Connection

HANUMANTHA PULIVARTHI to Child

This is a "connection" page, showing publications HANUMANTHA PULIVARTHI has written about Child.
Connection Strength

0.138
  1. Translocation t(7;12) as the sole chromosomal abnormality resulting in ACTB-GLI1 fusion in pediatric gastric pericytoma. Hum Pathol. 2016 07; 53:137-41.
    View in: PubMed
    Score: 0.015
  2. Cytogenetic landscape of paired neurospheres and traditional monolayer cultures in pediatric malignant brain tumors. Neuro Oncol. 2015 Jul; 17(7):965-77.
    View in: PubMed
    Score: 0.014
  3. Integrated multimodal genetic testing of Ewing sarcoma--a single-institution experience. Hum Pathol. 2013 Oct; 44(10):2010-9.
    View in: PubMed
    Score: 0.012
  4. Near-Haploid B-Cell Acute Lymphoblastic Leukemia in a Patient with Rubinstein-Taybi Syndrome. Pediatr Hematol Oncol. 2022 Nov; 39(8):747-754.
    View in: PubMed
    Score: 0.011
  5. Genomic profiling of plasmablastic lymphoma using array comparative genomic hybridization (aCGH): revealing significant overlapping genomic lesions with diffuse large B-cell lymphoma. J Hematol Oncol. 2009 Nov 12; 2:47.
    View in: PubMed
    Score: 0.010
  6. Pediatric myeloid sarcoma: a single institution clinicopathologic and molecular analysis. Pediatr Hematol Oncol. 2020 Feb; 37(1):76-89.
    View in: PubMed
    Score: 0.010
  7. Genetically transforming human mesenchymal stem cells to sarcomas: changes in cellular phenotype and multilineage differentiation potential. Cancer. 2009 Oct 15; 115(20):4795-806.
    View in: PubMed
    Score: 0.009
  8. Juvenile juxtacortical chondromyxoid fibroma of bone: a case report. Hum Pathol. 2008 Jun; 39(6):960-5.
    View in: PubMed
    Score: 0.009
  9. Medulloblastomas overexpress the p53-inactivating oncogene WIP1/PPM1D. J Neurooncol. 2008 Feb; 86(3):245-56.
    View in: PubMed
    Score: 0.008
  10. The utility of spectral karyotyping in the cytogenetic analysis of newly diagnosed pediatric acute lymphoblastic leukemia. Leukemia. 2002 Nov; 16(11):2222-7.
    View in: PubMed
    Score: 0.006
  11. Multicolor spectral karyotyping identifies novel translocations in childhood acute lymphoblastic leukemia. Leukemia. 2001 Mar; 15(3):468-72.
    View in: PubMed
    Score: 0.005
  12. A clinically relevant orthotopic xenograft model of ependymoma that maintains the genomic signature of the primary tumor and preserves cancer stem cells in vivo. Neuro Oncol. 2010 Jun; 12(6):580-94.
    View in: PubMed
    Score: 0.005
  13. Comparative genomic hybridization study of de novo myeloid neoplasia. Acta Haematol. 2000; 104(1):25-30.
    View in: PubMed
    Score: 0.005
  14. Clinical utility of array comparative genomic hybridization for detection of chromosomal abnormalities in pediatric acute lymphoblastic leukemia. Pediatr Blood Cancer. 2008 Aug; 51(2):171-7.
    View in: PubMed
    Score: 0.004
  15. Medulloblastoma outcome is adversely associated with overexpression of EEF1D, RPL30, and RPS20 on the long arm of chromosome 8. BMC Cancer. 2006 Sep 12; 6:223.
    View in: PubMed
    Score: 0.004
  16. Genome-wide array comparative genomic hybridization analysis reveals distinct amplifications in osteosarcoma. BMC Cancer. 2004 Aug 07; 4:45.
    View in: PubMed
    Score: 0.003
  17. Frequent amplification and rearrangement of chromosomal bands 6p12-p21 and 17p11.2 in osteosarcoma. Genes Chromosomes Cancer. 2004 Jan; 39(1):11-21.
    View in: PubMed
    Score: 0.003
  18. Cytogenetic analysis of a juvenile granulosa cell tumor. Cancer Genet Cytogenet. 1992 Jul 15; 61(2):207-9.
    View in: PubMed
    Score: 0.003
  19. Neural differentiation in small round cell tumors of bone and soft tissue with the translocation t(11;22)(q24;q12): an immunohistochemical study of 11 cases. Hum Pathol. 1990 Dec; 21(12):1245-51.
    View in: PubMed
    Score: 0.003
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.