FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

Gopalrao Velagaleti

Research Profile

Procedures

Disorders

Living Beings

Infants

Physiology

Anatomy

Co-author Network

Publications

TOP 3
Tahereh Dadfarnia; Mahmoud A Eltorky; Eduardo Eyzaguirre; Kelly D Carmichael; Gopalrao Velagaleti; Suimin Qiu
A t(1;9)(q10;q10) translocation with additional 6q23 and 9q22 rearrangements in a case of chondromyxoid fibroma.
Jill K Northup; Judy C Hawkins; Lillian H Lockhart; Reuben Matalon; Gopalrao Velagaleti
A complex chromosome rearrangement, der(6)ins(6)(p21.1q25.3q27)inv(6)(p25.3q27), in a child with cleidocranial dysplasia.
Anna D Asleson; Vickie Morgan; Stephen Smith; Gopalrao Velagaleti
Amplification of the RARA gene in acute myeloid leukemia: significant finding or coincidental observation?

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Geonetwork of Gopalrao Velagaleti (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

All Publications

2011: Tahereh Dadfarnia; Mahmoud A Eltorky; Eduardo Eyzaguirre; Kelly D Carmichael; Gopalrao Velagaleti; Suimin Qiu
A t(1;9)(q10;q10) translocation with additional 6q23 and 9q22 rearrangements in a case of chondromyxoid fibroma.
Cancer genetics 2011;204(12):666-70.
2011: Jill K Northup; Judy C Hawkins; Lillian H Lockhart; Reuben Matalon; Gopalrao Velagaleti
A complex chromosome rearrangement, der(6)ins(6)(p21.1q25.3q27)inv(6)(p25.3q27), in a child with cleidocranial dysplasia.
European journal of medical genetics 2011;54(4):e394-8.
2010: Anna D Asleson; Vickie Morgan; Stephen Smith; Gopalrao Velagaleti
Amplification of the RARA gene in acute myeloid leukemia: significant finding or coincidental observation?
Cancer genetics and cytogenetics 2010;202(1):33-7.
2010: Gopalrao Velagaleti; Vijay S Tonk; Nawar M Hakim; Xiaoke Wang; Hongying Zhang; Michele Erickson-Johnson; Fabiola Medeiros; Andre M Oliveira
Fusion of HMGA2 to COG5 in uterine leiomyoma.
Cancer genetics and cytogenetics 2010;202(1):11-6.
2010: Jill K Northup; Dena Matalon; Judy C Hawkins; Reuben Matalon; Gopalrao Velagaleti
Pericentric inversion, inv(14)(p11.2q22.3), in a 9-month old with features of Goldenhar syndrome.
Clinical dysmorphology 2010;19(4):185-9.
2010: Nicole L Hoppman-Chaney; D Brian Dawson; Lai Nguyen; Sunanda Sengupta; Kara Reynolds; Elizabeth McPherson; Gopalrao Velagaleti
Partial hexasomy for the Prader-Willi-Angelman syndrome critical region due to a maternally inherited large supernumerary marker chromosome.
American journal of medical genetics. Part A 2010;152A(8):2034-8.
2010: Thi Minh Thi Ha; Viet Nhan Nguyen; Noralane M Lindor; Reid G Meyer; Ruhi Rai; Gopalrao Velagaleti
A case of Down syndrome with mirror-image duplication of chromosome 21.
American journal of medical genetics. Part A 2010;152A(6):1580-2.
2010: Nicole L Hoppman-Chaney; Daniel Cherry; Charles Holladay; Jason Yuhas; Rich Wang; Gopalrao Velagaleti
Identification of a patient with 7q32 deletion-associated acute myeloid leukemia and an incidental t(8;14).
Cancer genetics and cytogenetics 2010;197(2):179-84.
2009: Zoran Gatalica; Stan L Lilleberg; Semir Vranic; Eduardo Eyzaguirre; Eduardo Orihuela; Gopalrao Velagaleti
Novel intronic germline FLCN gene mutation in a patient with multiple ipsilateral renal neoplasms.
Human pathology 2009;40(12):1813-9.
2009: Ercan Mihci; Gopalrao Velagaleti; Regina Ensenauer; Dusica Babovic-Vuksanovic
The phenotypic spectrum of trisomy 2: report of two new cases.
Clinical dysmorphology 2009;18(4):201-4.
2009: Neena L Champaigne; Nicole A Laird; Jill K Northup; Gopalrao Velagaleti
Molecular cytogenetic characterization of an interstitial de novo 13q deletion in a 3-month-old with severe pediatric gastroesophageal reflux.
American journal of medical genetics. Part A 2009;149A(4):751-4.
2008: Jill K Northup; Kären E Wain; Judy C Hawkins; Reuben Matalon; Gopalrao Velagaleti
First report of an interstitial deletion, del(5)(q33.1q35.1) in a girl with primary amenorrhea, seizures, and severe behavioral and developmental deficiencies.
American journal of medical genetics. Part A 2008;146A(19):2578-82.
2008: Anita S Kulharya; David B Flannery; Karen Norris; Carolyn Lovell; Brynn Levy; Gopalrao Velagaleti
Fine mapping of breakpoints in two unrelated patients with rare overlapping interstitial deletions of 9q with mild dysmorphic features.
American journal of medical genetics. Part A 2008;146A(17):2234-41.
2008: Gopalrao Velagaleti; Judy C Hawkins; Neli I Panova; Lillian H Lockhart
Partial trisomy and partial monosomy resulting from a reciprocal segregating in a large family.
Indian journal of pediatrics 2008;75(9):956-60.
2008: Susanna L Cooke; Jill K Northup; Neena L Champaige; William Zinser; Paul A W Edwards; Lillian H Lockhart; Gopalrao Velagaleti
Molecular cytogenetic characterization of a unique and complex de novo 8p rearrangement.
American journal of medical genetics. Part A 2008;146A(9):1166-72.
2008: Karmaine Millington; S David Hudnall; Jill K Northup; Neli I Panova; Gopalrao Velagaleti
Role of chromosome 1 pericentric heterochromatin (1q) in pathogenesis of myelodysplastic syndromes: report of 2 new cases.
Experimental and molecular pathology 2008;84(2):189-93.
2007: S David Hudnall; Jill K Northup; Neli I Panova; Kauser Suleman; Gopalrao Velagaleti
Prolonged preleukemic phase of chronic myelogenous leukemia.
Experimental and molecular pathology 2007;83(3):484-9.
2007: Jill K Northup; Kathleen Griffis; Judy Hawkins; Lillian H Lockhart; Gopalrao Velagaleti
Unusual pseudo dicentric, psu dic (1;19)(q10;q13.42), in a female with premature ovarian failure.
Fertility and sterility 2007;87(3):697.e5-8.
2007: Jill K Northup; Swarupa A Gadre; Yimin Ge; Lillian H Lockhart; Gopalrao Velagaleti
Do cytogenetic abnormalities precede morphologic abnormalities in a developing malignant condition?
European journal of haematology 2007;78(2):152-6.
2007: Zhiqin Wang; Gopalrao Velagaleti; Mahmoud A Eltorky; Wendell W Tang; Hal K Hawkins; Elizabeth A Jones; Jill K Northup; Neli I Panova; Suimin Qiu
Cytogenetic and molecular studies of an unusual case of multiple primary alveolar rhabdomyosarcomas: low-level chromosomal instability and reciprocal translocation t(6;11).
Experimental and molecular pathology 2007;82(1):58-62.
2006: Mark L Weiss; Satish Medicetty; Amber R Bledsoe; Raja Shekar Rachakatla; Michael Choi; Shosh Merchav; Yongquan Luo; Mahendra S Rao; Gopalrao Velagaleti; Deryl L Troyer
Human umbilical cord matrix stem cells: preliminary characterization and effect of transplantation in a rodent model of Parkinson's disease.
Stem cells (Dayton, Ohio) 2006;24(3):781-92.
2005: Vijay S Tonk; Golder N Wilson; Svetlana A Yatsenko; Pawel Stankiewicz; James R Lupski; Robert C Schutt; Jill K Northup; Gopalrao Velagaleti
Molecular cytogenetic characterization of a familial der(1)del(1)(p36.33)dup(1)(p36.33p36.22) with variable phenotype.
American journal of medical genetics. Part A 2005;139A(2):136-40.
2005: Gopalrao Velagaleti; Sally S Robinson; Bobby M Rouse; Vijay S Tonk; Lillian H Lockhart
Subtelomeric rearrangements in idiopathic mental retardation.
Indian journal of pediatrics 2005;72(8):679-85.
2005: Gabriel A Bien-Willner; Pawel Stankiewicz; James R Lupski; Jill K Northup; Gopalrao Velagaleti
Interphase FISH screening for the LCR-mediated common rearrangement of isochromosome 17q in primary myelofibrosis.
American journal of hematology 2005;79(4):309-13.
2005: Sankar Surendran; Dena Matalon; Stephen K Tyring; Peter L Rady; Gopalrao Velagaleti; Reuben Matalon
Altered expression of myocilin in the brain of a mouse model for phenylketonuria (PKU).
Neuroscience letters 2005;382(3):323-6.
2005: Gopalrao Velagaleti; Gabriel A Bien-Willner; Jill K Northup; Lillian H Lockhart; Judy C Hawkins; Syed M Jalal; Marjorie Withers; James R Lupski; Pawel Stankiewicz
Position effects due to chromosome breakpoints that map approximately 900 Kb upstream and approximately 1.3 Mb downstream of SOX9 in two patients with campomelic dysplasia.
American journal of human genetics 2005;76(4):652-62.
2005: Zoran Gatalica; Gopalrao Velagaleti; Helena Kuivaniemi; Gerard Tromp; Juan Palazzo; Kerry M Graves; Michelle Guigneaux; Thomas Wood; Mala Sinha; Bruce Luxon
Gene expression profile of an adenomyoepithelioma of the breast with a reciprocal translocation involving chromosomes 8 and 16.
Cancer genetics and cytogenetics 2005;156(1):14-22.
2004: Jessica M Linhart; Marjorie R Grafe; George R Saade; Gopalrao Velagaleti
Sonographic, pathologic and karyotypic findings in a rare case of placenta fenestrata.
Fetal diagnosis and therapy 2004;19(6):479-82.
2004: Melvyn S Soloff; Yow-Jiun Jeng; Monica Ilies; Solweig L Soloff; Michael G Izban; Thomas G Wood; Neli I Panova; Gopalrao Velagaleti; Garland D Anderson
Immortalization and characterization of human myometrial cells from term-pregnant patients using a telomerase expression vector.
Molecular human reproduction 2004;10(9):685-95.
2004: Gopalrao Velagaleti
Concerning 14q(22) deletion in a familial case of anophthalmia with polydactyly.
American journal of medical genetics. Part A 2004;126A(1):108;author reply 110.
2004: Gopalrao Velagaleti; Markku Miettinen; Zoran Gatalica
Malignant peripheral nerve sheath tumor with rhabdomyoblastic differentiation (malignant triton tumor) with balanced t(7;9)(q11.2;p24) and unbalanced translocation der(16)t(1;16)(q23;q13).
Cancer genetics and cytogenetics 2004;149(1):23-7.
2004: Vijay S Tonk; C A Jesurun; David L Morgan; Lillian H Lockhart; Gopalrao Velagaleti
Molecular cytogenetic characterization of a recombinant chromosome rec(22)dup(22q)inv(22)(p13q12.2).
American journal of medical genetics. Part A 2004;124A(1):92-5.
2003: Vijay S Tonk; Syed M Jalal; Jose Gonzalez; Amantia Kennedy; Gopalrao Velagaleti
Familial interstitial deletion of chromosome 4 (p15.2p16.1).
Annales de génétique 2003;46(4):453-8.
2003: Gopalrao Velagaleti; Jill K Tapper; Neli E Panova; Markku Miettinen; Zoran Gatalica
Cytogenetic findings in a case of nodular fasciitis of subclavicular region.
Cancer genetics and cytogenetics 2003;141(2):160-3.
2003: Gopalrao Velagaleti; Jill K Tapper; Bill A Rampy; Shuliu Zhang; Judy C Hawkins; Lillian H Lockhart
A rapid and noninvasive method for detecting tissue-limited mosaicism: detection of i(12)(p10) in buccal smear from a child with Pallister-Killian syndrome.
Genetic testing 2003;7(3):219-23.
2003: Vijay S Tonk; Herman E Wyandt; X Huang; N Patel; David L Morgan; MK Kukolich; Lillian H Lockhart; Gopalrao Velagaleti
Disease associated balanced chromosome rearrangements (DBCR): report of two new cases.
Annales de génétique 2003;46(1):37-43.
2003: Gopalrao Velagaleti; Syed M Jalal; Ron C Michaelis; Thomas F Rowe; Jerilynn R Nichols; Lillian H Lockhart
Molecular cytogenetic characterization of a de novo unbalanced translocation leading to trisomy 17q25-->qter and monosomy 18p11.3-->pter in a girl with dysmorphic features.
Clinical dysmorphology 2003;12(1):29-33.
2002: Jill K Tapper; Shuliu Zhang; Hassan M Harirah; Neli I Panova; Linda S Merryman; Judy C Hawkins; Lillian H Lockhart; Alfredo B Gei; Gopalrao Velagaleti
Prenatal diagnosis of a fetus with unbalanced translocation (4;13)(p16;q32) with overlapping features of Patau and Wolf-Hirschhorn syndromes.
Fetal diagnosis and therapy 2002;17(6):347-51.
2002: M Tarek Elghetany; Claudia P Molina; Jyoti Patel; Joe Martinez; Hanna Schwab; Gopalrao Velagaleti
Expression of CD4 on peripheral blood granulocytes. a novel finding in a case of myelodysplastic syndrome in association with t(5;12).
Cancer genetics and cytogenetics 2002;136(1):38-42.
2002: Shulan Li; Paul Malafiej; Brynn Levy; Radma Mahmood; Michael Field; Thomas Hughes; Lillian H Lockhart; Zhanhe Wu; Melissa Huang; Kurt Hirschhorn; Gopalrao Velagaleti; Art Daniel; Peter E Warburton
Chromosome 13q neocentromeres: molecular cytogenetic characterization of three additional cases and clinical spectrum.
American journal of medical genetics 2002;110(3):258-67.
2002: Brynn Levy; Syed M Jalal; Teresa M Dunn; Peter E Warburton; Vijay S Tonk; Kurt Hirschhorn; Lillian H Lockhart; T Hughes; Gopalrao Velagaleti
Unique case of mosaicism involving two morphologically similar marker chromosomes of different centric origin in a patient with developmental delay.
American journal of medical genetics 2002;108(3):198-204.
2002: Gopalrao Velagaleti; Syed M Jalal; MK Kukolich; Lillian H Lockhart; Vijay S Tonk
De novo supernumerary ring chromosome 7: first report of a non-mosaic patient and review of the literature.
Clinical genetics 2002;61(3):202-6.
2002: Melissa M Blann; Gopalrao Velagaleti; David L Morgan; Rodolfo E Martinez; Phillip A Conlin; Vijay S Tonk
Interstitial deletion of 20q in a patient with Waldenström macroglobulinemia following chemotherapy.
Cancer genetics and cytogenetics 2002;132(2):145-8.
2002: Derrick W Spell; Gopalrao Velagaleti; Dennie V Jones; William S Velasquez
Translocation (15;17) and trisomy 21 in the microgranular variant of acute promyelocytic leukemia.
Cancer genetics and cytogenetics 2002;132(1):74-6.
2001: Vijay S Tonk; Golder N Wilson; Gopalrao Velagaleti
Duplication 8 [inv dup(8)(p12p23)] with macrocephaly.
Annales de génétique 2001;44(4):195-9.
2001: Gopalrao Velagaleti; Lillian H Lockhart; Frank C Schmalstieg; Armond S Goldman
Trisomy 4 pter-q12 and monosomy of chromosome 13 pter-q12 in a male with deficiency of all blood lymphocyte populations.
American journal of medical genetics 2001;102(2):139-45.
2001: V Sovani; Gopalrao Velagaleti; Ewa Filipowicz; Zoran Gatalica; A S Knisely
Ossifying fibromyxoid tumor of soft parts: report of a case with novel cytogenetic findings.
Cancer genetics and cytogenetics 2001;127(1):1-6.
2000: M Kumar; HE Boggino; S David Hudnall; Gopalrao Velagaleti
Acute myeloid leukemia associated with hemophagocytic syndrome and t(4;7)(q21;q36).
Cancer genetics and cytogenetics 2000;122(1):26-9.
2000: Gopalrao Velagaleti; D L Morgan; Vijay S Tonk
Trisomy 5p. A case report and review.
Annales de génétique 2000;43(3-4):143-5.
2000: Gopalrao Velagaleti; A Kumar; Lillian H Lockhart; Reuben Matalon
Patent ductus arteriosus and microdeletion 22q11 in a patient with Klinefelter syndrome.
Annales de génétique 2000;43(2):105-7.
2000: BLANCHE ALTER; J P Caruso; R A Drachtman; T Uchida; Gopalrao Velagaleti; M Tarek Elghetany
Fanconi anemia: myelodysplasia as a predictor of outcome.
Cancer genetics and cytogenetics 2000;117(2):125-31.
1999: Gopalrao Velagaleti; Sugandhi A Tharapel; Avirachan T Tharapel
Validation of primed in situ labeling (PRINS) for interphase analysis: comparative studies with conventional fluorescence in situ hybridization and chromosome analyses.
Cancer genetics and cytogenetics 1999;108(2):100-6.
1999: Avirachan T Tharapel; Ron C Michaelis; Gopalrao Velagaleti; C H Laundon; Paula R Martens; P D Buchanan; K E Teague; Sugandhi A Tharapel; R Sid Wilroy
Chromosome duplications and deletions and their mechanisms of origin.
Cytogenetics and cell genetics 1999;85(3-4):285-90.
1998: Enikö K Pivnick; Robert A Kaufman; Gopalrao Velagaleti; Wendy M Gunther; D Abramovici
Infant with midline thoracoabdominal schisis and limb defects.
Teratology 1998;58(5):205-8.
1998: Enikö K Pivnick; W L Furman; Gopalrao Velagaleti; J J Jenkins; N A Chase; Raul C Ribeiro
Simultaneous adrenocortical carcinoma and ganglioneuroblastoma in a child with Turner syndrome and germline p53 mutation.
Journal of medical genetics 1998;35(4):328-32.
1998: Ron C Michaelis; Gopalrao Velagaleti; C Jones; Enikö K Pivnick; Mary C Phelan; E Boyd; J Tarleton; R Sid Wilroy; A Tunnacliffe; Avirachan T Tharapel
Most Jacobsen syndrome deletion breakpoints occur distal to FRA11B.
American journal of medical genetics 1998;76(3):222-8.
1997: Gopalrao Velagaleti; Sugandhi A Tharapel; Paula R Martens; Avirachan T Tharapel
Rapid identification of marker chromosomes using primed in situ labeling (PRINS).
American journal of medical genetics 1997;71(2):130-3.
1997: Owen P Phillips; Gopalrao Velagaleti; D E Emerson; Avirachan T Tharapel; Lee P Shulman
Confirmation of fetal aneuploidy with primed in situ hybridization on amniotic fluid during selective fetal reduction.
Prenatal diagnosis 1997;17(6):586-8.
1997: Sayee Rajangam; Ron C Michaelis; Gopalrao Velagaleti; S Lincoln; S Hegde; S Lewin; J Tarleton; IM Thomas; Avirachan T Tharapel
Down syndrome with biparental inheritance of der(14q21q) and maternally derived trisomy 21: confirmation by fluorescent in situ hybridization and microsatellite polymorphism analysis.
American journal of medical genetics 1997;70(1):43-7.
1997: Owen P Phillips; Gopalrao Velagaleti; Avirachan T Tharapel; Lee P Shulman
Discordant direct and culture results following chorionic villus sampling and the diagnosis of a third cell line in the fetus.
Prenatal diagnosis 1997;17(2):170-2.
1997: Gopalrao Velagaleti; N J Carpenter; Avirachan T Tharapel
Clinical applications of primed in situ labelling (PRINS) rapid identification of a marker chromosome in a fetus.
Annales de génétique 1997;40(3):154-7.
1996: Enikö K Pivnick; Gopalrao Velagaleti; R Sid Wilroy; M E Smith; S R Rose; R E Tipton; Avirachan T Tharapel
Jacobsen syndrome: report of a patient with severe eye anomalies, growth hormone deficiency, and hypothyroidism associated with deletion 11 (q23q25) and review of 52 cases.
Journal of medical genetics 1996;33(9):772-8.
1996: Gopalrao Velagaleti; S Harris; N J Carpenter; J Coldwell; B Say
Familial deletion of chromosome 18 (p11.2).
Annales de génétique 1996;39(4):201-4.