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Author Details

Juliet D French
QIMR Berghofer Medical Research Institute
2001
55
29
PMIDPaper TitleJournal TitlePublished Year
36713455CRISPR interference for sequence-specific regulation of fibroblast growth factor receptor A in <i>Schistosoma mansoni</i>.Front Immunol2023
36713455CRISPR interference for sequence-specific regulation of fibroblast growth factor receptor A in <i>Schistosoma mansoni</i>.Front Immunol2023
37144467Redefining normal breast cell populations using long noncoding RNAs.Nucleic Acids Res2023
37333134Preventing recurrence in Sonic Hedgehog Subgroup Medulloblastoma using the OLIG2 inhibitor CT-179.Res Sq2023
36991492CRISPR screens identify gene targets at breast cancer risk loci.Genome Biol2023
37487416Development of CRISPR/Cas13a-based assays for the diagnosis of Schistosomiasis.EBioMedicine2023
37487416Development of CRISPR/Cas13a-based assays for the diagnosis of Schistosomiasis.EBioMedicine2023
36991492CRISPR screens identify gene targets at breast cancer risk loci.Genome Biol2023
37144467Redefining normal breast cell populations using long noncoding RNAs.Nucleic Acids Res2023
37333134Preventing recurrence in Sonic Hedgehog Subgroup Medulloblastoma using the OLIG2 inhibitor CT-179.Res Sq2023
33337558CRISPR/Cas9-mediated genome editing of Schistosoma mansoni acetylcholinesterase.FASEB J2021
33145822CRISPR/Cas9: A new tool for the study and control of helminth parasites.Bioessays2021
33337558CRISPR/Cas9-mediated genome editing of Schistosoma mansoni acetylcholinesterase.FASEB J2021
33145822CRISPR/Cas9: A new tool for the study and control of helminth parasites.Bioessays2021
32871102eQTL Colocalization Analyses Identify NTN4 as a Candidate Breast Cancer Risk Gene.Am J Hum Genet2020
31910864Non-coding RNAs underlie genetic predisposition to breast cancer.Genome Biol2020
31910858Chromatin interactome mapping at 139 independent breast cancer risk signals.Genome Biol2020
32871102eQTL Colocalization Analyses Identify NTN4 as a Candidate Breast Cancer Risk Gene.Am J Hum Genet2020
32741549The Role of Noncoding Variants in Heritable Disease.Trends Genet2020
31910864Non-coding RNAs underlie genetic predisposition to breast cancer.Genome Biol2020
31910858Chromatin interactome mapping at 139 independent breast cancer risk signals.Genome Biol2020
32741549The Role of Noncoding Variants in Heritable Disease.Trends Genet2020
29633761Publisher Correction: Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation.Nat Commun2018
30323900MiR-29b-1-5p is altered in BRCA1 mutant tumours and is a biomarker in basal-like breast cancer.Oncotarget2018
29633761Publisher Correction: Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation.Nat Commun2018
30323900MiR-29b-1-5p is altered in BRCA1 mutant tumours and is a biomarker in basal-like breast cancer.Oncotarget2018
28777932Long Noncoding RNAs CUPID1 and CUPID2 Mediate Breast Cancer Risk at 11q13 by Modulating the Response to DNA Damage.Am J Hum Genet2017
28777932Long Noncoding RNAs CUPID1 and CUPID2 Mediate Breast Cancer Risk at 11q13 by Modulating the Response to DNA Damage.Am J Hum Genet2017
28978027Functional dissection of breast cancer risk-associated <i>TERT</i> promoter variants.Oncotarget2017
29059683Association analysis identifies 65 new breast cancer risk loci.Nature2017
28099932Allelic imbalance in human breast cancer.Oncotarget2017
28099932Allelic imbalance in human breast cancer.Oncotarget2017
29059683Association analysis identifies 65 new breast cancer risk loci.Nature2017
28978027Functional dissection of breast cancer risk-associated <i>TERT</i> promoter variants.Oncotarget2017
26840454Germline polymorphisms in an enhancer of PSIP1 are associated with progression-free survival in epithelial ovarian cancer.Oncotarget2016
26840454Germline polymorphisms in an enhancer of PSIP1 are associated with progression-free survival in epithelial ovarian cancer.Oncotarget2016
26928228Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170.Nat Genet2016
27378691Long-range regulators of the lncRNA HOTAIR enhance its prognostic potential in breast cancer.Hum Mol Genet2016
27135401Five endometrial cancer risk loci identified through genome-wide association analysis.Nat Genet2016
27087319Point Mutations in Exon 1B of APC Reveal Gastric Adenocarcinoma and Proximal Polyposis of the Stomach as a Familial Adenomatous Polyposis Variant.Am J Hum Genet2016
27043663MicroRNA-206 is differentially expressed in Brca1-deficient mice and regulates epithelial and stromal cell compartments of the mouse mammary gland.Oncogenesis2016
27259051A Common Variant at the 14q32 Endometrial Cancer Risk Locus Activates AKT1 through YY1 Binding.Am J Hum Genet2016
27601076Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus.Nat Commun2016
27600471Fine scale mapping of the 17q22 breast cancer locus using dense SNPs, genotyped within the Collaborative Oncological Gene-Environment Study (COGs).Sci Rep2016
28171565Endometriosis risk alleles at 1p36.12 act through inverse regulation of CDC42 and LINC00339.Hum Mol Genet2016
27640304Evidence that the 5p12 Variant rs10941679 Confers Susceptibility to Estrogen-Receptor-Positive Breast Cancer through FGF10 and MRPS30 Regulation.Am J Hum Genet2016
28171565Endometriosis risk alleles at 1p36.12 act through inverse regulation of CDC42 and LINC00339.Hum Mol Genet2016
27640304Evidence that the 5p12 Variant rs10941679 Confers Susceptibility to Estrogen-Receptor-Positive Breast Cancer through FGF10 and MRPS30 Regulation.Am J Hum Genet2016
27601076Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus.Nat Commun2016
27600471Fine scale mapping of the 17q22 breast cancer locus using dense SNPs, genotyped within the Collaborative Oncological Gene-Environment Study (COGs).Sci Rep2016
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Collaborators

Stacey L Edwards
QIMR Berghofer Medical Research Institute
Co-authored papers 40
Jonathan Beesley
QIMR Berghofer Medical Research Institute
Co-authored papers 20
Georgia Chenevix-Trench
QIMR Berghofer Medical Research Institute
Co-authored papers 20
Alison M Dunning
Co-authored papers 18
Douglas F Easton
University of Cambridge
Co-authored papers 17
Peter A Fasching
Otto-Friedrich-University Bamberg
Co-authored papers 15
Diether Lambrechts
Co-authored papers 15
Haran Sivakumaran
QIMR Berghofer Medical Research Institute
Co-authored papers 14
Paul D P Pharoah
Center for Cancer Genetic Epidemiology, University of Cambridge
Co-authored papers 14
Fergus J Couch
Mayo Clinic
Co-authored papers 14
Per Hall
Co-authored papers 14
Graham G Giles
Co-authored papers 14
Vessela N Kristensen
Faculty of Clinical Medicine, University of Oslo
Co-authored papers 14
Jenny Chang-Claude
German Cancer Research Center (DKFZ)
Co-authored papers 14
Xiao-Ou Shu
Co-authored papers 13
Wei Zheng
Co-authored papers 13
Irene L Andrulis
University of Toronto
Co-authored papers 13
Javier Ben??tez
Instituto de Salud Carlos III
Co-authored papers 12
Jan Lubinski
Pomeranian Medical University
Co-authored papers 12
Roger L Milne
Co-authored papers 12
Maya Ghoussaini
Wellcome Sanger Institute
Co-authored papers 12
Montserrat Garcia-Closas
National Cancer Institute
Co-authored papers 12
Paolo Radice
Ospedale Circolo e Fondazione Macchi
Co-authored papers 12
Anna H Wu
University of Southern California
Co-authored papers 12
Hoda Anton-Culver
University of California irvine
Co-authored papers 12
Jonine D Figueroa
The Usher Institute, The University of Edinburgh
Co-authored papers 12
Christopher A Haiman
University of Southern California
Co-authored papers 12
Qiuyin Cai
Co-authored papers 10
Sunil R Lakhani
University of Queensland
Co-authored papers 10
Chiu-Chen Tseng
Keck School of Medicine, University of Southern California
Co-authored papers 10
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