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Cureus|February 13, 2025
Variant Klinefelter Syndrome With Xq Trisomy (47,X,i(X)(q10),Y): A Case Report and Review of the LiteratureJagadeeshwar Ghatanatti, Somprakash Dhangar, Babu Rao VundintiIntractable & Rare Diseases Research|March 19, 2019
Partial trisomy 9 (9pter->9q22.1) and partial monosomy 14 (14pter- >14q11.2) due to paternal translocation t(9;14)(q22.1;q11.2) in a case of Dysmorphic featuresSomprakash Dhangar, Seema Korgaonkar, Babu Rao VundintiIntractable & Rare Diseases Research|August 27, 2020
array-CGH revealed gain of Yp11.2 in 49,XXXXY and gain of Xp22.33 in 48,XXYY karyotypes of two rare klinefelter variantsSomprakash Dhangar, Jagdeeshwar Ghatanatti, Babu Rao VundintiMolecular Biology Reports|July 10, 2019
Lack of association between functional polymorphism of DNA repair genes (XRCC1, XPD) and clinical response in Indian chronic myeloid leukemia patientsSomprakash Dhangar, Vinay Shanbhag, Chandrakala Shanmukhaiah, et al.Oncology|March 5, 2024
Comprehensive Study of Chromosomal Copy Number Variations and Genomic Variations Predicting Overall Survival in Myelodysplastic SyndromesNehakumari Maurya, Chandrakala Shanmukhaiah, Somprakash Dhangar, et al.Journal of Cancer Research and Therapeutics|April 3, 2023
Frequency and pattern of chromosomal abnormalities in acute myeloid leukemia from Western India: A retrospective studyBabu Rao Vundinti, Seema Korgaonkar, Somprakash Dhangar, et al.Journal of Human Reproductive Sciences|July 12, 2019
Chromosomal Aberrations in Primary Amenorrhea: A Retrospective StudySeema Korgaonkar, Somprakash Dhangar, Vinayak Kulkarni, et al.Molecular Human Reproduction|January 8, 2023
Comprehensive molecular analysis identifies eight novel variants in XY females with disorders of sex developmentVinayak Kulkarni, Selvaa Kumar Chellasamy, Somprakash Dhangar, et al.BMC Medical Genomics|January 4, 2022
Novel deletion of exon 3 in TYR gene causing Oculocutaneous albinism 1B in an Indian family along with intellectual disability associated with chromosomal copy number variationsSomprakash Dhangar, Purvi Panchal, Jagdeeshwar Ghatanatti, et al.Molecular Biology Reports|January 4, 2021
Severe telomere shortening in Fanconi anemia complementation group LAnjali Shah, Merin George, Somprakash Dhangar, et al.Pageof 2