Prenatal cell‐free DNA screening for fetal aneuploidy in pregnant women at average or high risk: Results from a large US clinical laboratory

por Guy, Carrie, Haji‐Sheikhi, Farnoosh, Rowland, Charles M., Anderson, Ben, Owen, Renius, Lacbawan, Felicitas L., Alagia, Damian P.
Publicado 2019

Effectiveness of Practices to Support Appropriate Laboratory Test Utilization: A Laboratory Medicine Best Practices Systematic Review and Meta-Analysis

por Rubinstein, Matthew, Hirsch, Robert, Bandyopadhyay, Kakali, Madison, Bereneice, Taylor, Thomas, Ranne, Anne, Linville, Millie, Donaldson, Keri, Lacbawan, Felicitas, Cornish, Nancy
Publicado 2018

NGS-defined measurable residual disease (MRD) after initial chemotherapy as a prognostic biomarker for acute myeloid leukemia

por Li, Yonghong, Solis-Ruiz, Jose, Yang, Fei, Long, Nicola, Tong, Carmen H., Lacbawan, Felicitas L., Racke, Frederick K., Press, Richard D.
Publicado 2023

Unique phenotype in a patient with CHARGE syndrome

por Jain, Shobhit, Kim, Hyung-Goo, Lacbawan, Felicitas, Meliciani, Irene, Wenzel, Wolfgang, Kurth, Ingo, Sharma, Josefina, Schoeneman, Morris, Ten, Svetlana, Layman, Lawrence C, Jacobson-Dickman, Elka
Publicado 2011

Development and validation of a high throughput SARS-CoV-2 whole genome sequencing workflow in a clinical laboratory

por Rosenthal, Sun Hee, Gerasimova, Anna, Ruiz-Vega, Rolando, Livingston, Kayla, Kagan, Ron M., Liu, Yan, Anderson, Ben, Owen, Renius, Bernstein, Laurence, Smolgovsky, Alla, Xu, Dong, Chen, Rebecca, Grupe, Andrew, Tanpaiboon, Pranoot, Lacbawan, Felicitas
Publicado 2022

Arginine to ornithine ratio as a diagnostic marker in patients with positive newborn screening for hyperargininemia

por Huang, Yue, Sharma, Rajesh, Feigenbaum, Annette, Lee, Chung, Sahai, Inderneel, Sanchez Russo, Rossana, Neira, Juanita, Brooks, Susan Sklower, Jackson, Kelly E., Wong, Derek, Cederbaum, Stephen, Lacbawan, Felicitas L., Rowland, Charles M., Tanpaiboon, Pranoot, Salazar, Denise
Publicado 2021

Analytical validation and performance characteristics of a 48-gene next-generation sequencing panel for detecting potentially actionable genomic alterations in myeloid neoplasms

por Rosenthal, Sun Hee, Gerasimova, Anna, Ma, Charles, Li, Hai-Rong, Grupe, Andrew, Chong, Hansook, Acab, Allan, Smolgovsky, Alla, Owen, Renius, Elzinga, Christopher, Chen, Rebecca, Sugganth, Daniel, Freitas, Tracey, Graham, Jennifer, Champion, Kristen, Bhattacharya, Anindya, Racke, Frederick, Lacbawan, Felicitas
Publicado 2021

Development and Validation of a 34-Gene Inherited Cancer Predisposition Panel Using Next-Generation Sequencing

por Rosenthal, Sun Hee, Sun, Weimin, Zhang, Ke, Liu, Yan, Nguyen, Quoclinh, Gerasimova, Anna, Nery, Camille, Cheng, Linda, Castonguay, Carolyn, Hiller, Elaine, Li, James, Elzinga, Christopher, Wolfson, David, Smolgovsky, Alla, Chen, Rebecca, Buller-Burckle, Arlene, Catanese, Joseph, Grupe, Andrew, Lacbawan, Felicitas, Owen, Renius
Publicado 2020

Absence of the ER Cation Channel TMEM38B/TRIC-B Disrupts Intracellular Calcium Homeostasis and Dysregulates Collagen Synthesis in Recessive Osteogenesis Imperfecta

por Cabral, Wayne A., Ishikawa, Masaki, Garten, Matthias, Makareeva, Elena N., Sargent, Brandi M., Weis, MaryAnn, Barnes, Aileen M., Webb, Emma A., Shaw, Nicholas J., Ala-Kokko, Leena, Lacbawan, Felicitas L., Högler, Wolfgang, Leikin, Sergey, Blank, Paul S., Zimmerberg, Joshua, Eyre, David R., Yamada, Yoshihiko, Marini, Joan C.
Publicado 2016