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Items: 1 to 50 of 324

1.

In case you missed it: The Prenatal Diagnosis editors bring you the most significant advances of 2018.

Ghidini A, Bianchi DW, Levy B, Van Mieghem T, Deprest J, Chitty LS.

Prenat Diagn. 2018 Dec 28. doi: 10.1002/pd.5407. [Epub ahead of print] No abstract available.

PMID:
30593668
2.

Neuroethics for the National Institutes of Health BRAIN Initiative.

Bianchi DW, Cooper JA, Gordon JA, Heemskerk J, Hodes R, Koob GF, Koroshetz WJ, Shurtleff D, Sieving PA, Volkow ND, Churchill JD, Ramos KM.

J Neurosci. 2018 Dec 12;38(50):10583-10585. doi: 10.1523/JNEUROSCI.2091-18.2018. No abstract available.

3.

Current controversies in prenatal diagnosis 2: NIPT results suggesting maternal cancer should always be disclosed.

Benn P, Plon SE, Bianchi DW.

Prenat Diagn. 2018 Nov 6. doi: 10.1002/pd.5379. [Epub ahead of print] No abstract available.

PMID:
30398677
4.

Disorganized Patterns of Sulcal Position in Fetal Brains with Agenesis of Corpus Callosum.

Tarui T, Madan N, Farhat N, Kitano R, Ceren Tanritanir A, Graham G, Gagoski B, Craig A, Rollins CK, Ortinau C, Iyer V, Pienaar R, Bianchi DW, Grant PE, Im K.

Cereb Cortex. 2018 Sep 1;28(9):3192-3203. doi: 10.1093/cercor/bhx191.

PMID:
30124828
5.

Characterization of three ciliopathy pedigrees expands the phenotype associated with biallelic C2CD3 variants.

Boczek NJ, Hopp K, Benoit L, Kraft D, Cousin MA, Blackburn PR, Madsen CD, Oliver GR, Nair AA, Na J, Bianchi DW, Beek G, Harris PC, Pichurin P, Klee EW.

Eur J Hum Genet. 2018 Dec;26(12):1797-1809. doi: 10.1038/s41431-018-0222-3. Epub 2018 Aug 10.

PMID:
30097616
6.

Sequencing of Circulating Cell-free DNA during Pregnancy.

Bianchi DW, Chiu RWK.

N Engl J Med. 2018 Aug 2;379(5):464-473. doi: 10.1056/NEJMra1705345. Review. No abstract available.

PMID:
30067923
7.

The 2017 Malcolm Ferguson-Smith Young Investigator Award.

Bianchi DW, Ghidini A, Levy B, Deprest J, Van Mieghem T, Chitty LS, McLean-Inglis AJL.

Prenat Diagn. 2018 Jun 27. doi: 10.1002/pd.5289. [Epub ahead of print] No abstract available.

PMID:
29952009
8.

The Inadvertent Discovery of Human Fetal Cell Microchimerism.

Bianchi DW.

Clin Chem. 2018 Sep;64(9):1400-1401. doi: 10.1373/clinchem.2017.273474. Epub 2018 Jun 25. Review. No abstract available.

PMID:
29941471
9.

Research on Underrepresented Populations-Reply.

Spong CY, Bianchi DW.

JAMA. 2018 May 15;319(19):2045. doi: 10.1001/jama.2018.4098. No abstract available.

PMID:
29800209
10.

Lifespan analysis of brain development, gene expression and behavioral phenotypes in the Ts1Cje, Ts65Dn and Dp(16)1/Yey mouse models of Down syndrome.

Aziz NM, Guedj F, Pennings JLA, Olmos-Serrano JL, Siegel A, Haydar TF, Bianchi DW.

Dis Model Mech. 2018 Jun 12;11(6). pii: dmm031013. doi: 10.1242/dmm.031013.

11.

Biological explanations for discordant noninvasive prenatal test results: Preliminary data and lessons learned.

Wilkins-Haug L, Zhang C, Cerveira E, Ryan M, Mil-Homens A, Zhu Q, Reddi H, Lee C, Bianchi DW.

Prenat Diagn. 2018 May;38(6):445-458. doi: 10.1002/pd.5260.

PMID:
29633279
12.

Association of National Institute of Child Health and Human Development Career Development Awards With Subsequent Research Project Grant Funding.

Twombly DA, Glavin SL, Guimond J, Taymans S, Spong CY, Bianchi DW.

JAMA Pediatr. 2018 Mar 1;172(3):226-231. doi: 10.1001/jamapediatrics.2017.4305.

13.

In case you missed it: The Prenatal Diagnosis editors bring you the most significant advances of 2017.

Levy B, Bianchi DW, Van Mieghem T, Deprest J, Ghidini A, Chitty LS.

Prenat Diagn. 2018 Jan;38(2):83-90. doi: 10.1002/pd.5210. Review. No abstract available.

PMID:
29322541
14.

Improving Public Health Requires Inclusion of Underrepresented Populations in Research.

Spong CY, Bianchi DW.

JAMA. 2018 Jan 23;319(4):337-338. doi: 10.1001/jama.2017.19138. No abstract available.

PMID:
29285540
15.

Unusual Prenatal Genomic Results Provide Proof-of-Principle of the Liquid Biopsy for Cancer Screening.

Bianchi DW.

Clin Chem. 2018 Feb;64(2):254-256. doi: 10.1373/clinchem.2017.282459. Epub 2017 Dec 13. No abstract available.

PMID:
29237713
16.

Cherchez la femme: maternal incidental findings can explain discordant prenatal cell-free DNA sequencing results.

Bianchi DW.

Genet Med. 2018 Sep;20(9):910-917. doi: 10.1038/gim.2017.219. Epub 2017 Dec 7. Review.

PMID:
29215645
17.

The conception of the ABCD study: From substance use to a broad NIH collaboration.

Volkow ND, Koob GF, Croyle RT, Bianchi DW, Gordon JA, Koroshetz WJ, Pérez-Stable EJ, Riley WT, Bloch MH, Conway K, Deeds BG, Dowling GJ, Grant S, Howlett KD, Matochik JA, Morgan GD, Murray MM, Noronha A, Spong CY, Wargo EM, Warren KR, Weiss SRB.

Dev Cogn Neurosci. 2018 Aug;32:4-7. doi: 10.1016/j.dcn.2017.10.002. Epub 2017 Oct 10. Review.

18.

Rare autosomal trisomies, revealed by maternal plasma DNA sequencing, suggest increased risk of feto-placental disease.

Pertile MD, Halks-Miller M, Flowers N, Barbacioru C, Kinnings SL, Vavrek D, Seltzer WK, Bianchi DW.

Sci Transl Med. 2017 Aug 30;9(405). pii: eaan1240. doi: 10.1126/scitranslmed.aan1240.

PMID:
28855395
19.

Cell-free DNA results lead to unexpected diagnosis.

Smith J, Kean V, Bianchi DW, Feldman G, Petrucelli N, Simon M, Gonik B.

Clin Case Rep. 2017 Jul 3;5(8):1323-1326. doi: 10.1002/ccr3.1051. eCollection 2017 Aug.

20.

Amniotic fluid transcriptomics reflects novel disease mechanisms in fetuses with myelomeningocele.

Tarui T, Kim A, Flake A, McClain L, Stratigis JD, Fried I, Newman R, Slonim DK, Bianchi DW.

Am J Obstet Gynecol. 2017 Nov;217(5):587.e1-587.e10. doi: 10.1016/j.ajog.2017.07.022. Epub 2017 Jul 20.

21.

Prenatal DNA Sequencing: Clinical, Counseling, and Diagnostic Laboratory Considerations.

Abou Tayoun AN, Spinner NB, Rehm HL, Green RC, Bianchi DW.

Prenat Diagn. 2018 Jan;38(1):26-32. doi: 10.1002/pd.5038. Epub 2017 Apr 17. Review.

PMID:
28345240
22.

In case you missed it: the Prenatal Diagnosis editors bring you the most significant advances of 2016.

Van Mieghem T, Bianchi DW, Levy B, Deprest J, Chitty LS, Ghidini A.

Prenat Diagn. 2017 Feb;37(2):117-122. doi: 10.1002/pd.5007. No abstract available.

PMID:
28205301
23.

Confined placental mosaicism for 22q11.2 deletion as the etiology for discordant positive NIPT results.

Bunnell M, Zhang C, Lee C, Bianchi DW, Wilkins-Haug L.

Prenat Diagn. 2017 Apr;37(4):416-419. doi: 10.1002/pd.5022. Epub 2017 Mar 8.

PMID:
28198030
24.

Prenatal testing for neuropsychiatric disorders.

Ghidini A, Bianchi DW.

Prenat Diagn. 2017 Jan;37(1):3-5. doi: 10.1002/pd.4998. No abstract available.

PMID:
28097708
25.

Should we 'open the kimono' to release the results of rare autosomal aneuploidies following noninvasive prenatal whole genome sequencing?

Bianchi DW.

Prenat Diagn. 2017 Feb;37(2):123-125. doi: 10.1002/pd.4993. Epub 2017 Jan 24.

PMID:
28010042
26.

Fetal therapy for Down syndrome: an ethical exploration.

de Wert G, Dondorp W, Bianchi DW.

Prenat Diagn. 2017 Mar;37(3):222-228. doi: 10.1002/pd.4995. Epub 2017 Feb 1.

PMID:
28004394
27.

Perinatal Natural History of the Ts1Cje Mouse Model of Down Syndrome: Growth Restriction, Early Mortality, Heart Defects, and Delayed Development.

Ferrés MA, Bianchi DW, Siegel AE, Bronson RT, Huggins GS, Guedj F.

PLoS One. 2016 Dec 8;11(12):e0168009. doi: 10.1371/journal.pone.0168009. eCollection 2016.

28.

Global transcriptome dysregulation in second trimester fetuses with FMR1 expansions.

Zwemer LM, Nolin SL, Okamoto PM, Eisenberg M, Wick HC, Bianchi DW.

Prenat Diagn. 2017 Jan;37(1):43-52. doi: 10.1002/pd.4928. Epub 2016 Oct 25.

29.

Noninvasive Prenatal DNA Testing: The Vanguard of Genomic Medicine.

Hui L, Bianchi DW.

Annu Rev Med. 2017 Jan 14;68:459-472. doi: 10.1146/annurev-med-072115-033220. Epub 2016 Oct 10. Review.

PMID:
27732785
30.

An Integrated Human/Murine Transcriptome and Pathway Approach To Identify Prenatal Treatments For Down Syndrome.

Guedj F, Pennings JL, Massingham LJ, Wick HC, Siegel AE, Tantravahi U, Bianchi DW.

Sci Rep. 2016 Sep 2;6:32353. doi: 10.1038/srep32353.

31.

Copy-Number Variation and False Positive Prenatal Screening Results.

Chudova DI, Sehnert AJ, Bianchi DW.

N Engl J Med. 2016 Jul 7;375(1):97-8. doi: 10.1056/NEJMc1509813. No abstract available.

PMID:
27406371
32.

Gene expression in term placentas is regulated more by spinal or epidural anesthesia than by late-onset preeclampsia or gestational diabetes mellitus.

Lekva T, Lyle R, Roland MC, Friis C, Bianchi DW, Jaffe IZ, Norwitz ER, Bollerslev J, Henriksen T, Ueland T.

Sci Rep. 2016 Jul 11;6:29715. doi: 10.1038/srep29715.

33.

The 2015 Malcolm Ferguson-Smith Young Investigator Award.

Ghidini A, Bianchi DW, Levy B, Deprest J, van Mieghem T, Chitty LS, McLean-Inglis A.

Prenat Diagn. 2016 Jul;36(7):599-600. doi: 10.1002/pd.4855. No abstract available.

PMID:
27381265
34.

Absence of Prenatal Forebrain Defects in the Dp(16)1Yey/+ Mouse Model of Down Syndrome.

Goodliffe JW, Olmos-Serrano JL, Aziz NM, Pennings JL, Guedj F, Bianchi DW, Haydar TF.

J Neurosci. 2016 Mar 9;36(10):2926-44. doi: 10.1523/JNEUROSCI.2513-15.2016.

35.

Males are from Mars, and females are from Venus: sex-specific fetal brain gene expression signatures in a mouse model of maternal diet-induced obesity.

Edlow AG, Guedj F, Pennings JL, Sverdlov D, Neri C, Bianchi DW.

Am J Obstet Gynecol. 2016 May;214(5):623.e1-623.e10. doi: 10.1016/j.ajog.2016.02.054. Epub 2016 Mar 3.

36.

Assessing the fetal effects of maternal obesity via transcriptomic analysis of cord blood: a prospective case-control study.

Edlow AG, Hui L, Wick HC, Fried I, Bianchi DW.

BJOG. 2016 Jan;123(2):180-9. doi: 10.1111/1471-0528.13795.

37.

Follow-up of multiple aneuploidies and single monosomies detected by noninvasive prenatal testing: implications for management and counseling.

Snyder HL, Curnow KJ, Bhatt S, Bianchi DW.

Prenat Diagn. 2016 Mar;36(3):203-9. doi: 10.1002/pd.4778. Epub 2016 Feb 8.

38.

In case you missed it: the Prenatal Diagnosis editors bring you the most significant advances of 2015.

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

Prenat Diagn. 2016 Jan;36(1):3-9. doi: 10.1002/pd.4758. No abstract available.

PMID:
26777520
39.

Maternal Malignancies Detected With Noninvasive Prenatal Testing--Reply.

Halks-Miller M, Chudova D, Bianchi DW.

JAMA. 2015 Nov 24;314(20):2192-3. doi: 10.1001/jama.2015.12925. No abstract available.

PMID:
26599192
40.

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 Nov;23(11):1592. doi: 10.1038/ejhg.2015.109. No abstract available.

41.

New Perspectives for the Rescue of Cognitive Disability in Down Syndrome.

Bartesaghi R, Haydar TF, Delabar JM, Dierssen M, Martínez-Cué C, Bianchi DW.

J Neurosci. 2015 Oct 14;35(41):13843-52. doi: 10.1523/JNEUROSCI.2775-15.2015.

42.

Next generation sequencing and the next generation: how genomics is revolutionizing reproduction.

Chitty LS, Bianchi DW.

Prenat Diagn. 2015 Oct;35(10):929-30. doi: 10.1002/pd.4679. Epub 2015 Sep 7. No abstract available.

PMID:
26443108
43.

Recommended pre-test counseling points for noninvasive prenatal testing using cell-free DNA: a 2015 perspective.

Sachs A, Blanchard L, Buchanan A, Norwitz E, Bianchi DW.

Prenat Diagn. 2015 Oct;35(10):968-71. doi: 10.1002/pd.4666. Epub 2015 Sep 3.

PMID:
26245889
44.

Noninvasive Prenatal Testing and Incidental Detection of Occult Maternal Malignancies.

Bianchi DW, Chudova D, Sehnert AJ, Bhatt S, Murray K, Prosen TL, Garber JE, Wilkins-Haug L, Vora NL, Warsof S, Goldberg J, Ziainia T, Halks-Miller M.

JAMA. 2015 Jul 14;314(2):162-9. doi: 10.1001/jama.2015.7120.

PMID:
26168314
45.

The 2014 Malcolm Ferguson-Smith Young Investigator Award.

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

Prenat Diagn. 2015 Jun;35(6):515-6. doi: 10.1002/pd.4612. No abstract available.

PMID:
26041253
46.

Pregnancy: Prepare for unexpected prenatal test results.

Bianchi DW.

Nature. 2015 Jun 4;522(7554):29-30. doi: 10.1038/522029a. No abstract available.

PMID:
26040879
47.

The fetal brain transcriptome and neonatal behavioral phenotype in the Ts1Cje mouse model of Down syndrome.

Guedj F, Pennings JL, Ferres MA, Graham LC, Wick HC, Miczek KA, Slonim DK, Bianchi DW.

Am J Med Genet A. 2015 Sep;167A(9):1993-2008. doi: 10.1002/ajmg.a.37156. Epub 2015 May 14.

48.

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.

49.

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; European Society of Human Genetics; American Society of Human Genetics.

Eur J Hum Genet. 2015 Nov;23(11):1438-50. doi: 10.1038/ejhg.2015.57. Epub 2015 Mar 18. Erratum in: Eur J Hum Genet. 2015 Nov;23(11):1592.

50.

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 Jul;213(1):59.e1-59.e172. doi: 10.1016/j.ajog.2015.03.023. Epub 2015 Mar 12.

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