Channel: Columbia University

This collection includes bioRxiv and medRxiv papers from authors at Columbia University.

5155 Articles

Loss-of-function in IRF2BPL is associated with neurological phenotypes

Marcogliese, P. C., Shashi, V., Spillmann, R. C., Stong, N., Rosenfeld, J. A., Koenig, M. K., Martinez-Agosto, J. A., Herzog, M., Chen, A. H., Dickson, P. I., Lin, H. J., Vera, M. U., Salamon, N., Ortiz, D., Infante, E., Steyaert, W., Dermaut, B., Poppe, B., Chung, H.-L., Zuo, Z., Lee, P.-T., Kanca, O., Xia, F., Yang, Y., Smith, E. C., Jasien, J., Kansagra, S., Spiridigliozzi, G., El-Dairi, M., Lark, R., Riley, K., Koeberl, D. D., Golden-Grant, K., Program for Undiagnosed Diseases (UD-PrOZA), , Undiagnosed Diseases Network, , Yamamoto, S., Wangler, M. F., Mirzaa, G., Hemelsoet, D., Lee, B.

10.1101/322495 — Posted: 2018-05-30

Enrichment of rare protein truncating variants in amyotrophic lateral sclerosis patients

Farhan, S. M. K., Howrigan, D. P., Abbott, L., Byrnes, A., Churchhouse, C., Phatnani, H., Smith, B., Topp, S., Rampersaud, E., Wu, G., Wuu, J., Gubitz, A., Kilm, J., Mordes, D., Ghosh, S., CReATe Consortium, , FALS Consortium, , ALSGENS Consortium, , Eggan, K., Rademakers, R., McCauley, J., Schule, R., Zuchner, S., Benatar, M., Taylor, J. P., Nalls, M., Traynor, B., Shaw, C., Goldstein, D., Harms, M., Daly, M., Neale, B.

10.1101/307835 — Posted: 2018-05-29

Neural Networks for Efficient Bayesian Decoding of Natural Images from Retinal Neurons

Parthasarathy, N., Batty, E., Falcon, W., Rutten, T., Rajpal, M., Chichilnisky, E. J., Paninski, L.

10.1101/153759 — Posted: 2018-05-28

D-amino acid-mediated translation arrest is modulated by the identity of the incoming aminoacyl-tRNA

Fleisher, R. C., Cornish, V. W., Gonzalez, R. L.

10.1101/323295 — Posted: 2018-05-27

Epigenetic selection and the DNA methylation signatures of adverse prenatal environments

Tobi, E., van den Heuvel, J., Zwaan, B., Lumey, L. H., Heijmans, B. T., Uller, T.

10.1101/321711 — Posted: 2018-05-25

Genetic determinants of risk and survival in pulmonary arterial hypertension

Rhodes, C., Batai, K., Bleda, M., Haimel, M., Southgate, L., Germain, M., Pauciulo, M., Hadinnapola, C., Girerd, B., Arora, A., Knight, J., Hanscombe, K., Karnes, J., Kaakinen, M., Gall, H., Ulrich, A., Harbaum, L., Aman, J., Cebola, I., Ferrer, J., NIHR BioResource Rare Diseases Consortium, , UK PAH Cohort Study Consortium, , US PAH Biobank Consortium, , Ahmad, F., Amouyel, P., Archer, S., Argula, R., Austin, E., Badesch, D., Bakshi, S., Barnett, C., Benza, R., Bhatt, N., Bogaard, H., Burger, C., Chakinala, M., Church, C., Coghlan, J., Condliffe, R., Corris, P., Danesino, C., Debette, S.

10.1101/317164 — Posted: 2018-05-21

Common Neural Code for Reward and Information Value

Kobayashi, K., Hsu, M.

10.1101/324665 — Posted: 2018-05-17

Quality Control and Integration of Genotypes from Two Calling Pipelines for Whole Genome Sequence Data in the Alzheimer’s Disease Sequencing Project

Naj, A. C., Lin, H., Vardarajan, B. N., White, S., Lancour, D., Ma, Y., Schmidt, M., Sun, F., Butkiewicz, M., Bush, W. S., Kunkle, B. W., Malamon, J., Amin, N., Choi, S. H., Hamilton-Nelson, K. L., van der Lee, S. J., Gupta, N., Koboldt, D. C., Saad, M., Wang, B., Nato, A. Q., Sohi, H. K., Kuzma, A., Alzheimer's Disease Sequencing Project (ADSP), , Wang, L.-S., Cupples, L. A., van Duijn, C., Seshadri, S., Schellenberg, G. D., Boerwinkle, E., Bis, J. C., Dupuis, J., Salerno, W. J., Wijsman, E. M., Martin, E., DeStefano, A. L.

10.1101/318857 — Posted: 2018-05-11

Neuronal morphologies built for reliable physiology in a rhythmic motor circuit

Otopalik, A. G., Marder, E.

10.1101/319582 — Posted: 2018-05-11

Widespread Alterations in Translation Elongation in the Brain of Juvenile Fmr1 Knock-Out Mice

Das Sharma, S., Metz, J. B., Li, H., Hobson, B. D., Hornstein, N., Sulzer, D., Tang, G., Sims, P. A.

10.1101/319368 — Posted: 2018-05-10

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