Van den Veyver IB - Search Results

1

International Society for Prenatal Diagnosis Updated Position Statement on the use of genome-wide sequencing for prenatal diagnosis.

Van den Veyver IB, Chandler N, Wilkins-Haug LE, Wapner RJ, Chitty LS; ISPD Board of Directors. Van den Veyver IB, et al. Prenat Diagn. 2022 May;42(6):796-803. doi: 10.1002/pd.6157. Prenat Diagn. 2022. PMID: 35583085 Review.

2

Comparative genomic hybridization and prenatal diagnosis.

Van den Veyver IB, Beaudet AL. Van den Veyver IB, et al. Curr Opin Obstet Gynecol. 2006 Apr;18(2):185-91. doi: 10.1097/01.gco.0000192986.22718.cc. Curr Opin Obstet Gynecol. 2006. PMID: 16601480 Review.

3

Prenatal diagnosis of chromosomal abnormalities using array-based comparative genomic hybridization.

Sahoo T, Cheung SW, Ward P, Darilek S, Patel A, del Gaudio D, Kang SH, Lalani SR, Li J, McAdoo S, Burke A, Shaw CA, Stankiewicz P, Chinault AC, Van den Veyver IB, Roa BB, Beaudet AL, Eng CM. Sahoo T, et al. Among authors: van den veyver ib. Genet Med. 2006 Nov;8(11):719-27. doi: 10.1097/01.gim.0000245576.47154.63. Genet Med. 2006. PMID: 17108764 Free article.

4

Clinical use of array comparative genomic hybridization (aCGH) for prenatal diagnosis in 300 cases.

Van den Veyver IB, Patel A, Shaw CA, Pursley AN, Kang SH, Simovich MJ, Ward PA, Darilek S, Johnson A, Neill SE, Bi W, White LD, Eng CM, Lupski JR, Cheung SW, Beaudet AL. Van den Veyver IB, et al. Prenat Diagn. 2009 Jan;29(1):29-39. doi: 10.1002/pd.2127. Prenat Diagn. 2009. PMID: 19012303 Free PMC article.

5

Genome-wide array-based copy number profiling in human placentas from unexplained stillbirths.

Harris RA, Ferrari F, Ben-Shachar S, Wang X, Saade G, Van Den Veyver I, Facchinetti F, Aagaard-Tillery K. Harris RA, et al. Prenat Diagn. 2011 Oct;31(10):932-44. doi: 10.1002/pd.2817. Epub 2011 Jul 5. Prenat Diagn. 2011. PMID: 21732394 Free PMC article.

6

Multiplex ligation-dependent probe amplification (MLPA) and prenatal diagnosis.

Willis AS, van den Veyver I, Eng CM. Willis AS, et al. Prenat Diagn. 2012 Apr;32(4):315-20. doi: 10.1002/pd.3860. Prenat Diagn. 2012. PMID: 22467161 Review.

7

Prenatal chromosomal microarray analysis in a diagnostic laboratory; experience with >1000 cases and review of the literature.

Breman A, Pursley AN, Hixson P, Bi W, Ward P, Bacino CA, Shaw C, Lupski JR, Beaudet A, Patel A, Cheung SW, Van den Veyver I. Breman A, et al. Prenat Diagn. 2012 Apr;32(4):351-61. doi: 10.1002/pd.3861. Prenat Diagn. 2012. PMID: 22467166 Review.

8

Detection of ≥1Mb microdeletions and microduplications in a single cell using custom oligonucleotide arrays.

Bi W, Breman A, Shaw CA, Stankiewicz P, Gambin T, Lu X, Cheung SW, Jackson LG, Lupski JR, Van den Veyver IB, Beaudet AL. Bi W, et al. Among authors: van den veyver ib. Prenat Diagn. 2012 Jan;32(1):10-20. doi: 10.1002/pd.2855. Prenat Diagn. 2012. PMID: 22470934

9

Current controversies in prenatal diagnosis 2: should incidental findings arising from prenatal testing always be reported to patients?

Bui TH, Raymond FL, Van den Veyver IB. Bui TH, et al. Among authors: van den veyver ib. Prenat Diagn. 2014 Jan;34(1):12-7. doi: 10.1002/pd.4275. Epub 2013 Dec 5. Prenat Diagn. 2014. PMID: 24214820 No abstract available.

10

Noninvasive prenatal screening by next-generation sequencing.

Gregg AR, Van den Veyver IB, Gross SJ, Madankumar R, Rink BD, Norton ME. Gregg AR, et al. Among authors: van den veyver ib. Annu Rev Genomics Hum Genet. 2014;15:327-47. doi: 10.1146/annurev-genom-090413-025341. Epub 2014 May 14. Annu Rev Genomics Hum Genet. 2014. PMID: 24849140 Review.

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