List of works - Lucia Inglada

Allelic variant at -79 (C>T) in CDKN1B (p27Kip1) confers an increased risk of thyroid cancer and alters mRNA levels.

scientific article

An epistatic interaction between the PAX8 and STK17B genes in papillary thyroid cancer susceptibility.

scientific article

DNA copy number profiling reveals different patterns of chromosomal instability within colorectal cancer according to the age of onset

scientific article published on 25 March 2015

DNA methylation profiling of well-differentiated thyroid cancer uncovers markers of recurrence free survival.

scientific article

Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma

scientific article (publication date: 19 June 2011)

Functional and in silico assessment of MAX variants of unknown significance

scientific article

Genetic anticipation is associated with telomere shortening in hereditary breast cancer.

scientific article

Genetic variation in the SLC19A1 gene and methotrexate toxicity in rheumatoid arthritis patients.

scientific article

Genome-wide association study identifies ephrin type A receptors implicated in paclitaxel induced peripheral sensory neuropathy

scientific journal article

Hematologic β-tubulin VI isoform exhibits genetic variability that influences paclitaxel toxicity.

scientific article

Impact of chemotherapy on telomere length in sporadic and familial breast cancer patients

scientific article published on 21 December 2014

Integrative analysis of miRNA and mRNA expression profiles in pheochromocytoma and paraganglioma identifies genotype-specific markers and potentially regulated pathways

scientific article published on 24 June 2013

MAX Mutations Cause Hereditary and Sporadic Pheochromocytoma and Paraganglioma

scientific article published on 27 March 2012

MicroRNA deep-sequencing reveals master regulators of follicular and papillary thyroid tumors.

scientific article published on 27 February 2015

Overexpression and activation of EGFR and VEGFR2 in medullary thyroid carcinomas is related to metastasis.

scientific article

Recommendations for somatic and germline genetic testing of single pheochromocytoma and paraganglioma based on findings from a series of 329 patients.

scientific article published on 12 August 2015

Regulatory polymorphisms in β-tubulin IIa are associated with paclitaxel-induced peripheral neuropathy.

scientific article published on 20 June 2012

Research resource: Transcriptional profiling reveals different pseudohypoxic signatures in SDHB and VHL-related pheochromocytomas

scientific article

SIRT1 promotes thyroid carcinogenesis driven by PTEN deficiency.

scientific article

Short telomeres are frequent in hereditary breast tumors and are associated with high tumor grade

scientific article published on 15 September 2013

Shorter telomere length is associated with increased ovarian cancer risk in both familial and sporadic cases.

scientific article published on 6 April 2012

The miR-200 family controls -tubulin III expression and is associated with paclitaxel-based treatment response and progression-free survival in ovarian cancer patients

scientific article published on 21 December 2010

The variant rs1867277 in FOXE1 gene confers thyroid cancer susceptibility through the recruitment of USF1/USF2 transcription factors

scientific article published on 4 September 2009

Thyroid cancer GWAS identifies 10q26.12 and 6q14.1 as novel susceptibility loci and reveals genetic heterogeneity among populations

scientific article published on 22 April 2015

Tumor microRNA expression profiling identifies circulating microRNAs for early breast cancer detection

scientific article published on 8 June 2015

Tumoral EPAS1 (HIF2A) mutations explain sporadic pheochromocytoma and paraganglioma in the absence of erythrocytosis

scientific article published on 14 February 2013

VEGF, VEGFR3, and PDGFRB protein expression is influenced by RAS mutations in medullary thyroid carcinoma.

scientific article

Whole-exome sequencing identifies MDH2 as a new familial paraganglioma gene.

scientific article

List of works by Lucia Inglada

Allelic variant at -79 (C>T) in CDKN1B (p27Kip1) confers an increased risk of thyroid cancer and alters mRNA levels.

An epistatic interaction between the PAX8 and STK17B genes in papillary thyroid cancer susceptibility.

DNA copy number profiling reveals different patterns of chromosomal instability within colorectal cancer according to the age of onset

DNA methylation profiling of well-differentiated thyroid cancer uncovers markers of recurrence free survival.

Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma

Functional and in silico assessment of MAX variants of unknown significance

Genetic anticipation is associated with telomere shortening in hereditary breast cancer.

Genetic variation in the SLC19A1 gene and methotrexate toxicity in rheumatoid arthritis patients.

Genome-wide association study identifies ephrin type A receptors implicated in paclitaxel induced peripheral sensory neuropathy

Hematologic β-tubulin VI isoform exhibits genetic variability that influences paclitaxel toxicity.

Impact of chemotherapy on telomere length in sporadic and familial breast cancer patients

Integrative analysis of miRNA and mRNA expression profiles in pheochromocytoma and paraganglioma identifies genotype-specific markers and potentially regulated pathways

MAX Mutations Cause Hereditary and Sporadic Pheochromocytoma and Paraganglioma

MicroRNA deep-sequencing reveals master regulators of follicular and papillary thyroid tumors.

Overexpression and activation of EGFR and VEGFR2 in medullary thyroid carcinomas is related to metastasis.

Recommendations for somatic and germline genetic testing of single pheochromocytoma and paraganglioma based on findings from a series of 329 patients.

Regulatory polymorphisms in β-tubulin IIa are associated with paclitaxel-induced peripheral neuropathy.

Research resource: Transcriptional profiling reveals different pseudohypoxic signatures in SDHB and VHL-related pheochromocytomas

SIRT1 promotes thyroid carcinogenesis driven by PTEN deficiency.

Short telomeres are frequent in hereditary breast tumors and are associated with high tumor grade

Shorter telomere length is associated with increased ovarian cancer risk in both familial and sporadic cases.

The miR-200 family controls -tubulin III expression and is associated with paclitaxel-based treatment response and progression-free survival in ovarian cancer patients

The variant rs1867277 in FOXE1 gene confers thyroid cancer susceptibility through the recruitment of USF1/USF2 transcription factors

Thyroid cancer GWAS identifies 10q26.12 and 6q14.1 as novel susceptibility loci and reveals genetic heterogeneity among populations

Tumor microRNA expression profiling identifies circulating microRNAs for early breast cancer detection

Tumoral EPAS1 (HIF2A) mutations explain sporadic pheochromocytoma and paraganglioma in the absence of erythrocytosis

VEGF, VEGFR3, and PDGFRB protein expression is influenced by RAS mutations in medullary thyroid carcinoma.

Whole-exome sequencing identifies MDH2 as a new familial paraganglioma gene.