymorphisms and male infertility--a meta-analysis and literature review

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Chromosomal mosaicism in human preimplantation embryos: a systematic review

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Assisted reproduction treatment and epigenetic inheritance.

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Chromosome instability is common in human cleavage-stage embryos.

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New array approaches to explore single cells genomes

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Does the European Union Tissues and Cells Directive improve quality in the in vitro fertilization laboratory? A case study in a tertiary referral center.

21 January 2018

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Cystic fibrosis transmembrane conductance regulator is vital to sperm fertilizing capacity and male fertility.

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Selection of single blastocysts for fresh transfer via standard morphology assessment alone and with array CGH for good prognosis IVF patients: results from a randomized pilot study

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CFTR mutations in men with congenital bilateral absence of the vas deferens (CBAVD): a systemic review and meta-analysis

21 January 2018

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Linking genome to epigenome

21 January 2018

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