Denise Batista
The Johns Hopkins University, School of Medicine

Denise Batista

30 Publications

This is a list of publications by this researcher, listed chronologically starting with the most recent first. New publications appear in this list weekly. The source of publications for this application is PubMed, so only PubMed publications are included.

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1.
2013

Justin A Bishop; Raluca Yonescu; Denise A S Batista; William H Westra; Syed Z Ali

Cytopathologic features of mammary analogue secretory carcinoma.
Cancer cytopathology 2013;121(5):228-33.
2.
2013

Ryan W Y Lee; Joann Bodurtha; Julie Cohen; Ali Fatemi; Denise Batista

Deletion 12p12 involving SOX5 in two children with developmental delay and dysmorphic features.
Pediatric neurology 2013;48(4):317-20.
3.
2013

Lindsay B Henderson; Virginia L Corson; Daniel O Saul; Cynthia Anderson; Sarah Millard; Denise A S Batista; Karin J Blakemore; Cheryl Descipio

First trimester diagnosis of holoprosencephaly secondary to a ring chromosome 7.
Case reports in genetics 2013;2013():578202.
4.
2012

Andres Jerez; Lukasz P Gondek; Anna M Jankowska; Hideki Makishima; Bartlomiej Przychodzen; Ramon V Tiu; Christine L O'Keefe; Azim M Mohamedali; Denise Batista; Mikkael A Sekeres; et al.

Topography, clinical, and genomic correlates of 5q myeloid malignancies revisited.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2012;30(12):1343-9.
5.
2011

Shuko Harada; Lindsay B Henderson; James R Eshleman; Christopher D Gocke; Peter Burger; Constance A Griffin; Denise A S Batista

Genomic changes in gliomas detected using single nucleotide polymorphism array in formalin-fixed, paraffin-embedded tissue: superior results compared with microsatellite analysis.
The Journal of molecular diagnostics : JMD 2011;13(5):541-8.
6.
2011

Natini Jinawath; Regina Zambrano; Elizabeth Wohler; Maria K Palmquist; Julie Hoover-Fong; Ada Hamosh; Denise A S Batista

Mosaic trisomy 13: understanding origin using SNP array.
Journal of medical genetics 2011;48(5):323-6.
7.
2011

Gerald Raymond; Elizabeth Wohler; Carolyn Dinsmore; Jeanne Cox; Michael Johnston; Denise Batista; Tao Wang

An interstitial duplication at 2q24.3 involving the SCN1A, SCN2A, SCN3A genes associated with infantile epilepsy.
American journal of medical genetics. Part A 2011;155A(4):920-3.
8.
2011

Regina M Zambrano; Elizabeth Wohler; Göran Annerén; Ann-Charlotte Thuresson; Garry R Cutting; Denise A Batista

Unbalanced translocation 9;16 in two children with dysmorphic features, and severe developmental delay: Evidence of cross-over within derivative chromosome 9 in patient #1.
European journal of medical genetics 2011;54(2):189-93.
9.
2010

Feng Li; Denise A S Batista; Irene Maumenee; Tao Wang

An unbalanced translocation between chromosomes 2p and 6p associated with Axenfeld-Rieger anomaly type 3, hearing loss, developmental delay, and distinct facial dysmorphism.
American journal of medical genetics. Part A 2010;152A(5):1318-21.
10.
2010

Feng Li; Yiping Shen; Udo Köhler; Freddie H Sharkey; Deepa Menon; Laurence Coulleaux; Valérie Malan; Marlène Rio; Dominic J McMullan; H Cox; et al.

Interstitial microduplication of Xp22.31: Causative of intellectual disability or benign copy number variant?
European journal of medical genetics 2010;53(2):93-9.
11.
2009

N Sobreira; M Cernach; D Batista; D Brunoni; A Perez

Pseudoaminopterin syndrome: clinical report with new characteristics.
American journal of medical genetics. Part A 2009;149A(12):2843-8.
12.
2009

Nara Sobreira; Michael F Walsh; Denise Batista; Tao Wang

Interstitial deletion 5q14.3-q21 associated with iris coloboma, hearing loss, dental anomaly, moderate intellectual disability, and attention deficit and hyperactivity disorder.
American journal of medical genetics. Part A 2009;149A(11):2581-3.
13.
2009

Feng Li; Emily C Lisi; Elizabeth S Wohler; Ada Hamosh; Denise A S Batista

3q29 interstitial microdeletion syndrome: an inherited case associated with cardiac defect and normal cognition.
European journal of medical genetics 2009;52(5):349-52.
14.
2009

Natini Jinawath; Alexis Norris-Kirby; B Douglas Smith; Christopher D Gocke; Denise A Batista; Constance A Griffin; Kathleen M Murphy

A rare e14a3 (b3a3) BCR-ABL fusion transcript in chronic myeloid leukemia: diagnostic challenges in clinical laboratory practice.
The Journal of molecular diagnostics : JMD 2009;11(4):359-63.
15.
2008

Veronica Mardo; Elizabeth E Squibb; Nancy Braverman; Julie E Hoover-Fong; Claude Migeon; Denise A S Batista; George H Thomas

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.
American journal of medical genetics. Part A 2008;146A(17):2293-7.
16.
2008

Matthew Georgy; Raluca Yonescu; Constance A Griffin; Denise A S Batista

Acute mixed lineage leukemia and a t(6;14)(q25;q32) in two adults.
Cancer genetics and cytogenetics 2008;185(1):28-31.
17.
2008

Emily C Lisi; Ada Hamosh; Kimberly F Doheny; Elizabeth Squibb; Barbara Jackson; Rebecca Galczynski; George H Thomas; Denise A S Batista

3q29 interstitial microduplication: a new syndrome in a three-generation family.
American journal of medical genetics. Part A 2008;146A(5):601-9.
18.
2007

E G Weir; M Ali Ansari-Lari; D A S Batista; C A Griffin; S Fuller; B D Smith; M J Borowitz

Acute bilineal leukemia: a rare disease with poor outcome.
Leukemia 2007;21(11):2264-70.
19.
2007

Reem Saadeh; Emily C Lisi; Denise A S Batista; Iain McIntosh; Julie E Hoover-Fong

Albinism and developmental delay: the need to test for 15q11-q13 deletion.
Pediatric neurology 2007;37(4):299-302.
20.
2006

Janis M Taube; Constance A Griffin; Raluca Yonescu; Laura Morsberger; Pedram Argani; Frederic B Askin; Denise A S Batista

Pleuropulmonary blastoma: cytogenetic and spectral karyotype analysis.
Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society 2006;9(6):453-61.
21.
2006

Denise A S Batista; Eric C Vonderheid; Anita Hawkins; Laura Morsberger; Patricia Long; Kathleen M Murphy; Constance A Griffin

Multicolor fluorescence in situ hybridization (SKY) in mycosis fungoides and Sézary syndrome: search for recurrent chromosome abnormalities.
Genes, chromosomes & cancer 2006;45(4):383-91.
22.
2005

Denise A S Batista; Anita Hawkins; Kathleen M Murphy; Constance A Griffin

BCR/ABL rearrangement in two cases of Philadelphia chromosome negative chronic myeloid leukemia: deletion on the derivative chromosome 9 may or not be present.
Cancer genetics and cytogenetics 2005;163(2):164-7.
23.
1997

K F Doheny; S A Rasmussen; J Rutberg; G L Semenza; J Stamberg; M Schwartz; D A Batista; G Stetten; G H Thomas

Segregation of a familial balanced (12;10) insertion resulting in Dup(10)(q21.2q22.1) and Del(10)(q21.2q22.1) in first cousins.
American journal of medical genetics 1997;69(2):188-93.
24.
1995

C M Tuck-Muller; H Chen; J E Martínez; C C Shen; S Li; C Kusyk; D A Batista; Y M Bhatnagar; E Dowling; W Wertelecki

Isodicentric Y chromosome: cytogenetic, molecular and clinical studies and review of the literature.
Human genetics 1995;96(1):119-29.
25.
1995

H Chen; C M Tuck-Muller; D A Batista; W Wertelecki

Identification of supernumerary ring chromosome 1 mosaicism using fluorescence in situ hybridization.
American journal of medical genetics 1995;56(2):219-33.
26.
1995

D A Batista; C Escallon; K J Blakemore; G Stetten

An accessory marker derived from chromosome 20 and its co-existence with a mosaic trisomy 20 cell line.
Prenatal diagnosis 1995;15(2):123-7.
27.
1994

D A Batista; G S Pai; G Stetten

Molecular analysis of a complex chromosomal rearrangement and a review of familial cases.
American journal of medical genetics 1994;53(3):255-63.
28.
1993

D A Batista; C M Tuck-Muller; J E Martinez; W G Kearns; P L Pearson; G Stetten

A complex chromosomal rearrangement detected prenatally and studied by fluorescence in situ hybridization.
Human genetics 1993;92(2):117-21.
29.
1993

C M Tuck-Muller; J E Martinez; D A Batista; W G Kearns; W Wertelecki

Duplication of the short arm of the X chromosome in mother and daughter.
Human genetics 1993;91(4):395-400.
30.
1983

D A Batista; A M Vianna-Morgante; A Richieri-Costa

Tetrasomy 18p: tentative delineation of a syndrome.
Journal of medical genetics 1983;20(2):144-7.

Denise Batista The Johns Hopkins University, School of Medicine

Denise Batista

30 Publications

Denise Batista
The Johns Hopkins University, School of Medicine