Published in Mol Cytogenet on February 08, 2010
Pregnancies from biopsied human preimplantation embryos sexed by Y-specific DNA amplification. Nature (1990) 6.18
Embryo morphology, developmental rates, and maternal age are correlated with chromosome abnormalities. Fertil Steril (1995) 3.49
Sex matters in meiosis. Science (2002) 2.98
In situ hybridization as a tool to study numerical chromosome aberrations in solid bladder tumors. Histochemistry (1988) 2.26
Comprehensive chromosomal analysis of human preimplantation embryos using whole genome amplification and single cell comparative genomic hybridization. Mol Hum Reprod (2000) 2.15
Chromosome analysis of blastomeres from human embryos by using comparative genomic hybridization. Hum Genet (2000) 1.83
Multicolour FISH detects frequent chromosomal mosaicism and chaotic division in normal preimplantation embryos from fertile patients. Hum Genet (1997) 1.77
Preimplantation genetic diagnosis for an insertional translocation carrier. Hum Reprod (2004) 1.53
Chromosomal mosaicism throughout human preimplantation development in vitro: incidence, type, and relevance to embryo outcome. Hum Reprod (2002) 1.42
Inter-sex variation in synaptonemal complex lengths largely determine the different recombination rates in male and female germ cells. Cytogenet Genome Res (2004) 1.40
Chromosome mosaicism in human embryos. Biol Reprod (1994) 1.29
Detection of aneuploidy and chromosomal mosaicism in human embryos during preimplantation sex determination by fluorescent in situ hybridisation, (FISH). Hum Mol Genet (1993) 1.28
Mechanisms of aneuploidy induction in human oogenesis and early embryogenesis. Cytogenet Genome Res (2005) 1.25
Chromosome mosaicism in cleavage-stage human embryos: evidence of a maternal age effect. Reprod Biomed Online (2003) 1.22
Mosaicism of autosomes and sex chromosomes in morphologically normal, monospermic preimplantation human embryos. Prenat Diagn (1995) 1.22
Centrioles in the beginning of human development. Proc Natl Acad Sci U S A (1991) 1.20
The human zygote inherits its mitotic potential from the male gamete. Hum Reprod (1994) 1.14
An 8.9 Mb 19p13 duplication associated with precocious puberty and a sporadic 3.9 Mb 2q23.3q24.1 deletion containing NR4A2 in mentally retarded members of a family with an intrachromosomal 19p-into-19q between-arm insertion. Eur J Hum Genet (2009) 1.11
Interchromosomal insertions. Identification of five cases and a review. Hum Genet (2000) 1.11
Meiotic outcomes in reciprocal translocation carriers ascertained in 3-day human embryos. Eur J Hum Genet (2002) 1.09
Intrachromosomal insertions: a case report and a review. Hum Genet (1992) 1.07
The origin of genetic defects in the human and their detection in the preimplantation embryo. Hum Reprod Update (1995) 1.00
Fluorescent in-situ hybridization to interphase nuclei of human preimplantation embryos with X and Y chromosome specific probes. Hum Reprod (1991) 0.99
Infertile couples with Robertsonian translocations: preimplantation genetic analysis of embryos reveals chaotic cleavage divisions. Hum Genet (1998) 0.98
Variable aneuploidy mechanisms in embryos from couples with poor reproductive histories undergoing preimplantation genetic screening. Hum Reprod (2007) 0.96
Preimplantation genetic diagnosis of chromosome abnormalities: implications from the outcome for couples with chromosomal rearrangements. Prenat Diagn (2003) 0.92
Analysis of chromosome segregation during preimplantation genetic diagnosis in both male and female translocation heterozygotes. Cytogenet Genome Res (2005) 0.91
Low-order polynomial trends of female-to-male map distance ratios along human chromosomes. Hum Hered (1998) 0.89
Highly abnormal cleavage divisions in preimplantation embryos from translocation carriers. Prenat Diagn (2000) 0.88
Transmission ratio distortion in offspring of mouse heterozygous carriers of a (7.18) Robertsonian translocation. Genetics (2004) 0.86
Meiotic and mitotic behaviour of a ring/deleted chromosome 22 in human embryos determined by preimplantation genetic diagnosis for a maternal carrier. Mol Cytogenet (2009) 0.84
Influence of sex on the meiotic segregation of a t(13;17) Robertsonian translocation: a case study in the pig. Hum Reprod (2009) 0.84
Intrachromosomal insertion of chromosome 7. Clin Genet (1992) 0.82
Chiasma distributions and chromosome segregation in male and female translocation heterozygous mice analysed using FISH. Chromosoma (1998) 0.81
Analysis of meiotic chromosome pairing in the female mouse using a novel minichromosome. Chromosome Res (1998) 0.81
Paternal contribution to aneuploidy in preimplantation embryos. Reprod Biomed Online (2009) 0.80
Pre-implantation genetic diagnosis. Br Med Bull (2000) 0.78
Segregation of a familial balanced (12;10) insertion resulting in Dup(10)(q21.2q22.1) and Del(10)(q21.2q22.1) in first cousins. Am J Med Genet (1997) 0.76
Cytogenetic analysis of human blastocysts with the use of FISH, CGH and aCGH: scientific data and technical evaluation. Hum Reprod (2010) 1.19
Preimplantation genetic diagnosis for myotonic dystrophy type 1: detection of crossover between the gene and the linked marker APOC2. Prenat Diagn (2007) 1.02
Meiotic and mitotic behaviour of a ring/deleted chromosome 22 in human embryos determined by preimplantation genetic diagnosis for a maternal carrier. Mol Cytogenet (2009) 0.84
Expression profiling of DNA repair genes in human oocytes and blastocysts using microarrays. Hum Reprod (2009) 0.83
Preimplantation genetic diagnosis for myotonic dystrophy type 1 in the UK. Neuromuscul Disord (2007) 0.78
Nuclear organisation in totipotent human nuclei and its relationship to chromosomal abnormality. J Cell Sci (2008) 0.78
Immunofluorescence staining of spindles, chromosomes, and kinetochores in human oocytes. Methods Mol Biol (2013) 0.78
Preimplantation genetic diagnosis for single gene disorders: experience with five single gene disorders. Prenat Diagn (2002) 0.77
Complete cytogenetic investigation of oocytes from a young cancer patient with the use of comparative genomic hybridisation reveals meiotic errors. Prenat Diagn (2006) 0.77
Preimplantation genetic diagnosis for retinoblastoma predisposition. Br J Ophthalmol (2007) 0.75
Factors influencing intracytoplasmic sperm injection (ICSI) outcome in men with azoospermia. BJU Int (2013) 0.75