Discovery of delta Scuti variables in eclipsing binary systems II. Southern TESS field search von Kahraman Aliçavuş, F, Çoban, Ç G, Çelik, E, Dogan, D S, Ekinci, O, Aliçavuş, F

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Single-lined eclipsing binaries with δ Scuti components: GQ Dra, RR Lep, and TYC 683-640-1 von Kahraman Aliçavuş, F, Aliçavuş, F, Çoban, Ç G, Handler, G, De Cat, P

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Photometry of GS UMa: a suspected {delta} Scuti variable von Kahraman Aliçavus, F., Raheem, A., Çoban, G. Ç., Tambulut, E. M., Gögülter, Ü., Bas, L., Çevirici, B.

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Discovery of Delta Scuti variables in eclipsing binary systems II.Southern TESS field search von F Kahraman Alicavus, Coban, G C, Celik, E, Dogan, D S, Ekinci, O, Alicavus, F

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Anthropogenic food resources foster the coexistence of distinct life history strategies: year-round sedentary and migratory brown bears von Cozzi, G., Chynoweth, M., Kusak, J., Çoban, E., Çoban, A., Ozgul, A., Şekercioğlu, Ç. H.

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A comprehensive study on narcissus tazetta subsp. tazetta L.: Chemo-profiling, isolation, anticholinesterase activity and molecular docking of amaryllidaceae alkaloids von Karakoyun, Ç., Bozkurt, B., Çoban, G., Masi, M., Cimmino, A., Evidente, A., Unver Somer, N.

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Insights into genetics, human biology and disease gleaned from family based genomic studies von Posey, Jennifer E., O’Donnell-Luria, Anne H., Chong, Jessica X., Harel, Tamar, Jhangiani, Shalini N., Coban Akdemir, Zeynep H., Buyske, Steven, Pehlivan, Davut, Carvalho, Claudia M. B., Baxter, Samantha, Sobreira, Nara, Liu, Pengfei, Wu, Nan, Rosenfeld, Jill A., Kumar, Sushant, Avramopoulos, Dimitri, White, Janson J., Doheny, Kimberly F., Witmer, P. Dane, Boehm, Corinne, Sutton, V. Reid, Muzny, Donna M., Boerwinkle, Eric, Günel, Murat, Nickerson, Deborah A., Mane, Shrikant, MacArthur, Daniel G., Gibbs, Richard A., Hamosh, Ada, Lifton, Richard P., Matise, Tara C., Rehm, Heidi L., Gerstein, Mark, Bamshad, Michael J., Valle, David, Lupski, James R.

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Absent B cells, agammaglobulinemia, and hypertrophic cardiomyopathy in folliculin-interacting protein 1 deficiency von Saettini, Francesco, Poli, Cecilia, Vengoechea, Jaime, Bonanomi, Sonia, Orellana, Julio C., Fazio, Grazia, Rodriguez, Fred H., Noguera, Loreani P., Booth, Claire, Jarur-Chamy, Valentina, Shams, Marissa, Iascone, Maria, Vukic, Maja, Gasperini, Serena, Quadri, Manuel, Barroeta Seijas, Amairelys, Rivers, Elizabeth, Mauri, Mario, Badolato, Raffaele, Cazzaniga, Gianni, Bugarin, Cristina, Gaipa, Giuseppe, Kroes, Wilma G.M., Moratto, Daniele, van Oostaijen-ten Dam, Monique M., Baas, Frank, van der Maarel, Silvère, Piazza, Rocco, Coban-Akdemir, Zeynep H., Lupski, James R., Yuan, Bo, Chinn, Ivan K., Daxinger, Lucia, Biondi, Andrea

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Synthesis and Antioxidant Properties of Novel Benzimidazole Derivatives von Ayhan-Kilcigil, Gülgün, Kus, Canan, Çoban, Tülay, Can-Eke, Benay, Iscan, Mumtaz

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Biallelic pathogenic variants in roundabout guidance receptor 1 associate with syndromic congenital anomalies of the kidney and urinary tract von Münch, Johannes, Engesser, Marie, Schönauer, Ria, Hamm, J. Austin, Hartig, Christin, Hantmann, Elena, Akay, Gulsen, Pehlivan, Davut, Mitani, Tadahiro, Coban Akdemir, Zeynep, Tüysüz, Beyhan, Shirakawa, Toshihiko, Dateki, Sumito, Claus, Laura R., van Eerde, Albertien M., Smol, Thomas, Devisme, Louise, Franquet, Hélène, Attié-Bitach, Tania, Wagner, Timo, Bergmann, Carsten, Höhn, Anne Kathrin, Shril, Shirlee, Pollack, Ari, Wenger, Tara, Scott, Abbey A., Paolucci, Sarah, Buchan, Jillian, Gabriel, George C., Posey, Jennifer E., Lupski, James R., Petit, Florence, McCarthy, Andrew A., Pazour, Gregory J., Lo, Cecilia W., Popp, Bernt, Halbritter, Jan

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Twelve-year trends in the prevalence and risk factors of diabetes and prediabetes in Turkish adults von Satman, Ilhan, Omer, Beyhan, Tutuncu, Yildiz, Kalaca, Sibel, Gedik, Selda, Dinccag, Nevin, Karsidag, Kubilay, Genc, Sema, Telci, Aysegul, Canbaz, Bulent, Turker, Fulya, Yilmaz, Temel, Cakir, Bekir, Tuomilehto, Jaakko

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A Toll-like receptor-independent antiviral response induced by double-stranded B-form DNA von Akira, Shizuo, Ishii, Ken J, Coban, Cevayir, Kato, Hiroki, Takahashi, Ken, Torii, Yuichi, Takeshita, Fumihiko, Ludwig, Holger, Sutter, Gerd, Suzuki, Koichi, Hemmi, Hiroaki, Sato, Shintaro, Yamamoto, Masahiro, Uematsu, Satoshi, Kawai, Taro, Takeuchi, Osamu

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Computer-Aided Detection Improves Adenomas per Colonoscopy for Screening and Surveillance Colonoscopy: A Randomized Trial von Shaukat, Aasma, Lichtenstein, David R., Somers, Samuel C., Chung, Daniel C., Perdue, David G., Gopal, Murali, Colucci, Daniel R., Phillips, Sloane A., Marka, Nicholas A., Church, Timothy R., Brugge, William R., Thompson, Robert, Chehade, Robert, Loew, Burr, Downing, Jackie, Vermillion, James, Borges, Lawrence, Rajbhandari, Ruma, Schafer, Theodore, Coban, Sahin, Richter, James, Carolan, Peter, Colizzo, Francis, Jeong, Tiffany, DelSignore, Marisa, Asher, Shreya, McCabe, Robert, Van Handel, Daniel, Cinnor, Birtukan, Mitlyng, Benjamin, Sherman, Cynthia, Feldshon, S. David, Lounsbury, Amy, Thompson, Ana, Duggirala, Anusha, Davies, Irena, Huang, Christopher, Bliss, Charles, Mohanty, Arpan, Sina, Oltion, Mendez, Jean, Iwan, Allison, Stromberg, Jennifer, Ng, Jonathan, Erisson, Lavi, Golland, Polina, Wang, Daniel, Wlodkowski, Evan, Carlin, Joseph, Javia, Perikumar, Chavali, Neelima, Wang, Austin, Little, Janine, Hunsberger, Cara

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Controlling genetic heterogeneity in gene-edited hematopoietic stem cells by single-cell expansion von Becker, Hans Jiro, Ishida, Reiko, Wilkinson, Adam C., Kimura, Takaharu, Lee, Michelle Sue Jann, Coban, Cevayir, Ota, Yasunori, Tanaka, Yosuke, Roskamp, Meike, Sano, Tsubasa, Tojo, Arinobu, Kent, David G., Yamazaki, Satoshi

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Biallelic loss-of-function variants in the splicing regulator NSRP1 cause a severe neurodevelopmental disorder with spastic cerebral palsy and epilepsy von Calame, Daniel G., Bakhtiari, Somayeh, Logan, Rachel, Coban-Akdemir, Zeynep, Du, Haowei, Mitani, Tadahiro, Fatih, Jawid M., Hunter, Jill V., Herman, Isabella, Pehlivan, Davut, Jhangiani, Shalini N., Person, Richard, Schnur, Rhonda E., Jin, Sheng Chih, Bilguvar, Kaya, Posey, Jennifer E., Koh, Sookyong, Firouzabadi, Saghar G., Alehabib, Elham, Tafakhori, Abbas, Esmkhani, Sahra, Gibbs, Richard A., Noureldeen, Mahmoud M., Zaki, Maha S., Marafi, Dana, Darvish, Hossein, Kruer, Michael C., Lupski, James R.

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Bi-allelic CCDC47 Variants Cause a Disorder Characterized by Woolly Hair, Liver Dysfunction, Dysmorphic Features, and Global Developmental Delay von Morimoto, Marie, Waller-Evans, Helen, Ammous, Zineb, Song, Xiaofei, Strauss, Kevin A., Pehlivan, Davut, Gonzaga-Jauregui, Claudia, Puffenberger, Erik G., Holst, Charles R., Karaca, Ender, Brigatti, Karlla W., Maguire, Emily, Coban-Akdemir, Zeynep H., Amagata, Akiko, Lau, C. Christopher, Chepa-Lotrea, Xenia, Macnamara, Ellen, Tos, Tulay, Isikay, Sedat, Nehrebecky, Michele, Overton, John D., Klein, Matthew, Markello, Thomas C., Posey, Jennifer E., Adams, David R., Lloyd-Evans, Emyr, Lupski, James R., Gahl, William A., Malicdan, May Christine V.

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P578 CDST (Clinical Decision Support Tool) is predictive of steroid-free clinical remission in patients with Crohn's disease treated with vedolizumab in a specific manner which is... von Buisson, A, Nancey, S, Dodel, M, Gay, C, Coban, D, Bazoge, M, Pereira, B, Boschetti, G

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High prevalence of multilocus pathogenic variation in neurodevelopmental disorders in the Turkish population von Mitani, Tadahiro, Isikay, Sedat, Gezdirici, Alper, Gulec, Elif Yilmaz, Punetha, Jaya, Fatih, Jawid M., Herman, Isabella, Akay, Gulsen, Du, Haowei, Calame, Daniel G., Ayaz, Akif, Tos, Tulay, Yesil, Gozde, Aydin, Hatip, Geckinli, Bilgen, Elcioglu, Nursel, Candan, Sukru, Sezer, Ozlem, Erdem, Haktan Bagis, Gul, Davut, Demiral, Emine, Elmas, Muhsin, Yesilbas, Osman, Kilic, Betul, Gungor, Serdal, Ceylan, Ahmet C., Bozdogan, Sevcan, Ozalp, Ozge, Cicek, Salih, Aslan, Huseyin, Yalcintepe, Sinem, Topcu, Vehap, Bayram, Yavuz, Grochowski, Christopher M., Jolly, Angad, Dawood, Moez, Duan, Ruizhi, Jhangiani, Shalini N., Doddapaneni, Harsha, Hu, Jianhong, Muzny, Donna M., Marafi, Dana, Akdemir, Zeynep Coban, Karaca, Ender, Carvalho, Claudia M.B., Gibbs, Richard A., Posey, Jennifer E., Lupski, James R., Pehlivan, Davut

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Elucidating the clinical spectrum and molecular basis of HYAL2 deficiency von Fasham, James, Lin, Siying, Ghosh, Promita, Radio, Francesca Clementina, Farrow, Emily G., Thiffault, Isabelle, Kussman, Jennifer, Zhou, Dihong, Hemming, Rick, Zahka, Kenneth, Chioza, Barry A., Rawlins, Lettie E., Wenger, Olivia K., Gunning, Adam C., Pizzi, Simone, Onesimo, Roberta, Zampino, Giuseppe, Barker, Emily, Osawa, Natasha, Rodriguez, Megan Christine, Neuhann, Teresa M., Zackai, Elaine H., Keena, Beth, Capasso, Jenina, Levin, Alex V., Bhoj, Elizabeth, Li, Dong, Hakonarson, Hakon, Wentzensen, Ingrid M., Jackson, Adam, Chandler, Kate E., Coban-Akdemir, Zeynep H., Posey, Jennifer E., Banka, Siddharth, Lupski, James R., Sheppard, Sarah E., Tartaglia, Marco, Triggs-Raine, Barbara, Crosby, Andrew H., Baple, Emma L.

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Human NK cell deficiency as a result of biallelic mutations in MCM10 von Mace, Emily M., Paust, Silke, Conte, Matilde I., Baxley, Ryan M., Schmit, Megan M., Patil, Sagar L., Guilz, Nicole C., Mukherjee, Malini, Pezzi, Ashley E., Chmielowiec, Jolanta, Tatineni, Swetha, Chinn, Ivan K., Akdemir, Zeynep Coban, Jhangiani, Shalini N., Muzny, Donna M., Stray-Pedersen, Asbjorg, Bradley, Rachel E., Moody, Mo, Connor, Philip P., Heaps, Adrian G., Steward, Colin, Banerjee, Pinaki P., Gibbs, Richard A., Borowiak, Malgorzata, Lupski, James R., Jolles, Stephen, Bielinsky, Anja K., Orange, Jordan S.

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