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발행년	- (예 : 2010-2015)

Mapping the NPHP-JBTS-MKS protein network reveals ciliopathy disease genes and pathways

Academic Journal

Sang, L.; Brauer, M.J.; Wen, X.; Scales, S.J.; Kwong, M.; Huntzicker, E.G.; Sfakianos, M.K.; Sandoval, W.; Bazan, J.F.; Kulkarni, P.; Jackson, P.K.; Miller, J.J.; Corbit, K.C.; Garcia-Gonzalo, F.R.; Seol, A.D.; Reiter, J.F.; Giles, R.H.; Otto, E.A.; O'Toole, J.F.; Held, S.; Hildebrandt, F.; Baye, L.M.; Slusarski, D.C.; Sheffield, V.C.; Reutter, H.M.; Lane, W.S.; Rafiq, M.A.; Noor, A.; Vincent, J.B.; Ansar, M.; Devi, A.R.R.; Doherty, D.A.

In: Cell. (Cell, 13 May 2011, 145(4):513-528)

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Hyperhomocysteinemia and the compound heterozygous state for methylene tetrahydrofolate reductase are independent risk factors for deep vein thrombosis among South Indians

Academic Journal

Naushad, S.M.; Jamal, M.N.J.; Angalena, R.; Prasad, C.K.; Devi, A.R.R.

In: Blood Coagulation and Fibrinolysis. (Blood Coagulation and Fibrinolysis, March 2007, 18(2):113-117)

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Farber lipogranulomatosis: Clinical and molecular genetic analysis reveals a novel mutation in an Indian family

Academic Journal

Devi, A.R.R.; Ratheesh, R.; Savithri, G.; Bashyam, M.; Gopikrishna, M.; Swarnalata, G.

In: Journal of Human Genetics. (Journal of Human Genetics, September 2006, 51(9):811-814)

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Molecular genetic analyses of β-thalassemia in South India reveals rare mutations in the β-globin gene

Academic Journal

Bashyam, M.D.; Gopikrishna, M.; Sangal, V.; Bashyam, L.; Devi, A.R.R.; Savithri, G.R.

In: Journal of Human Genetics. (Journal of Human Genetics, 2004, 49(8):408-413)

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Amplification of phenylalanine hydroxylase and cystathionine β-synthase transcripts in human peripheral lymphocytes by RT-PCR

Academic Journal

Devi, K.S.; Kondaiah, P.; Devi, A.R.R.

In: Biochemistry and Molecular Biology International. (Biochemistry and Molecular Biology International, July 1998, 45(4):643-650)

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Neonatal screening for amino acidaemias in Karnataka, South India

Academic Journal

Rao, N.A.; Devi, A.R.R.; Savithri, H.S.; Rao, S.V.; Bittles, A.H.

In: Clinical Genetics. (Clinical Genetics, July 1988, 34(1):60-63)

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Inbreeding and the incidence of childhood genetic disorders in Karnataka, South India

Academic Journal

Devi, A.R.R.; Rao, N.A.; Bittles, A.H.

In: Journal of Medical Genetics. (Journal of Medical Genetics, 1987, 24(6):362-365)

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Inbreeding and post-natal mortality in South India: Effects on the gene pool

Academic Journal

Buttles, A.H.; Devi, A.R.R.; Savithri, H.S.; Sridhar, R.; Rao, N.A.

In: Journal of Genetics. (Journal of Genetics, December 1985, 64(2-3):135-142)

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Corrigendum to: Spectrum of Mutations in the SMPD1 Gene in Asian Indian Patients with Acid Sphingomyelinase Deficient Niemann–Pick Disease (Am J Med Genet A., (2016), 170A, 10, 2719-2730, 10.1002/ajmg.a.37817)

Academic Journal

Ranganath, P.; Matta, D.; Bhavani, G.S.; Wangnekar, S.; Jain, J.M.N.; Verma, I.C.; Kabra, M.; Puri, R.D.; Danda, S.; Gupta, N.; Girisha, K.M.; Sankar, V.H.; Patil, S.J.; Devi, A.R.R.; Bhat, M.; Gowrishankar, K.; Mandal, K.; Aggarwal, S.; Tamhankar, P.M.; Tilak, P.; Phadke, S.R.; Dalal, A.

In: American Journal of Medical Genetics, Part A. (American Journal of Medical Genetics, Part A, 1 March 2017, 173(3):829)

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