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L. Marcato · SciRah

Researcher profile · Semantic Scholar

L. Marcato

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L. Marcato — researcher profile on SciRah

h-index: 9
Works: 15
Citations: 300

Most-cited papers

Prenatal BACs‐on‐Beads™: a new technology for rapid detection of aneuploidies and microdeletions in prenatal diagnosis
F. Vialard, G. Simoni, A. Aboura, S. De Toffol +13 more
2011Prenatal Diagnosis53 citations
Semantic Scholar
Implications of fetoplacental mosaicism on cell‐free DNA testing for sex chromosome aneuploidies
F. Grati, Komal K. Bajaj, V. Zanatta, F. Malvestiti +7 more
2017Prenatal Diagnosis48 citations
Semantic Scholar
Prenatal BACs‐on‐BeadsTM: the prospective experience of five prenatal diagnosis laboratories
F. Vialard, G. Simoni, D. M. Gomes, Azzedine Abourra +12 more
2012Prenatal Diagnosis48 citations Open access
Semantic Scholar
Fetal mesenchymal stromal cells from cryopreserved human chorionic villi: cytogenetic and molecular analysis of genome stability in long-term cultures.
E. A. Roselli, S. Lazzati, Federico Iseppon, M. Manganini +5 more
2013Cytotherapy41 citations
Semantic Scholar
Application of a new molecular technique for the genetic evaluation of products of conception
F. Grati, D. M. Gomes, D. Ganesamoorthy, L. Marcato +14 more
2013Prenatal Diagnosis24 citations
Semantic Scholar
De novo small supernumerary marker chromosomes detected on 143 000 consecutive prenatal diagnoses: chromosomal distribution, frequencies, and characterization combining molecular cytogenetics approaches
F. Malvestiti, S. De Toffol, B. Grimi, S. Chinetti +11 more
2014Prenatal Diagnosis22 citations
Semantic Scholar
Prenatal phenotype of Williams–Beuren syndrome and of the reciprocal duplication syndrome
L. Marcato, L. Turolla, E. Pompilii, C. Dupont +16 more
2014Clinical Case Reports21 citations Open access
Semantic Scholar
QF‐PCR as a substitute for karyotyping of cytotrophoblast for the analysis of chorionic villi: advantages and limitations from a cytogenetic retrospective audit of 44,727 first‐trimester prenatal diagnoses
F. Grati, F. Malvestiti, B. Grimi, E. Gaetani +15 more
2013Prenatal Diagnosis18 citations
Semantic Scholar
First Trimester Screening for Common Trisomies and Microdeletion 22q11.2 Syndrome Using Cell-Free DNA: A Prospective Clinical Study
K. Kagan, M. Hoopmann, Theresa Pfaff, N. Prodan +8 more
2020Fetal Diagnosis and Therapy15 citations
Semantic Scholar
Cryptic 13q34 and 4q35.2 Deletions in an Italian Family
F. Riccardi, G. Rivolta, V. Uliana, F. Grati +10 more
2015Cytogenetic and Genome Research8 citations
Semantic Scholar
A pharmacogenetic-driven approach for controlled ovarian hyperstimulation by FSH treatment.
R. Colognato, R. Aiello, F. Dulcetti, A. Ruggeri +7 more
2014Minerva Ginecologica2 citations
Semantic Scholar
OC11.10: Diagnostic cytogenetics and cytogenomics confirmations following a cfDNA test with a high‐risk or inconclusive result
D. De Siero, B. Malvestiti, L. Marcato, Jose Ferreira +9 more
20200 citations Open access
Semantic Scholar
VP30.01: Cell‐free DNA screening for 22q11.2DS by targeted method based on microarray quantitation in the average risk population: results from a single European laboratory
L. Marcato, B. Malvestiti, S. Saragozza, S. Crippa +5 more
20200 citations Open access
Semantic Scholar
VP29.06: Cell‐free DNA screening for fetal aneuploidy by targeted method based on microarray quantitation as primary test in the average risk population: results from a single European laboratory
B. Malvestiti, S. Crippa, L. Marcato, S. Saragozza +7 more
20200 citations Open access
Semantic Scholar
Response to “QF‐PCR as a substitute for karyotyping of cytotrophoblast for the analysis of chorionic villi: advantages and limitations from a cytogenetic retrospective audit of 44 727 first‐trimester prenatal diagnoses”
F. Grati, F. Malvestiti, B. Grimi, E. Gaetani +15 more
2013Prenatal Diagnosis0 citations
Semantic Scholar

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