When phenotype does not match genotype: importance of “real-time” refining of phenotypic information for exome data interpretation von Basel-Salmon, Lina, Ruhrman-Shahar, Noa, Orenstein, Naama, Goldberg, Yael, Gonzaga-Jauregui, Claudia, Shuldiner, Alan R., Sukenik-Halevy, Rivka, Maya, Idit, Magal, Nurit, Hagari, Ofir, Azulay, Noy, Lidzbarsky, Gabriel Arie, Bazak, Lily

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Investigation of hydrodynamic characteristics of Li jet flowing along concave flow channel using LES for A-FNS von Hoashi, Eiji, Hagari, Daichi, Ogino, Yosuke, Okita, Takafumi, Oyaizu, Makoto, Ochiai, Kentaro

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The role of phenotype-based search approaches using public online databases in diagnostics of Mendelian disorders von Fellner, Avi, Ruhrman-Shahar, Noa, Orenstein, Naama, Lidzbarsky, Gabriel, Shuldiner, Alan R., Gonzaga-Jauregui, Claudia, Brown-Shalev, Hadar, Hagari-Bechar, Ofir, Bazak, Lily, Basel-Salmon, Lina

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The Diagnostic Yield and Implications of Targeted Founder Pathogenic Variant Testing in an Israeli Cohort von Abu Shtaya, Aasem, Kedar, Inbal, Mattar, Samar, Mahamid, Ahmad, Basel-Salmon, Lina, Farage Barhom, Sarit, Naftaly Nathan, Sofia, Magal, Nurit, Azulay, Noy, Levy Zalcberg, Michal, Chen-Shtoyerman, Rakefet, Segol, Ori, Seri, Mor, Reznick Levi, Gili, Shkedi-Rafid, Shiri, Vinkler, Chana, Netzer, Iris, Hagari Bechar, Ofir, Chamma, Liat, Liberman, Sari, Goldberg, Yael

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DYRK1B haploinsufficiency in a family with metabolic syndrome and abnormal cognition von Orenstein, Naama, Gofin, Yoel, Shomron, Noam, Ruhrman‐Shahar, Noa, Magal, Nurit, Hagari, Ofir, Azulay, Noy, Bazak, Lily, Goldberg, Yael, Basel‐Salmon, Lina

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The prevalence of prenatal sonographic findings in postnatal diagnostic exome sequencing performed for neurocognitive phenotypes: A cohort study von Sukenik‐Halevy, Rivka, Perlman, Sharon, Ruhrman‐Shahar, Noa, Engel, Offra, Orenstein, Naama, Gonzaga‐Jauregui, Claudia, Shuldiner, Alan R., Magal, Nurit, Hagari, Ofir, Azulay, Noy, Lidzbarsky, Gabriel Arie, Bazak, Lily, Basel‐Salmon, Lina

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Biallelic variants in ETV2 in a family with congenital heart defects, vertebral abnormalities and preaxial polydactyly von Basel-Salmon, Lina, Ruhrman-Shahar, Noa, Barel, Ortal, Hagari, Ofir, Marek-Yagel, Dina, Azulai, Noy, Bazak, Lily, Svirsky, Ran, Reznik-wolf, Haike, Lidzbarsky, Gabriel Arie, Shohat, Mordechai

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The genetic landscape of Lynch syndrome in the Israeli population von Shtaya, Aasem Abu, Nathan, Sofia Naftaly, Kedar, Inbal, Friedman, Eitan, Half, Elizabeth, Lidzbarsky, Gabi, Levi, Gili Reznick, Laish, Ido, Katz, Lior, Bazak, Lily, Peretz, Lilach Peled, Salmon, Lina Basel, Douiev, Liza, Kalis, Marina Lifshitc, Schechter, Menachem, Barzily-Rokni, Michal, Samra, Nadra Nasser, Abu-Freha, Naim, Hagari-Bechar, Ofir, Segol, Ori, Mattar, Samar, Barhom, Sarit Farage, Mordechai, Shikma, Rafid, Shiri Shkedi, Shalev, Stavit A., Peretz-Yablonski, Tamar, Levi, Zohar, Bruchim, Revital, Vinkler, Chana, Bernstein-Molho, Rinat, Lieberman, Sari, Goldberg, Yael

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Clustered variants in the 5′ coding region of TRA2B cause a distinctive neurodevelopmental syndrome von Ramond, Francis, Dalgliesh, Caroline, Grimmel, Mona, Wechsberg, Oded, Vetro, Annalisa, Guerrini, Renzo, FitzPatrick, David, Poole, Rebecca L., Lebrun, Marine, Bayat, Allan, Grasshoff, Ute, Bertrand, Miriam, Witt, Dennis, Turnpenny, Peter D., Faundes, Víctor, Santa María, Lorena, Mendoza Fuentes, Carolina, Mabe, Paulina, Hussain, Shaun A., Mullegama, Sureni V., Torti, Erin, Oehl-Jaschkowitz, Barbara, Salmon, Lina Basel, Orenstein, Naama, Shahar, Noa Ruhrman, Hagari, Ofir, Bazak, Lily, Hoffjan, Sabine, Prada, Carlos E., Haack, Tobias, Elliott, David J.

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Axillary apocrine carcinoma with benign apocrine tumours: a case report involving a pathological and immunohistochemical study and review of the literature von Miyamoto, T, Hagari, Y, Inoue, S, Watanabe, T, Yoshino, T

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The diagnostic efficacy of exome data analysis using fixed neurodevelopmental gene lists: Implications for prenatal setting von Sukenik‐Halevy, Rivka, Ruhrman‐Shahar, Noa, Orenstein, Naama, Gonzaga‐Jauregui, Claudia, Shuldiner, Alan R., Magal, Nurit, Hagari, Ofir, Azulay, Noy, Lidzbarsky, Gabriel A., Bazak, Lily, Basel‐Salmon, Lina

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Heat Transfer and Pressure Losses of W-Shaped Small Ribs at High Reynolds Numbers for Combustor Liner von Hagari, Tomoko, Ishida, Katsuhiko, Oda, Takeo, Douura, Yasushi, Kinoshita, Yasuhiro

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Activity of the Type 1 5α-Reductase Exhibits Regional Differences in Isolated Sebaceous Glands and Whole Skin von Thiboutot, Diane, Harris, Georgianna, Iles, Vicki, Cimis, George, Gilliland, Kathyrn, Hagari, Shinobu

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Controller and control method for internal combustion engine von Hagari, Hideki

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Febrile ulceronecrotic Mucha–Habermann disease: a case report and a review of the literature von Miyamoto, T, Takayama, N, Kitada, S, Hagari, Y, Mihara, M

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Acral pseudolymphomatous angiokeratoma of children: immunohistochemical and clonal analyses of the infiltrating cells von Hagari, Yoshitaka, Hagari, Shinobu, Kambe, Naoto, Kawaguchi, Toshio, Nakamoto, Shu, Mihara, Motoyuki

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Controller and control method for internal combustion engine von Hagari, Hideki

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Controller and control method for internal combustion engine von Hagari, Hideki

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Schätzvorrichtung und Verfahren für eine Zylinderansaugluftmenge eines Verbrennungsmotors von Hagari, Hideki

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Controller and control method for internal combustion engine von Hagari, Hideki

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