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Items: 1 to 50 of 252

1.

Fecal microbiota transplantation in ulcerative colitis.

Blanchaert C, Strubbe B, Peeters H.

Acta Gastroenterol Belg. 2019 Oct-Dec;82(4):519-528. Review.

PMID:
31950808
2.

The clinical relevance of intragenic NRXN1 deletions.

Cosemans N, Vandenhove L, Vogels A, Devriendt K, Van Esch H, Van Buggenhout G, Olivié H, de Ravel T, Ortibus E, Legius E, Aerssens P, Breckpot J, R Vermeesch J, Shen S, Fitzgerald J, Gallagher L, Peeters H.

J Med Genet. 2020 Jan 13. pii: jmedgenet-2019-106448. doi: 10.1136/jmedgenet-2019-106448. [Epub ahead of print]

PMID:
31932357
3.

Increased Ca2+ signaling in NRXN1α +/- neurons derived from ASD induced pluripotent stem cells.

Avazzadeh S, McDonagh K, Reilly J, Wang Y, Boomkamp SD, McInerney V, Krawczyk J, Fitzgerald J, Feerick N, O'Sullivan M, Jalali A, Forman EB, Lynch SA, Ennis S, Cosemans N, Peeters H, Dockery P, O'Brien T, Quinlan LR, Gallagher L, Shen S.

Mol Autism. 2019 Dec 30;10:52. doi: 10.1186/s13229-019-0303-3. eCollection 2019.

4.

Belgian IBD Research Group (BIRD) Position Statement 2019 on the Use of Adalimumab Biosimilars in Inflammatory Bowel Diseases.

Somers M, Bossuyt P, Ferrante M, Peeters H, Baert F; for BIRD (Belgian IBD Research and Development).

J Crohns Colitis. 2019 Dec 26. pii: jjz209. doi: 10.1093/ecco-jcc/jjz209. [Epub ahead of print]

PMID:
31875891
5.

Beclomethasone dipropionate in microscopic colitis: Results of an exploratory open-label multicentre study (COLCO).

Corte T, Janssens E, D'Hondt A, Thorrez K, Arts J, Dejaegher K, D'Heygere F, Holvoet A, van Besien B, Harlet L, Peeters H, Moerkercke WV, Baert F.

United European Gastroenterol J. 2019 Nov;7(9):1183-1188. doi: 10.1177/2050640619860965. Epub 2019 Jul 12.

6.

Monoclonal gammopathy of renal significance (MGRS) histopathologic classification, diagnostic workup, and therapeutic options.

Amaador K, Peeters H, Minnema MC, Nguyen TQ, Dendooven A, Vos JMI, Croockewit AJ, van de Donk NWCJ, Jacobs JFM, Wetzels JFM, Sprangers B, Abrahams AC.

Neth J Med. 2019 Sep;77(7):243-254.

7.

The East Flanders Prospective Twin Survey (EFPTS): 55 Years Later.

Derom C, Thiery E, Rutten BPF, Peeters H, Gielen M, Bijnens E, Vlietinck R, Weyers S.

Twin Res Hum Genet. 2019 Sep 9:1-6. doi: 10.1017/thg.2019.64. [Epub ahead of print]

PMID:
31496455
8.

Measuring the Pancreatic β Cell Mass in Vivo with Exendin SPECT during Hyperglycemia and Severe Insulitis.

Joosten L, Brom M, Peeters H, Bos D, Himpe E, Bouwens L, Boerman O, Gotthardt M.

Mol Pharm. 2019 Sep 3;16(9):4024-4030. doi: 10.1021/acs.molpharmaceut.9b00728. Epub 2019 Aug 8.

PMID:
31345042
9.

[Adolescent with a schizophreniform disorder and recurrent 16p11.2 duplication].

Castelein L, Steyaert J, Peeters H, van Buggenhout G.

Tijdschr Psychiatr. 2019;61(6):421-425. Dutch.

10.

Maternal copy-number variations in the DMD gene as secondary findings in noninvasive prenatal screening.

Brison N, Storms J, Villela D, Claeys KG, Dehaspe L, de Ravel T, De Waele L, Goemans N, Legius E, Peeters H, Van Esch H, Race V, Robert Vermeesch J, Devriendt K, Van Den Bogaert K.

Genet Med. 2019 Dec;21(12):2774-2780. doi: 10.1038/s41436-019-0564-4. Epub 2019 Jun 14.

PMID:
31197268
11.

Long-term Clinical Effectiveness of Ustekinumab in Patients with Crohn's Disease Who Failed Biologic Therapies: A National Cohort Study.

Liefferinckx C, Verstockt B, Gils A, Noman M, Van Kemseke C, Macken E, De Vos M, Van Moerkercke W, Rahier JF, Bossuyt P, Dutré J, Humblet E, Staessen D, Peeters H, Van Hootegem P, Louis E, Franchimont D, Baert F, Vermeire S; Belgian Inflammatory Bowel Disease Research and Development Group [BIRD group].

J Crohns Colitis. 2019 Oct 28;13(11):1401-1409. doi: 10.1093/ecco-jcc/jjz080.

PMID:
30989232
12.

Spatially Dense 3D Facial Heritability and Modules of Co-heritability in a Father-Offspring Design.

Hoskens H, Li J, Indencleef K, Gors D, Larmuseau MHD, Richmond S, Zhurov AI, Hens G, Peeters H, Claes P.

Front Genet. 2018 Nov 19;9:554. doi: 10.3389/fgene.2018.00554. eCollection 2018.

13.

Six NSCL/P Loci Show Associations With Normal-Range Craniofacial Variation.

Indencleef K, Roosenboom J, Hoskens H, White JD, Shriver MD, Richmond S, Peeters H, Feingold E, Marazita ML, Shaffer JR, Weinberg SM, Hens G, Claes P.

Front Genet. 2018 Oct 25;9:502. doi: 10.3389/fgene.2018.00502. eCollection 2018.

14.

NFIB Haploinsufficiency Is Associated with Intellectual Disability and Macrocephaly.

Schanze I, Bunt J, Lim JWC, Schanze D, Dean RJ, Alders M, Blanchet P, Attié-Bitach T, Berland S, Boogert S, Boppudi S, Bridges CJ, Cho MT, Dobyns WB, Donnai D, Douglas J, Earl DL, Edwards TJ, Faivre L, Fregeau B, Genevieve D, Gérard M, Gatinois V, Holder-Espinasse M, Huth SF, Izumi K, Kerr B, Lacaze E, Lakeman P, Mahida S, Mirzaa GM, Morgan SM, Nowak C, Peeters H, Petit F, Pilz DT, Puechberty J, Reinstein E, Rivière JB, Santani AB, Schneider A, Sherr EH, Smith-Hicks C, Wieland I, Zackai E, Zhao X, Gronostajski RM, Zenker M, Richards LJ.

Am J Hum Genet. 2018 Nov 1;103(5):752-768. doi: 10.1016/j.ajhg.2018.10.006.

15.

Olfactory function in patients with nonsyndromic orofacial clefts and their unaffected relatives.

Roosenboom J, Hermans R, Lammens F, Samain JL, Devriendt K, Vander Poorten V, Hellings PW, Jorissen M, Peeters H, Claes P, Hens G.

Am J Med Genet A. 2018 Nov;176(11):2375-2381. doi: 10.1002/ajmg.a.40348. Epub 2018 Oct 22.

PMID:
30345654
16.

Intra-individual comparison of gadolinium-enhanced MRI using pseudo-golden-angle radial acquisition with gadoxetic acid-enhanced MRI for diagnosis of HCCs using LI-RADS.

Kim YC, Min JH, Kim YK, Lee SJ, Ahn S, Kim E, Peeters H.

Eur Radiol. 2019 Apr;29(4):2058-2068. doi: 10.1007/s00330-018-5771-x. Epub 2018 Oct 15.

PMID:
30324388
17.

A comprehensive clinical and genetic study in 127 patients with ID in Kinshasa, DR Congo.

Lumaka A, Race V, Peeters H, Corveleyn A, Coban-Akdemir Z, Jhangiani SN, Song X, Mubungu G, Posey J, Lupski JR, Vermeesch JR, Lukusa P, Devriendt K.

Am J Med Genet A. 2018 Sep;176(9):1897-1909. doi: 10.1002/ajmg.a.40382. Epub 2018 Aug 8.

18.

Validation of 111In-Exendin SPECT for the Determination of the β-Cell Mass in BioBreeding Diabetes-Prone Rats.

Brom M, Joosten L, Frielink C, Peeters H, Bos D, van Zanten M, Boerman O, Gotthardt M.

Diabetes. 2018 Oct;67(10):2012-2018. doi: 10.2337/db17-1312. Epub 2018 Jul 25.

19.

Usefulness of fragile X checklist and CGG distribution in specialized institutions in Kinshasa, DR Congo.

Lumaka A, Lubala TK, Race V, Peeters H, Lukusa P, Devriendt K.

J Community Genet. 2019 Jan;10(1):153-159. doi: 10.1007/s12687-018-0374-4. Epub 2018 Jul 4.

20.

Noise-robust assessment of SNP array based CNV calls through local noise estimation of log R ratios.

Cosemans N, Claes P, Brison N, Vermeesch JR, Peeters H.

Stat Appl Genet Mol Biol. 2018 Apr 28;17(2). pii: /j/sagmb.2018.17.issue-2/sagmb-2017-0026/sagmb-2017-0026.xml. doi: 10.1515/sagmb-2017-0026.

PMID:
29708886
21.

The ethics of patenting autism genes.

Hens K, Noens I, Peeters H, Steyaert J.

Nat Rev Genet. 2018 May;19(5):247-248. doi: 10.1038/nrg.2018.17. Epub 2018 Mar 26. No abstract available.

PMID:
29576616
22.

Efficacy of switching to infliximab in patients with Crohn's disease with loss of response to adalimumab.

Peeters H, Louis E, Baert F, Dewit O, Coche JC, Ferrante M, Lambrecht G, Colard A, Van Gossum A, Bossuyt P, Moreels T, Vander Cruyssen B, Gils A, De Vos M.

Acta Gastroenterol Belg. 2018 Jan-Mar;81(1):15-21.

23.

ZNF462 and KLF12 are disrupted by a de novo translocation in a patient with syndromic intellectual disability and autism spectrum disorder.

Cosemans N, Vandenhove L, Maljaars J, Van Esch H, Devriendt K, Baldwin A, Fryns JP, Noens I, Peeters H.

Eur J Med Genet. 2018 Jul;61(7):376-383. doi: 10.1016/j.ejmg.2018.02.002. Epub 2018 Feb 7.

PMID:
29427787
24.

Predicting fetoplacental chromosomal mosaicism during non-invasive prenatal testing.

Brison N, Neofytou M, Dehaspe L, Bayindir B, Van Den Bogaert K, Dardour L, Peeters H, Van Esch H, Van Buggenhout G, Vogels A, de Ravel T, Legius E, Devriendt K, Vermeesch JR.

Prenat Diagn. 2018 Mar;38(4):258-266. doi: 10.1002/pd.5223. Epub 2018 Feb 19.

PMID:
29388226
25.

EGFRvIII expression triggers a metabolic dependency and therapeutic vulnerability sensitive to autophagy inhibition.

Jutten B, Keulers TG, Peeters HJM, Schaaf MBE, Savelkouls KGM, Compter I, Clarijs R, Schijns OEMG, Ackermans L, Teernstra OPM, Zonneveld MI, Colaris RME, Dubois L, Vooijs MA, Bussink J, Sotelo J, Theys J, Lammering G, Rouschop KMA.

Autophagy. 2018;14(2):283-295. doi: 10.1080/15548627.2017.1409926. Epub 2018 Jan 29.

26.

Compound heterozygous loss-of-function mutations in KIF20A are associated with a novel lethal congenital cardiomyopathy in two siblings.

Louw JJ, Nunes Bastos R, Chen X, Verdood C, Corveleyn A, Jia Y, Breckpot J, Gewillig M, Peeters H, Santoro MM, Barr F, Devriendt K.

PLoS Genet. 2018 Jan 22;14(1):e1007138. doi: 10.1371/journal.pgen.1007138. eCollection 2018 Jan.

27.

Enhanced Specific Activity by Multichelation of Exendin-3 Leads To Improved Image Quality and In Vivo Beta Cell Imaging.

Joosten L, Brom M, Peeters H, Heskamp S, Béhé M, Boerman O, Gotthardt M.

Mol Pharm. 2018 Feb 5;15(2):486-494. doi: 10.1021/acs.molpharmaceut.7b00853. Epub 2017 Dec 21.

28.

A case of regional migratory osteoporosis.

Spierings J, Bours S, Peeters HRM.

Osteoporos Int. 2018 Feb;29(2):507-510. doi: 10.1007/s00198-017-4240-8. Epub 2017 Oct 24.

29.

Testing the face shape hypothesis in twins discordant for nonsyndromic orofacial clefting.

Roosenboom J, Indencleef K, Hens G, Peeters H, Christensen K, Marazita ML, Claes P, Leslie EJ, Weinberg SM.

Am J Med Genet A. 2017 Nov;173(11):2886-2892. doi: 10.1002/ajmg.a.38471. Epub 2017 Sep 8.

30.

Long-term Outcomes with Anti-TNF Therapy and Accelerated Step-up in the Prospective Pediatric Belgian Crohn's Disease Registry (BELCRO).

Wauters L, Smets F, De Greef E, Bontems P, Hoffman I, Hauser B, Alliet P, Arts W, Peeters H, Van Biervliet S, Paquot I, Van de Vijver E, De Vos M, Bossuyt P, Rahier JF, Dewit O, Moreels T, Franchimont D, Muls V, Fontaine F, Louis E, Coche JC, Baert F, Paul J, Vermeire S, Veereman G.

Inflamm Bowel Dis. 2017 Sep;23(9):1584-1591. doi: 10.1097/MIB.0000000000001193.

31.

Hotspots of missense mutation identify neurodevelopmental disorder genes and functional domains.

Geisheker MR, Heymann G, Wang T, Coe BP, Turner TN, Stessman HAF, Hoekzema K, Kvarnung M, Shaw M, Friend K, Liebelt J, Barnett C, Thompson EM, Haan E, Guo H, Anderlid BM, Nordgren A, Lindstrand A, Vandeweyer G, Alberti A, Avola E, Vinci M, Giusto S, Pramparo T, Pierce K, Nalabolu S, Michaelson JJ, Sedlacek Z, Santen GWE, Peeters H, Hakonarson H, Courchesne E, Romano C, Kooy RF, Bernier RA, Nordenskjöld M, Gecz J, Xia K, Zweifel LS, Eichler EE.

Nat Neurosci. 2017 Aug;20(8):1043-1051. doi: 10.1038/nn.4589. Epub 2017 Jun 19.

32.

Variants in TTC25 affect autistic trait in patients with autism spectrum disorder and general population.

Vojinovic D, Brison N, Ahmad S, Noens I, Pappa I, Karssen LC, Tiemeier H, van Duijn CM, Peeters H, Amin N.

Eur J Hum Genet. 2017 Aug;25(8):982-987. doi: 10.1038/ejhg.2017.82. Epub 2017 May 17.

33.

Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases.

Stessman HA, Xiong B, Coe BP, Wang T, Hoekzema K, Fenckova M, Kvarnung M, Gerdts J, Trinh S, Cosemans N, Vives L, Lin J, Turner TN, Santen G, Ruivenkamp C, Kriek M, van Haeringen A, Aten E, Friend K, Liebelt J, Barnett C, Haan E, Shaw M, Gecz J, Anderlid BM, Nordgren A, Lindstrand A, Schwartz C, Kooy RF, Vandeweyer G, Helsmoortel C, Romano C, Alberti A, Vinci M, Avola E, Giusto S, Courchesne E, Pramparo T, Pierce K, Nalabolu S, Amaral DG, Scheffer IE, Delatycki MB, Lockhart PJ, Hormozdiari F, Harich B, Castells-Nobau A, Xia K, Peeters H, Nordenskjöld M, Schenck A, Bernier RA, Eichler EE.

Nat Genet. 2017 Apr;49(4):515-526. doi: 10.1038/ng.3792. Epub 2017 Feb 13.

34.

Facial dysmorphism is influenced by ethnic background of the patient and of the evaluator.

Lumaka A, Cosemans N, Lulebo Mampasi A, Mubungu G, Mvuama N, Lubala T, Mbuyi-Musanzayi S, Breckpot J, Holvoet M, de Ravel T, Van Buggenhout G, Peeters H, Donnai D, Mutesa L, Verloes A, Lukusa Tshilobo P, Devriendt K.

Clin Genet. 2017 Aug;92(2):166-171. doi: 10.1111/cge.12948. Epub 2017 Jan 16.

PMID:
27925162
35.

Executive functioning and local-global visual processing: candidate endophenotypes for autism spectrum disorder?

Van Eylen L, Boets B, Cosemans N, Peeters H, Steyaert J, Wagemans J, Noens I.

J Child Psychol Psychiatry. 2017 Mar;58(3):258-269. doi: 10.1111/jcpp.12637. Epub 2016 Nov 2.

PMID:
27804132
36.

Accuracy and clinical value of maternal incidental findings during noninvasive prenatal testing for fetal aneuploidies.

Brison N, Van Den Bogaert K, Dehaspe L, van den Oever JM, Janssens K, Blaumeiser B, Peeters H, Van Esch H, Van Buggenhout G, Vogels A, de Ravel T, Legius E, Devriendt K, Vermeesch JR.

Genet Med. 2017 Mar;19(3):306-313. doi: 10.1038/gim.2016.113. Epub 2016 Sep 1.

PMID:
27584908
37.

Genetic testing and counseling in the case of an autism diagnosis: A caregivers perspective.

Hens K, Peeters H, Dierickx K.

Eur J Med Genet. 2016 Sep;59(9):452-8. doi: 10.1016/j.ejmg.2016.08.007. Epub 2016 Aug 17.

PMID:
27544064
38.

CREBBP mutations in individuals without Rubinstein-Taybi syndrome phenotype.

Menke LA, van Belzen MJ, Alders M, Cristofoli F; DDD Study, Ehmke N, Fergelot P, Foster A, Gerkes EH, Hoffer MJ, Horn D, Kant SG, Lacombe D, Leon E, Maas SM, Melis D, Muto V, Park SM, Peeters H, Peters DJ, Pfundt R, van Ravenswaaij-Arts CM, Tartaglia M, Hennekam RC.

Am J Med Genet A. 2016 Oct;170(10):2681-93. doi: 10.1002/ajmg.a.37800. Epub 2016 Jun 17.

PMID:
27311832
39.

The ethics of complexity. Genetics and autism, a literature review.

Hens K, Peeters H, Dierickx K.

Am J Med Genet B Neuropsychiatr Genet. 2016 Apr;171B(3):305-16. doi: 10.1002/ajmg.b.32432. Epub 2016 Feb 12. Review.

PMID:
26870917
40.

Shooting a moving target. Researching autism genes: An interview study with professionals.

Hens K, Peeters H, Dierickx K.

Eur J Med Genet. 2016 Jan;59(1):32-8. doi: 10.1016/j.ejmg.2015.12.009. Epub 2015 Dec 23.

PMID:
26721322
41.

Review: Facial endophenotypes in non-syndromic orofacial clefting.

Roosenboom J, Claes P, Devriendt K, Dormaar T, Peeters H, Saey I, Schoenaers J, Vander Poorten V, Verdonck A, Hens G.

B-ENT. 2015;11(3):173-82. Review.

PMID:
26601549
42.

Platelet studies in autism spectrum disorder patients and first-degree relatives.

Bijl N, Thys C, Wittevrongel C, De la Marche W, Devriendt K, Peeters H, Van Geet C, Freson K.

Mol Autism. 2015 Oct 23;6:57. doi: 10.1186/s13229-015-0051-y. eCollection 2015.

43.

The Influence of Microdeletions and Microduplications of 16p11.2 on Global Transcription Profiles.

Kusenda M, Vacic V, Malhotra D, Rodgers L, Pavon K, Meth J, Kumar RA, Christian SL, Peeters H, Cho SS, Addington A, Rapoport JL, Sebat J.

J Child Neurol. 2015 Dec;30(14):1947-53. doi: 10.1177/0883073815602066. Epub 2015 Sep 20.

44.

GABARAPL1 is required for increased EGFR membrane expression during hypoxia.

Keulers TG, Schaaf MB, Peeters HJ, Savelkouls KG, Vooijs MA, Bussink J, Jutten B, Rouschop KM.

Radiother Oncol. 2015 Sep;116(3):417-22. doi: 10.1016/j.radonc.2015.06.023. Epub 2015 Jul 8.

PMID:
26164772
45.

Facial Characteristics and Olfactory Dysfunction: Two Endophenotypes Related to Nonsyndromic Cleft Lip and/or Palate.

Roosenboom J, Saey I, Peeters H, Devriendt K, Claes P, Hens G.

Biomed Res Int. 2015;2015:863429. doi: 10.1155/2015/863429. Epub 2015 May 6.

46.

Clinical implementation of NIPT - technical and biological challenges.

Brady P, Brison N, Van Den Bogaert K, de Ravel T, Peeters H, Van Esch H, Devriendt K, Legius E, Vermeesch JR.

Clin Genet. 2016 May;89(5):523-30. doi: 10.1111/cge.12598. Epub 2015 May 4. Review.

PMID:
25867715
47.

Canonical autophagy does not contribute to cellular radioresistance.

Schaaf MB, Jutten B, Keulers TG, Savelkouls KG, Peeters HJ, van den Beucken T, van Schooten FJ, Godschalk RW, Vooijs M, Rouschop KM.

Radiother Oncol. 2015 Mar;114(3):406-12. doi: 10.1016/j.radonc.2015.02.019. Epub 2015 Mar 13.

PMID:
25779723
48.

Homozygous missense mutation in STYXL1 associated with moderate intellectual disability, epilepsy and behavioural complexities.

Isrie M, Zamani Esteki M, Peeters H, Voet T, Van Houdt J, Van Paesschen W, Van Esch H.

Eur J Med Genet. 2015 Apr;58(4):205-10. doi: 10.1016/j.ejmg.2015.02.006. Epub 2015 Feb 24.

PMID:
25724587
49.

Disruptive de novo mutations of DYRK1A lead to a syndromic form of autism and ID.

van Bon BW, Coe BP, Bernier R, Green C, Gerdts J, Witherspoon K, Kleefstra T, Willemsen MH, Kumar R, Bosco P, Fichera M, Li D, Amaral D, Cristofoli F, Peeters H, Haan E, Romano C, Mefford HC, Scheffer I, Gecz J, de Vries BB, Eichler EE.

Mol Psychiatry. 2016 Jan;21(1):126-32. doi: 10.1038/mp.2015.5. Epub 2015 Feb 24.

50.

Noninvasive prenatal testing using a novel analysis pipeline to screen for all autosomal fetal aneuploidies improves pregnancy management.

Bayindir B, Dehaspe L, Brison N, Brady P, Ardui S, Kammoun M, Van der Veken L, Lichtenbelt K, Van den Bogaert K, Van Houdt J, Peeters H, Van Esch H, de Ravel T, Legius E, Devriendt K, Vermeesch JR.

Eur J Hum Genet. 2015 Oct;23(10):1286-93. doi: 10.1038/ejhg.2014.282. Epub 2015 Jan 14.

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