Department of Genetic Centre
Started in 2006
Rearch Publication in the Last One Year
| Sr No. | Research Publication - National/International |
|---|---|
| 1. | Sharma N, Singh M, Kaur G, Thapa BR, Prasad R. Identification and characterization of CFTR gene mutations in Indian CF patients. Annals of Human Genetics, 2008(in press). |
| 2. | Sharma N, Singh M., Acharya N, Singh SK, Thapa BR, Kaur G, Prasad R. Implication of cystic fibrosis transmembrane conductance regulator gene in infertile family members of Indian CF patients. Biochemical Genetics; 46(11-12):847-856, 2008. |
| 3. | Gurjit Kaur, Soumya Mishra, Alka Sehgal, Rajendra Prasad, Alterations in lipid peroxidation and antioxidant status in pregnancy with preeclampsia. Mol Cell Biochem; 313:37-44, 2008. |
| 4. | Kaur G, Singh Chavan B, Gupta D, Sinhmar V, Prasad R, Tripathi A, Garg PD, Gupta R, Khurana H, Gautam S, Margoob MA, Aneja J, An association study of dopaminergic (DRD2) and serotoninergic (5-HT2) gene polymorphism and schizophrenia in a North Indian population, Asian Journal of Psychiatry (2018). |
| 5. | Chavan BS, Kaur G , Gupta D , Aneja J.A Prospective Study to Evaluate the Effect of CYP2D6 Polymorphism on Plasma level of Risperidone and its Metabolite in North Indian Patients with Schizophrenia. Indian J Psycho Med(2018) 40: 335-342. |
| 6. | Kaur G, Gupta D, Chavan BS, Sinhmar V, Prasad R, Tripathi A, Garg PD, Gupta R, Khurana H, Gautam S, Margoob MA, Aneja J. Identification of genetic correlates of response to Risperidone: Findings of a multicentric schizophrenia study from India. Asian J Psychiatr (2017) 29: 174-182. |
| 7. | Sahni S, Chavan BS, Sidana A, Kalra P, Kaur G. Comparative study of clozapine versus risperidone in treatment-naïve first episode schizophrenia: A pilot study. Indian J Med Res (2016) 144: 697-703. |
| 8. | Kaur G, Thakur K, Kataria S, Singh TR, Chavan BS, et al. Current and future perspective of Newborn screening: an Indian scenario. J Pediatr Endocrinol Metab (2016) 29(1):5-13. |
| 9. | Anand D, Kaur G, Sehgal A, Rani S, Mathur M. Role of Vitamin D and calcium supplementation in pregnancy alone or in combination. IJRDPL; (2015). 4(1); 1341-1343. |
| 10. | Geetha TS., Michealraj KA, Kabra M, KaurG, Juyal RC, Thelma BK. Targeted Deep Resequencing IdentifiesMID2 Mutation for X-Linked Intellectual Disability with Varied Disease Severity in Large Kindred from India. Human Mutation (IF: 5.686) (2014) 35 (1):41–44. |
| 11. | Chawla D, Jain S, Kaur G, Sinhmar V, Guglani V. Accuracy of transcutaneous bilirubin measurement in preterm low-birth-weight neonates. European Journal of Pediatrics (2014) 173( 2): 173-179 |
| 12. | Kaur G, Srivastav S, Sharma S, Huria A, Goel P, et al. Maternal Serum Median Levels of Alpha-Fetoprotein, Human Chorionic Gonadotropin and Unconjugated Estriol in Second Trimester from North-West Indian Pregnant Women. Indian J Med Res. (2013) 138(1):83-88. |
| 13. | Kaur G, Srivastav J, Kaur A, Huria A, Goel P, et al. Maternal serum second trimester screening for chromosomal disorders and neural tube defects in a government hospital of North India. Prenat Diagn. (2012) 11:1-5. |
| 14. | Singh R, Thapa BR, Kaur G, Prasad R. Biochemical and molecular characterization of GALT gene from Indian galactosemia patients: Identification of 10 novel mutations and their structural and functional implications. Clin Chim Acta. 2012 Sep 25;414C:191-196. |
| 15. | Singh R, Thapa BR, Kaur G, Prasad R. Frequency Distribution of Q188R, N314D, Duarte 1, and Duarte 2 GALT Variant Alleles in an Indian Galactosemia Population. Biochem Genet. 2012 Jul 15. |
| 16. | Singh R, Ram J, Kaur G, Prasad R. Galactokinase Deficiency Induced Cataracts in Indian Infants: Identification of 4 novel Mutations in GALK Gene. Curr Eye Res. 2012 May 25. |
| 17. | Kaur G, Srivastav J, Jain S, Chawla D, Chavan B.S, et al. Preliminary Report on Neonatal Screening for Congenital Hypothyroidism, Congenital adrenal hyperplasia and Glucose-6-Phosphate Dehydrogenase deficiency: A Chandigarh Experience. Indian J Pediatr (2010) 77:969–973. |