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The forkhead-box family of transcription factors: key molecular players in colorectal cancer pathogenesis

Molecular cancer, 2019-01, Vol.18 (1), p.5-5, Article 5

Laissue, Paul

2019

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The multisystemic functions of FOXD1 in development and disease

Journal of molecular medicine (Berlin, Germany), 2018-08, Vol.96 (8), p.725-739

2018

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ATG7 and ATG9A loss-of-function variants trigger autophagy impairment and ovarian failure

Genetics in medicine, 2019-04, Vol.21 (4), p.930-938

2019

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Novel genes and mutations in patients affected by recurrent pregnancy loss

PloS one, 2017-10, Vol.12 (10), p.e0186149-e0186149

2017

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The molecular complexity of primary ovarian insufficiency aetiology and the use of massively parallel sequencing

Molecular and cellular endocrinology, 2018-01, Vol.460, p.170-180

Laissue, Paul

2018

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Aetiological coding sequence variants in non-syndromic premature ovarian failure: From genetic linkage analysis to next generation sequencing

Molecular and cellular endocrinology, 2015-08, Vol.411, p.243-257

Laissue, Paul

2015

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Undertreatment Strongly Decreases Prognosis of Breast Cancer in Elderly Women

Journal of clinical oncology, 2003-10, Vol.21 (19), p.3580-3587

2003

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Next generation sequencing in women affected by nonsyndromic premature ovarian failure displays new potential causative genes and mutations

Fertility and sterility, 2015-07, Vol.104 (1), p.154-162.e2

2015

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Endothelial cell dysfunction and cardiac hypertrophy in the STOX1 model of preeclampsia

Scientific reports, 2016-01, Vol.6 (1), p.19196-19196, Article 19196

2016

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Structural Modelling of KCNQ1 and KCNH2 Double Mutant Proteins, Identified in Two Severe Long QT Syndrome Cases, Reveals New Insights into Cardiac Channelopathies

International journal of molecular sciences, 2021-11, Vol.22 (23), p.12861

2021

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FOXD1 mutations are related to repeated implantation failure, intra-uterine growth restriction and preeclampsia

Molecular medicine (Cambridge, Mass.), 2019-08, Vol.25 (1), p.37-37, Article 37

2019

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Linking genotype to trophoblast phenotype in preeclampsia and HELLP syndrome associated with STOX1 genetic variants

iScience, 2024-03, Vol.27 (3), p.109260-109260, Article 109260

2024

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Recent advances in the study of genes involved in non-syndromic premature ovarian failure

Molecular and cellular endocrinology, 2008-01, Vol.282 (1), p.101-111

2008

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Possible Genetic Determinants of Response to Phenytoin in a Group of Colombian Patients With Epilepsy

Frontiers in pharmacology, 2020-05, Vol.11, p.555-555

2020

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THBD sequence variants potentially related to recurrent pregnancy loss

Reproductive biology and endocrinology, 2017-12, Vol.15 (1), p.92-92, Article 92

2017

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Copy number variation profiling in pharmacogenetics CYP-450 and GST genes in Colombian population

BMC medical genomics, 2019-07, Vol.12 (1), p.110-110, Article 110

2019

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Genetic Variants Contributing to Early Recurrent Pregnancy Loss Etiology Identified by Sequencing Approaches

Reproductive sciences (Thousand Oaks, Calif.), 2020-08, Vol.27 (8), p.1541-1552

2020

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A Pharmacogenomic Dissection of a Rosuvastatin-Induced Rhabdomyolysis Case Evokes the Polygenic Nature of Adverse Drug Reactions

Pharmacogenomics and personalized medicine, 2020-01, Vol.13, p.59-70

2020

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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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Whole-exome sequencing enables rapid determination of xeroderma pigmentosum molecular etiology

PloS one, 2013-06, Vol.8 (6), p.e64692-e64692

2013

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Molecular Mechanisms of Trophoblast Dysfunction Mediated by Imbalance between STOX1 Isoforms

iScience, 2020-05, Vol.23 (5), p.101086-101086, Article 101086

2020

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Centimorgan-Range One-Step Mapping of Fertility Traits Using Interspecific Recombinant Congenic Mice

Genetics (Austin), 2007-07, Vol.176 (3), p.1907-1921

2007

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A first description of the Colombian national registry for rare diseases

BMC research notes, 2017-10, Vol.10 (1), p.514-514, Article 514

2017

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Genetic Variants Contributing to Early Recurrent Pregnancy Loss Etiology Identified by Sequencing Approaches

Reproductive sciences (Thousand Oaks, Calif.), 2019-03, p.1933719119831769-1933719119831769

2019

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Refined mapping of a quantitative trait locus on chromosome 1 responsible for mouse embryonic death

PloS one, 2012-08, Vol.7 (8), p.e43356-e43356

2012

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The forkhead-box family of transcription factors: key molecular players in colorectal cancer pathogenesis

The multisystemic functions of FOXD1 in development and disease

ATG7 and ATG9A loss-of-function variants trigger autophagy impairment and ovarian failure

Novel genes and mutations in patients affected by recurrent pregnancy loss

The molecular complexity of primary ovarian insufficiency aetiology and the use of massively parallel sequencing

Aetiological coding sequence variants in non-syndromic premature ovarian failure: From genetic linkage analysis to next generation sequencing

Undertreatment Strongly Decreases Prognosis of Breast Cancer in Elderly Women

Next generation sequencing in women affected by nonsyndromic premature ovarian failure displays new potential causative genes and mutations

Endothelial cell dysfunction and cardiac hypertrophy in the STOX1 model of preeclampsia

Structural Modelling of KCNQ1 and KCNH2 Double Mutant Proteins, Identified in Two Severe Long QT Syndrome Cases, Reveals New Insights into Cardiac Channelopathies

FOXD1 mutations are related to repeated implantation failure, intra-uterine growth restriction and preeclampsia

Linking genotype to trophoblast phenotype in preeclampsia and HELLP syndrome associated with STOX1 genetic variants

Recent advances in the study of genes involved in non-syndromic premature ovarian failure

Possible Genetic Determinants of Response to Phenytoin in a Group of Colombian Patients With Epilepsy

THBD sequence variants potentially related to recurrent pregnancy loss

Copy number variation profiling in pharmacogenetics CYP-450 and GST genes in Colombian population

Genetic Variants Contributing to Early Recurrent Pregnancy Loss Etiology Identified by Sequencing Approaches

A Pharmacogenomic Dissection of a Rosuvastatin-Induced Rhabdomyolysis Case Evokes the Polygenic Nature of Adverse Drug Reactions

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

Whole-exome sequencing enables rapid determination of xeroderma pigmentosum molecular etiology

Molecular Mechanisms of Trophoblast Dysfunction Mediated by Imbalance between STOX1 Isoforms

Centimorgan-Range One-Step Mapping of Fertility Traits Using Interspecific Recombinant Congenic Mice

A first description of the Colombian national registry for rare diseases

Genetic Variants Contributing to Early Recurrent Pregnancy Loss Etiology Identified by Sequencing Approaches

Refined mapping of a quantitative trait locus on chromosome 1 responsible for mouse embryonic death

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