Clinical exome sequencing for fetuses with ultrasound abnormalities and a suspected Mendelian disorder
Normand, Elizabeth A, Braxton, Alicia, Nassef, Salma, Ward, Patricia A, Vetrini, Francesco, He, Weimin, Patel, Vipulkumar, Qu, Chunjing, Westerfield, Lauren E, Stover, Samantha, Dharmadhikari, Avinash V, Muzny, Donna M, Gibbs, Richard A, Dai, Hongzheng, Meng, Linyan, Wang, Xia, Xiao, Rui, Liu, Pengfei, Bi, Weimin, Xia, Fan, Walkiewicz, Magdalena, Van den Veyver, Ignatia B, Eng, Christine M, Yang, Yaping
Published in Genome medicine (28.09.2018)
Published in Genome medicine (28.09.2018)
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Journal Article
P793: Pre- and post-implementation of protocol for genetics evaluation for intrauterine fetal demise at Texas Children’s Hospital
Mizerik, Elizabeth, Adams, April, Shay, Lena, Westerfield, Lauren, Parobek, Christian, Smith, Janice
Published in Genetics in Medicine Open (2024)
Published in Genetics in Medicine Open (2024)
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Journal Article
Prenatal testing in pregnancies conceived by in vitro fertilization with pre‐implantation genetic testing
Arian, Sara E., Erfani, Hadi, Westerfield, Lauren E., Buffie, Alexandra, Nassef, Salma, Gibbons, William E., Van den Veyver, Ignatia B.
Published in Prenatal diagnosis (01.06.2020)
Published in Prenatal diagnosis (01.06.2020)
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Journal Article
Clinical characterization of individuals with the distal 1q21.1 microdeletion
Edwards, Stacey D., Schulze, Katharina V., Rosenfeld, Jill A., Westerfield, Lauren E., Gerard, Amanda, Yuan, Bo, Grigorenko, Elena L., Posey, Jennifer E., Bi, Weimin, Liu, Pengfei
Published in American journal of medical genetics. Part A (01.05.2021)
Published in American journal of medical genetics. Part A (01.05.2021)
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Journal Article
Reproductive genetic counseling challenges associated with diagnostic exome sequencing in a large academic private reproductive genetic counseling practice
Westerfield, Lauren E., Stover, Samantha R., Mathur, Veena S., Nassef, Salma A., Carter, Tiffiney G., Yang, Yaping, Eng, Christine M., Van den Veyver, Ignatia B.
Published in Prenatal diagnosis (01.10.2015)
Published in Prenatal diagnosis (01.10.2015)
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Journal Article
P284: Compound heterozygosity for loss-of-function variants in GDF1 provides a molecular diagnosis in a patient with heterotaxy syndrome
Rossi, Vittoria, Luo, Xi, Nunez, Kristin Cardiel, Yi, Ruiyang, Mizerik, Elizabeth, Westerfield, Lauren, Lalani, Seema, Bekheirnia, Mir Reza
Published in Genetics in Medicine Open (2023)
Published in Genetics in Medicine Open (2023)
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Journal Article
Prenatal Diagnostic Exome Sequencing: a Review
Westerfield, Lauren E., Braxton, Alicia A., Walkiewicz, Magdalena
Published in Current genetic medicine reports (2017)
Published in Current genetic medicine reports (2017)
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Journal Article
Bi-allelic Mutations in NADSYN1 Cause Multiple Organ Defects and Expand the Genotypic Spectrum of Congenital NAD Deficiency Disorders
Szot, Justin O., Campagnolo, Carla, Cao, Ye, Iyer, Kavitha R., Cuny, Hartmut, Drysdale, Thomas, Flores-Daboub, Josue A., Bi, Weimin, Westerfield, Lauren, Liu, Pengfei, Leung, Tse Ngong, Choy, Kwong Wai, Chapman, Gavin, Xiao, Rui, Siu, Victoria M., Dunwoodie, Sally L.
Published in American journal of human genetics (02.01.2020)
Published in American journal of human genetics (02.01.2020)
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Journal Article
Clinical characterization of individuals with the distal 1q21.1 microdeletion
Edwards, Stacey, Schulze, Katharina, Rosenfeld, Jill, Westerfield, Lauren, Gerard, Amanda, Yuan, Bo, Grigorenko, Elena, Posey, Jennifer, Bi, Weimin, Liu, Pengfei
Published in Molecular genetics and metabolism (01.04.2021)
Published in Molecular genetics and metabolism (01.04.2021)
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Journal Article
eP120 - Clinical characterization of individuals with the distal 1q21.1 microdeletion
Edwards, Stacey, Schulze, Katharina, Rosenfeld, Jill, Westerfield, Lauren, Gerard, Amanda, Yuan, Bo, Grigorenko, Elena, Posey, Jennifer, Bi, Weimin, Liu, Pengfei
Published in Molecular genetics and metabolism (01.04.2021)
Published in Molecular genetics and metabolism (01.04.2021)
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Journal Article
1 Multicenter, prospective cohort of genome sequencing in 750 fetal structural anomalies
Wapner, Ronald J., Giordano, Jessica L., de Voest, Jessica, Gilmore, Kelly L., Westerfield, Lauren, Tinfow, Alexandra, Galloway, Stephanie, Tolusso, Leandra, Wong, Beatrix, Jackson, Farrah, Bonesteele, Grant, Wittman, Theresa, Stevens, Blair, Stover, Samantha, Johnson, Anthony, Leslie, Nancy Doan, Swarr, Daniel, Caughey, Aaron B., Chung, Wendy, Clifton, Rebecca, Van den Veyver, Ignatia B., Vora, Neeta L.
Published in American journal of obstetrics and gynecology (01.01.2024)
Published in American journal of obstetrics and gynecology (01.01.2024)
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Journal Article
Expanded carrier screening for reproductive risk assessment: An evidence‐based practice guideline from the National Society of Genetic Counselors
Sagaser, Katelynn G., Malinowski, Jennifer, Westerfield, Lauren, Proffitt, Jennifer, Hicks, Melissa A., Toler, Tomi L., Blakemore, Karin J., Stevens, Blair K., Oakes, Lisa M.
Published in Journal of genetic counseling (01.06.2023)
Published in Journal of genetic counseling (01.06.2023)
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Journal Article
Information is power: The experiences, attitudes and needs of individuals who chose to have prenatal genomic sequencing for fetal anomalies
Kernie, Catherine G., Wynn, Julia, Rosenbaum, Allison, Voest, Jessica, Galloway, Stephanie, Giordano, Jessica, Stover, Samantha, Westerfield, Lauren, Gilmore, Kelly, Wapner, Ronald J., Van den Veyver, Ignatia B., Vora, Neeta L., Clifton, Rebecca G., Caughey, Aaron B., Chung, Wendy K.
Published in Prenatal diagnosis (01.06.2022)
Published in Prenatal diagnosis (01.06.2022)
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Journal Article
A family affair—Severe fetal and neonatal hemolytic anemia due to novel alpha‐spectrin mutations in two siblings
Donepudi, Roopali, Westerfield, Lauren, Stonecipher, Ashley, A. Nassr, Ahmed, Cortes, Magdalena S., Espinoza, Jimmy, Belfort, Michael, Shamshirsaz, Alireza
Published in American journal of medical genetics. Part A (01.03.2020)
Published in American journal of medical genetics. Part A (01.03.2020)
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Journal Article