INCREDB ID : 479
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Kamlesh Guleria, Ph.D.
Assistant Professor 
 
Guru Nanak Dev University, Amritsar
Department of Human Genetics
Amritsar - 143 005   
Punjab   
 
E-mail: guleria_k@yahoo.com
Phone: 0183-2258803-09 Ext. 3240
Mobile: 09815948779
Fax: 0183-2258819; 2258820
 
URL: http://www.gndu.ac.in/gndu2014/ShowFacultyDetailProforma2.asp?id=2015101530&d=18
 
Publications:
1. Kapahi, R., Manjari, M., Uppal, M. S., Singh, N. R., Sambyal, V. and Guleria, K.  Association of -2549 insertion/deletion polymorphism of vascular endothelial growth factor with breast cancer in North Indian patients. Genetic Testing and Molecular Biomarkers. 2013.  17, 242-248. [PubMed]
2. Guleria, K., Sharma, S., Manjari, M., Uppal, M. S., Singh, N. R. and Sambyal, V.  p.R72P, PIN3 Ins16bp polymorphisms of TP53 and CCR5?32 in north Indian breast cancer patients. Asian Pacific Journal of Cancer Prevention : APJCP. 2012.  13, 3305-3311. [PubMed]
3. Al-Balool, H. H., Weber, D., Liu, Y., Wade, M., Guleria, K., Nam, P. L., Clayton, J., Rowe, W., Coxhead, J., Irving, J., Elliott, D. J., Hall, A. G., Santibanez-Koref, M. and Jackson, M. S.  Post-transcriptional exon shuffling events in humans can be evolutionarily conserved and abundant. Genome Research. 2011.  21, 1788-1799. [PubMed]
4. Saxena, R., Kohli, S., Guleria, K. and Verma, I. C.  Novel human pathological mutations. Gene symbol: TP53. Disease: Li-Fraumeni syndrome. Human Genetics. 2010.  127, 480. [PubMed]
5. Guleria, K., Sperling, K., Singh, D., Varon, R., Singh, J. R. and Vanita, V.  A novel mutation in the connexin 46 (GJA3) gene associated with autosomal dominant congenital cataract in an Indian family. Molecular Vision. 2007.  13, 1657-1665. [PubMed]
6. Guleria, K., Vanita, V., Singh, D. and Singh, J. R.  A novel "pearl box" cataract associated with a mutation in the connexin 46 (GJA3) gene. Molecular Vision. 2007.  13, 797-803. [PubMed]
7. Vanita, V., Hejtmancik, J. F., Hennies, H. C., Guleria, K., Nurnberg, P., Singh, D., Sperling, K. and Singh, J. R.  Sutural cataract associated with a mutation in the ferritin light chain gene (FTL) in a family of Indian origin. Molecular Vision. 2006.  12, 93-99. [PubMed]
 

 
Grant Support:
Project Title Role Funding Agency Sanction Number Sanction Date
Assessment of VEGF Polymorphisms and Serum Vascular Endothelial Growth Factor (sVEGF-C) level as Prognostic Marker for Breast Cancer Principal Investigator Department of Biotechnology, Government of India 2009-2013
Assessment of HIF-1α and TP53 polymorphisms and their serum levels in Breast Cancer Patients Co-PI University Grants Commission, India 2011-2014
Assessment of HIF-1α and TP53 as prognostic markers in esophageal cancer - A Multidisciplinary Approach Co-PI Department of Science & Technology, Government of India 2012-2015
Risk Assessment for Cancer University Grants Commission, India 2012-2017

 
 
My CV:   Download
 
Education 
::
Ph.D.
Honors and Awards
::
Young aspiring cataract research scientist award from Senju Pharmaceutical Co., Ltd. Japan in the 5th “Asian Cataract Research Conference”, June 23-26, 2004 Seoul, South Korea
::
Vocational Service Award from Rotary Club Amritsar, October, 24, 2008
Member
::
Human Genome Organization
::
Indian Society of Human Genetics
::
Indian Association of Cancer Research
::
Punjab Academy of Sciences
  Last modified on : Dec 14, 2015
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