Integrated model of de novo and inherited genetic variants yields greater power to identify risk genes von He, Xin, Sanders, Stephan J, Liu, Li, De Rubeis, Silvia, Lim, Elaine T, Sutcliffe, James S, Schellenberg, Gerard D, Gibbs, Richard A, Daly, Mark J, Buxbaum, Joseph D, State, Matthew W, Devlin, Bernie, Roeder, Kathryn

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Contribution of SHANK3 Mutations to Autism Spectrum Disorder von Moessner, Rainald, Marshall, Christian R., Sutcliffe, James S., Skaug, Jennifer, Pinto, Dalila, Vincent, John, Zwaigenbaum, Lonnie, Fernandez, Bridget, Roberts, Wendy, Szatmari, Peter, Scherer, Stephen W.

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Effects of indoor air movement and ambient temperature on mosquito (Anopheles gambiae) behaviour around bed nets: implications for malaria prevention initiatives von Sutcliffe, James F., Yin, Shaoman

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Behavioural responses of females of two anopheline mosquito species to human-occupied, insecticide-treated and untreated bed nets von Sutcliffe, James F, Yin, Shaoman

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A Bayesian framework that integrates multi-omics data and gene networks predicts risk genes from schizophrenia GWAS data von Wang, Quan, Chen, Rui, Cheng, Feixiong, Wei, Qiang, Ji, Ying, Yang, Hai, Zhong, Xue, Tao, Ran, Wen, Zhexing, Sutcliffe, James S., Liu, Chunyu, Cook, Edwin H., Cox, Nancy J., Li, Bingshan

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Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci von Sanders, Stephan J., He, Xin, Willsey, A. Jeremy, Ercan-Sencicek, A. Gulhan, Samocha, Kaitlin E., Cicek, A. Ercument, Murtha, Michael T., Bal, Vanessa H., Bishop, Somer L., Dong, Shan, Goldberg, Arthur P., Jinlu, Cai, Keaney, John F., Klei, Lambertus, Mandell, Jeffrey D., Moreno-De-Luca, Daniel, Poultney, Christopher S., Robinson, Elise B., Smith, Louw, Solli-Nowlan, Tor, Su, Mack Y., Teran, Nicole A., Walker, Michael F., Werling, Donna M., Beaudet, Arthur L., Cantor, Rita M., Fombonne, Eric, Geschwind, Daniel H., Grice, Dorothy E., Lord, Catherine, Lowe, Jennifer K., Mane, Shrikant M., Martin, Donna M., Morrow, Eric M., Talkowski, Michael E., Sutcliffe, James S., Walsh, Christopher A., Yu, Timothy W., Ledbetter, David H., Martin, Christa Lese, Cook, Edwin H., Buxbaum, Joseph D., Daly, Mark J., Devlin, Bernie, Roeder, Kathryn, State, Matthew W.

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Autism gene variant causes hyperserotonemia, serotonin receptor hypersensitivity, social impairment and repetitive behavior von Veenstra-VanderWeele, Jeremy, Muller, Christopher L, Iwamoto, Hideki, Sauer, Jennifer E, Owens, W. Anthony, Shah, Charisma R, Cohen, Jordan, Mannangatti, Padmanabhan, Jessen, Tammy, Thompson, Brent J, Ye, Ran, Kerr, Travis M, Carneiro, Ana M, Crawley, Jacqueline N, Sanders-Bush, Elaine, McMahon, Douglas G, Ramamoorthy, Sammanda, Daws, Lynette C, Sutcliffe, James S, Blakely, Randy D

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Impact of Body Temperature Before and After Endovascular Thrombectomy for Large Vessel Occlusion Stroke von Diprose, William K, Liem, Bernard, Wang, Michael T.M, Sutcliffe, James A, Brew, Stefan, Caldwell, James R, McGuinness, Ben, Campbell, Doug, Barber, P Alan

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Shorter sleep duration is associated with social impairment and comorbidities in ASD von Veatch, Olivia J., Sutcliffe, James S., Warren, Zachary E., Keenan, Brendan T., Potter, Melissa H., Malow, Beth A.

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A Novel Human CAMK2A Mutation Disrupts Dendritic Morphology and Synaptic Transmission, and Causes ASD-Related Behaviors von Stephenson, Jason R, Wang, Xiaohan, Perfitt, Tyler L, Parrish, Walker P, Shonesy, Brian C, Marks, Christian R, Mortlock, Douglas P, Nakagawa, Terunaga, Sutcliffe, James S, Colbran, Roger J

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Strong Association of De Novo Copy Number Mutations with Autism von Sebat, Jonathan, Lakshmi, B, Malhotra, Dheeraj, Troge, Jennifer, Lese-Martin, Christa, Walsh, Tom, Yamrom, Boris, Yoon, Seungtai, Krasnitz, Alex, Kendall, Jude, Leotta, Anthony, Pai, Deepa, Zhang, Ray, Lee, Yoon-Ha, Hicks, James, Spence, Sarah J, Lee, Annette T, Puura, Kaija, Lehtimäki, Terho, Ledbetter, David, Gregersen, Peter K, Bregman, Joel, Sutcliffe, James S, Jobanputra, Vaidehi, Chung, Wendy, Warburton, Dorothy, King, Mary-Claire, Skuse, David, Geschwind, Daniel H, Gilliam, T. Conrad, Ye, Kenny, Wigler, Michael

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A Genetic Variant That Disrupts MET Transcription Is Associated with Autism von Campbell, Daniel B., Sutcliffe, James S., Ebert, Philip J., Militerni, Roberto, Bravaccio, Carmela, Trillo, Simona, Elia, Maurizio, Schneider, Cindy, Melmed, Raun, Sacco, Roberto, Persico, Antonio M., Levitt, Pat

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Genetics. Insights into the pathogenesis of autism von Sutcliffe, James S

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Relationship between maternal serotonin levels and autism-associated genetic variants von Jutla, Amandeep, Shuffrey, Lauren C, Guter, Stephen J, O'Reilly, Kally C, Anderson, George M, Sutcliffe, James S, Cook, Edwin H, Veenstra-VanderWeele, Jeremy

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Enhanced activity of human serotonin transporter variants associated with autism von Prasad, Harish C, Steiner, Jennifer A, Sutcliffe, James S, Blakely, Randy D

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Common genetic variants, acting additively, are a major source of risk for autism von Klei, Lambertus, Sanders, Stephan J, Murtha, Michael T, Hus, Vanessa, Lowe, Jennifer K, Willsey, A Jeremy, Moreno-De-Luca, Daniel, Yu, Timothy W, Fombonne, Eric, Geschwind, Daniel, Grice, Dorothy E, Ledbetter, David H, Lord, Catherine, Mane, Shrikant M, Martin, Christa Lese, Martin, Donna M, Morrow, Eric M, Walsh, Christopher A, Melhem, Nadine M, Chaste, Pauline, Sutcliffe, James S, State, Matthew W, Cook, Jr, Edwin H, Roeder, Kathryn, Devlin, Bernie

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Allelic Heterogeneity at the Serotonin Transporter Locus ( SLC6A4) Confers Susceptibility to Autism and Rigid-Compulsive Behaviors von Sutcliffe, James S., Delahanty, Ryan J., Prasad, Harish C., McCauley, Jacob L., Han, Qiao, Jiang, Lan, Li, Chun, Folstein, Susan E., Blakely, Randy D.

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Long COVID-19 and Peripheral Serotonin: A Commentary and Reconsideration von Anderson, George M, Cook, Edwin H, Blakely, Randy D, Sutcliffe, James S, Veenstra-VanderWeele, Jeremy

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A phenome‐wide association study of polygenic scores for attention deficit hyperactivity disorder across two genetic ancestries in electronic health record data von Niarchou, Maria, Sealock, Julia M., Straub, Peter, Sanchez‐Roige, Sandra, Sutcliffe, James S., Davis, Lea K.

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Analysis of CHRNA7 rare variants in autism spectrum disorder susceptibility von Bacchelli, Elena, Battaglia, Agatino, Cameli, Cinzia, Lomartire, Silvia, Tancredi, Raffaella, Thomson, Susanne, Sutcliffe, James S, Maestrini, Elena

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