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Nabeel Affara

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Benjamin M Skinner; Kim Lachani; Carole A Sargent; Nabeel A Affara
Regions of XY homology in the pig X chromosome and the boundary of the pseudoautosomal region.
Claire R Quilter; C P Reiter; Carole A Sargent; Olwen I Southwood; Meenakshi R Bagga; J Bauer; G Evans; Darren K Griffin; E L Hutchinson; Alan J Mileham; Nabeel A Affara
An association and haplotype analysis of porcine maternal infanticide: a model for human puerperal psychosis?
Julie Cocquet; Peter Ellis; Shantha K Mahadevaiah; Daniel Vaiman; Nabeel A Affara; Paul S Burgoyne
A genetic basis for a postmeiotic X versus Y chromosome intragenomic conflict in the mouse.

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All Publications

2013: Benjamin M Skinner; Kim Lachani; Carole A Sargent; Nabeel A Affara
Regions of XY homology in the pig X chromosome and the boundary of the pseudoautosomal region.
BMC genetics 2013;14():3.
2012: Claire R Quilter; C P Reiter; Carole A Sargent; Olwen I Southwood; Meenakshi R Bagga; J Bauer; G Evans; Darren K Griffin; E L Hutchinson; Alan J Mileham; Nabeel A Affara
An association and haplotype analysis of porcine maternal infanticide: a model for human puerperal psychosis?
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2012;159B(8):908-27.
2012: Julie Cocquet; Peter Ellis; Shantha K Mahadevaiah; Daniel Vaiman; Nabeel A Affara; Paul S Burgoyne
A genetic basis for a postmeiotic X versus Y chromosome intragenomic conflict in the mouse.
PLoS genetics 2012;8(9):e1002900.
2012: Batbayar Khulan; Stephen Owens; Andrew M Prentice; Benjamin M Skinner; Julien Bauer; Gusztav Belteki; Miguel Constancia; Wendy N Cooper; David D Dunger; Nabeel A Affara
Periconceptional maternal micronutrient supplementation is associated with widespread gender related changes in the epigenome: a study of a unique resource in the Gambia.
Human molecular genetics 2012;21(9):2086-101.
2012: Wendy N Cooper; Nabeel A Affara; Gusztav Belteki; Miguel Constância; Cathy E Elks; Batbayar Khulan; Ken K Ong; Stephen Owens; Andrew M Prentice; Veronica Seidel; David D Dunger
DNA methylation profiling at imprinted loci after periconceptional micronutrient supplementation in humans: results of a pilot randomized controlled trial.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2012;26(5):1782-90.
2011: Peter Ellis; Joanne Bacon; Nabeel A Affara
Association of Sly with sex-linked gene amplification during mouse evolution: a side effect of genomic conflict in spermatids?
Human molecular genetics 2011;20(15):3010-21.
2011: Alem S Gabriel; Terry J Hassold; Alan R Thornhill; Nabeel A Affara; Alan H Handyside; Darren K Griffin
An algorithm for determining the origin of trisomy and the positions of chiasmata from SNP genotype data.
Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology 2011;19(2):155-63.
2010: Julie Cocquet; Peter Ellis; Yasuhiro Yamauchi; Jonathan M Riel; Thomas P S Karacs; Aine Rattigan; Obah A Ojarikre; Nabeel A Affara; Monika A Ward; Paul S Burgoyne
Deficiency in the multicopy Sycp3-like X-linked genes Slx and Slxl1 causes major defects in spermatid differentiation.
Molecular biology of the cell 2010;21(20):3497-505.
2010: Claire R Quilter; A C Karcanias; Meenakshi R Bagga; S Duncan; A Murray; Gerard S Conway; Carole A Sargent; Nabeel A Affara
Analysis of X chromosome genomic DNA sequence copy number variation associated with premature ovarian failure (POF).
Human reproduction (Oxford, England) 2010;25(8):2139-50.
2010: Alexandra M Lopes; Ricardo N Miguel; Carole A Sargent; Peter Ellis; António Amorim; Nabeel A Affara
The human RPS4 paralogue on Yq11.223 encodes a structurally conserved ribosomal protein and is preferentially expressed during spermatogenesis.
BMC molecular biology 2010;11():33.
2010: Alexandra M Lopes; Paul S Burgoyne; Andrew Ojarikre; Julien Bauer; Carole A Sargent; António Amorim; Nabeel A Affara
Transcriptional changes in response to X chromosome dosage in the mouse: implications for X inactivation and the molecular basis of Turner Syndrome.
BMC genomics 2010;11():82.
2009: Julie Cocquet; Peter Ellis; Yasuhiro Yamauchi; Shantha K Mahadevaiah; Nabeel A Affara; Monika A Ward; Paul S Burgoyne
The multicopy gene Sly represses the sex chromosomes in the male mouse germline after meiosis.
PLoS biology 2009;7(11):e1000244.
2009: Osman Jafer; S Zhang; Carole A Sargent; M A Mellencamp; G Evans; Alan J Mileham; Graham S Plastow; Nabeel A Affara
Identification of SNPs in porcine genes expressed during porcine respiratory and reproductive syndrome virus infection.
Animal genetics 2009;40(4):580-2.
2009: Lydia Ferguson; Peter Ellis; Nabeel A Affara
Two novel mouse genes mapped to chromosome Yp are expressed specifically in spermatids.
Mammalian genome : official journal of the International Mammalian Genome Society 2009;20(4):193-206.
2009: J F Yuan; S J Zhang; Osman Jafer; Robert A Furlong; O E Chausiaux; Carole A Sargent; G H Zhang; Nabeel A Affara
Global transcriptional response of pig brain and lung to natural infection by Pseudorabies virus.
BMC microbiology 2009;9():246.
2009: Tiffany J Morris; Mark Vickers; Peter Gluckman; Stewart Gilmour; Nabeel A Affara
Transcriptional profiling of rats subjected to gestational undernourishment: implications for the developmental variations in metabolic traits.
PloS one 2009;4(9):e7271.
2009: Antonio M Ramos; R P M A Crooijmans; Nabeel A Affara; Andreia J Amaral; Alan L Archibald; Jonathan E Beever; Christian Bendixen; Carol Churcher; Richard Clark; Patrick Dehais; Mark S Hansen; Jakob Hedegaard; Zhi-Liang Hu; Hindrik H Kerstens; Andy S Law; Hendrik-Jan Megens; Denis Milan; Danny J Nonneman; Gary A Rohrer; Max F Rothschild; Tim P L Smith; Robert D Schnabel; Curt P Van Tassell; Jeremy F Taylor; Ralph T Wiedmann; Lawrence B Schook; Martien A M Groenen
Design of a high density SNP genotyping assay in the pig using SNPs identified and characterized by next generation sequencing technology.
PloS one 2009;4(8):e6524.
2008: Claire R Quilter; Colin L Gilbert; Gina L Oliver; Osman Jafer; Robert A Furlong; Sarah C Blott; Anna E Wilson; Carole A Sargent; Alan J Mileham; Nabeel A Affara
Gene expression profiling in porcine maternal infanticide: a model for puerperal psychosis.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2008;147B(7):1126-37.
2008: Oriane E Chausiaux; Margaret H Abel; Fiona O Baxter; Walid T Khaled; Peter Ellis; Harry M Charlton; Nabeel A Affara
Hypogonadal mouse, a model to study the effects of the endogenous lack of gonadotropins on apoptosis.
Biology of reproduction 2008;78(1):77-90.
2007: Claire R Quilter; Sarah C Blott; Anna E Wilson; Meenakshi R Bagga; Carole A Sargent; Gina L Oliver; Olwen I Southwood; Colin L Gilbert; Alan J Mileham; Nabeel A Affara
Porcine maternal infanticide as a model for puerperal psychosis.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2007;144B(7):862-8.
2007: Peter Ellis; Robert A Furlong; Sarah J Conner; Jackson C Kirkman-Brown; Masoud Afnan; Christopher L R Barratt; Darren K Griffin; Nabeel A Affara
Coordinated transcriptional regulation patterns associated with infertility phenotypes in men.
Journal of medical genetics 2007;44(8):498-508.
2007: A C Karcanias; Koichi Ichimura; Michael John Mitchell; Carole A Sargent; Nabeel A Affara
Analysis of sex chromosome abnormalities using X and Y chromosome DNA tiling path arrays.
Journal of medical genetics 2007;44(7):429-36.
2007: Peter Ellis; Lydia Ferguson; Emily Clemente; Nabeel A Affara
Bidirectional transcription of a novel chimeric gene mapping to mouse chromosome Yq.
BMC evolutionary biology 2007;7():171.
2006: Emily Clemente; Robert A Furlong; Kate L Loveland; Nabeel A Affara
Gene expression study in the juvenile mouse testis: identification of stage-specific molecular pathways during spermatogenesis.
Mammalian genome : official journal of the International Mammalian Genome Society 2006;17(9):956-75.
2006: Louise van der Weyden; Mark J Arends; Oriane E Chausiaux; Peter Ellis; Ulrike C Lange; M Azim Surani; Nabeel A Affara; Yoshinori Murakami; David J Adams; Allan Bradley
Loss of TSLC1 causes male infertility due to a defect at the spermatid stage of spermatogenesis.
Molecular and cellular biology 2006;26(9):3595-609.
2006: Peter Ellis; Nabeel A Affara
Spermatogenesis and sex chromosome gene content: an evolutionary perspective.
Human fertility (Cambridge, England) 2006;9(1):1-7.
2005: Peter Ellis; Emily Clemente; Penny Ball; Aminata Touré; Lydia Ferguson; James M A Turner; Kate L Loveland; Nabeel A Affara; Paul S Burgoyne
Deletions on mouse Yq lead to upregulation of multiple X- and Y-linked transcripts in spermatids.
Human molecular genetics 2005;14(18):2705-15.
2005: Aminata Touré; Emily Clemente; Peter Ellis; Shantha K Mahadevaiah; Obah A Ojarikre; Penny A F Ball; Louise Reynard; Kate L Loveland; Paul S Burgoyne; Nabeel A Affara
Identification of novel Y chromosome encoded transcripts by testis transcriptome analysis of mice with deletions of the Y chromosome long arm.
Genome biology 2005;6(12):R102.
2004: Alireza Fazeli; Nabeel A Affara; Mike Hubank; William V Holt
Sperm-induced modification of the oviductal gene expression profile after natural insemination in mice.
Biology of reproduction 2004;71(1):60-5.
2004: Patricia Blanco-Arias; Carole A Sargent; Nabeel A Affara
A comparative analysis of the pig, mouse, and human PCDHX genes.
Mammalian genome : official journal of the International Mammalian Genome Society 2004;15(4):296-306.
2004: Peter Ellis; Robert A Furlong; A Wilson; S Morris; D Carter; G Oliver; Cristin G Print; Paul S Burgoyne; Kate L Loveland; Nabeel A Affara
Modulation of the mouse testis transcriptome during postnatal development and in selected models of male infertility.
Molecular human reproduction 2004;10(4):271-81.
2004: Patricia Blanco-Arias; Carole A Sargent; Nabeel A Affara
Protocadherin X ( PCDHX) and Y ( PCDHY) genes; multiple mRNA isoforms encoding variant signal peptides and cytoplasmic domains.
Mammalian genome : official journal of the International Mammalian Genome Society 2004;15(1):41-52.
2003: Nicola M Hall; Graeme M Brown; Robert A Furlong; Carole A Sargent; Michael John Mitchell; Dominique Rocha; Nabeel A Affara
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.
Mammalian genome : official journal of the International Mammalian Genome Society 2003;14(7):437-47.
2003: Nabeel A Affara
Resource and hardware options for microarray-based experimentation.
Briefings in functional genomics & proteomics 2003;2(1):7-20.
2002: Claire R Quilter; Sarah C Blott; Alan J Mileham; Nabeel A Affara; Carole A Sargent; Darren K Griffin
A mapping and evolutionary study of porcine sex chromosome genes.
Mammalian genome : official journal of the International Mammalian Genome Society 2002;13(10):588-94.
2002: Patricia Blanco-Arias; Carole A Sargent; Nabeel A Affara
The human-specific Yp11.2/Xq21.3 homology block encodes a potentially functional testis-specific TGIF-like retroposon.
Mammalian genome : official journal of the International Mammalian Genome Society 2002;13(8):463-8.
2001: Norman L J Ross; J Yang; Carole A Sargent; CA Boucher; S Nanko; Rekha Wadekar; N A Williams; Nabeel A Affara; Timothy J Crow
Triplication of several PAR1 genes and part of the Homo sapiens specific Yp11.2/Xq21.3 region of homology in a 46,X,t(X;Y)(p22.33;p11.2) male with schizophrenia.
Journal of medical genetics 2001;38(10):710-9.
2001: CA Boucher; Carole A Sargent; T Ogata; Nabeel A Affara
Breakpoint analysis of Turner patients with partial Xp deletions: implications for the lymphoedema gene location.
Journal of medical genetics 2001;38(9):591-8.
2001: P Blanco; Carole A Sargent; CA Boucher; G Howell; M Ross; Nabeel A Affara
A novel poly(A)-binding protein gene (PABPC5) maps to an X-specific subinterval in the Xq21.3/Yp11.2 homology block of the human sex chromosomes.
Genomics 2001;74(1):1-11.
2001: Dominique Rocha; Nabeel A Affara
Insights into the molecular basis of male infertility.
Indian journal of physiology and pharmacology 2001;45(2):136-47.
2001: Carole A Sargent; CA Boucher; P Blanco; I J Chalmers; L Highet; N Hall; N Ross; T Crow; Nabeel A Affara
Characterization of the human Xq21.3/Yp11 homology block and conservation of organization in primates.
Genomics 2001;73(1):77-85.
2000: Nabeel A Affara; Michael John Mitchell
The role of human and mouse Y chromosome genes in male infertility.
Journal of endocrinological investigation 2000;23(10):630-45.
2000: P Blanco; M Shlumukova; Carole A Sargent; Mark A Jobling; Nabeel A Affara; Matthew E Hurles
Divergent outcomes of intrachromosomal recombination on the human Y chromosome: male infertility and recurrent polymorphism.
Journal of medical genetics 2000;37(10):752-8.
2000: P Blanco; Carole A Sargent; CA Boucher; Michael John Mitchell; Nabeel A Affara
Conservation of PCDHX in mammals; expression of human X/Y genes predominantly in brain.
Mammalian genome : official journal of the International Mammalian Genome Society 2000;11(10):906-14.
2000: Carole A Sargent; A Kidd; S Moore; J Dean; G T Besley; Nabeel A Affara
Five cases of isolated glycerol kinase deficiency, including two families: failure to find genotype:phenotype correlation.
Journal of medical genetics 2000;37(6):434-41.
2000: Emma R Woodward; Alexander Buchberger; Steven C Clifford; L D Hurst; Nabeel A Affara; Eamonn R Maher
Comparative sequence analysis of the VHL tumor suppressor gene.
Genomics 2000;65(3):253-65.
2000: Emma R Woodward; Steven C Clifford; Dewi Astuti; Nabeel A Affara; Eamonn R Maher
Familial clear cell renal cell carcinoma (FCRC): clinical features and mutation analysis of the VHL, MET, and CUL2 candidate genes.
Journal of medical genetics 2000;37(5):348-53.
1999: Carole A Sargent; CA Boucher; Stefan Kirsch; G Brown; Birgit Weiss; Anita Trundley; Paul S Burgoyne; N Saut; C Durand; N Levy; Philippe Terriou; Timothy B Hargreave; H Cooke; Michael John Mitchell; Gudrun A Rappold; Nabeel A Affara
The critical region of overlap defining the AZFa male infertility interval of proximal Yq contains three transcribed sequences.
Journal of medical genetics 1999;36(9):670-7.
1999: J Wong; P Blanco; Nabeel A Affara
An exon map of the AZFc male infertility region of the human Y chromosome.
Mammalian genome : official journal of the International Mammalian Genome Society 1999;10(1):57-61.
1998: Mark A Jobling; G A Williams; G A Schiebel; G A Pandya; G A McElreavey; G A Salas; Gudrun A Rappold; Nabeel A Affara; Chris Tyler-Smith
A selective difference between human Y-chromosomal DNA haplotypes.
Current biology : CB 1998;8(25):1391-4.
1998: Michael Jones; K N Tirosvoutis; C Bowgen; P Davey; S Moore; Susan Naylor; Nabeel A Affara
Regional assignment and expression analysis of 29 expressed sequence tags mapped to chromosome 3.
Genomics 1998;53(3):400-5.
1998: IE Ehrmann; PS Ellis; S Mazeyrat; SM Duthie; Neil Brockdorff; Marie-Geneviève Mattei; M A Gavin; Nabeel A Affara; Graeme M Brown; Elizabeth Simpson; Michael John Mitchell; D M Scott
Characterization of genes encoding translation initiation factor eIF-2gamma in mouse and human: sex chromosome localization, escape from X-inactivation and evolution.
Human molecular genetics 1998;7(11):1725-37.
1998: S Mazeyrat; N Saut; Carole A Sargent; Sean M Grimmond; guy Longepied; IE Ehrmann; PS Ellis; Andy Greenfield; Nabeel A Affara; Michael John Mitchell
The mouse Y chromosome interval necessary for spermatogonial proliferation is gene dense with syntenic homology to the human AZFa region.
Human molecular genetics 1998;7(11):1713-24.
1998: Steven C Clifford; A H Prowse; Nabeel A Affara; C H Buys; Eamonn R Maher
Inactivation of the von Hippel-Lindau (VHL) tumour suppressor gene and allelic losses at chromosome arm 3p in primary renal cell carcinoma: evidence for a VHL-independent pathway in clear cell renal tumourigenesis.
Genes, chromosomes & cancer 1998;22(3):200-9.
1998: Graeme M Brown; M Leversha; M Hulten; Malcolm A Ferguson-Smith; Nabeel A Affara; Robert A Furlong
Genetic analysis of meiotic recombination in humans by use of sperm typing: reduced recombination within a heterozygous paracentric inversion of chromosome 9q32-q34.3.
American journal of human genetics 1998;62(6):1484-92.
1998: I Milisav; Nabeel A Affara
A potential human axonemal dynein heavy-chain gene maps to 17q25.
Mammalian genome : official journal of the International Mammalian Genome Society 1998;9(5):404-7.
1998: SF Slaney; I J Chalmers; Nabeel A Affara; Lyn S Chitty
An autosomal or X linked mutation results in true hermaphrodites and 46,XX males in the same family.
Journal of medical genetics 1998;35(1):17-22.
1998: Graeme M Brown; Robert A Furlong; Carole A Sargent; R P Erickson; guy Longepied; Michael John Mitchell; Michael Jones; Timothy B Hargreave; H J Cooke; Nabeel A Affara
Characterisation of the coding sequence and fine mapping of the human DFFRY gene and comparative expression analysis and mapping to the Sxrb interval of the mouse Y chromosome of the Dffry gene.
Human molecular genetics 1998;7(1):97-107.
1997: Emma R Woodward; Charis Eng; R McMahon; R Voutilainen; Nabeel A Affara; bruce ponder; Eamonn R Maher
Genetic predisposition to phaeochromocytoma: analysis of candidate genes GDNF, RET and VHL.
Human molecular genetics 1997;6(7):1051-6.
1997: A H Prowse; AR Webster; Frances M Richards; Stéphane Richard; Sylviane Olschwang; F Resche; Nabeel A Affara; Eamonn R Maher
Somatic inactivation of the VHL gene in Von Hippel-Lindau disease tumors.
American journal of human genetics 1997;60(4):765-71.
1997: HR Burkin; Dean J Burkin; P M Davey; Darren K Griffin; Nabeel A Affara
Mapping, sequence, and expression analysis of the human fertilin beta gene (FTNB).
Genomics 1997;40(1):190-2.
1997: Michael Jones; Y Zhang; K N Tirosvoutis; P M Davey; AR Webster; D Walsh; Nigel K Spurr; Nabeel A Affara
Chromosomal assignment of 311 sequences transcribed in human adult testis.
Genomics 1997;40(1):155-67.
1997: Peter H Vogt; Nabeel A Affara; P Davey; M Hammer; M A Jobling; Y F Lau; Michael John Mitchell; Werner Schempp; Chris Tyler-Smith; G Williams; P Yen; Gudrun A Rappold
Report of the Third International Workshop on Y Chromosome Mapping 1997. Heidelberg, Germany, April 13-16, 1997.
Cytogenetics and cell genetics 1997;79(1-2):1-20.
1996: Michael Jones; Robert A Furlong; HR Burkin; I J Chalmers; Graeme M Brown; O Khwaja; Nabeel A Affara
The Drosophila developmental gene fat facets has a human homologue in Xp11.4 which escapes X-inactivation and has related sequences on Yq11.2.
Human molecular genetics 1996;5(11):1695-701.
1996: I Milisav; Michael Jones; Nabeel A Affara
Characterization of a novel human dynein-related gene that is specifically expressed in testis.
Mammalian genome : official journal of the International Mammalian Genome Society 1996;7(9):667-72.
1996: Robert A Furlong; C Y Zhou; Malcolm A Ferguson-Smith; Nabeel A Affara
Characterization of a kinesin-related gene ATSV, within the tuberous sclerosis locus (TSC1) candidate region on chromosome 9Q34.
Genomics 1996;33(3):421-9.
1996: Carole A Sargent; H Briggs; I J Chalmers; Bronwen Lambson; E Walker; Nabeel A Affara
The sequence organization of Yp/proximal Xq homologous regions of the human sex chromosomes is highly conserved.
Genomics 1996;32(2):200-9.
1996: B Zbar; T Kishida; F Chen; L Schmidt; Eamonn R Maher; Frances M Richards; P A Crossey; AR Webster; Nabeel A Affara; Malcolm A Ferguson-Smith; H Brauch; D Glavac; Hartmut P H Neumann; S Tisherman; J J Mulvihill; D J Gross; T Shuin; J Whaley; BR Seizinger; N Kley; Sylviane Olschwang; Cécile Boisson; Stéphane Richard; C H Lips; M Lerman
Germline mutations in the Von Hippel-Lindau disease (VHL) gene in families from North America, Europe, and Japan.
Human mutation 1996;8(4):348-57.
1996: Nabeel A Affara; Jack alvarez; W Brown; H Cooke; P Davey; Nathan Ellis; J M Graves; M Jones; Michael John Mitchell; G Rappold; Chris Tyler-Smith; P Yen; Y F Lau
Report of the Second International Workshop on Y Chromosome Mapping 1995.
Cytogenetics and cell genetics 1996;73(1-2):33-76.
1995: K Foster; R J Osborne; R A Huddart; Nabeel A Affara; Malcolm A Ferguson-Smith; Eamonn R Maher
Molecular genetic analysis of the von Hippel-Lindau disease (VHL) tumour suppressor gene in gonadal tumours.
European journal of cancer (Oxford, England : 1990) 1995;31A(13-14):2392-5.
1995: Frances M Richards; S J Payne; B Zbar; Nabeel A Affara; Malcolm A Ferguson-Smith; Eamonn R Maher
Molecular analysis of de novo germline mutations in the von Hippel-Lindau disease gene.
Human molecular genetics 1995;4(11):2139-43.
1995: Michael Jones; P M Davey; H Aplin; Nabeel A Affara
Expression analysis, genomic structure, and mapping to 7q31 of the human sperm adhesion molecule gene SPAM1.
Genomics 1995;29(3):796-800.
1995: K N Tirosvoutis; A Divane; M Jones; Nabeel A Affara
Characterization of a novel zinc finger gene (ZNF165) mapping to 6p21 that is expressed specifically in testis.
Genomics 1995;28(3):485-90.
1995: I Wang; Dominique Weil; Jacqueline Levilliers; Nabeel A Affara; ALBERT DE LA CHAPELLE; Christine Petit
Prevalence and molecular analysis of two hot spots for ectopic recombination leading to XX maleness.
Genomics 1995;28(1):52-8.
1995: S Herrell; F J Novo; R Charlton; Nabeel A Affara
Development and physical analysis of YAC contigs covering 7 Mb of Xp22.3-p22.2.
Genomics 1995;25(2):526-37.
1995: C Y Zhou; K Y Wu; MA Leversha; Robert A Furlong; Malcolm A Ferguson-Smith; Nabeel A Affara
Physical analysis of the tuberous sclerosis region in 9q34.
Genomics 1995;25(1):304-8.
1994: Carole A Sargent; I J Chalmers; MA Leversha; Nabeel A Affara
A rearrangement on chromosome 5 of an expressed human beta-glucuronidase pseudogene.
Mammalian genome : official journal of the International Mammalian Genome Society 1994;5(12):791-6.
1994: K Foster; A Prowse; Anke Van den Berg; S Fleming; M M Hulsbeek; P A Crossey; Frances M Richards; P Cairns; Nabeel A Affara; Malcolm A Ferguson-Smith
Somatic mutations of the von Hippel-Lindau disease tumour suppressor gene in non-familial clear cell renal carcinoma.
Human molecular genetics 1994;3(12):2169-73.
1994: Graeme M Brown; Robert A Furlong; Nabeel A Affara
A dinucleotide repeat polymorphism at the D9S749 locus.
Human molecular genetics 1994;3(9):1713.
1994: Carole A Sargent; C Young; S Marsh; Malcolm A Ferguson-Smith; Nabeel A Affara
The glycerol kinase gene family: structure of the Xp gene, and related intronless retroposons.
Human molecular genetics 1994;3(8):1317-24.
1994: P A Crossey; Frances M Richards; K Foster; J S Green; A Prowse; F Latif; M I Lerman; B Zbar; Nabeel A Affara; Malcolm A Ferguson-Smith
Identification of intragenic mutations in the von Hippel-Lindau disease tumour suppressor gene and correlation with disease phenotype.
Human molecular genetics 1994;3(8):1303-8.
1994: Nabeel A Affara; E Bentley; P Davey; A Pelmear; Michael Jones
The identification of novel gene sequences of the human adult testis.
Genomics 1994;22(1):205-10.
1994: M E Phipps; F Latif; A Prowse; S J Payne; J Dietz-Band; M Leversha; Nabeel A Affara; Anthony T Moore; J Tolmie; A Schinzel
Molecular genetic analysis of the 3p- syndrome.
Human molecular genetics 1994;3(6):903-8.
1994: Frances M Richards; P A Crossey; M E Phipps; K Foster; F Latif; G Evans; J Sampson; M I Lerman; B Zbar; Nabeel A Affara
Detailed mapping of germline deletions of the von Hippel-Lindau disease tumour suppressor gene.
Human molecular genetics 1994;3(4):595-8.
1994: K Foster; P A Crossey; P Cairns; J W Hetherington; Frances M Richards; Michael Jones; E Bentley; Nabeel A Affara; Malcolm A Ferguson-Smith; Eamonn R Maher
Molecular genetic investigation of sporadic renal cell carcinoma: analysis of allele loss on chromosomes 3p, 5q, 11p, 17 and 22.
British journal of cancer 1994;69(2):230-4.
1994: Nabeel A Affara; Y F Lau; H Briggs; P Davey; M H Jones; O Khwaja; Michael John Mitchell; Carole A Sargent
Report and abstracts of the First International Workshop on Y Chromosome Mapping 1994. Cambridge, England, April 2-5, 1994.
Cytogenetics and cell genetics 1994;67(4):359-402.
1993: Chris Tyler-Smith; R J Oakey; Zoia Larin; R B Fisher; M Crocker; Nabeel A Affara; M A Ferguson-Smith; M Muenke; Orsetta Zuffardi; Mark A Jobling
Localization of DNA sequences required for human centromere function through an analysis of rearranged Y chromosomes.
Nature genetics 1993;5(4):368-75.
1993: J E Lyall; Graeme M Brown; Robert A Furlong; Malcolm A Ferguson-Smith; Nabeel A Affara
A method for creating chromosome-specific plasmid libraries enriched in clones containing [CA]n microsatellite repeat sequences directly from flow-sorted chromosomes.
Nucleic acids research 1993;21(19):4641-2.
1993: M E Phipps; Eamonn R Maher; Nabeel A Affara; F Latif; M A Leversha; M E Ferguson-Smith; Y Nakamura; M Lerman; B Zbar; Malcolm A Ferguson-Smith
Physical mapping of chromosome 3p25-p26 by fluorescence in situ hybridisation (FISH).
Human genetics 1993;92(1):18-22.
1993: Frances M Richards; M E Phipps; F Latif; M Yao; P A Crossey; K Foster; W M Linehan; Nabeel A Affara; M I Lerman; B Zbar
Mapping the Von Hippel-Lindau disease tumour suppressor gene: identification of germline deletions by pulsed field gel electrophoresis.
Human molecular genetics 1993;2(7):879-82.
1993: Robert A Furlong; D R Goudie; Nigel P Carter; J E Lyall; Nabeel A Affara; Malcolm A Ferguson-Smith
Analysis of four microsatellite markers on the long arm of chromosome 9 by meiotic recombination in flow-sorted single sperm.
American journal of human genetics 1993;52(6):1191-9.
1993: Nabeel A Affara; I J Chalmers; Malcolm A Ferguson-Smith
Analysis of the SRY gene in 22 sex-reversed XY females identifies four new point mutations in the conserved DNA binding domain.
Human molecular genetics 1993;2(6):785-9.
1993: D R Goudie; M A Yuille; MA Leversha; Robert A Furlong; Nigel P Carter; M J Lush; Nabeel A Affara; Malcolm A Ferguson-Smith
Multiple self-healing squamous epitheliomata (ESS1) mapped to chromosome 9q22-q31 in families with common ancestry.
Nature genetics 1993;3(2):165-9.
1993: Carole A Sargent; Nabeel A Affara; E Bentley; A Pelmear; D M Bailey; P Davey; D Dow; MA Leversha; H Aplin; G T Besley
Cloning of the X-linked glycerol kinase deficiency gene and its identification by sequence comparison to the Bacillus subtilis homologue.
Human molecular genetics 1993;2(2):97-106.
1993: R M Harris; Nigel P Carter; B Griffiths; D Goudie; R M Hampson; J R W Yates; Nabeel A Affara; Malcolm A Ferguson-Smith
Physical mapping within the tuberous sclerosis linkage group in region 9q32-q34.
Genomics 1993;15(2):265-74.
1993: J R W Yates; J P Warner; J A Smith; F Deymeer; J P Azulay; Irena Hausmanowa-Petrusewicz; Jacek Zaremba; Janina Borkowska; Nabeel A Affara; Malcolm A Ferguson-Smith
Emery-Dreifuss muscular dystrophy: linkage to markers in distal Xq28.
Journal of medical genetics 1993;30(2):108-11.
1992: Bronwen Lambson; Nabeel A Affara; Michael John Mitchell; Malcolm A Ferguson-Smith
Evolution of DNA sequence homologies between the sex chromosomes in primate species.
Genomics 1992;14(4):1032-40.
1992: D M Bailey; Nabeel A Affara; Malcolm A Ferguson-Smith
The X-Y homologous gene amelogenin maps to the short arms of both the X and Y chromosomes and is highly conserved in primates.
Genomics 1992;14(1):203-5.
1992: Robert A Furlong; J E Lyall; M J Lush; Nabeel A Affara; Malcolm A Ferguson-Smith
Four dinucleotide repeat polymorphisms on chromosome 9 (D9S143-146).
Human molecular genetics 1992;1(6):447.
1992: A J O'Reilly; Nabeel A Affara; Elizabeth Simpson; Phillip R Chandler; E Goulmy; Malcolm A Ferguson-Smith
A molecular deletion map of the Y chromosome long arm defining X and autosomal homologous regions and the localisation of the HYA locus to the proximal region of the Yq euchromatin.
Human molecular genetics 1992;1(6):379-85.
1992: M A Yuille; D R Goudie; Nabeel A Affara; Malcolm A Ferguson-Smith
Additional polymorphism at a CHR 9 reference locus (D9S12).
Human molecular genetics 1992;1(5):351.
1992: J E Lyall; Robert A Furlong; M A Yuille; D R Goudie; MA Leversha; Nabeel A Affara; Malcolm A Ferguson-Smith
A dinucleotide repeat polymorphism at the D9S127 locus.
Nucleic acids research 1992;20(4):925.
1992: Robert A Furlong; J E Lyall; D R Goudie; MA Leversha; Nabeel A Affara; Malcolm A Ferguson-Smith
A dinucleotide repeat polymorphism at the D9S109 locus.
Nucleic acids research 1992;20(4):925.
1991: M A Yuille; MA Leversha; D R Goudie; Nabeel A Affara; Malcolm A Ferguson-Smith
Microsatellite polymorphism at the D9S12 locus.
Nucleic acids research 1991;19(18):5097.
1991: S L Lloyd; C A Sargent; J Chalmers; E Lim; S S Habeebu; Nabeel A Affara
An X-linked zinc finger gene mapping to Xq21.1-q21.3 closely related to ZFX and ZFY: possible origins from a common ancestral gene.
Nucleic acids research 1991;19(18):4835-41.
1991: Nabeel A Affara
Sex and the single Y.
BioEssays : news and reviews in molecular, cellular and developmental biology 1991;13(9):475-8.
1991: Eamonn R Maher; E Bentley; J R W Yates; F Latif; M Lerman; B Zbar; Nabeel A Affara; Malcolm A Ferguson-Smith
Mapping of the von Hippel-Lindau disease locus to a small region of chromosome 3p by genetic linkage analysis.
Genomics 1991;10(4):957-60.
1991: M North; C Sargent; J O'Brien; K Taylor; J Wolfe; Nabeel A Affara; Malcolm A Ferguson-Smith
Comparison of ZFY and ZFX gene structure and analysis of alternative 3' untranslated regions of ZFY.
Nucleic acids research 1991;19(10):2579-86.
1991: M A Yuille; D R Goudie; Nabeel A Affara; Malcolm A Ferguson-Smith
Rapid determination of sequences flanking microsatellites.
Nucleic acids research 1991;19(8):1950.
1990: M A Yuille; R M Hampson; R M Harris; Nabeel A Affara; J R W Yates; Malcolm A Ferguson-Smith
CA repeat polymorphism at the ASS locus.
Nucleic acids research 1990;18(24):7472.
1990: R S Newman; Nabeel A Affara; J R W Yates; Michael John Mitchell; Malcolm A Ferguson-Smith
Physical mapping of deletion breakpoints in patients with X-linked ichthyosis: evidence for clustering of distal and proximal breakpoints.
Proceedings. Biological sciences / The Royal Society 1990;242(1305):231-9.
1990: Malcolm A Ferguson-Smith; M A North; Nabeel A Affara; H Briggs
The secret of sex.
Lancet 1990;336(8718):809-10.
1990: N E Abbas; J E Toublanc; C Boucekkine; M Toublanc; Nabeel A Affara; J C Job; Marc Fellous
A possible common origin of "Y-negative" human XX males and XX true hermaphrodites.
Human genetics 1990;84(4):356-60.
1990: Malcolm A Ferguson-Smith; A Cooke; Nabeel A Affara; E Boyd; J L Tolmie
Genotype-phenotype correlations in XX males and their bearing on current theories of sex determination.
Human genetics 1990;84(2):198-202.
1990: Nigel P Carter; M E Ferguson-Smith; Nabeel A Affara; H Briggs; Malcolm A Ferguson-Smith
Study of X chromosome abnormality in XX males using bivariate flow karyotype analysis and flow sorted dot blots.
Cytometry 1990;11(1):202-7.
1989: Nabeel A Affara; D Chambers; J O'Brien; S S Habeebu; M Kalaitsidaki; Jack alvarez; Malcolm A Ferguson-Smith
Evidence for distinguishable transcripts of the putative testis determining gene (ZFY) and mapping of homologous cDNA sequences to chromosomes X,Y and 9.
Nucleic acids research 1989;17(8):2987-99.
1989: Michael John Mitchell; D Simon; Nabeel A Affara; M Ferguson-Smith; Philip Avner; Jack alvarez
Localization of murine X and autosomal sequences homologous to the human Y located testis-determining region.
Genetics 1989;121(4):803-9.
1989: Robert Feil; E Gillard; Nabeel A Affara; Malcolm A Ferguson-Smith; J L Mandel
A probe from an X-Y homology region detects RFLPs in Xq13-q22.
Nucleic acids research 1989;17(3):1279.
1988: Malcolm A Ferguson-Smith; Nabeel A Affara
Accidental X-Y recombination and the aetiology of XX males and true hermaphrodites.
Philosophical transactions of the Royal Society of London. Series B, Biological sciences 1988;322(1208):133-44.
1988: A Cooke; E F Gillard; J R W Yates; Michael John Mitchell; David A Aitken; D M Weir; Nabeel A Affara; Malcolm A Ferguson-Smith
X chromosome deletions detectable by flow cytometry in some patients with steroid sulphatase deficiency (X-linked ichthyosis).
Human genetics 1988;79(1):49-52.
1988: Margit Burmeister; Anthony P Monaco; E F Gillard; G J van Ommen; Nabeel A Affara; Malcolm A Ferguson-Smith; Louis Kunkel; Hans Lehrach
A 10-megabase physical map of human Xp21, including the Duchenne muscular dystrophy gene.
Genomics 1988;2(3):189-202.
1987: J R W Yates; D R Goudie; E F Gillard; David A Aitken; Nabeel A Affara; J F Clayton; P A Tippett; Malcolm A Ferguson-Smith
Multipoint linkage analysis of steroid sulfatase (X-linked ichthyosis) and distal Xp markers.
Genomics 1987;1(1):52-9.
1987: E F Gillard; Nabeel A Affara; J R W Yates; D R Goudie; J Lambert; David A Aitken; Malcolm A Ferguson-Smith
Deletion of a DNA sequence in eight of nine families with X-linked ichthyosis (steroid sulphatase deficiency).
Nucleic acids research 1987;15(10):3977-85.
1987: Malcolm A Ferguson-Smith; Nabeel A Affara; R Ellen Magenis
Ordering of Y-specific sequences by deletion mapping and analysis of X-Y interchange males and females.
Development (Cambridge, England) 1987;101 Suppl():41-50.
1986: J R W Yates; Nabeel A Affara; D M Jamieson; Malcolm A Ferguson-Smith; Irena Hausmanowa-Petrusewicz; Jacek Zaremba; Janina Borkowska; A W Johnston; K Kelly
Emery-Dreifuss muscular dystrophy: localisation to Xq27.3----qter confirmed by linkage to the factor VIII gene.
Journal of medical genetics 1986;23(6):587-90.