Director
Publications
Molecular Biology Lab
Proteomics
Metabolomics
Infractructure
Phd
funding
Collaborators
visitors gallery
Trainees
 
Aunsha Uttarili, Ph.D.
Research Scientist
 
Institute of Bioinformatics
Discoverer Building, International Tech Park, Whitefield
Bangalore - 560 066
E-mail: anusha at ibioinformatics dot org
Phone: +91-80-28416140 Fax: +91-80-28416132
 
Education
Ph.D. in Human/Medical Genetics from Manipal Academy of Higher Education, Manipal, Karnataka, India
M.Sc. in Biochemistry from Andhra University, Visakhapatnam, Andhra Pradesh, India
 

Positions Held

Research Scientist, Institute of Bioinformatics, Bangalore, India, 2019-Present
National Post-Doctoral Fellow, Kasturba Medical College and Hospital, Manipal, India, India 2016-2018 
 

Area of Specialization

Human and Medical Genetics
Medical Genomics
 

Publications

Research papers: 11

Uttarilli, A., Amalakanti, S., Kommoju, P.R., Sharma, S., Goyal, P., Manjunath, G.K., Upadhayay, V., Parveen, A., Tandon, R., Prasad, K.S., Dakal, T.C., Ben Shlomo, I., Yousef, M., Neerathilingam, M., Kumar, A. (2021). Super-rapid race for saving lives by developing COVID-19 vaccines. Journal of Integrative Bioinformatics. 18(1), 27-43. [PubMed]

Mishra, S., Uttarilli, A., Girisha, K.M. (2021). Mongolian spots in GM1 gangliosidosis: a pictorial report. Clinical Dysmorphology. 30(1), 6-9. [PubMed]

Uttarilli, A., Shah H., Bhavani, G,S., Upadhyai, P., Shukla, A., Girisha, K.M. (2019). Phenotyping and genotyping of skeletal dysplasias: Evolution of a center and a decade of experience in India. Bone. 6(11):12 0, 204-211. [PubMed]

Uttarilli, A., Pasumathi, D., Ranganath, P., Dalal, A.B. (2016). Functional characterization of novel mutations in Indian patients with Maroteaux-Lamy syndrome (mucopolysaccharidoses Type VI). Gene. 30(1):599, 19-27. [PubMed]

Uttarilli, A., Ranganath, P., Matta, D., Nurul, Jain, J, M.d., Prasad, K., Babu AS., Girisha, K.M., Verma, I.C., Phadke, S.R., Mandal, K., Puri, R.D., Aggarwal, S., Danda, S., Sankar, V.H., Kapoor, S., Bhat, M., Gowrishankar, K., Hasan, A.Q., Nair, M., Nampoothiri, S., Dalal, A. (2016). Identification and characterization of 20 novel pathogenic variants in 60 unrelated Indian patients with mucopolysaccharidoses type I and type II. Clinical Genetics. 90(6), 496-508. [PubMed]

Uttarilli, A., Ranganath, P., Jain, S.J., Prasad, C.K., Sinha, A., Verma, I.C., Phadke, S.R., Puri, D.R., Danda, S., Muranjan, M.N., Jevalikar, G., Nagarajaram, H.A., Dalal, A.B. (2015). Novel mutations of the arylsulphatase B (ARSB) gene in Indian patients with Mucopolysaccharidosis Type VI. Indian Journal of Medical Research. 142(4), 414-425. [PubMed]

Gupta, A., Uttarilli, A., Dalal, A., Girisha, K.M. (2015). Hunter syndrome with late age of presentation: clinical description of a case and review of literature. Bio Medical Journal Case Reports. 14(5). [PubMed]

Kantaputra, P.N., Kayserili, H., Guven, Y., Kantaputra, W., Balci, M.C., Tanpaiboon, P., Tananuvat, N., Uttarilli, A., Dalal, A. (2014). Clinical manifestations of 17 patients affected with mucopolysaccharidosis type VI and eight novel ARSB mutations. American Journal of Medical Genetics A. 164A(6), 1443-1453. [PubMed]

Kantaputra, P.N., Kayserili, H., Güven, Y., Kantaputra, W., Balci, M.C., Tanpaiboon, P., Tananuvat, N., Uttarilli, A., Dalal, A. (2014). Oral manifestations of 17 patients affected with mucopolysaccharidosis type VI. Journal of Inherited Metabolic Disease. 37(2), 263-268. [PubMed]

Aggarwal, S., Uttarilli, A., Dalal, A.B. (2013). GAPO syndrome with deafness: new feature or incidental finding?. Clinical Dysmorphology. 161-163. [PubMed]

 

Research Support

 

Title of Project

Funding Agency

 

Role
1

Genetics of syndromic and non-syndromic conotruncal heart defects in pediatric patients

Department of Biotechnology, Government of India

 

PI
1

Generation of induced pluripotent stem cell (iPSC) models of conotruncal heart defects (CTDs) to investigate the disease-relevant molecular mechanisms using advanced proteomics and metabolomics approaches

Science and Engineering Research Board (SERB), India

 

PI