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ArticlesPeer ReviewedFull Text
Oncofertility: insights from IVF specialists—a worldwide web-based survey analysis
Author / Creator:Shoham, Gon ; Levy-Toledano, Rachel ; Leong, Milton ; Weissman, Ariel ; Yaron, Yuval ; Shoham, Zeev
Publisher:New York: Springer US
Journal title:Journal of assisted reproduction and genetics, 2019-05, Vol.36 (5), p.1013-1021
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ArticlesPeer ReviewedFull Text
Ethnicity has a multiplex impact upon the risk of a full mutation expansion among female heterozygotes for FMR1 premutation
Author / Creator:Domniz, Noam ; Levavi, Liat Ries ; Berkenstadt, Michal ; Pras, Elon ; Cohen, Yoram ; Raanani, Hila ; Goldstein, Dana Brabbing ; Yaron, Yuval ; Elizur, Shai ; Ben-Shachar, Shay
Publisher:New York: Elsevier Inc
Journal title:Genetics in medicine, 2021-06, Vol.23 (6), p.1023-1027
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Community data-driven approach to identify pathogenic founder variants for pan-ethnic carrier screening panels
Author / Creator:Einhorn, Yaron ; Einhorn, Moshe ; Kurolap, Alina ; Steinberg, Dror ; Mory, Adi ; Bazak, Lily ; Paperna, Tamar ; Grinshpun-Cohen, Julia ; Basel-Salmon, Lina ; Weiss, Karin ; Singer, Amihood ; Yaron, Yuval ; Baris Feldman, Hagit
Publisher:England: BioMed Central
Journal title:Human genomics, 2023-03, Vol.17 (1), p.30-30, Article 30
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Evaluation of the digital genetic assistant in technology assisted genetic counseling for genetic carrier screening
Author / Creator:Yaron, Yuval ; Ofen Glassner, Vered ; Berkenstadt, Michal ; Goldstein, Nurit ; Reznik Wolf, Haike ; Ries Levavi, Liat ; Abo Gutstein, Liat ; Furman, Yael ; Anouchi, Mori ; Delmar, Galit ; Behar, Doron M. ; Pras, Elon ; Reches, Adi ; Kurolap, Alina ; Baris Feldman, Hagit
Publisher:London: Nature Publishing Group UK
Journal title:NPJ digital medicine, 2025-03, Vol.8 (1), p.183-8, Article 183
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Yaron, Yuval, Sibelius Violin Contest prize
Publisher:London: Novello
Journal title:The Musical Times, 1976-01, Vol.117, p.238
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ArticlesPeer ReviewedFull Text
Improving preimplantation genetic diagnosis (PGD) reliability by selection of sperm donor with the most informative haplotype
Author / Creator:Malcov, Mira ; Gold, Veronica ; Peleg, Sagit ; Frumkin, Tsvia ; Azem, Foad ; Amit, Ami ; Ben-Yosef, Dalit ; Yaron, Yuval ; Reches, Adi ; Barda, Shimi ; Kleiman, Sandra E. ; Yogev, Leah ; Hauser, Ron
Publisher:England: BioMed Central
Journal title:Reproductive biology and endocrinology, 2017-04, Vol.15 (1), p.31-31, Article 31
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Newspaper ArticlesFull Text
Tel Aviv team spots baby's sex just 16 days after conception: Daily Edition
Author / Creator:Siegel, Judy
Publisher:Jerusalem: The Jerusalem Post Ltd
Journal title:The Jerusalem post, 2002-01-31
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Brachydactyly A-1 mutations restricted to the central region of the N-terminal active fragment of Indian Hedgehog
Author / Creator:Byrnes, Ashley M ; Racacho, Lemuel ; Grimsey, Allison ; Hudgins, Louanne ; Kwan, Andrea C ; Sangalli, Michel ; Kidd, Alexa ; Yaron, Yuval ; Lau, Yu-Lung ; Nikkel, Sarah M ; Bulman, Dennis E
Publisher:Cham: Springer International Publishing
Journal title:European journal of human genetics : EJHG, 2009-09, Vol.17 (9), p.1112-1120
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Yaron, Yuval. International Violin Competition of Indianapolis prize winner
Publisher:London: Novello
Journal title:The Musical Times, 1982-01, Vol.123, p.841
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Studies detect gender in fetus's first 16 days
Author / Creator:Schwartz, Avigail
Publisher:Jerusalem: Jerusalem Report
Journal title:The Jerusalem report, 2002-03, p.7
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Newspaper ArticlesFull Text
BARTOK PROVIDES FUEL FOR POWERFUL PERFORMANCE
Author / Creator:Ury Eppstein, Michael Ajzenstadt, Max Stern, Benjamin Bar-Am
Publisher:Jerusalem: The Jerusalem Post Ltd
Journal title:The Jerusalem post, 1994-05-17
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ArticlesPeer ReviewedFull Text
Two novel mutations identified in familial cases with Donohue syndrome
Author / Creator:Falik Zaccai, Tzipora C. ; Kalfon, Limor ; Klar, Aharon ; Elisha, Mordechai Ben ; Hurvitz, Haggit ; Weingarten, Galina ; Chechik, Emelia ; Fleisher Sheffer, Vered ; Haj Yahya, Raid ; Meidan, Gal ; Gross‐Kieselstein, Eva ; Bauman, Dvora ; Hershkovitz, Sylvia ; Yaron, Yuval ; Orr‐Urtreger, Avi ; Wertheimer, Efrat
Publisher:United States: John Wiley & Sons, Inc
Journal title:Molecular genetics & genomic medicine, 2014-01, Vol.2 (1), p.64-72
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ArticlesPeer ReviewedFull Text
Whole-exome sequencing in fetuses with central nervous system abnormalities
Author / Creator:Reches, Adi ; Hiersch, Liran ; Simchoni, Sharon ; Barel, Dalit ; Greenberg, Rotem ; Ben Sira, Liat ; Malinger, Gustavo ; Yaron, Yuval
Publisher:New York: Nature Publishing Group US
Journal title:Journal of perinatology, 2018-10, Vol.38 (10), p.1301-1308
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ArticlesPeer ReviewedFull Text
Expanded targeted preconception screening panel in Israel: findings and insights
Author / Creator:Reches, Adi ; Ofen Glassner, Vered ; Goldstein, Nurit ; Yeshaya, Josepha ; Delmar, Galit ; Portugali, Ellie ; Hallas, Tova ; Weinstein, Amit ; Kurolap, Alina ; Berkenstadt, Michal ; Mantsour, Tal ; Abu-Gutstein, Liat ; Ries-Levavi, Liat ; Reznik-Wolf, Haike ; Behar, Doron Moshe ; Yaron, Yuval ; Pras, Elon ; Baris Feldman, Hagit
Publisher:England: BMJ Publishing Group Ltd
Journal title:Journal of medical genetics, 2024-08, Vol.61 (8), p.783-787
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ArticlesPeer ReviewedFull Text
Whole Genome Sequencing Applied in Familial Hamartomatous Polyposis Identifies Novel Structural Variations
Author / Creator:Kariv, Revital ; Dahary, Dvir ; Yaron, Yuval ; Petel-Galil, Yael ; Malcov, Mira ; Rosner, Guy
Publisher:Basel: MDPI AG
Journal title:Genes, 2022-08, Vol.13 (8), p.1408
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Mutations in TMEM216 perturb ciliogenesis and cause Joubert, Meckel and related syndromes
Author / Creator:Valente, Enza Maria ; Logan, Clare V ; Mougou-Zerelli, Soumaya ; Lee, Jeong Ho ; Silhavy, Jennifer L ; Brancati, Francesco ; Iannicelli, Miriam ; Travaglini, Lorena ; Romani, Sveva ; Illi, Barbara ; Adams, Matthew ; Szymanska, Katarzyna ; Mazzotta, Annalisa ; Lee, Ji Eun ; Tolentino, Jerlyn C ; Swistun, Dominika ; Salpietro, Carmelo D ; Fede, Carmelo ; Gabriel, Stacey ; Russ, Carsten ; Cibulskis, Kristian ; Sougnez, Carrie ; Hildebrandt, Friedhelm ; Otto, Edgar A ; Held, Susanne ; Diplas, Bill H ; Davis, Erica E ; Mikula, Mario ; Strom, Charles M ; Ben-Zeev, Bruria ; Lev, Dorit ; Sagie, Tally Lerman ; Michelson, Marina ; Yaron, Yuval ; Krause, Amanda ; Boltshauser, Eugen ; Elkhartoufi, Nadia ; Roume, Joelle ; Shalev, Stavit ; Munnich, Arnold ; Saunier, Sophie ; Inglehearn, Chris ; Saad, Ali ; Alkindy, Adila ; Thomas, Sophie ; Vekemans, Michel ; Dallapiccola, Bruno ; Katsanis, Nicholas ; Johnson, Colin A ; Attié-Bitach, Tania ; Gleeson, Joseph G
Publisher:New York: Nature Publishing Group US
Journal title:Nature genetics, 2010-07, Vol.42 (7), p.619-625
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ArticlesPeer ReviewedFull Text
Evaluation of Fetal Echogenic Bowel in the Second Trimester
Author / Creator:Yaron, Yuval ; Hassan, Sonia ; Geva, Eli ; Kupferminc, Michael J. ; Yavetz, Haim ; Evans, Mark I.
Publisher:Basel, Switzerland: Karger
Journal title:Fetal diagnosis and therapy, 1999-05, Vol.14 (3), p.176-180
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Parental Origin of the Retained X Chromosome in Monosomy X Miscarriages and Ongoing Pregnancies
Author / Creator:Grande, Maribel ; Stergiotou, Iosifina ; Pauta, Montse ; Marquès, Borja ; Badenas, Cèlia ; Soler, Anna ; Yaron, Yuval ; Borrell, Antoni
Publisher:Basel, Switzerland: S. Karger AG
Journal title:Fetal diagnosis and therapy, 2019-01, Vol.45 (2), p.118-124
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Paternal deletion of the 11p15.5 centromeric-imprinting control region is associated with alteration of imprinted gene expression and recurrent severe intrauterine growth restriction
Author / Creator:De Crescenzo, Agostina ; Sparago, Angela ; Cerrato, Flavia ; Palumbo, Orazio ; Carella, Massimo ; Miceli, Marco ; Bronshtein, Moshe ; Riccio, Andrea ; Yaron, Yuval
Publisher:London: BMJ Publishing Group Ltd
Journal title:Journal of medical genetics, 2013-02, Vol.50 (2), p.99-103
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Screening for germline mutations in breast/ovarian cancer susceptibility genes in high-risk families in Israel
Author / Creator:Yablonski-Peretz, Tamar ; Paluch-Shimon, Shani ; Gutman, Lior Soussan ; Kaplan, Yulia ; Dvir, Addie ; Barnes-Kedar, Inbal ; Kadouri, Luna ; Semenisty, Valeriya ; Efrat, Noa ; Neiman, Victoria ; Glasser, Yafit ; Michaelson-Cohen, Rachel ; Katz, Lior ; Kaufman, Bella ; Golan, Talia ; Reish, Orit ; Hubert, Ayala ; Safra, Tamar ; Yaron, Yuval ; Friedman, Eitan
Publisher:New York: Springer US
Journal title:Breast cancer research and treatment, 2016-01, Vol.155 (1), p.133-138
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Showing 1 to 20 of 53 results

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Oncofertility: insights from IVF specialists—a worldwide web-based survey analysis

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Ethnicity has a multiplex impact upon the risk of a full mutation expansion among female heterozygotes for FMR1 premutation

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Community data-driven approach to identify pathogenic founder variants for pan-ethnic carrier screening panels

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Evaluation of the digital genetic assistant in technology assisted genetic counseling for genetic carrier screening

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Yaron, Yuval, Sibelius Violin Contest prize

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Improving preimplantation genetic diagnosis (PGD) reliability by selection of sperm donor with the most informative haplotype

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Tel Aviv team spots baby's sex just 16 days after conception: Daily Edition

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Brachydactyly A-1 mutations restricted to the central region of the N-terminal active fragment of Indian Hedgehog

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Yaron, Yuval. International Violin Competition of Indianapolis prize winner

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Studies detect gender in fetus's first 16 days

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BARTOK PROVIDES FUEL FOR POWERFUL PERFORMANCE

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Two novel mutations identified in familial cases with Donohue syndrome

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Whole-exome sequencing in fetuses with central nervous system abnormalities

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Expanded targeted preconception screening panel in Israel: findings and insights

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Whole Genome Sequencing Applied in Familial Hamartomatous Polyposis Identifies Novel Structural Variations

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Mutations in TMEM216 perturb ciliogenesis and cause Joubert, Meckel and related syndromes

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Evaluation of Fetal Echogenic Bowel in the Second Trimester

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Parental Origin of the Retained X Chromosome in Monosomy X Miscarriages and Ongoing Pregnancies

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Paternal deletion of the 11p15.5 centromeric-imprinting control region is associated with alteration of imprinted gene expression and recurrent severe intrauterine growth restriction

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Screening for germline mutations in breast/ovarian cancer susceptibility genes in high-risk families in Israel

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