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Why do singletons conceived after assisted reproduction technology have adverse perinatal outcome? Systematic review and meta-analysis

Human reproduction update, 2013-03, Vol.19 (2), p.87-104

2013

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Obstetric and neonatal complications in pregnancies conceived after oocyte donation: a systematic review and meta‐analysis

BJOG : an international journal of obstetrics and gynaecology, 2017-03, Vol.124 (4), p.561-572

2017

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Obstetric and neonatal outcome after oocyte donation in 106 women with Turner syndrome: a Nordic cohort study

Human reproduction (Oxford), 2013-06, Vol.28 (6), p.1598-1609

2013

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Children born after cryopreservation of embryos or oocytes: a systematic review of outcome data

Human reproduction (Oxford), 2009-09, Vol.24 (9), p.2158-2172

2009

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Cyclin D1 expression is associated with poor prognostic features in estrogen receptor positive breast cancer

Breast cancer research and treatment, 2009-01, Vol.113 (1), p.75-82

2009

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High cyclin B1 expression is associated with poor survival in breast cancer

British journal of cancer, 2009-04, Vol.100 (7), p.1055-1060

2009

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Recent developments in genetics and medically assisted reproduction: from research to clinical applications

European journal of human genetics : EJHG, 2018-01, Vol.26 (1), p.12-33

2018

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Familial Cutaneous Leiomyomatosis Is a Two-Hit Condition Associated with Renal Cell Cancer of Characteristic Histopathology

The American journal of pathology, 2001-09, Vol.159 (3), p.825-829

2001

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A population-based study of the incidence of müllerian aplasia in Finland

Fertility and sterility, 2001-09, Vol.76 (3), p.624-625

2001

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p53, CHK2, and CHK1 genes in Finnish families with Li-Fraumeni syndrome : Further evidence of CHK2 in inherited cancer predisposition

Cancer research (Chicago, Ill.), 2001-08, Vol.61 (15), p.5718-5722

2001

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Safety issues in assisted reproduction technology: Should ICSI patients have genetic testing before treatment? A practical proposition to help patient information

Human reproduction (Oxford), 2004-03, Vol.19 (3), p.472-476

2004

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The frequency and outcome of breast cancer risk-reducing surgery in finnish BRCA1 and BRCA2 mutation carriers

Scandinavian journal of surgery, 2014-03, Vol.103 (1), p.34-40

2014

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Clinical features of primary ovarian failure caused by a point mutation in the follicle-stimulating hormone receptor gene

The journal of clinical endocrinology and metabolism, 1996-10, Vol.81 (10), p.3722-3726

1996

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Men homozygous for an inactivating mutation of the follicle-stimulating hormone (FSH) receptor gene present variable suppression of spermatogenesis and fertility

Nature genetics, 1997-02, Vol.15 (2), p.205-206

1997

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Altered Expression of MLH1, MSH2, and MSH6 in Predisposition to Hereditary Nonpolyposis Colorectal Cancer

Journal of clinical oncology, 2003-10, Vol.21 (19), p.3629-3637

2003

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The DNA damage signalling kinase ATM is aberrantly reduced or lost in BRCA1 BRCA2-deficient and ER PR ERBB2-triple-negative breast cancer

Oncogene, 2008-04, Vol.27 (17), p.2501-2506

2008

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Breast-Cancer Risk in Families with Mutations in PALB2

The New England journal of medicine, 2014-08, Vol.371 (6), p.497-506

2014

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Mutation in the follicle-stimulating hormone receptor gene causes hereditary hypergonadotropic ovarian failure

Cell, 1995-09, Vol.82 (6), p.959-968

1995

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Gene‐panel testing of breast and ovarian cancer patients identifies a recurrent RAD51C duplication

Clinical genetics, 2018-03, Vol.93 (3), p.595-602

2018

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Finnish Fanconi anemia mutations and hereditary predisposition to breast and prostate cancer

Clinical genetics, 2015-07, Vol.88 (1), p.68-73

2015

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Evaluation of the role of Finnish ataxia-telangiectasia mutations in hereditary predisposition to breast cancer

Carcinogenesis (New York), 2007-05, Vol.28 (5), p.1040-1045

2007

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Increased risk of cancer in patients with fumarate hydratase germline mutation

Journal of medical genetics, 2006-06, Vol.43 (6), p.523-526

2006

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Overabundant FANCD2, alone and combined with NQO1, is a sensitive marker of adverse prognosis in breast cancer

Annals of oncology, 2013-11, Vol.24 (11), p.2780-2785

2013

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Inhibin: a candidate gene for premature ovarian failure

Human reproduction (Oxford), 2000-12, Vol.15 (12), p.2644-2649

2000

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A two-decade experience of head and neck paragangliomas in a whole population-based single centre cohort

European archives of oto-rhino-laryngology, 2015-08, Vol.272 (8), p.2045-2053

2015

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Why do singletons conceived after assisted reproduction technology have adverse perinatal outcome? Systematic review and meta-analysis

Obstetric and neonatal complications in pregnancies conceived after oocyte donation: a systematic review and meta‐analysis

Obstetric and neonatal outcome after oocyte donation in 106 women with Turner syndrome: a Nordic cohort study

Children born after cryopreservation of embryos or oocytes: a systematic review of outcome data

Cyclin D1 expression is associated with poor prognostic features in estrogen receptor positive breast cancer

High cyclin B1 expression is associated with poor survival in breast cancer

Recent developments in genetics and medically assisted reproduction: from research to clinical applications

Familial Cutaneous Leiomyomatosis Is a Two-Hit Condition Associated with Renal Cell Cancer of Characteristic Histopathology

A population-based study of the incidence of müllerian aplasia in Finland

p53, CHK2, and CHK1 genes in Finnish families with Li-Fraumeni syndrome : Further evidence of CHK2 in inherited cancer predisposition

Safety issues in assisted reproduction technology: Should ICSI patients have genetic testing before treatment? A practical proposition to help patient information

The frequency and outcome of breast cancer risk-reducing surgery in finnish BRCA1 and BRCA2 mutation carriers

Clinical features of primary ovarian failure caused by a point mutation in the follicle-stimulating hormone receptor gene

Men homozygous for an inactivating mutation of the follicle-stimulating hormone (FSH) receptor gene present variable suppression of spermatogenesis and fertility

Altered Expression of MLH1, MSH2, and MSH6 in Predisposition to Hereditary Nonpolyposis Colorectal Cancer

The DNA damage signalling kinase ATM is aberrantly reduced or lost in BRCA1 BRCA2-deficient and ER PR ERBB2-triple-negative breast cancer

Breast-Cancer Risk in Families with Mutations in PALB2

Mutation in the follicle-stimulating hormone receptor gene causes hereditary hypergonadotropic ovarian failure

Gene‐panel testing of breast and ovarian cancer patients identifies a recurrent RAD51C duplication

Finnish Fanconi anemia mutations and hereditary predisposition to breast and prostate cancer

Evaluation of the role of Finnish ataxia-telangiectasia mutations in hereditary predisposition to breast cancer

Increased risk of cancer in patients with fumarate hydratase germline mutation

Overabundant FANCD2, alone and combined with NQO1, is a sensitive marker of adverse prognosis in breast cancer

Inhibin: a candidate gene for premature ovarian failure

A two-decade experience of head and neck paragangliomas in a whole population-based single centre cohort

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