Clinically actionable incidental and secondary parental genomic findings after proband exome sequencing: Yield and dilemmas by Lina Basel-Salmon, Noa Ruhrman-Shahar, Naama Orenstein, Michal Levy, Gabriel A. Lidzbarsky, Nurit A. Batzir, Marina Lifshitc-Kalis, Sarit Farage-Barhom, Gali Abel, Mayra Petasny, Dana Brabbing-Goldstein, Avi Fellner, Lily Bazak

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Potential Founder Variants in COL4A4 Identified in Bukharian Jews Linked to Autosomal Dominant and Autosomal Recessive Alport Syndrome by Michal Levy, Lily Bazak, Noa Lev-El, Rotem Greenberg, Nesia Kropach, Lina Basel-Salmon, Idit Maya

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P766: A combined Bayesian inference and machine-learning approach for prenatal screening by cell free DNA of monogenic disorders by Noa Liscovitch-Brauer, Ravit Mesika, Tom Rabinowitz, Hadas Volkov, Meitar Grad, Reut Tomashov Matar, Lina Basel-Salmon, Oren Tadmor, Amir Beker, Noam Shomron

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P762: Short-read haplotype-assisted genotyping for prenatal screening of monogenic disorders* by Noa Liscovitch-Brauer, Tom Rabinowitz, Sapir Bornstein, Lilach Schneor, Ravit Mesika, Meitar Grad, Reut Tomashov Matar, Lina Basel-Salmon, Oren Tadmor, Amir Beker, Noam Shomron

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Nonmalignant Features Associated with Inherited Colorectal Cancer Syndromes-Clues for Diagnosis by Diana Haimov, Sari Lieberman, Sergi Castellvi-Bel, Maartje Nielsen, Yael Goldberg

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Identification of a novel mutation in the PNLIP gene in two brothers with congenital pancreatic lipase deficiency by Doron M. Behar, Lina Basel-Vanagaite, Fabian Glaser, Marielle Kaplan, Shay Tzur, Nurit Magal, Tal Eidlitz-Markus, Yishay Haimi-Cohen, Galit Sarig, Concetta Bormans, Mordechai Shohat, Avraham Zeharia

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Refining the Phenotypic Spectrum of KMT5B-Associated Developmental Delay by Aviva Eliyahu, Aviva Eliyahu, Ortal Barel, Ortal Barel, Lior Greenbaum, Lior Greenbaum, Lior Greenbaum, Gal Zaks Hoffer, Gal Zaks Hoffer, Yael Goldberg, Yael Goldberg, Annick Raas-Rothschild, Annick Raas-Rothschild, Amihood Singer, Ifat Bar-Joseph, Ifat Bar-Joseph, Vered Kunik, Elisheva Javasky, Elisheva Javasky, Orna Staretz-Chacham, Orna Staretz-Chacham, Naomi Pode-Shakked, Naomi Pode-Shakked, Naomi Pode-Shakked, Lily Bazak, Lily Bazak, Lily Bazak, Noa Ruhrman-Shahar, Noa Ruhrman-Shahar, Elon Pras, Elon Pras, Moshe Frydman, Moshe Frydman, Mordechai Shohat, Mordechai Shohat, Ben Pode-Shakked, Ben Pode-Shakked, Ben Pode-Shakked

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Prenatal gender-customized head circumference nomograms result in reclassification of microcephaly and macrocephalyAJOG Global Reports at a Glance by Rivka Sukenik-Halevy, MD, Ella Golbary Kinory, MS, Tamar Laron Kenet, MD, Dana Brabbing-Goldstein, MD, Yinon Gilboa, MD, Lina Basel-Salmon, MD, PhD, Sharon Perlman, MD

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Central nervous system metastases in breast cancer patients with germline BRCA pathogenic variants compared to non-carriers: a matched-pair analysis by Matan Ben-Zion Berliner, Shlomit Yust-Katz, Inbar Lavie, Yael Goldberg, Inbal Kedar, Rinat Yerushalmi

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Going against the flow: Motivations of professionals with critical views on vaccination by Elisha Ety, Guetzkow Josh, Shir-Raz Yaffa, Ronel Natti

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Molecular functions of MCM8 and MCM9 and their associated pathologies by Noah Cornelis Helderman, Diantha Terlouw, Laia Bonjoch, Mariano Golubicki, Marina Antelo, Hans Morreau, Tom van Wezel, Sergi Castellví-Bel, Yael Goldberg, Maartje Nielsen

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Autosomal Recessive Rod–Cone Dystrophy with Mild Extra-Ocular Manifestations Due to a Splice-Affecting Variant in <i>BBS9</i> by Iris Deitch, Sofia Itskov, Daan Panneman, Aasem Abu Shtaya, Tal Saban, Yael Goldberg, Miriam Ehrenberg, Frans P. M. Cremers, Susanne Roosing, Tamar Ben-Yosef

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Real-World Experiences with Taliglucerase Alfa Home Infusions for Patients with Gaucher Disease: A Global Cohort Study by Shoshana Revel-Vilk, Royston Mansfield, Neta Feder-Krengel, Noya Machtiger-Azoulay, David Kuter, Jeff Szer, Hanna Rosenbaum, David Cavalcanti Ferreira, Noa Ruhrman-Shahar, Michael Wajnrajch, Ari Zimran

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Expanding the phenotype of familial hypocalciuric hypercalcemia type 3: Case report and review of the literature by Lior Baraf, Noa Shefer Averbuch, Lior Carmon, Auryan Szalat, Rivka Sukenik-Halevy, Merav Fraenkel

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Vici syndrome in Israel: Clinical and molecular insights by Odelia Chorin, Odelia Chorin, Odelia Chorin, Yoel Hirsch, Rachel Rock, Rachel Rock, Rachel Rock, Liat Salzer Sheelo, Liat Salzer Sheelo, Yael Goldberg, Yael Goldberg, Hanna Mandel, Hanna Mandel, Tova Hershkovitz, Tova Hershkovitz, Nicole Fleischer, Lior Greenbaum, Lior Greenbaum, Lior Greenbaum, Uriel Katz, Uriel Katz, Ortal Barel, Ortal Barel, Nasrin Hamed, Nasrin Hamed, Bruria Ben-Zeev, Bruria Ben-Zeev, Shoshana Greenberger, Shoshana Greenberger, Shoshana Greenberger, Nadra Nasser Samra, Nadra Nasser Samra, Michal Stern Zimmer, Michal Stern Zimmer, Michal Stern Zimmer, Annick Raas-Rothschild, Annick Raas-Rothschild, Ben Pode-Shakked, Ben Pode-Shakked, Ben Pode-Shakked

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Correlations between pathogenic variants in DNA repair genes and anticancer treatment efficacy in stage IV non‐small cell lung cancer: A large real‐world cohort and review of the l... by Itamar Averbuch, Roi Tschernichovsky, Oded Icht, Daniel A. Goldstein, Raz Mutai, Elizabeth Dudnik, Ofer Rotem, Nir Peled, Aaron M. Allen, Smadar Laufer‐Geva, Yael Goldberg, Alona Zer

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Abdominal Desmoid: Course, Severe Outcomes, and Unique Genetic Background in a Large Local Series by Gilad Ophir, Shamai Sivan, Strul Hana, Rosner Guy, Gluck Nathan, Fliss Isakov Naomi, Klausner Joseph, Wolf Ido, Merimsky Ofer, Goldberg Yael, Levi Zohar, Zer Alona, Kariv Revital

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