Author details

Full Name

HÃ©lÃ¨ne BlanchÃ©

Affiliation

ORCID

Career Start Year

1987

Papers

108

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37383672	Genetic factors for differentiated thyroid cancer in French Polynesia: new candidate loci.		2023
37954429	SARS-CoV-2 seroprevalence in French 9-year-old children and their parents after the first lockdown in 2020.		2023
37686494	A Case-Only Genome-Wide Interaction Study of Smoking and Bladder Cancer Risk: Results from the COBLAnCE Cohort.		2023
35304543	A high-throughput real-time PCR tissue-of-origin test to distinguish blood from lymphoblastoid cell line DNA for (epi)genomic studies.	Scientific Reports	2022
36350653	Long-lasting Symptoms After an Acute COVID-19 Infection and Factors Associated With Their Resolution.	JAMA network open	2022
35434687	Persistent symptoms after the first wave of COVID-19 in relation to SARS-CoV-2 serology and experience of acute symptoms: A nested survey in a population-based cohort.	Lancet Regional Health - Europe, The	2022
35632699	Seroprevalence of SARS-CoV-2 IgG Antibodies and Factors Associated with SARS-CoV-2 IgG Neutralizing Activity among Primary Health Care Workers 6 Months after Vaccination Rollout in France.	Viruses	2022
34747982	Association of Self-reported COVID-19 Infection and SARS-CoV-2 Serology Test Results With Persistent Physical Symptoms Among French Adults During the COVID-19 Pandemic.	JAMA Internal Medicine	2022
34453524	Corrigendum to: Antibody status and cumulative incidence of SARS-CoV-2 infection among adults in three regions of France following the first lockdown and associated risk factors: a multicohort study.	International Journal of Epidemiology	2021
33491046	Exome-Wide Association Study Identifies FN3KRP and PGP as New Candidate Longevity Genes.	J Gerontol A Biol Sci Med Sci	2021
34293141	Antibody status and cumulative incidence of SARS-CoV-2 infection among adults in three regions of France following the first lockdown and associated risk factors: a multicohort study.	International Journal of Epidemiology	2021
33893282	Publisher Correction: A meta-analysis of genome-wide association studies identifies multiple longevity genes.	Nat Commun	2021
33677556	Genome-wide association analysis in dilated cardiomyopathy reveals two new players in systolic heart failure on chromosomes 3p25.1 and 22q11.23.	Eur Heart J	2021
33998042	Evaluation of saliva as a source of accurate whole-genome and microbiome sequencing data.	Genetic Epidemiology	2021
33827984	Role of DNA Repair Variants and Diagnostic Radiology Exams in Differentiated Thyroid Cancer Risk: A Pooled Analysis of Two Case-Control Studies.	Cancer Epidemiology Biomarkers and Prevention	2021
34358061	Nationwide Seroprevalence of SARS-CoV-2 IgG Antibodies among Four Groups of Primary Health-Care Workers and Their Household Contacts 6 Months after the Initiation of the COVID-19 Vaccination Campaign in France: SeroPRIM Study Protocol.	Pathogens	2021
32506468	Circadian genes polymorphisms, night work and prostate cancer risk: Findings from the EPICAP study.	International Journal of Cancer	2020
32193295	Insights into human genetic variation and population history from 929 diverse genomes.	Science	2020
30825406	Where are the missing gene defects in inherited retinal disorders? Intronic and synonymous variants contribute at least to 4% of CACNA1F-mediated inherited retinal disorders.	Hum Mutat	2019
31624180	Adaptive archaic introgression of copy number variants and the discovery of previously unknown human genes.	Science	2019
30605491	The influence of obesity-related factors in the etiology of renal cell carcinoma-A mendelian randomization study.	PLoS Med	2019
31413261	A meta-analysis of genome-wide association studies identifies multiple longevity genes.	Nat Commun	2019
29688594	Whole-genome sequencing in patients with ciliopathies uncovers a novel recurrent tandem duplication in IFT140.	Hum Mutat	2018
29853305	Corrigendum re "Genetic Variants Related to Longer Telomere Length are Associated with Increased Risk of Renal Cell Carcinoma" [Eur Urol 2017;72:747-54].	Eur Urol	2018
29621323	Performance comparison of three DNA extraction kits on human whole-exome data from formalin-fixed paraffin-embedded normal and tumor samples.	PLoS ONE	2018
29339726	Publisher Correction: Identification and characterization of two functional variants in the human longevity gene FOXO3.	Nat Commun	2018
29234056	Identification and characterization of two functional variants in the human longevity gene FOXO3.	Nat Commun	2017
28598434	Genome-wide association study identifies multiple risk loci for renal cell carcinoma.	Nat Commun	2017
28797570	Genetic Variants Related to Longer Telomere Length are Associated with Increased Risk of Renal Cell Carcinoma.	Eur Urol	2017
28973654	A novel duplication of PRMD13 causes North Carolina macular dystrophy: overexpression of PRDM13 orthologue in drosophila eye reproduces the human phenotype.	Human Molecular Genetics	2017
28830573	Assessment of the prognostic role of a 94-single nucleotide polymorphisms risk score in early breast cancer in the SIGNAL/PHARE prospective cohort: no correlation with clinico-pathological characteristics and outcomes.	Breast Cancer Research	2017
28649644	Constitutional variants are not associated with HER2-positive breast cancer: results from the SIGNAL/PHARE clinical cohort.	NPJ Breast Cancer	2017
27764800	GWAS in the SIGNAL/PHARE clinical cohort restricts the association between the FGFR2 locus and estrogen receptor status to HER2-negative breast cancer patients.	Oncotarget	2016
26831756	HSP110 T17 simplifies and improves the microsatellite instability testing in patients with colorectal cancer.	Journal of Medical Genetics	2016
27004735	Immunochip analysis identifies association of the RAD50/IL13 region with human longevity.	Aging Cell	2016
27406316	A whole-genome sequence and transcriptome perspective on HER2-positive breast cancers.	Nat Commun	2016
26657656	Aristolochic acid exposure in Romania and implications for renal cell carcinoma.	Br J Cancer	2016
26633630	Corrigendum: A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma.	Nature	2016
26691988	A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants.	Nat Genet	2016
26116798	Diagnosis of Constitutional Mismatch Repair-Deficiency Syndrome Based on Microsatellite Instability and Lymphocyte Tolerance to Methylating Agents.	Gastroenterology	2015
25849217	Common variants at 9q22.33, 14q13.3, and ATM loci, and risk of differentiated thyroid cancer in the French Polynesian population.	PLoS ONE	2015
25631097	NF1 single and multi-exons copy number variations in neurofibromatosis type 1.	Journal of Human Genetics	2015
25657019	BioCAST/IFCT-1002: epidemiological and molecular features of lung cancer in never-smokers.	European Respiratory Journal	2015
24688116	Genome-wide association meta-analysis of human longevity identifies a novel locus conferring survival beyond 90 years of age.	Hum Mol Genet	2014
25351205	Variation in genomic landscape of clear cell renal cell carcinoma across Europe.	Nat Commun	2014
24352235	The complete genome sequence of a Neanderthal from the Altai Mountains.	Nature	2014
24341918	The co-occurrence of mtDNA mutations on different oxidative phosphorylation subunits, not detected by haplogroup analysis, affects human longevity and is population specific.	Aging Cell	2014
25013125	Noninvasive diagnosis of actionable mutations by deep sequencing of circulating free DNA in lung cancer from never-smokers: a proof-of-concept study from BioCAST/IFCT-1002.	Clinical Cancer Research	2014
23286790	Genome-wide linkage analysis for human longevity: Genetics of Healthy Aging Study.	Aging Cell	2013
23913538	NF1 molecular characterization and neurofibromatosis type I genotype-phenotype correlation: the French experience.	Human Mutation	2013