Deletions of NRXN1 (neurexin-1) predispose to a wide spectrum of developmental disorders von Ching, Michael S.L., Shen, Yiping, Tan, Wen-Hann, Jeste, Shafali S., Morrow, Eric M., Chen, Xiaoli, Mukaddes, Nahit M., Yoo, Seung-Yun, Hanson, Ellen, Hundley, Rachel, Austin, Christina, Becker, Ronald E., Berry, Gerard T., Driscoll, Katherine, Engle, Elizabeth C., Friedman, Sandra, Gusella, James F., Hisama, Fuki M., Irons, Mira B., Lafiosca, Tina, LeClair, Elaine, Miller, David T., Neessen, Michael, Picker, Jonathan D., Rappaport, Leonard, Rooney, Cynthia M., Sarco, Dean P., Stoler, Joan M., Walsh, Christopher A., Wolff, Robert R., Zhang, Ting, Nasir, Ramzi H., Wu, Bai-Lin

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Evaluation of SMN protein, transcript, and copy number in the biomarkers for spinal muscular atrophy (BforSMA) clinical study von Crawford, Thomas O, Paushkin, Sergey V, Kobayashi, Dione T, Forrest, Suzanne J, Joyce, Cynthia L, Finkel, Richard S, Kaufmann, Petra, Swoboda, Kathryn J, Tiziano, Danilo, Lomastro, Rosa, Li, Rebecca H, Trachtenberg, Felicia L, Plasterer, Thomas, Chen, Karen S

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Updated International Tuberous Sclerosis Complex Diagnostic Criteria and Surveillance and Management Recommendations von Northrup, Hope, Aronow, Mary E., Bebin, E. Martina, Bissler, John, Darling, Thomas N., de Vries, Petrus J., Frost, Michael D., Gosnell, Elizabeth S., Gupta, Nishant, Jansen, Anna C., Jóźwiak, Sergiusz, Kingswood, J. Chris, Knilans, Timothy K., McCormack, Francis X., Pounders, Ashley, Roberds, Steven L., Rodriguez-Buritica, David F., Roth, Jonathan, Sampson, Julian R., Sparagana, Steven, Thiele, Elizabeth Anne, Weiner, Howard L., Wheless, James W., Towbin, Alexander J., Krueger, Darcy A., Annear, Nicholas M.P., Aronow, Mary E., Bebin, E. Martina, Bissler, John J., Budde, Klemens, Byars, Anna, Chugani, Harry, Cowen, Edward W., Crino, Peter B., Curatolo, Paolo, Darling, Thomas N., de Vries, Petrus, Dilling, Daniel F., Dunn, David W., Ekong, Rosmary, Ess, Kevin C., Franz, David N., Frost, Michael, Gosnell, Elizabeth, Guay-Woodford, Lisa, Gupta, Nishant, Haddad, Luciana, Halbert, Anne, Hebert, Adelaide A., Henske, Elizabeth P., Hook, Dena, Hulbert, John, Jansen, Anna, Johnson, Simon R., Jóźwiak, Sergiusz, King, Bryan, Knilans, Timothy K., Koenig, Mary Kay, Korf, Bruce, Krueger, Darcy A., McCormack, Francis X., Moss, Joel, Mowat, David, Mowrey, Kate, Nabbout, Rima, Nellist, Mark D., Northrup, Hope, O'Callaghan, Finbar, Patel, Uday, Pounders, Ashley, Roach, E. Steve, Roberds, Steven L., Rodriguez-Buritica, David, Romp, Robb, Roth, Jonathan, Rozenberg, Micaela, Ruoss, Stephen J., Sahin, Mustafa, Sampson, Julian, Samuels, Joshua A., Sauter, Matthias, Smith, Catherine A., Soltani, Keyomaurs, Sparagana, Steven, Srivastava, Shoba, Stuart, Clare, Teng, Joyce M.C., Thiele, Elizabeth A., Towbin, Alexander J., Trout, Andrew, van Eeghen, Agnies, Vanclooster, Stephanie, Wang, Henry Z., Wataya-Kaneda, Mari, Weiner, Howard L., Wheless, James W., Witman, Patricia, Wright, Tim, Wu, Joyce Y., Young, Lisa

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Polymicrogyria is Associated With Pathogenic Variants in PTEN von Shao, Diane D., Achkar, Christelle M., Lai, Abbe, Srivastava, Siddharth, Doan, Ryan N., Rodan, Lance H., Chen, Allen Y., Poduri, Annapurna, Yang, Edward, Walsh, Christopher A., Irons, Mira B., Johnson, Ervin L., Ojeda, Mayra Martinez, Olson, Heather E., Sahin, Mustafa, Stredny, Coral M., Tan, Wen‐Hann

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Biomarkers to Enable Therapeutics Development in Neurodevelopmental Disorders

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Tuberous Sclerosis Complex Surveillance and Management: Recommendations of the 2012 International Tuberous Sclerosis Complex Consensus Conference von Krueger, Darcy A., MD PhD, Northrup, Hope, MD

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Early diagnosed but late treated subungual melanoma von SAHIN, Mustafa T, OZTURKCAN, Serap, SEYHAN, Ahmet, DEMIRELI, Peyker, TUREL-ERMERTCAN, Aylin

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Epilepsy and Neurodevelopmental Comorbidities in Tuberous Sclerosis Complex: A Natural History Study von Gupta, Ajay, de Bruyn, Gwendolyn, Tousseyn, Simon, Krishnan, Balu, Lagae, Lieven, Agarwal, Nitin, Minnesota Epilepsy Group, Frost, Michael, Sparagana, Steven, LaJoie, Josiane, Riviello, James, Devinsky, Orrin, Thiele, Elizabeth, McClintock, William, Kohrman, Michael, Brown, Candida, Kuperman, Rachel, Wu, Joyce, Northrup, Hope, Bebin, E. Martina, Korf, Bruce, Gupta, Ajay, Levisohn, Paul, Koh, Susan, O'Neil Miller, Ian, Duchowny, Michael, Ashwal, Stephen, Jansen, Anna, Crino, Peter, Pollard, John, Nathanson, Kate, Sahin, Mustafa, Krueger, Darcy A., Wong, Michael, Jeong, Anna

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IFSO Worldwide Survey 2020–2021: Current Trends for Bariatric and Metabolic Procedures von Angrisani, Luigi, Santonicola, Antonella, Iovino, Paola, Palma, Rossella, Kow, Lilian, Prager, Gerhard, Ramos, Almino, Shikora, Scott

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Exome Sequencing and the Identification of New Genes and Shared Mechanisms in Polymicrogyria von Akula, Shyam K, Chen, Allen Y, Neil, Jennifer E, Shao, Diane D, Mo, Alisa, Hylton, Norma K, DiTroia, Stephanie, Ganesh, Vijay S, Smith, Richard S, O’Kane, Katherine, Yeh, Rebecca C, Marciano, Jack H, Kirkham, Samantha, Kenny, Connor J, Song, Janet H. T, Al Saffar, Muna, Millan, Francisca, Harris, David J, Murphy, Andrea V, Klemp, Kara C, Braddock, Stephen R, Brand, Harrison, Wong, Isaac, Talkowski, Michael E, O’Donnell-Luria, Anne, Lai, Abbe, Hill, Robert Sean, Mochida, Ganeshwaran H, Doan, Ryan N, Barkovich, A. James, Yang, Edward, Amrom, Dina, Andermann, Eva, Poduri, Annapurna, Walsh, Christopher A

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Candidate proteins, metabolites and transcripts in the Biomarkers for Spinal Muscular Atrophy (BforSMA) clinical study von Finkel, Richard S, Crawford, Thomas O, Swoboda, Kathryn J, Kaufmann, Petra, Juhasz, Peter, Li, Xiaohong, Guo, Yu, Li, Rebecca H, Trachtenberg, Felicia, Forrest, Suzanne J, Kobayashi, Dione T, Chen, Karen S, Joyce, Cynthia L, Plasterer, Thomas

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Study protocol: retrospectively mining multisite clinical data to presymptomatically predict seizure onset for individual patients with Sturge-Weber von Vedmurthy, Pooja, Pinto, Anna L R, Lin, Doris D M, Comi, Anne M, Ou, Yangming, Sahin, Mustafa, Ellen Grant, P., Boyer, Katrina, Takeoka, Masanori, Cohen, Bernard, Ewen, Joshua, Kossoff, Eric, Reidy, Teressa Garcia, Suskauer, Stacy, Zabel, Andrew

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Diffusion Tensor Imaging Abnormalities in the Uncinate Fasciculus and Inferior Longitudinal Fasciculus in Phelan-McDermid Syndrome von Bassell, Julia, Srivastava, Siddharth, Prohl, Anna K., Scherrer, Benoit, Kapur, Kush, Filip-Dhima, Rajna, Berry-Kravis, Elizabeth, Soorya, Latha, Thurm, Audrey, Powell, Craig M., Bernstein, Jonathan A., Buxbaum, Joseph D., Kolevzon, Alexander, Warfield, Simon K., Sahin, Mustafa, Sahin, Mustafa, Kolevzon, Alexander, Buxbaum, Joseph, Berry Kravis, Elizabeth, Soorya, Latha, Thurm, Audrey, Powell, Craig, Bernstein, Jonathan A., Warfield, Simon, Scherrer, Benoit, Filip-Dhima, Rajna, Dies, Kira, Siper, Paige, Hanson, Ellen, Phillips, Jennifer M., White, Stormi P.

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Rigor and reproducibility in human brain organoid research: Where we are and where we need to go von Sandoval, Soraya O., Cappuccio, Gerarda, Kruth, Karina, Osenberg, Sivan, Khalil, Saleh M., Méndez-Albelo, Natasha M., Padmanabhan, Krishnan, Wang, Daifeng, Niciu, Mark J., Bhattacharyya, Anita, Stein, Jason L., Sousa, André M.M., Waxman, Elisa A., Buttermore, Elizabeth D., Whye, Dosh, Sirois, Carissa L., Anderson, Stewart, Anita, Bhattacharyya, Buttermore, Elizabeth, Chang, Qiang, French, Deborah, Hashimoto-Torii, Kazue, Kornblum, Harley, Kroll, Kristin, Lachman, Herbert M., Maletic-Savatic, Mirjana, Niciu, Mark, Novitch, Bennett, Padmanabhan, Krishnan, Proschel, Chris, Sahin, Mustafa, Sousa, Andre, Stein, Jason, Wang, Daifeng, Waxman, Elisa, Whye, Dosh, Williams, Aislinn, Zhao, Xinyu, Williams, Aislinn, Maletic-Savatic, Mirjana, Zhao, Xinyu

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Parent-reported measure of repetitive behavior in Phelan-McDermid syndrome von Srivastava, Siddharth, Condy, Emma, Carmody, Erin, Filip-Dhima, Rajna, Kapur, Kush, Bernstein, Jonathan A., Berry-Kravis, Elizabeth, Powell, Craig M., Soorya, Latha, Thurm, Audrey, Buxbaum, Joseph D., Sahin, Mustafa, Kolevzon, Alexander

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Drug-Resistant Epilepsy in Tuberous Sclerosis Complex Is Associated With TSC2 Genotype: More Findings From the Preventing Epilepsy Using Vigatrin (PREVeNT) Trial von Farach, Laura S., Richard, Melissa A., Wulsin, Aynara C., Bebin, Elizabeth M., Krueger, Darcy A., Sahin, Mustafa, Porter, Brenda E., McPherson, Tarrant O., Peters, Jurriaan M., O'Kelley, Sarah, Taub, Katherine S., Rajaraman, Rajsekar, Randle, Stephanie C., McClintock, William M., Koenig, Mary Kay, Frost, Michael D., Werner, Klaus, Nolan, Danielle A., Wong, Michael, Cutter, Gary, Northrup, Hope, Au, Kit Sing, Bebin, E. Martina, Krueger, Darcy, Sahin, Mustafa, Flamini, Robert, Sergott, Robert C., Cutter, Gary, McPherson, Tarrant, Peri, Kalyani, Krefting, Jessica, Porter, Brenda, Peters, Jurriaan M., Taub, Katherine, Litt, Brian, Wu, Joyce, Lagory, Denise, Korf, Bruce, Messiaen, Ludwig, O'Kelley, Sarah, Biasini, Fred, Byars, Anna, Roberds, Steven L., Rushing, Gabrielle, Griffith, Molly, Davis, Peter, Hansen, Ellen, Arcasoy, Emine, Phillips, Jennifer, Solidum, Rayann, Rajaraman, Rajsekar, Gulsrud, Amanda, Solis, Natalie, Randle, Stephanie, Patrick, Kristina, Lee-Eng, Jacqueline, Frost, Mike D., Branson, Janet, Ellis, Sarah, Wong, Michael, White, Desiree, Novak, Olga, Fasciola, Ashley, Werner, Klaus, Lorenzi, Jill, Layer, Marcus, Thomas, Allison, Chanbers, Emily, McClintock, William M., Berl, Madison, Elling, Nancy, Kassoff, Bergen, Hardie, Kinaya, Nolan, Danielle, DeBastos, Angela, Batchelder, Christine, Koening, Mary Kay, Northrup, Hope, Au, Kit Su, Pearson, Deborah, Mansour, Rosleen, Farach, Laura, Salazar, Elida

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The Brain Gene Registry: a data snapshot von Baldridge, Dustin, Kaster, Levi, Sancimino, Catherine, Srivastava, Siddharth, Molholm, Sophie, Gupta, Aditi, Oh, Inez, Lanzotti, Virginia, Grewal, Daleep, Riggs, Erin Rooney, Savatt, Juliann M, Hauck, Rachel, Sveden, Abigail, Constantino, John N, Piven, Joseph, Gurnett, Christina A, Chopra, Maya, Hazlett, Heather, Payne, Philip R O

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Pediatric Neurocritical Care: A Neurology Consultation Model and Implication for Education and Training von LaRovere, Kerri L., MD, Graham, Robert J., MD, Tasker, Robert C., MBBS, MD

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Assessment of acceptability of the COVID-19 vaccine based on the health belief model among Malaysians-A qualitative approach von Rani, Mohd Dzulkhairi Mohd, Mohamed, Nurul Azmawati, Solehan, Hana Maizuliana, Ithnin, Muslimah, Ariffien, Abd Rasyid, Isahak, Ilina

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Both Maternal and Pup Genotype Influence Ultrasonic Vocalizations and Early Developmental Milestones in Tsc2^(+/-) Mice von Greene-Colozzi, Emily A., Sadowski, Abbey R., Chadwick, Elyza, Tsai, Peter T., Sahin, Mustafa

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