Educational Utility of Social Media for Laparoscopic Surgery in India: A Cross-Sectional Survey of Popular Indian Communities on Facebook [Response to Letter] by Rajan D, Pillai VG, Varghese P

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STUDY OF LONG-TERM TREND IN RIVER DISCHARGE OF SUTLEJ RIVER (N-W HIMALAYAN REGION) by Dharmaveer Singh, Rajan D. Gupta, Sanjay K. Jain

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Melioidosis in India. by Kang, G, Rajan, D, Ramakrishna, B, Aucken, H, Dance, D

Bicarbonate boosts flash response amplitude to augment absolute sensitivity and extend dynamic range in murine retinal rods by Rajan D. Adhikari, Amanda M. Kossoff, M. Carter Cornwall, Clint L. Makino

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aCGH.Spline--an R package for aCGH dye bias normalization. by Fitzgerald, T, Larcombe, L, Le Scouarnec, S, Clayton, S, Rajan, D, Carter, N, Redon, R

Reverse-ChIP Techniques for Identifying Locus-Specific Proteomes: A Key Tool in Unlocking the Cancer Regulome by Tim M. G. MacKenzie, Rocío Cisneros, Rajan D. Maynard, Michael P. Snyder

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MPI-enabled Shape Optimization of Panels Subjected to Air Blast Loading by Argod V., Belegundu A. D., Aziz A., Agrawala V., Jain R., Rajan D.

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Phenotypic characteristics of peripheral immune cells of Myalgic encephalomyelitis/chronic fatigue syndrome via transmission electron microscopy: A pilot study. by Fereshteh Jahanbani, Rajan D Maynard, Justin Cyril Sing, Shaghayegh Jahanbani, John J Perrino, Damek V Spacek, Ronald W Davis, Michael P Snyder

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Making new genetic diagnoses with old data: iterative reanalysis and reporting from genome-wide data in 1,133 families with developmental disorders by Wright, C, McRae, J, Clayton, S, Gallone, G, Aitken, S, FitzGerald, T, Jones, P, Prigmore, E, Rajan, D, Lord, J, Sifrim, A, Kelsell, R, Parker, M, Barrett, J, Hurles, M, FitzPatrick, R, Firth, H, on behalf of the DDD Study

Genetic diagnosis of developmental disorders in the DDD study: a scalable analysis of genome-wide research data. by Wright, C, Fitzgerald, T, Jones, W, Clayton, S, McRae, J, van Kogelenberg, M, King, D, Ambridge, K, Barrett, D, Bayzetinova, T, Bevan, A, Bragin, E, Chatzimichali, E, Gribble, S, Jones, P, Krishnappa, N, Mason, L, Miller, R, Morley, K, Parthiban, V, Prigmore, E, Rajan, D, Sifrim, A, Swaminathan, G, Tivey, A

Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing. by Sifrim, A, Hitz, M, Wilsdon, A, Breckpot, J, Al Turki, S, Thienpont, B, McRae, J, Fitzgerald, T, Singh, T, Swaminathan, G, Prigmore, E, Rajan, D, Abdul-Khaliq, H, Banka, S, Bauer, U, Bentham, J, Berger, F, Bhattacharya, S, Bu'Lock, F, Canham, N, Colgiu, I, Cosgrove, C, Cox, H, Daehnert, I, Daly, A, Danesh, J, Fryer, A, Gewillig, M, Hobson, E, Hoff, K, Homfray, T, Kahlert, A, Ketley, A, Kramer, H, Lachlan, K, Lampe, A, Louw, J, Manickara, A, Manase, D, McCarthy, K, Metcalfe, K, Moore, C, Newbury-Ecob, R, Omer, S, Ouwehand, W, Park, S, Parker, M, Pickardt, T, Pollard, M, Robert, L, Roberts, D, Sambrook, J, Setchfield, K, Stiller, B, Thornborough, C, Toka, O, Watkins, H, Williams, D, Wright, M, Mital, S, Daubeney, P, Keavney, B, Goodship, J, Abu-Sulaiman, R, Klaassen, S, Wright, C, Firth, H, Barrett, J, Devriendt, K, FitzPatrick, D, Brook, J, Hurles, M