Prenatal Diagnosis by Chromosomal Microarray Analysis

per Levy, Brynn, Wapner, Ronald
Publicat a Fertil Steril (2018)

Noninvasive Prenatal Testing: The Future Is Now

per Norwitz, Errol R, Levy, Brynn
Publicat 2013

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

per Fantauzzo, Katherine A., Kurban, Mazen, Levy, Brynn, Christiano, Angela M.
Publicat 2012

Chromosomal Mosaicism: Origins and Clinical Implications in Preimplantation and Prenatal Diagnosis

per Levy, Brynn, Hoffman, Eva, McCoy, Rajiv C., Grati, Francesca Romana
Publicat a Prenat Diagn (2021)

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

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

Glut1 Deficiency: Inheritance Pattern Determined by Haploinsufficiency

per Rotstein, Michael, Engelstad, Kristin, Yang, Hong, Wang, Dong, Levy, Brynn, Chung, Wendy K., De Vivo, Darryl C.
Publicat 2010

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

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

Copy Number Variations on Chromosome 4q26–27 Are Associated with Cantu Syndrome

per Kurban, Mazen, Kim, Chong Ae, Kiuru, Maija, Fantauzzo, Katherine, Cabral, Rita, Abbas, Ossama, Levy, Brynn, Christiano, Angela M.
Publicat 2012

At the dawn of personalized reproductive medicine: opportunities and challenges with incorporating multigene panel testing into fertility care

per Yurttas Beim, Piraye, Parfitt, David-Emlyn, Tan, Lei, Sugarman, Elaine A., Hu-Seliger, Tina, Clementi, Caterina, Levy, Brynn
Publicat a J Assist Reprod Genet (2017)

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

per Wei, Shan, Levy, Brynn, Hoffman, Nataly, Cujar, Claudia, Rodney-Sandy, Reunet, Wapner, Ronald, D'Alton, Mary, Williams, Zev
Publicat a Biotechniques (2020)

Genome-wide analysis of abdominal and pleural malignant mesothelioma with DNA arrays reveals both common and distinct regions of copy number alteration

per Borczuk, Alain C., Pei, Jianming, Taub, Robert N., Levy, Brynn, Nahum, Odelia, Chen, Jinli, Chen, Katherine, Testa, Joseph R.
Publicat a Cancer Biol Ther (2016)

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

per Ravi, Harini, McNeill, Gabriel, Goel, Shruti, Meltzer, Steven D., Hunkapiller, Nathan, Ryan, Allison, Levy, Brynn, Demko, Zachary P.
Publicat a PLoS One (2018)

Duplication of the ZIC2 gene is not associated with holoprosencephaly

per Jobanputra, Vaidehi, Burke, Alanna, Kwame, Anyane-Yeboa, Shanmugham, Anita, Shirazi, Maryam, Brown, Stephen, Warburton, Peter E., Levy, Brynn, Warburton, Dorothy
Publicat 2011

Prevalence and Physical Distribution of SRY in the gonads of a Woman with Turner Syndrome: Phenotypic Presentation, Tubal Formation, and Malignancy Risk

per Baer, Tamar G., Freeman, Christopher E., Cujar, Claudia, Mansukhani, Mahesh, Singh, Bahadur, Chen, Xiaowei, Abellar, Rosanna, Oberfield, Sharon E, Levy, Brynn
Publicat a Horm Res Paediatr (2017)

Non-invasive prenatal aneuploidy testing at chromosomes 13, 18, 21, X, and Y, using targeted sequencing of polymorphic loci

per Zimmermann, Bernhard, Hill, Matthew, Gemelos, George, Demko, Zachary, Banjevic, Milena, Baner, Johan, Ryan, Allison, Sigurjonsson, Styrmir, Chopra, Nikhil, Dodd, Michael, Levy, Brynn, Rabinowitz, Matthew
Publicat 2012

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

per 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
Publicat a Oncotarget (2016)

Restoration of replication fork stability in BRCA1- and BRCA2-deficient cells by inactivation of SNF2-family fork remodelers

per Taglialatela, Angelo, Alvarez, Silvia, Leuzzi, Giuseppe, Sannino, Vincenzo, Ranjha, Lepakshi, Huang, Jen-Wei, Madubata, Chioma, Anand, Roopesh, Levy, Brynn, Rabadan, Raul, Cejka, Petr, Costanzo, Vincenzo, Ciccia, Alberto
Publicat a Mol Cell (2017)

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

per 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
Publicat a PLoS Curr (2017)

Induced pluripotent stem cells (iPSC) created from skin fibroblasts of patients with Prader-Willi Syndrome (PWS) retain the molecular signature of PWS

per Burnett, Lisa C., LeDuc, Charles A., Sulsona, Carlos R., Paull, Daniel, Eddiry, Sanaa, Levy, Brynn, Salles, Jean Pierre, Tauber, Maithe, Driscoll, Daniel J., Egli, Dieter, Leibel, Rudolph L.
Publicat a Stem Cell Res (2016)

Genomic imbalances in pediatric patients with chronic kidney disease

per Verbitsky, Miguel, Sanna-Cherchi, Simone, Fasel, David A., Levy, Brynn, Kiryluk, Krzysztof, Wuttke, Matthias, Abraham, Alison G., Kaskel, Frederick, Köttgen, Anna, Warady, Bradley A., Furth, Susan L., Wong, Craig S., Gharavi, Ali G.
Publicat a J Clin Invest (2015)