Novel ATP6V1B1 and ATP6V0A4 mutations in autosomal recessive distal renal tubular acidosis with new evidence for hearing loss von Stover, E H, Borthwick, K J, Bavalia, C, Eady, N, Fritz, D M, Rungroj, N, Giersch, A B S, Morton, C C, Axon, P R, Akil, I, Al-Sabban, E A, Baguley, D M, Bianca, S, Bakkaloglu, A, Bircan, Z, Chauveau, D, Clermont, M-J, Guala, A, Hulton, S A, Kroes, H, Li Volti, G, Mir, S, Mocan, H, Nayir, A, Ozen, S, Rodriguez Soriano, J, Sanjad, S A, Tasic, V, Taylor, C M, Topaloglu, R, Smith, A N, Karet, F E

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Consensus interpretation of the p.Met34Thr and p.Val37Ile variants in GJB2 by the ClinGen Hearing Loss Expert Panel von Shen, Jun, Oza, Andrea M., del Castillo, Ignacio, Duzkale, Hatice, Matsunaga, Tatsuo, Pandya, Arti, Kang, Hyunseok P., Mar-Heyming, Rebecca, Guha, Saurav, Moyer, Krista, Lo, Christine, Kenna, Margaret, Alexander, John J., Zhang, Yan, Hirsch, Yoel, Luo, Minjie, Cao, Ye, Wai Choy, Kwong, Cheng, Yen-Fu, Avraham, Karen B., Hu, Xinhua, Garrido, Gema, Moreno-Pelayo, Miguel A., Greinwald, John, Zhang, Kejian, Zeng, Yukun, Brownstein, Zippora, Basel-Salmon, Lina, Davidov, Bella, Frydman, Moshe, Weiden, Tzvi, Nagan, Narasimhan, Willis, Alecia, Hemphill, Sarah E., Grant, Andrew R., Siegert, Rebecca K., DiStefano, Marina T., Amr, Sami S., Rehm, Heidi L., Abou Tayoun, Ahmad N.

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Novel ATP6V1B1 and ATP6VOA4 mutations in autosomal recessive distal renal tubular acidosis with new evidence for hearing loss von STOVER, E. H, BORTHWICK, K. J, AL-SABBAN, E. A, BAGULEY, D. M, BIANCA, S, BAKKALOGLU, A, BIRCAN, Z, CHAUVEAU, D, CLERMONT, M-J, GUALA, A, HULTON, S. A, KROES, H, BAVALIA, C, LI VOLTI, G, MIR, S, MOCAN, H, NAYIR, A, OZEN, S, RODRIGUEZ SORIANO, J, SANJAD, S. A, TASIC, V, TAYLOR, C. M, TOPALOGLU, R, EADY, N, SMITH, A. N, KARET, F. E, FRITZ, D. M, RUNGROJ, N, GIERSCH, A. B. S, MORTON, C. C, AXON, P. R, AKIL, I

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A 3-D virtual human thermoregulatory model to predict whole-body and organ-specific heat-stress responses von Unnikrishnan, Ginu, Hatwar, Rajeev, Hornby, Samantha, Laxminarayan, Srinivas, Gulati, Tushar, Belval, Luke N., Giersch, Gabrielle E. W., Kazman, Josh B., Casa, Douglas J., Reifman, Jaques

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Commentary on Mosaic Copy Number Variation in a Patient with Cerebral and Pulmonary Arteriovenous Malformations and Recurrent Epistaxis von Giersch, Anne B S

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Leveraging Unique Chromosomal Microarray Probes to Accurately Detect Copy Number at the Highly Homologous 15q15.3 Deafness-Infertility Syndrome Locus von Sack, Laura M, Mertens, Lauren, Murphy, Elissa, Hutchinson, Laura, Giersch, Anne B S, Mason-Suares, Heather

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Corrigendum to “Self and time in individuals with schizophrenia: A motor component?” [Schizophr. Res. 272 (2024) 12–19 (October)] von Foerster, Francois R., Joos, E., Martin, B., Coull, J.T., Giersch, A.

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A targeted Coch missense mutation: a knock-in mouse model for DFNA9 late-onset hearing loss and vestibular dysfunction von Robertson, Nahid G., Jones, Sherri M., Sivakumaran, Theru A., Giersch, Anne B.S., Jurado, Sara A., Call, Linda M., Miller, Constance E., Maison, Stéphane F., Liberman, M. Charles, Morton, Cynthia C.

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Self and time in individuals with schizophrenia: A motor component? von Foerster, Francois R., Joos, E., Martin, B., Coull, J.T., Giersch, A.

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Genome-wide association meta-analysis identifies 48 risk variants and highlights the role of the stria vascularis in hearing loss von Trpchevska, Natalia, Freidin, Maxim B., Broer, Linda, Oosterloo, Berthe C., Yao, Shuyang, Zhou, Yitian, Vona, Barbara, Bishop, Charles, Bizaki-Vallaskangas, Argyro, Canlon, Barbara, Castellana, Fabio, Chasman, Daniel I., Cherny, Stacey, Christensen, Kaare, Concas, Maria Pina, Correa, Adolfo, Elkon, Ran, Metspalu, Andres, Nelis, Mari, Mägi, Reedik, Esko, Tõnu, Mengel-From, Jonas, Gao, Yan, Giersch, Anne B.S., Girotto, Giorgia, Gudjonsson, Alexander, Gudnason, Vilmundur, Heard-Costa, Nancy L., Hertzano, Ronna, Hjelmborg, Jacob v.B., Hjerling-Leffler, Jens, Hoffman, Howard J., Kaprio, Jaakko, Kettunen, Johannes, Krebs, Kristi, Kähler, Anna K., Lallemend, Francois, Launer, Lenore J., Lee, I-Min, Leonard, Hampton, Li, Chuan-Ming, Lowenheim, Hubert, Magnusson, Patrik K.E., van Meurs, Joyce, Milani, Lili, Morton, Cynthia C., Mäkitie, Antti, Nalls, Mike A., Nardone, Giuseppe Giovanni, Nygaard, Marianne, Palviainen, Teemu, Pratt, Sheila, Quaranta, Nicola, Rämö, Joel, Saarentaus, Elmo, Sardone, Rodolfo, Satizabal, Claudia L., Schweinfurth, John M., Seshadri, Sudha, Shiroma, Eric, Shulman, Eldad, Simonsick, Eleanor, Spankovich, Christopher, Tropitzsch, Anke, Lauschke, Volker M., Sullivan, Patrick F., Goedegebure, Andre, Cederroth, Christopher R., Williams, Frances M.K., Nagtegaal, Andries Paul

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An Integrated Framework for Ecological Drought across Riverscapes of North America von KOVACH, RYAN P., DUNHAM, JASON B., AL-CHOKHACHY, ROBERT, SNYDER, CRAIG D., LETCHER, BENJAMIN H., YOUNG, JOHN A., BEEVER, ERIK A., PEDERSON, GREG T., LYNCH, ABIGAIL J., HITT, NATHANIEL P., KONRAD, CHRIS P., JAEGER, KRISTIN L., REA, ALAN H., SEPULVEDA, ADAM J., LAMBERT, PATRICK M., STOKER, JASON, GIERSCH, JOSEPH J., MUHLFELD, CLINT C.

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The Burden and Benefits of Knowledge: Ethical Considerations Surrounding Population-Based Newborn Genome Screening for Hearing von Mitchell, Calli O., Rivera-Cruz, Greysha, Chau, Matthew Hoi Kin, Dong, Zirui, Choy, Kwong Wai, Shen, Jun, Amr, Sami, Giersch, Anne B. S., Morton, Cynthia C.

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Warming undermines emergence success in a threatened alpine stonefly: A multi‐trait perspective on vulnerability to climate change von Shah, Alisha A., Hotaling, Scott, Lapsansky, Anthony B., Malison, Rachel L., Birrell, Jackson H., Keeley, Tylor, Giersch, J. Joseph, Tronstad, Lusha M., Woods, H. Arthur

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Hearing and vestibular deficits in the Coch(-/-) null mouse model: comparison to the Coch(G88E/G88E) mouse and to DFNA9 hearing and balance disorder von Jones, Sherri M, Robertson, Nahid G, Given, Shelly, Giersch, Anne B S, Liberman, M Charles, Morton, Cynthia C

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Model update and validation of a mistuned high-pressure compressor blisk von Beirow, B., Kühhorn, A., Figaschewsky, F., Hönisch, P., Giersch, T., Schrape, S.

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Overview of the PALM model system 6.0 von Maronga, Björn, Banzhaf, Sabine, Burmeister, Cornelia, Esch, Thomas, Forkel, Renate, Fröhlich, Dominik, Fuka, Vladimir, Gehrke, Katrin Frieda, Geletic, Jan, Giersch, Sebastian, Gronemeier, Tobias, Groß, Günter, Heldens, Wieke, Hellsten, Antti, Hoffmann, Fabian, Inagaki, Atsushi, Kadasch, Eckhard, Kanani-Sühring, Farah, Ketelsen, Klaus, Khan, Basit Ali, Knigge, Christoph, Knoop, Helge, Krc, Pavel, Kurppa, Mona, Maamari, Halim, Matzarakis, Andreas, Mauder, Matthias, Pallasch, Matthias, Pavlik, Dirk, Pfafferott, Jens, Resler, Jaroslav, Rissmann, Sascha, Russo, Emmanuele, Salim, Mohamed, Schrempf, Michael, Schwenkel, Johannes, Seckmeyer, Gunther, Schubert, Sebastian, Sühring, Matthias, von Tils, Robert, Vollmer, Lukas, Ward, Simon, Witha, Björn, Wurps, Hauke, Zeidler, Julian, Raasch, Siegfried

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Analysis of mistuned forced response in an axial high-pressure compressor rig with focus on Tyler–Sofrin modes von Figaschewsky, F., Kühhorn, A., Beirow, B., Giersch, T., Schrape, S.

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Low time resolution in schizophrenia Lengthened windows of simultaneity for visual, auditory and bimodal stimuli von FOUCHER, J. R, LACAMBRE, M, PHAM, B.-T, GIERSCH, A, ELLIOTT, M. A

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Hearing and vestibular deficits in the Coch-/- null mouse model: Comparison to the CochG88E/G88E mouse and to DFNA9 hearing and balance disorder von JONES, Sherri M, ROBERTSON, Nahid G, GIVEN, Shelly, GIERSCH, Anne B. S, LIBERMAN, M. Charles, MORTON, Cynthia C

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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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