• 457 Citations
  • 12 h-Index
1990 …2019
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Publications 1990 2019

  • 457 Citations
  • 12 h-Index
  • 39 Article
  • 1 Chapter
2019

Molecular Pathway and Fluorescence In Situ Hybridization Testing of ERBB2 (HER2) Gene Amplification in Invasive Ductal Carcinoma of Breast

Jodlowski, T. & Ramesh, K. H., Mar 15 2019, Molecular Diagnostics in Cancer Patients. Springer Singapore, p. 237-268 32 p.

Research output: Chapter in Book/Report/Conference proceedingChapter

Carcinoma, Ductal, Breast
Gene Amplification
Fluorescence In Situ Hybridization
2018

Rheumatoid arthritis in an adult patient with mosaic distal 18q-, 18p- and ring chromosome 18

Arora, S., Chau, A., Ramesh, K. H. & Jagannath, A. D., Jan 1 2018, In : F1000Research. 6, 1940.

Research output: Contribution to journalArticle

Chromosomes
IgA Deficiency
Chromosomes, Human, Pair 18
Rheumatoid Arthritis
Pulmonary diseases
2017
1 Citation (Scopus)
Synovial Sarcoma
Stomach
2016
2 Citations (Scopus)

Fine-needle aspiration biopsy of prostate synovial sarcoma: A case report and review of the literature

Maleki, S., Cajigas, A., Moss, J., Ramesh, K. H. & Khader, S. N., 2016, (Accepted/In press) In : Diagnostic Cytopathology.

Research output: Contribution to journalArticle

Synovial Sarcoma
Fine Needle Biopsy
Prostate
Needle Biopsy
Fluorescence In Situ Hybridization
2015
Ewing's Sarcoma
Oncogene Proteins
2014
8 Citations (Scopus)

A de novo 10.79 Mb interstitial deletion at 2q13q14.2 involving PAX8 causing hypothyroidism and mullerian agenesis: A novel case report and literature review

Ma, D., Marion, R. W., Punjabi, N. P., Pereira, E., Samanich, J., Agarwal, C., Li, J., Huang, C. K., Ramesh, K. H., Cannizzaro, L. A. & Naeem, R. C., 2014, In : Molecular Cytogenetics. 7, 1, 85.

Research output: Contribution to journalArticle

Hypothyroidism
Chromosomes
Genes
Thyroid Gland
Urogenital Abnormalities
3 Citations (Scopus)

Epidemiologic study of myelodysplastic syndromes in a multiethnic, inner city cohort

Sridharan, A., Jain, R., Bachhuber, M. A., Yu, Y., Ramesh, K. H., Gundabolu, K., Friedman, E. W. & Verma, A. K., Aug 23 2014, In : Experimental Hematology and Oncology. 3, 1, p. 1-6 6 p., 22.

Research output: Contribution to journalArticle

Myelodysplastic Syndromes
Hispanic Americans
Epidemiologic Studies
Survival
Thrombocytopenia
2012
5 Citations (Scopus)
Dextrocardia
Atrial Heart Septal Defects
Ribs
Karyotype
Craniofacial Abnormalities
13 Citations (Scopus)

Hepatoblastoma in a mosaic trisomy 18 patient

Pereira, E. M., Marion, R. W., Ramesh, K. H., Kim, J. S., Ewart, M. R. & Ricafort, R., May 2012, In : Journal of Pediatric Hematology/Oncology. 34, 4

Research output: Contribution to journalArticle

Hepatoblastoma
Karyotype
Trisomy 18
Drug Therapy
Neoplasms
2011
12 Citations (Scopus)

Alpha- and beta-synucleins are new diagnostic tools for acute erythroid leukemia and acute megakaryoblastic leukemia

Maitta, R. W., Wolgast, L. R., Wang, Q., Zhang, H., Bhattacharyya, P., Gong, J. Z., Sunkara, J., Albanese, J. M., Pizzolo, J. G., A.Cannizzaro, L., Ramesh, K. H. & Ratech, H., Feb 2011, In : American Journal of Hematology. 86, 2, p. 230-234 5 p.

Research output: Contribution to journalArticle

Neoplasm Proteins
Megakaryocyte-Erythroid Progenitor Cells
gamma-Synuclein
beta-Synuclein
Synucleins
8 Citations (Scopus)

Spectrin isoforms: Differential expression in normal hematopoiesis and alterations in neoplastic bone marrow disorders

Wolgast, L. R., Cannizzarro, L. A., Ramesh, K. H., Xue, X. N., Wang, D., Bhattacharyya, P. K., Gong, J. Z., McMahon, C., Albanese, J. M., Sunkara, J. L. & Ratech, H., Aug 2011, In : American Journal of Clinical Pathology. 136, 2, p. 300-308 9 p.

Research output: Contribution to journalArticle

Spectrin
Hematopoiesis
Protein Isoforms
Bone Marrow
Leukemia, Megakaryoblastic, Acute
79 Citations (Scopus)

Widespread hypomethylation occurs early and synergizes with gene amplification during esophageal carcinogenesis

Alvarez, H., Opalinska, J., Zhou, L., Sohal, D., Fazzari, M. J., Yu, Y., Montagna, C., Montgomery, E. A., Canto, M., Dunbar, K. B., Wang, J., Roa, J. C., Mo, Y., Bhagat, T., Ramesh, K. H., Cannizzaro, L., Mollenhauer, J., Thompson, R. F., Suzuki, M., Meltzer, S. & 4 others, Melnick, A., Greally, J. M., Maitra, A. & Verma, A., Mar 2011, In : PLoS Genetics. 7, 3, e1001356.

Research output: Contribution to journalArticle

Barrett Esophagus
Gene Amplification
methylation
Epigenomics
carcinogenesis
2009
12 Citations (Scopus)

Association of MLL amplification with poor outcome in acute myeloid leukemia

Maitta, R. W., Cannizzaro, L. A. & Ramesh, K. H., Jul 1 2009, In : Cancer Genetics and Cytogenetics. 192, 1, p. 40-43 4 p.

Research output: Contribution to journalArticle

Acute Myeloid Leukemia
Chromosome Aberrations
Staining and Labeling
Chromosomes, Human, Pair 16
Chromosomes, Human, Pair 11
2008
11 Citations (Scopus)

The combination of clofarabine and cytarabine in pediatric relapsed acute lymphoblastic leukemia: A case report

Gidwani, P., Ramesh, K. H., Liu, Y. & Kolb, E. A., Mar 2008, In : Chemotherapy. 54, 2, p. 120-124 5 p.

Research output: Contribution to journalArticle

Cytarabine
Precursor Cell Lymphoblastic Leukemia-Lymphoma
Pediatrics
Leukemia
Purine Nucleosides
2007

Cytogenetic and Genome Research: Preface

Cannizzaro, L. A. & Ramesh, K. H., Nov 2007, In : Cytogenetic and Genome Research. 118, 2-4, p. 91 1 p.

Research output: Contribution to journalArticle

Cytogenetics
Genome
Research
2006
15 Citations (Scopus)

AIDS and non-AIDS diffuse large B-cell lymphomas express different antigen profiles

Madan, R., Gormley, R., Dulau, A., Xu, D., Walsh, D., Ramesh, K. H., Cannizaro, L., Tamas, E. F., Kumar, P., Sparano, J. A., LeValley, A., Xue, X. N., Bhattacharyya, P. K., Ioachim, H. L. & Ratech, H., Mar 2006, In : Modern Pathology. 19, 3, p. 438-446 9 p.

Research output: Contribution to journalArticle

Lymphoma, Large B-Cell, Diffuse
Germinal Center
Acquired Immunodeficiency Syndrome
Antigens
B-Lymphocytes
2005
22 Citations (Scopus)

Germinal center and activated B-cell profiles separate Burkitt lymphoma and diffuse large B-cell lymphoma in AIDS and non-AIDS cases

Gormley, R. P., Madan, R., Dulau, A. E., Xu, D., Tamas, E. F., Bhattacharyya, P. K., LeValley, A., Xue, X. N., Kumar, P., Sparano, J. A., Ramesh, K. H., Pulijaal, V., Cannizzaro, L., Walsh, D., Ioachim, H. L. & Ratech, H., Nov 2005, In : American Journal of Clinical Pathology. 124, 5, p. 790-798 9 p.

Research output: Contribution to journalArticle

Germinal Center
Burkitt Lymphoma
Lymphoma, Large B-Cell, Diffuse
Acquired Immunodeficiency Syndrome
B-Lymphocytes
2004
16 Citations (Scopus)

Acute promyelocytic leukemia cell line AP-1060 established as a cytokine-dependent culture from a patient clinically resistant to all-trans retinoic acid and arsenic trioxide

Sun, Y., Kim, S. H., Zhou, D. C., Ding, W., Paietta, E. M., Guidez, F., Zelent, A., Ramesh, K. H., Cannizzaro, L., Warrell, R. P. & Gallagher, R. E., Jul 2004, In : Leukemia. 18, 7, p. 1258-1269 12 p.

Research output: Contribution to journalArticle

Acute Promyelocytic Leukemia
Tretinoin
Cytokines
Cell Line
Ethylnitrosourea
2003
20 Citations (Scopus)

Evidence for expression of early myeloid antigens in mature, non-blast myeloid cells in myelodysplasia

Xu, D., Schultz, C., Akker, Y., Cannizzaro, L., Ramesh, K. H., Du, J. & Ratech, H., Sep 1 2003, In : American Journal of Hematology. 74, 1, p. 9-16 8 p.

Research output: Contribution to journalArticle

Myelodysplastic Syndromes
Myeloid Cells
Antigens
Chromosome Aberrations
Bone Marrow
2001
5 Citations (Scopus)

Characterization of t(11;19)(q23;p13.3) by fluorescence in situ hybridization analysis in a pediatric patient with therapy-related acute myelogenous leukemia

Cheng, L., Ramesh, K. H., Radel, E., Ratech, H., Wei, D. & Cannizzaro, L. A., 2001, In : Cancer Genetics and Cytogenetics. 129, 1, p. 17-22 6 p.

Research output: Contribution to journalArticle

Etoposide
Fluorescence In Situ Hybridization
Acute Myeloid Leukemia
Pediatrics
Drug Therapy
1998
15 Citations (Scopus)

FHIT gene transcript alterations occur frequently in myeloproliferative and myelodysplastic diseases

Luan, X., Ramesh, K. H. & Cannizzaro, L. A., 1998, In : Cytogenetics and Cell Genetics. 81, 3-4, p. 183-188 6 p.

Research output: Contribution to journalArticle

Myelodysplastic-Myeloproliferative Diseases
Genes
Exons
Leukemia
Biopsy
2 Citations (Scopus)

Origin of human chromosome 2 revisited

Samonte, R. V., Ramesh, K. H. & Verma, R. S., Apr 1998, In : Journal of Genetics. 77, 1, p. 41-44 4 p.

Research output: Contribution to journalArticle

Chromosomes, Human, Pair 2
Human Chromosomes
Hominidae
Chromosomes
DNA Probes
1997
6 Citations (Scopus)

Clonal chromosome aberrations with monosomy of chromosome 8 in a case of grade III chondrosarcoma

Ptaszynski, K., Ramesh, K. H. & Cannizzaro, L. A., Aug 1997, In : Cancer Genetics and Cytogenetics. 97, 1, p. 60-63 4 p.

Research output: Contribution to journalArticle

Monosomy
Chromosomes, Human, Pair 8
Chondrosarcoma
Chromosome Aberrations
Chromosomes, Human, Pair 12
9 Citations (Scopus)

Comparative mapping of human alphoid satellite DNA repeat sequences in the great apes

Samonte, R. V., Ramesh, K. H. & Verma, R. S., 1997, In : Genetica. 101, 2, p. 97-104 8 p.

Research output: Contribution to journalArticle

Satellite DNA
satellite DNA
Hominidae
Pongidae
Gorilla gorilla
Hypogonadism
Crohn Disease
Sex-Determining Region Y Protein
Chromosomes
Euchromatin
Hypogonadism
Y Chromosome
X Chromosome
Crohn Disease
Sex-Determining Region Y Protein
2 Citations (Scopus)

Rapid denaturation improves chromosome morphology and permits multiple hybridizations during fluorescence in situ hybridization

Ramesh, K. H., Macera, M. J. & Verma, R. S., May 1997, In : Biotechnic and Histochemistry. 72, 3, p. 141-143 3 p.

Research output: Contribution to journalArticle

Nucleic Acid Denaturation
Pyrimidines
Purines
Human Chromosomes
Metaphase
1996
5 Citations (Scopus)

A de novo interstitial deletion of chromosome 15 band q25 as revealed by FISH-technique

Verma, R. S., Kleyman, S. M., Giridharan, R. & Ramesh, K. H., Jun 1996, In : Clinical Genetics. 49, 6, p. 303-305 3 p.

Research output: Contribution to journalArticle

Hypertelorism
Chromosomes, Human, Pair 15
Microcephaly
Muscle Hypotonia
Telomerase
1 Citation (Scopus)

Assignment of human MYCN proto-oncogene to chromosome band 12q24 in higher primates

Ramesh, K. H., Gupta, S. & Verma, R. S., Oct 24 1996, In : Gene. 177, 1-2, p. 169-172 4 p.

Research output: Contribution to journalArticle

Proto-Oncogenes
Primates
Chromosomes
Chromosomes, Human, Pair 2
Human Chromosomes
27 Citations (Scopus)
Satellite DNA
Chromosomes, Human, Pair 9
Reunion
Calcium Gluconate
Nucleic Acid Repetitive Sequences
7 Citations (Scopus)

Centromeric alphoid sequences are breakage prone resulting in pericentromeric inversion heteromorphism of qh region of chromosome 1

Verma, R. S., Ramesh, K. H., Mathews, T., Kleyman, S. M. & Conte, R. A., 1996, In : Annales de Genetique. 39, 4, p. 205-208 4 p.

Research output: Contribution to journalArticle

Chromosomes, Human, Pair 1
Chromosomes, Human, Pair 9
Fluorescence In Situ Hybridization
Constriction
3 Citations (Scopus)

Characterization of a derivative chromosome 17 by FISH-technique

Ramesh, K. H., Shah, H. O., Sherman, J., Lin, J. H. & Verma, R. S., 1996, In : Annales de Genetique. 39, 3, p. 177-180 4 p.

Research output: Contribution to journalArticle

Chromosomes, Human, Pair 17
Fluorescence In Situ Hybridization
Micrognathism
Chromosomes
Septum Pellucidum
2 Citations (Scopus)

Mapping the homolog of the human Rb1 gene to Chromosome 14 of higher primates

Verma, R. S., Ramesh, K. H., Samonte, R. V. & Conte, R. A., 1996, In : Mammalian Genome. 7, 8, p. 591-592 2 p.

Research output: Contribution to journalArticle

Chromosomes, Human, Pair 14
Primates
Genes
Cosmids
Retinoblastoma
35 Citations (Scopus)

Molecular cytogenetic characterization of breakpoints involving pericentric inversions of human chromosome 9

Samonte, R. V., Conte, R. A., Ramesh, K. H. & Verma, R. S., 1996, In : Human Genetics. 98, 5, p. 576-580 5 p.

Research output: Contribution to journalArticle

Satellite DNA
Chromosomes, Human, Pair 9
Human Chromosomes
Cytogenetics
Reunion
11 Citations (Scopus)

Origine paternelle du chromosome 18 surnumeraire dans la trisomie 18

Ramesh, K. H. & Verma, R. S., 1996, In : Annales de Genetique. 39, 2, p. 110-112 3 p.

Research output: Contribution to journalArticle

Chromosomes, Human, Pair 18
Meiosis
Trisomy
Age Distribution
Mitosis
1995
3 Citations (Scopus)

Are we fishing in troubled waters?

Verma, R. S., Batish, S. D., Ramesh, K. H. & Gogineni, S. K., 1995, In : Cellular and Molecular Biology Research. 41, 2, p. 81-84 4 p.

Research output: Contribution to journalArticle

False Positive Reactions
Chromosome Banding
Chromosomes, Human, Pair 17
Chromosome Aberrations
Water
1994
25 Citations (Scopus)

Chromosome aberrations in lymphocytes from women irradiated for benign and malignant gynecological disease

Kleinerman, R. A., Littlefield, L. G., Tarone, R. E., Sayer, A. M., Cookfair, D. L., Wactawski-Wende, J., Inskip, P. D., Block, A. W., Ramesh, K. H. & Boice, J. D., 1994, In : Radiation Research. 139, 1, p. 40-46 7 p.

Research output: Contribution to journalArticle

chromosome aberrations
lymphocytes
Chromosome Aberrations
cancer
uterine cervical neoplasms
1993
14 Citations (Scopus)

Chromosome instability and the FAMMM syndrome

Lynch, H. T., Fusaro, R. M., Sandberg, A. A., Bixenman, H. A., Johnsen, L. R., Lynch, J. F., Ramesh, K. H. & Leppert, M., 1993, In : Cancer Genetics and Cytogenetics. 71, 1, p. 27-39 13 p.

Research output: Contribution to journalArticle

Dysplastic Nevus Syndrome
Chromosomal Instability
Nevus
Genetic Translocation
Skin
1992
12 Citations (Scopus)

Cytogenetic damage in peripheral blood lymphocytes of cancer patients prior to radiotherapy

Ramesh, K. H. & Bhargava, M. K., 1992, In : Cancer Genetics and Cytogenetics. 60, 1, p. 86-88 3 p.

Research output: Contribution to journalArticle

Cytogenetics
Radiotherapy
Lymphocytes
Chromosome Aberrations
Neoplasms
1990
46 Citations (Scopus)

A guide to fragile sites on human chromosomes

Hecht, F., Ramesh, K. H. & Lockwood, D. H., 1990, In : Cancer Genetics and Cytogenetics. 44, 1, p. 37-45 9 p.

Research output: Contribution to journalArticle

Human Chromosomes
Chromosomes
Aphidicolin
Chromosomes, Human, Pair 21
Chromosomes, Human, Pair 3