Revisiting mutagenesis at non-B DNA motifs in the human genome von McGinty, R. J., Sunyaev, S. R.

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Guidelines for investigating causality of sequence variants in human disease von MacArthur, D. G., Manolio, T. A., Dimmock, D. P., Rehm, H. L., Shendure, J., Abecasis, G. R., Adams, D. R., Altman, R. B., Antonarakis, S. E., Ashley, E. A., Barrett, J. C., Biesecker, L. G., Conrad, D. F., Cooper, G. M., Cox, N. J., Daly, M. J., Gerstein, M. B., Goldstein, D. B., Hirschhorn, J. N., Leal, S. M., Pennacchio, L. A., Stamatoyannopoulos, J. A., Sunyaev, S. R., Valle, D., Voight, B. F., Winckler, W., Gunter, C.

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Inferring causality and functional significance of human coding DNA variants von SUNYAEV, Shamil R

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Prediction of deleterious human alleles von Sunyaev, S, Ramensky, V, Koch, I, Lathe, 3rd, W, Kondrashov, A S, Bork, P

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Charting the Proteomes of Organisms with Unsequenced Genomes by MALDI-Quadrupole Time-of-Flight Mass Spectrometry and BLAST Homology Searching von Shevchenko, Andrej, Sunyaev, Shamil, Loboda, Alexander, Shevchenko, Anna, Bork, Peer, Ens, Werner, Standing, Kenneth G

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AnFiSA: An open-source computational platform for the analysis of sequencing data for rare genetic disease von Bouzinier, M.A., Etin, D., Trifonov, S.I., Evdokimova, V.N., Ulitin, V., Shen, J., Kokorev, A., Ghazani, A.A., Chekaluk, Y., Albertyn, Z., Giersch, A., Morton, C.C., Abraamyan, F., Bendapudi, P.K., Sunyaev, S., Undiagnosed Diseases Network, Brigham Genomic Medicine, SEQuencing a Baby for an Optimal Outcome, Quantori, Krier, J.B.

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Large scale variation in the rate of germ-line de novo mutation, base composition, divergence and diversity in humans von Smith, Thomas C A, Arndt, Peter F, Eyre-Walker, Adam

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Sequencing studies in human genetics: design and interpretation von Goldstein, David B., Allen, Andrew, Keebler, Jonathan, Margulies, Elliott H., Petrou, Steven, Petrovski, Slavé, Sunyaev, Shamil

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Gain-of-function mutations in the mechanically activated ion channel PIEZO2 cause a subtype of Distal Arthrogryposis von Coste, Bertrand, Houge, Gunnar, Murray, Michael F., Stitziel, Nathan, Bandell, Michael, Giovanni, Monica A., Philippakis, Anthony, Hoischen, Alexander, Riemer, Gunnar, Steen, Unni, Steen, Vidar Martin, Mathur, Jayanti, Cox, James, Lebo, Matthew, Rehm, Heidi, Weiss, Scott T., Wood, John N., Maas, Richard L., Sunyaev, Shamil R., Patapoutian, Ardem

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Computational analysis of human genome polymorphism von Ramensky, V. E, Sunyaev, S. R

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Impact of selection, mutation rate and genetic drift on human genetic variation von Sunyaev, Shamil, Kondrashov, Fyodor A., Bork, Peer, Ramensky, Vasily

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Extremely Rare Polymorphisms in Saccharomyces cerevisiae Allow Inference of the Mutational Spectrum von Zhu, Yuan O, Sherlock, Gavin, Petrov, Dmitri A

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Extremely low-coverage sequencing and imputation increases power for genome-wide association studies von Pasaniuc, Bogdan, Rohland, Nadin, McLaren, Paul J, Garimella, Kiran, Zaitlen, Noah, Li, Heng, Gupta, Namrata, Neale, Benjamin M, Daly, Mark J, Sklar, Pamela, Sullivan, Patrick F, Bergen, Sarah, Moran, Jennifer L, Hultman, Christina M, Lichtenstein, Paul, Magnusson, Patrik, Purcell, Shaun M, Haas, David W, Liang, Liming, Sunyaev, Shamil, Patterson, Nick, de Bakker, Paul I W, Reich, David, Price, Alkes L

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Polygenic adaptation on height is overestimated due to uncorrected stratification in genome-wide association studies von Sohail, Mashaal, Maier, Robert M, Ganna, Andrea, Bloemendal, Alex, Martin, Alicia R, Turchin, Michael C, Chiang, Charleston Wk, Hirschhorn, Joel, Daly, Mark J, Patterson, Nick, Neale, Benjamin, Mathieson, Iain, Reich, David, Sunyaev, Shamil R

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Towards a structural basis of human non-synonymous single nucleotide polymorphisms von Sunyaev, S, Ramensky, V, Bork, P

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SNP frequencies in human genes: an excess of rare alleles and differing modes of selection von Sunyaev, Shamil R., Lathe III, Warren C., Ramensky, Vasily E., Bork, Peer

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A universal trend of amino acid gain and loss in protein evolution von Kondrashov, Alexey S, Sunyaev, Shamil, Jordan, I. King, Kondrashov, Fyodor A, Adzhubei, Ivan A, Wolf, Yuri I, Koonin, Eugene V

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Human non‐synonymous SNPs: server and survey von Ramensky, Vasily, Bork, Peer, Sunyaev, Shamil

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Protein evolution Causes of trends in amino-acid gain and loss (Reply) von Jordan, I. K, Koonin, E. V, Sunyaev, S, Kondrashov, A. S, Kondrashov, F. A, Adzhubei, I. A, Wolf, Y. I

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Dobzhansky-Muller Incompatibilities in Protein Evolution von Kondrashov, Alexey S., Sunyaev, Shamil, Kondrashov, Fyodor A.

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