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Page 1
Whole Exome Sequencing in a Population of Fetuses With Structural Anomalies.
Burrill N, Schindewolf E, Pilchman L, Wright R, Crane H, Gebb J, Khalek N, Soni S, Paidas Teefey C, Oliver ER, Linn R, Moldenhauer JS. Burrill N, et al. Among authors: schindewolf e. Prenat Diagn. 2025 Mar;45(3):310-317. doi: 10.1002/pd.6735. Epub 2025 Jan 1. Prenat Diagn. 2025. PMID: 39743338
Expanding Genetic Counselor Roles: A Model for Global Research Development.
Muraresku CC, McCormick EM, Rockart L, Blaine Crowley T, Asher S, Back A, Baldino SM, Bedoukian E, Britt AD, Burrill N, Cacioppo C, Clark DF, Clark ME, Conway L, Dratch L, Dubbs HA, Engelhardt NM, Ginn N, Gray C, Hartman T, Hathaway ER, Helbig KL, Hoffman-Andrews L, Kasperski S, Keena BA, Keller KN, Long JM, Lulis L, Lusk L, McGinn DE, Mueller R, Paul RA, Pilchman L, Powers J, Raible SE, Reichert S, Rippert AL, Arnold AG, Ruggiero SM, Schindewolf E, Sullivan KR, Terek S, Wang B, Wells M, Wisniewski N, Wright R, Wood EM, Woyciechowski S, Zelley K, Valverde KD, McDonald-McGinn DM. Muraresku CC, et al. Among authors: schindewolf e. Genes (Basel). 2024 Jul 1;15(7):867. doi: 10.3390/genes15070867. Genes (Basel). 2024. PMID: 39062646 Free PMC article.
Amniocentesis in pregnancies at or beyond 24 weeks: an international multicenter study.
Zemet R, Maktabi MA, Tinfow A, Giordano JL, Heisler TM, Yan Q, Plaschkes R, Stokes J, Walsh JM, Corcoran S, Schindewolf E, Miller K, Talati AN, Miller KA, Blakemore K, Swanson K, Ramm J, Bedei I, Sparks TN, Jelin AC, Vora NL, Gebb JS, Crosby DA, Berkenstadt M, Weisz B, Wapner RJ, Van Den Veyver IB. Zemet R, et al. Among authors: schindewolf e. Am J Obstet Gynecol. 2025 Apr;232(4):402.e1-402.e16. doi: 10.1016/j.ajog.2024.06.025. Epub 2024 Jun 22. Am J Obstet Gynecol. 2025. PMID: 38914189 Free PMC article.
Risk of meningomyelocele mediated by the common 22q11.2 deletion.
Vong KI, Lee S, Au KS, Crowley TB, Capra V, Martino J, Haller M, Araújo C, Machado HR, George R, Gerding B, James KN, Stanley V, Jiang N, Alu K, Meave N, Nidhiry AS, Jiwani F, Tang I, Nisal A, Jhamb I, Patel A, Patel A, McEvoy-Venneri J, Barrows C, Shen C, Ha YJ, Howarth R, Strain M, Ashley-Koch AE, Azam M, Mumtaz S, Bot GM, Finnell RH, Kibar Z, Marwan AI, Melikishvili G, Meltzer HS, Mutchinick OM, Stevenson DA, Mroczkowski HJ, Ostrander B, Schindewolf E, Moldenhauer J, Zackai EH, Emanuel BS, Garcia-Minaur S, Nowakowska BA, Stevenson RE, Zaki MS, Northrup H, McNamara HK, Aldinger KA, Phelps IG, Deng M, Glass IA; Spina Bifida Sequencing Consortium‡; Morrow B, McDonald-McGinn DM, Sanna-Cherchi S, Lamb DJ, Gleeson JG. Vong KI, et al. Among authors: schindewolf e. Science. 2024 May 3;384(6695):584-590. doi: 10.1126/science.adl1624. Epub 2024 May 2. Science. 2024. PMID: 38696583 Free PMC article.
Prenatal cardiac findings and 22q11.2 deletion syndrome: Fetal detection and evaluation.
Goldmuntz E, Bassett AS, Boot E, Marino B, Moldenhauer JS, Óskarsdóttir S, Putotto C, Rychik J, Schindewolf E, McDonald-McGinn DM, Blagowidow N. Goldmuntz E, et al. Among authors: schindewolf e. Prenat Diagn. 2024 Jun;44(6-7):804-814. doi: 10.1002/pd.6566. Epub 2024 Apr 9. Prenat Diagn. 2024. PMID: 38593251 Free PMC article. Review.
33 results