PUBLICATIONS
Naushad S M, Jamal NJ, Angalena R, Prasad CK, Devi AR. Hyperhomocysteinemia and the compound heterozygous state for methylene tetrahydrofolate reductase are independent risk factors for deep vein thrombosis among South Indians. Blood Coagul Fibrinolysis. 2007 Mar;18(2):113-7
Naushad SM, Jamal MNJ, Angalena R, Krishna Prasad C, Radha Rama Devi A. Hyperhomocysteinemia and compound heterozygous status for MTHFR are independent risk factors for Deep vein thrombosis among South Indian subjects. Blood Coagulation and Fibrinolysis 2006 (In Press).
NBSdb: New Born Screening Database (2004) Buddhaditta Bose, Gyan Rajkumar, M. Narendar Pavan, A RadhaRama Devi, H.A. Nagarajaram Indian Journal of Medical Informatics online.
Prevalence and distribution of high-risk human papilloma virus (HPV) types in invasive squamous cell carcinoma of the cervix and in normal women in Andhra Pradesh, India: Pavani Sowjanya, Meenkashi Jain , Usha Rani Poli, S Padma, Manik Das, Keerti V Shah , BN Rao, Radha Rama Devi, Patti E Gravitt ,and Gayatri Ramakrishna, BMC Infectious Diseases 2005, 5:116 doi:10.1186/1471-2334-5-116. Highly accessed, Online
A RadhaRama Devi, M Gopikrishna, R Ratheesh, G Savithri, G Swarnalata and MD Bashyam. (2006). Farber lipogranulomatosis-clinical and molecular genetic analysis reveals a novel mutation In an Indian family. J Hum Genet. (In press).
Radha Rama Devi A, Naushad SM, Prasad KC. Evaluation of total plasma homocysteine in Indian newborns using heel-prick samples. Indian J Pediatr. 2006 Jun;73(6):503-8.
Murali Dharan Bashyam, Leena Bashyam, Gorinabele R Savithri, Munimanda Gopikrishna, Vartul Sangal, Akela Radha Rama Devi. (2004) Molecular genetic analyses of b-thalassemia in South India reveals rare mutations in the b-globin gene. Journal of Human Genetics, 49:408-413.
A.Radha Rama Devi, V. Govindiah, G. Ramakrishna and S.M. Naushad. "Prevalence of Methylene tetrahydrofolate reductase polymorphism in South Indian population." Current Science 86(3) 440-443.
A. Radha Rama Devi and S.M. Naushad. 2004, "Newborn screening in India". The Indian Journal of Pediatrics 71(2). 157-160.
Prabhakara K, Wyandt HE, Huang XL, Prasad KS, Ramadevi AR (2004) Recurrent proximal 18p monosomy and 18q trisomy in a family with a maternal pericentric inversion of chromosome 18.# Ann Genet 47: 297-303.
Prabhakara K, Angelena M, Ramadevi AR (2004) Familial (9;11)(p22;p15.3)pat translocation and XX sex reversal in a phenotypic boy with cryptorchidism and delayed development. Genetic Counseling 51(4), 355-357.
Prabhakara K, Ramadevi AR (2004) Premature centromere division versus C-anaphases in cultures: Need for consensus and guidelines. American Journal of Medical Genetics 124(3):331.
Kumar KS, Govindaiah V, Naushad SE, Devi RR, Jyothy A. 2003. Plasma homocysteine levels correlated to interactions between folate states and methylene tretrahydrofolate reductase gene mutation in women with unexplained pregnancy loss. Journal of Obstetrics and Gynaecology 23: 55-58.
Mandal AK, Prabhakara K, Raddy ABM, Ramadevi AR, Panicker SG .2003. Congenital glaucoma associated with 22p+ variant in a dysmorphic child. Indian Journal of Ophthalomology 51(4), 355-357.
Prabhakara K, Dutta U, Ramadevi AR 2002. Partial 15q22 trisomy due to segregation of maternal 10;15 reciprocal translocation. Indian Pediatrics 39 : 1050-1054.
Ramadevi AR, Prabhakara K, Dutta U. 2002. Familial (11;21)pat balanced translocation in a female child with regression of mile stones. Ann Genet 45:13-15.
Ramadevi AR, Naik U, Dutta U, Srikanth, Prabhakara K. 2002. De novo pericentric inversion of chromosome 4, inv(4p16q12), in boy with piebaldism and mental retardation. Am J Med Genet 113:190-192.
Prabhakara K, Padman P, Dutta U, Angeleena M, Sekher K, Radha Ramadevi A. 2002. Meiotic impairment in an oligozoosperic male with translocation t(5;13). In the Proceedings of National Conference of Expanding Horizons of Human Genetics Eds: Bhasin MK, Kalla AK, pp55-60.
Devi KS, Ramadevi AR, Kondaiah P (1998) Amplification of phenylalanine hydroxylase and cystathionine beta-synthase transcripts in human peripheral lymphocytes by RT-PCR. Biochem Mol Biol Int 45: 643-50.
Bhaskaran S, Naseerullah MK, Manjunatha KR, Chetan GK, Arati R, Rao GV, Girimaji SR, Srinath S, Sheshadri S, Ramadevi AR (1998) Triplet repeat polymorphism & fragile X syndrome in the Indian context. Ind J Med Res 107: 29-36.
Savithri HS, Ramadevi AR, Bittles AH, Rao NA (1994) An unusual distribution of glucose-6-phosphate dehydrogenase deficiency of South Indian newborn population. Ind J Biochem Biophy 31: 358-360.
Ramachandra L, Ramadevi AR, Rao MRS ( 1993 ) An 18 mer sequence in a rat 1.3kbp EcoR1 detects genetic polymorphism in humans. Current Sci 65: 569-571.
Bittles AH, Ramadevi AR, Rao NA (1988) Consanguinity, twinning and secondary sex ratio in the population of Karnataka. Ann Hum Biol 15:455-460.
Ramadevi AR, Rao NA (1988) Neonatal screening for amnioacidemias in Karantaka, South India. Clin Genet 34: 60-63.
Ramadevi AR, Rao NA, Bittles AH (1987) Consanguinity and the incidence of childhood genetic diseases in Karnataka. J Med Gen 24, 362-365.
Rao NA, Ramadevi AR, Savithri HS, Rao SV, Bittles AH (1987) Newborn screening for amnioacidemias in Karanataka, South India. Proc 4th Intl Cong Inborn Errors of Metabolism.Sendai, Japan.
Bittles AH, Ramadevi AR, Sridhar R, Rao NA (1985) Inbreeding and postnatal mortality in South India. J Genet 64: 135-142.
Bittles AH, Ramadevi AR, Rao NA (1985) Consguinity and postnatal mortality in Karnataka. Proc 5th Cong Eur Anthropol Assoc, 30.
Bittles AH, Ramadevi AR, Rao VS, Rao NA (1983) A newborn screening program for the detection of amnioacid disorders in South India. Biochem Rev 52: 24.
Bittles AH, Ramadevi AR, Rao NA (1983) The study of inborn errors of metabolism in human populations. Proc. 15th Intl Cong Gen Ple &Symp Seas, 65.
Ramadevi AR, Rao NA, Bittles AH (1982) Inbreeding in the state of Karanataka, South India. Hum Hered, 32, 8-10.
Ramadevi AR, Rao NA, Bittles AH (1981) Consanguinity fecundity and postnatal mortality in Karantaka. Ann Hum Biol: 8: 469-472.
Ramadevi AR (1970) A case of Juvenile amytropic lateral sclerosis.Indian Pediatrics.
Ramadevi AR (1969) A case of cystecercosis in humans. Mediscope.
CHAPTERS IN BOOKS
A.Radha Rama Devi, 2004,Environment and Fetal Effects, in Health and Environment,Published by Osmania University,Hyderabad.
A.Radha Rama Devi, 2004, Clinical Application of Cytogenetics ,Trends in Cytology and Genetics,Published by Osmania University.
Ramadevi AR. 2003. Newborn Screening For Inborn Errors Of Metabolism Trends In Clinical Biochemistry And Laboratory Medicine. Publication of Association of Clinical Biochemists of India
Prabhakara K, Ramadevi AR. 2001. Cytogenetics of male infertility. In: The Infertility Manual. Eds: Rao KA, Brinsden P, Federation Indian Societies of Obstetrics & Gynaecology (FOGSI), pp134-143.
Rao NA, Savithri HS, Ramadevi AR, Bittles AH (1998) Consanguinity - A common heritage? The effects on the health and well being of Indian population. In: Consanguinity in Indian heritage. Edited by: Balasubrarmaniam D, Rao NA. University Press, Hyderabad.
Ramadevi AR (1998) Prenatal diagnosis of inborn errors of metabolism. In: Hand Book of Prenatal Diagnosis & Reproductive Genetics. Edited by: Rao KA, Federation of Obstetrics & Gynaecological Societies of India (FOGSI).
Ramadevi AR (1997) Management of inborn errors of metabolism. In: Genetics and Foetal Medicine. Edited by: Rao KA, Federation of Obstetrics & Gynaecolgical Societies of India (FOGSI).
Bittles AH, Ramadevi AR, Sridhar R, Rao NA (1986) Inbreeding and incidence of recessive disorders in the population of Karnataka, South India. In: Genetic Variation and its Maintenance, Edited by: Roberts DF, Stefano GF. Cambridge University Press, New York, 221-228.
Ramadevi AR, Rao NA, Bittles AH (1983) Newborn screening for aminoacidopathies in South India. In: Neonatal Screening. Edited by: Naurse H, Irie M. Expcerpta Medica, Amsterdam, 493-495.
INVITED ARTICLES
NBSdb: New Born Screening Database (2004) Buddhaditta Bose, Gyan Rajkumar, M. Narendar Pavan, A RadhaRama Devi, H.A. Nagarajaram Indian Journal of Medical Informatics online.