Acute Kidney Injury Due to Collapsing Glomerulopathy Following COVID-19 Infection von Peleg, Yonatan, Kudose, Satoru, D’Agati, Vivette, Siddall, Eric, Ahmad, Syeda, Nickolas, Thomas, Kisselev, Sergey, Gharavi, Ali, Canetta, Pietro

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Candidate sequence variants and fetal hemoglobin in children with sickle cell disease treated with hydroxyurea von Green, Nancy S, Ender, Katherine L, Pashankar, Farzana, Driscoll, Catherine, Giardina, Patricia J, Mullen, Craig A, Clark, Lorraine N, Manwani, Deepa, Crotty, Jennifer, Kisselev, Sergey, Neville, Kathleen A, Hoppe, Carolyn, Barral, Sandra

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Promoter methylation-mediated inactivation of PCDH10 in acute lymphoblastic leukemia contributes to chemotherapy resistance von Narayan, Gopeshwar, Freddy, Allen J., Xie, Dongxu, Liyanage, Hema, Clark, Lorraine, Kisselev, Sergey, Un Kang, Ji, Nandula, Subhadra V., McGuinn, Catherine, Subramaniyam, Shivakumar, Alobeid, Bachir, Satwani, Prakash, Savage, David, Bhagat, Govind, Murty, Vundavalli V.

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Increasing Generative Artificial Intelligence Competency among Students Enrolled in Doctoral Nursing Research Coursework von Reading Turchioe, Meghan, Kisselev, Sergey, Van Bulck, Liesbet, Bakken, Suzanne

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Identification of candidate genes for familial early-onset essential tremor von Liu, Xinmin, Hernandez, Nora, Kisselev, Sergey, Floratos, Aris, Sawle, Ashley, Ionita-Laza, Iuliana, Ottman, Ruth, Louis, Elan D, Clark, Lorraine N

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Candidate Gene Analysis for Alzheimer’s Disease in Adults with Down syndrome von Lee, Joseph H, Lee, Annie J, Dang, Lam-Ha, Pang, Deborah, Kisselev, Sergey, Krinsky-McHale, Sharon J, Zigman, Warren B, Luchsinger, José A, Silverman, Wayne, Tycko, Benjamin, Clark, Lorraine N, Schupf, Nicole

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Reorganization of corticostriatal circuits in healthy G2019S LRRK2 carriers von Helmich, Rick C, Thaler, Avner, van Nuenen, Bart F.L, Gurevich, Tanya, Mirelman, Anat, Marder, Karen S, Bressman, Susan, Orr-Urtreger, Avi, Giladi, Nir, Bloem, Bastiaan R, Toni, Ivan

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Replication of the LINGO1 gene association with essential tremor in a North American population von CLARK, Lorraine N, PARK, Naeun, KISSELEV, Sergey, RIOS, Eileen, LEE, Joseph H, LOUIS, Elan D

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Candidate genes for Alzheimer's disease are associated with individual differences in plasma levels of beta amyloid peptides in adults with Down syndrome von Schupf, Nicole, Lee, Annie, Park, Naeun, Dang, Lam-Ha, Pang, Deborah, Yale, Alexander, Oh, David Kyung-Taek, Krinsky-McHale, Sharon J, Jenkins, Edmund C, Luchsinger, José A, Zigman, Warren B, Silverman, Wayne, Tycko, Benjamin, Kisselev, Sergey, Clark, Lorraine, Lee, Joseph H

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REM sleep behavior disorder, as assessed by questionnaire, in G2019S LRRK2 mutation PD and carriers von Saunders-Pullman, Rachel, Alcalay, Roy N., Mirelman, Anat, Wang, Cuiling, Luciano, Marta San, Ortega, Roberto A., Glickman, Amanda, Raymond, Deborah, Mejia-Santana, Helen, Doan, Nancy, Johannes, Brooke, Yasinovsky, Kira, Ozelius, Laurie, Clark, Lorraine, Orr-Utreger, Avi, Marder, Karen, Giladi, Nir, Bressman, Susan B.

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Lower cognitive performance in healthy G2019S LRRK2 mutation carriers von THALER, Avner, MIRELMAN, Anat, GUREVICH, Tanya, SIMON, Ely, ORR-URTREGER, Avi, MARDER, Karen, BRESSMAN, Susan, GILADI, Nir

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PCDH10 promoter hypermethylation is frequent in most histologic subtypes of mature lymphoid malignancies and occurs early in lymphomagenesis von Narayan, Gopeshwar, Xie, Dongxu, Freddy, Allen J., Ishdorj, Ganchimeg, Do, Catherine, Satwani, Prakash, Liyanage, Hema, Clark, Lorraine, Kisselev, Sergey, Nandula, Subhadra V., Scotto, Luigi, Alobeid, Bachir, Savage, David, Tycko, Benjamin, O'Connor, Owen A., Bhagat, Govind, Murty, Vundavalli V.

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A voxel-based morphometry and diffusion tensor imaging analysis of asymptomatic Parkinson's disease-related G2019S LRRK2 mutation carriers von Thaler, Avner, Artzi, Moran, Mirelman, Anat, Jacob, Yael, Helmich, Rick C., van Nuenen, Bart F.L., Gurevich, Tanya, Orr-Urtreger, Avi, Marder, Karen, Bressman, Susan, Bloem, Bastiaan R., Hendler, Talma, Giladi, Nir, Ben Bashat, Dafna

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Distribution of mononucleotide repeats in bacterial chromosomes: A/T-tracts dominate on G/C-tracts von Kisselev, Sergey Sergeevich, Komarov, Vladislav Mikhailovich, Masulis, Irina Stanislavovna, Ozoline, Olga Nikolaevna

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Variants in candidate genes for Alzheimer's disease are associated with declining plasma abeta peptides in adults with down syndrome von Schupf, Nicole, Dang, Lam-Ha, Lee, Annie, Pang, Deborah, Zigman, Warren B, Luchsinger, Jose A, Krinsky-McHale, Sharon, Silverman, Wayne, Tycko, Benjamin, Kisselev, Sergey, Clark, Lorraine, Lee, Joseph H

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P1‐268: Variants in candidate genes for Alzheimer's disease are associated with declining plasma abeta peptides in adults with down syndrome von Schupf, Nicole, Dang, Lam-Ha, Lee, Annie, Pang, Deborah, Zigman, Warren B., Luchsinger, Jose A., Krinsky-McHale, Sharon, Silverman, Wayne, Tycko, Benjamin, Kisselev, Sergey, Clark, Lorraine, Lee, Joseph H.

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Exome sequencing identified MYO1E and NEIL1 as candidate genes for human autosomal recessive steroid-resistant nephrotic syndrome von Sanna-Cherchi, Simone, Burgess, Katelyn E., Nees, Shannon N., Caridi, Gianluca, Weng, Patricia L., Dagnino, Monica, Bodria, Monica, Carrea, Alba, Allegretta, Maddalena A., Kim, Hyunjae R., Perry, Brittany J., Gigante, Maddalena, Clark, Lorraine N., Kisselev, Sergey, Cusi, Daniele, Gesualdo, Loreto, Allegri, Landino, Scolari, Francesco, D'Agati, Vivette, Shapiro, Lawrence S., Pecoraro, Carmine, Palomero, Teresa, Ghiggeri, Gian M., Gharavi, Ali G.

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Neuropsychological Profile of Parkin Mutation Carriers with and without Parkinson Disease: The CORE-PD Study von Caccappolo, Elise, Alcalay, Roy N., Mejia-Santana, Helen, Tang, Ming-X., Rakitin, Brian, Rosado, Llency, Louis, Elan D., Comella, Cynthia L., Colcher, Amy, Jennings, Danna, Nance, Martha A., Bressman, Susan, Scott, William K., Tanner, Caroline M., Mickel, Susan F., Andrews, Howard F., Waters, Cheryl, Fahn, Stanley, Cote, Lucien J., Frucht, Steven, Ford, Blair, Rezak, Michael, Novak, Kevin, Friedman, Joseph H., Pfeiffer, Ronald F., Marsh, Laura, Hiner, Brad, Siderowf, Andrew D., Ross, Barbara M., Verbitsky, Miguel, Kisselev, Sergey, Ottman, Ruth, Clark, Lorraine N., Marder, Karen S.

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Increased rate of sporadic and recurrent rare genic copy number variants in Parkinson's disease among Ashkenazi Jews von Liu, Xinmin, Cheng, Rong, Ye, Xin, Verbitsky, Miguel, Kisselev, Sergey, Mejia‐Santana, Helen, Louis, Elan D., Cote, Lucien J., Andrews, Howard F., Waters, Cheryl H., Ford, Blair, Fahn, Stanley, Marder, Karen, Lee, Joseph H., Clark, Lorraine N.

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Gene-Wise Association of Variants in Four Lysosomal Storage Disorder Genes in Neuropathologically Confirmed Lewy Body Disease: e0125204 von Clark, Lorraine N, Chan, Robin, Cheng, Rong, Liu, Xinmin, Park, Naeun, Parmalee, Nancy, Kisselev, Sergey, Cortes, Etty, Torres, Paola A, Pastores, Gregory M

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