Tumor-Infiltrating Macrophages in Post-Transplant, Relapsed Classical Hodgkin Lymphoma Are Donor-Derived
Crane, Genevieve M, Samols, Mark A, Morsberger, Laura A, Yonescu, Raluca, Thiess, Michele L, Batista, Denise A S, Ning, Yi, Burns, Kathleen H, Vuica-Ross, Milena, Borowitz, Michael J, Gocke, Christopher D, Ambinder, Richard F, Duffield, Amy S
Published in PloS one (29.09.2016)
Published in PloS one (29.09.2016)
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Journal Article
Cytopathologic features of mammary analogue secretory carcinoma
Bishop, Justin A, Yonescu, Raluca, Batista, Denise A S, Westra, William H, Ali, Syed Z
Published in Cancer cytopathology (01.05.2013)
Published in Cancer cytopathology (01.05.2013)
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Journal Article
Mutations in FARS2 and non-fatal mitochondrial dysfunction in two siblings
Vernon, Hilary J, McClellan, Rebecca, Batista, Denise AS, Naidu, Sakkubai
Published in American journal of medical genetics. Part A (01.05.2015)
Published in American journal of medical genetics. Part A (01.05.2015)
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Journal Article
3q29 interstitial microduplication: A new syndrome in a three-generation family
Lisi, Emily C., Hamosh, Ada, Doheny, Kimberly F., Squibb, Elizabeth, Jackson, Barbara, Galczynski, Rebecca, Thomas, George H., Batista, Denise A.S.
Published in American journal of medical genetics. Part A (01.03.2008)
Published in American journal of medical genetics. Part A (01.03.2008)
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Journal Article
Multicolor fluorescence in situ hybridization (SKY) in mycosis fungoides and Sézary syndrome: Search for recurrent chromosome abnormalities
Batista, Denise A S., Vonderheid, Eric C., Hawkins, Anita, Morsberger, Laura, Long, Patricia, Murphy, Kathleen M., Griffin, Constance A.
Published in Genes chromosomes & cancer (01.04.2006)
Published in Genes chromosomes & cancer (01.04.2006)
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Journal Article
The Use of High-Density SNP Array to Map Homozygosity in Consanguineous Families to Efficiently Identify Candidate Genes: Application to Woodhouse-Sakati Syndrome
Applegate, Carolyn, Batista, Denise A. S., Wohler, Elizabeth, Sheridan, Molly B., Hoover-Fong, Julie
Published in Case reports in genetics (01.01.2015)
Published in Case reports in genetics (01.01.2015)
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Journal Article
Molecular cytogenetic analysis of a de novo interstitial deletion of chromosome 10q (q25.3q26.13) in a male child with ambiguous genitalia: Evidence for a new critical region for genital development
Mardo, Veronica, Squibb, Elizabeth E., Braverman, Nancy, Hoover-Fong, Julie E., Migeon, Claude, Batista, Denise A.S., Thomas, George H.
Published in American journal of medical genetics. Part A (01.09.2008)
Published in American journal of medical genetics. Part A (01.09.2008)
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Journal Article
Mutations in Alström protein impair terminal differentiation of cardiomyocytes
Shenje, Lincoln T., Andersen, Peter, Halushka, Marc K., Lui, Cecillia, Fernandez, Laviel, Collin, Gayle B., Amat-Alarcon, Nuria, Meschino, Wendy, Cutz, Ernest, Chang, Kenneth, Yonescu, Raluca, Batista, Denise A. S., Chen, Yan, Chelko, Stephen, Crosson, Jane E., Scheel, Janet, Vricella, Luca, Craig, Brian D., Marosy, Beth A., Mohr, David W., Hetrick, Kurt N., Romm, Jane M., Scott, Alan F., Valle, David, Naggert, Jürgen K., Kwon, Chulan, Doheny, Kimberly F., Judge, Daniel P.
Published in Nature communications (04.03.2014)
Published in Nature communications (04.03.2014)
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Journal Article
Sacrococcygeal teratomas: clinico-pathological characteristics and isochromosome 12p status
Gurda, Grzegorz T, VandenBussche, Christopher J, Yonescu, Raluca, Gonzalez-Roibon, Nilda, Ellis, Carla L, Batista, Denise A S, Netto, George J
Published in Modern pathology (01.04.2014)
Published in Modern pathology (01.04.2014)
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Journal Article
First Trimester Diagnosis of Holoprosencephaly Secondary to a Ring Chromosome 7
Henderson, Lindsay B., Corson, Virginia L., Saul, Daniel O., Anderson, Cynthia, Millard, Sarah, Batista, Denise A. S., Blakemore, Karin J., DeScipio, Cheryl
Published in Case reports in genetics (01.01.2013)
Published in Case reports in genetics (01.01.2013)
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Journal Article
Albinism and Developmental Delay: The Need to Test for 15q11-q13 Deletion
Saadeh, Reem, MD, Lisi, Emily C., MS, Batista, Denise A.S., PhD, McIntosh, Iain, PhD, Hoover-Fong, Julie E., MD
Published in Pediatric neurology (01.10.2007)
Published in Pediatric neurology (01.10.2007)
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Journal Article
Creation and characterization of an airway epithelial cell line for stable expression of CFTR variants
Gottschalk, Laura B, Vecchio-Pagan, Briana, Sharma, Neeraj, Han, Sangwoo T, Franca, Arianna, Wohler, Elizabeth S, Batista, Denise A.S, Goff, Loyal A, Cutting, Garry R
Published in Journal of cystic fibrosis (01.05.2016)
Published in Journal of cystic fibrosis (01.05.2016)
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Journal Article
Genetic Profiling by Single-Nucleotide Polymorphism-Based Array Analysis Defines Three Distinct Subtypes of Orbital Meningioma
Ho, Cheng-Ying, Mosier, Stacy, Safneck, Janice, Salomao, Diva R., Miller, Neil R., Eberhart, Charles G., Gocke, Christopher D., Batista, Denise A. S., Rodriguez, Fausto J.
Published in Brain pathology (Zurich, Switzerland) (01.03.2015)
Published in Brain pathology (Zurich, Switzerland) (01.03.2015)
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Journal Article
Genomic changes in gliomas detected using single nucleotide polymorphism array in formalin-fixed, paraffin-embedded tissue: superior results compared with microsatellite analysis
Harada, Shuko, Henderson, Lindsay B, Eshleman, James R, Gocke, Christopher D, Burger, Peter, Griffin, Constance A, Batista, Denise A S
Published in The Journal of molecular diagnostics : JMD (01.09.2011)
Published in The Journal of molecular diagnostics : JMD (01.09.2011)
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Journal Article
Mosaic trisomy 13: understanding origin using SNP array
Jinawath, Natini, Zambrano, Regina, Wohler, Elizabeth, Palmquist, Maria K, Hoover-Fong, Julie, Hamosh, Ada, Batista, Denise A S
Published in Journal of medical genetics (01.05.2011)
Published in Journal of medical genetics (01.05.2011)
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Journal Article
Interstitial microduplication of Xp22.31: Causative of intellectual disability or benign copy number variant?
Li, Feng, Shen, Yiping, Köhler, Udo, Sharkey, Freddie H, Menon, Deepa, Coulleaux, Laurence, Malan, Valérie, Rio, Marlène, McMullan, Dominic J, Cox, H, Fagan, Kerry A, Gaunt, Lorraine, Metcalfe, Kay, Heinrich, Uwe, Hislop, Gordon, Maye, Una, Sutcliffe, Maxine, Wu, Bai-Lin, Thiel, Brian D, Mulchandani, Surabhi, Conlin, Laura K, Spinner, Nancy B, Murphy, Kathleen M, Batista, Denise A.S
Published in European journal of medical genetics (01.03.2010)
Published in European journal of medical genetics (01.03.2010)
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Journal Article
An unbalanced translocation between chromosomes 2p and 6p associated with Axenfeld-Rieger anomaly type 3, hearing loss, developmental delay, and distinct facial dysmorphism
Li, Feng, Batista, Denise A.S., Maumenee, Irene, Wang, Tao
Published in American journal of medical genetics. Part A (01.05.2010)
Published in American journal of medical genetics. Part A (01.05.2010)
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Journal Article