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Items: 1 to 20 of 232

1.

How can zygotes segregate entire parental genomes into distinct blastomeres? The zygote metaphase revisited.

Destouni A, Vermeesch JR.

Bioessays. 2017 Apr;39(4). doi: 10.1002/bies.201600226. Review.

PMID:
28247957
2.

Mutational Processes Shaping the Genome in Early Human Embryos.

Voet T, Vermeesch JR.

Cell. 2017 Feb 23;168(5):751-753. doi: 10.1016/j.cell.2017.02.008.

PMID:
28235191
3.

Principles guiding embryo selection following genome-wide haplotyping of preimplantation embryos.

Dimitriadou E, Melotte C, Debrock S, Esteki MZ, Dierickx K, Voet T, Devriendt K, de Ravel T, Legius E, Peeraer K, Meuleman C, Vermeesch JR.

Hum Reprod. 2017 Feb 2:1-11. doi: 10.1093/humrep/dex011. [Epub ahead of print] No abstract available.

PMID:
28158716
4.

Detecting mosaicism in trophectoderm biopsies.

Sermon KD, Spits C, Mertzanidou A, Vermeesch JR, Fiorentino F.

Hum Reprod. 2017 Jan 1. doi: 10.1093/humrep/dew346. [Epub ahead of print] No abstract available.

PMID:
28043945
5.

Detecting AGG Interruptions in Male and Female FMR1 Premutation Carriers by Single-Molecule Sequencing.

Ardui S, Race V, Zablotskaya A, Hestand MS, Van Esch H, Devriendt K, Matthijs G, Vermeesch JR.

Hum Mutat. 2017 Mar;38(3):324-331. doi: 10.1002/humu.23150.

PMID:
27883256
6.

Current controversies in prenatal diagnosis 3: industry drives innovation in research and clinical application of genetic prenatal diagnosis and screening.

Evans MI, Vermeesch JR.

Prenat Diagn. 2016 Dec;36(13):1172-1177. doi: 10.1002/pd.4967. No abstract available.

PMID:
27862087
7.

Prenatal and pre-implantation genetic diagnosis.

Vermeesch JR, Voet T, Devriendt K.

Nat Rev Genet. 2016 Sep 15;17(10):643-56. doi: 10.1038/nrg.2016.97. Review.

PMID:
27629932
8.

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.

PMID:
27584908
9.

Copy number variation analysis in adults with catatonia confirms haploinsufficiency of SHANK3 as a predisposing factor.

Breckpot J, Vercruyssen M, Weyts E, Vandevoort S, D'Haenens G, Van Buggenhout G, Leempoels L, Brischoux-Boucher E, Van Maldergem L, Renieri A, Mencarelli MA, D'Angelo C, Mericq V, Hoffer MJ, Tauber M, Molinas C, Castiglioni C, Brison N, Vermeesch JR, Danckaerts M, Sienaert P, Devriendt K, Vogels A.

Eur J Med Genet. 2016 Sep;59(9):436-43. doi: 10.1016/j.ejmg.2016.08.003.

PMID:
27519580
10.

Variant discovery and breakpoint region prediction for studying the human 22q11.2 deletion using BAC clone and whole genome sequencing analysis.

Guo X, Delio M, Haque N, Castellanos R, Hestand MS, Vermeesch JR, Morrow BE, Zheng D.

Hum Mol Genet. 2016 Sep 1;25(17):3754-3767. doi: 10.1093/hmg/ddw221.

PMID:
27436579
11.

Maternal vitamin B12 deficiency and abnormal cell-free DNA results in pregnancy.

Schuring-Blom H, Lichtenbelt K, van Galen K, Elferink M, Weiss M, Vermeesch JR, Page-Christiaens L.

Prenat Diagn. 2016 Aug;36(8):790-3. doi: 10.1002/pd.4863. No abstract available.

PMID:
27328203
12.

A catalog of hemizygous variation in 127 22q11 deletion patients.

Hestand MS, Nowakowska BA, Vergaelen E, Van Houdt J, Dehaspe L, Suhl JA, Del-Favero J, Mortier G, Zackai E, Swillen A, Devriendt K, Gur RE, McDonald-McGinn DM, Warren ST, Emanuel BS, Vermeesch JR.

Hum Genome Var. 2016 Jan 14;3:15065. doi: 10.1038/hgv.2015.65.

13.

The why, the how and the when of PGS 2.0: current practices and expert opinions of fertility specialists, molecular biologists, and embryologists.

Sermon K, Capalbo A, Cohen J, Coonen E, De Rycke M, De Vos A, Delhanty J, Fiorentino F, Gleicher N, Griesinger G, Grifo J, Handyside A, Harper J, Kokkali G, Mastenbroek S, Meldrum D, Meseguer M, Montag M, Munné S, Rienzi L, Rubio C, Scott K, Scott R, Simon C, Swain J, Treff N, Ubaldi F, Vassena R, Vermeesch JR, Verpoest W, Wells D, Geraedts J.

Mol Hum Reprod. 2016 Aug;22(8):845-57. doi: 10.1093/molehr/gaw034. Review.

PMID:
27256483
14.

Zygotes segregate entire parental genomes in distinct blastomere lineages causing cleavage-stage chimerism and mixoploidy.

Destouni A, Zamani Esteki M, Catteeuw M, Tšuiko O, Dimitriadou E, Smits K, Kurg A, Salumets A, Van Soom A, Voet T, Vermeesch JR.

Genome Res. 2016 May;26(5):567-78. doi: 10.1101/gr.200527.115.

15.

Identification of Intellectual Disability Genes in Female Patients with a Skewed X-Inactivation Pattern.

Fieremans N, Van Esch H, Holvoet M, Van Goethem G, Devriendt K, Rosello M, Mayo S, Martinez F, Jhangiani S, Muzny DM, Gibbs RA, Lupski JR, Vermeesch JR, Marynen P, Froyen G.

Hum Mutat. 2016 Aug;37(8):804-11. doi: 10.1002/humu.23012.

PMID:
27159028
16.

Reciprocal 22q11.2 Deletion and Duplication in Siblings with Karyotypically Normal Parents.

Demaerel W, Hosseinzadeh M, Nouri N, Sedghi M, Dimitriadou E, Salehi M, Abdali H, Memarzadeh M, Zamani M, Vermeesch JR.

Cytogenet Genome Res. 2016;148(1):1-5. doi: 10.1159/000445089.

PMID:
27055209
17.

A Distinct Class of Chromoanagenesis Events Characterized by Focal Copy Number Gains.

Masset H, Hestand MS, Van Esch H, Kleinfinger P, Plaisancié J, Afenjar A, Molignier R, Schluth-Bolard C, Sanlaville D, Vermeesch JR.

Hum Mutat. 2016 Jul;37(7):661-8. doi: 10.1002/humu.22984.

PMID:
26936114
18.

Polymerase specific error rates and profiles identified by single molecule sequencing.

Hestand MS, Van Houdt J, Cristofoli F, Vermeesch JR.

Mutat Res. 2016 Feb-Mar;784-785:39-45. doi: 10.1016/j.mrfmmm.2016.01.003.

PMID:
26829216
19.

Pulmonary transcriptome analysis in the surgically induced rabbit model of diaphragmatic hernia treated with fetal tracheal occlusion.

Engels AC, Brady PD, Kammoun M, Finalet Ferreiro J, DeKoninck P, Endo M, Toelen J, Vermeesch JR, Deprest J.

Dis Model Mech. 2016 Feb;9(2):221-8. doi: 10.1242/dmm.021626.

20.

Non-invasive detection of genomic imbalances in Hodgkin/Reed-Sternberg cells in early and advanced stage Hodgkin's lymphoma by sequencing of circulating cell-free DNA: a technical proof-of-principle study.

Vandenberghe P, Wlodarska I, Tousseyn T, Dehaspe L, Dierickx D, Verheecke M, Uyttebroeck A, Bechter O, Delforge M, Vandecaveye V, Brison N, Verhoef GE, Legius E, Amant F, Vermeesch JR.

Lancet Haematol. 2015 Feb;2(2):e55-65. doi: 10.1016/S2352-3026(14)00039-8.

PMID:
26687610

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