Prenatal Diagnosis by Chromosomal Microarray Analysis

Por Levy, Brynn, Wapner, Ronald
Publicado no Fertil Steril (2018)

Noninvasive Prenatal Testing: The Future Is Now

Por Norwitz, Errol R, Levy, Brynn
Publicado em 2013

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 em 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 em 2010

Glut1 Deficiency: Inheritance Pattern Determined by Haploinsufficiency

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

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 em 2013

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

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

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

Por Yurttas Beim, Piraye, Parfitt, David-Emlyn, Tan, Lei, Sugarman, Elaine A., Hu-Seliger, Tina, Clementi, Caterina, Levy, Brynn
Publicado no J Assist Reprod Genet (2017)

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 no Biotechniques (2020)

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

Por Borczuk, Alain C., Pei, Jianming, Taub, Robert N., Levy, Brynn, Nahum, Odelia, Chen, Jinli, Chen, Katherine, Testa, Joseph R.
Publicado no Cancer Biol Ther (2016)

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 no PLoS One (2018)

Duplication of the ZIC2 gene is not associated with holoprosencephaly

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

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

Por Baer, Tamar G., Freeman, Christopher E., Cujar, Claudia, Mansukhani, Mahesh, Singh, Bahadur, Chen, Xiaowei, Abellar, Rosanna, Oberfield, Sharon E, Levy, Brynn
Publicado no Horm Res Paediatr (2017)

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

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

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 no Oncotarget (2016)

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

Por 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
Publicado no Mol Cell (2017)

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 no PLoS Curr (2017)

Genomic imbalances in pediatric patients with chronic kidney disease

Por 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.
Publicado no J Clin Invest (2015)

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 no Oncotarget (2016)

Position effect on FGF13 associated with X-linked congenital generalized hypertrichosis

Por DeStefano, Gina M., Fantauzzo, Katherine A., Petukhova, Lynn, Kurban, Mazen, Tadin-Strapps, Marija, Levy, Brynn, Warburton, Dorothy, Cirulli, Elizabeth T., Han, Yujun, Sun, Xiaoyun, Shen, Yufeng, Shirazi, Maryam, Jobanputra, Vaidehi, Cepeda-Valdes, Rodrigo, Cesar Salas-Alanis, Julio, Christiano, Angela M.
Publicado em 2013