Polarizable atomic multipole X-ray refinement: application to peptide crystals

por Schnieders, Michael J., Fenn, Timothy D., Pande, Vijay S., Brunger, Axel T.
Publicado 2009

Endothelial Lipase Variant, T111I, Does Not Alter Inhibition by Angiopoietin-like Proteins

por Sylvers-Davie, Kelli L., Bierstedt, Kaleb C., Schnieders, Michael J., Davies, Brandon S. J.
Publicado 2023

Progressive alignment of crystals: reproducible and efficient assessment of crystal structure similarity

por Nessler, Aaron J., Okada, Okimasa, Hermon, Mitchell J., Nagata, Hiroomi, Schnieders, Michael J.
Publicado 2022

In Silico and In Vivo Analysis of Amino Acid Substitutions That Cause Laminopathies

por Hinz, Benjamin E., Walker, Sydney G., Xiong, Austin, Gogal, Rose A., Schnieders, Michael J., Wallrath, Lori L.
Publicado 2021

Germline landscape of RPA1, RPA2 and RPA3 variants in pediatric malignancies: identification of RPA1 as a novel cancer predisposition candidate gene

por Sharma, Richa, Oak, Ninad, Chen, Wenan, Gogal, Rose, Kirschner, Martin, Beier, Fabian, Schnieders, Michael J., Spies, Maria, Nichols, Kim E., Wlodarski, Marcin
Publicado 2023

Nanophthalmos patient with a THR518MET mutation in MYRF, a case report

por Hagedorn, Joshua, Avdic, Armin, Schnieders, Michael J., Roos, Benjamin R., Kwon, Young H., Drack, Arlene V., Boese, Erin A., Fingert, John H.
Publicado 2020

LADD syndrome with glaucoma is caused by a novel gene

por Simpson, Allie, Avdic, Armin, Roos, Ben R., DeLuca, Adam, Miller, Kathy, Schnieders, Michael J., Scheetz, Todd E., Alward, Wallace L.M., Fingert, John H.
Publicado 2017

Tinker-HP: a massively parallel molecular dynamics package for multiscale simulations of large complex systems with advanced point dipole polarizable force fields

por Lagardère, Louis, Jolly, Luc-Henri, Lipparini, Filippo, Aviat, Félix, Stamm, Benjamin, Jing, Zhifeng F., Harger, Matthew, Torabifard, Hedieh, Cisneros, G. Andrés, Schnieders, Michael J., Gresh, Nohad, Maday, Yvon, Ren, Pengyu Y., Ponder, Jay W., Piquemal, Jean-Philip
Publicado 2017

Genomic Landscape and Mutational Signatures of Deafness-Associated Genes

por 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.
Publicado 2018

Assessing variants of uncertain significance implicated in hearing loss using a comprehensive deafness proteome

por 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.
Publicado 2023

Whole-genome sequencing reveals de-novo mutations associated with nonsyndromic cleft lip/palate

por Awotoye, Waheed, Mossey, Peter A., Hetmanski, Jacqueline B., Gowans, Lord J. J., Eshete, Mekonen A., Adeyemo, Wasiu L., Alade, Azeez, Zeng, Erliang, Adamson, Olawale, Naicker, Thirona, Anand, Deepti, Adeleke, Chinyere, Busch, Tamara, Li, Mary, Petrin, Aline, Aregbesola, Babatunde S., Braimah, Ramat O., Oginni, Fadekemi O., Oladele, Ayodeji O., Oladayo, Abimbola, Kayali, Sami, Olotu, Joy, Hassan, Mohaned, Pape, John, Donkor, Peter, Arthur, Fareed K. N., Obiri-Yeboah, Solomon, Sabbah, Daniel K., Agbenorku, Pius, Plange-Rhule, Gyikua, Oti, Alexander Acheampong, Gogal, Rose A., Beaty, Terri H., Taub, Margaret, Marazita, Mary L., Schnieders, Michael J., Lachke, Salil A., Adeyemo, Adebowale A., Murray, Jeffrey C., Butali, Azeez
Publicado 2022