Works by ten Kate, Leo P.

Results: 34

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

Published in:

2010

By:

ten Kate, Leo P.

Publication type:

Letter

Segregation ratio in cranio-cerebello-cardiac syndrome.

Published in:

European Journal of Human Genetics, 2006, v. 14, n. 9, p. 1054, doi. 10.1038/sj.ejhg.5201660

By:

Stellingwerff, Harm-Jan;
van Hagen, Johanna M.;
ten Kate, Leo P.

Publication type:

Article

The difference between observed and expected prevalence of MCAD deficiency in The Netherlands: a genetic epidemiological study.

Published in:

European Journal of Human Genetics, 2005, v. 13, n. 8, p. 947, doi. 10.1038/sj.ejhg.5201428

By:

Derks, Terry G. J.;
Duran, Marinus;
Waterham, Hans R.;
Reijngoud, Dirk-Jan;
ten Kate, Leo P.;
Smit, G. Peter A.

Publication type:

Article

A genome-wide scan for preeclampsia in the Netherlands.

Published in:

European Journal of Human Genetics, 2001, v. 9, n. 10, p. 758, doi. 10.1038/sj.ejhg.5200706

By:

Lachmeijer, Augusta MA;
Arngrímsson, Reynir;
Bastiaans, Esther J;
Frigge, Michael L;
Pals, Gerald;
Sigurdardóttir, Sigrun;
Stéfansson, Hreinn;
Pálsson, Birgir;
Nicolae, Dan;
Kong, Augustin;
Aarnoudse, Jan G;
Gulcher, Jeff R;
Dekker, Guustaaf A;
ten Kate, Leo P;
Stéfansson, Kári

Publication type:

Article

Efficacy of cascade testing for fragile X syndrome.

Published in:

Journal of Medical Screening, 1999, v. 6, n. 2, p. 70, doi. 10.1136/jms.6.2.70

By:

Wildhagen, Mark F.;
Van Os, Theo A. M.;
Polder, Johan J.;
ten Kate, Leo P.;
Habbema, J. Dik F.

Publication type:

Article

Community attitudes to cystic fibrosis carrier screening.

Published in:

Prenatal Diagnosis, 1990, v. 10, n. 4, p. 275, doi. 10.1002/pd.1970100413

By:

ten Kate, Leo P.;
Tumstra, Tjeerd

Publication type:

Article

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

Published in:

2011

By:

Borry, Pascal;
Henneman, Lidewij;
Lakeman, Phillis;
ten Kate, Leo P.;
Cornel, Martina C.;
Howard, Heidi C.

Publication type:

journal article

Current practice and future interest of GPs and prospective parents in pre-conception care in The Netherlands.

Published in:

Family Practice, 2004, v. 21, n. 3, p. 307

By:

Francis AM Poppelaars;
Martina C Cornel;
Leo P ten Kate

Publication type:

Article

The parent-of-origin effect of 10q22 in pre-eclamptic females coincides with two regions clustered for genes with down-regulated expression in androgenetic placentas.

Published in:

Molecular Human Reproduction, 2004, v. 10, n. 8, p. 589, doi. 10.1093/molehr/gah080

By:

Oudejans, Cees B.M.;
Mulders, Joyce;
Lachmeijer, Augusta M.A.;
van Dijk, Marie;
Könst, Andrea A.M.;
Westerman, Bart A.;
van Wijk, Inge J.;
Leegwater, Peter A.J.;
Kato, Hidenori D.;
Matsuda, Takao;
Wake, Norio;
Dekker, Gustaaf A.;
Pals, Gerard;
ten Kate, Leo P.;
Blankenstein, Marinus A.

Publication type:

Article

Screening for Cystic Fibrosis.

Published in:

Acta Paediatrica, 1987, v. 76, n. 2, p. 209, doi. 10.1111/j.1651-2227.1987.tb10449.x

By:

DANKERT-ROELSE, JEANNETTE E.;
TE MEERMAN, GERARD J.;
MARTIJN, ALBERT;
TEN KATE, LEO P.;
KNOL, KLAAS

Publication type:

Article

Malignant hemangiopericytoma in three kindred members of one family.

Published in:

1988

By:

Plukker, John Th.;
Koops, Heimen Schraffordt;
Molenaar, Ineke;
Vermey, Albert;
Kate, Leo P. Ten;
Oldhoff, Jan;
Plukker, J T;
Koops, H S;
Molenaar, I;
Vermey, A;
ten Kate, L P;
Oldhoff, J

Publication type:

journal article

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

Published in:

European Journal of Human Genetics, 2014, v. 22, n. 4, p. 452, doi. 10.1038/ejhg.2013.167

By:

Teeuw, Marieke E;
Loukili, Ghariba;
Bartels, Edien AC;
ten Kate, Leo P;
Cornel, Martina C;
Henneman, Lidewij

Publication type:

Article

Comment on Gialluisi et al.

Published in:

European Journal of Human Genetics, 2014, v. 22, n. 2, p. 157, doi. 10.1038/ejhg.2013.152

By:

ten Kate, Leo P;
Teeuw, Marieke;
Henneman, Lidewij;
Cornel, Martina C

Publication type:

Article

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

Published in:

European Journal of Human Genetics, 2012, v. 20, n. 7, p. 729, doi. 10.1038/ejhg.2012.1

By:

Koolen, David A;
Dupont, Juliette;
de Leeuw, Nicole;
Vissers, Lisenka ELM;
van den Heuvel, Simone PA;
Bradbury, Alyson;
Steer, James;
de Brouwer, Arjan PM;
ten Kate, Leo P;
Nillesen, Willy M;
de Vries, Bert BA;
Parker, Michael J

Publication type:

Article

Congenital hepatic fibrosis in autosomal-dominant polycystic kidney disease.

Published in:

Kidney International, 1990, v. 38, n. 5, p. 880, doi. 10.1038/ki.1990.286

By:

Cobben, Jan M.;
Breuning, Martijn H.;
Schoots, Coen;
ten Kate, Leo P.;
Zerres, Klaus

Publication type:

Article

Does informed decision making influence psychological outcomes after receiving a positive screening outcome?

Published in:

Prenatal Diagnosis, 2009, v. 29, n. 3, p. 271, doi. 10.1002/pd.2186

By:

Kleinveld, Johanna H.;
Ten Kate, Leo P.;
van den Berg, Matthijs;
van Vugt, John M. G.;
Timmermans, Daniëlle R. M.

Publication type:

Article

Does offering and performing prenatal screening influence women's attachment to their unborn child? A longitudinal randomized controlled trial.

Published in:

Prenatal Diagnosis, 2007, v. 27, n. 8, p. 757, doi. 10.1002/pd.1775

By:

Kleinveld, Johanna H.;
Timmermans, Daniëlle R. M.;
van den Berg, Matthijs;
van Eijk, Jacques Th. M.;
Ten Kate, Leo P.

Publication type:

Article

Does prenatal screening influence anxiety levels of pregnant women? A longitudinal randomised controlled trial.

Published in:

Prenatal Diagnosis, 2006, v. 26, n. 4, p. 354, doi. 10.1002/pd.1419

By:

Kleinveld, Johanna H.;
Timmermans, Danielle R. M.;
de Smit, Denhard J.;
J. Adér, Herman;
van der Wal, Gerrit;
ten Kate, Leo P.

Publication type:

Article

Human Uteroglobin Gene Polymorphisms and Genetic Susceptibility to Asthma.

Published in:

Annals of the New York Academy of Sciences, 2000, v. 923, n. 1, p. 303, doi. 10.1111/j.1749-6632.2000.tb05538.x

By:

CHOI, MOONSUK;
ZHANG, ZHONGJIAN;
TEN KATE, LEO P.;
COLLEE, J. MARGRIET;
GERRITSEN, J.;
MUKHERJEE, ANIL B.

Publication type:

Article

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

Published in:

Human Heredity, 2016, v. 80, n. 2, p. 69, doi. 10.1159/000438862

By:

Jonker, Marianne A.;
Teeuw, Marieke E.;
Kelmemi, Wided;
Kharrat, Maher;
Chaabouni-Bouhamed, Habiba;
Ten Kate, Leo P.

Publication type:

Article

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

Published in:

Human Heredity, 2014, v. 77, n. 1-4, p. 161, doi. 10.1159/000360761

By:

ten Kate, Leo P.;
Teeuw, Marieke E.;
Henneman, Lidewij;
Cornel, Martina C.

Publication type:

Article

Comparison of Single-Entry and Double-Entry Two-Step Couple Screening for Cystic Fibrosis Carriers.

Published in:

Human Heredity, 1996, v. 46, n. 1, p. 20, doi. 10.1159/000154320

By:

ten Kate, Leo P.;
Verheij, Joke B.G.M.;
Wildhagen, Mark F.;
Hilderink, Henk B.M.;
Kooij, Loes;
Verzijl, Jan Gerben;
Habbema, Dik F.

Publication type:

Article

Mendelian Phenotypes in the Netherlands.

Published in:

Human Heredity, 1993, v. 43, n. 4, p. 223, doi. 10.1159/000154135

By:

Verheij, Joke B.G.M.;
Ten Kate, Leo P.

Publication type:

Article

Family Distances as a Measure of Hidden Consanguinity.

Published in:

Human Heredity, 1991, v. 41, n. 1, p. 12, doi. 10.1159/000153967

By:

Swaving, Janny;
Groenewegen, Alex;
Kamstra, Aukje;
te Meerman, Gerard J.;
ten Kate, Leo P.

Publication type:

Article

Family Distances and Human Lymphocyte Antigens.

Published in:

Human Heredity, 1987, v. 37, n. 6, p. 359, doi. 10.1159/000153735

By:

Nauta, Maarten J.;
van Treuren, Rob;
ten Kate, Leo P.;
te Meerman, Gerard J.;
Amaro, Joe D'

Publication type:

Article

LINKAGE AND ASSOCIATION STUDIES OF IL1B AND IL1RN GENE POLYMORPHISMS IN PREECLAMPSIA.

Published in:

Hypertension in Pregnancy, 2002, v. 21, n. 1, p. 23, doi. 10.1081/PRG-120002907

By:

Lachmeijer, Augusta M.A.;
Nosti-Escanilla, Maria P.;
Bastiaans, Esther B.;
Pals, G.;
Sandkuijl, Lodewijk A.;
Kostense, Pieter J.;
Aarnoudse, Jan G.;
Crusius, J. Bart A.;
Peña, A. Salvador;
Dekker, Guustaaf A.;
Arngrímsson, Reynir;
ten Kate, Leo P.

Publication type:

Article

Decreased scattering coefficient of blue sclerae.

Published in:

Clinical Genetics, 1985, v. 27, n. 2, p. 187, doi. 10.1111/j.1399-0004.1985.tb00209.x

By:

Lanting, Peter J. H.;
Borsboom, Peter C. F.;
Meerman, Gerard J. te;
Kate, Leo P. ten

Publication type:

Article

Family distances can reveal hidden consanguinity.

Published in:

Clinical Genetics, 1983, v. 24, n. 1, p. 29, doi. 10.1111/j.1399-0004.1983.tb00065.x

By:

Kate, Leo P. ten;
Rutgers-Janssen, Roelien

Publication type:

Article

The significance of different types of information in calculating the probability that a female relative of a Duchenne muscular dystrophy patient is a carrier.

Published in:

Clinical Genetics, 1981, v. 20, n. 4, p. 281, doi. 10.1111/j.1399-0004.1981.tb01034.x

By:

Kate, Leo P. ten;
Offringa, Pieter J.

Publication type:

Article

Reflections on Termination of Pregnancy for Genetic or Non-Genetic Congenital Disorders.

Published in:

Currents of Encounter, 2013, v. 48, p. 135

By:

Ten Kate, Leo P.

Publication type:

Article

Screening for cystic fibrosis and its evaluation.

Published in:

British Medical Bulletin, 1998, v. 54, n. 4, p. 857, doi. 10.1093/oxfordjournals.bmb.a011734

By:

Wildhagen, Mark F;
Kate, Leo P ten;
Habbema, J Dik F

Publication type:

Article

Challenges in the care for consanguineous couples: an exploratory interview study among general practitioners and midwives.

Published in:

BMC Family Practice, 2012, v. 13, n. 1, p. 105, doi. 10.1186/1471-2296-13-105

By:

Teeuw, Marieke E.;
Hagelaar, Anouk;
ten Kate, Leo P.;
Cornel, Martina C.;
Henneman, Lidewij

Publication type:

Article

Evidence for a second gene for primary microcephaly at MCPH5 on chromosome 1.

Published in:

Hereditas, 2003, v. 139, n. 1, p. 64, doi. 10.1111/j.1601-5223.2003.01682.x

By:

Wallerman, Ola;
Van Eeghen, Agnies;
Ten Kate, Leo P.;
Wadelius, Claes

Publication type:

Article

Do cosanguineous parents of a child affected byan autosomal recessive disease have more DNAidentical-by-descent than similarly-related parentswith healthy offspring? Design of a case-controlstudy.

Published in:

BMC Medical Genetics, 2010, v. 11, p. 113, doi. 10.1186/1471-2350-11-113

By:

Teeuw, Marieke E.;
Henneman, Lidewij;
Bochdanovits, Zoltan;
Heutink, Peter;
Kuik, Dirk J.;
Cornel, Martina C.;
ten Kate, Leo P.

Publication type:

Article