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Denise Batista

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Procedures

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Justin A Bishop; William H Westra; Raluca Yonescu; Denise A S Batista; Syed Z Ali
Cytopathologic features of mammary analogue secretory carcinoma.
Ryan W Y Lee; Joann Bodurtha; Julie Cohen; Ali Fatemi; Denise A S Batista
Deletion 12p12 involving SOX5 in two children with developmental delay and dysmorphic features.
Lindsay B Henderson; Sarah Millard; Daniel O Saul; Cynthia Anderson; Denise A S Batista; Karin J Blakemore; VIRGINIA CORSON; Cheryl DeScipio
First trimester diagnosis of holoprosencephaly secondary to a ring chromosome 7.

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All Publications

2013: Justin A Bishop; William H Westra; Raluca Yonescu; Denise A S Batista; Syed Z Ali
Cytopathologic features of mammary analogue secretory carcinoma.
Cancer cytopathology 2013;121(5):228-33.
2013: Ryan W Y Lee; Joann Bodurtha; Julie Cohen; Ali Fatemi; Denise A S Batista
Deletion 12p12 involving SOX5 in two children with developmental delay and dysmorphic features.
Pediatric neurology 2013;48(4):317-20.
2013: Lindsay B Henderson; Sarah Millard; Daniel O Saul; Cynthia Anderson; Denise A S Batista; Karin J Blakemore; VIRGINIA CORSON; Cheryl DeScipio
First trimester diagnosis of holoprosencephaly secondary to a ring chromosome 7.
Case reports in genetics 2013;2013():578202.
2012: Andres Jerez; Denise A S Batista; Lukasz Gondek; Anna Jankowska; Hideki Makishima; A MICHAEL MCDEVITT; Azim Mohamedali; Ghulam J Mufti; Christine L O'Keefe; Bartlomiej Przychodzen; Mikkael A Sekeres; Ramon Tiu; Jaroslaw P Maciejewski
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.
2011: Shuko Harada; Lindsay B Henderson; Peter C Burger; James R Eshleman; Christopher D Gocke; 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.
2011: Natini Jinawath; Regina Zambrano; Elizabeth Wohler; Maria K Palmquist; Julie E 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.
2011: Gerald V Raymond; Elizabeth Wohler; Carolyn Dinsmore; Jeanne Cox; Michael V Johnston; Denise A S 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.
2011: Regina M Zambrano; Elizabeth Wohler; Göran Annerén; Ann-Charlotte Thuresson; Garry R Cutting; Denise A S 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.
2010: Feng Li; Denise A S Batista; Irene H 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.
2010: Feng Li; Yiping Shen; Udo Köhler; Freddie H Sharkey; DEEPA MENON; Laurence Coulleaux; Valérie Malan; Marlène Rio; Dominic J McMullan; H Cox; Kerry A Fagan; Lorraine Gaunt; Kay Metcalfe; Uwe Heinrich; Gordon Hislop; Una Maye; Maxine Sutcliffe; Bai-Lin Wu; Brian D Thiel; Surabhi Mulchandani; Laura K Conlin; Nancy B Spinner; KATHLEEN MURPHY; Denise A S Batista
Interstitial microduplication of Xp22.31: Causative of intellectual disability or benign copy number variant?
European journal of medical genetics 2010;53(2):93-9.
2009: N Sobreira; M Cernach; Denise A S Batista; D Brunoni; A Perez
Pseudoaminopterin syndrome: clinical report with new characteristics.
American journal of medical genetics. Part A 2009;149A(12):2843-8.
2009: Nara Sobreira; Michael F Walsh; Denise A S 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.
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.
2009: Natini Jinawath; Alexis Norris-Kirby; B Douglas Smith; Christopher D Gocke; Denise A S Batista; Constance A Griffin; KATHLEEN 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.
2008: Veronica Mardo; Elizabeth E Squibb; Nancy Braverman; Julie E Hoover-Fong; Claude J 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.
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.
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.
2007: Edward G Weir; M Ali Ansari-Lari; Denise A S Batista; Constance A Griffin; S Fuller; B Douglas Smith; Michael J Borowitz
Acute bilineal leukemia: a rare disease with poor outcome.
Leukemia 2007;21(11):2264-70.
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.
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.
2006: Denise A S Batista; Eric Vonderheid; Anita E Hawkins; Laura Morsberger; Patricia Long; KATHLEEN 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.
2005: Denise A S Batista; Anita E Hawkins; KATHLEEN 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.
1997: Kimberly F Doheny; S A Rasmussen; Julie Rutberg; Gregg L Semenza; J Stamberg; M Schwartz; Denise A S Batista; Gail Stetten; George 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.
1995: Cathy M Tuck-Muller; H Chen; José E Martínez; C C Shen; Shibo Li; C Kusyk; Denise A S Batista; Yogendra Bhatnagar; E Dowling; Wladimir Wertelecki
Isodicentric Y chromosome: cytogenetic, molecular and clinical studies and review of the literature.
Human genetics 1995;96(1):119-29.
1995: H Chen; Cathy M Tuck-Muller; Denise A S Batista; Wladimir Wertelecki
Identification of supernumerary ring chromosome 1 mosaicism using fluorescence in situ hybridization.
American journal of medical genetics 1995;56(2):219-33.
1995: Denise A S Batista; C Escallon; Karin J Blakemore; Gail 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.
1994: Denise A S Batista; G Shashidhar Pai; Gail Stetten
Molecular analysis of a complex chromosomal rearrangement and a review of familial cases.
American journal of medical genetics 1994;53(3):255-63.
1993: Denise A S Batista; Cathy M Tuck-Muller; J E Martinez; William G Kearns; P L Pearson; Gail Stetten
A complex chromosomal rearrangement detected prenatally and studied by fluorescence in situ hybridization.
Human genetics 1993;92(2):117-21.
1993: Cathy M Tuck-Muller; J E Martinez; Denise A S Batista; William G Kearns; Wladimir Wertelecki
Duplication of the short arm of the X chromosome in mother and daughter.
Human genetics 1993;91(4):395-400.
1983: Denise A S Batista; A M Vianna-Morgante; A Richieri-Costa
Tetrasomy 18p: tentative delineation of a syndrome.
Journal of medical genetics 1983;20(2):144-7.