PubRank

Iu B Iurov

Author PubWeight™ 11.61‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 [Identification of candidate genes of autism on the basis of molecular cytogenetic and in silico studies of the genome organization of chromosomal regions involved in unbalanced rearrangements]. Genetika 2010 0.87
2 [Variations of heterochromatic chromosomal regions and chromosome abnormalities in children with autism: identification of genetic markers in autistic spectrum disorders]. Zh Nevrol Psikhiatr Im S S Korsakova 2006 0.80
3 [Subchromosomal microdeletion identified by molecular karyotyping using DNA microarrays (array CGH) in Rett syndrome girls negative for MECP2 gene mutations]. Zh Nevrol Psikhiatr Im S S Korsakova 2013 0.78
4 [Analysis of germ cell populations in ejaculate of men infected with herpes simplex virus]. Ontogenez 2008 0.78
5 [Genotype-phenotype correlations in Rett syndrome: the study of Russian cohort of patients]. Zh Nevrol Psikhiatr Im S S Korsakova 2002 0.78
6 [Genomic abnormalities in children with mental retardation and autism: the use of comparative genomic hybridization in situ (HRCGH) and molecular karyotyping with DNA-microchips (array CGH)]. Zh Nevrol Psikhiatr Im S S Korsakova 2013 0.77
7 [X chromosome inactivation pattern in elderly women over 70 years of age]. Tsitol Genet 2005 0.76
8 [Molecular cytogenetic research on the polymorphism of segments of the constitutive heterochromatin in human chromosomes]. Genetika 1988 0.76
9 [Cytogenetic, molecular cytogenetic, clinical and genealogical study of mothers of children with autism: a search for family genetic markers of autistic disorders]. Zh Nevrol Psikhiatr Im S S Korsakova 2009 0.76
10 [Chromosome abnormalities in schizophrenia]. Zh Nevrol Psikhiatr Im S S Korsakova 2006 0.76
11 [Current methods of molecular cytogenetics in pre- and postnatal diagnosis of chromosome aberrations]. Klin Lab Diagn 2000 0.76
12 [Chromosomal mosaicism in spontaneous abortions: analysis of 650 cases]. Genetika 2010 0.76
13 [Molecular cytogenetic pre- and postnatal diagnosis of chromosomal abnormalities]. Vestn Ross Akad Med Nauk 1999 0.76
14 [Diagnosis of numerical chromosomal aberrations in the cells of spontaneous abortions by multicolor fluorescence in situ hybridization (MFISH)]. Klin Lab Diagn 2005 0.76
15 [Molecular cytogenetic methods for studying interphase chromosomes in human brain cells]. Genetika 2010 0.75
16 [Molecular cytogenetic studies of chromosomal abnormalities and disorders in nervous and mental diseases: search for biological markers for diagnosis]. Vestn Ross Akad Med Nauk 2001 0.75
17 [Genomic instability in the brain: etiology, pathogenesis and new biological markers of psychiatric disorders]. Vestn Ross Akad Med Nauk 2012 0.75
18 [Method of diagnosing aneuploidies using in situ hybridization: analysis of interphase nuclei]. Biull Eksp Biol Med 1991 0.75
19 [Nervous and mental diseases in boys and mutations in MECP2 gene]. Zh Nevrol Psikhiatr Im S S Korsakova 2004 0.75
20 [Rate of DNA replication and size of replicons in human diploid cells]. Mol Biol (Mosk) 1979 0.75
21 [Contemporary views on Rett's syndrome: clinical, cytogenetic and molecular studies]. Zh Nevrol Psikhiatr Im S S Korsakova 1999 0.75
22 [Quantitative analysis of chromosomal localization of two human cloned satellite DNA III sequences by in situ hybridization]. Genetika 1989 0.75
23 [Molecular genetic polymorphism of the genes of neurotransmitter systems in schizophrenics with early manifestation of the disease]. Zh Nevrol Psikhiatr Im S S Korsakova 2001 0.75
24 [Multidisciplinary approach to the study of a family with many children including several schizophrenics]. Zh Nevropatol Psikhiatr Im S S Korsakova 1992 0.75
25 [A case of deletion of the short arm of the chromosome 21 (21p-) (christchurch chromosome) discovered prenatally:clinical and cytogenetic data]. Tsitol Genet 2004 0.75
26 [The search for a mutation in the gene coding the beta-amyloid protein precursor gene in patients with Alzheimer-type dementias]. Zh Nevrol Psikhiatr Im S S Korsakova 1996 0.75
27 [Use of a cloned alphoid repetitive sequence of human DNA in studying the polymorphism of heterochromatin regions of chromosomes]. Genetika 1988 0.75
28 [Clones sequences of satellite DNA III specific for the centromere heterochromatin of human chromosome 9]. Mol Gen Mikrobiol Virusol 1986 0.75
29 [Chromosomal anomalies in children with undifferentiated forms of metal retardation based on molecular cytogenetic research data]. Tsitol Genet 1994 0.75
30 [Mental retardation syndrome due to fragile X chromosome: diagnostic and genetic problems]. Zh Nevrol Psikhiatr Im S S Korsakova 1998 0.75
31 [Study of alpha-satellite DNA in cosmid libraries, specific for chromosomes 13, 21, and 22, using fluorescence in situ hybridization]. Genetika 1998 0.75
32 [Chromosome organization of human alphoid DNA]. Dokl Akad Nauk SSSR 1986 0.75
33 [Unusual case of 18p- syndrome: diagnosis using a cloned DNA fragment]. Tsitol Genet 1986 0.75
34 Species specific variant of human centromeric DNA repeats: localization on chromosome 18 and recent amplification in human ancestral line. Mol Gen Mikrobiol Virusol 1989 0.75
35 [Molecular cytogenetic study of Robertsonian translocation 13;14 and Down syndrome in a 3-year-old infant]. Tsitol Genet 2005 0.75
36 [Structural analysis of the Alu-containing DNA fragment with disperse distribution in human chromosomes]. Genetika 1984 0.75
37 [Original molecular cytogenetic approach to determining spontaneous chromosomal mutations in the interphase cells to evaluate the mutagenic activity of environmental factors]. Gig Sanit 2011 0.75
38 [Replication of chromosomal DNA in Chinese hamster cells, cultivated at different temperatures]. Tsitologiia 1977 0.75
39 [Molecular-cytogenetic diagnosis of hereditary diseases associated with diverse anomalies of X chromosome]. Pediatriia 1989 0.75
40 [Serotonin type 2a (5-HTR2A) receptor gene polymorphism and personality traits in patients with endogenous psychoses]. Genetika 2001 0.75
41 [Quantitative analysis of fluorescence in situ hybridization (FISH) signals for molecular cytogenetic diagnosis]. Klin Lab Diagn 2005 0.75
42 [Cloned fragment of human repetitive DNA specific for the centromere heterochromatin of chromosome 3]. Mol Gen Mikrobiol Virusol 1986 0.75
43 [Interindividual hyperpolymorphism of autosomal satellites III of human DNA]. Genetika 1990 0.75
44 [Development of an original computer program FISHMet: use for molecular cytogenetic diagnosis and genome mapping by fluorescent in situ hybridization (FISH)]. Klin Lab Diagn 2000 0.75
45 [Optimization of the conditions for the in situ hybridization of cloned DNA sequences and for the differential staining of human chromosomes]. Biull Eksp Biol Med 1984 0.75
46 [Discovery of a new family of human alpha-satellite DNA]. Dokl Akad Nauk 1992 0.75
47 [Human alpha-satellite DNA specific to chromosomes 13 and 21: use for the analysis of polymorphism of acrocentric chromosomes and the origin of the additional chromosome 21 in Down's syndrome]. Genetika 1991 0.75
48 [Correlation of polymorphism of heterochromatin segments with hybridization on chromosome preparations of various cloned repeated human DNA sequences]. Genetika 1989 0.75
49 [Instability of chromosomes in human nerve cells (normal and with neuromental diseases)]. Genetika 2010 0.75
50 [A review of the data from cytogenetic and molecular cytogenetic research on human supernumerary minichromosomes]. Tsitol Genet 1995 0.75
51 [DNA replication in cultured amniotic fluid cells]. Biull Eksp Biol Med 1981 0.75
52 [Serotonin receptor gene allele polymorphism (5HTR2A) and clinical pathogenetic characteristics in patients with schizophrenia and schizophrenia spectrum disorders]. Zh Nevrol Psikhiatr Im S S Korsakova 2000 0.75
53 [An analysis of human marker chromosomes originating from chromosome 21 by using in situ hybridization]. Tsitol Genet 1996 0.75
54 [Cloned fragment of human alphoid DNA--a molecular marker of the pericentromeric region of chromosome 18]. Genetika 1986 0.75
55 [Molecular genetics of the human brain]. Vestn Ross Akad Med Nauk 1992 0.75
56 [Cytogenetic and molecular genetic diagnostics of Rett syndrome in children]. Zh Nevrol Psikhiatr Im S S Korsakova 1998 0.75
57 [A method of analyzing the chromosome localization of repetitive nucleotide sequences by using hybridization in situ]. Genetika 1988 0.75
58 [Characteristics of DNA replication in the long-term culture of human cells at the stationary phase]. Tsitologiia 1987 0.75
59 [DNA replication in a primary culture of human hepatocytes]. Dokl Akad Nauk SSSR 1976 0.75
60 [A familial case of mental retardation syndrome linked to fragile X chromosome]. Zh Nevrol Psikhiatr Im S S Korsakova 1998 0.75
61 [Rate of DNA synthesis and the size of replication units in cell culture of Drosophila melanogaster]. Mol Biol (Mosk) 1979 0.75
62 [A cytogenetic study of the human chorion for the purpose of the prenatal diagnosis of hereditary diseases]. Tsitologiia 1990 0.75