Skip to content

Home Search Authors Pakistan News Saved

SciRah

SciRah does not host or store research papers. Results come live from free, official scholarly APIs, and every paper links back to its original source.

Data sources

OpenAlex
Semantic Scholar
Crossref
CORE
arXiv
PubMed

Privacy policy Terms of service

I. Maya · SciRah

Researcher profile · Semantic Scholar

I. Maya

Share profile

I. Maya — researcher profile on SciRah

h-index: 19
Works: 85
Citations: 1,442

Most-cited papers

Multiple congenital anomalies-hypotonia-seizures syndrome is caused by a mutation in PIGN
G. Maydan, I. Noyman, Adi Har‐Zahav, Z. Ben Neriah +12 more
2011Journal of Medical Genetics158 citations
Semantic Scholar
Diagnostic utility of array‐based comparative genomic hybridization (aCGH) in a prenatal setting
I. Maya, B. Davidov, Liron Gershovitz, Yael Zalzstein +4 more
2010Prenatal Diagnosis92 citations
Semantic Scholar
RIN2 deficiency results in macrocephaly, alopecia, cutis laxa, and scoliosis: MACS syndrome.
L. Basel-Vanagaite, O. Sarig, D. Hershkovitz, D. Fuchs-Telem +17 more
2009American Journal of Human Genetics88 citations Open access
Semantic Scholar
When genotype is not predictive of phenotype: implications for genetic counseling based on 21,594 chromosomal microarray analysis examinations
I. Maya, R. Sharony, S. Yacobson, S. Kahana +8 more
2017Genetics in Medicine70 citations Open access
Semantic Scholar
Cut‐off value of nuchal translucency as indication for chromosomal microarray analysis
I. Maya, S. Yacobson, S. Kahana, J. Yeshaya +6 more
2017Ultrasound in Obstetrics and Gynecology63 citations Open access
Semantic Scholar
Chromosomal microarray vs. NIPS: analysis of 5541 low-risk pregnancies
L. Sagi-Dain, L. Cohen-Vig, S. Kahana, S. Yacobson +6 more
2019Genetics in Medicine60 citations Open access
Semantic Scholar
Prenatal screening: current practice, new developments, ethical challenges.
Antina de Jong, I. Maya, J. V. van Lith
2015Bioethics57 citations
Semantic Scholar
Chromosomal Microarray Analysis Results From Pregnancies With Various Ultrasonographic Anomalies.
L. Sagi-Dain, I. Maya, A. Reches, A. Frumkin +11 more
2018Obstetrics and Gynecology53 citations Open access
Semantic Scholar
Noncoding copy-number variations are associated with congenital limb malformation
Ricarda Flöttmann, Bjørt K. Kragesteen, Sinje Geuer, Magdalena Socha +23 more
2017Genetics in Medicine49 citations Open access
Semantic Scholar
Microcephaly thin corpus callosum intellectual disability syndrome caused by mutated TAF2.
S. Hellman-Aharony, P. Smirin-Yosef, Ayelet Halevy, M. Pasmanik-Chor +8 more
2013Pediatric Neurology40 citations
Semantic Scholar
Chromosomal microarray analysis in fetuses with aberrant right subclavian artery
I. Maya, S. Kahana, J. Yeshaya, T. Tenne +7 more
2017Ultrasound in Obstetrics and Gynecology39 citations Open access
Semantic Scholar
SOBP is mutated in syndromic and nonsyndromic intellectual disability and is highly expressed in the brain limbic system.
E. Birk, Adi Har‐Zahav, Chiara Manzini, M. Pasmanik-Chor +18 more
2010American Journal of Human Genetics35 citations Open access
Semantic Scholar
Exome sequencing in every pregnancy? Results of trio exome sequencing in structurally normal fetuses
M. Levy, Shira Lifshitz, Mirela Goldenberg-Fumanov, Lily Bazak +6 more
2024Prenatal Diagnosis32 citations Open access
Semantic Scholar
Homozygous MED25 mutation implicated in eye–intellectual disability syndrome
L. Basel-Vanagaite, P. Smirin-Yosef, Jenna Lee Essakow, S. Tzur +17 more
2015Human Genetics32 citations
Semantic Scholar
Delineation of a KDM2B-related neurodevelopmental disorder and its associated DNA methylation signature
R. V. van Jaarsveld, Jack Reilly, M. Cornips, M. A. Hadders +55 more
2022Genetics in Medicine30 citations Open access
Semantic Scholar
Chromosomal Microarray Analysis (CMA) a Clinical Diagnostic Tool in the Prenatal and Postnatal Settings.
N. A. Batzir, M. Shohat, I. Maya
2015Pediatric Endocrinology Reviews: diabetes, nutrition, metabolism25 citations
Semantic Scholar
Microarray analysis has no additional value in fetal aberrant right subclavian artery: description of 268 pregnancies and systematic literature review
L. Sagi-Dain, A. Singer, S. Josefsberg, A. Peleg +6 more
2019Ultrasound in Obstetrics and Gynecology24 citations Open access
Semantic Scholar
Microarray analysis in pregnancies with isolated echogenic bowel.
A. Singer, I. Maya, A. Koifman, Nadra Nasser Samra +4 more
2018Early Human Development21 citations
Semantic Scholar
When phenotype does not match genotype: importance of “real-time” refining of phenotypic information for exome data interpretation
L. Basel-Salmon, N. Ruhrman-Shahar, N. Orenstein, Y. Goldberg +9 more
2020Genetics in Medicine20 citations Open access
Semantic Scholar
Should We Report 15q11.2 BP1-BP2 Deletions and Duplications in the Prenatal Setting?
I. Maya, S. Perlman, M. Shohat, S. Kahana +6 more
2020Journal of Clinical Medicine19 citations Open access
Semantic Scholar
Risk of Clinically Significant Chromosomal Microarray Analysis Findings in Fetuses With Nuchal Translucency From 3.0 mm Through 3.4 mm.
L. Sagi-Dain, A. Singer, S. Ben-Shachar, Sagi Josefsberg Ben Yehoshua +3 more
2020Obstetrics and Gynecology19 citations Open access
Semantic Scholar
Cytogenetic analysis in fetuses with late onset abnormal sonographic findings
R. Bardin, E. Hadar, L. Haizler-Cohen, R. Gabbay-Benziv +8 more
2017Journal of Perinatal Medicine19 citations
Semantic Scholar
Non-visualization of fetal gallbladder in microarray era – a retrospective cohort study and review of the literature
L. Sagi-Dain, A. Singer, Y. Hadid, R. Sharony +5 more
2019Journal of Maternal-Fetal & Neonatal Medicine18 citations
Semantic Scholar
Clinical utility of expanded non‐invasive prenatal screening compared with chromosomal microarray analysis in over 8000 pregnancies without major structural anomaly
I. Maya, L. Salzer Sheelo, D. Brabbing-Goldstein, R. Matar +6 more
2023Ultrasound in Obstetrics and Gynecology17 citations
Semantic Scholar
What have we learned from 691 prenatal chromosomal microarrays for ventricular septal defects?
I. Maya, A. Singer, H. Yonath, A. Reches +4 more
2020Acta Obstetricia et Gynecologica Scandinavica17 citations
Semantic Scholar
Prenatal clubfoot increases the risk for clinically significant chromosomal microarray results - Analysis of 269 singleton pregnancies.
A. Singer, I. Maya, Ehud Banne, H. Baris Feldman +3 more
2020Early Human Development17 citations
Semantic Scholar
Microarray analysis in pregnancies with isolated unilateral kidney agenesis
L. Sagi-Dain, I. Maya, A. Peleg, A. Reches +5 more
2018Pediatric Research17 citations
Semantic Scholar
Prenatal microarray analysis in right aortic arch—a retrospective cohort study and review of the literature
I. Maya, A. Singer, H. Baris, Y. Goldberg +4 more
2018Journal of Perinatology17 citations
Semantic Scholar
Abnormal brain magnetic resonance imaging in two patients with Smith–Magenis syndrome
I. Maya, C. Vinkler, O. Konen, L. Kornreich +6 more
2014American Journal of Medical Genetics. Part A17 citations
Semantic Scholar
Residual risk for clinically significant copy number variants in low-risk pregnancies, following exclusion of NIPS-detectable findings.
I. Maya, Liat Salzer Sheelo, D. Brabbing-Goldstein, R. Matar +6 more
2021American Journal of Obstetrics and Gynecology16 citations
Semantic Scholar
Chromosomal microarray should be performed for cases of fetal short long bones detected prenatally
K. Tzadikevitch-Geffen, A. Singer, I. Maya, L. Sagi-Dain +6 more
2020Archives of Gynecology and Obstetrics16 citations Open access
Semantic Scholar
The rare 13q33–q34 microdeletions: eight new patients and review of the literature
L. Sagi-Dain, Y. Goldberg, A. Peleg, R. Sukenik-Halevy +7 more
2019Human Genetics16 citations
Semantic Scholar
A de-novo interstitial microduplication involving 2p16.1-p15 and mirroring 2p16.1-p15 microdeletion syndrome: Clinical and molecular analysis.
A. Mimouni-Bloch, J. Yeshaya, S. Kahana, I. Maya +1 more
2015European journal of paediatric neurology16 citations
Semantic Scholar
The yield of chromosomal microarray analysis among pregnancies terminated due to fetal malformations
Y. Pasternak, Y. Daykan, T. Tenne, E. Reinstein +5 more
2020Journal of Maternal-Fetal & Neonatal Medicine15 citations
Semantic Scholar
High-frequency low-penetrance copy-number variant classification: should we revise the existing guidelines?
I. Maya, L. Basel-Salmon, A. Singer, L. Sagi-Dain
2020Genetics in Medicine14 citations Open access
Semantic Scholar
Residual Risk for Clinically Significant Copy Number Variants in Low-Risk Pregnancies, Following Exclusion of Noninvasive Prenatal Screening–Detectable Findings
I. Maya, Liat Salzer Sheelo, D. Brabbing-Goldstein, R. Matar +6 more
2022Obstetrical & Gynecological Survey13 citations
Semantic Scholar
Isolated fetal horseshoe kidney does not seem to increase the risk for abnormal chromosomal microarray results.
L. Sagi-Dain, I. Maya, T. Falik-Zaccai, Michal Feingold-Zadok +6 more
2018European Journal of Obstetrics, Gynecology, and Reproductive Biology13 citations
Semantic Scholar
Microcephaly-thin corpus callosum syndrome maps to 8q23.2-q24.12.
Ayelet Halevy, L. Basel-Vanagaite, A. Shuper, S. Helman +9 more
2012Pediatric Neurology13 citations
Semantic Scholar
Chromosomal Microarray Analysis in Pregnancies With Corpus Callosum or Posterior Fossa Anomalies
L. Greenbaum, I. Maya, L. Sagi-Dain, R. Sukenik-Halevy +6 more
2021Neurology: Genetics12 citations Open access
Semantic Scholar
Homozygous deletion of RAG1, RAG2 and 5′ region TRAF6 causes severe immune suppression and atypical osteopetrosis
M. Weisz Hubshman, L. Basel-Vanagaite, A. Krauss, O. Konen +16 more
2017Clinical Genetics12 citations
Semantic Scholar
Prenatal and postnatal chromosomal microarray analysis in 885 cases of various congenital heart defects
L. Salzer-Sheelo, Uri Polak, A. Barg, S. Kahana +9 more
2022Archives of Gynecology and Obstetrics10 citations
Semantic Scholar
The yield of chromosomal microarray in pregnancies with congenital cardiac defects and normal NIPS.
L. Sagi-Dain, A. Singer, R. Segel, Racheli Berger +2 more
2021American Journal of Obstetrics and Gynecology10 citations
Semantic Scholar
The yield of chromosomal microarray testing for cases of abnormal fetal head circumference
Y. Pasternak, A. Singer, I. Maya, L. Sagi-Dain +6 more
2020Journal of Perinatal Medicine10 citations
Semantic Scholar
Chromosomal microarray findings in pregnancies with an isolated pelvic kidney
L. Sagi-Dain, A. Singer, A. Frumkin, A. Shalata +8 more
2018Journal of Perinatal Medicine10 citations Open access
Semantic Scholar
Balanced chromosomal rearrangements offer insights into coding and noncoding genomic features associated with developmental disorders
Chelsea Lowther, M. Mehrjouy, Ryan L. Collins, M. Bak +151 more
2022medRxiv8 citations Open access
Semantic Scholar
The Yield of Chromosomal Microarray in Pregnancies Complicated with Fetal Growth Restriction Can Be Predicted According to Clinical Parameters
K. Tzadikevitch-Geffen, A. Singer, I. Maya, S. Ben-Shachar +6 more
2020Fetal Diagnosis and Therapy7 citations
Semantic Scholar
Microarray findings in pregnancies with oligohydramnios – a retrospective cohort study and literature review
A. Singer, I. Maya, R. Sukenik-Halevy, T. Tenne +3 more
2019Journal of Perinatal Medicine7 citations
Semantic Scholar
The effect of polyhydramnios degree on chromosomal microarray results: a retrospective cohort analysis of 742 singleton pregnancies
L. Sagi-Dain, A. Singer, T. Falik-Zaccai, A. Peleg +4 more
2021Archives of Gynecology and Obstetrics6 citations
Semantic Scholar
Ten points to consider when providing genetic counseling for variants of incomplete penetrance and variable expressivity detected in a prenatal setting
I. Maya, R. Sukenik-Halevy, L. Basel-Salmon, L. Sagi-Dain
2020Acta Obstetricia et Gynecologica Scandinavica6 citations
Semantic Scholar
Chromosomal Microarray Analysis Compared With Noninvasive Prenatal Testing in Pregnancies With Abnormal Maternal Serum Screening
L. Sagi-Dain, Liat Salzer Sheelo, D. Brabbing-Goldstein, R. Matar +6 more
2022Obstetrics and Gynecology5 citations
Semantic Scholar

Frequent co-authors

Invite them to SciRah by sharing their profile.

L. Sagi-Dain×27
Invite
L. Sagi-Dain — researcher profile on SciRah
A. Singer×19
Invite
A. Singer — researcher profile on SciRah
S. Ben-Shachar×17
Invite
S. Ben-Shachar — researcher profile on SciRah
S. Kahana×12
Invite
S. Kahana — researcher profile on SciRah

L. Basel-Salmon

×12

Invite

L. Basel-Salmon — researcher profile on SciRah

Invite

M. Shohat — researcher profile on SciRah

L. Basel-Vanagaite×11

Invite

L. Basel-Vanagaite — researcher profile on SciRah

Invite

T. Tenne — researcher profile on SciRah

I. Agmon-Fishman×9

Invite

I. Agmon-Fishman — researcher profile on SciRah

Invite

S. Yacobson — researcher profile on SciRah

R. Sukenik-Halevy×7

Invite

R. Sukenik-Halevy — researcher profile on SciRah

Invite

J. Yeshaya — researcher profile on SciRah