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Results: 1 to 20 of 277

1.

Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening. Summary and recommendations.

Dondorp W, de Wert G, Bombard Y, Bianchi DW, Bergmann C, Borry P, Chitty LS, Fellmann F, Forzano F, Hall A, Henneman L, Howard HC, Lucassen A, Ormond K, Peterlin B, Radojkovic D, Rogowski W, Soller M, Tibben A, Tranebjærg L, van El CG, Cornel MC.

Eur J Hum Genet. 2015 Apr 1. doi: 10.1038/ejhg.2015.56. [Epub ahead of print] No abstract available.

PMID:
25828867
2.

Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening.

Dondorp W, de Wert G, Bombard Y, Bianchi DW, Bergmann C, Borry P, Chitty LS, Fellmann F, Forzano F, Hall A, Henneman L, Howard HC, Lucassen A, Ormond K, Peterlin B, Radojkovic D, Rogowski W, Soller M, Tibben A, Tranebjærg L, van El CG, Cornel MC.

Eur J Hum Genet. 2015 Mar 18. doi: 10.1038/ejhg.2015.57. [Epub ahead of print]

PMID:
25782669
3.

The pathway not taken: understanding 'omics data in the perinatal context.

Edlow AG, Slonim DK, Wick HC, Hui L, Bianchi DW.

Am J Obstet Gynecol. 2015 Mar 12. pii: S0002-9378(15)00243-4. doi: 10.1016/j.ajog.2015.03.023. [Epub ahead of print]

PMID:
25772209
4.

The Amniotic Fluid Transcriptome as a Guide to Understanding Fetal Disease.

Zwemer LM, Bianchi DW.

Cold Spring Harb Perspect Med. 2015 Feb 13;5(4). pii: a023101. doi: 10.1101/cshperspect.a023101. Review.

PMID:
25680981
5.

CSAX: Characterizing Systematic Anomalies in eXpression Data.

Noto K, Majidi S, Edlow AG, Wick HC, Bianchi DW, Slonim DK.

J Comput Biol. 2015 Feb 4. [Epub ahead of print]

PMID:
25651392
6.
7.

In case you missed it: the Prenatal Diagnosis editors bring you the most significant advances of 2014.

Faas BH, Ghidini A, Van Mieghem T, Chitty LS, Deprest J, Bianchi DW.

Prenat Diagn. 2015 Jan;35(1):29-34. doi: 10.1002/pd.4551. No abstract available.

PMID:
25594313
8.

Fetal sex chromosome testing by maternal plasma DNA sequencing: clinical laboratory experience and biology.

Bianchi DW, Parsa S, Bhatt S, Halks-Miller M, Kurtzman K, Sehnert AJ, Swanson A.

Obstet Gynecol. 2015 Feb;125(2):375-82. doi: 10.1097/AOG.0000000000000637.

PMID:
25568992
9.

Current controversies in prenatal diagnosis 1: NIPT for chromosome abnormalities should be offered to women with low a priori risk.

Van Lith JM, Faas BH, Bianchi DW.

Prenat Diagn. 2015 Jan;35(1):8-14. doi: 10.1002/pd.4530.

PMID:
25393690
10.

DNA sequencing versus standard prenatal aneuploidy screening.

Bianchi DW, Rava RP, Sehnert AJ.

N Engl J Med. 2014 Aug 7;371(6):578. doi: 10.1056/NEJMc1405486. No abstract available.

11.

The 2013 Malcolm Ferguson-Smith Young Investigator Award.

Bianchi DW, Chitty LS, Deprest J, Faas BH, Ghidini A, Cousens RK.

Prenat Diagn. 2014 Aug;34(8):717-8. doi: 10.1002/pd.4440. No abstract available.

PMID:
25087736
12.

Analysis of adult cerebral cortex and hippocampus transcriptomes reveals unique molecular changes in the Ts1Cje mouse model of down syndrome.

Guedj F, Pennings JL, Wick HC, Bianchi DW.

Brain Pathol. 2015 Jan;25(1):11-23. doi: 10.1111/bpa.12151. Epub 2014 Jul 25.

PMID:
24916381
13.

RNA-Seq and expression microarray highlight different aspects of the fetal amniotic fluid transcriptome.

Zwemer LM, Hui L, Wick HC, Bianchi DW.

Prenat Diagn. 2014 Oct;34(10):1006-14. doi: 10.1002/pd.4417. Epub 2014 Jun 29.

PMID:
24852236
14.

Amniotic fluid RNA gene expression profiling provides insights into the phenotype of Turner syndrome.

Massingham LJ, Johnson KL, Scholl TM, Slonim DK, Wick HC, Bianchi DW.

Hum Genet. 2014 Sep;133(9):1075-82. doi: 10.1007/s00439-014-1448-y. Epub 2014 May 22.

PMID:
24850140
15.

Antenatal noninvasive DNA testing: clinical experience and impact.

Ferres MA, Hui L, Bianchi DW.

Am J Perinatol. 2014 Aug;31(7):577-82. doi: 10.1055/s-0034-1371706. Epub 2014 Mar 28. Review.

PMID:
24683075
16.

Prenatal treatment of Down syndrome: a reality?

Guedj F, Bianchi DW, Delabar JM.

Curr Opin Obstet Gynecol. 2014 Apr;26(2):92-103. doi: 10.1097/GCO.0000000000000056. Review.

PMID:
24573065
17.

DNA sequencing versus standard prenatal aneuploidy screening.

Bianchi DW, Parker RL, Wentworth J, Madankumar R, Saffer C, Das AF, Craig JA, Chudova DI, Devers PL, Jones KW, Oliver K, Rava RP, Sehnert AJ; CARE Study Group.

N Engl J Med. 2014 Feb 27;370(9):799-808. doi: 10.1056/NEJMoa1311037.

18.

Maternal obesity affects fetal neurodevelopmental and metabolic gene expression: a pilot study.

Edlow AG, Vora NL, Hui L, Wick HC, Cowan JM, Bianchi DW.

PLoS One. 2014 Feb 18;9(2):e88661. doi: 10.1371/journal.pone.0088661. eCollection 2014.

19.

DFLAT: functional annotation for human development.

Wick HC, Drabkin H, Ngu H, Sackman M, Fournier C, Haggett J, Blake JA, Bianchi DW, Slonim DK.

BMC Bioinformatics. 2014 Feb 7;15:45. doi: 10.1186/1471-2105-15-45.

20.

Review: cell-free fetal DNA in the maternal circulation as an indication of placental health and disease.

Taglauer ES, Wilkins-Haug L, Bianchi DW.

Placenta. 2014 Feb;35 Suppl:S64-8. doi: 10.1016/j.placenta.2013.11.014. Epub 2013 Dec 1. Review.

PMID:
24388429
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