Lista de obras - Fabienne Lesueur - Dominio Público Uruguay

A Greek Family with a Follicular Variant of Familial Papillary Thyroid Carcinoma: TCO, MNG1, fPTC/PRN, and NMTC1 Excluded as Susceptibility Loci

scientific article published on 01 December 2005

A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma

artículo científico publicado en 2011

A Transcriptome-Wide Association Study Among 97,898 Women to Identify Candidate Susceptibility Genes for Epithelial Ovarian Cancer Risk

article

A common variant within the HNF1B gene is associated with overall survival of multiple myeloma patients: results from the IMMEnSE consortium and meta-analysis.

artículo científico publicado en 2016

A gene predisposing to familial thyroid tumors with cell oxyphilia maps to chromosome 19p13.2.

artículo científico publicado en 1998

A germline oncogenic MITF mutation and tumor susceptibility.

artículo científico

A polygenic risk score for multiple myeloma risk prediction

artículo científico publicado en 2022

A sample storage management system for biobanks.

artículo científico publicado en 2010

ABRAXAS (FAM175A) and Breast Cancer Susceptibility: No Evidence of Association in the Breast Cancer Family Registry

artículo científico publicado en 2016

ADAM33, a new candidate for psoriasis susceptibility

artículo científico publicado en 2007

Abstract 5103: Transcriptional profiling in clear cell renal cell carcinoma (ccRCC). Focus on Czech Republic

Allelic association of the human homologue of the mouse modifier Ptprj with breast cancer

artículo científico publicado en 2005

Allelic loss on chromosomes 2q21 and 19p 13.2 in oxyphilic thyroid tumors

An association study of 22 candidate genes in psoriasis families reveals shared genetic factors with other autoimmune and skin disorders

artículo científico publicado en 2009

Association of Genomic Domains in BRCA1 and BRCA2 with Prostate Cancer Risk and Aggressiveness

artículo científico publicado en 2019

Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of breast cancer risk at locus 11q22.3.

artículo científico publicado en 2016

Association of single-nucleotide polymorphisms in the cell cycle genes with breast cancer in the British population

artículo científico publicado en 2008

At least three genes account for familial papillary thyroid carcinoma: TCO and MNG1 excluded as susceptibility loci from a large Tasmanian family

article

BRCA1 and BRCA2 Pathogenic Sequence Variants in Women of African Origin or Ancestry

artículo científico publicado en 2019

Breast and Prostate Cancer Risks for Male BRCA1 and BRCA2 Pathogenic Variant Carriers Using Polygenic Risk Scores

artículo científico publicado en 2022

COMPLEXO: identifying the missing heritability of breast cancer via next generation collaboration

artículo científico publicado en 2013

Cancer Risks Associated With Germline PALB2 Pathogenic Variants: An International Study of 524 Families

artículo científico publicado en 2019

Cancer Risks Associated With and Pathogenic Variants

artículo científico publicado en 2022

Characterization of the Cancer Spectrum in Men With Germline BRCA1 and BRCA2 Pathogenic Variants: Results From the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA)

artículo científico publicado en 2020

Circulating concentrations of insulin-like growth factor-I, insulin-like growth factor-binding protein-3, genetic polymorphisms and mammographic density in premenopausal Mexican women: results from the ESMaestras cohort

artículo científico publicado en 2013

Circulating plasma phospholipid fatty acids and risk of pancreatic cancer in a large European cohort

artículo científico publicado en 2018

Classification of missense substitutions in the BRCA genes: a database dedicated to Ex-UVs.

artículo científico publicado en 2011

Common ERBB2 polymorphisms and risk of breast cancer in a white British population: a case-control study

artículo científico publicado en 2005

Common Variants in RB1 Gene and Risk of Invasive Ovarian Cancer

article

Common gene variants within 3'-untranslated regions as modulators of multiple myeloma risk and survival

scientific article published on 05 November 2020

Common variants at 9q22.33, 14q13.3, and ATM loci, and risk of differentiated thyroid cancer in the French Polynesian population

artículo científico publicado en 2015

Common variants at the 9q22.33, 14q13.3 and ATM loci, and risk of differentiated thyroid cancer in the Cuban population

artículo científico publicado en 2015

Common variation in EMSY and risk of breast and ovarian cancer: a case-control study using HapMap tagging SNPs

artículo científico publicado en 2005

Comprehensive investigation of genetic variation in the 8q24 region and multiple myeloma risk in the IMMEnSE consortium

artículo científico publicado en 2012

Confirmation of Psoriasis Susceptibility Loci on Chromosome 6p21 and 20p13 in French Families

artículo científico publicado en 2007

Contribution of ATM and FOXE1 (TTF2) to risk of papillary thyroid carcinoma in Belarusian children exposed to radiation

artículo científico publicado en 2013

DICER1 mutations in familial multinodular goiter with and without ovarian Sertoli-Leydig cell tumors

artículo científico publicado en 2011

Description and validation of high-throughput simultaneous genotyping and mutation scanning by high-resolution melting curve analysis

artículo científico publicado en 2009

Detecting differential allelic expression using high-resolution melting curve analysis: application to the breast cancer susceptibility gene CHEK2.

artículo científico publicado en 2011

Determining the effectiveness of High Resolution Melting analysis for SNP genotyping and mutation scanning at the TP53 locus

artículo científico publicado en 2009

Effects of common germline genetic variation in cell cycle control genes on breast cancer survival: results from a population-based cohort

artículo científico publicado en 2008

Erratum: Corrigendum: A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma

artículo científico publicado en 2015

Evaluation of Polygenic Risk Scores for Breast and Ovarian Cancer Risk Prediction in BRCA1 and BRCA2 Mutation Carriers

artículo científico publicado en 2017

Evidence for interaction between the TCO and NMTC1 loci in familial non-medullary thyroid cancer.

artículo científico publicado en 2004

Exome sequencing identifies germline variants in DIS3 in familial multiple myeloma.

artículo científico publicado en 2019

FOXE1 Polymorphism Interacts with Dietary Iodine Intake in Differentiated Thyroid Cancer Risk in the Cuban Population

artículo científico publicado en 2016

Familial breast cancer and DNA repair genes: insights into known and novel susceptibility genes from the GENESIS study, and implications for multigene panel testing

article

Fine-Scale Mapping at 9p22.2 Identifies Candidate Causal Variants That Modify Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers

artículo científico publicado en 2016

Fine-mapping of 150 breast cancer risk regions identifies 178 high confidence target genes

article

Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes

artículo científico publicado en 2020

Fine-mapping of two differentiated thyroid carcinoma susceptibility loci at 9q22.33 and 14q13.3 detects novel candidate functional SNPs in Europeans from metropolitan France and Melanesians from New Caledonia

artículo científico publicado en 2016

GEMO, a National Resource to Study Genetic Modifiers of Breast and Ovarian Cancer Risk in and Pathogenic Variant Carriers

GENESIS: a French national resource to study the missing heritability of breast cancer

artículo científico publicado en 2016

Gene and pathway level analyses of iCOGS variants highlight novel signalling pathways underlying familial breast cancer susceptibility

artículo científico publicado en 2020

Gene expression signature associated with BRAF mutations in human primary cutaneous melanomas

artículo científico publicado en 2008

Genetic Variants and Multiple Myeloma Risk: IMMEnSE Validation of the Best Reported Associations--An Extensive Replication of the Associations from the Candidate Gene Era

article

Genetic heterogeneity in familial nonmedullary thyroid carcinoma: exclusion of linkage to RET, MNG1, and TCO in 56 families. NMTC Consortium.

artículo científico publicado en 1999

Genetic polymorphisms in genes of class switch recombination and multiple myeloma risk and survival: an IMMEnSE study

article

Genetic susceptibility to radiation-related differentiated thyroid cancers: a systematic review of literature

artículo científico publicado en 2019

Genetically determined telomere length and multiple myeloma risk and outcome

artículo científico publicado en 2021

Genetics and molecular epidemiology of multiple myeloma: the rationale for the IMMEnSE consortium (review).

artículo científico

Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer

article

Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses

scientific article published on 18 May 2020

Germline Homozygous Mutations at Codon 804 in theRETProtooncogene in Medullary Thyroid Carcinoma/Multiple Endocrine Neoplasia Type 2A Patients

artículo científico publicado en 2005

HapMap-based study of the 17q21 ERBB2 amplicon in susceptibility to breast cancer

artículo científico publicado en 2006

Height and Body Mass Index as Modifiers of Breast Cancer Risk in BRCA1/2 Mutation Carriers: A Mendelian Randomization Study

artículo científico publicado en 2019

Histology of familial thyroid tumours linked to a gene mapping to chromosome 19p13.2.

scientific article published on 01 November 1999

Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer

artículo científico publicado en 2017

Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus

artículo científico publicado en 2016

Identification of miRSNPs associated with the risk of multiple myeloma.

artículo científico publicado en 2016

Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer

artículo científico publicado en 2017

Impact of polymorphic variation at 7p15.3, 3p22.1 and 2p23.3 loci on risk of multiple myeloma

In silico analysis of missense substitutions using sequence-alignment based methods

artículo científico publicado en 2008

Integrative genome-wide gene expression profiling of clear cell renal cell carcinoma in Czech Republic and in the United States

artículo científico publicado en 2013

Investigation of DNA repair-related SNPs underlying susceptibility to papillary thyroid carcinoma reveals MGMT as a novel candidate gene in Belarusian children exposed to radiation.

artículo científico publicado en 2017

MITF: a genetic key to melanoma and renal cell carcinoma?

artículo científico publicado en 2012

Mapping of a gene predisposing to familial thyroid tumors with cell oxyphilia to chromosome 19 and exclusion of JUN B as a candidate gene

article

Mendelian randomisation study of height and body mass index as modifiers of ovarian cancer risk in 22,588 BRCA1 and BRCA2 mutation carriers

scientific article published on 19 June 2019

Morphology and genomic hallmarks of breast tumours developed by ATM deleterious variant carriers.

artículo científico publicado en 2018

Multigene testing of moderate-risk genes: be mindful of the missense

artículo científico publicado en 2016

Mutational Spectrum in a Worldwide Study of 29,700 Families with BRCA1 or BRCA2 Mutations

artículo científico publicado en 2018

NBT-II carcinoma behaviour is not dependent on cell-cell communication through gap junctions.

artículo científico publicado en 2002

New founder germline mutations of CDKN2A in melanoma-prone families and multiple primary melanoma development in a patient receiving levodopa treatment.

artículo científico publicado en 2007

No evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testing

scientific article published on 26 February 2016

Novel mutations in ALOX12B in patients with autosomal recessive congenital ichthyosis and evidence for genetic heterogeneity on chromosome 17p13.

artículo científico publicado en 2006

Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants

artículo científico publicado en 2020

Polymorphisms in RET and Its Coreceptors and Ligands as Genetic Modifiers of Multiple Endocrine Neoplasia Type 2A

scientific article published on 01 January 2006

Polymorphisms in regulators of xenobiotic transport and metabolism genes PXR and CAR do not affect multiple myeloma risk: a case-control study in the context of the IMMEnSE consortium

artículo científico publicado en 2013

Polymorphisms in the initiators of RET (rearranged during transfection) signaling pathway and susceptibility to sporadic medullary thyroid carcinoma

artículo científico publicado en 2005

Protective effect of copy number polymorphism of glutathione S-transferase T1 gene on melanoma risk in presence of CDKN2A mutations, MC1R variants and host-related phenotypes

artículo científico publicado en 2009

RAD51 and breast cancer susceptibility: no evidence for rare variant association in the Breast Cancer Family Registry study

artículo científico publicado en 2012

RET rearrangements in familial papillary thyroid carcinomas

scientific article published on 01 September 2001

Rare key functional domain missense substitutions in MRE11A, RAD50, and NBN contribute to breast cancer susceptibility: results from a Breast Cancer Family Registry case-control mutation-screening study

artículo científico publicado en 2014

Rare mutations in RINT1 predispose carriers to breast and Lynch syndrome-spectrum cancers

artículo científico publicado en 2014

Rare mutations in XRCC2 increase the risk of breast cancer

artículo científico publicado en 2012

Rare, evolutionarily unlikely missense substitutions in ATM confer increased risk of breast cancer

artículo científico publicado en 2009

Rare, evolutionarily unlikely missense substitutions in CHEK2 contribute to breast cancer susceptibility: results from a breast cancer family registry case-control mutation-screening study

artículo científico publicado en 2011

Risk of multiple myeloma is associated with polymorphisms within telomerase genes and telomere length.

artículo científico publicado en 2014

Single-nucleotide polymorphisms in the RB1 gene and association with breast cancer in the British population

artículo científico publicado en 2006

Sipa1 is a candidate for underlying the metastasis efficiency modifier locus Mtes1.

artículo científico publicado en 2005

Specific haplotypes of the RET proto-oncogene are over-represented in patients with sporadic papillary thyroid carcinoma.

artículo científico publicado en 2002

Succinate dehydrogenase D variants do not constitute a risk factor for developing C cell hyperplasia or sporadic medullary thyroid carcinoma

artículo científico publicado en 2004

Telomere length, ATM mutation status and cancer risk in Ataxia-Telangiectasia families

artículo científico publicado en 2017

The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer

scientific article published on 01 November 2019

The FOXE1 locus is a major genetic determinant for familial nonmedullary thyroid carcinoma

artículo científico publicado en 2013

The Spectrum of FANCM Protein Truncating Variants in European Breast Cancer Cases

scientific article published on 26 January 2020

The contribution of large genomic deletions at the CDKN2A locus to the burden of familial melanoma

artículo científico publicado en 2008

Transcriptome-wide association study of breast cancer risk by estrogen-receptor status

artículo científico publicado en 2020

Type 2 diabetes-related variants influence the risk of developing multiple myeloma: results from the IMMEnSE consortium

artículo científico publicado en 2015

[Recommendations for genetic testing and management of individuals genetically at-risk of cutaneous melanoma].

artículo científico publicado en 2014

Lista de obras de Fabienne Lesueur

A Greek Family with a Follicular Variant of Familial Papillary Thyroid Carcinoma: TCO, MNG1, fPTC/PRN, and NMTC1 Excluded as Susceptibility Loci

A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma

A Transcriptome-Wide Association Study Among 97,898 Women to Identify Candidate Susceptibility Genes for Epithelial Ovarian Cancer Risk

A common variant within the HNF1B gene is associated with overall survival of multiple myeloma patients: results from the IMMEnSE consortium and meta-analysis.

A gene predisposing to familial thyroid tumors with cell oxyphilia maps to chromosome 19p13.2.

A germline oncogenic MITF mutation and tumor susceptibility.

A polygenic risk score for multiple myeloma risk prediction

A sample storage management system for biobanks.

ABRAXAS (FAM175A) and Breast Cancer Susceptibility: No Evidence of Association in the Breast Cancer Family Registry

ADAM33, a new candidate for psoriasis susceptibility

Abstract 5103: Transcriptional profiling in clear cell renal cell carcinoma (ccRCC). Focus on Czech Republic

Allelic association of the human homologue of the mouse modifier Ptprj with breast cancer

Allelic loss on chromosomes 2q21 and 19p 13.2 in oxyphilic thyroid tumors

An association study of 22 candidate genes in psoriasis families reveals shared genetic factors with other autoimmune and skin disorders

Association of Genomic Domains in BRCA1 and BRCA2 with Prostate Cancer Risk and Aggressiveness

Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of breast cancer risk at locus 11q22.3.

Association of single-nucleotide polymorphisms in the cell cycle genes with breast cancer in the British population

At least three genes account for familial papillary thyroid carcinoma: TCO and MNG1 excluded as susceptibility loci from a large Tasmanian family

BRCA1 and BRCA2 Pathogenic Sequence Variants in Women of African Origin or Ancestry

Breast and Prostate Cancer Risks for Male BRCA1 and BRCA2 Pathogenic Variant Carriers Using Polygenic Risk Scores

COMPLEXO: identifying the missing heritability of breast cancer via next generation collaboration

Cancer Risks Associated With Germline PALB2 Pathogenic Variants: An International Study of 524 Families

Cancer Risks Associated With and Pathogenic Variants

Characterization of the Cancer Spectrum in Men With Germline BRCA1 and BRCA2 Pathogenic Variants: Results From the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA)

Circulating concentrations of insulin-like growth factor-I, insulin-like growth factor-binding protein-3, genetic polymorphisms and mammographic density in premenopausal Mexican women: results from the ESMaestras cohort

Circulating plasma phospholipid fatty acids and risk of pancreatic cancer in a large European cohort

Classification of missense substitutions in the BRCA genes: a database dedicated to Ex-UVs.

Common ERBB2 polymorphisms and risk of breast cancer in a white British population: a case-control study

Common Variants in RB1 Gene and Risk of Invasive Ovarian Cancer

Common gene variants within 3'-untranslated regions as modulators of multiple myeloma risk and survival

Common variants at 9q22.33, 14q13.3, and ATM loci, and risk of differentiated thyroid cancer in the French Polynesian population

Common variants at the 9q22.33, 14q13.3 and ATM loci, and risk of differentiated thyroid cancer in the Cuban population

Common variation in EMSY and risk of breast and ovarian cancer: a case-control study using HapMap tagging SNPs

Comprehensive investigation of genetic variation in the 8q24 region and multiple myeloma risk in the IMMEnSE consortium

Confirmation of Psoriasis Susceptibility Loci on Chromosome 6p21 and 20p13 in French Families

Contribution of ATM and FOXE1 (TTF2) to risk of papillary thyroid carcinoma in Belarusian children exposed to radiation

DICER1 mutations in familial multinodular goiter with and without ovarian Sertoli-Leydig cell tumors

Description and validation of high-throughput simultaneous genotyping and mutation scanning by high-resolution melting curve analysis

Detecting differential allelic expression using high-resolution melting curve analysis: application to the breast cancer susceptibility gene CHEK2.

Determining the effectiveness of High Resolution Melting analysis for SNP genotyping and mutation scanning at the TP53 locus

Effects of common germline genetic variation in cell cycle control genes on breast cancer survival: results from a population-based cohort

Erratum: Corrigendum: A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma

Evaluation of Polygenic Risk Scores for Breast and Ovarian Cancer Risk Prediction in BRCA1 and BRCA2 Mutation Carriers

Evidence for interaction between the TCO and NMTC1 loci in familial non-medullary thyroid cancer.

Exome sequencing identifies germline variants in DIS3 in familial multiple myeloma.

FOXE1 Polymorphism Interacts with Dietary Iodine Intake in Differentiated Thyroid Cancer Risk in the Cuban Population

Familial breast cancer and DNA repair genes: insights into known and novel susceptibility genes from the GENESIS study, and implications for multigene panel testing

Fine-Scale Mapping at 9p22.2 Identifies Candidate Causal Variants That Modify Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers

Fine-mapping of 150 breast cancer risk regions identifies 178 high confidence target genes

Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes

Fine-mapping of two differentiated thyroid carcinoma susceptibility loci at 9q22.33 and 14q13.3 detects novel candidate functional SNPs in Europeans from metropolitan France and Melanesians from New Caledonia

GEMO, a National Resource to Study Genetic Modifiers of Breast and Ovarian Cancer Risk in and Pathogenic Variant Carriers

GENESIS: a French national resource to study the missing heritability of breast cancer

Gene and pathway level analyses of iCOGS variants highlight novel signalling pathways underlying familial breast cancer susceptibility

Gene expression signature associated with BRAF mutations in human primary cutaneous melanomas

Genetic Variants and Multiple Myeloma Risk: IMMEnSE Validation of the Best Reported Associations--An Extensive Replication of the Associations from the Candidate Gene Era

Genetic heterogeneity in familial nonmedullary thyroid carcinoma: exclusion of linkage to RET, MNG1, and TCO in 56 families. NMTC Consortium.

Genetic polymorphisms in genes of class switch recombination and multiple myeloma risk and survival: an IMMEnSE study

Genetic susceptibility to radiation-related differentiated thyroid cancers: a systematic review of literature

Genetically determined telomere length and multiple myeloma risk and outcome

Genetics and molecular epidemiology of multiple myeloma: the rationale for the IMMEnSE consortium (review).

Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer

Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses

Germline Homozygous Mutations at Codon 804 in theRETProtooncogene in Medullary Thyroid Carcinoma/Multiple Endocrine Neoplasia Type 2A Patients

HapMap-based study of the 17q21 ERBB2 amplicon in susceptibility to breast cancer

Height and Body Mass Index as Modifiers of Breast Cancer Risk in BRCA1/2 Mutation Carriers: A Mendelian Randomization Study

Histology of familial thyroid tumours linked to a gene mapping to chromosome 19p13.2.

Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer

Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus

Identification of miRSNPs associated with the risk of multiple myeloma.

Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer

Impact of polymorphic variation at 7p15.3, 3p22.1 and 2p23.3 loci on risk of multiple myeloma

In silico analysis of missense substitutions using sequence-alignment based methods

Integrative genome-wide gene expression profiling of clear cell renal cell carcinoma in Czech Republic and in the United States

Investigation of DNA repair-related SNPs underlying susceptibility to papillary thyroid carcinoma reveals MGMT as a novel candidate gene in Belarusian children exposed to radiation.

MITF: a genetic key to melanoma and renal cell carcinoma?

Mapping of a gene predisposing to familial thyroid tumors with cell oxyphilia to chromosome 19 and exclusion of JUN B as a candidate gene

Mendelian randomisation study of height and body mass index as modifiers of ovarian cancer risk in 22,588 BRCA1 and BRCA2 mutation carriers

Morphology and genomic hallmarks of breast tumours developed by ATM deleterious variant carriers.