Polarizable atomic multipole X-ray refinement: weighting schemes for macromolecular diffraction von Fenn, T. D., Schnieders, M. J.

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The Use of Variant Maps to Explore Domain-Specific Mutations of FGFR1 von Lansdon, L.A., Bernabe, H.V., Nidey, N., Standley, J., Schnieders, M.J., Murray, J.C.

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A smooth and differentiable bulk-solvent model for macromolecular diffraction von Fenn, T. D., Schnieders, M. J., Brunger, A. T.

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A novel mutation (LEU396ARG) in OPA1 is associated with a severe phenotype in a large dominant optic atrophy pedigree von Schnieders, M J, Goar, W, Griess, M, Roos, B R, Scheetz, T E, Stone, E M, Fingert, J H

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Assessing the accuracy of a prototype drill guide for fibular graft placement in femoral head necrosis von Schnieders, M J, Dave, S B, Morrow, D E, Heiner, A D, Pedersen, D R, Brown, T D

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Genomic Landscape and Mutational Signatures of Deafness-Associated Genes von Azaiez, Hela, Booth, Kevin T., Ephraim, Sean S., Crone, Bradley, Black-Ziegelbein, Elizabeth A., Marini, Robert J., Shearer, A. Eliot, Sloan-Heggen, Christina M., Kolbe, Diana, Casavant, Thomas, Schnieders, Michael J., Nishimura, Carla, Braun, Terry, Smith, Richard J.H.

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Force Field X: A computational microscope to study genetic variation and organic crystals using theory and experiment von Gogal, Rose A., Nessler, Aaron J., Thiel, Andrew C., Bernabe, Hernan V., Corrigan Grove, Rae A., Cousineau, Leah M., Litman, Jacob M., Miller, Jacob M., Qi, Guowei, Speranza, Matthew J., Tollefson, Mallory R., Fenn, Timothy D., Michaelson, Jacob J., Okada, Okimasa, Piquemal, Jean-Philip, Ponder, Jay W., Shen, Jana, Smith, Richard J. H., Yang, Wei, Ren, Pengyu, Schnieders, Michael J.

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Assessing variants of uncertain significance implicated in hearing loss using a comprehensive deafness proteome von Tollefson, Mallory R., Gogal, Rose A., Weaver, A. Monique, Schaefer, Amanda M., Marini, Robert J., Azaiez, Hela, Kolbe, Diana L., Wang, Donghong, Weaver, Amy E., Casavant, Thomas L., Braun, Terry A., Smith, Richard J. H., Schnieders, Michael J.

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METTL23 Variants and Patients With Normal-Tension Glaucoma von Scheetz, Todd. E, Tollefson, Mallory R, Roos, Ben R, Boese, Erin A, Pouw, Andrew E, Stone, Edwin M, Schnieders, Michael J, Fingert, John H

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GJA3 Genetic Variation and Autosomal Dominant Congenital Cataracts and Glaucoma Following Cataract Surgery von Boese, Erin A, Drack, Arlene V, Roos, Benjamin R, Alward, Wallace L. M, Tollefson, Mallory R, Schnieders, Michael J, Scheetz, Todd E, Boldt, H. Culver, Stone, Edwin M, Fingert, John H

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PDZD7 and hearing loss: More than just a modifier von Booth, Kevin T., Azaiez, Hela, Kahrizi, Kimia, Simpson, Allen C., Tollefson, William T.A., Sloan, Christina M., Meyer, Nicole C., Babanejad, Mojgan, Ardalani, Fariba, Arzhangi, Sanaz, Schnieders, Michael J., Najmabadi, Hossein, Smith, Richard J.H.

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Toward polarizable AMOEBA thermodynamics at fixed charge efficiency using a dual force field approach: application to organic crystals von Nessler, Ian J, Litman, Jacob M, Schnieders, Michael J

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Dead-End Elimination with a Polarizable Force Field Repacks PCNA Structures von LuCore, Stephen D., Litman, Jacob M., Powers, Kyle T., Gao, Shibo, Lynn, Ava M., Tollefson, William T.A., Fenn, Timothy D., Washington, M. Todd, Schnieders, Michael J.

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Rapid Validation of Whole-Slide Imaging for Primary Histopathology Diagnosis: A Roadmap for the SARS-CoV-2 Pandemic Era von Samuelson, Megan I, Chen, Stephanie J, Boukhar, Sarag A, Schnieders, Eric M, Walhof, Mackenzie L, Bellizzi, Andrew M, Robinson, Robert A, Rajan, Anand

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Rapid Validation of Whole-Slide Imaging for Primary Histopathology Diagnosis von Samuelson, Megan I, Chen, Stephanie J, Boukhar, Sarag A, Schnieders, Eric M, Walhof, Mackenzie L, Bellizzi, Andrew M, Robinson, Robert A, Rajan K D, Anand

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Hypomorphic mutations in TRNT1 cause retinitis pigmentosa with erythrocytic microcytosis von DeLuca, Adam P, Whitmore, S Scott, Barnes, Jenna, Sharma, Tasneem P, Westfall, Trudi A, Scott, C Anthony, Weed, Matthew C, Wiley, Jill S, Wiley, Luke A, Johnston, Rebecca M, Schnieders, Michael J, Lentz, Steven R, Tucker, Budd A, Mullins, Robert F, Scheetz, Todd E, Stone, Edwin M, Slusarski, Diane C

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Structural Insights into Hearing Loss Genetics from Polarizable Protein Repacking von Tollefson, Mallory R., Litman, Jacob M., Qi, Guowei, O’Connell, Claire E., Wipfler, Matthew J., Marini, Robert J., Bernabe, Hernan V., Tollefson, William T.A., Braun, Terry A., Casavant, Thomas L., Smith, Richard J.H., Schnieders, Michael J.

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LADD syndrome with glaucoma is caused by a novel gene von Simpson, Allie, Avdic, Armin, Roos, Ben R, DeLuca, Adam, Miller, Kathy, Schnieders, Michael J, Scheetz, Todd E, Alward, Wallace L M, Fingert, John H

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Metal Hydride Vibrations: The Trans Effect of the Hydride von Schnieders, David, Tsui, Brian T. H, Sung, Molly M. H, Bortolus, Mark R, Schrobilgen, Gary J, Neugebauer, Johannes, Morris, Robert H

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Microalbuminuria and tubular proteinuria as risk predictors of cardiovascular morbidity and mortality in essential hypertension: final results of a prospective long-term study (MAR... von Schrader, Joachim, Lüders, Stephan, Kulschewski, Anke, Hammersen, Frank, Züchner, Christel, Venneklaas, Ulla, Schrandt, Günter, Schnieders, Marion, Rangoonwala, Badrudin, Berger, Jürgen, Dominiak, Peter, Zidek, Walter

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