Works by Yaron, Yuval

Results: 89

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

Published in:

Journal of Assisted Reproduction & Genetics, 2019, v. 36, n. 5, p. 1013, doi. 10.1007/s10815-019-01419-8

By:

Shoham, Gon;
Levy-Toledano, Rachel;
Leong, Milton;
Weissman, Ariel;
Yaron, Yuval;
Shoham, Zeev

Publication type:

Article

A Missense Variant in KIF14 Results in Two Gene Isoforms by Affecting Normal Gene Splicing.

Published in:

Prenatal Diagnosis, 2025, v. 45, n. 2, p. 231, doi. 10.1002/pd.6744

By:

Trigubov, Dorin;
Ofen‐Glassner, Vered;
Levy, Bar;
Mory, Adi;
Wolman, Igal;
Yaron, Yuval;
Birnbaum, Roee;
Kurolap, Alina

Publication type:

Article

Prenatal Diagnosis of a KIDINS220 De Novo Heterozygous Variant in a Fetus With a Complex CNS Anomaly.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 12, p. 1518, doi. 10.1002/pd.6682

By:

Miremberg, Hadas;
Birnbaum, Roee;
Trigubov, Dorin;
Botvinik, Adi;
Yaron, Yuval;
Mory, Adi;
Malinger, Gustavo;
Haratz, Karina Krajden

Publication type:

Article

Exploring the factors affecting classification and reporting of uncertain prenatal microarray findings, using a "virtual fetus" model‐a pilot study.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 4, p. 511, doi. 10.1002/pd.6535

By:

Michaelson‐Cohen, Rachel;
Salzer, Liat Sheelo;
Brabbing‐Goldstein, Dana;
Yaron, Yuval;
Reches, Adi;
Yonath, Hagith;
Regev, Miriam;
Shani, Hagit;
Altarescu, Gheona;
Segel, Reeval;
Sukenik‐Halevy, Rivka;
Daum, Hagit;
Harel, Tamar;
Meiner, Vardiella;
Basel‐Salmon, Lina;
Sagi‐Dain, Lena;
Maya, Idit

Publication type:

Article

Monogenic conditions and central nervous system anomalies: A prospective study, systematic review and meta‐analysis.

Published in:

Prenatal Diagnosis, 2024, v. 44, n. 4, p. 422, doi. 10.1002/pd.6466

By:

Blayney, Gillian V.;
Laffan, Eoghan;
Jacob, Preethi A.;
Baptiste, Caitlin D.;
Gabriel, Heinz;
Sparks, Teresa N.;
Yaron, Yuval;
Norton, Mary E.;
Diderich, Karin;
Wang, Yiming;
Chong, Karen;
Chitayat, David;
Saini, Neelam;
Aggarwal, Shagun;
Pauta, Montse;
Borrell, Antoni;
Gilmore, Kelly;
Chandler, Natalie J.;
Allen, Stephanie;
Vora, Neeta

Publication type:

Article

SMARCC1 is a susceptibility gene for congenital hydrocephalus with an autosomal dominant inheritance mode and incomplete penetrance.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 10, p. 1374, doi. 10.1002/pd.6426

By:

Hourvitz, Noa;
Kurolap, Alina;
Mory, Adi;
Haratz, Karina Krajden;
Kidron, Dvora;
Malinger, Gustavo;
Baris Feldman, Hagit;
Yaron, Yuval

Publication type:

Article

International Society for Prenatal Diagnosis 2022 debate 3—Fetal genome sequencing should be offered to all pregnant patients.

Published in:

Prenatal Diagnosis, 2023, v. 43, n. 4, p. 428, doi. 10.1002/pd.6247

By:

Van den Veyver, Ignatia B.;
Yaron, Yuval;
Deans, Zandra C.

Publication type:

Article

Upgrading an intronic TMEM67 variant of unknown significance to likely pathogenic through RNA studies and community data sharing.

Published in:

Prenatal Diagnosis, 2022, v. 42, n. 12, p. 1484, doi. 10.1002/pd.6248

By:

Kurolap, Alina;
Mory, Adi;
Simchoni, Sharon;
Krajden Haratz, Karina;
Malinger, Gustavo;
Birnbaum, Roee;
Baris Feldman, Hagit;
Yaron, Yuval

Publication type:

Article

A founding father of reproductive genetics: Eugene Pergament (1933–2022).

Published in:

2022

By:

Cuckle, Howard;
Benn, Peter;
Yaron, Yuval

Publication type:

Obituary

Non‐immune hydrops fetalis caused by PIEZO1 compound heterozygous deletions detected only by exome sequencing.

Published in:

Prenatal Diagnosis, 2022, v. 42, n. 7, p. 890, doi. 10.1002/pd.6142

By:

Reytan, Sivan;
Zunz Henig, Noa;
Yinon, Yoav;
Avnet, Hagai;
Kurolap, Alina;
Yaron, Yuval;
Baris Feldman, Hagit

Publication type:

Article

Economic impact of using maternal plasma cell‐free DNA testing to guide further workup in recurrent pregnancy loss.

Published in:

Prenatal Diagnosis, 2021, v. 41, n. 10, p. 1215, doi. 10.1002/pd.5972

By:

Peng, Siyang;
Bhatt, Sucheta;
Borrell, Antoni;
Yaron, Yuval

Publication type:

Article

International Society for Prenatal Diagnosis Position Statement: cell free (cf)DNA screening for Down syndrome in multiple pregnancies.

Published in:

Prenatal Diagnosis, 2021, v. 41, n. 10, p. 1222, doi. 10.1002/pd.5832

By:

Palomaki, Glenn E.;
Chiu, Rossa W.K.;
Pertile, Mark D.;
Sistermans, Erik A.;
Yaron, Yuval;
Vermeesch, Joris Robert;
Vora, Neeta L.;
Best, Robert G.;
Wilkins‐Haug, Louise

Publication type:

Article

Comprehensive clinical and molecular assessment of 32 probands with congenital contractural arachnodactyly: Report of 14 novel mutations and review of the literature.

Published in:

Human Mutation, 2009, v. 30, n. 3, p. 334, doi. 10.1002/humu.20854

By:

Callewaert, Bert L.;
Loeys, Bart L.;
Ficcadenti, Anna;
Vermeer, Sascha;
Landgren, Magnus;
Kroes, Hester Y.;
Yaron, Yuval;
Pope, Michael;
Foulds, Nicola;
Boute, Odile;
Galán, Francisco;
Kingston, Helen;
Van der Aa, Nathalie;
Salcedo, Iratxe;
Swinkels, Marielle E.;
Wallgren-Pettersson, Carina;
Gabrielli, Orazio;
De Backer, Julie;
Coucke, Paul J.;
De Paepe, Anne M.

Publication type:

Article

MECP2 Mutations in Israel: Implications for molecular analysis, genetic counseling, and prenatal diagnosis in Rett syndrome.

Published in:

Human Mutation, 2002, v. 20, n. 4, p. 323, doi. 10.1002/humu.9069

By:

Yaron, Yuval;
Ben Zeev, Bruria;
Shomrat, Ruth;
Bercovich, Dani;
Naiman, Tova;
Orr-Urtreger, Avi

Publication type:

Article

Molecular analysis of the APC gene in 71 Israeli families: 17 novel mutations.

Published in:

Human Mutation, 2002, v. 19, n. 6, p. 664, doi. 10.1002/humu.9037

By:

Gavert, Nancy;
Yaron, Yuval;
Naiman, Tova;
Bercovich, Dani;
Rozen, Paul;
Shomrat, Ruth;
Legum, Cyril;
Orr-Urtreger, Avi

Publication type:

Article

Novel mutations in the emerin gene in Israeli families.

Published in:

Human Mutation, 2001, v. 17, n. 6, p. 522, doi. 10.1002/humu.1139

By:

Nevo, Yoram;
Ahituv, Sarit;
Yaron, Yuval;
Kedmi, Merav;
Shomrat, Ruth;
Legum, Cyril;
Orr-Urtreger, Avi

Publication type:

Article

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

Published in:

2022

By:

Kariv, Revital;
Dahary, Dvir;
Yaron, Yuval;
Petel-Galil, Yael;
Malcov, Mira;
Rosner, Guy

Publication type:

Case Study

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

Published in:

European Journal of Human Genetics, 2009, v. 17, n. 9, p. 1112, doi. 10.1038/ejhg.2009.18

By:

Byrnes, Ashley M.;
Racacho, Lemuel;
Grimsey, Allison;
Hudgins, Louanne;
Kwan, Andrea C.;
Sangalli, Michel;
Kidd, Alexa;
Yaron, Yuval;
Yu-Lung Lau;
Nikkel, Sarah M.;
Bulman, Dennis E.

Publication type:

Article

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

Published in:

Reproductive Biology & Endocrinology, 2017, v. 15, p. 1, doi. 10.1186/s12958-017-0247-4

By:

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

Publication type:

Article

Loeys-Dietz Syndrome in Pregnancy: A Case Description and Report of a Novel Mutation.

Published in:

Fetal Diagnosis & Therapy, 2009, v. 26, n. 1, p. 35, doi. 10.1159/000236357

By:

Gutman, Guy;
Baris, Hagit N.;
Hirsch, Raphael;
Mandel, Dror;
Yaron, Yuval;
Lessing, Joseph B.;
Kuperminc, Michael J.

Publication type:

Article

Rapid Prenatal Diagnosis of Aneuploidy for Chromosomes 21, 18, 13, and X by Quantitative Fluorescence Polymerase Chain Reaction.

Published in:

Fetal Diagnosis & Therapy, 2006, v. 21, n. 4, p. 326, doi. 10.1159/000092459

By:

Ochshorn, Yifat;
Bar-Shira, Anat;
Jonish, Anat;
Yaron, Yuval

Publication type:

Article

Preimplantation Genetic Diagnosis of Canavan Disease.

Published in:

Fetal Diagnosis & Therapy, 2005, v. 20, n. 5, p. 465, doi. 10.1159/000086834

By:

Yaron, Yuval;
Schwartz, Tamar;
Mey-Raz, Nava;
Amit, Ami;
Lessing, Joseph B.;
Malcov, Mira

Publication type:

Article

2nd-Trimester Maternal Serum Human Chorionic Gonadotropin and α-Fetoprotein Levels in Male and Female Fetuses with Down Syndrome.

Published in:

Fetal Diagnosis & Therapy, 2005, v. 20, n. 3, p. 235, doi. 10.1159/000083911

By:

Lehavi, Ofer;
Aizenstein, Orna;
Evans, Mark I.;
Yaron, Yuval

Publication type:

Article

Nomograms for the sonographic measurement of the fetal philtrum and chin.

Published in:

2005

By:

Gull, Ilan;
Wolman, Igal;
Merlob, Paul;
Jaffa, Ariel J.;
Lessing, Joseph B.;
Yaron, Yuval

Publication type:

journal article

Multiplex Nested PCR for Preimplantation Genetic Diagnosis of Spinal Muscular Atrophy.

Published in:

Fetal Diagnosis & Therapy, 2004, v. 19, n. 2, p. 199, doi. 10.1159/000075151

By:

Malcov, Mira;
Schwartz, Tamar;
Mei-Raz, Nava;
Yosef, Dalit Ben;
Amit, Ami;
Lessing, Joseph B.;
Shomrat, Ruth;
Orr-Urtreger, Avi;
Yaron, Yuval

Publication type:

Article

A Comparison between Maternal Serum Free β-Human Chorionic Gonadotrophin and Pregnancy-Associated Plasma Protein A Levels in First-Trimester Twin and Singleton Pregnancies.

Published in:

Fetal Diagnosis & Therapy, 2004, v. 19, n. 2, p. 174, doi. 10.1159/000075145

By:

Mashiach, Roy;
Orr-Urtreger, Avi;
Yaron, Yuval

Publication type:

Article

First trimester maternal serum free human chorionic gonadotropin as a predictor of adverse pregnancy outcome.

Published in:

2002

By:

Yaron, Yuval;
Ochshorn, Yifat;
Heifetz, Sigal;
Lehavi, Ofer;
Sapir, Yaron;
Orr-Urtreger, Avi

Publication type:

journal article

Spontaneous abortions in couples declining multifetal pregnancy reduction.

Published in:

2002

By:

Evans, Mark I.;
Wapner, Ronald J.;
Ayoub, Melissa A.;
Shalhoub, Alex G.;
Feldman, Baruch;
Yaron, Yuval

Publication type:

journal article

Intracardiac echogenic focus: no apparent association with structural cardiac abnormality.

Published in:

2000

By:

Wolman, Igal;
Jaffa, Ariel;
Geva, Eli;
Diamant, Shmuel;
Strauss, Simon;
Lessing, Joseph B.;
Yaron, Yuval;
Wolman, I;
Jaffa, A;
Geva, E;
Diamant, S;
Strauss, S;
Lessing, J B;
Yaron, Y

Publication type:

journal article

Treatment of heterotopic cervical and intrauterine pregnancy.

Published in:

2000

By:

Carreno, Carlos A.;
King, Mary;
Johnson, Mark P.;
Yaron, Yuval;
Diamond, Michael P.;
Bush, Dana;
Evans, Mark I.;
Carreno, C A;
King, M;
Johnson, M P;
Yaron, Y;
Diamond, M P;
Bush, D;
Evans, M I

Publication type:

journal article

Evaluation of fetal echogenic bowel in the second trimester.

Published in:

1999

By:

Yaron, Yuval;
Hassan, Sonia;
Geva, Eli;
Kupferminc, Michael J.;
Yavetz, Haim;
Evans, Mark I.;
Yaron, Y;
Hassan, S;
Geva, E;
Kupferminc, M J;
Yavetz, H;
Evans, M I

Publication type:

journal article

Differential effect of advanced maternal age on prenatal diagnosis of trisomies 13, 18 and 21.

Published in:

1999

By:

Drugan, Arie;
Yaron, Yuval;
Zamir, Ronit;
Ebrahim, Salah A.D.;
Johnson, Mark P.;
Evans, Mark I.;
Drugan, A;
Yaron, Y;
Zamir, R;
Ebrahim, S A;
Johnson, M P;
Evans, M I

Publication type:

journal article

Distribution of neural tube defects as a function of maternal weight: no apparent correlation.

Published in:

1999

By:

Feldman, Baruch;
Yaron, Yuval;
Critchfield, Gregory;
Leon, Jorge;
O'Brien, Joseph E.;
Johnson, Mark P.;
Evans, Mark I.;
Feldman, B;
Yaron, Y;
Critchfield, G;
Leon, J;
O'Brien, J E;
Johnson, M P;
Evans, M I

Publication type:

journal article

Prenatal diagnosis of cloacal dysgenesis sequence: differential diagnosis from other forms of fetal obstructive uropathy.

Published in:

1998

By:

Qureshi, Faisal;
Jacques, Suzanne M.;
Yaron, Yuval;
Kramer, Ralph L.;
Evans, Mark I.;
Johnson, Mark P.;
Qureshi, F;
Jacques, S M;
Yaron, Y;
Kramer, R L;
Evans, M I;
Johnson, M P

Publication type:

journal article

Pastoral care utilization among women electing pregnancy termination for fetal anomalies.

Published in:

1998

By:

Brady, Teresa B.;
Lidums, Sue;
Yaron, Yuval;
Evans, Mark I.;
Johnson, Mark P.;
Kramer, Ralph L.;
Brady, T B;
Lidums, S;
Yaron, Y;
Evans, M I;
Johnson, M P;
Kramer, R L

Publication type:

journal article

Maternal weight differences do not explain ethnic differences in biochemical screening.

Published in:

1998

By:

Bryant-Greenwood, Peter K.;
O'Brien, Joseph E.;
Huang, Xiaohua;
Yaron, Yuval;
Ayoub, Mazin;
Johnson, Mark P.;
Evans, Mark I.;
Bryant-Greenwood, P K;
O'Brien, J E;
Huang, X;
Yaron, Y;
Ayoub, M;
Johnson, M P;
Evans, M I

Publication type:

journal article

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

Published in:

NPJ Digital Medicine, 2025, v. 8, n. 1, p. 1, doi. 10.1038/s41746-025-01573-7

By:

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

Publication type:

Article

Preimplantation genetic diagnosis for fragile X syndrome using multiplex nested PCR.

Published in:

Reproductive BioMedicine Online (Reproductive Healthcare Limited), 2007, v. 14, n. 4, p. 515, doi. 10.1016/S1472-6483(10)60901-7

By:

Malcov, Mira;
Naiman, Tova;
Yosef, Dalit Ben;
Carmon, Ariella;
Mey-Raz, Nava;
Amit, Ami;
Vagman, Israel;
Yaron, Yuval

Publication type:

Article

SECOND-TRIMESTER MATERNAL SERUM ALPHA-FETOPROTEIN, HUMAN CHORIONIC GONADOTROPIN, AND UNCONJUGATED OESTRIOL AFTER EARLY TRANSVAGINAL MULTIFETAL PREGNANCY REDUCTION.

Published in:

Prenatal Diagnosis, 1996, v. 16, n. 8, p. 723, doi. 10.1002/(SICI)1097-0223(199608)16:8<723::AID-PD942>3.0.CO;2-W

By:

GROUTZ, ASNAT;
AMIT, AMI;
YARON, YUVAL;
YOVEL, ISRAEL;
WOLMAN, IGAL;
LEGUM, CYRIL;
LESSING, JOSEPH B.

Publication type:

Article

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

Published in:

2019

By:

Grande, Maribel;
Stergiotou, Iosifina;
Pauta, Montse;
Marquès, Borja;
Badenas, Cèlia;
Soler, anna;
Yaron, Yuval;
Borrell, antoni

Publication type:

journal article

Israeli Society of Medical Genetics NIPT Committee Opinion 072013: Non-Invasive Prenatal Testing of Cell-Free DNA in Maternal Plasma for Detection of Fetal Aneuploidy.

Published in:

Fetal Diagnosis & Therapy, 2014, v. 36, n. 3, p. 242, doi. 10.1159/000360420

By:

Michaelson-Cohen, Rachel;
Gershoni-Baruch, Ruth;
Sharoni, Reuven;
Shochat, Mordechai;
Yaron, Yuval;
Singer, amihood

Publication type:

Article

Reply: cfDNA testing in recurrent pregnancy loss: a new step in the right way but still raw for the clinical area.

Published in:

2021

By:

Yaron, Yuval;
Borrell, Antoni

Publication type:

Letter

Maternal plasma genome-wide cell-free DNA can detect fetal aneuploidy in early and recurrent pregnancy loss and can be used to direct further workup.

Published in:

2020

By:

Yaron, Yuval;
Pauta, Montse;
Badenas, Celia;
Soler, Anna;
Borobio, Virginia;
Illanes, Carmen;
Paz-y-Miño, Fernanda;
Martinez-Portilla, Raigam;
Borrell, Antoni

Publication type:

journal article

Methodological drawbacks in the alleged association between foetal sonographic anomalies and autism.

Published in:

2022

By:

Sagi-Dain, Lena;
Weisz, Boaz;
Krajden, Karina Haratz;
Singer, Amihood;
Yaron, Yuval;
Maymon, Ron;
Haratz Krajden, Karina

Publication type:

Editorial

Clinical and screening implications of the I1307K adenomatous polyposis coli gene variant in Israeli Ashkenazi Jews with familial colorectal neoplasia. Evidence for a founder effect.

Published in:

2002

By:

Rozen, Paul;
Naiman, Tova;
Strul, Hana;
Taussky, Philipp;
Karminsky, Nataly;
Shomrat, Ruth;
Samuel, Ziona;
Yaron, Yuval;
Orr-Urtreger, Avi

Publication type:

journal article

The genetic and clinical outcome of isolated fetal muscular ventricular septal defect (VSD).

Published in:

2019

By:

Svirsky, Ran;
Brabbing-Goldstein, Dana;
Rozovski, Uri;
Kapusta, Livia;
Reches, Adi;
Yaron, Yuval

Publication type:

journal article

Does the number of previous miscarriages influence the incidence of chromosomal aberrations in spontaneous pregnancy loss?

Published in:

2017

By:

Goldstein, Myriam;
Svirsky, Ran;
Reches, Adi;
Yaron, Yuval

Publication type:

journal article

Maternal serum HCG is higher in the presence of a female fetus as early as week 3 post-fertilization.

Published in:

2002

By:

Yaron, Yuval;
Lehavi, Ofer;
Orr-Urtreger, Avi;
Gull, Ilan;
Lessing, Joseph B.;
Amit, Ami;
Ben-Yosef, Dalit

Publication type:

journal article

How many embryos to transfer in patients undergoing IVF?

Published in:

1996

By:

Azem, Foad;
Yaron, Yuval;
Amit, Ami;
Yovel, Israel;
Barak, Yona;
Peyser, M.Reuben;
David, Menachem P.;
Lessing, J.B.;
Azem, F;
Yaron, Y;
Amit, A;
Yovel, I;
Barak, Y;
Peyser, M R;
David, M P

Publication type:

Letter

The prevalence and expression of inherited connexin 26 mutations associated with nonsyndromic hearing loss in the Israeli population.

Published in:

Human Genetics, 2000, v. 106, n. 1, p. 50, doi. 10.1007/s004390051009

By:

Sobe, Tama;
Vreugde, Sarah;
Shahin, Hashem;
Berlin, Mira;
Davis, Noa;
Kanaan, Moien;
Yaron, Yuval;
Orr-Urtreger, Avi;
Frydman, Moshe;
Shohat, Mordechai;
Avraham, Karen B.

Publication type:

Article