Detection of gene mutations and gene–gene fusions in circulating cell‐free DNA of glioblastoma patients: an avenue for clinically relevant diagnostic analysis von Palande, Vikrant, Siegal, Tali, Detroja, Rajesh, Gorohovski, Alessandro, Glass, Rainer, Flueh, Charlotte, Kanner, Andrew A., Laviv, Yoseph, Har‐Nof, Sagi, Levy‐Barda, Adva, Viviana Karpuj, Marcela, Kurtz, Marina, Perez, Shira, Raviv Shay, Dorith, Frenkel‐Morgenstern, Milana

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Sequence variation in PPP1R13L results in a novel form of cardio‐cutaneous syndrome von Falik‐Zaccai, Tzipora C, Barsheshet, Yiftah, Mandel, Hanna, Segev, Meital, Lorber, Avraham, Gelberg, Shachaf, Kalfon, Limor, Ben Haroush, Shani, Shalata, Adel, Gelernter‐Yaniv, Liat, Chaim, Sarah, Raviv Shay, Dorith, Khayat, Morad, Werbner, Michal, Levi, Inbar, Shoval, Yishay, Tal, Galit, Shalev, Stavit, Reuveni, Eli, Avitan‐Hersh, Emily, Vlodavsky, Eugene, Appl‐Sarid, Liat, Goldsher, Dorit, Bergman, Reuven, Segal, Zvi, Bitterman‐Deutsch, Ora, Avni, Orly

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Detection of Cell-Free DNA in Blood Plasma Samples of Cancer Patients von Palande, Vikrant, Raviv Shay, Dorith, Frenkel-Morgenstern, MILANA

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Sequence variation in PPP1R13L results in a novel form of cardio‐cutaneous syndrome von Falik‐Zaccai, Tzipora C, Barsheshet, Yiftah, Mandel, Hanna, Segev, Meital, Lorber, Avraham, Gelberg, Shachaf, Kalfon, Limor, Ben Haroush, Shani, Shalata, Adel, Gelernter‐Yaniv, Liat, Chaim, Sarah, Raviv Shay, Dorith, Khayat, Morad, Werbner, Michal, Levi, Inbar, Shoval, Yishay, Tal, Galit, Shalev, Stavit, Reuveni, Eli, Avitan‐Hersh, Emily, Vlodavsky, Eugene, Appl‐Sarid, Liat, Goldsher, Dorit, Bergman, Reuven, Segal, Zvi, Bitterman‐Deutsch, Ora, Avni, Orly

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mouse model for human hearing loss DFNB30 due to loss of function of myosin IIIA von Walsh, Vanessa L, Raviv, Dorith, Dror, Amiel A, Shahin, Hashem, Walsh, Tom, Kanaan, Moien N, Avraham, Karen B, King, Mary-Claire

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Hearing loss: a common disorder caused by many rare alleles von Raviv, Dorith, Dror, Amiel A., Avraham, Karen B.

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ChiTaRS 5.0: the comprehensive database of chimeric transcripts matched with druggable fusions and 3D chromatin maps von Balamurali, Deepak, Gorohovski, Alessandro, Detroja, Rajesh, Palande, Vikrant, Raviv-Shay, Dorith, Frenkel-Morgenstern, Milana

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PATH-24. DETECTION OF POINT MUTATIONS AND GENE FUSIONS FROM CIRCULATING CELL-FREE DNA (CFDNA) OF GLIOBLASTOMA (GBM) PATIENTS von Frenkel-Morgenstern, Milana, Palande, Vikrant, Detroja, Rajesh, Gorohovski, Alessandro, Glass, Rainer, Flueh, Charlotte, Kanner, Andrew A, Laviv, Yoseph, Nof, Sagi Har, Levy-Barda, Adva, Benouaich-Amiel, Alexandra, Yust-Katz, Shlomit, Kurtz, Marina, Perez, Shira, Shay, Dorith Raviv, Siegal, Tali

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ChiTaRS-3.1-the enhanced chimeric transcripts and RNA-seq database matched with protein-protein interactions von Gorohovski, Alessandro, Tagore, Somnath, Palande, Vikrant, Malka, Assaf, Raviv-Shay, Dorith, Frenkel-Morgenstern, Milana

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Design principles of gene evolution for niche adaptation through changes in protein–protein interaction networks von Carmi, Gon, Tagore, Somnath, Gorohovski, Alessandro, Sivan, Aviad, Raviv-Shay, Dorith, Frenkel-Morgenstern, Milana

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Detection of Cell-Free DNA in Blood Plasma Samples of Cancer Patients von Palande, Vikrant, Raviv Shay, Dorith, Frenkel-Morgenstern, MILANA

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Erratum To: Sequence variation in PPP1R13L results in a novel form of cardio‐cutaneous syndrome von Falik‐Zaccai, Tzipora C, Barsheshet, Yiftah, Mandel, Hanna, Segev, Meital, Lorber, Avraham, Gelberg, Shachaf, Kalfon, Limor, Ben Haroush, Shani, Shalata, Adel, Gelernter‐Yaniv, Liat, Chaim, Sarah, Raviv Shay, Dorith, Khayat, Morad, Werbner, Michal, Levi, Inbar, Shoval, Yishay, Tal, Galit, Shalev, Stavit, Reuveni, Eli, Avitan‐Hersh, Emily, Vlodavsky, Eugene, Appl‐Sarid, Liat, Goldsher, Dorit, Bergman, Reuven, Segal, Zvi, Bitterman‐Deutsch, Ora, Avni, Orly

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Sequence variation in PPP 1R13L results in a novel form of cardio‐cutaneous syndrome von Falik‐Zaccai, Tzipora C, Barsheshet, Yiftah, Mandel, Hanna, Segev, Meital, Lorber, Avraham, Gelberg, Shachaf, Kalfon, Limor, Ben Haroush, Shani, Shalata, Adel, Gelernter‐Yaniv, Liat, Chaim, Sarah, Raviv Shay, Dorith, Khayat, Morad, Werbner, Michal, Levi, Inbar, Shoval, Yishay, Tal, Galit, Shalev, Stavit, Reuveni, Eli, Avitan‐Hersh, Emily, Vlodavsky, Eugene, Appl‐Sarid, Liat, Goldsher, Dorit, Bergman, Reuven, Segal, Zvi, Bitterman‐Deutsch, Ora, Avni, Orly

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Sequence variation in PPP 1R13L results in a novel form of cardio‐cutaneous syndrome von Falik‐Zaccai, Tzipora C, Barsheshet, Yiftah, Mandel, Hanna, Segev, Meital, Lorber, Avraham, Gelberg, Shachaf, Kalfon, Limor, Ben Haroush, Shani, Shalata, Adel, Gelernter‐Yaniv, Liat, Chaim, Sarah, Raviv Shay, Dorith, Khayat, Morad, Werbner, Michal, Levi, Inbar, Shoval, Yishay, Tal, Galit, Shalev, Stavit, Reuveni, Eli, Avitan‐Hersh, Emily, Vlodavsky, Eugene, Appl‐Sarid, Liat, Goldsher, Dorit, Bergman, Reuven, Segal, Zvi, Bitterman‐Deutsch, Ora, Avni, Orly

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METHODS AND BIOMARKERS FOR DIAGNOSTICS, DISEASE MONITORING, PERSONALIZED DRUG DISCOVERY AND TARGETED THERAPY OF AUTOIMMUNE DISEASE CONDITIONS von RAVIV SHAY, Dorith, PALANDE, Vikrant, DETROJA, Rajesh, FRENKEL-MORGENSTERN, Milana

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METHODS AND BIOMARKERS FOR DIAGNOSTICS, DISEASE MONITORING, PERSONALIZED DRUG DISCOVERY AND TARGETED THERAPY OF AUTOIMMUNE DISEASE CONDITIONS von RAVIV SHAY, Dorith, PALANDE, Vikrant, DETROJA, Rajesh, FRENKEL-MORGENSTERN, Milana

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