Exome sequencing as first‐tier test for fetuses with severe central nervous system structural anomalies von Yaron, Y., Ofen Glassner, V., Mory, A., Zunz Henig, N., Kurolap, A., Bar Shira, A., Brabbing Goldstein, D., Marom, D., Ben Sira, L., Baris Feldman, H., Malinger, G., Krajden Haratz, K., Reches, A.

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Study of Thin Film LiNbO3 Laterally Excited Bulk Acoustic Resonators von Yandrapalli, Soumya, Eroglu, Seniz Esra Kucuk, Plessky, Victor, Atakan, H. Baris, Villanueva, Luis Guillermo

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Non-parabolic conical rotations von Çolakoğlu, H. Barış, Öztürk, İskender, Özdemir, Mustafa

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Midline facial soft tissue thickness database of Turkish population: MRI study von Sipahioğlu, Serdar, Ulubay, Hakan, Diren, H. Barış

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Multi-well plate lid for single-step pooling of 96 samples for high-throughput barcode-based sequencing von Boder-Pasche, Stéphanie, Demir, Mustafa, Heub, Sarah, Garzuel, Manon, Ischer, Réal, Migliozzi, Daniel, Graf, Siegfried, Schmid, Noa, Atakan, H. Baris, Gudkova, Daria, Alpern, Daniel, Dainese, Riccardo, Deplancke, Bart, Weder, Gilles

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Refugee women’s well-being, needs and challenges: implications for health policymakers von Qutranji, L, Silahlı, N Y, Baris, H E, Boran, P

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Calm in the midst of cytokine storm: a collaborative approach to the diagnosis and treatment of hemophagocytic lymphohistiocytosis and macrophage activation syndrome von Halyabar, Olha, Chang, Margaret H, Schoettler, Michelle L, Schwartz, Marc A, Baris, Ezgi H, Benson, Leslie A, Biggs, Catherine M, Gorman, Mark, Lehmann, Leslie, Lo, Mindy S, Nigrovic, Peter A, Platt, Craig D, Priebe, Gregory P, Rowe, Jared, Sundel, Robert P, Surana, Neeraj K, Weinacht, Katja G, Mann, Alison, Yuen, Jenny Chan, Meleedy-Rey, Patricia, Starmer, Amy, Banerjee, Taruna, Dedeoglu, Fatma, Degar, Barbara A, Hazen, Melissa M, Henderson, Lauren A

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The safety of live-attenuated vaccines in patients using IL-1 or IL-6 blockade: an international survey von Jeyaratnam, Jerold, Ter Haar, Nienke M, Lachmann, Helen J, Kasapcopur, Ozgur, Ombrello, Amanda K, Rigante, Donato, Dedeoglu, Fatma, Baris, Ezgi H, Vastert, Sebastiaan J, Wulffraat, Nico M, Frenkel, Joost

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Expanding the MYBPC1 phenotypic spectrum: a novel homozygous mutation causes arthrogryposis multiplex congenita von Ekhilevitch, N., Kurolap, A., Oz-Levi, D., Mory, A., Hershkovitz, T., Ast, G., Mandel, H., Baris, H.N.

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From phenotyping to genotyping - bioinformatics for the busy clinician von Reches, A., Weiss, K., Bazak, L., Baris Feldman, H., Maya, I.

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Occurrence of Two Non-indigenous Alien Sea Slugs, Bursatella leachii (Blainville, 1817) and Melibe viridis (Kelaart, 1858) (Gastropoda: Heterobranchia), from the Canakkale Strait,... von Ozalp, Baris H., Ovalis, Panayotis, Culha, Mehmet

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The gastrointestinal manifestation of constitutional mismatch repair deficiency syndrome: from a single adenoma to polyposis-like phenotype and early onset cancer von Levi, Z., Kariv, R., Barnes-Kedar, I., Goldberg, Y., Half, E., Morgentern, S., Eli, B., Baris, H.N., Vilkin, A., Belfer, R.G., Niv, Y., Elhasid, R., Dvir, R., Abu-Freha, N., Cohen, S.

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Non-syndromic retinitis pigmentosa due to mutations in the mucopolysaccharidosis type IIIC gene, heparan-alpha-glucosaminide N-acetyltransferase (HGSNAT) von Haer-Wigman, Lonneke, Newman, Hadas, Leibu, Rina, Bax, Nathalie M, Baris, Hagit N, Rizel, Leah, Banin, Eyal, Massarweh, Amir, Roosing, Susanne, Lefeber, Dirk J, Zonneveld-Vrieling, Marijke N, Isakov, Ofer, Shomron, Noam, Sharon, Dror, Den Hollander, Anneke I, Hoyng, Carel B, Cremers, Frans P M, Ben-Yosef, Tamar

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Thirty Minutes of Running Exercise Decreases T2 Signal Intensity but Not Thickness of the Knee Joint Cartilage: A 3.0-T Magnetic Resonance Imaging Study von Karanfil, Yiğitcan, Babayeva, Naila, Dönmez, Gürhan, Diren, H. Barış, Eryılmaz, Muzaffer, Doral, Mahmut Nedim, Korkusuz, Feza

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Genetic features of Lynch syndrome in the Israeli population von Goldberg, Y., Barnes-Kedar, I., Lerer, I., Halpern, N., Plesser, M., Hubert, A., Kadouri, L., Goldshmidt, H., Solar, I., Strul, H., Rosner, G., Baris, H.N., Peretz, T., Levi, Z., Kariv, R.

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A PRELIMINARY BIODIVERSITY SURVEY IN THREE SHIPWRECKS IN THE DARDANELLES (MARMARA SEA, TURKEY) von Ozalp, H Baris, Alparslan, Mustafa, Okudan-Aslan, Emine Sukran, Aysel, Orkun, Aysel, Veysel

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Pre-assessment of zoobenthos diversity from the only hard coral Marine Reserve in the Turkish Seas (Çanakkale Strait, Turkey) von Özalp, H. Barış, Demir, Volkan, Evcen, Alper, Önen-Tarantini, Senem, Montesanto, Federica, Erdoğan, Sevil, Çulha, Mehmet, Koçak, Ferah

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Endovenous laser ablation for saphenous vein insufficiency: Short- and mid-term results of 230 procedures von Altin, Firat H, Aydin, Selim, Erkoc, Kamuran, Gunes, Tevfik, Eygi, Bortecin, Kutas, Baris H

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A novel GJB6 missense mutation in hidrotic ectodermal dysplasia 2 (Clouston syndrome) broadens its genotypic basis von Baris, H.N., Zlotogorski, A., Peretz-Amit, G., Doviner, V., Shohat, M., Reznik-Wolf, H., Pras, E.

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Founder mutation for Huntington disease in Caucasus Jews von Melamed, O., Behar, D. M., Bram, C., Magal, N., Pras, E., Reznik-Wolf, H., Borochowitz, Z. U., Davidov, B., Mor-Cohen, R., Baris, H. N.

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