Published in Tsitol Genet on February 17, 2005
Skewed X-chromosome inactivation in patients with esophageal carcinoma. Diagn Pathol (2013) 0.80
Unexplained autism is frequently associated with low-level mosaic aneuploidy. J Med Genet (2007) 1.29
Visualization of interphase chromosomes in postmitotic cells of the human brain by multicolour banding (MCB). Chromosome Res (2006) 1.18
Multicolor fluorescent in situ hybridization on post-mortem brain in schizophrenia as an approach for identification of low-level chromosomal aneuploidy in neuropsychiatric diseases. Brain Dev (2001) 1.14
Molecular cytogenetics and cytogenomics of brain diseases. Curr Genomics (2008) 1.12
SEQSEE: a comprehensive program suite for protein sequence analysis. Comput Appl Biosci (1994) 1.07
High resolution multicolor fluorescence in situ hybridization using cyanine and fluorescein dyes: rapid chromosome identification by directly fluorescently labeled alphoid DNA probes. Hum Genet (1996) 1.05
Somatic genome variations in health and disease. Curr Genomics (2010) 1.04
CAMRA: chemical shift based computer aided protein NMR assignments. J Biomol NMR (1998) 0.96
Structure-based thermodynamic analysis of the dissociation of protein phosphatase-1 catalytic subunit and microcystin-LR docked complexes. Protein Sci (2000) 0.95
Variability in the heterochromatin regions of the chromosomes and chromosomal anomalies in children with autism: identification of genetic markers of autistic spectrum disorders. Neurosci Behav Physiol (2007) 0.93
Cytogenetic and molecular-cytogenetic studies of Rett syndrome (RTT): a retrospective analysis of a Russian cohort of RTT patients (the investigation of 57 girls and three boys). Brain Dev (2001) 0.88
Somatic cell genomics of brain disorders: a new opportunity to clarify genetic-environmental interactions. Cytogenet Genome Res (2013) 0.88
Ultrastructure of Babesia WA1 (Apicomplexa: Piroplasma) during infection of erythrocytes in a hamster model. J Parasitol (2006) 0.87
Non-disjunction of chromosome 21, alphoid DNA variation, and sociogenetic features of Down syndrome. Tsitol Genet (2006) 0.87
18p- syndrome: an unusual case and diagnosis by in situ hybridization with chromosome 18-specific alphoid DNA sequence. Hum Genet (1986) 0.86
Ontogenetic variation of the human genome. Curr Genomics (2010) 0.86
Trisomy 21 mosaicism: we may all have a touch of Down syndrome. Cytogenet Genome Res (2013) 0.86
Prenatal diagnosis of trisomy 21 using interphase fluorescence in situ hybridization of post-replicated cells with site-specific cosmid and cosmid contig probes. Prenat Diagn (1995) 0.86
Dynamic mosaicism manifesting as loss, gain and rearrangement of an isodicentric Y chromosome in a male child with growth retardation and abnormal external genitalia. Cytogenet Genome Res (2008) 0.85
Cytogenetic, molecular-cytogenetic, and clinical-genealogical studies of the mothers of children with autism: a search for familial genetic markers for autistic disorders. Neurosci Behav Physiol (2010) 0.84
Cytogenetic and molecular-cytogenetic investigation of Rett syndrome: analysis of 31 cases. Neuroreport (1996) 0.82
[Depressions and disorders of depressive spectrum in general medical practice. Results of the COMPAS program]. Kardiologiia (2004) 0.80
Chimerism and multiple numerical chromosome imbalances in a spontaneously aborted fetus. Tsitol Genet (2007) 0.80
[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
Effects of simvastatin on the phospholipid composition of high-density lipoproteins in patients with hypercholesterolemia. Bull Exp Biol Med (2001) 0.79
[Epigenetic study of Rett's syndrome as an adequate model for autistic disorders]. Zh Nevrol Psikhiatr Im S S Korsakova (2005) 0.79
Analysis of alphoid DNA variation and kinetochore size in human chromosome 21: evidence against pathological significance of alphoid satellite DNA diminutions. Tsitol Genet (1999) 0.79
Rapid chromosomal analysis of germ-line cells by FISH: an investigation of an infertile male with large-headed spermatozoa. Mol Hum Reprod (1996) 0.79
[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
[The use of molecular cytogenetic and cytogenetic techniques for the diagnosis of Prader-Willi and Angelman syndrome]. Zh Nevrol Psikhiatr Im S S Korsakova (2014) 0.78
[Analysis of germ cell populations in ejaculate of men infected with herpes simplex virus]. Ontogenez (2008) 0.78
[Effect of thiol-oxidizing agents on several enzymes in rat liver mitochondria]. Ukr Biokhim Zh (1976) 0.78
[Genotype-phenotype correlations in Rett syndrome: the study of Russian cohort of patients]. Zh Nevrol Psikhiatr Im S S Korsakova (2002) 0.78
Clinical, neurophysiological and immunological correlations in classical Rett syndrome. Brain Dev (2001) 0.78
[Risk factors of chronic venous insufficiency of the lower extremities and possibilities of its medication in therapeutic practice]. Ter Arkh (2006) 0.78
[Clinico-epidemiological program of the study of depression in cardiological practice in patients with arterial hypertension and ischemic heart disease (COORDINATA)]. Kardiologiia (2007) 0.77
Oxidation of plasma low-density lipoproteins from coronary patients with various forms of hypercholesterolemia. Bull Exp Biol Med (2003) 0.77
Two new cases of the Christchurch (Ch1) chromosome 21: evidence for clinical consequences of de novo deletion 21P-. Tsitol Genet (2002) 0.77
16q subtelomeric deletion in proband with congenital malformations and mental retardation. Tsitol Genet (2001) 0.77
[Dynamics of changes in anomalous human cells during prolonged cultivation in the stationary phase. Trisomy 7 cells]. Biull Eksp Biol Med (1977) 0.77
[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
Rapid identification of marker chromosomes by in situ hybridization under different stringency conditions. Anal Cell Pathol (1994) 0.77
[Depression in cardiological practice: pilot results from a multicenter clinico-epidemiological trial in hypertensive patients with ischemic heart disease (koordinata)]. Ter Arkh (2006) 0.77
Pericentric inversion inv(7)(p11q21.1): report on two cases and genotype-phenotype correlations. Tsitol Genet (2006) 0.76
Fluorescence intensity profiles of in situ hybridization signals depict genome architecture within human interphase nuclei. Tsitol Genet (2009) 0.76
[Molecular cytogenetic research on the polymorphism of segments of the constitutive heterochromatin in human chromosomes]. Genetika (1988) 0.76
Molecular-cytogenetic investigation of skewed chromosome X inactivation in Rett syndrome. Brain Dev (2001) 0.76
Association of serum apolipoprotein A-II concentration with combined hyperlipidemia and impaired glucose tolerance. Bull Exp Biol Med (2006) 0.76
[Current methods of molecular cytogenetics in pre- and postnatal diagnosis of chromosome aberrations]. Klin Lab Diagn (2000) 0.76
Double color in situ hybridization of alpha-satellite chromosome 13, 21 specific cosmid clones for a rapid screening of their specificity. Tsitol Genet (1998) 0.76
[Chromosome abnormalities in schizophrenia]. Zh Nevrol Psikhiatr Im S S Korsakova (2006) 0.76
[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
[Molecular cytogenetic pre- and postnatal diagnosis of chromosomal abnormalities]. Vestn Ross Akad Med Nauk (1999) 0.76
[Chromosomal mosaicism in spontaneous abortions: analysis of 650 cases]. Genetika (2010) 0.76
[Diagnosis of numerical chromosomal aberrations in the cells of spontaneous abortions by multicolor fluorescence in situ hybridization (MFISH)]. Klin Lab Diagn (2005) 0.76
[Molecular cytogenetic methods for studying interphase chromosomes in human brain cells]. Genetika (2010) 0.75
Phospholipid composition of high-density lipoproteins reflects lipolysis of triglyceride-rich lipoproteins during hyperlipidemia. Bull Exp Biol Med (2001) 0.75
[Instability of chromosomes in human nerve cells (normal and with neuromental diseases)]. Genetika (2010) 0.75
[Molecular-cytogenetic diagnosis of hereditary diseases associated with diverse anomalies of X chromosome]. Pediatriia (1989) 0.75
[Stationary populations of genetically different homonuclear strains of human cells]. Biull Eksp Biol Med (1978) 0.75
[Mental retardation syndrome due to fragile X chromosome: diagnostic and genetic problems]. Zh Nevrol Psikhiatr Im S S Korsakova (1998) 0.75
[Study of alpha-satellite DNA in cosmid libraries, specific for chromosomes 13, 21, and 22, using fluorescence in situ hybridization]. Genetika (1998) 0.75
[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
[Prenatal diagnosis of hereditary diseases]. Med Sestra (1988) 0.75
[Contemporary views on Rett's syndrome: clinical, cytogenetic and molecular studies]. Zh Nevrol Psikhiatr Im S S Korsakova (1999) 0.75