d-Amino Acids and Classical Neurotransmitters in Healthy and Type 2 Diabetes-Affected Human Pancreatic Islets of Langerhans von Lee, Cindy J, Schnieders, Jack H, Rubakhin, Stanislav S, Patel, Amit V, Liu, Chengyang, Naji, Ali, Sweedler, Jonathan V

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Neuroimmune activation and increased brain aging in chronic pain patients after the COVID-19 pandemic onset von Brusaferri, Ludovica, Alshelh, Zeynab, Schnieders, Jack H., Sandström, Angelica, Mohammadian, Mehrbod, Morrissey, Erin J., Kim, Minhae, Chane, Courtney A., Grmek, Grace C., Murphy, Jennifer P., Bialobrzewski, Julia, DiPietro, Alexa, Klinke, Julie, Zhang, Yi, Torrado-Carvajal, Angel, Mercaldo, Nathaniel, Akeju, Oluwaseun, Wu, Ona, Rosen, Bruce R., Napadow, Vitaly, Hadjikhani, Nouchine, Loggia, Marco L.

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Multichannel spectroscopy and hyperspectral imaging for improved steel surface states monitoring and cost savings (MULTISAVE): final report von Roquelet, C, Teppola, P, Juuti, M, Finta, C, Jussila, J, Hyvärinen, T, Schnieders, H, Grundmeier, G, Liu, C, Fricout, Gabriel, Ferte, M

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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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High-Throughput Genetic Testing for Thrombotic Microangiopathies and C3 Glomerulopathies von Bu, Fengxiao, Borsa, Nicolo Ghiringhelli, Jones, Michael B, Takanami, Erika, Nishimura, Carla, Hauer, Jill J, Azaiez, Hela, Black-Ziegelbein, Elizabeth A, Meyer, Nicole C, Kolbe, Diana L, Li, Yingyue, Frees, Kathy, Schnieders, Michael J, Thomas, Christie, Nester, Carla, Smith, Richard J H

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

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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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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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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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Nanophthalmos patient with a THR518MET mutation in MYRF, a case report von Hagedorn, Joshua, Avdic, Armin, Schnieders, Michael J, Roos, Benjamin R, Kwon, Young H, Drack, Arlene V, Boese, Erin A, Fingert, John 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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Direct involvement of phosphatidylinositol 4-phosphate in secretion in the yeast Saccharomyces cerevisiae von Hama, H, Schnieders, E.A, Thorner, J, Takemoto, J.Y, DeWald, D.B

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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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Cell Type-specific Expression of LINE-1 Open Reading Frames 1 and 2 in Fetal and Adult Human Tissues von Ergün, Süleyman, Buschmann, Christian, Heukeshoven, Jochen, Dammann, Kristin, Schnieders, Frank, Lauke, Heidrun, Chalajour, Fariba, Kilic, Nerbil, Strätling, Wolf H., Schumann, Gerald G.

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Automatic identification of clinically important Aspergillus species by artificial intelligence-based image recognition: proof-of-concept study von Tsang, Chi-Ching, Zhao, Chenyang, Liu, Yueh, Lin, Ken P K, Tang, James Y M, Cheng, Kar-On, Chow, Franklin W N, Yao, Weiming, Chan, Ka-Fai, Poon, Sharon N L, Wong, Kelly Y C, Zhou, Lianyi, Mak, Oscar T N, Lee, Jeremy C Y, Zhao, Suhui, Ngan, Antonio H Y, Wu, Alan K L, Fung, Kitty S C, Que, Tak-Lun, Teng, Jade L L, Schnieders, Dirk, Yiu, Siu-Ming, Lau, Susanna K P, Woo, Patrick C Y

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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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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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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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