Trps1 and Its Target Gene Sox9 Regulate Epithelial Proliferation in the Developing Hair Follicle and Are Associated with Hypertrichosis

por Fantauzzo, Katherine A., Kurban, Mazen, Levy, Brynn, Christiano, Angela M.
Publicado 2012

SNP microarray-based 24 chromosome aneuploidy screening is significantly more consistent than FISH

por Treff, Nathan R., Levy, Brynn, Su, Jing, Northrop, Lesley E., Tao, Xin, Scott, Richard T.
Publicado 2010

3q27.1 microdeletion causes prenatal and postnatal growth restriction and neurodevelopmental abnormalities

por Barua, Subit, Pereira, Elaine M., Jobanputra, Vaidehi, Anyane-Yeboa, Kwame, Levy, Brynn, Liao, Jun
Publicado 2022

3′ UTR Deletion of FBXO28 in a Patient with Brain Abnormalities and Developmental Delay

por Bi, Xin, Mulhern, Maureen S., Spiegel, Erica, Wapner, Ronald J., Levy, Brynn, Bain, Jennifer M., Liao, Jun
Publicado 2023

Incidental identification of balanced translocation carrier patients through comprehensive chromosome screening of IVF-derived blastocysts

por Treff, Nathan R., Forman, Eric J., Katz-Jaffe, Mandy G., Schoolcraft, William B., Levy, Brynn, Scott, Richard T.
Publicado 2013

A rapid and simple bead-bashing-based method for genomic DNA extraction from mammalian tissue

por Wei, Shan, Levy, Brynn, Hoffman, Nataly, Cujar, Claudia, Rodney-Sandy, Reunet, Wapner, Ronald, D'Alton, Mary, Williams, Zev
Publicado 2020

Validation of a SNP-based non-invasive prenatal test to detect the fetal 22q11.2 deletion in maternal plasma samples

por Ravi, Harini, McNeill, Gabriel, Goel, Shruti, Meltzer, Steven D., Hunkapiller, Nathan, Ryan, Allison, Levy, Brynn, Demko, Zachary P.
Publicado 2018

Implementation of Nanopore sequencing as a pragmatic workflow for copy number variant confirmation in the clinic

por Greer, Stephanie U., Botello, Jacquelin, Hongo, Donna, Levy, Brynn, Shah, Premal, Rabinowitz, Matthew, Miller, Danny E., Im, Kate, Kumar, Akash
Publicado 2023

Case Report: Prenatal Identification of a De Novo Mosaic Neocentric Marker Resulting in 13q31.1→qter Tetrasomy in a Mildly Affected Girl

por Dharmadhikari, Avinash V., Pereira, Elaine M., Andrews, Carli C ., Macera, Michael, Harkavy, Nina, Wapner, Ronald, Jobanputra, Vaidehi, Levy, Brynn, Ganapathi, Mythily, Liao, Jun
Publicado 2022

Integration of a Cross-Ancestry Polygenic Model With Clinical Risk Factors Improves Breast Cancer Risk Stratification

por Tshiaba, Placede T., Ratman, Dariusz K., Sun, Jiayi M., Tunstall, Tate S., Levy, Brynn, Shah, Premal S., Weitzel, Jeffrey N., Rabinowitz, Matthew, Kumar, Akash, Im, Kate M.
Publicado 2023

Genetic landscape of T- and NK-cell post-transplant lymphoproliferative disorders

por Margolskee, Elizabeth, Jobanputra, Vaidehi, Jain, Preti, Chen, Jinli, Ganapathi, Karthik, Nahum, Odelia, Levy, Brynn, Morscio, Julie, Murty, Vundavalli, Tousseyn, Thomas, Alobeid, Bachir, Mansukhani, Mahesh, Bhagat, Govind
Publicado 2016

Analytical and Clinical Validity Study of FirstStepDx PLUS: A Chromosomal Microarray Optimized for Patients with Neurodevelopmental Conditions

por Hensel, Charles, Vanzo, Rena, Martin, Megan, Dixon, Sean, Lambert, Christophe, Levy, Brynn, Nelson, Lesa, Peiffer, Andy, Ho, Karen S., Rushton, Patricia, Serrano, Moises, South, Sarah, Ward, Kenneth, Wassman, Edward
Publicado 2017

Whole-genome risk prediction of common diseases in human preimplantation embryos

por Kumar, Akash, Im, Kate, Banjevic, Milena, Ng, Pauline C., Tunstall, Tate, Garcia, Geronimo, Galhardo, Luisa, Sun, Jiayi, Schaedel, Oren N., Levy, Brynn, Hongo, Donna, Kijacic, Dusan, Kiehl, Michelle, Tran, Nam D., Klatsky, Peter C., Rabinowitz, Matthew
Publicado 2022

The genetic landscape of dural marginal zone lymphomas

por Ganapathi, Karthik A., Jobanputra, Vaidehi, Iwamoto, Fabio, Jain, Preti, Chen, Jinli, Cascione, Luciano, Nahum, Odelia, Levy, Brynn, Xie, Yi, Khattar, Pallavi, Hoehn, Daniela, Bertoni, Francesco, Murty, Vundavalli V., Pittaluga, Stefania, Jaffe, Elaine S., Alobeid, Bachir, Mansukhani, Mahesh M., Bhagat, Govind
Publicado 2016

Optical genome mapping in acute myeloid leukemia: a multicenter evaluation

por Levy, Brynn, Baughn, Linda B., Akkari, Yassmine, Chartrand, Scott, LaBarge, Brandon, Claxton, David, Lennon, P. Alan, Cujar, Claudia, Kolhe, Ravindra, Kroeger, Kate, Pitel, Beth, Sahajpal, Nikhil, Sathanoori, Malini, Vlad, George, Zhang, Lijun, Fang, Min, Kanagal-Shamanna, Rashmi, Broach, James R.
Publicado 2022

Reliable detection of subchromosomal deletions and duplications using cell‐based noninvasive prenatal testing

por Vossaert, Liesbeth, Wang, Qun, Salman, Roseen, Zhuo, Xinming, Qu, Chunjing, Henke, David, Seubert, Ron, Chow, Jennifer, U'ren, Lance, Enright, Brennan, Stilwell, Jackie, Kaldjian, Eric, Yang, Yaping, Shaw, Chad, Levy, Brynn, Wapner, Ronald, Breman, Amy, Van den Veyver, Ignatia, Beaudet, Arthur
Publicado 2018

Validation Studies for Single Circulating Trophoblast Genetic Testing as a Form of Noninvasive Prenatal Diagnosis

por Vossaert, Liesbeth, Wang, Qun, Salman, Roseen, McCombs, Anne K., Patel, Vipulkumar, Qu, Chunjing, Mancini, Michael A., Edwards, Dean P., Malovannaya, Anna, Liu, Pengfei, Shaw, Chad A., Levy, Brynn, Wapner, Ronald J., Bi, Weimin, Breman, Amy M., Van den Veyver, Ignatia B., Beaudet, Arthur L.
Publicado 2019

Guiding the global evolution of cytogenetic testing for hematologic malignancies

por Akkari, Yassmine M.N., Baughn, Linda B., Dubuc, Adrian M., Smith, Adam C., Mallo, Mar, Dal Cin, Paola, Diez Campelo, Maria, Gallego, Marta S., Granada Font, Isabel, Haase, Detlef T., Schlegelberger, Brigitte, Slavutsky, Irma, Mecucci, Cristina, Levine, Ross L., Hasserjian, Robert P., Solé, Francesc, Levy, Brynn, Xu, Xinjie
Publicado 2022

Mutations in the Cholesterol Transporter Gene ABCA5 Are Associated with Excessive Hair Overgrowth

por DeStefano, Gina M., Kurban, Mazen, Anyane-Yeboa, Kwame, Dall'Armi, Claudia, Di Paolo, Gilbert, Feenstra, Heather, Silverberg, Nanette, Rohena, Luis, López-Cepeda, Larissa D., Jobanputra, Vaidehi, Fantauzzo, Katherine A., Kiuru, Maija, Tadin-Strapps, Marija, Sobrino, Antonio, Vitebsky, Anna, Warburton, Dorothy, Levy, Brynn, Salas-Alanis, Julio C., Christiano, Angela M.
Publicado 2014

Identification of novel genomic imbalances in Saudi patients with congenital heart disease

por Al-Hassnan, Zuhair N., Albawardi, Waad, Almutairi, Faten, AlMass, Rawan, AlBakheet, Albandary, Mustafa, Osama M., AlQuait, Laila, Shinwari, Zarghuna M. A., Wakil, Salma, Salih, Mustafa A., Al-Fayyadh, Majid, Hassan, Saeed M., Aljoufan, Mansour, Al-Nakhli, Osima, Levy, Brynn, AlMaarik, Balsam, Al-Hakami, Hana A., Alsagob, Maysoon, Colak, Dilek, Kaya, Namik
Publicado 2018