De novo variants in CNOT3 cause a variable neurodevelopmental disorder
Martin, R, Splitt, M, Genevieve, D, Aten, E, Collins, A, de Bie, C I, Faivre, L, Foulds, N, Giltay, J, Ibitoye, R, Joss, S, Kennedy, J, Kerr, B, Kivuva, E, Koopmans, M, Newbury-Ecob, R, Jean-Marçais, N, Peeters, E A J, Smithson, S, Tomkins, S, Tranmauthem, F, Piton, A, van Haeringen, A
Published in European journal of human genetics : EJHG (01.11.2019)
Published in European journal of human genetics : EJHG (01.11.2019)
Get full text
Journal Article
An unanticipated copy number variant of chromosome 15 disrupting SMAD3 reveals a three-generation family at serious risk for aortic dissection
Hilhorst-Hofstee, Y, Scholte, AJHA, Rijlaarsdam, MEB, van Haeringen, A, Kroft, LJ, Reijnierse, M, Ruivenkamp, CAL, Versteegh, MIM, Pals, G, Breuning, MH
Published in Clinical genetics (01.04.2013)
Published in Clinical genetics (01.04.2013)
Get full text
Journal Article
Determining the genome-wide kinship coefficient seems unhelpful in distinguishing consanguineous couples with a high versus low risk for adverse reproductive outcome
Kelmemi, W, Teeuw, M E, Bochdanovits, Z, Ouburg, S, Jonker, M A, Alkuraya, F, Hashem, M, Kayserili, H, van Haeringen, A, Sheridan, E, Masri, A, Cobben, J M, Rizzu, P, Kostense, P J, Dommering, C J, Henneman, L, Bouhamed-Chaabouni, H, Heutink, P, Ten Kate, L P, Cornel, M C
Published in BMC medical genetics (20.07.2015)
Published in BMC medical genetics (20.07.2015)
Get full text
Journal Article
Field comparison of real-time polymerase chain reaction and bacterial culture for identification of bovine mastitis bacteria
Koskinen, M.T., Wellenberg, G.J., Sampimon, O.C., Holopainen, J., Rothkamp, A., Salmikivi, L., van Haeringen, W.A., Lam, T.J.G.M., Pyörälä, S.
Published in Journal of dairy science (01.12.2010)
Published in Journal of dairy science (01.12.2010)
Get full text
Journal Article
single nucleotide polymorphism set for paternal identification to reduce the costs of trait recording in commercial pig breeding
Harlizius, B, Lopes, M.S, Duijvesteijn, N, van de Goor, L.H.P, van Haeringen, W.A, Panneman, H, Guimarães, S.E.F, Merks, J.W.M, Knol, E.F
Published in Journal of animal science (01.06.2011)
Published in Journal of animal science (01.06.2011)
Get full text
Journal Article
Population studies of 16 bovine STR loci for forensic purposes
van de Goor, L. H. P., Koskinen, M. T., van Haeringen, W. A.
Published in International journal of legal medicine (01.01.2011)
Published in International journal of legal medicine (01.01.2011)
Get full text
Journal Article
Sleep deprivation or postnatal depression in later infancy: Separating the chicken from the egg
ARMSTRONG, KL, HAERINGEN, AR VAN, DADDS, MR, CASH, R
Published in Journal of paediatrics and child health (01.06.1998)
Published in Journal of paediatrics and child health (01.06.1998)
Get full text
Journal Article
Population studies of 17 equine STR for forensic and phylogenetic analysis
van de Goor, L. H. P., van Haeringen, W. A., Lenstra, J. A.
Published in Animal genetics (01.12.2011)
Published in Animal genetics (01.12.2011)
Get full text
Journal Article
Identification of critical regions and candidate genes for cardiovascular malformations and cardiomyopathy associated with deletions of chromosome 1p36
Zaveri, Hitisha P, Beck, Tyler F, Hernández-García, Andrés, Shelly, Katharine E, Montgomery, Tara, van Haeringen, Arie, Anderlid, Britt-Marie, Patel, Chirag, Goel, Himanshu, Houge, Gunnar, Morrow, Bernice E, Cheung, Sau Wai, Lalani, Seema R, Scott, Daryl A
Published in PloS one (15.01.2014)
Published in PloS one (15.01.2014)
Get full text
Journal Article
Andersen-Tawil syndrome: Overlapping clinical features with Noonan syndrome?
van der Werf - ’t Lam, A.S., van Haeringen, A., Rinnen, T., Robles de Medina, R.M., Wilde, A.A.M., Hennekam, R.C., Barge - Schaapveld, D.Q.C.M.
Published in European journal of medical genetics (01.01.2022)
Published in European journal of medical genetics (01.01.2022)
Get full text
Journal Article
Cytogenetic screening of livestock populations in Europe: an overview
Ducos, A., Revay, T., Kovacs, A., Hidas, A., Pinton, A., Bonnet-Garnier, A., Molteni, L, Slota, E., Switonski, M., Arruga, M.V., van Haeringen, W.A., Nicolae, I., Chaves, R., Guedes-Pinto, H., Andersson, M., Iannuzzi, L.
Published in Cytogenetic and Genome Research (01.01.2008)
Published in Cytogenetic and Genome Research (01.01.2008)
Get full text
Journal Article
Array-CGH detection of micro rearrangements in mentally retarded individuals: clinical significance of imbalances present both in affected children and normal parents
Rosenberg, C, Knijnenburg, J, Bakker, E, Vianna-Morgante, A M, Sloos, W, Otto, P A, Kriek, M, Hansson, K, Krepischi-Santos, A C V, Fiegler, H, Carter, N P, Bijlsma, E K, van Haeringen, A, Szuhai, K, Tanke, H J
Published in Journal of medical genetics (01.02.2006)
Published in Journal of medical genetics (01.02.2006)
Get full text
Journal Article
Genetic diversity, evolutionary history and implications for conservation of the lion (Panthera leo) in West and Central Africa
Bertola, L.D, van Hooft, W.F, Vrieling, K, Uit de Weerd, D.R, York, D.S, Bauer, H, Prins, H.H.T, Funston, P.J, Udo de Haes, H.A, Leirs, H, van Haeringen, W.A, Sogbohossou, E, Tumenta, P.N, de Iongh, H.H
Published in Journal of biogeography (01.07.2011)
Published in Journal of biogeography (01.07.2011)
Get full text
Journal Article
Extending the phenotype of recurrent rearrangements of 16p11.2: Deletions in mentally retarded patients without autism and in normal individuals
Bijlsma, E.K, Gijsbers, A.C.J, Schuurs-Hoeijmakers, J.H.M, van Haeringen, A, Fransen van de Putte, D.E, Anderlid, B.-M, Lundin, J, Lapunzina, P, Pérez Jurado, L.A, Delle Chiaie, B, Loeys, B, Menten, B, Oostra, A, Verhelst, H, Amor, D.J, Bruno, D.L, van Essen, A.J, Hordijk, R, Sikkema-Raddatz, B, Verbruggen, K.T, Jongmans, M.C.J, Pfundt, R, Reeser, H.M, Breuning, M.H, Ruivenkamp, C.A.L
Published in European journal of medical genetics (01.03.2009)
Published in European journal of medical genetics (01.03.2009)
Get full text
Journal Article
Clinical spectrum of SIX3-associated mutations in holoprosencephaly: correlation between genotype, phenotype and function
Lacbawan, F, Solomon, B D, Roessler, E, El-Jaick, K, Domené, S, Vélez, J I, Zhou, N, Hadley, D, Balog, J Z, Long, R, Fryer, A, Smith, W, Omar, S, McLean, S D, Clarkson, K, Lichty, A, Clegg, N J, Delgado, M R, Levey, E, Stashinko, E, Potocki, L, VanAllen, M I, Clayton-Smith, J, Donnai, D, Bianchi, D W, Juliusson, P B, Njølstad, P R, Brunner, H G, Carey, J C, Hehr, U, Müsebeck, J, Wieacker, P F, Postra, A, Hennekam, R C M, van den Boogaard, M-J H, van Haeringen, A, Paulussen, A, Herbergs, J, Schrander-Stumpel, C T R M, Janecke, A R, Chitayat, D, Hahn, J, McDonald-McGinn, D M, Zackai, E H, Dobyns, W B, Muenke, M
Published in Journal of medical genetics (01.06.2009)
Published in Journal of medical genetics (01.06.2009)
Get full text
Journal Article
Bones in human CYP26B1 deficiency and rats with hypervitaminosis A phenocopy Vegfa overexpression
Lind, Thomas, Lugano, Roberta, Gustafson, Ann-Marie, Norgård, Maria, van Haeringen, Arie, Dimberg, Anna, Melhus, Håkan, Robertson, Stephen P., Andersson, Göran
Published in Bone Reports (01.12.2018)
Published in Bone Reports (01.12.2018)
Get full text
Journal Article