bioRxiv/medRxiv TRiP Review Activity

204 Reviews — eLife — Genetics

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A simple and effective F0 knockout method for rapid screening of behaviour and other complex phenotypes
Kroll, F., Powell, G. T., Ghosh, M., Antinucci, P., Hearn, T. J., Tunbak, H., Lim, S., Dennis, H. W., Fernandez, J. M., Hoffman, E. J., Whitmore, D., Dreosti, E., Wilson, S. W., Rihel, J.
10.1101/2020.06.04.133462 — Posted: 2020-06-05 — Discussion: 2020-09-11  eLife
Selective constraints and pathogenicity of mitochondrial DNA variants inferred from a novel database of 196,554 unrelated individuals
Bolze, A., Mendez, F., White, S., Tanudjaja, F., Isaksson, M., Rashkin, M., Bowes, J., Cirulli, E. T., Metcalf, W. J., Grzymski, J. J., Lee, W., Lu, J., Washington, N. L.
10.1101/798264 — Posted: 2019-10-08 — Discussion: 2020-09-01  eLife
Interpreting the pathogenicity of Joubert Syndrome missense variants in Caenorhabditis elegans
Lange, K. I., Tsiropoulou, S., Kucharska, K., Blacque, O. E.
10.1101/2020.05.22.110668 — Posted: 2020-05-22 — Discussion: 2020-07-31  eLife
A missense in HSF2BP causing Primary Ovarian Insufficiency affects meiotic recombination by its novel interactor C19ORF57/MIDAP
Felipe-Medina, N., Caburet, S., Sanchez-Saez, F., Codezo, Y. B., de Rooij, D. G., Gomez-H, L., Garcia-Valiente, R., Todeschini, A. L., Duque, P., Shalev, S., Sanchez-Martin, M. A., Llano, E., Veitia, R., Pendas, A. M.
10.1101/2020.03.05.978007 — Posted: 2020-03-05 — Discussion: 2020-05-06  eLife

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