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Sarah Ennis

Research Profile

Concepts & Ideas

Genes & Molecular Sequences

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Physiology

Chemicals & Drugs

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X Chromosome

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Publications

TOP 3
N Weston-Bell; Niklas Zojer; T Cezard; ANDREW COLLINS; Sarah Ennis; J Gibson; M John; H Ludwig; S Pfeifer; Surinder S Sahota
Exome sequencing in tracking clonal evolution in multiple myeloma following therapy.
Jane Gibson; William Tapper; Sarah Ennis; Andrew Collins
Exome-based linkage disequilibrium maps of individual genes: functional clustering and relationship to disease.
Ioannis Politopoulos; Jane Gibson; William Tapper; Sarah Ennis; Diana Eccles; ANDREW COLLINS
Composite likelihood-based meta-analysis of breast cancer association studies.

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All Publications

2013: N Weston-Bell; Niklas Zojer; T Cezard; ANDREW COLLINS; Sarah Ennis; J Gibson; M John; H Ludwig; S Pfeifer; Surinder S Sahota
Exome sequencing in tracking clonal evolution in multiple myeloma following therapy.
Leukemia 2013;27(5):1188-91.
2013: Jane Gibson; William Tapper; Sarah Ennis; Andrew Collins
Exome-based linkage disequilibrium maps of individual genes: functional clustering and relationship to disease.
Human genetics 2013;132(2):233-43.
2011: Ioannis Politopoulos; Jane Gibson; William Tapper; Sarah Ennis; Diana Eccles; ANDREW COLLINS
Composite likelihood-based meta-analysis of breast cancer association studies.
Journal of human genetics 2011;56(5):377-82.
2011: Ioannis Politopoulos; Jane Gibson; William Tapper; Sarah Ennis; Diana Eccles; ANDREW COLLINS
Genome-wide association of breast cancer: composite likelihood with imputed genotypes.
European journal of human genetics : EJHG 2011;19(2):194-9.
2010: Jane Gibson; Angela Cree; ANDREW COLLINS; Andrew Lotery; Sarah Ennis
Determination of a gene and environment risk model for age-related macular degeneration.
The British journal of ophthalmology 2010;94(10):1382-7.
2008: Sarah Ennis; Catherine Jomary; Robert Mullins; Angela Cree; Xiaoli Chen; Alex Macleod; Stephen Jones; ANDREW COLLINS; Edwin Stone; Andrew J Lotery
Association between the SERPING1 gene and age-related macular degeneration: a two-stage case-control study.
Lancet 2008;372(9652):1828-34.
2008: S V Goverdhan; Sarah Ennis; S R Hannan; K C Madhusudhana; A J Cree; Andrew J Luff; Andrew J Lotery
Interleukin-8 promoter polymorphism -251A/T is a risk factor for age-related macular degeneration.
The British journal of ophthalmology 2008;92(4):537-40.
2007: Sarah Ennis; A Murray; G Brightwell; Newton E Morton; Patricia A Jacobs
Closely linked cis-acting modifier of expansion of the CGG repeat in high risk FMR1 haplotypes.
Human mutation 2007;28(12):1216-24.
2007: Sarah Ennis; Srini Goverdhan; Angela Cree; Josephine Hoh; ANDREW COLLINS; Andrew J Lotery
Fine-scale linkage disequilibrium mapping of age-related macular degeneration in the complement factor H gene region.
The British journal of ophthalmology 2007;91(7):966-70.
2007: Sarah Ennis
Linkage disequilibrium as a tool for detecting signatures of natural selection.
Methods in molecular biology (Clifton, N.J.) 2007;376():59-70.
2007: Newton Morton; Nikolas Maniatis; Weihua Zhang; Sarah Ennis; ANDREW COLLINS
Genome scanning by composite likelihood.
American journal of human genetics 2007;80(1):19-28.
2006: Sarah Ennis; A Murray; Sheila Youings; G Brightwell; David Herrick; S Ring; Marcus E Pembrey; Newton E Morton; Patricia A Jacobs
An investigation of FRAXA intermediate allele phenotype in a longitudinal sample.
Annals of human genetics 2006;70(Pt 2):170-80.
2006: Sarah Ennis; Daniel Ward; Anna Murray
Nonlinear association between CGG repeat number and age of menopause in FMR1 premutation carriers.
European journal of human genetics : EJHG 2006;14(2):253-5.
2006: James Self; Sarah Ennis; ANDREW COLLINS; Fatima Shawkat; Christopher M Harris; David Anthony Mackey; Peter R Hodgkins; I Karen Temple; Xiaoli Chen; Andrew J Lotery
Fine mapping of the X-linked recessive congenital idiopathic nystagmus locus at Xq24-q26.3.
Molecular vision 2006;12():1211-6.
2005: William Tapper; ANDREW COLLINS; Jane Gibson; Nikolas Maniatis; Sarah Ennis; Newton E Morton
A map of the human genome in linkage disequilibrium units.
Proceedings of the National Academy of Sciences of the United States of America 2005;102(33):11835-9.
2005: John A Crolla; Sheila Youings; Sarah Ennis; Patricia A Jacobs
Supernumerary marker chromosomes in man: parental origin, mosaicism and maternal age revisited.
European journal of human genetics : EJHG 2005;13(2):154-60.
2004: Sheila Youings; Katrina Ellis; Sarah Ennis; John Barber; Patricia Jacobs
A study of reciprocal translocations and inversions detected by light microscopy with special reference to origin, segregation, and recurrent abnormalities.
American journal of medical genetics. Part A 2004;126A(1):46-60.
2002: Nikolas Maniatis; ANDREW COLLINS; Chun-Fang Xu; Linda C McCarthy; D R Hewett; William Tapper; Sarah Ennis; Xiayi Ke; Newton E Morton
The first linkage disequilibrium (LD) maps: delineation of hot and cold blocks by diplotype analysis.
Proceedings of the National Academy of Sciences of the United States of America 2002;99(4):2228-33.
2001: Sarah Ennis; Nikolas Maniatis; ANDREW COLLINS
Allelic association and disease mapping.
Briefings in bioinformatics 2001;2(4):375-87.
2001: Sarah Ennis; ANDREW COLLINS; William Tapper; A Murray; JN Macpherson; Newton E Morton
Allelic association discriminates draft orders.
Annals of human genetics 2001;65(Pt 5):503-4.
2001: Newton E Morton; W Zhang; Patricia Taillon-Miller; Sarah Ennis; Pui-Yan Kwok; ANDREW COLLINS
The optimal measure of allelic association.
Proceedings of the National Academy of Sciences of the United States of America 2001;98(9):5217-21.
2001: ANDREW COLLINS; Sarah Ennis; Patricia Taillon-Miller; Pui-Yan Kwok; Newton E Morton
Allelic association with SNPs: metrics, populations, and the linkage disequilibrium map.
Human mutation 2001;17(4):255-62.
2001: Sarah Ennis; A Murray; Newton E Morton
Haplotypic determinants of instability in the FRAX region: Concatenated mutation or founder effect?
Human mutation 2001;18(1):61-9.
2000: Sarah Ennis; ANDREW COLLINS; A Murray; JN Macpherson; Newton E Morton
Allelic association in the FRAX region.
Annals of human genetics 2000;64(Pt 6):513-8.
2000: A Murray; Sarah Ennis; Sheila Youings; AJ Sharrock; C Lewis; MC Pound; JN Macpherson; Nicholas R Dennis; Newton E Morton; Patricia A Jacobs
Stability and haplotype analysis of the FRAXE region.
European journal of human genetics : EJHG 2000;8(8):583-9.
2000: A Murray; Sarah Ennis; N Morton
No evidence for parent of origin influencing premature ovarian failure in fragile X premutation carriers.
American journal of human genetics 2000;67(1):253-4; author reply 256-8.
2000: Sheila Youings; A Murray; Nicholas R Dennis; Sarah Ennis; C Lewis; N McKechnie; MC Pound; AJ Sharrock; Patricia Jacobs
FRAXA and FRAXE: the results of a five year survey.
Journal of medical genetics 2000;37(6):415-21.
2000: A Murray; Sarah Ennis; F MacSwiney; J Webb; Newton E Morton
Reproductive and menstrual history of females with fragile X expansions.
European journal of human genetics : EJHG 2000;8(4):247-52.