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The Intersection of the Genetic Architectures of Orofacial Clefts and Normal Facial Variation.
Published in:
Frontiers in Genetics, 2021, v. 11, p. N.PAG, doi. 10.3389/fgene.2021.626403
By:
- Indencleef, Karlijne;
- Hoskens, Hanne;
- Lee, Myoung Keun;
- White, Julie D.;
- Liu, Chenxing;
- Eller, Ryan J.;
- Naqvi, Sahin;
- Wehby, George L.;
- Moreno Uribe, Lina M.;
- Hecht, Jacqueline T.;
- Long, Ross E.;
- Christensen, Kaare;
- Deleyiannis, Frederic W.;
- Walsh, Susan;
- Shriver, Mark D.;
- Richmond, Stephen;
- Wysocka, Joanna;
- Peeters, Hilde;
- Shaffer, John R.;
- Marazita, Mary L.
Publication type:
Article
Orthognathic surgery in patients with systemic diseases.
Published in:
Oral & Maxillofacial Surgery, 2023, v. 27, n. 2, p. 235, doi. 10.1007/s10006-022-01054-1
By:
- Brijs, Katrien;
- Peeters, Hilde;
- Politis, Constantinus
Publication type:
Article
The Influence of Microdeletions and Microduplications of 16p11.2 on Global Transcription Profiles.
Published in:
Journal of Child Neurology, 2015, v. 30, n. 14, p. 1947, doi. 10.1177/0883073815602066
By:
- Kusenda, Mary;
- Vacic, Vladimir;
- Malhotra, Dheeraj;
- Rodgers, Linda;
- Pavon, Kevin;
- Meth, Jennifer;
- Kumar, Ravinesh A.;
- Christian, Susan L.;
- Peeters, Hilde;
- Cho, Shawn S.;
- Addington, Anjene;
- Rapoport, Judith L.;
- Sebat, Jonathan
Publication type:
Article
Reasons affecting the uptake of reproductive genetic carrier screening among nonpregnant reproductive‐aged women in Flanders (Belgium).
Published in:
Journal of Genetic Counseling, 2022, v. 31, n. 5, p. 1043, doi. 10.1002/jgc4.1575
By:
- Van Steijvoort, Eva;
- Demuynck, Remke;
- Peeters, Hilde;
- Vandecruys, Hilde;
- Verguts, Jasper;
- Peeraer, Karen;
- Matthijs, Gert;
- Borry, Pascal
Publication type:
Article
The East Flanders Prospective Twin Survey (EFPTS): 55 Years Later.
Published in:
2019
By:
- Derom, Catherine;
- Thiery, Evert;
- Rutten, Bart P.F.;
- Peeters, Hilde;
- Gielen, Marij;
- Bijnens, Esmée;
- Vlietinck, Robert;
- Weyers, Steven
Publication type:
journal article
The East Flanders Prospective Twin Survey (EFPTS): An Actual Perception.
Published in:
Twin Research & Human Genetics, 2013, v. 16, n. 1, p. 58, doi. 10.1017/thg.2012.75
By:
- Derom, Catherine;
- Thiery, Evert;
- Peeters, Hilde;
- Vlietinck, Robert;
- Defoort, Paul;
- Frijns, Jean-Pierre
Publication type:
Article
The ethics of complexity. Genetics and autism, a literature review.
Published in:
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 3, p. 305, doi. 10.1002/ajmg.b.32432
By:
- Hens, Kristien;
- Peeters, Hilde;
- Dierickx, Kris
Publication type:
Article
Association of CDH11 with non-syndromic ASD.
Published in:
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2014, v. 165B, n. 5, p. 391, doi. 10.1002/ajmg.b.32243
By:
- Crepel, An;
- De Wolf, Veerle;
- Brison, Nathalie;
- Ceulemans, Berten;
- Walleghem, Didier;
- Peuteman, Gilian;
- Lambrechts, Diether;
- Steyaert, Jean;
- Noens, Ilse;
- Devriendt, Koen;
- Peeters, Hilde
Publication type:
Article
Taking the risk. A systematic review of ethical reasons and moral arguments in the clinical use of polygenic risk scores.
Published in:
American Journal of Medical Genetics. Part A, 2024, v. 194, n. 7, p. 1, doi. 10.1002/ajmg.a.63584
By:
- Andreoli, Lara;
- Peeters, Hilde;
- Van Steen, Kristel;
- Dierickx, Kris
Publication type:
Article
Olfactory function in patients with nonsyndromic orofacial clefts and their unaffected relatives.
Published in:
American Journal of Medical Genetics. Part A, 2018, v. 176, n. 11, p. 2375, doi. 10.1002/ajmg.a.40348
By:
- Roosenboom, Jasmien;
- Hermans, Robert;
- Lammens, Frederik;
- Samain, Jean Louis;
- Devriendt, Koen;
- Vander Poorten, Vincent;
- Hellings, Peter W.;
- Jorissen, Mark;
- Peeters, Hilde;
- Claes, Peter;
- Hens, Greet
Publication type:
Article
A comprehensive clinical and genetic study in 127 patients with ID in Kinshasa, DR Congo.
Published in:
American Journal of Medical Genetics. Part A, 2018, v. 176, n. 9, p. 1897, doi. 10.1002/ajmg.a.40382
By:
- Lumaka, Aimé;
- Race, Valerie;
- Peeters, Hilde;
- Corveleyn, Anniek;
- Coban‐Akdemir, Zeynep;
- Jhangiani, Shalini N.;
- Song, Xiaofei;
- Mubungu, Gerrye;
- Posey, Jennifer;
- Lupski, James R.;
- Vermeesch, Joris R.;
- Lukusa, Prosper;
- Devriendt, Koenraad
Publication type:
Article
Testing the face shape hypothesis in twins discordant for nonsyndromic orofacial clefting.
Published in:
American Journal of Medical Genetics. Part A, 2017, v. 173, n. 11, p. 2886, doi. 10.1002/ajmg.a.38471
By:
- Roosenboom, Jasmien;
- Indencleef, Karlijne;
- Hens, Greet;
- Peeters, Hilde;
- Christensen, Kaare;
- Marazita, Mary L.;
- Claes, Peter;
- Leslie, Elizabeth J.;
- Weinberg, Seth M.
Publication type:
Article
CREBBP mutations in individuals without Rubinstein-Taybi syndrome phenotype.
Published in:
American Journal of Medical Genetics. Part A, 2016, v. 170A, n. 10, p. 2681, doi. 10.1002/ajmg.a.37800
By:
- Menke, Leonie A.;
- van Belzen, Martine J.;
- Alders, Marielle;
- Cristofoli, Francesca;
- Ehmke, Nadja;
- Fergelot, Patricia;
- Foster, Alison;
- Gerkes, Erica H.;
- Hoffer, Mariëtte J. V.;
- Horn, Denise;
- Kant, Sarina G.;
- Lacombe, Didier;
- Leon, Eyby;
- Maas, Saskia M.;
- Melis, Daniela;
- Muto, Valentina;
- Park, Soo‐Mi;
- Peeters, Hilde;
- Peters, Dorien J. M.;
- Pfundt, Rolph
Publication type:
Article
A complex Xp11.22 deletion in a patient with syndromic autism: Exploration of FAM120C as a positional candidate gene for autism.
Published in:
American Journal of Medical Genetics. Part A, 2014, v. 164A, n. 12, p. 3035, doi. 10.1002/ajmg.a.36752
By:
- De Wolf, Veerle;
- Crepel, An;
- Schuit, Frans;
- van Lommel, LeENtje;
- Ceulemans, BertEN;
- Steyaert, Jean;
- SeuntjENs, Eve;
- Peeters, Hilde;
- DevriENdt, KoEN
Publication type:
Article
Genetic counseling for susceptibility loci and neurodevelopmental disorders: The del15q11.2 as an example.
Published in:
American Journal of Medical Genetics. Part A, 2013, v. 161A, n. 11, p. 2846, doi. 10.1002/ajmg.a.36209
By:
- De Wolf, Veerle;
- Brison, Nathalie;
- Devriendt, Koenraad;
- Peeters, Hilde
Publication type:
Article
Refining analyses of copy number variation identifies specific genes associated with developmental delay.
Published in:
Nature Genetics, 2014, v. 46, n. 10, p. 1063, doi. 10.1038/ng.3092
By:
- Coe, Bradley P;
- Witherspoon, Kali;
- Baker, Carl;
- Krumm, Nik;
- Shendure, Jay;
- Lockhart, Paul J;
- Scheffer, Ingrid E;
- Tervo, Raymond;
- Peeters, Hilde;
- Thompson, Elizabeth;
- Haan, Eric;
- O'Roak, Brian J;
- Fichera, Marco;
- Gécz, Jozef;
- Eichler, Evan E;
- Rosenfeld, Jill A;
- Torchia, Beth S;
- van Bon, Bregje W M;
- Vulto-van Silfhout, Anneke T;
- Vissers, Lisenka E L M
Publication type:
Article
Mutations in lectin complement pathway genes COLEC11 and MASP1 cause 3MC syndrome.
Published in:
Nature Genetics, 2011, v. 43, n. 3, p. 197, doi. 10.1038/ng.757
By:
- Rooryck, Caroline;
- Diaz-Font, Anna;
- Osborn, Daniel P. S.;
- Chabchoub, Elyes;
- Hernandez-Hernandez, Victor;
- Shamseldin, Hanan;
- Kenny, Joanna;
- Waters, Aoife;
- Jenkins, Dagan;
- Kaissi, Ali Al;
- Leal, Gabriela F.;
- Dallapiccola, Bruno;
- Carnevale, Franco;
- Bitner-Glindzicz, Maria;
- Lees, Melissa;
- Hennekam, Raoul;
- Stanier, Philip;
- Burns, Alan J.;
- Peeters, Hilde;
- Alkuraya, Fowzan S.
Publication type:
Article
Compound heterozygous loss-of-function mutations in KIF20A are associated with a novel lethal congenital cardiomyopathy in two siblings.
Published in:
PLoS Genetics, 2018, v. 14, n. 1, p. 1, doi. 10.1371/journal.pgen.1007138
By:
- Louw, Jacoba J.;
- Nunes Bastos, Ricardo;
- Chen, Xiaowen;
- Verdood, Céline;
- Corveleyn, Anniek;
- Jia, Yaojuan;
- Breckpot, Jeroen;
- Gewillig, Marc;
- Peeters, Hilde;
- Santoro, Massimo M.;
- Barr, Francis;
- Devriendt, Koenraad
Publication type:
Article
Noise-robust assessment of SNP array based CNV calls through local noise estimation of log R ratios.
Published in:
Statistical Applications in Genetics & Molecular Biology, 2018, v. 17, n. 2, p. N.PAG, doi. 10.1515/sagmb-2017-0026
By:
- Cosemans, Nele;
- Claes, Peter;
- Brison, Nathalie;
- Vermeesch, Joris Robert;
- Peeters, Hilde
Publication type:
Article
Aarskog syndrome: from prenatal features towards postnatal diagnosis.
Published in:
2011
By:
- Witters, Ingrid;
- Peeters, Hilde;
- Willekes, Christine;
- Coumans, Audrey;
- Sieprath, Peter;
- Boshoff, Derize;
- Fryns, Jean-Pierre
Publication type:
Journal Article
3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies.
Published in:
PLoS Genetics, 2021, v. 17, n. 5, p. 1, doi. 10.1371/journal.pgen.1009528
By:
- Hoskens, Hanne;
- Liu, Dongjing;
- Naqvi, Sahin;
- Lee, Myoung Keun;
- Eller, Ryan J.;
- Indencleef, Karlijne;
- White, Julie D.;
- Li, Jiarui;
- Larmuseau, Maarten H. D.;
- Hens, Greet;
- Wysocka, Joanna;
- Walsh, Susan;
- Richmond, Stephen;
- Shriver, Mark D.;
- Shaffer, John R.;
- Peeters, Hilde;
- Weinberg, Seth M.;
- Claes, Peter
Publication type:
Article
Noninvasive prenatal testing using a novel analysis pipeline to screen for all autosomal fetal aneuploidies improves pregnancy management.
Published in:
European Journal of Human Genetics, 2015, v. 23, n. 10, p. 1286, doi. 10.1038/ejhg.2014.282
By:
- Bayindir, Baran;
- Dehaspe, Luc;
- Brison, Nathalie;
- Brady, Paul;
- Ardui, Simon;
- Kammoun, Molka;
- Van der Veken, Lars;
- Lichtenbelt, Klaske;
- Van den Bogaert, Kris;
- Van Houdt, Jeroen;
- Peeters, Hilde;
- Van Esch, Hilde;
- de Ravel, Thomy;
- Legius, Eric;
- Devriendt, Koen;
- Vermeesch, Joris R
Publication type:
Article
Haploinsufficiency of ANKRD11 causes mild cognitive impairment, short stature and minor dysmorphisms.
Published in:
2012
By:
- Isrie, Mala;
- Hendriks, Yvonne;
- Gielissen, Nicole;
- Sistermans, Erik A;
- Willemsen, Marjolein H;
- Peeters, Hilde;
- Vermeesch, Joris R;
- Kleefstra, Tjitske;
- Van Esch, Hilde
Publication type:
Letter
Platelet studies in autism spectrum disorder patients and first-degree relatives.
Published in:
Molecular Autism, 2015, v. 6, p. 1, doi. 10.1186/s13229-015-0051-y
By:
- Bijl, Nora;
- Thys, Chantal;
- Wittevrongel, Christine;
- De la Marche, Wouter;
- Devriendt, Koenraad;
- Peeters, Hilde;
- Van Geet, Chris;
- Freson, Kathleen
Publication type:
Article
Toward 3D facial analysis for recognizing Mendelian causes of autism spectrum disorder.
Published in:
Clinical Genetics, 2024, v. 106, n. 5, p. 603, doi. 10.1111/cge.14595
By:
- Sleyp, Yoeri;
- Matthews, Harold S.;
- Vanneste, Michiel;
- Vandenhove, Laura;
- Delanote, Valentine;
- Hoskens, Hanne;
- Indencleef, Karlijne;
- Teule, Hanne;
- Larmuseau, Maarten H. D.;
- Steyaert, Jean;
- Devriendt, Koenraad;
- Claes, Peter;
- Peeters, Hilde
Publication type:
Article
Time trends in the natural dizygotic twinning rate.
Published in:
Human Reproduction, 2011, v. 26, n. 8, p. 2247, doi. 10.1093/humrep/der180
By:
- Derom, Catherine;
- Gielen, Marij;
- Peeters, Hilde;
- Frijns, Jean-Pierre;
- Zeegers, Maurice P.A.
Publication type:
Article
Large-scale open-source three-dimensional growth curves for clinical facial assessment and objective description of facial dysmorphism.
Published in:
Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-91465-z
By:
- Matthews, Harold S.;
- Palmer, Richard L.;
- Baynam, Gareth S.;
- Quarrell, Oliver W.;
- Klein, Ophir D.;
- Spritz, Richard A.;
- Hennekam, Raoul C.;
- Walsh, Susan;
- Shriver, Mark;
- Weinberg, Seth M.;
- Hallgrimsson, Benedikt;
- Hammond, Peter;
- Penington, Anthony J.;
- Peeters, Hilde;
- Claes, Peter D.
Publication type:
Article
Spatially Dense 3D Facial Heritability and Modules of Co-heritability in a Father-Offspring Design.
Published in:
Frontiers in Genetics, 2018, p. N.PAG, doi. 10.3389/fgene.2018.00554
By:
- Hoskens, Hanne;
- Li, Jiarui;
- Indencleef, Karlijne;
- Gors, Dorothy;
- Larmuseau, Maarten H. D.;
- Richmond, Stephen;
- Zhurov, Alexei I.;
- Hens, Greet;
- Peeters, Hilde;
- Claes, Peter
Publication type:
Article
Six NSCL/P Loci Show Associations With Normal-Range Craniofacial Variation.
Published in:
Frontiers in Genetics, 2018, p. N.PAG, doi. 10.3389/fgene.2018.00502
By:
- Indencleef, Karlijne;
- Roosenboom, Jasmien;
- Hoskens, Hanne;
- White, Julie D.;
- Shriver, Mark D.;
- Richmond, Stephen;
- Peeters, Hilde;
- Feingold, Eleanor;
- Marazita, Mary L.;
- Shaffer, John R.;
- Weinberg, Seth M.;
- Hens, Greet;
- Claes, Peter
Publication type:
Article
Homozygous and heterozygous disruptions of ANK3: at the crossroads of neurodevelopmental and psychiatric disorders.
Published in:
Human Molecular Genetics, 2013, v. 22, n. 10, p. 1960, doi. 10.1093/hmg/ddt043
By:
- Iqbal, Zafar;
- Vandeweyer, Geert;
- van der Voet, Monique;
- Waryah, Ali Muhammad;
- Zahoor, Muhammad Yasir;
- Besseling, Judith A.;
- Roca, Laura Tomas;
- Vulto-van Silfhout, Anneke T.;
- Nijhof, Bonnie;
- Kramer, Jamie M.;
- Van der Aa, Nathalie;
- Ansar, Muhammad;
- Peeters, Hilde;
- Helsmoortel, Céline;
- Gilissen, Christian;
- Vissers, Lisenka E. L. M.;
- Veltman, Joris A.;
- de Brouwer, Arjan P. M.;
- Kooy, R. Frank;
- Riazuddin, Sheikh
Publication type:
Article
Exploring attitudes and experiences with reproductive genetic carrier screening among couples seeking medically assisted reproduction: a longitudinal survey study.
Published in:
Journal of Assisted Reproduction & Genetics, 2024, v. 41, n. 2, p. 451, doi. 10.1007/s10815-023-03010-8
By:
- Van Steijvoort, Eva;
- Cassou, Mathilde;
- De Schutter, Camille;
- Dimitriadou, Eftychia;
- Peeters, Hilde;
- Peeraer, Karen;
- Matthijs, Gert;
- Borry, Pascal
Publication type:
Article
Somatic embryogenesis from mature Bambusa balcooa Roxburgh as basis for mass production of elite forestry bamboos.
Published in:
Plant Cell, Tissue & Organ Culture, 2007, v. 91, n. 2, p. 115, doi. 10.1007/s11240-007-9236-1
By:
- Koen Gillis;
- Johan Gielis;
- Hilde Peeters;
- Emmy Dhooghe;
- Jan Oprins
Publication type:
Article
Multiple pilomatricomas with somatic CTNNB1 mutations in children with constitutive mismatch repair deficiency.
Published in:
Genes, Chromosomes & Cancer, 2013, v. 52, n. 7, p. 656, doi. 10.1002/gcc.22061
By:
- Chmara, Magdalena;
- Wernstedt, Annekatrin;
- Wasag, Bartosz;
- Peeters, Hilde;
- Renard, Marleen;
- Beert, Eline;
- Brems, Hilde;
- Giner, Tina;
- Bieber, Imke;
- Hamm, Henning;
- Sciot, Raf;
- Wimmer, Katharina;
- Legius, Eric
Publication type:
Article
Interest in expanded carrier screening among individuals and couples in the general population: systematic review of the literature.
Published in:
2020
By:
- Steijvoort, Eva Van;
- Chokoshvili, Davit;
- Cannon, Jeffrey W;
- Peeters, Hilde;
- Peeraer, Karen;
- Matthijs, Gert;
- Borry, Pascal;
- Van Steijvoort, Eva;
- W Cannon, Jeffrey
Publication type:
journal article
Predicting fetoplacental chromosomal mosaicism during non-invasive prenatal testing.
Published in:
2018
By:
- Brison, Nathalie;
- Neofytou, Maria;
- Dehaspe, Luc;
- Bayindir, Baran;
- Van Den Bogaert, Kris;
- Dardour, Leila;
- Peeters, Hilde;
- Van Esch, Hilde;
- Van Buggenhout, Griet;
- Vogels, Annick;
- de Ravel, Thomy;
- Legius, Eric;
- Devriendt, Koen;
- Vermeesch, Joris R.
Publication type:
journal article
Executive functioning and local-global visual processing: candidate endophenotypes for autism spectrum disorder?
Published in:
Journal of Child Psychology, 2017, v. 58, n. 3, p. 258, doi. 10.1111/jcpp.12637
By:
- Van Eylen, Lien;
- Boets, Bart;
- Cosemans, Nele;
- Peeters, Hilde;
- Steyaert, Jean;
- Wagemans, Johan;
- Noens, Ilse
Publication type:
Article
Sesn1 is a novel gene for left–right asymmetry and mediating nodal signaling.
Published in:
Human Molecular Genetics, 2006, v. 15, n. 22, p. 3369, doi. 10.1093/hmg/ddl413
By:
- Peeters, Hilde;
- Voz, Marianne L.;
- Verschueren, Kristin;
- De Cat, Bart;
- Pendeville, Hélène;
- Thienpont, Bernard;
- Schellens, Ann;
- Belmont, John W.;
- David, Guido;
- Van De Ven, Wim J.M.;
- Fryns, Jean-Pierre;
- Gewillig, Marc;
- Huylebroeck, Danny;
- Peers, Bernard;
- Devriendt, Koen
Publication type:
Article
Increased Ca2+ signaling in NRXN1α+/− neurons derived from ASD induced pluripotent stem cells.
Published in:
Molecular Autism, 2019, v. 10, n. 1, p. 1, doi. 10.1186/s13229-019-0303-3
By:
- Avazzadeh, Sahar;
- McDonagh, Katya;
- Reilly, Jamie;
- Wang, Yanqin;
- Boomkamp, Stephanie D.;
- McInerney, Veronica;
- Krawczyk, Janusz;
- Fitzgerald, Jacqueline;
- Feerick, Niamh;
- O'Sullivan, Matthew;
- Jalali, Amirhossein;
- Forman, Eva B.;
- Lynch, Sally A.;
- Ennis, Sean;
- Cosemans, Nele;
- Peeters, Hilde;
- Dockery, Peter;
- O'Brien, Timothy;
- Quinlan, Leo R.;
- Gallagher, Louise
Publication type:
Article
Validation of a Telephone Zygosity Questionnaire in Twins of Known Zygosity.
Published in:
Behavior Genetics, 1998, v. 28, n. 3, p. 159, doi. 10.1023/A:1021416112215
By:
- Peeters, Hilde;
- Van Gestel, Sofie;
- Vlietinck, Robert;
- Derom, Catherine;
- Derom, Robert
Publication type:
Article
8p21.3 deletions are rare causes of non-syndromic autism spectrum disorder.
Published in:
Neurogenetics, 2021, v. 22, n. 3, p. 207, doi. 10.1007/s10048-021-00635-8
By:
- Cosemans, Nele;
- Maljaars, Jarymke;
- Vogels, Annick;
- Holvoet, Maureen;
- Devriendt, Koen;
- Steyaert, Jean;
- Van Den Bogaert, Kris;
- Noens, Ilse;
- Peeters, Hilde
Publication type:
Article

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