Potential di‐genic contribution to guttate leukoderma as the predominant feature of epidermolysis bullosa simplex by Koren, Tamar, Zagairy, Fadia, Tatour, Yasmin, Belhanes‐Peled, Hila, Khayat, Morad, Krausz, Judit, Danial‐Farran, Nada, Ziv, Michael, Cohen‐Barak, Eran

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Parental mosaic cutaneous‐gonadal GJB2 mutation: From epidermal nevus to inherited ichthyosis‐deafness syndrome by Cohen‐Barak, Eran, Mwassi, Bannan, Zagairy, Fadia, Danial‐Farran, Nada, Khayat, Morad, Tatour, Yasmin, Ziv, Michael

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Acral peeling in Nagashima type palmo‐plantar keratosis patients reveals the role of serine protease inhibitor B 7 in keratinocyte adhesion by Cohen‐Barak, Eran, Azzam, Wassim, Koetsier, Jennifer L., Danial‐Farran, Nada, Barcan, Moran, Hriesh, Maysa, Khayat, Morad, Edison, Natalia, Krausz, Judith, Gafni‐Amsalem, Chen, Kubo, Akiharu, Godsel, Lisa M., Ziv, Michael, Allon‐Shalev, Stavit

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The landscape of autosomal recessive variants in an isolated community: Implications for population screening for reproductive purposes by Khayat, Morad, Danial‐Farran, Nada, Chervinsky, Elena, Zehavi, Yoav, Peled‐Peretz, Lilach, Gafni‐Amsalem, Chen, Hakrosh, Shadia, Abu‐Leil Zouabi, Olfat, Tamir, Liron, Mamlouk, Efrat, Zlotogora, Joël, Shalev, Stavit A.

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Concomitant variants in NF1, LZTR1 and GNAZ genes probably contribute to the aggressiveness of plexiform neurofibroma and warrant treatment with MEK inhibitor by Cohen‐Barak, Eran, Toledano‐Alhadef, Hagit, Danial‐Farran, Nada, Livneh, Ido, Mwassi, Banan, Hriesh, Maysa, Zagairy, Fadia, Gafni‐Amsalem, Chen, Bashir, Husam, Khayat, Morad, Warrour, Nassim, Sher, Osnat, Marom, Daphna, Postovsky, Sergey, Dujovny, Tal, Ziv, Michael, Shalev, Stavit A.

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Spectrum of genes for inherited hearing loss in the Israeli Jewish population, including the novel human deafness gene ATOH1 by Brownstein, Zippora, Gulsuner, Suleyman, Walsh, Tom, Martins, Fábio T.A., Taiber, Shahar, Isakov, Ofer, Lee, Ming K., Bordeynik‐Cohen, Mor, Birkan, Maria, Chang, Weise, Casadei, Silvia, Danial‐Farran, Nada, Abu‐Rayyan, Amal, Carlson, Ryan, Kamal, Lara, Arnthórsson, Asgeir Ö., Sokolov, Meirav, Gilony, Dror, Lipschitz, Noga, Frydman, Moshe, Davidov, Bella, Macarov, Michal, Sagi, Michal, Vinkler, Chana, Poran, Hana, Sharony, Reuven, Samra, Nadra, Zvi, Na'ama, Baris‐Feldman, Hagit, Singer, Amihood, Handzel, Ophir, Hertzano, Ronna, Ali‐Naffaa, Doaa, Ruhrman‐Shahar, Noa, Madgar, Ory, Sofrin‐Drucker, Efrat, Peleg, Amir, Khayat, Morad, Shohat, Mordechai, Basel‐Salmon, Lina, Pras, Elon, Lev, Dorit, Wolf, Michael, Steingrimsson, Eirikur, Shomron, Noam, Kelley, Matthew W., Kanaan, Moien N., Allon‐Shalev, Stavit, King, Mary‐Claire, Avraham, Karen B.

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Homozygote loss-of-function variants in the human COCH gene underlie hearing loss by Danial-Farran, Nada, Chervinsky, Elena, Nadar-Ponniah, Prathamesh T, Cohen Barak, Eran, Taiber, Shahar, Khayat, Morad, Avraham, Karen B, Shalev, Stavit A

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Genetics of hearing loss in the Arab population of Northern Israel by Danial-Farran, Nada, Brownstein, Zippora, Gulsuner, Suleyman, Tammer, Luna, Khayat, Morad, Aleme, Ola, Chervinsky, Elena, Zoubi, Olfat Aboleile, Walsh, Tom, Ast, Gil, King, Mary-Claire, Avraham, Karen B, Shalev, Stavit A

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Bi-allelic variants in the ESAM tight-junction gene cause a neurodevelopmental disorder associated with fetal intracranial hemorrhage by Lecca, Mauro, Pehlivan, Davut, Suñer, Damià Heine, Weiss, Karin, Coste, Thibault, Zweier, Markus, Oktay, Yavuz, Danial-Farran, Nada, Rosti, Vittorio, Bonasoni, Maria Paola, Malara, Alessandro, Contrò, Gianluca, Zuntini, Roberta, Pollazzon, Marzia, Pascarella, Rosario, Neri, Alberto, Fusco, Carlo, Marafi, Dana, Mitani, Tadahiro, Posey, Jennifer Ellen, Bayramoglu, Sadik Etka, Gezdirici, Alper, Hernandez-Rodriguez, Jessica, Cladera, Emilia Amengual, Miravet, Elena, Roldan-Busto, Jorge, Ruiz, María Angeles, Bauzá, Cristofol Vives, Ben-Sira, Liat, Sigaudy, Sabine, Begemann, Anaïs, Unger, Sheila, Güngör, Serdal, Hiz, Semra, Sonmezler, Ece, Zehavi, Yoav, Jerdev, Michael, Balduini, Alessandra, Zuffardi, Orsetta, Horvath, Rita, Lochmüller, Hanns, Rauch, Anita, Garavelli, Livia, Tournier-Lasserve, Elisabeth, Spiegel, Ronen, Lupski, James R., Errichiello, Edoardo

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Molecular characterization of methicillin-resistant Staphylococcus aureus strains isolated from patients with hospital readmissions by Eghbaria, Saleh, Schnitser, Kathy, Danial-Farran, Nada, Keness, Yoram, Bisharat, Naiel

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