HIGH FLOW DEEPSET INSERT SAFETY VALVE von VICK, JR, KHANOUKI, Hadi Arabnejad, GASSEN, Matthew

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Metal to metal tubular connection with controlled support structure von Jason Lee Peacock, Anthony Phan, Matthew Gassen, James Dan Vick Jr

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Metal to metal tubular connection with controlled support structure von Jason Lee Peacock, Anthony Phan, Matthew Gassen, JR., James Dan Vick

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HIGH FLOW DEEPSET INSERT SAFETY VALVE von MATTHEW GASSEN, HADI ARABNEJAD KHANOUKI, JAMES DAN JR. VICK

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High Flow Deepset Insert Safety Valve von Vick, JR., James Dan, Khanouki, Hadi Arabnejad, Gassen, Matthew

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METAL TO METAL TUBULAR CONNECTION WITH CONTROLLED SUPPORT STRUCTURE von PHAN, ANTHONY, VICK JR, JAMES DAN, PEACOCK, JASON LEE, GASSEN, MATTHEW

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Metal to metal tubular connection with controlled support structure von Phan, Anthony, Peacock, Jason Lee, Vick, Jr., James Dan, Gassen, Matthew

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Metal To Metal Tubular Connection With Controlled Support Structure von Phan, Anthony, Vick, JR., James Dan, Peacock, Jason Lee, Gassen, Matthew

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METAL TO METAL TUBULAR CONNECTION WITH CONTROLLED SUPPORT STRUCTURE von VICK, JR, PHAN, Anthony, PEACOCK, Jason Lee, GASSEN, Matthew

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SOUPAPE DE SÉCURITÉ À INSERT PROFONDE À HAUT DÉBIT von VICK Jr., James Dan, KHANOUKI, Hadi Arabnejad, GASSEN, Matthew

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Connexion tubulaire métal sur métal avec structure de support contrôlée von PHAN, Anthony, VICK, James Dan, PEACOCK, Jason Lee, GASSEN, Matthew

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Mutations in SPATA5 Are Associated with Microcephaly, Intellectual Disability, Seizures, and Hearing Loss von Tanaka, Akemi J., Cho, Megan T., Millan, Francisca, Juusola, Jane, Retterer, Kyle, Joshi, Charuta, Niyazov, Dmitriy, Garnica, Adolfo, Gratz, Edward, Deardorff, Matthew, Wilkins, Alisha, Ortiz-Gonzalez, Xilma, Mathews, Katherine, Panzer, Karin, Brilstra, Eva, van Gassen, Koen L.I., Volker-Touw, Catharina M.L., van Binsbergen, Ellen, Sobreira, Nara, Hamosh, Ada, McKnight, Dianalee, Monaghan, Kristin G., Chung, Wendy K.

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Single-Nucleus Transcriptome Profiling of Dorsolateral Prefrontal Cortex: Mechanistic Roles for Neuronal Gene Expression, Including the 17q21.31 Locus, in PTSD Stress Response von Chatzinakos, Chris, Pernia, Cameron D, Morrison, Filomene G, Iatrou, Artemis, McCullough, Kenneth M, Schuler, Heike, Snijders, Clara, Bajaj, Thomas, DiPietro, Christopher P, Soliva Estruch, Marina, Gassen, Nils C, Anastasopoulos, Constantin, Bharadwaj, Rahul A, Bowlby, Benjamin C, Hartmann, Jakob, Maihofer, Adam X, Nievergelt, Caroline M, Ressler, Nicholas M, Wolf, Erika J, Carlezon, Jr, William A, Krystal, John H, Kleinman, Joel E, Girgenti, Matthew J, Huber, Bertrand R, Kellis, Manolis, Logue, Mark W, Miller, Mark W, Ressler, Kerry J, Daskalakis, Nikolaos P

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Biallelic variants in CSMD1 are implicated in a neurodevelopmental disorder with intellectual disability and variable cortical malformations von Werren, Elizabeth A., Peirent, Emily R., Jantti, Henna, Guxholli, Alba, Srivastava, Kinshuk Raj, Orenstein, Naama, Narayanan, Vinodh, Wiszniewski, Wojciech, Dawidziuk, Mateusz, Gawlinski, Pawel, Umair, Muhammad, Khan, Amjad, Khan, Shahid Niaz, Geneviève, David, Lehalle, Daphné, van Gassen, K. L. I., Giltay, Jacques C., Oegema, Renske, van Jaarsveld, Richard H., Rafiullah, Rafiullah, Rappold, Gudrun A., Rabin, Rachel, Pappas, John G., Wheeler, Marsha M., Bamshad, Michael J., Tsan, Yao-Chang, Johnson, Matthew B., Keegan, Catherine E., Srivastava, Anshika, Bielas, Stephanie L.

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B56δ-related protein phosphatase 2A dysfunction identified in patients with intellectual disability von Houge, Gunnar, Haesen, Dorien, Vissers, Lisenka E L M, Mehta, Sarju, Parker, Michael J, Wright, Michael, Vogt, Julie, McKee, Shane, Tolmie, John L, Cordeiro, Nuno, Kleefstra, Tjitske, Willemsen, Marjolein H, Reijnders, Margot R F, Berland, Siren, Hayman, Eli, Lahat, Eli, Brilstra, Eva H, van Gassen, Koen L I, Zonneveld-Huijssoon, Evelien, de Bie, Charlotte I, Hoischen, Alexander, Eichler, Evan E, Holdhus, Rita, Steen, Vidar M, Døskeland, Stein Ove, Hurles, Matthew E, FitzPatrick, David R, Janssens, Veerle

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De novo substitutions of TRPM3 cause intellectual disability and epilepsy von Dyment, David A, Terhal, Paulien A, Rustad, Cecilie F, Tveten, Kristian, Griffith, Christopher, Jayakar, Parul, Shinawi, Marwan, Ellingwood, Sara, Smith, Rosemarie, van Gassen, Koen, McWalter, Kirsty, Innes, A Micheil, Lines, Matthew A

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De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual Disability von Küry, Sébastien, van Woerden, Geeske M., Besnard, Thomas, Proietti Onori, Martina, Latypova, Xénia, Towne, Meghan C., Cho, Megan T., Ploeg, Melissa A., Sanders, Stephan, Stessman, Holly A.F., Pujol, Aurora, Distel, Ben, Robak, Laurie A., Bernstein, Jonathan A., Denommé-Pichon, Anne-Sophie, Lesca, Gaëtan, Sellars, Elizabeth A., Berg, Jonathan, Carré, Wilfrid, Busk, Øyvind Løvold, van Bon, Bregje W.M., Waugh, Jeff L., Deardorff, Matthew, Hoganson, George E., Bosanko, Katherine B., Johnson, Diana S., Dabir, Tabib, Holla, Øystein Lunde, Sarkar, Ajoy, Tveten, Kristian, de Bellescize, Julitta, Braathen, Geir J., Terhal, Paulien A., Grange, Dorothy K., van Haeringen, Arie, Lam, Christina, Mirzaa, Ghayda, Burton, Jennifer, Bhoj, Elizabeth J., Douglas, Jessica, Santani, Avni B., Nesbitt, Addie I., Helbig, Katherine L., Andrews, Marisa V., Begtrup, Amber, Tang, Sha, van Gassen, Koen L.I., Juusola, Jane, Foss, Kimberly, Enns, Gregory M., Moog, Ute, Hinderhofer, Katrin, Paramasivam, Nagarajan, Lincoln, Sharyn, Kusako, Brandon H., Lindenbaum, Pierre, Charpentier, Eric, Nowak, Catherine B., Cherot, Elouan, Simonet, Thomas, Ruivenkamp, Claudia A.L., Hahn, Sihoun, Brownstein, Catherine A., Xia, Fan, Schmitt, Sébastien, Deb, Wallid, Bonneau, Dominique, Nizon, Mathilde, Chelly, Jamel, Rudolf, Gabrielle, Sanlaville, Damien, Parent, Philippe, Gilbert-Dussardier, Brigitte, Toutain, Annick, Sutton, Vernon R., Thies, Jenny, Peart-Vissers, Lisenka E.L.M., Boisseau, Pierre, Vincent, Marie, Grabrucker, Andreas M., Dubourg, Christèle, Tan, Wen-Hann, Verbeek, Nienke E., Granzow, Martin, Santen, Gijs W.E., Shendure, Jay, Pasquier, Laurent, Redon, Richard, Yang, Yaping, State, Matthew W., Kleefstra, Tjitske, Cogné, Benjamin, Petrovski, Slavé, Retterer, Kyle, Eichler, Evan E., Rosenfeld, Jill A., Agrawal, Pankaj B., Bézieau, Stéphane, Odent, Sylvie, Mercier, Sandra

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De Novo Mutations in YWHAG Cause Early-Onset Epilepsy von Guella, Ilaria, McKenzie, Marna B., Evans, Daniel M., Buerki, Sarah E., Toyota, Eric B., Van Allen, Margot I., Adam, Shelin, Boelman, Cyrus, Bolbocean, Corneliu, Candido, Tara, Eydoux, Patrice, Horvath, Gabriella, Huh, Linda, Nelson, Tanya N., Sinclair, Graham, van Karnebeek, Clara, Vercauteren, Suzanne, Suri, Mohnish, Elmslie, Frances, Simon, Marleen E.H., van Gassen, Koen L.I., Héron, Delphine, Keren, Boris, Nava, Caroline, Connolly, Mary B., Demos, Michelle, Farrer, Matthew J.

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A multi-site study of the relationship between photoperiod and ovulation rate using Natural Cycles data von Shanmugam, Divya, Espinosa, Matthew, Gassen, Jeffrey, van Lamsweerde, Agathe, Pearson, Jack T., Benhar, Eleonora, Hill, Sarah

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A genetic variant of fatty acid amide hydrolase (FAAH) exacerbates hormone-mediated orexigenic feeding in mice von Balsevich, Georgia, Petrie, Gavin N, Heinz, Daniel E, Singh, Arashdeep, Aukema, Robert J, Hunker, Avery C, Vecchiarelli, Haley A, Yau, Hiulan, Sticht, Martin, Thompson, Roger J, Lee, Francis S, Zweifel, Larry S, Chelikani, Prasanth K, Gassen, Nils C, Hill, Matthew N

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