GIS based approach to analyze soil liquefaction and amplification: A case study in Eskisehir, Turkey von Okur, Volkan

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Dynamic Properties of Clean Sand Modified with Granulated Rubber von Okur, Volkan, Umu, Seyfettin Umut

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Clinical and genomic characterization of 8p cytogenomic disorders von Okur, Volkan, Hamm, Laura, Kavus, Haluk, Mebane, Caroline, Robinson, Scott, Levy, Brynn, Chung, Wendy K.

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Dynamic Behavior of Soft Subgrade Soils Treated with Boron Waste von Okur, Volkan, Akinci, Kubra

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De novo variants in HK1 associated with neurodevelopmental abnormalities and visual impairment von Okur, Volkan, Cho, Megan T, van Wijk, Richard, van Oirschot, Brigitte, Picker, Jonathan, Coury, Stephanie A, Grange, Dorothy, Manwaring, Linda, Krantz, Ian, Muraresku, Colleen Clark, Hulick, Peter J, May, Holley, Pierce, Eric, Place, Emily, Bujakowska, Kinga, Telegrafi, Aida, Douglas, Ganka, Monaghan, Kristin G, Begtrup, Amber, Wilson, Ashley, Retterer, Kyle, Anyane-Yeboa, Kwame, Chung, Wendy K

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Predictive functional, statistical and structural analysis of CSNK2A1 and CSNK2B variants linked to neurodevelopmental diseases von Unni, Prasida, Friend, Jack, Weinberg, Janice, Okur, Volkan, Hochscherf, Jennifer, Dominguez, Isabel

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A Study on the Rheological Properties of Recycled Rubber-Modified Asphalt Mixtures von Karacasu, Murat, Er, Arzu, Okur, Volkan

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P775: Maternally inherited 11p15 duplication involving only part of the ICR1 H19/IGF2 domain: Unraveling mild Russell-Silver syndrome phenotype von Thomas-Wilson, Amanda, Harkavy, Nina, Schwanke, Corbin, Schoof, Jonathan, Srinivasa, Sowmya Thirumalai, Guha, Saurav, Rehman, Atteeq, Okur, Volkan, Giordano, Jessica, Elias, Abdallah, Wapner, Ronald, Jobanputra, Vaidehi

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P764: RNA sequencing improves assessment of variants of uncertain significance from fetal genome and exome sequencing von Rehman, Atteeq, Thomas-Wilson, Amanda, Mau-Them, Frederic Tran, Tolusso, Leandra, Abyankar, Avinash, Guha, Saurav, Okur, Volkan, Felice, Vanessa, Hopkin, Robert, Wilson, Ashley, Han, Ted, Guan, Qiaoning, Giordano, Jessica, Bréhin, Anne-Claire, Wapner, Ronald, Jobanputra, Vaidehi

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O44: Genome sequencing as a first-tier prenatal diagnostic test von Jobanputra, Vaidehi, Giordano, Jessica, Pervola, Josie, Wilson, Ashley, Guha, Saurav, Thomas-Wilson, Amanda, Rehman, Atteeq, Okur, Volkan, Han, Ted, Esteves, Cecilia, Tinfow, Alexandra, Galloway, Stephanie, Srinivasa, Sowmya T., Khan, Shahid, Brace, Poppy, Nava, Caroline, Perrin, Hannah, Elder, Bruce, Hegedus, Endre, Felice, Vanessa, Phadke, Shruti, Abhyankar, Avinash, Wapner, Ronald

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P780: Improving peripartum health is an unappreciated advantage of prenatal genome sequencing von Giordano, Jessica, Pervola, Josie, Wilson, Ashley, Rehman, Atteeq, Thomas-Wilson, Amanda, Guha, Saurav, Okur, Volkan, Tinfow, Alexandra, Galloway, Stephanie, Perrin, Hannah, Esteves, Cecilia, Brace, Poppy, Baptiste, Caitlin, Srinivasa, Sowmya Thirumalai, Khan, Shahid, Elder, Bruce, Hegedus, Endre, Felice, Vanessa, Phadke, Shruti, Abhyankar, Avinash, Jobanputra, Vaidehi, Wapner, Ronald

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P589: Diagnostic yield of digital gene panel from genome sequencing in common multifactorial endocrine and metabolic disorders von Okur, Volkan, Srinivasa, Sowmya Thirumalai, Halstrom, Amanda, Falcone, John, Rehman, Atteeq, Thomas-Wilson, Amanda, Guha, Saurav, Phadke, Shruti, Abhyankar, Avinash, Wilson, Ashley, Nava, Caroline, Khan, Shahid, Hurd, Maurice, Stewart, Sarah, Claudio, Katerine, Jablonski, Anne, Manohar, Jyothi, Kumar, Sonal, Yeung, Michele, Dakin, Gregory, Bellorin-Marin, Omar, Afaneh, Cheguevara, Hudgins, Lisa, Pena, Jessica, Wei, Esther, Gingras, Laura, King, Alexandra, Tung, Judy, Chen, Shuibing, Smith, Ryan, MacDonald, Theresa, Ritter, Megan, Alonso, Lauro, Elemento, Olivier, Udler, Miriam, Goncalves, Marcus, Jobanputra, Vaidehi

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De novo variants in H3-3A and H3-3B are associated with neurodevelopmental delay, dysmorphic features, and structural brain abnormalities von Okur, Volkan, Chen, Zefu, Vossaert, Liesbeth, Peacock, Sandra, Rosenfeld, Jill, Zhao, Lina, Du, Haowei, Calamaro, Emily, Gerard, Amanda, Zhao, Sen, Kelsay, Jill, Lahr, Ashley, Mighton, Chloe, Porter, Hillary M., Siemon, Amy, Silver, Josh, Svihovec, Shayna, Fong, Chin-To, Grant, Christina L., Lerner-Ellis, Jordan, Manickam, Kandamurugu, Madan-Khetarpal, Suneeta, McCandless, Shawn E., Morel, Chantal F., Schaefer, G. Bradley, Berry-Kravis, Elizabeth M., Gates, Ryan, Gomez-Ospina, Natalia, Qiu, Guixing, Zhang, Terry Jianguo, Wu, Zhihong, Meng, Linyan, Liu, Pengfei, Scott, Daryl A., Lupski, James R., Eng, Christine M., Wu, Nan, Yuan, Bo

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A study of the local site effects on the ground response for the city of Eskişehir, Turkey von Ci̇velekler, Ebru, Okur, Volkan D., Afacan, Kamil B.

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Early-Onset Parkinsonism Is a Manifestation of thePPP2R5Dp.E200KMutation von Kim, Christine Y., Wirth, Thomas, Hubsch, Cecile, Nemeth, Andrea H., Okur, Volkan, Anheim, Mathieu, Drouot, Nathalie, Tranchant, Christine, Rudolf, Gabrielle, Chelly, Jamel, Tatton-Brown, Katrina, Blauwendraat, Cornelis, Vonsattel, Jean Paul G., Cortes, Etty, Alcalay, Roy N., Chung, Wendy K.

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Early‐Onset Parkinsonism Is a Manifestation of the PPP2R5D p.E200K Mutation von Kim, Christine Y., Wirth, Thomas, Hubsch, Cécile, Németh, Andrea H., Okur, Volkan, Anheim, Mathieu, Drouot, Nathalie, Tranchant, Christine, Rudolf, Gabrielle, Chelly, Jamel, Tatton‐Brown, Katrina, Blauwendraat, Cornelis, Vonsattel, Jean Paul G., Cortes, Etty, Alcalay, Roy N., Chung, Wendy K.

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The impact of hereditary cancer gene panels on clinical care and lessons learned von Okur, Volkan, Chung, Wendy K

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Pulmonary hypertension in patients with 9q34.3 microdeletion‐associated Kleefstra syndrome von Okur, Volkan, Nees, Shannon, Chung, Wendy K., Krishnan, Usha

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Neuropathological Findings in a Case of Parkinsonism and Developmental Delay Associated with a Monoallelic Variant in PLXNA1 von O'Shea, Sarah A., Hickman, Richard A., Cortes, Etty, Vonsattel, Jean Paul, Fahn, Stanley, Okur, Volkan, Alcalay, Roy N., Chung, Wendy K.

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Recessive Rare Variants in Deoxyhypusine Synthase, an Enzyme Involved in the Synthesis of Hypusine, Are Associated with a Neurodevelopmental Disorder von Ganapathi, Mythily, Padgett, Leah R., Yamada, Kentaro, Devinsky, Orrin, Willaert, Rebecca, Person, Richard, Au, Ping-Yee Billie, Tagoe, Julia, McDonald, Marie, Karlowicz, Danielle, Wolf, Barry, Lee, Joanna, Shen, Yufeng, Okur, Volkan, Deng, Liyong, LeDuc, Charles A., Wang, Jiayao, Hanner, Ashleigh, Mirmira, Raghavendra G., Park, Myung Hee, Mastracci, Teresa L., Chung, Wendy K.

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