Titel	Veröffentlichungsdatum	Sprache	Zitate
Chromosomal mosaicism goes global	2008/01/01	English	89
Cytogenetic contribution to uniparental disomy (UPD)	2010/01/01	English	86
Genomic SNP array as a gold standard for prenatal diagnosis of foetal ultrasound abnormalities	2012/01/01	English	57
Exosome-delivered microRNAs of “chromosome 19 microRNA cluster” as immunomodulators in pregnancy and tumorigenesis	2012/01/01	English	56
On the origin of trisomy 21 Down syndrome	2008/01/01	English	51
Chromosome distribution in human sperm – a 3D multicolor banding-study	2008/01/01	English	50
Molecular karyotyping by array CGH in a Russian cohort of children with intellectual disability, autism, epilepsy and congenital anomalies	2012/01/01	English	44
Array CGH as a first line diagnostic test in place of karyotyping for postnatal referrals - results from four years’ clinical application for over 8,700 patients	2013/01/01	English	42
Karyotypic analysis and FISH mapping of microsatellite motifs reveal highly differentiated XX/XY sex chromosomes in the pink-tailed worm-lizard (Aprasia parapulchella, Pygopodidae, Squamata)	2013/01/01	English	39
GIN'n'CIN hypothesis of brain aging: deciphering the role of somatic genetic instabilities and neural aneuploidy during ontogeny	2009/01/01	English	36
Selection of euploid blastocysts for cryopreservation with array comparative genomic hybridization (aCGH) results in increased implantation rates in subsequent frozen and thawed embryo transfer cycles	2013/01/01	English	35
Assessment of ERBB2 and EGFR gene amplification and protein expression in gastric carcinoma by immunohistochemistry and fluorescence in situ hybridization	2011/01/01	English	33
Genetic testing for hearing loss in the United States should include deletion/duplication analysis for the deafness/infertility locus at 15q15.3	2013/01/01	English	32
Fluorescence in situ hybridization in combination with the comet assay and micronucleus test in genetic toxicology	2010/01/01	English	31
Intragenic deletion of RBFOX1 associated with neurodevelopmental/neuropsychiatric disorders and possibly other clinical presentations	2013/01/01	English	30
Diagnostic utility of novel combined arrays for genome-wide simultaneous detection of aneuploidy and uniparental isodisomy in losses of pregnancy	2014/01/01	English	27
Complex small supernumerary marker chromosomes – an update	2013/01/01	English	27
Chromosome aberrations in a large series of spontaneous miscarriages in the German population and review of the literature	2014/01/01	English	26
Incidence and patterns of ALK FISH abnormalities seen in a large unselected series of lung carcinomas	2012/01/01	English	25
Chromosome 22q11.2 microdeletion in monozygotic twins with discordant phenotype and deletion size	2012/01/01	English	25
The accuracy of chromosomal microarray testing for identification of embryonic mosaicism in human blastocysts	2014/01/01	English	23
Small supernumerary marker chromosomes (sSMC) in humans; are there B chromosomes hidden among them	2008/01/01	English	23
8p23.1 duplication syndrome differentiated from copy number variation of the defensin cluster at prenatal diagnosis in four new families	2010/01/01	English	22
MLPA for confirmation of array CGH results and determination of inheritance	2010/01/01	English	21
Phylogenetic insight into subgenera Idaeobatus and Malachobatus (Rubus, Rosaceae) inferring from ISH analysis	2015/01/01	English	21
Xq28 (MECP2) microdeletions are common in mutation-negative females with Rett syndrome and cause mild subtypes of the disease	2013/01/01	English	21
On the origin of crossover interference: A chromosome oscillatory movement (COM) model	2011/01/01	English	20
On the paternal origin of trisomy 21 Down syndrome	2010/01/01	English	20
Best diagnostic approach for the genetic evaluation of fetuses after intrauterine death in first, second or third trimester: QF-PCR, karyotyping and/or genome wide SNP array analysis	2014/01/01	English	20
A novel deletion in proximal 22q associated with cardiac septal defects and microcephaly: a case report	2009/01/01	English	19