Goldberg JD - Search Results

1

Genome-wide fetal aneuploidy detection by maternal plasma DNA sequencing.

Bianchi DW, Platt LD, Goldberg JD, Abuhamad AZ, Sehnert AJ, Rava RP; MatErnal BLood IS Source to Accurately diagnose fetal aneuploidy (MELISSA) Study Group. Bianchi DW, et al. Among authors: goldberg jd. Obstet Gynecol. 2012 May;119(5):890-901. doi: 10.1097/AOG.0b013e31824fb482. Obstet Gynecol. 2012. PMID: 22362253 Clinical Trial.

2

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. Bianchi DW, et al. JAMA. 2015 Jul 14;314(2):162-9. doi: 10.1001/jama.2015.7120. JAMA. 2015. PMID: 26168314

3

Massively parallel sequencing of maternal plasma DNA in 113 cases of fetal nuchal cystic hygroma.

Bianchi DW, Prosen T, Platt LD, Goldberg JD, Abuhamad AZ, Rava RP, Sehnert AJ; MatErnal BLood IS Source to Accurately diagnose fetal aneuploidy (MELISSA) Study Group*. Bianchi DW, et al. Among authors: goldberg jd. Obstet Gynecol. 2013 May;121(5):1057-1062. doi: 10.1097/AOG.0b013e31828ba3d8. Obstet Gynecol. 2013. PMID: 23635743 Clinical Trial.

4

Impact of noninvasive prenatal testing in regionally dispersed medical centers in the United States.

Platt LD, Janicki MB, Prosen T, Goldberg JD, Adashek J, Figueroa R, Rodis J, Liao W, Sehnert AJ, Snyder HL, Warsof SL. Platt LD, et al. Among authors: goldberg jd. Am J Obstet Gynecol. 2014 Oct;211(4):368.e1-7. doi: 10.1016/j.ajog.2014.03.065. Epub 2014 Apr 3. Am J Obstet Gynecol. 2014. PMID: 24705127

5

Fetal aneuploidy detection by maternal plasma DNA sequencing: a technology assessment.

Walsh JM, Goldberg JD. Walsh JM, et al. Among authors: goldberg jd. Prenat Diagn. 2013 Jun;33(6):514-20. doi: 10.1002/pd.4109. Prenat Diagn. 2013. PMID: 23686655 Review.

6

Noninvasive prenatal screening at low fetal fraction: comparing whole-genome sequencing and single-nucleotide polymorphism methods.

Artieri CG, Haverty C, Evans EA, Goldberg JD, Haque IS, Yaron Y, Muzzey D. Artieri CG, et al. Among authors: goldberg jd. Prenat Diagn. 2017 May;37(5):482-490. doi: 10.1002/pd.5036. Epub 2017 Apr 26. Prenat Diagn. 2017. PMID: 28317136

7

Routine screening for fetal anomalies: expectations.

Goldberg JD. Goldberg JD. Obstet Gynecol Clin North Am. 2004 Mar;31(1):35-50. doi: 10.1016/S0889-8545(03)00118-9. Obstet Gynecol Clin North Am. 2004. PMID: 15062446 Review.

8

Fetal screening and whole genome sequencing: where are the limits?

Hancock S, Johansen Taber K, Goldberg JD. Hancock S, et al. Among authors: goldberg jd. Expert Rev Mol Diagn. 2021 May;21(5):433-435. doi: 10.1080/14737159.2021.1919087. Epub 2021 Apr 26. Expert Rev Mol Diagn. 2021. PMID: 33866903 No abstract available.

9

Noninvasive prenatal screening for patients with high body mass index: Evaluating the impact of a customized whole genome sequencing workflow on sensitivity and residual risk.

Muzzey D, Goldberg JD, Haverty C. Muzzey D, et al. Among authors: goldberg jd. Prenat Diagn. 2020 Feb;40(3):333-341. doi: 10.1002/pd.5603. Epub 2019 Dec 20. Prenat Diagn. 2020. PMID: 31697845 Free PMC article.

10

Response to "Noninvasive prenatal screening at low fetal fraction: comparing whole-genome sequencing and single-nucleotide polymorphism methods".

Muzzey D, Haverty C, Evans EA, Goldberg JD. Muzzey D, et al. Among authors: goldberg jd. Prenat Diagn. 2017 Jul;37(7):727-728. doi: 10.1002/pd.5071. Prenat Diagn. 2017. PMID: 28675624 Free PMC article. No abstract available.

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