PubRank

Emmanouil Manolakos

Author PubWeight™ 13.44‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Characterization of a prenatally assessed de novo supernumerary minute ring chromosome 20 in a phenotypically normal male. Mol Cytogenet 2009 1.43
2 Uterine arteriovenous malformations induced after diagnostic curettage: a systematic review. Arch Gynecol Obstet 2011 1.42
3 Unexpected results in the constitution of small supernumerary marker chromosomes. Eur J Med Genet 2012 0.97
4 Prenatal diagnosis of proximal partial trisomy 1q confirmed by comparative genomic hybridization array: molecular cytogenetic analysis, fetal pathology and review of the literature. Birth Defects Res A Clin Mol Teratol 2014 0.85
5 Detection of congenital heart defects throughout pregnancy; impact of first trimester ultrasound screening for cardiac abnormalities. J Matern Fetal Neonatal Med 2012 0.85
6 An interstitial 4q31.21q31.22 microdeletion associated with developmental delay: case report and literature review. Cytogenet Genome Res 2014 0.83
7 Dual testing with QF-PCR and karyotype analysis for prenatal diagnosis of chromosomal abnormalities. Evaluation of 13,500 cases with consideration of using QF-PCR as a stand-alone test according to referral indications. Prenat Diagn 2012 0.82
8 Recipient CTLA-4*CT60-AA genotype is a prognostic factor for acute graft-versus-host disease in hematopoietic stem cell transplantation for thalassemia. Hum Immunol 2011 0.81
9 Common structural features characterize interstitial intrachromosomal Xp and 18q triplications. Am J Med Genet A 2011 0.81
10 Complex Rearrangement Involving Three Chromosomes, Four Breakpoints and a 2.7-Mb Deletion in the 18q Segment Observed in a Girl with Mild Learning Difficulties. Cytogenet Genome Res 2015 0.81
11 Prenatal detection of TAR syndrome in a fetus with compound inheritance of an RBM8A SNP and a 334‑kb deletion: a case report. Mol Med Rep 2013 0.80
12 Sonographic antenatal diagnosis of congenital dacryocystoceles. J Clin Ultrasound 2012 0.79
13 Prenatal diagnosis of a fetus with ring chromosome 15 characterized by array-CGH. Prenat Diagn 2009 0.78
14 Prenatal diagnosis of a fetus with 7q11.23 deletion detected by multiplex ligation-dependent probe amplification (MLPA) screening. Prenat Diagn 2008 0.77
15 Prenatal diagnosis of Wolf-Hirschhorn syndrome confirmed by comparative genomic hybridization array: report of two cases and review of the literature. Mol Cytogenet 2012 0.75
16 Characterization of a prenatally assessed de novo supernumerary minute ring chromosome 20 in a phenotypically normal male. Mol Cytogenet 2009 0.75
17 Deletion of 4.4 Mb at 2q33.2q33.3 May Cause Growth Deficiency in a Patient with Mental Retardation, Facial Dysmorphic Features and Speech Delay. Cytogenet Genome Res 2015 0.75
18 A 725 kb deletion at 22q13.1 chromosomal region including SOX10 gene in a boy with a neurologic variant of Waardenburg syndrome type 2. Eur J Med Genet 2012 0.75
19 A fetus with ring chromosome 21 characterized by aCGH shows no clinical findings after birth. Prenat Diagn 2010 0.75