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Binuja Varma
Binuja Varma
Principal Scientist
在 tcs.com 的电子邮件经过验证
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引用次数
引用次数
年份
Common variants of FTO and the risk of obesity and type 2 diabetes in Indians
G Chauhan, R Tabassum, A Mahajan, OP Dwivedi, Y Mahendran, I Kaur, ...
Journal of human genetics 56 (10), 720-726, 2011
842011
Genetic susceptibility to schizophrenia: role of dopaminergic pathway gene polymorphisms
M Gupta, C Chauhan, P Bhatnagar, S Gupta, S Grover, PK Singh, ...
Pharmacogenomics 10 (2), 277-291, 2009
622009
Genetic profile of patients with epilepsy on first-line antiepileptic drugs and potential directions for personalized treatment
S Grover, M Gourie-Devi, R Baghel, S Sharma, K Bala, M Gupta, ...
Pharmacogenomics 11 (7), 927-941, 2010
542010
Chromosome 22q11. 2 microdeletion in monozygotic twins with discordant phenotype and deletion size
A Halder, M Jain, I Chaudhary, B Varma
Molecular cytogenetics 5, 1-8, 2012
512012
Ayurgenomics for stratified medicine: TRISUTRA consortium initiative across ethnically and geographically diverse Indian populations
B Prasher, B Varma, A Kumar, BK Khuntia, R Pandey, A Narang, P Tiwari, ...
Journal of ethnopharmacology 197, 274-293, 2017
362017
Spectrum of large copy number variations in 26 diverse Indian populations: potential involvement in phenotypic diversity
P Gautam, P Jha, D Kumar, S Tyagi, B Varma, D Dash, A Mukhopadhyay, ...
Human genetics 131, 131-143, 2012
222012
Genetic determinants of immune-response to a polysaccharide vaccine for typhoid
PP Majumder, HF Staats, N Sarkar-Roy, B Varma, T Ghosh, S Maiti, ...
The HUGO journal 3, 17-30, 2009
182009
Frequency spectrum of rare and clinically relevant markers in multiethnic Indian populations (ClinIndb): A resource for genomic medicine in India
A Narang, B Uppilli, A Vivekanand, S Naushin, A Yadav, K Singhal, ...
Human Mutation 41 (11), 1833-1847, 2020
142020
Targeted exome sequencing in anti-factor H antibody negative HUS reveals multiple variations
RW Thergaonkar, A Narang, BS Gurjar, P Tiwari, M Puraswani, H Saini, ...
Clinical and Experimental Nephrology 22, 653-660, 2018
142018
Human brain harbors single nucleotide somatic variations in functionally relevant genes possibly mediated by oxidative stress
A Sharma, AH Ansari, R Kumari, R Pandey, R Rehman, B Mehani, ...
F1000Research 5, 2016
62016
The somatic chromosomes of five species of Aristolochia
AK Sharma, B Varma
Phyton. Rev. Internac. Bot. Expt. Argentina 12, 101-108, 1959
61959
Floury leaf spot of Bean caused by Ramularia phaseolina Petrak.
HS Sohi, SL Sharma, BR Verma, KB Sachdeva
51965
Polymorphisms in renin-angiotensin-aldosterone system and vascular endothelial growth factor may cross talk in preeclampsia: a pilot study of maternal and fetal dyads in Indian …
S Sharma, S Bhaskaran, SB Tripathi, N Vaid, B Varma
Int J Res Med Sci 4, 1666-72, 2016
22016
Genetic discovery in vesicoureteral reflux using exome sequencing: A pilot study
RW Thergaonkar, V Manchanda, G Bansal, A Yadav, J Singh, B Varma, ...
Medical Journal Armed Forces India, 2024
2024
Unique mutation and gene expression in High Hyperdiploid Acute Lymphoblastic Leukaemia with whole chromosome uniparental isodisomy
M Parihar, D Ganguli, A Banerjee, R Islam, S Basu, C Bhattacharya, ...
2022
Development of a targeted sequencing panel for Indian patients with acute Lymphoblastic Leukaemia
D Ganguli, M Parihar, R Islam, D Saha, A Basu, P Roy, S Dhar, N Arora, ...
Pediatric Hematology Oncology Journal 2 (2), S3-S4, 2017
2017
Targeted exome sequencing in patients with atypical hemolytic uremic syndrome (aHUS) and negative anti-complement factor H (FH) antibodies reveals multiple variations
R Thergaonkar, A Narang, BS Gurjar, M Puraswani, A Sinha, A Yadav, ...
PEDIATRIC NEPHROLOGY 31 (10), 1742-1742, 2016
2016
Identification Of Mutations In Bcr-Abl Gene In Newly Diagnosed Indian Patients With Chronic Myelogenous Leukemia (CML)
BVMJ Aggarwal Shyam, Binuja Verma
Blood 122 (5), 169, 2013
2013
Feto-Maternal Polymorphisms in Genes of Renin Angiotensin System and Angiogenesis Pathway in Preeclampsia/Eclampsia
N Vaid, S Bhaskaran, A Suneja, K Narayanswamy, B Varma
HYPERTENSION IN PREGNANCY 27 (4), 692-692, 2008
2008
Human brain harbors single nucleotide somatic variations
A Sharma, AH Ansan, R Kumari, R Pandey, R Rehman, B Mehani, ...
Proc Natl Acad Sci US A 98 (5), 2532-2537, 2001
2001
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