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Author Details
Full Name
Maya Ghoussaini
Affiliation
Wellcome Sanger Institute
ORCID
Career Start Year
2005
Papers
55
H Index
35
Expertise
CM4AI Collaborator
Trey Ideker (CM4AI)
PMID
Paper Title
Journal Title
Published Year
36399499
The next-generation Open Targets Platform: reimagined, redesigned, rebuilt.
Nucleic Acids Res
2023
37945903
Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants.
Nat Genet
2023
37308670
Mapping interindividual dynamics of innate immune response at single-cell resolution.
Nat Genet
2023
36963162
Future prospects for human genetics and genomics in drug discovery.
Curr Opin Struct Biol
2023
35772218
Multi-ancestry Mendelian randomization of omics traits revealing drug targets of COVID-19 severity.
EBioMedicine
2022
35804044
Human genetics evidence supports two-thirds of the 2021 FDA-approved drugs.
Nat Rev Drug Discov
2022
33045747
Open Targets Genetics: systematic identification of trait-associated genes using large-scale genetics and functional genomics.
Nucleic Acids Res
2021
33664506
Population-scale single-cell RNA-seq profiling across dopaminergic neuron differentiation.
Nat Genet
2021
34402426
A proteome-wide genetic investigation identifies several SARS-CoV-2-exploited host targets of clinical relevance.
Elife
2021
34711957
An open approach to systematically prioritize causal variants and genes at all published human GWAS trait-associated loci.
Nat Genet
2021
34146516
Functional annotation of the 2q35 breast cancer risk locus implicates a structural variant in influencing activity of a long-range enhancer element.
Am J Hum Genet
2021
34083789
A map of transcriptional heterogeneity and regulatory variation in human microglia.
Nat Genet
2021
33196847
Open Targets Platform: supporting systematic drug-target identification and prioritisation.
Nucleic Acids Res
2021
33398198
Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction.
Nat Genet
2021
33473200
Publisher Correction: Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction.
Nat Genet
2021
33289971
Mining a GWAS of Severe Covid-19.
N Engl J Med
2020
33060197
Comparative host-coronavirus protein interaction networks reveal pan-viral disease mechanisms.
Science
2020
33289972
Mining a GWAS of Severe Covid-19.
N Engl J Med
2020
29633761
Publisher Correction: Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation.
Nat Commun
2018
29915430
A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer.
Nat Genet
2018
29059683
Association analysis identifies 65 new breast cancer risk loci.
Nature
2017
26928228
Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170.
Nat Genet
2016
27640304
Evidence that the 5p12 Variant rs10941679 Confers Susceptibility to Estrogen-Receptor-Positive Breast Cancer through FGF10 and MRPS30 Regulation.
Am J Hum Genet
2016
27601076
Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus.
Nat Commun
2016
27600471
Fine scale mapping of the 17q22 breast cancer locus using dense SNPs, genotyped within the Collaborative Oncological Gene-Environment Study (COGs).
Sci Rep
2016
27117709
Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer.
Nat Commun
2016
27459855
Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus.
Breast Cancer Res
2016
27087578
Fine-scale mapping of 8q24 locus identifies multiple independent risk variants for breast cancer.
Int J Cancer
2016
25168388
Identification and characterization of novel associations in the CASP8/ALS2CR12 region on chromosome 2 with breast cancer risk.
Hum Mol Genet
2015
26354892
Fine-scale mapping of the 4q24 locus identifies two independent loci associated with breast cancer risk.
Cancer Epidemiol Biomarkers Prev
2015
26073781
Polymorphisms in a Putative Enhancer at the 10q21.2 Breast Cancer Risk Locus Regulate NRBF2 Expression.
Am J Hum Genet
2015
25652398
Fine-mapping identifies two additional breast cancer susceptibility loci at 9q31.2.
Hum Mol Genet
2015
25529635
Fine-scale mapping of the 5q11.2 breast cancer locus reveals at least three independent risk variants regulating MAP3K1.
Am J Hum Genet
2015
25248036
Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation.
Nat Commun
2014
23540573
Functional variants at the 11q13 risk locus for breast cancer regulate cyclin D1 expression through long-range enhancers.
Am J Hum Genet
2013
24290378
Fine-scale mapping of the FGFR2 breast cancer risk locus: putative functional variants differentially bind FOXA1 and E2F1.
Am J Hum Genet
2013
23973388
Inherited genetic susceptibility to breast cancer: the beginning of the end or the end of the beginning?
Am J Pathol
2013
23778136
Loss-of-function mutations in SIM1 contribute to obesity and Prader-Willi-like features.
J Clin Invest
2013
23535731
Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer.
Nat Genet
2013
23535732
Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array.
Nat Genet
2013
23535729
Large-scale genotyping identifies 41 new loci associated with breast cancer risk.
Nat Genet
2013
22267197
Genome-wide association analysis identifies three new breast cancer susceptibility loci.
Nat Genet
2012
22859399
9q31.2-rs865686 as a susceptibility locus for estrogen receptor-positive breast cancer: evidence from the Breast Cancer Association Consortium.
Cancer Epidemiol Biomarkers Prev
2012
21814516
A functional variant at a prostate cancer predisposition locus at 8q24 is associated with PVT1 expression.
PLoS Genet
2011
20075856
Analysis of the SIM1 contribution to polygenic obesity in the French population.
Obesity (Silver Spring)
2010
20852631
A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor-negative breast cancer in the general population.
Nat Genet
2010
20453838
Genome-wide association study identifies five new breast cancer susceptibility loci.
Nat Genet
2010
19519208
Polygenic susceptibility to breast cancer: current state-of-the-art.
Future Oncol
2009
19401419
Common variation in SIM1 is reproducibly associated with BMI in Pima Indians.
Diabetes
2009
19330027
Newly discovered breast cancer susceptibility loci on 3p24 and 17q23.2.
Nat Genet
2009
1 - 50 of 55
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