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Items: 1 to 20 of 193

1.

Clinical experience with single-nucleotide polymorphism-based non-invasive prenatal screening for 22q11.2 deletion syndrome.

Gross SJ, Stosic M, McDonald-McGinn DM, Bassett AS, Norvez A, Dhamankar R, Kobara K, Kirkizlar E, Zimmermann B, Wayham N, Babiarz JE, Ryan A, Jinnett KN, Demko Z, Benn P.

Ultrasound Obstet Gynecol. 2016 Feb;47(2):177-83. doi: 10.1002/uog.15754. Epub 2016 Jan 5.

2.

Efficacy of a proprietary formulation of fipronil/(S)-methoprene/cyphenothrin against Ixodes scapularis tick infestations on dogs.

Carithers D, Everett WR, Gross SJ, Solanki R.

Parasit Vectors. 2015 Jul 17;8:379. doi: 10.1186/s13071-015-0992-1.

3.

Prenatal screening: Focus on more specific fetal testing.

Gross SJ, Kareht S, Ryan A.

Nature. 2015 Jul 16;523(7560):290. doi: 10.1038/523290d. No abstract available.

PMID:
26178955
4.

Positive predictive values and false-positive results in noninvasive prenatal screening.

Dar P, Gross SJ, Benn P.

Am J Obstet Gynecol. 2015 Oct;213(4):595-6. doi: 10.1016/j.ajog.2015.06.006. Epub 2015 Jun 9. No abstract available.

PMID:
26070701
5.

Noninvasive prenatal testing for 22q11.2 deletion syndrome: deeper sequencing increases the positive predictive value.

Gross SJ, Ryan A, Benn P.

Am J Obstet Gynecol. 2015 Aug;213(2):254-5. doi: 10.1016/j.ajog.2015.05.028. Epub 2015 May 15. No abstract available.

PMID:
25986033
6.

Reply: To PMID 25111587.

Dar P, Gross SJ, Benn P.

Am J Obstet Gynecol. 2015 Aug;213(2):253-4. doi: 10.1016/j.ajog.2015.04.040. Epub 2015 May 1. No abstract available.

PMID:
25940611
7.

Detection of complete molar pregnancy by single-nucleotide polymorphism-based non-invasive prenatal testing.

Simon AL, Su B, Demko Z, Rabinowitz M, Harmon ER, Gross SJ.

Ultrasound Obstet Gynecol. 2015 Oct;46(4):506-7. doi: 10.1002/uog.14854. Epub 2015 Aug 24. No abstract available.

PMID:
25810270
8.

Expanding the scope of noninvasive prenatal testing: detection of fetal microdeletion syndromes.

Wapner RJ, Babiarz JE, Levy B, Stosic M, Zimmermann B, Sigurjonsson S, Wayham N, Ryan A, Banjevic M, Lacroute P, Hu J, Hall MP, Demko Z, Siddiqui A, Rabinowitz M, Gross SJ, Hill M, Benn P.

Am J Obstet Gynecol. 2015 Mar;212(3):332.e1-9. doi: 10.1016/j.ajog.2014.11.041. Epub 2014 Dec 2.

9.

Detection of triploid, molar, and vanishing twin pregnancies by a single-nucleotide polymorphism-based noninvasive prenatal test.

Curnow KJ, Wilkins-Haug L, Ryan A, Kırkızlar E, Stosic M, Hall MP, Sigurjonsson S, Demko Z, Rabinowitz M, Gross SJ.

Am J Obstet Gynecol. 2015 Jan;212(1):79.e1-9. doi: 10.1016/j.ajog.2014.10.012. Epub 2014 Oct 15.

10.

The genetics of diabetic pregnancy.

Bajaj K, Gross SJ.

Best Pract Res Clin Obstet Gynaecol. 2015 Jan;29(1):102-9. doi: 10.1016/j.bpobgyn.2014.08.008. Epub 2014 Aug 26. Review.

PMID:
25438929
11.

Predictive validity of the Bayley, Third Edition at 2 years for intelligence quotient at 4 years in preterm infants.

Bode MM, DʼEugenio DB, Mettelman BB, Gross SJ.

J Dev Behav Pediatr. 2014 Nov-Dec;35(9):570-5. doi: 10.1097/DBP.0000000000000110.

PMID:
25370298
12.

Pregnancy associated plasma protein-A2: a novel biomarker for Down syndrome.

Munnangi S, Gross SJ, Madankumar R, Salcedo G, Reznik SE.

Placenta. 2014 Nov;35(11):900-6. doi: 10.1016/j.placenta.2014.08.001. Epub 2014 Aug 12.

13.

Clinical experience and follow-up with large scale single-nucleotide polymorphism-based noninvasive prenatal aneuploidy testing.

Dar P, Curnow KJ, Gross SJ, Hall MP, Stosic M, Demko Z, Zimmermann B, Hill M, Sigurjonsson S, Ryan A, Banjevic M, Kolacki PL, Koch SW, Strom CM, Rabinowitz M, Benn P.

Am J Obstet Gynecol. 2014 Nov;211(5):527.e1-527.e17. doi: 10.1016/j.ajog.2014.08.006. Epub 2014 Aug 8.

14.

Cognitive and Antipsychotic Medication Use in Monoallelic GBA-Related Parkinson Disease.

Barrett MJ, Shanker VL, Severt WL, Raymond D, Gross SJ, Schreiber-Agus N, Kornreich R, Ozelius LJ, Bressman SB, Saunders-Pullman R.

JIMD Rep. 2014;16:31-8. doi: 10.1007/8904_2014_315. Epub 2014 May 22.

15.

Noninvasive prenatal screening by next-generation sequencing.

Gregg AR, Van den Veyver IB, Gross SJ, Madankumar R, Rink BD, Norton ME.

Annu Rev Genomics Hum Genet. 2014;15:327-47. doi: 10.1146/annurev-genom-090413-025341. Epub 2014 May 14. Review.

PMID:
24849140
16.

Carrier testing for Ashkenazi Jewish disorders in the prenatal setting: navigating the genetic maze.

Ferreira JC, Schreiber-Agus N, Carter SM, Klugman S, Gregg AR, Gross SJ.

Am J Obstet Gynecol. 2014 Sep;211(3):197-204. doi: 10.1016/j.ajog.2014.02.001. Epub 2014 Feb 5. Review.

PMID:
24508465
17.

ACMG statement on noninvasive prenatal screening for fetal aneuploidy.

Gregg AR, Gross SJ, Best RG, Monaghan KG, Bajaj K, Skotko BG, Thompson BH, Watson MS.

Genet Med. 2013 May;15(5):395-8. doi: 10.1038/gim.2013.29. Epub 2013 Apr 4.

PMID:
23558255
18.

The p.L302P mutation in the lysosomal enzyme gene SMPD1 is a risk factor for Parkinson disease.

Gan-Or Z, Ozelius LJ, Bar-Shira A, Saunders-Pullman R, Mirelman A, Kornreich R, Gana-Weisz M, Raymond D, Rozenkrantz L, Deik A, Gurevich T, Gross SJ, Schreiber-Agus N, Giladi N, Bressman SB, Orr-Urtreger A.

Neurology. 2013 Apr 23;80(17):1606-10. doi: 10.1212/WNL.0b013e31828f180e. Epub 2013 Mar 27.

19.

ACMG Policy Statement. Risk categorization for oversight of laboratory-developed tests for inherited conditions.

Monaghan KG, Benkendorf J, Cherry AM, Gross SJ, Richards CS, Sutton VR, Watson MS; Laboratory Quality Assurance Committee of the American College of Medical Genetics and Genomics; Professional Practice and Guidelines Committee of the American College of Medical Genetics and Genomics.

Genet Med. 2013 Apr;15(4):314-5. doi: 10.1038/gim.2012.178. Epub 2013 Jan 24. No abstract available.

PMID:
23348768
20.

Transcranial sonography and functional imaging in glucocerebrosidase mutation Parkinson disease.

Barrett MJ, Hagenah J, Dhawan V, Peng S, Stanley K, Raymond D, Deik A, Gross SJ, Schreiber-Agus N, Mirelman A, Marder K, Ozelius LJ, Eidelberg D, Bressman SB, Saunders-Pullman R; LRRK2 Ashkenazi Jewish Consortium.

Parkinsonism Relat Disord. 2013 Feb;19(2):186-91. doi: 10.1016/j.parkreldis.2012.09.007. Epub 2012 Oct 10.

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