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Deficiency of knowledge of genetics and genetic tests among general practitioners, gynecologists, and pediatricians: A global problem

Genetics in medicine, 2005-11, Vol.7 (9), p.605-610

2005

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Informed decision making in the context of prenatal screening

Patient education and counseling, 2006-10, Vol.63 (1), p.110-117

2006

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Estimating the Total Pathogenic Allele Frequency of Autosomal Recessive Disorders in Case of Consanguinity

Human heredity, 2015-01, Vol.80 (2), p.69-78

2015

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Do consanguineous parents of a child affected by an autosomal recessive disease have more DNA identical-by-descent than similarly-related parents with healthy offspring? Design of a case-control study

BMC medical genetics, 2010-07, Vol.11 (1), p.113-113, Article 113

2010

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Preconceptional genetic carrier testing and the commercial offer directly-to-consumers

Human reproduction (Oxford), 2011-05, Vol.26 (5), p.972-977

2011

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Consanguineous marriage and reproductive risk: attitudes and understanding of ethnic groups practising consanguinity in Western society

European journal of human genetics : EJHG, 2014-04, Vol.22 (4), p.452-457

2014

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Psychomotor developmental delay and epilepsy in an offspring of father–daughter incest: quantification of the causality probability

International journal of legal medicine, 2014-09, Vol.128 (5), p.749-750

ten Kate, Leo P.

2014

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Are pregnant women making informed choices about prenatal screening?

Genetics in medicine, 2005-05, Vol.7 (5), p.332-338

2005

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Confidence of primary care physicians in their ability to carry out basic medical genetic tasks—a European survey in five countries—Part 1

Journal of community genetics, 2011-03, Vol.2 (1), p.1-11

2011

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Comment on Gialluisi et al

European journal of human genetics : EJHG, 2014-02, Vol.22 (2), p.157-157

2014

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Benchmarks for Cystic Fibrosis carrier screening: A European consensus document

Journal of cystic fibrosis, 2010-05, Vol.9 (3), p.165-178

2010

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Psychomotor developmental delay and epilepsy in an offspring of father–daughter incest: quantification of the causality probability

International journal of legal medicine, 2010-11, Vol.124 (6), p.667-668

ten Kate, Leo P.

2010

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Three-month follow-up of Western and non-Western participants in a study on preconceptional ancestry-based carrier couple screening for cystic fibrosis and hemoglobinopathies in the Netherlands

Genetics in medicine, 2008-11, Vol.10 (11), p.820-830

2008

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Consanguinity and Endogamy in the Netherlands: Demographic and Medical Genetic Aspects

Human heredity, 2014-01, Vol.77 (1/4), p.161-166

2014

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Genetic risk

Journal of community genetics, 2012-07, Vol.3 (3), p.159-166

ten Kate, Leo P.

2012

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With expanded carrier screening, founder populations run the risk of being overlooked

Journal of community genetics, 2017-10, Vol.8 (4), p.327-333

2017

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Searching for preeclampsia genes: the current position

European journal of obstetrics & gynecology and reproductive biology, 2002-11, Vol.105 (2), p.94-113

2002

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Earliest trace, so far, of community genetics as a distinct concept

Journal of community genetics, 2012-10, Vol.3 (4), p.331-331

ten Kate, Leo P.

2012

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First steps in exploring prospective exome sequencing of consanguineous couples

European journal of medical genetics, 2014-11, Vol.57 (11), p.613-616

2014

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Two families with sibling recurrence of the 17q21.31 microdeletion syndrome due to low-grade mosaicism

European journal of human genetics : EJHG, 2012-07, Vol.20 (7), p.729-733

2012

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Genetics Education for Non-Genetic Health Care Professionals in the Netherlands (2002)

Community genetics, 2006-09, Vol.9 (4), p.246-250

2006

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A short history of the first 3 years of the Community Genetics Network and its newsletter

Journal of community genetics, 2011-09, Vol.2 (3), p.111-115

2011

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Erratum to: A short history of the first three years of the Community Genetics Network and its Newsletter

Journal of community genetics, 2011-12, Vol.2 (4), p.259-259

2011

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Birth defects after incestuous mating: Calculating the probability of causality and reflecting on the desirability of genetic testing

European journal of medical genetics, 2013-05, Vol.56 (5), p.243-244

2013

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Deficiency of knowledge of genetics and genetic tests among general practitioners, gynecologists, and pediatricians: A global problem

Informed decision making in the context of prenatal screening

Estimating the Total Pathogenic Allele Frequency of Autosomal Recessive Disorders in Case of Consanguinity

Consanguineous marriages, pearls and perils: Geneva International Consanguinity Workshop Report

Do consanguineous parents of a child affected by an autosomal recessive disease have more DNA identical-by-descent than similarly-related parents with healthy offspring? Design of a case-control study

Preconceptional genetic carrier testing and the commercial offer directly-to-consumers

Consanguineous marriage and reproductive risk: attitudes and understanding of ethnic groups practising consanguinity in Western society

Psychomotor developmental delay and epilepsy in an offspring of father–daughter incest: quantification of the causality probability

Are pregnant women making informed choices about prenatal screening?

Confidence of primary care physicians in their ability to carry out basic medical genetic tasks—a European survey in five countries—Part 1

Comment on Gialluisi et al

Benchmarks for Cystic Fibrosis carrier screening: A European consensus document

Psychomotor developmental delay and epilepsy in an offspring of father–daughter incest: quantification of the causality probability

Three-month follow-up of Western and non-Western participants in a study on preconceptional ancestry-based carrier couple screening for cystic fibrosis and hemoglobinopathies in the Netherlands

Consanguinity and Endogamy in the Netherlands: Demographic and Medical Genetic Aspects

Genetic risk

With expanded carrier screening, founder populations run the risk of being overlooked

Searching for preeclampsia genes: the current position

Earliest trace, so far, of community genetics as a distinct concept

First steps in exploring prospective exome sequencing of consanguineous couples

Two families with sibling recurrence of the 17q21.31 microdeletion syndrome due to low-grade mosaicism

Genetics Education for Non-Genetic Health Care Professionals in the Netherlands (2002)

A short history of the first 3 years of the Community Genetics Network and its newsletter

Erratum to: A short history of the first three years of the Community Genetics Network and its Newsletter

Birth defects after incestuous mating: Calculating the probability of causality and reflecting on the desirability of genetic testing

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