A study of ontology-based risk management framework of construction projects through project life cycle von Tserng, H. Ping, Yin, Samuel Y.L., Dzeng, R.J., Wou, B., Tsai, M.D., Chen, W.Y.

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Whole-exome sequencing in the evaluation of fetal structural anomalies: a prospective cohort study von Petrovski, Slavé, Aggarwal, Vimla, Giordano, Jessica L, Stosic, Melissa, Wou, Karen, Bier, Louise, Spiegel, Erica, Brennan, Kelly, Stong, Nicholas, Jobanputra, Vaidehi, Ren, Zhong, Zhu, Xiaolin, Mebane, Caroline, Nahum, Odelia, Wang, Quanli, Kamalakaran, Sitharthan, Malone, Colin, Anyane-Yeboa, Kwame, Miller, Russell, Levy, Brynn, Goldstein, David B, Wapner, Ronald J

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Promises, pitfalls and practicalities of prenatal whole exome sequencing von Best, Sunayna, Wou, Karen, Vora, Neeta, Van der Veyver, Ignatia B., Wapner, Ronald, Chitty, Lyn S.

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The associations between the response efficacy and objective and subjective change in physical activity and diet in the Information and Risk Modification trial von Wou, C., Silarova, B., Griffin, S., Usher-Smith, J.A.

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Variants in STXBP3 are Associated with Very Early Onset Inflammatory Bowel Disease, Bilateral Sensorineural Hearing Loss and Immune Dysregulation von Ouahed, Jodie, Kelsen, Judith R, Spessott, Waldo A, Kooshesh, Kameron, Sanmillan, Maria L, Dawany, Noor, Sullivan, Kathleen E, Hamilton, Kathryn E, Slowik, Voytek, Nejentsev, Sergey, Neves, João Farela, Flores, Helena, Chung, Wendy K, Wilson, Ashley, Anyane-Yeboa, Kwame, Wou, Karen, Jain, Preti, Field, Michael, Tollefson, Sophia, Dent, Maiah H, Li, Dalin, Naito, Takeo, McGovern, Dermot P B, Kwong, Andrew C, Taliaferro, Faith, Ordovas-Montanes, Jose, Horwitz, Bruce H, Kotlarz, Daniel, Klein, Christoph, Evans, Jonathan, Dorsey, Jill, Warner, Neil, Elkadri, Abdul, Muise, Aleixo M, Goldsmith, Jeffrey, Thompson, Benjamin, Engelhardt, Karin R, Cant, Andrew J, Hambleton, Sophie, Barclay, Andrew, Toth-Petroczy, Agnes, Vuzman, Dana, Carmichael, Nikkola, Bodea, Corneliu, Cassa, Christopher A, Devoto, Marcella, Maas, Richard L, Behrens, Edward M, Giraudo, Claudio G, Snapper, Scott B

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Single cell and spatial transcriptomics highlight the interaction of club-like cells with immunosuppressive myeloid cells in prostate cancer von Kiviaho, Antti, Eerola, Sini K., Kallio, Heini M. L., Andersen, Maria K., Hoikka, Miina, Tiihonen, Aliisa M., Salonen, Iida, Spotbeen, Xander, Giesen, Alexander, Parker, Charles T. A., Taavitsainen, Sinja, Hantula, Olli, Marttinen, Mikael, Hermelo, Ismaïl, Ismail, Mazlina, Midtbust, Elise, Wess, Maximilian, Devlies, Wout, Sharma, Abhibhav, Krossa, Sebastian, Häkkinen, Tomi, Afyounian, Ebrahim, Vandereyken, Katy, Kint, Sam, Kesseli, Juha, Tolonen, Teemu, Tammela, Teuvo L. J., Viset, Trond, Størkersen, Øystein, Giskeødegård, Guro F., Rye, Morten B., Murtola, Teemu, Erickson, Andrew, Latonen, Leena, Bova, G. Steven, Mills, Ian G., Joniau, Steven, Swinnen, Johannes V., Voet, Thierry, Mirtti, Tuomas, Attard, Gerhardt, Claessens, Frank, Visakorpi, Tapio, Rautajoki, Kirsi J., Tessem, May-Britt, Urbanucci, Alfonso, Nykter, Matti

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Discovery of novel heart rate-associated loci using the Exome Chip von van den Berg, Marten E, Warren, Helen R, Cabrera, Claudia P, Verweij, Niek, Mifsud, Borbala, Haessler, Jeffrey, Bihlmeyer, Nathan A, Fu, Yi-Ping, Weiss, Stefan, Lin, Henry J, Grarup, Niels, Li-Gao, Ruifang, Pistis, Giorgio, Shah, Nabi, Brody, Jennifer A, Müller-Nurasyid, Martina, Lin, Honghuang, Mei, Hao, Smith, Albert V, Lyytikäinen, Leo-Pekka, Hall, Leanne M, van Setten, Jessica, Trompet, Stella, Prins, Bram P, Isaacs, Aaron, Radmanesh, Farid, Marten, Jonathan, Entwistle, Aiman, Kors, Jan A, Silva, Claudia T, Alonso, Alvaro, Bis, Joshua C, de Boer, Rudolf, de Haan, Hugoline G, de Mutsert, Renée, Dedoussis, George, Dominiczak, Anna F, Doney, Alex S F, Ellinor, Patrick T, Eppinga, Ruben N, Felix, Stephan B, Guo, Xiuqing, Hagemeijer, Yanick, Hansen, Torben, Harris, Tamara B, Heckbert, Susan R, Huang, Paul L, Hwang, Shih-Jen, Kähönen, Mika, Kanters, Jørgen K, Kolcic, Ivana, Launer, Lenore J, Li, Man, Yao, Jie, Linneberg, Allan, Liu, Simin, Macfarlane, Peter W, Mangino, Massimo, Morris, Andrew D, Mulas, Antonella, Murray, Alison D, Nelson, Christopher P, Orrú, Marco, Padmanabhan, Sandosh, Peters, Annette, Porteous, David J, Poulter, Neil, Psaty, Bruce M, Qi, Lihong, Raitakari, Olli T, Rivadeneira, Fernando, Roselli, Carolina, Rudan, Igor, Sattar, Naveed, Sever, Peter, Sinner, Moritz F, Soliman, Elsayed Z, Spector, Timothy D, Stanton, Alice V, Stirrups, Kathleen E, Taylor, Kent D, Tobin, Martin D, Uitterlinden, André, Vaartjes, Ilonca, Hoes, Arno W, van der Meer, Peter, Völker, Uwe, Waldenberger, Melanie, Xie, Zhijun, Zoledziewska, Magdalena, Tinker, Andrew, Polasek, Ozren, Rosand, Jonathan, Jamshidi, Yalda, van Duijn, Cornelia M, Zeggini, Eleftheria, Jukema, J Wouter, Asselbergs, Folkert W, Samani, Nilesh J, Lehtimäki, Terho

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Refining the phenotype associated with GNB1 mutations: Clinical data on 18 newly identified patients and review of the literature von Hemati, Parisa, Revah‐Politi, Anya, Bassan, Haim, Petrovski, Slavé, Bilancia, Colleen G., Ramsey, Keri, Griffin, Nicole G., Bier, Louise, Cho, Megan T., Rosello, Monica, Lynch, Sally Ann, Colombo, Sophie, Weber, Astrid, Haug, Marte, Heinzen, Erin L., Sands, Tristan T., Narayanan, Vinodh, Primiano, Michelle, Aggarwal, Vimla S., Millan, Francisca, Sattler‐Holtrop, Shannon G., Caro‐Llopis, Alfonso, Pillar, Nir, Baker, Janice, Freedman, Rebecca, Kroes, Hester Y., Sacharow, Stephanie, Stong, Nick, Lapunzina, Pablo, Schneider, Michael C., Mendelsohn, Nancy J., Singleton, Amanda, Loik Ramey, Valerie, Wou, Karen, Kuzminsky, Alla, Monfort, Sandra, Weisz Hubshman, Monika, Doyle, Samantha, Iglesias, Alejandro, Martinez, Francisco, Mckenzie, Fiona, Orellana, Carmen, Gassen, Koen L.I., Palomares, Maria, Bazak, Lily, Lee, Andy, Bircher, Ana, Basel‐Vanagaite, Lina, Hafström, Maria, Houge, Gunnar, Goldstein, David B., Anyane‐Yeboa, Kwame

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Sa2008 - Mutations in Stxbp3 Contribute to Very Early Onset of IBD Immunodeficieny and Hearing Loss von Kelsen, Judith R., Ouahed, Jodie, Spessott, Waldo, Kooshesh, Kameron, Sanmillan, Maria, Dawany, Noor, Sullivan, Kathleen E., Hamilton, Kathryn E., Slowik, Voyteck, Nejentsev, Sergey, Neves, João Farela, Flores, Helena, Chung, Wendy, Wilson, Ashley, Yeboa, Kwame Anyane, Wou, Karen, Jain, Preti, Tollefson, Sophia, Evans, Jonathan S., Warner, Neil E., Muise, Aleixo, Toth-Petroczy, Agnes, Vuzman, Dana, Carmichael, Nikkola, Bodea, Corneliu, Cassa, Christopher, Devoto, Marcella, Mass, Richard, Behrens, Edward, Snapper, Scott B., Giraudo, Claudio

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A prevalent variant in PPP1R3A impairs glycogen synthesis and reduces muscle glycogen content in humans and mice von Savage, David B, Zhai, Lanmin, Ravikumar, Balasubramanian, Choi, Cheol Soo, Snaar, Johanna E, McGuire, Amanda C, Wou, Sung-Eun, Medina-Gomez, Gemma, Kim, Sheene, Bock, Cheryl B, Segvich, Dyann M, Solanky, Bhavana, Deelchand, Dinesh, Vidal-Puig, Antonio, Wareham, Nicholas J, Shulman, Gerald I, Karpe, Fredrik, Taylor, Roy, Pederson, Bartholomew A, Roach, Peter J, O'Rahilly, Stephen, DePaoli-Roach, Anna A

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Whole exome sequencing identifies a homozygous POLG2 missense variant in an infant with fulminant hepatic failure and mitochondrial DNA depletion von Varma, Hemant, Faust, Phyllis L, Iglesias, Alejandro D, Lagana, Stephen M, Wou, Karen, Hirano, Michio, DiMauro, Salvatore, Mansukani, Mahesh M, Hoff, Kirsten E, Nagy, Peter L, Copeland, William C, Naini, Ali B

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25 MUTATIONS IN STXBP3 CONTRIBUTE TO VERY EARLY ONSET OF IBD, IMMUNODEFICIENCY AND HEARING LOSS von Kelsen, Judith R., Ouahed, Jodie, Spessott, Waldo A., Kooshesh, Kameron, Sanmillan, Maria L., Dawany, Noor, Sullivan, Kathleen E., Hamilton, Kathryn, Slowik, Voytek, Nejentsev, Sergey, Farela Neves, João, Flores, Helena, Chung, Wendy K., Wilson, Ashley, Yeboa, Kwame Anyane, Wou, Karen, Jain, Preti, Tollefson, Sophia, Evans, Jonathan, Warner, Neil, Muise, Alexio, Goldsmith, Jeffrey, Toth-Petroczy, Agnes, Vuzman, Dana, Carmichael, Nikkola, Bodea, Corneliu, Cassa, Christopher, Devoto, Marcella, Maas, Richard L., Behrens, Edward M., Snapper, Scott B., Giraudo, Claudio G.

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25 MUTATIONS IN STXBP3 CONTRIBUTE TO VERY EARLY ONSET OF IBD, IMMUNODEFICIENCY AND HEARING LOSS von Kelsen, Judith R, Ouahed, Jodie, Spessott, Waldo A, Kooshesh, Kameron, Sanmillan, Maria L, Dawany, Noor, Sullivan, Kathleen E, Hamilton, Kathryn, Slowik, Voytek, Nejentsev, Sergey, Neves, João Farela, Flores, Helena, Chung, Wendy K, Wilson, Ashley, Yeboa, Kwame Anyane, Wou, Karen, Jain, Preti, Tollefson, Sophia, Evans, Jonathan, Warner, Neil, Muise, Alexio, Goldsmith, Jeffrey, Toth-Petroczy, Agnes, Vuzman, Dana, Carmichael, Nikkola, Bodea, Corneliu, Cassa, Christopher, Devoto, Marcella, Maas, Richard L, Behrens, Edward M, Snapper, Scott B, Giraudo, Claudio G

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Correction: a prevalent variant in PPP1R3A impairs glycogen synthesis and reduces muscle glycogen content in humans and mice von Savage, David B, Zhai, Lanmin, Ravikumar, Balasubramanian, Choi, Cheol Soo, Snaar, Johanna E, McGuire, Amanda C, Wou, Sung-Eun, Medina-Gomez, Gemma, Kim, Sheene, Bock, Cheryl B, Segvich, Dyann M, Solanky, Bhavana, Deelchand, Dinesh, Vidal-Puig, Antonio, Wareham, Nicholas J, Shulman, Gerald I, Karpe, Fredrik, Taylor, Roy, Pederson, Bartholomew A, Roach, Peter J, O'Rahilly, Stephen, DePaoli-Roach, Anna A

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Interleukin‐10 haplotype associated with total serum IgE in atopic dermatitis patients von Shin, H. D., Park, B. L., Kim, L. H., Kim, J.‐S., Kim, J.‐W.

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Successful treatment of Vulvar Bowen's disease with topical imiquimod 5% cream von Kim, Yeon Jeong, Kim, Jin Wou, Koh, Bo Kyung

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Correction: A Prevalent Variant in Impairs Glycogen Synthesis and Reduces Muscle Glycogen Content in Humans and Mice von David B Savage, Lanmin Zhai, Balasubramanian Ravikumar, Cheol Soo Choi, Johanna E Snaar, Amanda C McGuire, Sung-Eun Wou, Gemma Medina-Gomez, Sheene Kim, Cheryl B Bock, Dyann M Segvich, Bhavana Solanky, Dinesh Deelchand, Antonio Vidal-Puig, Nicholas J Wareham, Gerald I Shulman, Fredrik Karpe, Roy Taylor, Bartholomew A Pederson, Peter J Roach, Stephen O'Rahilly, Anna A DePaoli-Roach

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Correction: A Prevalent Variant in PPP1R3A Impairs Glycogen Synthesis and Reduces Muscle Glycogen Content in Humans and Mice von Savage, David B, Zhai, Lanmin, Ravikumar, Balasubramanian, Choi, Cheol Soo, Snaar, Johanna E, McGuire, Amanda C, Wou, Sung-Eun, Medina-Gomez, Gemma, Kim, Sheene, Bock, Cheryl B, Segvich, Dyann M, Solanky, Bhavana, Deelchand, Dinesh, Vidal-Puig, Antonio, Wareham, Nicholas J, Shulman, Gerald I, Karpe, Fredrik, Taylor, Roy, Pederson, Bartholomew A, Roach, Peter J, O'Rahilly, Stephen, DePaoli-Roach, Anna A

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Solitary premature sebaceous hyperplasia associated with acneiform eruption von Choi, Moon Jung, Kim, Jin Wou, Koh, Bo Kyung

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Effect of Dispersion on the Coloring Properties of Aluminum Dye Lakes von Wou, Lyndon L.-S., Mulley, B.A.

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