Nabeel A Affara

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Nabeel A



Publications in SciGraph latest 50 shown

  • 2017-12 Origin and phylogenetic status of the local Ashanti Dwarf pig (ADP) of Ghana based on genetic analysis in BMC GENOMICS
  • 2015-12 Expansion of the HSFY gene family in pig lineages in BMC GENOMICS
  • 2015-03 Karyomapping—a comprehensive means of simultaneous monogenic and cytogenetic PGD: comparison with standard approaches in real time for Marfan syndrome in JOURNAL OF ASSISTED REPRODUCTION AND GENETICS
  • 2014-12 Thrifty metabolic programming in rats is induced by both maternal undernutrition and postnatal leptin treatment, but masked in the presence of both: implications for models of developmental programming in BMC GENOMICS
  • 2013-12 Regions of XY homology in the pig X chromosome and the boundary of the pseudoautosomal region in BMC GENETICS
  • 2013-12 Genome wide analysis reveals single nucleotide polymorphisms associated with fatness and putative novel copy number variants in three pig breeds in BMC GENOMICS
  • 2011-02 An algorithm for determining the origin of trisomy and the positions of chiasmata from SNP genotype data in CHROMOSOME RESEARCH
  • 2010-12 The human RPS4 paralogue on Yq11.223 encodes a structurally conserved ribosomal protein and is preferentially expressed during spermatogenesis in BMC MOLECULAR BIOLOGY
  • 2010-12 Transcriptional changes in response to X chromosome dosage in the mouse: implications for X inactivation and the molecular basis of Turner Syndrome in BMC GENOMICS
  • 2009-04 Two novel mouse genes mapped to chromosome Yp are expressed specifically in spermatids in MAMMALIAN GENOME
  • 2007-12 Bidirectional transcription of a novel chimeric gene mapping to mouse chromosome Yq in BMC EVOLUTIONARY BIOLOGY
  • 2006-09 Gene expression study in the juvenile mouse testis: identification of stage-specific molecular pathways during spermatogenesis in MAMMALIAN GENOME
  • 2005-12 Identification of novel Y chromosome encoded transcripts by testis transcriptome analysis of mice with deletions of the Y chromosome long arm in GENOME BIOLOGY
  • 2004-04 A comparative analysis of the pig, mouse, and human PCDHX genes in MAMMALIAN GENOME
  • 2004-01 Protocadherin X (PCDHX) and Y (PCDHY) genes; multiple mRNA isoforms encoding variant signal peptides and cytoplasmic domains in MAMMALIAN GENOME
  • 2003-07 Usp9y (ubiquitin-specific protease 9 gene on the Y) is associated with a functional promoter and encodes an intact open reading frame homologous to Usp9x that is under selective constraint in MAMMALIAN GENOME
  • 2002-10 A mapping and evolutionary study of porcine sex chromosome gene in MAMMALIAN GENOME
  • 2002-08 The human-specific Yp11.2/Xq21.3 homology block encodes a potentially functional testis-specific TGIF-like retroposon in MAMMALIAN GENOME
  • 2000-11 The role of human and mouse Y chromosome genes in male infertility in JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
  • 2000-10 Conservation of PCDHX in mammals; expression of human X/Y genes predominantly in brain in MAMMALIAN GENOME
  • 1999-01 An exon map of the AZFc male infertility region of the human Y Chromosome in MAMMALIAN GENOME
  • 1998-05 A potential human axonemal dynein heavy-chain gene maps to 17q25 in MAMMALIAN GENOME
  • 1996-09 Characterization of a novel human dynein-related gene that is specifically expressed in testis in MAMMALIAN GENOME
  • 1994-12 A rearrangement on Chromosome 5 of an expressed human β-glucuronidase pseudogene in MAMMALIAN GENOME
  • 1994-02 Molecular genetic investigation of sporadic renal cell carcinoma: analysis of allele loss on chromosomes 3p, 5q, 11p, 17 and 22 in BRITISH JOURNAL OF CANCER
  • 1994-01 Molecular genetic investigations of the mechanism of tumourigenesis in von Hippel-Lindau disease: analysis of allele loss in VHL tumours in HUMAN GENETICS
  • 1993-12 Localization of DNA sequences required for human centromere function through an analysis of rearranged Y chromosomes in NATURE GENETICS
  • 1993-08 Physical mapping of chromosome 3p25-p26 by flourescence in situ hybridisation (FISH) in HUMAN GENETICS
  • 1993-02 Multiple self–healing squamous epitheliomata (ESS1) mapped to chromosome 9q22–q31 in families with common ancestry in NATURE GENETICS
  • 1990-03 A possible common origin of “Y-negative” human XX males and XX true hermaphrodites in HUMAN GENETICS
  • 1990-01 Genotype-phenotype correlations in XX males and their bearing on current theories of sex determination in HUMAN GENETICS
  • 1988-05 X Chromosome deletions detectable by flow cytometry in some patients with steroid sulphatase deficiency (X-linked ichthyosis) in HUMAN GENETICS
  • 1985-08 Multipoint linkage analysis of the short arm of the human X chromosome in families with X-linked muscular dystrophy in HUMAN GENETICS
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