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Papuan mitochondrial genomes and the settlement of Sahul

Journal of human genetics, 2020-10, Vol.65 (10), p.875-887

2020

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Genome-Wide Methylation Analysis Identifies Specific Epigenetic Marks In Severely Obese Children

Scientific reports, 2017-04, Vol.7 (1), p.46311-46311, Article 46311

2017

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Experimental evolution links post-transcriptional regulation to Leishmania fitness gain

PLoS pathogens, 2022-03, Vol.18 (3), p.e1010375-e1010375

2022

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A Case-Only Genome-Wide Interaction Study of Smoking and Bladder Cancer Risk: Results from the COBLAnCE Cohort

Cancers, 2023-08, Vol.15 (17), p.4218

2023

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Genome-wide linkage in a highly consanguineous pedigree reveals two novel loci on chromosome 7 for non-syndromic familial Premature Ovarian Failure

PloS one, 2012-03, Vol.7 (3), p.e33412-e33412

2012

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Prediction of treatment (tx)-induced fatigue in breast cancer (BC) patients (pts) using machine learning on genome-wide association (GWAS) data in the prospective CANTO cohort

Journal of clinical oncology, 2019-05, Vol.37 (15_suppl), p.11515-11515

2019

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dUTPase ( DUT ) Is Mutated in a Novel Monogenic Syndrome With Diabetes and Bone Marrow Failure

Diabetes (New York, N.Y.), 2017-04, Vol.66 (4), p.1086-1096

2017

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Evidence of Austronesian Genetic Lineages in East Africa and South Arabia: Complex Dispersal from Madagascar and Southeast Asia

Genome biology and evolution, 2019-03, Vol.11 (3), p.748-758

2019

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Lentiviral transduction of CD34(+) cells induces genome-wide epigenetic modifications

PloS one, 2012-11, Vol.7 (11), p.e48943-e48943

2012

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Copy number variations alter methylation and parallel IGF2 overexpression in adrenal tumors

Endocrine-related cancer, 2015-12, Vol.22 (6), p.953-967

2015

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Major Loci on Chromosomes 8q and 3q Control Interferon γ Production Triggered by Bacillus Calmette-Guerin and 6-kDa Early Secretory Antigen Target, Respectively, in Various Populations

The Journal of infectious diseases, 2016-04, Vol.213 (7), p.1173-1179

2016

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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 : BCR, 2017-08, Vol.19 (1), p.98-98, Article 98

2017

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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, 2016-11, Vol.7 (47), p.77358-77364

2016

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A GWAS in uveal melanoma identifies risk polymorphisms in the CLPTM1L locus

Npj genomic medicine, 2017-03, Vol.2 (1), p.1-7, Article 5

2017

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Human genetic structure in Northwest France provides new insights into West European historical demography

Nature communications, 2024-08, Vol.15 (1), p.6710-18, Article 6710

2024

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Accelerated genome sequencing with controlled costs for infants in intensive care units: a feasibility study in a French hospital network

European journal of human genetics : EJHG, 2022-05, Vol.30 (5), p.567-576

2022

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Genome-wide association analysis in dilated cardiomyopathy reveals two new players in systolic heart failure on chromosomes 3p25.1 and 22q11.23

European heart journal, 2021-05, Vol.42 (20), p.2000-2011

2021

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Constitutional variants are not associated with HER2-positive breast cancer: results from the SIGNAL/PHARE clinical cohort

NPJ breast cancer, 2017-02, Vol.3 (1), p.4-4, Article 4

2017

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Modifying a Game to Study the Impact of an Hostile Environments on Foraging Behavior

Proceedings of the 18th International Conference on the Foundations of Digital Games, 2023, p.1-4

2023

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Prediction of Breast Cancer Treatment-Induced Fatigue by Machine Learning Using Genome-Wide Association Data

JNCI cancer spectrum, 2020-10, Vol.4 (5), p.pkaa039

2020

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Prediction of Breast Cancer Treatment\textendashInduced Fatigue by Machine Learning Using Genome-Wide Association Data

JNCI cancer spectrum, 2020-10, Vol.4 (5)

2020

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Papuan mitochondrial genomes and the settlement of Sahul

Genome-Wide Methylation Analysis Identifies Specific Epigenetic Marks In Severely Obese Children

Mutations and variants of ONECUT1 in diabetes

Experimental evolution links post-transcriptional regulation to Leishmania fitness gain

Germline CYBB mutations that selectively affect macrophages in kindreds with X-linked predisposition to tuberculous mycobacterial disease

A Case-Only Genome-Wide Interaction Study of Smoking and Bladder Cancer Risk: Results from the COBLAnCE Cohort

Human adenylate kinase 2 deficiency causes a profound hematopoietic defect associated with sensorineural deafness

Genome-wide linkage in a highly consanguineous pedigree reveals two novel loci on chromosome 7 for non-syndromic familial Premature Ovarian Failure

Prediction of treatment (tx)-induced fatigue in breast cancer (BC) patients (pts) using machine learning on genome-wide association (GWAS) data in the prospective CANTO cohort

dUTPase ( DUT ) Is Mutated in a Novel Monogenic Syndrome With Diabetes and Bone Marrow Failure

Evidence of Austronesian Genetic Lineages in East Africa and South Arabia: Complex Dispersal from Madagascar and Southeast Asia

Lentiviral transduction of CD34(+) cells induces genome-wide epigenetic modifications

Copy number variations alter methylation and parallel IGF2 overexpression in adrenal tumors

Major Loci on Chromosomes 8q and 3q Control Interferon γ Production Triggered by Bacillus Calmette-Guerin and 6-kDa Early Secretory Antigen Target, Respectively, in Various Populations

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

GWAS in the SIGNAL/PHARE clinical cohort restricts the association between the FGFR2 locus and estrogen receptor status to HER2-negative breast cancer patients

A GWAS in uveal melanoma identifies risk polymorphisms in the CLPTM1L locus

Human genetic structure in Northwest France provides new insights into West European historical demography

Accelerated genome sequencing with controlled costs for infants in intensive care units: a feasibility study in a French hospital network

Genome-wide association analysis in dilated cardiomyopathy reveals two new players in systolic heart failure on chromosomes 3p25.1 and 22q11.23

Constitutional variants are not associated with HER2-positive breast cancer: results from the SIGNAL/PHARE clinical cohort

Modifying a Game to Study the Impact of an Hostile Environments on Foraging Behavior

Prediction of Breast Cancer Treatment-Induced Fatigue by Machine Learning Using Genome-Wide Association Data

Prediction of Breast Cancer Treatment\textendashInduced Fatigue by Machine Learning Using Genome-Wide Association Data

Human Adenylate Kinase 2 Deficiency Causes a Profound Haematopoietic Defect Associated with Sensorineural Deafness

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