Tetrasomy 18p: tentative delineation of a syndrome

Por Batista, Denise A S, Vianna-Morgante, Angela M, Richieri-Costa, A
Publicado em 1983

The Use of High-Density SNP Array to Map Homozygosity in Consanguineous Families to Efficiently Identify Candidate Genes: Application to Woodhouse-Sakati Syndrome

Por Sheridan, Molly B., Wohler, Elizabeth, Batista, Denise A. S., Applegate, Carolyn, Hoover-Fong, Julie
Publicado no Case Rep Genet (2015)

Cytopathologic Features of Mammary Analogue Secretory Carcinoma

Por Bishop, Justin A., Yonescu, Raluca, Batista, Denise A. S., Westra, William H., Ali, Syed Z.
Publicado em 2012

Albinism and Developmental Delay: The Need to Test for 15q11–q13 deletion

Por Saadeh, Reem, Lisi, Emily C., Batista, Denise A.S., McIntosh, Iain, Hoover-Fong, Julie E.
Publicado em 2007

Genomic Changes in Gliomas Detected Using Single Nucleotide Polymorphism Array in Formalin-Fixed, Paraffin-Embedded Tissue: Superior Results Compared with Microsatellite Analysis

Por Harada, Shuko, Henderson, Lindsay B., Eshleman, James R., Gocke, Christopher D., Burger, Peter, Griffin, Constance A., Batista, Denise A.S.
Publicado em 2011

A Rare e14a3 (b3a3) BCR-ABL Fusion Transcript in Chronic Myeloid Leukemia: Diagnostic Challenges in Clinical Laboratory Practice

Por Jinawath, Natini, Norris-Kirby, Alexis, Smith, B. Douglas, Gocke, Christopher D., Batista, Denise A., Griffin, Constance A., Murphy, Kathleen M.
Publicado em 2009

Myoclonus-dystonia and Silver-Russell syndrome resulting from maternal uniparental disomy of chromosome 7

Por Sheridan, Molly B., Telegrafi, Aida Bytyci, Stinnett, Victoria, Umeh, Chizoba C., Mari, Zoltan, Dawson, Ted M., Bodurtha, Joann, Batista, Denise A.S.
Publicado em 2013

First Trimester Diagnosis of Holoprosencephaly Secondary to a Ring Chromosome 7

Por Henderson, Lindsay B., Corson, Virginia L., Saul, Daniel O., Anderson, Cynthia, Millard, Sarah, Batista, Denise A. S., Blakemore, Karin J., DeScipio, Cheryl
Publicado em 2013

Severe infantile epileptic encephalopathy due to mutations in PLCB1: expansion of the genotypic and phenotypic disease spectrum

Por Ngoh, Adeline, McTague, Amy, Wentzensen, Ingrid M, Meyer, Esther, Applegate, Carolyn, Kossoff, Eric H, Batista, Denise A, Wang, Tao, Kurian, Manju A
Publicado no Dev Med Child Neurol (2014)

Creation and characterization of an airway epithelial cell line for stable expression of CFTR variants

Por 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.
Publicado no J Cyst Fibros (2015)

Genetic Profiling by Single‐Nucleotide Polymorphism‐Based Array Analysis Defines Three Distinct Subtypes of Orbital Meningioma

Por 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.
Publicado no Brain Pathol (2014)

Loss of the Mismatched Human Leukocyte Antigen Haplotype in Two Acute Myelogenous Leukemia Relapses after Haploidentical Bone Marrow Transplantation with Posttransplantation Cyclop...

Por McCurdy, Shannon R., Iglehart, Brian S., Batista, Denise A., Gocke, Christopher D., Ning, Yi, Knaus, Hanna A., Jackson, Annette M., Leffell, Mary S., Luznik, Leo, Gojo, Ivana
Publicado no Leukemia (2016)

Tumor-Infiltrating Macrophages in Post-Transplant, Relapsed Classical Hodgkin Lymphoma Are Donor-Derived

Por 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.
Publicado no PLoS One (2016)

Deletion of MAP2K2/MEK2: A novel mechanism for a RASopathy?

Por Nowaczyk, Małgorzata J.M., Thompson, Brandi A., Zeesman, Susan, Moog, Ute, Sanchez-Lara, Pedro A., Magoulas, Pilar L., Falk, Rena E., Fong, Julie Hoover, Batista, Denise A.S., Amudhavalli, Shivarajan M., White, Sue M., Graham, Gail E., Rauen, Katherine A.
Publicado no Clin Genet (2013)

Mutations in Alström Protein Impair Terminal Differentiation of Cardiomyocytes

Por 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.
Publicado em 2014