A Multi-Disciplinary Approach for the Electrical and Thermal Characterization of Battery Packs—Case Study for an Electric Race Car von Santarelli, Claudio, Helbig, Christopher, Li, An, Honel, Benoit, Nyhues, Thomas, Böhm, Fabian

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SCN3A‐Related Neurodevelopmental Disorder: A Spectrum of Epilepsy and Brain Malformation von Zaman, Tariq, Helbig, Katherine L., Clatot, Jérôme, Thompson, Christopher H., Kang, Seok Kyu, Stouffs, Katrien, Jansen, Anna E., Verstraete, Lieve, Jacquinet, Adeline, Parrini, Elena, Guerrini, Renzo, Fujiwara, Yuh, Miyatake, Satoko, Ben‐Zeev, Bruria, Bassan, Haim, Reish, Orit, Marom, Daphna, Hauser, Natalie, Vu, Thuy‐Anh, Ackermann, Sally, Spencer, Careni E., Lippa, Natalie, Srinivasan, Shraddha, Charzewska, Agnieszka, Hoffman‐Zacharska, Dorota, Fitzpatrick, David, Harrison, Victoria, Vasudevan, Pradeep, Joss, Shelagh, Pilz, Daniela T., Fawcett, Katherine A., Helbig, Ingo, Matsumoto, Naomichi, Kearney, Jennifer A., Fry, Andrew E., Goldberg, Ethan M.

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The Human Phenotype Ontology in 2021 von Köhler, Sebastian, Gargano, Michael, Matentzoglu, Nicolas, Carmody, Leigh C, Lewis-Smith, David, Vasilevsky, Nicole A, Danis, Daniel, Balagura, Ganna, Baynam, Gareth, Brower, Amy M, Callahan, Tiffany J, Chute, Christopher G, Est, Johanna L, Galer, Peter D, Ganesan, Shiva, Griese, Matthias, Haimel, Matthias, Pazmandi, Julia, Hanauer, Marc, Harris, Nomi L, Hartnett, Michael J, Hastreiter, Maximilian, Hauck, Fabian, He, Yongqun, Jeske, Tim, Kearney, Hugh, Kindle, Gerhard, Klein, Christoph, Knoflach, Katrin, Krause, Roland, Lagorce, David, McMurry, Julie A, Miller, Jillian A, Munoz-Torres, Monica C, Peters, Rebecca L, Rapp, Christina K, Rath, Ana M, Rind, Shahmir A, Rosenberg, Avi Z, Segal, Michael M, Seidel, Markus G, Smedley, Damian, Talmy, Tomer, Thomas, Yarlalu, Wiafe, Samuel A, Xian, Julie, Yüksel, Zafer, Helbig, Ingo, Mungall, Christopher J, Haendel, Melissa A, Robinson, Peter N

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Biallelic VARS variants cause developmental encephalopathy with microcephaly that is recapitulated in vars knockout zebrafish von Siekierska, Aleksandra, Stamberger, Hannah, Deconinck, Tine, Oprescu, Stephanie N., Partoens, Michèle, Zhang, Yifan, Sourbron, Jo, Adriaenssens, Elias, Mullen, Patrick, Wiencek, Patrick, Hardies, Katia, Lee, Jeong-Soo, Giong, Hoi-Khoanh, Distelmaier, Felix, Elpeleg, Orly, Helbig, Katherine L., Hersh, Joseph, Isikay, Sedat, Jordan, Elizabeth, Karaca, Ender, Kecskes, Angela, Lupski, James R., Kovacs-Nagy, Reka, May, Patrick, Narayanan, Vinodh, Pendziwiat, Manuela, Ramsey, Keri, Rangasamy, Sampathkumar, Shinde, Deepali N., Spiegel, Ronen, Timmerman, Vincent, von Spiczak, Sarah, Helbig, Ingo, Weckhuysen, Sarah, Francklyn, Christopher, Antonellis, Anthony, de Witte, Peter, De Jonghe, Peter

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Ylide‐Functionalized Phosphines: Strong Donor Ligands for Homogeneous Catalysis von Scherpf, Thorsten, Schwarz, Christopher, Scharf, Lennart T., Zur, Jana‐Alina, Helbig, Andreas, Gessner, Viktoria H.

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The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data von Köhler, Sebastian, Doelken, Sandra C, Mungall, Christopher J, Bauer, Sebastian, Firth, Helen V, Bailleul-Forestier, Isabelle, Black, Graeme C M, Brown, Danielle L, Brudno, Michael, Campbell, Jennifer, FitzPatrick, David R, Eppig, Janan T, Jackson, Andrew P, Freson, Kathleen, Girdea, Marta, Helbig, Ingo, Hurst, Jane A, Jähn, Johanna, Jackson, Laird G, Kelly, Anne M, Ledbetter, David H, Mansour, Sahar, Martin, Christa L, Moss, Celia, Mumford, Andrew, Ouwehand, Willem H, Park, Soo-Mi, Riggs, Erin Rooney, Scott, Richard H, Sisodiya, Sanjay, Van Vooren, Steven, Wapner, Ronald J, Wilkie, Andrew O M, Wright, Caroline F, Vulto-van Silfhout, Anneke T, de Leeuw, Nicole, de Vries, Bert B A, Washingthon, Nicole L, Smith, Cynthia L, Westerfield, Monte, Schofield, Paul, Ruef, Barbara J, Gkoutos, Georgios V, Haendel, Melissa, Smedley, Damian, Lewis, Suzanna E, Robinson, Peter N

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Assessing the landscape of STXBP1-related disorders in 534 individuals von Xian, Julie, Parthasarathy, Shridhar, Ruggiero, Sarah M, Balagura, Ganna, Fitch, Eryn, Helbig, Katherine, Gan, Jing, Ganesan, Shiva, Kaufman, Michael C, Ellis, Colin A, Lewis-Smith, David, Galer, Peter, Cunningham, Kristin, O'Brien, Margaret, Cosico, Mahgenn, Baker, Kate, Darling, Alejandra, Veiga de Goes, Fernanda, El Achkar, Christelle M, Doering, Jan Henje, Furia, Francesca, García-Cazorla, Ángeles, Gardella, Elena, Geertjens, Lisa, Klein, Courtney, Kolesnik-Taylor, Anna, Lammertse, Hanna, Lee, Jeehun, Mackie, Alexandra, Misra-Isrie, Mala, Olson, Heather, Sexton, Emma, Sheidley, Beth, Smith, Lacey, Sotero, Luiza, Stamberger, Hannah, Syrbe, Steffen, Thalwitzer, Kim Marie, van Berkel, Annemiek, van Haelst, Mieke, Yuskaitis, Christopher, Weckhuysen, Sarah, Prosser, Ben, Son Rigby, Charlene, Demarest, Scott, Pierce, Samuel, Zhang, Yuehua, Møller, Rikke S, Bruining, Hilgo, Poduri, Annapurna, Zara, Federico, Verhage, Matthijs, Striano, Pasquale, Helbig, Ingo

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Dynamic imaging of the hepatitis C virus NS5A protein during a productive infection von Eyre, Nicholas S, Fiches, Guillaume N, Aloia, Amanda L, Helbig, Karla J, McCartney, Erin M, McErlean, Christopher S P, Li, Kui, Aggarwal, Anupriya, Turville, Stuart G, Beard, Michael R

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Representativeness of Eddy-Covariance flux footprints for areas surrounding AmeriFlux sites von Chu, Housen, Luo, Xiangzhong, Ouyang, Zutao, Chan, W. Stephen, Dengel, Sigrid, Biraud, Sébastien C., Torn, Margaret S., Metzger, Stefan, Kumar, Jitendra, Arain, M. Altaf, Arkebauer, Tim J., Baldocchi, Dennis, Bernacchi, Carl, Billesbach, Dave, Black, T. Andrew, Blanken, Peter D., Bohrer, Gil, Bracho, Rosvel, Brown, Shannon, Brunsell, Nathaniel A., Chen, Jiquan, Chen, Xingyuan, Clark, Kenneth, Desai, Ankur R., Duman, Tomer, Durden, David, Fares, Silvano, Forbrich, Inke, Gamon, John A., Gough, Christopher M., Griffis, Timothy, Helbig, Manuel, Hollinger, David, Humphreys, Elyn, Ikawa, Hiroki, Iwata, Hiroki, Ju, Yang, Knowles, John F., Knox, Sara H., Kobayashi, Hideki, Kolb, Thomas, Law, Beverly, Lee, Xuhui, Litvak, Marcy, Liu, Heping, Munger, J. William, Noormets, Asko, Novick, Kim, Oberbauer, Steven F., Oechel, Walter, Oikawa, Patty, Papuga, Shirley A., Pendall, Elise, Prajapati, Prajaya, Prueger, John, Quinton, William L, Richardson, Andrew D., Russell, Eric S., Scott, Russell L., Starr, Gregory, Staebler, Ralf, Stoy, Paul C., Stuart-Haëntjens, Ellen, Sonnentag, Oliver, Sullivan, Ryan C., Suyker, Andy, Ueyama, Masahito, Vargas, Rodrigo, Wood, Jeffrey D., Zona, Donatella

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Combining Machine Learning and Backgrounded Membrane Imaging: A Case Study in Comparing and Classifying Different Types of Biopharmaceutically Relevant Particles von Calderon, Christopher P., Krhač Levačić, Ana, Helbig, Constanze, Wuchner, Klaus, Menzen, Tim

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P347: RareResolve: Gene-humanized animal models for resolving pathogenicity in variants of uncertain significance (VUS) von Hopkins, Christopher, Brock, Trisha, McCormick, Kathryn, Helbig, Ingo, Bainbridge, Matthew

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Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies von Abou-Khalil, Bassel, Auce, Pauls, Avbersek, Andreja, Bahlo, Melanie, Balding, David J., Bast, Thomas, Baum, Larry, Becker, Albert J., Becker, Felicitas, Berghuis, Bianca, Berkovic, Samuel F., Boysen, Katja E., Bradfield, Jonathan P., Brody, Lawrence C., Buono, Russell J., Campbell, Ellen, Cascino, Gregory D., Catarino, Claudia B., Cavalleri, Gianpiero L., Cherny, Stacey S., Chinthapalli, Krishna, Coffey, Alison J., Compston, Alastair, Coppola, Antonietta, Cossette, Patrick, Craig, John J., de Haan, Gerrit-Jan, De Jonghe, Peter, de Kovel, Carolien G. F., Delanty, Norman, Depondt, Chantal, Devinsky, Orrin, Dlugos, Dennis J., Doherty, Colin P., Elger, Christian E., Eriksson, Johan G., Ferraro, Thomas N., Feucht, Martha, Francis, Ben, Franke, Andre, French, Jacqueline A., Freytag, Saskia, Gaus, Verena, Geller, Eric B., Gieger, Christian, Glauser, Tracy, Glynn, Simon, Goldstein, David B., Gui, Hongsheng, Guo, Youling, Haas, Kevin F., Hakonarson, Hakon, Hallmann, Kerstin, Haut, Sheryl, Heinzen, Erin L., Helbig, Ingo, Hengsbach, Christian, Hjalgrim, Helle, Iacomino, Michele, Ingason, Andrés, Jamnadas-Khoda, Jennifer, Johnson, Michael R., Kälviäinen, Reetta, Kantanen, Anne-Mari, Kasperavičiūte, Dalia, Kasteleijn-Nolst Trenite, Dorothee, Kirsch, Heidi E., Knowlton, Robert C., Koeleman, Bobby P. C., Krause, Roland, Krenn, Martin, Kunz, Wolfram S., Kuzniecky, Ruben, Kwan, Patrick, Lal, Dennis, Lau, Yu-Lung, Lehesjoki, Anna-Elina, Lerche, Holger, Leu, Costin, Lieb, Wolfgang, Lindhout, Dick, Lo, Warren D., Lopes-Cendes, Iscia, Lowenstein, Daniel H., Malovini, Alberto, Marson, Anthony G., Mayer, Thomas, McCormack, Mark, Mills, James L., Mirza, Nasir, Moerzinger, Martina, Møller, Rikke S., Molloy, Anne M., Muhle, Hiltrud, Newton, Mark, Ng, Ping-Wing, Nöthen, Markus M., Nürnberg, Peter, O’Brien, Terence J., Oliver, Karen L.

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A structurally precise mechanism links an epilepsy-associated KCNC2 potassium channel mutation to interneuron dysfunction von Clatot, Jerome, Currin, Christopher B, Liang, Qiansheng, Pipatpolkai, Tanadet, Massey, Shavonne L, Helbig, Ingo, Delemotte, Lucie, Vogels, Tim P, Covarrubias, Manuel, Goldberg, Ethan M

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SvAnna: efficient and accurate pathogenicity prediction of coding and regulatory structural variants in long-read genome sequencing von Danis, Daniel, Jacobsen, Julius O B, Balachandran, Parithi, Zhu, Qihui, Yilmaz, Feyza, Reese, Justin, Haimel, Matthias, Lyon, Gholson J, Helbig, Ingo, Mungall, Christopher J, Beck, Christine R, Lee, Charles, Smedley, Damian, Robinson, Peter N

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FBXO28 causes developmental and epileptic encephalopathy with profound intellectual disability von Schneider, Amy L., Myers, Candace T., Muir, Alison M., Calvert, Sophie, Basinger, Alice, Perry, M. Scott, Rodan, Lance, Helbig, Katherine L., Chambers, Chelsea, Gorman, Kathleen M., King, Mary D., Donkervoort, Sandra, Soldatos, Ariane, Bönnemann, Carsten G., Spataro, Nino, Gabau, Elisabeth, Arellano, Montserrat, Cappuccio, Gerarda, Brunetti‐Pierri, Nicola, Rossignol, Elsa, Hamdan, Fadi F., Michaud, Jacques L., Balak, Christopher, Mefford, Heather C., Scheffer, Ingrid E.

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RIA fractions contain mesenchymal stroma cells with high osteogenic potency von Kuehlfluck, Pamela, Moghaddam, Arash, Helbig, Lars, Child, Christopher, Wildemann, Britt, Schmidmaier, Gerhard

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Validation of the German version of the Ford Insomnia Response to Stress Test von Dieck, Arne, Helbig, Susanne, Drake, Christopher L., Backhaus, Jutta

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Comprehensive multi-omic profiling of somatic mutations in malformations of cortical development von Chung, Changuk, Yang, Xiaoxu, Bae, Taejeong, Vong, Keng Ioi, Mittal, Swapnil, Donkels, Catharina, Westley Phillips, H., Li, Zhen, Marsh, Ashley P. L., Breuss, Martin W., Ball, Laurel L., Garcia, Camila Araújo Bernardino, George, Renee D., Gu, Jing, Xu, Mingchu, Barrows, Chelsea, James, Kiely N., Stanley, Valentina, Nidhiry, Anna S., Khoury, Sami, Howe, Gabrielle, Riley, Emily, Xu, Xin, Copeland, Brett, Wang, Yifan, Kim, Se Hoon, Kang, Hoon-Chul, Schulze-Bonhage, Andreas, Haas, Carola A., Urbach, Horst, Prinz, Marco, Limbrick, David D., Gurnett, Christina A., Smyth, Matthew D., Sattar, Shifteh, Nespeca, Mark, Gonda, David D., Imai, Katsumi, Takahashi, Yukitoshi, Chen, Hsin-Hung, Tsai, Jin-Wu, Conti, Valerio, Guerrini, Renzo, Devinsky, Orrin, Silva, Wilson A., Machado, Helio R., Mathern, Gary W., Abyzov, Alexej, Baldassari, Sara, Baulac, Stéphanie, Gleeson, Joseph G.

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Rare dysfunctional SCN2A variants are associated with malformation of cortical development von Clatot, Jérôme, Thompson, Christopher H, Sotardi, Susan, Jiang, Jinan, Trivisano, Marina, Balestrini, Simona, Ward, D Isum, Ginn, Natalie, Guaragni, Brunetta, Malerba, Laura, Vakrinou, Angeliki, Sherer, Mia, Helbig, Ingo, Somarowthu, Ala, Sisodiya, Sanjay M, Ben-Shalom, Roy, Guerrini, Renzo, Specchio, Nicola, George, Jr, Alfred L, Goldberg, Ethan M

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Community oncologists' perceptions and utilization of large-panel genomic tumor testing von Anderson, Eric C, Hinton, Alexandra C, Lary, Christine W, Fenton, Anny T H R, Antov, Andrey, Edelman, Emily, Helbig, Petra, Reed, Kate, Miesfeldt, Susan, Thomas, Christian A, Hall, Michael J, Roberts, J Scott, Rueter, Jens, Han, Paul K J

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