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Urvashi Surti

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Amanda L Wilson; Elias Campo; John K Choi; Grzegorz K Przybylski; Urvashi Surti; Steven H Swerdlow; Massimo M Trucco; S Branden Van Oss; Raymond E Felgar
Intestinal γδ T-cell lymphomas are most frequently of type II enteropathy-associated T-cell type.
Jie Hu; Sally J Kochmar; Suneeta Madan-Khetarpal; Marianne McGuire; Malini Sathanoori; Urvashi Surti
Co-existence of 9p deletion and Silver-Russell syndromes in a patient with maternally inherited cryptic complex chromosome rearrangement involving chromosomes 4, 9, and 11.
Jun Liao; Malini Sathanoori; Svetlana A Yatsenko; Lori Hoffner; W Allen Hogge; Jie Hu; Sally J Kochmar; Urvashi Surti
Prenatal detection of del(10)(q11.2) mosaicism in chorionic villus specimens likely caused by a common chromosomal fragile site FRA10G is associated with a normal phenotype.

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2013: Amanda L Wilson; Elias Campo; John K Choi; Grzegorz K Przybylski; Urvashi Surti; Steven H Swerdlow; Massimo M Trucco; S Branden Van Oss; Raymond E Felgar
Intestinal γδ T-cell lymphomas are most frequently of type II enteropathy-associated T-cell type.
Human pathology 2013;44(6):1131-45.
2013: Jie Hu; Sally J Kochmar; Suneeta Madan-Khetarpal; Marianne McGuire; Malini Sathanoori; Urvashi Surti
Co-existence of 9p deletion and Silver-Russell syndromes in a patient with maternally inherited cryptic complex chromosome rearrangement involving chromosomes 4, 9, and 11.
American journal of medical genetics. Part A 2013;161A(1):179-84.
2012: Jun Liao; Malini Sathanoori; Svetlana A Yatsenko; Lori Hoffner; W Allen Hogge; Jie Hu; Sally J Kochmar; Urvashi Surti
Prenatal detection of del(10)(q11.2) mosaicism in chorionic villus specimens likely caused by a common chromosomal fragile site FRA10G is associated with a normal phenotype.
Prenatal diagnosis 2012;32(12):1166-9.
2012: Sara A Monaghan; Urvashi Surti; Ketah Doty; Fiona E Craig
Altered neutrophil maturation patterns that limit identification of myelodysplastic syndromes.
Cytometry. Part B, Clinical cytometry 2012;82(4):217-28.
2012: Kimberly Bunce; Tianjiao Chu; W Allen Hogge; Urvashi Surti; David G Peters
Discovery of epigenetic biomarkers for the noninvasive diagnosis of fetal disease.
Prenatal diagnosis 2012;32(6):542-9.
2012: Lori Hoffner; Urvashi Surti
The genetics of gestational trophoblastic disease: a rare complication of pregnancy.
Cancer genetics 2012;205(3):63-77.
2012: Fiona E Craig; Sara A Monaghan; Urvashi Surti; Steven H Swerdlow
ZAP-70 and Bcl-2 expression in B lymphoblastic leukemia cells and hematogones.
Cytometry. Part B, Clinical cytometry 2012;82(2):85-92.
2012: Megan M McGuire; Lori Hoffner; Mirka Jones; Urvashi Surti; Alexander Yatsenko; Aleksandar Rajkovic
Whole exome sequencing in a random sample of North American women with leiomyomas identifies MED12 mutations in majority of uterine leiomyomas.
PloS one 2012;7(3):e33251.
2012: Heidi L Thorson; Beth Torchia; Sally J Kochmar; Malini Sathanoori; Urvashi Surti; Aleksandar Rajkovic
Prenatal diagnosis of 2q32 deletion syndrome characterized by multiple segmental deletions and complex chromosomal rearrangement involving chromosomes 2, 5 and 7.
Fetal diagnosis and therapy 2012;31(3):196-200.
2012: Karen E Hermetz; Jannine Cody; Urvashi Surti; M Katharine Rudd
A recurrent translocation is mediated by homologous recombination between HERV-H elements.
Molecular cytogenetics 2012;5(1):6.
2012: Nancy W Hendrix; Timothy P Canavan; Michele Clemens; Urvashi Surti; Aleksandar Rajkovic
Prenatally diagnosed 17q12 microdeletion syndrome with a novel association with congenital diaphragmatic hernia.
Fetal diagnosis and therapy 2012;31(2):129-33.
2011: David Peters; Patricia Shaw; Urvashi Surti; Svetlana A Yatsenko; Kimberly Bunce; Tianjiao Chu; Mary Dunkel; Nancy Hendrix; W Allen Hogge; Aleksandar Rajkovic
Noninvasive prenatal diagnosis of a fetal microdeletion syndrome.
The New England journal of medicine 2011;365(19):1847-8.
2011: Jun Liao; Suneeta Madan-Khetarpal; Urvashi Surti; Stephanie J DeWard; Jie Hu
A small homozygous microdeletion of 15q13.3 including the CHRNA7 gene in a girl with a spectrum of severe neurodevelopmental features.
American journal of medical genetics. Part A 2011;155A(11):2795-800.
2011: Mariana M Cajaiba; Lori Hoffner; Jaqueline Hoover; Trevor Macpherson; Suneeta Madan-Khetarpal; Selma Witchel; Urvashi Surti
Prenatal diagnosis of trisomy 6 rescue resulting in paternal UPD6 with novel placental findings.
American journal of medical genetics. Part A 2011;155A(8):1996-2002.
2011: Christiane Messaed; JianHua Qian; Cecile Rittore; Philippe Sauthier; Ariel Schneider; Rima Slim; Urvashi Surti; Isabelle Touitou; Raphael B Di Roberto; Jocelyne Arseneau; Rashmi Bagga; Kurt Bernishke; William Buckett; Wafaa Chebaro; Moy Fong Chen; Annie Cheung; Philippe Coullin; James C Engert; Lori Hoffner; Nga Man Lau
NLRP7 in the spectrum of reproductive wastage: rare non-synonymous variants confer genetic susceptibility to recurrent reproductive wastage.
Journal of medical genetics 2011;48(8):540-8.
2011: Sarah E Gibson; Nancy Lee Harris; Paola Dal Cin; Judith A Ferry; Urvashi Surti; Steven H Swerdlow; Robert P Hasserjian
Reassessment of small lymphocytic lymphoma in the era of monoclonal B-cell lymphocytosis.
Haematologica 2011;96(8):1144-52.
2011: Sarah E Gibson; Steven H Swerdlow; Fiona E Craig; Urvashi Surti; James R Cook; Michael A Nalesnik; Chris Lowe; Katrina M Wood; Chris M Bacon
EBV-positive extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue in the posttransplant setting: a distinct type of posttransplant lymphoproliferative disorder?
The American journal of surgical pathology 2011;35(6):807-15.
2011: Melanie E Ochalski; Natalie Engle; Anthony Wakim; Britt J Ravnan; Lori Hoffner; Aleksandar Rajkovic; Urvashi Surti
Complex X chromosome rearrangement delineated by array comparative genome hybridization in a woman with premature ovarian insufficiency.
Fertility and sterility 2011;95(7):2433.e9-15.
2011: Jie Hu; Sally J Kochmar; Suneeta Madan-Khetarpal; Malini Sathanoori; Alvaro H Serrano Russi; Stephanie J Deward; Urvashi Surti
Three supernumerary marker chromosomes in a patient with developmental delay, mental retardation, and dysmorphic features.
Genetics research international 2011;2011():185271.
2011: Tianjiao Chu; Daniel Handley; Kimberly Bunce; Urvashi Surti; W Allen Hogge; David G Peters
Structural and regulatory characterization of the placental epigenome at its maternal interface.
PloS one 2011;6(2):e14723.
2010: Brian Teague; Michael S Waterman; Steven Goldstein; Konstantinos Potamousis; Shiguo Zhou; Susan Reslewic; Deepayan Sarkar; Anton Valouev; Chris Churas; Jeffrey M Kidd; Scott Kohn; Rod Runnheim; Casey Lamers; Dan Forrest; Michael A Newton; Evan E Eichler; Marijo Kent-First; Urvashi Surti; Miron Livny; David C Schwartz
High-resolution human genome structure by single-molecule analysis.
Proceedings of the National Academy of Sciences of the United States of America 2010;107(24):10848-53.
2010: Lori Hoffner; W Tony Parks; Steven H Swerdlow; Jason C Carson; Urvashi Surti
Simultaneous detection of imprinted gene expression (p57(KIP2)) and molecular cytogenetics (FICTION) in the evaluation of molar pregnancies.
The Journal of reproductive medicine 2010;55(5-6):219-28.
2010: Shobhit Madan; Suneeta Madan-Khetarpal; Sang C Park; Urvashi Surti; Ariel L Bailey; Juliann McConnell; Sameh S Tadros
Left ventricular non-compaction on MRI in a patient with 22q11.2 distal deletion.
American journal of medical genetics. Part A 2010;152A(5):1295-9.
2010: Eumenia Costa da Cunha Castro; Cristina Blazquez; Jaime Boyd; Hernán Correa; J-P de Chadarevian; Raymond E Felgar; Nicole Graf; Norman Levy; Eric J Lowe; John T Manning; Maria A Proytcheva; Christof Senger; Katayoon Shayan; Jaroslav Sterba; Alice Werner; Urvashi Surti; Ronald Jaffe
Clinicopathologic features of histiocytic lesions following ALL, with a review of the literature.
Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society 2010;13(3):225-37.
2010: Scott D Dufresne; Raymond E Felgar; Rachel L Sargent; Urvashi Surti; Susanne M Gollin; Ellen D McPhail; James R Cook; Steven H Swerdlow
Defining the borders of splenic marginal zone lymphoma: a multiparameter study.
Human pathology 2010;41(4):540-51.
2010: Joel F Gradowski; Elaine S Jaffe; Roger A Warnke; Stefania Pittaluga; Urvashi Surti; Leena A Gole; Steven H Swerdlow
Follicular lymphomas with plasmacytic differentiation include two subtypes.
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2010;23(1):71-9.
2009: Jill A Rosenfeld; Kathleen Leppig; Blake C Ballif; Heidi Thiese; Christine Erdie-Lalena; Erawati V Bawle; Sujatha Sastry; J Edward Spence; Anne Bandholz; Urvashi Surti; Jonathan (Jon) Zonana; Kory L Keller; Wendy Meschino; Bassem A Bejjani; Beth S Torchia; Lisa Shaffer
Genotype-phenotype analysis of TCF4 mutations causing Pitt-Hopkins syndrome shows increased seizure activity with missense mutations.
Genetics in medicine : official journal of the American College of Medical Genetics 2009;11(11):797-805.
2009: Tianjiao Chu; Brian Burke; Kimberly Bunce; Urvashi Surti; W Allen Hogge; David G Peters
A microarray-based approach for the identification of epigenetic biomarkers for the noninvasive diagnosis of fetal disease.
Prenatal diagnosis 2009;29(11):1020-30.
2009: Sara E Monaco; Lisa A Teot; Raymond E Felgar; Urvashi Surti; Guoping Cai
Fluorescence in situ hybridization studies on direct smears: an approach to enhance the fine-needle aspiration biopsy diagnosis of B-cell non-Hodgkin lymphomas.
Cancer 2009;117(5):338-48.
2009: Dionysios Papachristou; Alka Palekar; Urvashi Surti; Kathleen Cieply; Richard L McGough; Uma N M Rao
Malignant granular cell tumor of the ulnar nerve with novel cytogenetic and molecular genetic findings.
Cancer genetics and cytogenetics 2009;191(1):46-50.
2009: Henry Armah; Anil V Parwani; Urvashi Surti; Sheldon Bastacky
Xp11.2 translocation renal cell carcinoma occurring during pregnancy with a novel translocation involving chromosome 19: a case report with review of the literature.
Diagnostic pathology 2009;4():15.
2008: Craig Horbinski; Erika M Carter; Patricia L Heard; Malini Sathanoori; Jie Hu; Jerry Vockley; Shelly Gunn; Daniel Hale; Urvashi Surti; Jannine Cody
Molecular and clinical characterization of a recurrent cryptic unbalanced t(4q;18q) resulting in an 18q deletion and 4q duplication.
American journal of medical genetics. Part A 2008;146A(22):2898-904.
2008: Rachel Lynn Sargent; James R Cook; Nadine I Aguilera; Urvashi Surti; Susan L Abbondanzo; Susanne M Gollin; Steven H Swerdlow
Fluorescence immunophenotypic and interphase cytogenetic characterization of nodal lymphoplasmacytic lymphoma.
The American journal of surgical pathology 2008;32(11):1643-53.
2008: Melina B Flanagan; Malini Sathanoori; Urvashi Surti; Lorinda A Soma; Steven H Swerdlow
Cytogenetic abnormalities detected by fluorescence in situ hybridization on paraffin-embedded chronic lymphocytic leukemia/small lymphocytic lymphoma lymphoid tissue biopsy specimens.
American journal of clinical pathology 2008;130(4):620-7.
2008: Mamatha Chivukula; Rohit Bhargava; Adam Brufsky; Urvashi Surti; David J Dabbs
Clinical importance of HER2 immunohistologic heterogeneous expression in core-needle biopsies vs resection specimens for equivocal (immunohistochemical score 2+) cases.
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2008;21(4):363-8.
2008: Joan M Striebel; Rohit Bhargava; Craig Horbinski; Urvashi Surti; David J Dabbs
The equivocally amplified HER2 FISH result on breast core biopsy: indications for further sampling do affect patient management.
American journal of clinical pathology 2008;129(3):383-90.
2008: Lori Hoffner; Jeanette Dunn; Nicole Esposito; Trevor Macpherson; Urvashi Surti
P57KIP2 immunostaining and molecular cytogenetics: combined approach aids in diagnosis of morphologically challenging cases with molar phenotype and in detecting androgenetic cell lines in mosaic/chimeric conceptions.
Human pathology 2008;39(1):63-72.
2007: Cristina R Antonescu; Paola Dal Cin; Khedoudja Nafa; Lisa A Teot; Urvashi Surti; Christopher D Fletcher; Marc Ladanyi
EWSR1-CREB1 is the predominant gene fusion in angiomatoid fibrous histiocytoma.
Genes, chromosomes & cancer 2007;46(12):1051-60.
2007: Heather E Hall; Ernest R Chan; ANDREW COLLINS; LuAnn Judis; Sofia Shirley; Urvashi Surti; Lori Hoffner; Annette E Cockwell; Patricia A Jacobs; Terry J Hassold
The origin of trisomy 13.
American journal of medical genetics. Part A 2007;143A(19):2242-8.
2007: Heather E Hall; Urvashi Surti; Lori Hoffner; Sofia Shirley; Eleanor Feingold; Terry J Hassold
The origin of trisomy 22: evidence for acrocentric chromosome-specific patterns of nondisjunction.
American journal of medical genetics. Part A 2007;143A(19):2249-55.
2007: Blake C Ballif; Sara A Hornor; Elizabeth Jenkins; Suneeta Madan-Khetarpal; Urvashi Surti; Kelly E Jackson; Alexander Asamoah; Pamela L Brock; Gordon C Gowans; Robert L Conway; John M Graham; Livija Medne; Elaine H Zackai; Tamim H Shaikh; Joel Geoghegan; Rebecca R Selzer; Peggy S Eis; Bassem A Bejjani; Lisa Shaffer
Discovery of a previously unrecognized microdeletion syndrome of 16p11.2-p12.2.
Nature genetics 2007;39(9):1071-3.
2007: Malini Sathanoori; Jie Hu; V Murthy; Abigail L Byrnes; J Vockley; R Safier; J Bedoyan; S M Jalal; H Huber; Urvashi Surti
Cryptic duplication of 12q24.33 --> qter in a child with Angelman syndrome-simultaneous occurrence of two unrelated cytogenetic events.
American journal of medical genetics. Part A 2007;143A(9):985-94.
2007: Yakov Gologorsky; Daniel Gologorsky; Anna S Yarygina; Urvashi Surti; Matthew J Zirwas
Familial multiple lipomatosis: report of a new family.
Cutis; cutaneous medicine for the practitioner 2007;79(3):227-32.
2007: Henry Armah; Richard L McGough; Mark A Goodman; Susanne M Gollin; Urvashi Surti; Anil V Parwani; Uma N M Rao
Chondromyxoid fibroma of rib with a novel chromosomal translocation: a report of four additional cases at unusual sites.
Diagnostic pathology 2007;2():44.
2006: Susan E Ingraham; Roy A Lynch; Urvashi Surti; Joni L Rutter; Alan J Buckler; Sohaib A Khan; Anil G Menon; Pierig Lepont
Identification and characterization of novel human transcripts embedded within HMGA2 in t(12;14)(q15;q24.1) uterine leiomyoma.
Mutation research 2006;602(1-2):43-53.
2006: Urvashi Surti; Lori Hoffner; Marta Kolthoff; Jeanette Dunn; Jennifer Hunt; Lynn Sniezek; Trevor Macpherson
Persistent gestational trophoblastic disease after an androgenetic/biparental fetal chimera: a case report and review.
International journal of gynecological pathology : official journal of the International Society of Gynecological Pathologists 2006;25(4):366-72.
2006: Jie Hu; Malini Sathanoori; Sally J Kochmar; Urvashi Surti
Application of multicolor banding for identification of complex chromosome 18 rearrangements.
The Journal of molecular diagnostics : JMD 2006;8(4):521-5; quiz 528.
2006: Michael D Graf; Laurie A Christ; James T Mascarello; P Mowrey; M Pettenati; Gail Stetten; P Storto; Urvashi Surti; Daniel L Van Dyke; Gail H Vance; Daynna J Wolff; Stuart Schwartz
Redefining the risks of prenatally ascertained supernumerary marker chromosomes: a collaborative study.
Journal of medical genetics 2006;43(8):660-4.
2006: Katherine Neiswanger; Paul M Hohler; Lori B Hively-Thomas; Elizabeth McPherson; W Allen Hogge; Urvashi Surti
Variable outcomes in mosaic trisomy 16: five case reports and literature analysis.
Prenatal diagnosis 2006;26(5):454-61.
2006: Kalyani R Vats; Chandra Ishwad; Ish Singla; Ashutosh Vats; Robert E Ferrell; Demetrius Ellis; Michael Moritz; Urvashi Surti; Parul Jayakar; Donald R Frederick; Abhay Vats
A locus for renal malformations including vesico-ureteric reflux on chromosome 13q33-34.
Journal of the American Society of Nephrology : JASN 2006;17(4):1158-67.
2005: Urvashi Surti; Lyndon M Hill; Jeanette Dunn; Tracy L Prosen; Lori Hoffner
Twin pregnancy with a chimeric androgenetic and biparental placenta in one twin displaying placental mesenchymal dysplasia phenotype.
Prenatal diagnosis 2005;25(11):1048-56.
2005: Jie Hu; Uma N M Rao; Suhagi Jasani; Vinish Khanna; Kenneth Yaw; Urvashi Surti
Loss of DNA copy number of 10q is associated with aggressive behavior of leiomyosarcomas: a comparative genomic hybridization study.
Cancer genetics and cytogenetics 2005;161(1):20-7.
2005: Elizabeth McPherson; Katherine Neiswanger; Urvashi Surti
Tetrasomy 9q in an infant with cleft palate and multiple anomalies.
Clinical dysmorphology 2005;14(3):145-7.
2005: Bong K Kim; Urvashi Surti; Amit Pandya; Jack Cohen; Michael S Rabkin; Steven H Swerdlow
Clinicopathologic, immunophenotypic, and molecular cytogenetic fluorescence in situ hybridization analysis of primary and secondary cutaneous follicular lymphomas.
The American journal of surgical pathology 2005;29(1):69-82.
2005: Jie Hu; Sofia Shekhter-Levin; Peter H Shaw; Carolyn Bay; Sally J Kochmar; Urvashi Surti
A case of myelodysplastic syndrome with acquired monosomy 7 in a child with a constitutional t(1;19) and a mosaicism for trisomy 21.
Cancer genetics and cytogenetics 2005;156(1):62-7.
2003: Giulia C Kennedy; Hajime Matsuzaki; Shoulian Dong; Wei-min Liu; Jing Huang; Guoying Liu; Xing Su; Manqiu Cao; Wenwei Chen; Jane Zhang; Weiwei Liu; Geoffrey Yang; Xiaojun Di; Thomas B Ryder; Zhijun He; Urvashi Surti; Michael S Phillips; michael Boyce-jacino; Stephen P A Fodor; Keith W Jones
Large-scale genotyping of complex DNA.
Nature biotechnology 2003;21(10):1233-7.
2003: W Allen Hogge; Abigail L Byrnes; Mark C Lanasa; Urvashi Surti
The clinical use of karyotyping spontaneous abortions.
American journal of obstetrics and gynecology 2003;189(2):397-400; discussion 400-2.
2003: Abhay Vats; Chandra Ishwad; Kalyani R Vats; Michael Moritz; Demetrius Ellis; Christine Mueller; Urvashi Surti; Maria Z Parizhskaya; Manuel P Meza; Leah Burke; Francis X Schneck; Malika Saxena; Robert E Ferrell
Steroid-resistant nephrotic syndrome and congenital anomalies of kidneys: evidence of locus on chromosome 13q.
Kidney international 2003;64(1):17-24.
2003: Jie Hu; Vinish Khanna; Mirka W Jones; Urvashi Surti
Comparative study of primary and recurrent ovarian serous carcinomas: comparative genomic hybridization analysis with a potential application for prognosis.
Gynecologic oncology 2003;89(3):369-75.
2003: Bong K Kim; Urvashi Surti; Amit G Pandya; Steven H Swerdlow
Primary and secondary cutaneous diffuse large B-cell lymphomas: a multiparameter analysis of 25 cases including fluorescence in situ hybridization for t(14;18) translocation.
The American journal of surgical pathology 2003;27(3):356-64.
2002: S Dhandha; W Allen Hogge; Urvashi Surti; Elizabeth McPherson
Three cases of tetrasomy 9p.
American journal of medical genetics 2002;113(4):375-80.
2002: J Hu; Elizabeth McPherson; Urvashi Surti; S L Hasegawa; Sriya Gunawardena; Susanne M Gollin
Tetrasomy 15q25.3 --> qter resulting from an analphoid supernumerary marker chromosome in a patient with multiple anomalies and bilateral Wilms tumors.
American journal of medical genetics 2002;113(1):82-8.
2002: Jie Hu; Vinish Khanna; Mirka M W Jones; Urvashi Surti
Genomic imbalances in ovarian borderline serous and mucinous tumors.
Cancer genetics and cytogenetics 2002;139(1):18-23.
2002: Jian-Bing Fan; Urvashi Surti; Patricia Taillon-Miller; Linda Hsie; Giulia C Kennedy; Lori Hoffner; Thomas B Ryder; David G Mutch; Pui-Yan Kwok
Paternal origins of complete hydatidiform moles proven by whole genome single-nucleotide polymorphism haplotyping.
Genomics 2002;79(1):58-62.
2001: Jie Hu; Vinish Khanna; M Jones; Urvashi Surti
Genomic alterations in uterine leiomyosarcomas: potential markers for clinical diagnosis and prognosis.
Genes, chromosomes & cancer 2001;31(2):117-24.
2000: MV Zaragoza; Urvashi Surti; Raymond W Redline; Elise A Millie; Aravinda Chakravarti; Terry J Hassold
Parental origin and phenotype of triploidy in spontaneous abortions: predominance of diandry and association with the partial hydatidiform mole.
American journal of human genetics 2000;66(6):1807-20.
2000: Anna Estop; Kathleen Cieply; Santiago Munne; Urvashi Surti; A Wakim; Eleanor Feingold
Is there an interchromosomal effect in reciprocal translocation carriers? Sperm FISH studies.
Human genetics 2000;106(5):517-24.
2000: PA Mowery-Rushton; J M Hanchett; W B Zipf; P K Rogan; Urvashi Surti
Mosaicism in Prader-Willi syndrome.
American journal of medical genetics 2000;90(2):177.
1998: Elizabeth McPherson; Michele Clemens; Lori Hoffner; Urvashi Surti
Sacral tumors in Schinzel-Giedion syndrome.
American journal of medical genetics 1998;79(1):62-3.
1998: Roy A Lynch; MB Piper; A Bankier; Bindu Bhugra; Urvashi Surti; J Liu; Alan J Buckler; Paul H Dear; Anil G Menon
Genomic and functional map of the chromosome 14 t(12;14) breakpoint cluster region in uterine leiomyoma.
Genomics 1998;52(1):17-26.
1998: K Suryanarayan; Katherine O'Hanlan; Urvashi Surti; Chandra Ishwad; Kent W Nowels; D Letourneau; Neyssa M Marina
Nongestational choriocarcinoma in the postpartum period: a case report.
Journal of pediatric hematology/oncology 1998;20(2):169-73.
1998: Susan M Sell; O Altungoz; A A Prowse; Aurelia Meloni-Ehrig; Urvashi Surti; Avery A Sandberg
Molecular analysis of chromosome 7q21.3 in uterine leiomyoma: analysis using markers with linkage to insulin resistance.
Cancer genetics and cytogenetics 1998;100(2):165-8.
1997: Elizabeth McPherson; G Laneri; M M Clemens; Sally J Kochmar; Urvashi Surti
Apparently balanced t(1;7)(q21.3;q34) in an infant with Coffin-Siris syndrome.
American journal of medical genetics 1997;71(4):430-3.
1997: Elena Pegoraro; J Whitaker; PA Mowery-Rushton; Urvashi Surti; Mark C Lanasa; Eric Hoffman
Familial skewed X inactivation: a molecular trait associated with high spontaneous-abortion rate maps to Xq28.
American journal of human genetics 1997;61(1):160-70.
1997: Chandra Ishwad; Robert E Ferrell; K Hanley; J Davare; Aurelia Meloni-Ehrig; Avery A Sandberg; Urvashi Surti
Two discrete regions of deletion at 7q in uterine leiomyomas.
Genes, chromosomes & cancer 1997;19(3):156-60.
1997: PA Mowery-Rushton; M P Stadler; Sally J Kochmar; Elizabeth McPherson; Urvashi Surti; W Allen Hogge
The use of interphase FISH for prenatal diagnosis of Pallister-Killian syndrome.
Prenatal diagnosis 1997;17(3):255-65.
1996: P A Mowery-Rushton; J M Hanchett; W B Zipf; P K Rogan; Urvashi Surti
Identification of mosaicism in Prader-Willi syndrome using fluorescent in situ hybridization.
American journal of medical genetics 1996;66(4):403-12.
1996: M Clemens; J T Martsolf; J G Rogers; P Mowery-Rushton; Urvashi Surti; Elizabeth McPherson
Pitt-Rogers-Danks syndrome: the result of a 4p microdeletion.
American journal of medical genetics 1996;66(1):95-100.
1996: W Allen Hogge; Urvashi Surti; Sally J Kochmar; P Mowery-Rushton; K Cumbie
Molecular cytogenetics: an essential component of modern prenatal diagnosis.
American journal of obstetrics and gynecology 1996;175(2):352-6; discussion 356-7.
1996: Uma N M Rao; Urvashi Surti; L Hoffner; Kenneth Yaw
Cytogenetic and histologic correlation of peripheral nerve sheath tumors of soft tissue.
Cancer genetics and cytogenetics 1996;88(1):17-25.
1996: P A Mowery-Rushton; D J Driscoll; R D Nicholls; Joseph Locker; Urvashi Surti
DNA methylation patterns in human tissues of uniparental origin using a zinc-finger gene (ZNF127) from the Angelman/Prader-Willi region.
American journal of medical genetics 1996;61(2):140-6.
1995: Anna Estop; P A Mowery-Rushton; Kathleen Cieply; Sally J Kochmar; C R Sherer; M Clemens; Urvashi Surti; Elizabeth McPherson
Identification of an unbalanced cryptic translocation t(9;17)(q34.3;p13.3) in a child with dysmorphic features.
Journal of medical genetics 1995;32(10):819-22.
1995: Chandra Ishwad; Robert E Ferrell; J Davare; Aurelia Meloni-Ehrig; Avery A Sandberg; Urvashi Surti
Molecular and cytogenetic analysis of chromosome 7 in uterine leiomyomas.
Genes, chromosomes & cancer 1995;14(1):51-5.
1995: P N Rauk; Urvashi Surti; James M Roberts; G Michalopoulos
Mitogenic effect of basic fibroblast growth factor and estradiol on cultured human myometrial and leiomyoma cells.
American journal of obstetrics and gynecology 1995;173(2):571-7.
1995: Yavuz Ozisik; Aurelia Meloni-Ehrig; O Altungoz; Urvashi Surti; Avery A Sandberg
Translocation (6;10)(p21;q22) in uterine leiomyomas.
Cancer genetics and cytogenetics 1995;79(2):136-8.
1994: Yavuz Ozisik; Aurelia Meloni-Ehrig; J F Stone; Avery A Sandberg; Urvashi Surti
Spontaneous expression of the chromosome fragile site at 10q23 in leiomyoma.
Cancer genetics and cytogenetics 1994;74(1):73-5.
1994: L Hoffner; R Deka; Aravinda Chakravarti; Urvashi Surti
Cytogenetics and origins of pediatric germ cell tumors.
Cancer genetics and cytogenetics 1994;74(1):54-8.
1994: Anna Estop; V Bansal; A Lin; F Levinson; S M Karlin; Urvashi Surti; S L Wenger; M W Steele
Three unrelated cases of paracentric inversions of 1p in individuals with abnormal phenotypes.
American journal of medical genetics 1994;49(4):410-3.
1994: Sharon L Wenger; Urvashi Surti; N A Nwokoro; M W Steele
Cytogenetic characterization of cat eye syndrome marker chromosome.
Annales de génétique 1994;37(1):33-6.
1993: Yavuz Ozisik; Aurelia Meloni-Ehrig; Urvashi Surti; Avery A Sandberg
Deletion 7q22 in uterine leiomyoma. A cytogenetic review.
Cancer genetics and cytogenetics 1993;71(1):1-6.
1993: Yavuz Ozisik; Aurelia Meloni-Ehrig; Urvashi Surti; Avery A Sandberg
Involvement of 10q22 in leiomyoma.
Cancer genetics and cytogenetics 1993;69(2):132-5.
1993: Yavuz Ozisik; Aurelia Meloni-Ehrig; A A Sandberg; Urvashi Surti; H Tobon; J Devare
Cytogenetic findings in a symplastic leiomyoma.
Cancer genetics and cytogenetics 1993;67(1):79-80.
1993: Yavuz Ozisik; Aurelia Meloni-Ehrig; M Powell; Urvashi Surti; Avery A Sandberg
Chromosome 7 biclonality in uterine leiomyoma.
Cancer genetics and cytogenetics 1993;67(1):59-64.
1992: J Hu; Urvashi Surti; H Tobon
Cytogenetic analysis of a uterine lipoleiomyoma.
Cancer genetics and cytogenetics 1992;62(2):200-2.
1992: Aurelia Meloni-Ehrig; Urvashi Surti; A M Contento; J Davare; Avery A Sandberg
Uterine leiomyomas: cytogenetic and histologic profile.
Obstetrics and gynecology 1992;80(2):209-17.
1992: L Hoffner; S Shen-Schwarz; R Deka; Aravinda Chakravarti; Urvashi Surti
Genetics and biology of human ovarian teratomas. III. Cytogenetics and origins of malignant ovarian germ cell tumors.
Cancer genetics and cytogenetics 1992;62(1):58-65.
1992: R A Becker; Urvashi Surti; Sharon L Wenger
Sister chromatid exchange and chromosome breakage in complete hydatidiform moles.
Cancer genetics and cytogenetics 1992;62(1):53-7.
1992: Yavuz Ozisik; Aurelia Meloni-Ehrig; Urvashi Surti; J Davare; Avery A Sandberg
Inversion (X)(p22q13) in a uterine leiomyoma.
Cancer genetics and cytogenetics 1992;61(2):131-3.
1991: Aurelia Meloni-Ehrig; Urvashi Surti; Avery A Sandberg
Deletion of chromosome 13 in leiomyomas of the uterus.
Cancer genetics and cytogenetics 1991;53(2):199-203.
1991: M Kiechle-Schwarz; C Sreekantaiah; C S Berger; S Pedron; M T Medchill; Urvashi Surti; Avery A Sandberg
Nonrandom cytogenetic changes in leiomyomas of the female genitourinary tract. A report of 35 cases.
Cancer genetics and cytogenetics 1991;53(1):125-36.
1991: H Tobon; Urvashi Surti; G J Naus; L Hoffner; R W Hemphill
Squamous cell carcinoma in situ arising in an ovarian mature cystic teratoma. Report of one case with histopathologic, cytogenetic, and flow cytometric DNA content analysis.
Archives of pathology & laboratory medicine 1991;115(2):172-4.
1990: Urvashi Surti; L Hoffner; Aravinda Chakravarti; R E Ferrell
Genetics and biology of human ovarian teratomas. I. Cytogenetic analysis and mechanism of origin.
American journal of human genetics 1990;47(4):635-43.
1990: Ranjan Deka; Aravinda Chakravarti; Urvashi Surti; E Hauselman; J Reefer; P P Majumder; Robert E Ferrell
Genetics and biology of human ovarian teratomas. II. Molecular analysis of origin of nondisjunction and gene-centromere mapping of chromosome I markers.
American journal of human genetics 1990;47(4):644-55.
1990: M Kiechle-Schwarz; C S Berger; Urvashi Surti; Avery A Sandberg
Rearrangement of band 10q22 in leiomyoma and leiomyosarcoma of the uterus.
Cancer genetics and cytogenetics 1990;47(1):95-100.
1990: E D Ruchelli; S Shen-Schwarz; J Martin; Urvashi Surti
Correlation between pathologic and ultrasound findings in first trimester spontaneous abortions.
Pediatric pathology / affiliated with the International Paediatric Pathology Association 1990;10(5):743-56.
1989: Urvashi Surti; R Habibian
Chromosomal rearrangement in choriocarcinoma cell lines.
Cancer genetics and cytogenetics 1989;38(2):229-40.
1989: Aravinda Chakravarti; P P Majumder; Susan A Slaugenhaupt; Ranjan Deka; AC Warren; Urvashi Surti; Robert E Ferrell; S E Antonarakis
Gene-centromere mapping and the study of non-disjunction in autosomal trisomies and ovarian teratomas.
Progress in clinical and biological research 1989;311():45-79.
1989: S Shen-Schwarz; L M Hill; Urvashi Surti; S Marchese
Deletion of terminal portion of 6q: report of a case with unusual malformations.
American journal of medical genetics 1989;32(1):81-6.
1987: R Habibian; Urvashi Surti
Cytogenetics of trophoblasts from complete hydatidiform moles.
Cancer genetics and cytogenetics 1987;29(2):271-87.
1981: M L Berman; H Tobon; Urvashi Surti
Primary malignant melanoma of the vagina: clinical, light and electron microscopic observations.
American journal of obstetrics and gynecology 1981;139(8):963-5.