Search | Virtual Health Library

1.

Systematic evaluation of genome sequencing for the diagnostic assessment of autism spectrum disorder and fetal structural anomalies.

Lowther, Chelsea; Valkanas, Elise; Giordano, Jessica L; Wang, Harold Z; Currall, Benjamin B; O'Keefe, Kathryn; Pierce-Hoffman, Emma; Kurtas, Nehir E; Whelan, Christopher W; Hao, Stephanie P; Weisburd, Ben; Jalili, Vahid; Fu, Jack; Wong, Isaac; Collins, Ryan L; Zhao, Xuefang; Austin-Tse, Christina A; Evangelista, Emily; Lemire, Gabrielle; Aggarwal, Vimla S; Lucente, Diane; Gauthier, Laura D; Tolonen, Charlotte; Sahakian, Nareh; Stevens, Christine; An, Joon-Yong; Dong, Shan; Norton, Mary E; MacKenzie, Tippi C; Devlin, Bernie; Gilmore, Kelly; Powell, Bradford C; Brandt, Alicia; Vetrini, Francesco; DiVito, Michelle; Sanders, Stephan J; MacArthur, Daniel G; Hodge, Jennelle C; O'Donnell-Luria, Anne; Rehm, Heidi L; Vora, Neeta L; Levy, Brynn; Brand, Harrison; Wapner, Ronald J; Talkowski, Michael E.

Am J Hum Genet ; 110(9): 1454-1469, 2023 09 07.

Article in English | MEDLINE | ID: mdl-37595579

2.

Treatment for Mild Chronic Hypertension during Pregnancy.

Tita, Alan T; Szychowski, Jeff M; Boggess, Kim; Dugoff, Lorraine; Sibai, Baha; Lawrence, Kirsten; Hughes, Brenna L; Bell, Joseph; Aagaard, Kjersti; Edwards, Rodney K; Gibson, Kelly; Haas, David M; Plante, Lauren; Metz, Torri; Casey, Brian; Esplin, Sean; Longo, Sherri; Hoffman, Matthew; Saade, George R; Hoppe, Kara K; Foroutan, Janelle; Tuuli, Methodius; Owens, Michelle Y; Simhan, Hyagriv N; Frey, Heather; Rosen, Todd; Palatnik, Anna; Baker, Susan; August, Phyllis; Reddy, Uma M; Kinzler, Wendy; Su, Emily; Krishna, Iris; Nguyen, Nicki; Norton, Mary E; Skupski, Daniel; El-Sayed, Yasser Y; Ogunyemi, Dotum; Galis, Zorina S; Harper, Lorie; Ambalavanan, Namasivayam; Geller, Nancy L; Oparil, Suzanne; Cutter, Gary R; Andrews, William W.

N Engl J Med ; 386(19): 1781-1792, 2022 05 12.

Article in English | MEDLINE | ID: mdl-35363951

3.

The Role of cfDNA Biomarkers and Patient Data in the Early Prediction of Preeclampsia: Artificial Intelligence Model.

Khalil, Asma; Bellesia, Giovanni; Norton, Mary E; Jacobsson, Bo; Haeri, Sina; Egbert, Melissa; Malone, Fergal D; Wapner, Ronald J; Roman, Ashley; Faro, Revital; Madankumar, Rajeevi; Strong, Noel; Silver, Robert M; Vohra, Nidhi; Hyett, Jon; Macpherson, Cora; Prigmore, Brittany; Ahmed, Ebad; Demko, Zach; Ortiz, J Bryce; Souter, Vivienne; Dar, Pe'er.

Am J Obstet Gynecol ; 2024 Mar 01.

Article in English | MEDLINE | ID: mdl-38432413

4.

Prenatal vs postnatal diagnosis of 22q11.2 deletion syndrome: cardiac and noncardiac outcomes through 1 year of age.

Freud, Lindsay R; Galloway, Stephanie; Crowley, T Blaine; Moldenhauer, Julie; Swillen, Ann; Breckpot, Jeroen; Borrell, Antoni; Vora, Neeta L; Cuneo, Bettina; Hoffman, Hilary; Gilbert, Lisa; Nowakowska, Beata; Geremek, Maciej; Kutkowska-Kazmierczak, Anna; Vermeesch, Joris R; Devriendt, Koen; Busa, Tiffany; Sigaudy, Sabine; Vigneswaran, Trisha; Simpson, John M; Dungan, Jeffrey; Gotteiner, Nina; Gloning, Karl-Philipp; Digilio, Maria Cristina; Unolt, Marta; Putotto, Carolina; Marino, Bruno; Repetto, Gabriela; Fadic, Magdalena; Garcia-Minaur, Sixto; Achón Buil, Ana; Thomas, Mary Ann; Fruitman, Deborah; Beecroft, Taylor; Hui, Pui Wah; Oskarsdottir, Solveig; Bradshaw, Rachael; Criebaum, Amanda; Norton, Mary E; Lee, Tiffany; Geiger, Miwa; Dunnington, Leslie; Isaac, Jacqueline; Wilkins-Haug, Louise; Hunter, Lindsey; Izzi, Claudia; Toscano, Marika; Ghi, Tullio; McGlynn, Julie; Romana Grati, Francesca.

Am J Obstet Gynecol ; 230(3): 368.e1-368.e12, 2024 Mar.

Article in English | MEDLINE | ID: mdl-37717890

5.

The utility of gene sequencing in identifying an underlying genetic disorder in prenatally suspected lower urinary tract obstruction.

Brar, Bobby K; Blakemore, Karin; Hertenstein, Christine; Miller, Jena L; Miller, Kristen A; Shamseldin, Hanan; Maddirevula, Sateesh; Hays, Thomas; Lianoglou, Billie; Dukhovny, Stephanie; Baker, Linda A; Sparks, Teresa N; Wapner, Ronald; Alkuraya, Fowzan S; Norton, Mary E; Jelin, Angie C.

Prenat Diagn ; 44(2): 196-204, 2024 02.

Article in English | MEDLINE | ID: mdl-37594370

6.

Monogenic conditions and central nervous system anomalies: A prospective study, systematic review and meta-analysis.

Blayney, Gillian V; Laffan, Eoghan; Jacob, Preethi A; Baptiste, Caitlin D; Gabriel, Heinz; Sparks, Teresa N; Yaron, Yuval; Norton, Mary E; Diderich, Karin; Wang, Yiming; Chong, Karen; Chitayat, David; Saini, Neelam; Aggarwal, Shagun; Pauta, Montse; Borrell, Antoni; Gilmore, Kelly; Chandler, Natalie J; Allen, Stephanie; Vora, Neeta; Noor, Abdul; Monaghan, Caitriona; Kilby, Mark D; Wapner, Ronald J; Chitty, Lyn S; Mone, Fionnuala.

Prenat Diagn ; 44(4): 422-431, 2024 Apr.

Article in English | MEDLINE | ID: mdl-38054560

7.

Exome Sequencing for Prenatal Diagnosis in Nonimmune Hydrops Fetalis.

Sparks, Teresa N; Lianoglou, Billie R; Adami, Rebecca R; Pluym, Ilina D; Holliman, Kerry; Duffy, Jennifer; Downum, Sarah L; Patel, Sachi; Faubel, Amanda; Boe, Nina M; Field, Nancy T; Murphy, Aisling; Laurent, Louise C; Jolley, Jennifer; Uy, Cherry; Slavotinek, Anne M; Devine, Patrick; Hodoglugil, Ugur; Van Ziffle, Jessica; Sanders, Stephan J; MacKenzie, Tippi C; Norton, Mary E.

N Engl J Med ; 383(18): 1746-1756, 2020 10 29.

Article in English | MEDLINE | ID: mdl-33027564

8.

Performance of prenatal cfDNA screening for sex chromosomes.

Martin, Kimberly; Dar, Pe'er; MacPherson, Cora; Egbert, Melissa; Demko, Zachary; Parmar, Sheetal; Hashimoto, Katelyn; Haeri, Sina; Malone, Fergal; Wapner, Ronald J; Roman, Ashley S; Khalil, Asma; Faro, Revital; Madankumar, Rajeevi; Strong, Noel; Silver, Robert M; Vohra, Nidhi; Hyett, Jon; Rabinowitz, Matt; Kao, Charlly; Hakonarson, Hakon; Jacobsson, Bo; Norton, Mary E.

Genet Med ; 25(8): 100879, 2023 08.

Article in English | MEDLINE | ID: mdl-37154148

9.

Prenatal exome and genome sequencing for fetal structural abnormalities.

Vora, Neeta L; Norton, Mary E.

Am J Obstet Gynecol ; 228(2): 140-149, 2023 02.

Article in English | MEDLINE | ID: mdl-36027950

10.

Society for Maternal-Fetal Medicine Consult Series #64: Systemic lupus erythematosus in pregnancy.

Silver, Robert; Craigo, Sabrina; Porter, Flint; Osmundson, Sarah S; Kuller, Jeffrey A; Norton, Mary E.

Am J Obstet Gynecol ; 228(3): B41-B60, 2023 03.

Article in English | MEDLINE | ID: mdl-36084704

11.

Obstetrical, perinatal, and genetic outcomes associated with nonreportable prenatal cell-free DNA screening results.

Norton, Mary E; MacPherson, Cora; Demko, Zachary; Egbert, Melissa; Malone, Fergal; Wapner, Ronald J; Roman, Ashley S; Khalil, Asma; Faro, Revital; Madankumar, Rajeevi; Strong, Noel; Haeri, Sina; Silver, Robert; Vohra, Nidhi; Hyett, Jon; Martin, Kimberly; Rabinowitz, Matthew; Jacobsson, Bo; Dar, Pe'er.

Am J Obstet Gynecol ; 229(3): 300.e1-300.e9, 2023 09.

Article in English | MEDLINE | ID: mdl-36965866

12.

Access to prenatal exome sequencing for fetal malformations: A qualitative landscape analysis in the US.

Sahin-Hodoglugil, Nuriye N; Lianoglou, Billie R; Ackerman, Sara; Sparks, Teresa N; Norton, Mary E.

Prenat Diagn ; 43(11): 1394-1405, 2023 10.

Article in English | MEDLINE | ID: mdl-37752660

13.

A systematic review and meta-analysis of cell-free DNA testing for detection of fetal sex chromosome aneuploidy.

Shear, Matthew A; Swanson, Kate; Garg, Ria; Jelin, Angie C; Boscardin, John; Norton, Mary E; Sparks, Teresa N.

Prenat Diagn ; 43(2): 133-143, 2023 02.

Article in English | MEDLINE | ID: mdl-36588186

14.

Impact of high-risk prenatal screening results for 22q11.2 deletion syndrome on obstetric and neonatal management: Secondary analysis from the SMART study.

Martin, Kimberly; Norton, Mary E; MacPherson, Cora; Demko, Zachary; Egbert, Melissa; Haeri, Sina; Malone, Fergal; Wapner, Ronald J; Roman, Ashley S; Khalil, Asma; Faro, Revital; Madankumar, Rajeevi; Strong, Noel; Silver, Robert; Vohra, Nidhi; Hyett, Jon; Kao, Charlly; Hakonarson, Hakon; Jacobson, Bo; Dar, Pe'er.

Prenat Diagn ; 43(13): 1574-1580, 2023 12.

Article in English | MEDLINE | ID: mdl-38066724

15.

Cell-free DNA Screening for Aneuploidy.

Norton, Mary E.

Clin Obstet Gynecol ; 66(3): 557-567, 2023 09 01.

Article in English | MEDLINE | ID: mdl-37650668

16.

Understanding Preterm Birth in Pregnancies Complicated by Nonimmune Hydrops Fetalis.

Swanson, Kate; Norton, Mary E; Downum, Sarah L; Gonzalez-Velez, Juan M; Sparks, Teresa N.

Am J Perinatol ; 40(9): 917-922, 2023 07.

Article in English | MEDLINE | ID: mdl-36603834

17.

Evaluation of Hypoglycemia in Neonates of Women at Risk for Late Preterm Delivery: An Antenatal Late Preterm Steroids Trial Cohort Study.

Gyamfi-Bannerman, Cynthia; Jablonski, Kathleen A; Blackwell, Sean C; Tita, Alan T N; Reddy, Uma M; Jain, Lucky; Saade, George R; Rouse, Dwight J; Clark, Erin A S; Thorp, John M; Chien, Edward K; Peaceman, Alan M; Gibbs, Ronald S; Swamy, Geeta K; Norton, Mary E; Casey, Brian M; Caritis, Steve N; Tolosa, Jorge E; Sorokin, Yoram; VanDorsten, J Peter.

Am J Perinatol ; 40(5): 532-538, 2023 04.

Article in English | MEDLINE | ID: mdl-34044454

18.

Universal Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Testing for Obstetric Inpatient Units Across the United States.

Gilner, Jennifer; Kansal, Namita; Biggio, Joseph R; Delaney, Shani; Grotegut, Chad A; Hardy, Erica; Hirshberg, Adi; Kachikis, Alisa; LaCourse, Sylvia M; Martin, Jane; Metz, Torri D; Miller, Emily S; Norton, Mary E; Sinkey, Rachel; Sobhani, Nasim C; Son, Shannon L; Srinivas, Sindhu; Tita, Alan; Werner, Erika F; Hughes, Brenna L.

Clin Infect Dis ; 75(1): e322-e328, 2022 08 24.

Article in English | MEDLINE | ID: mdl-34791093

19.

The difficulties of broad data sharing in genomic medicine: Empirical evidence from diverse participants in prenatal and pediatric clinical genomics research.

Norstad, Matthew; Outram, Simon; Brown, Julia E H; Zamora, Astrid N; Koenig, Barbara A; Risch, Neil; Norton, Mary E; Slavotinek, Anne; Ackerman, Sara L.

Genet Med ; 24(2): 410-418, 2022 02.

Article in English | MEDLINE | ID: mdl-34906477

20.

Perspectives and preferences regarding genomic secondary findings in underrepresented prenatal and pediatric populations: A mixed-methods approach.

Rego, Shannon; Hoban, Hannah; Outram, Simon; Zamora, Astrid N; Chen, Flavia; Sahin-Hodoglugil, Nuriye; Anguiano, Beatriz; Norstad, Matthew; Yip, Tiffany; Lianoglou, Billie; Sparks, Teresa N; Norton, Mary E; Koenig, Barbara A; Slavotinek, Anne M; Ackerman, Sara L.

Genet Med ; 24(6): 1206-1216, 2022 06.

Article in English | MEDLINE | ID: mdl-35396980

Virtual Health Library

United States - Mexico Border

Your selection (0)

Export format:

Export: