Paul Laissue
Laissue, Paul, 1975-....
VIAF ID: 210276336 (Personal)
Permalink: http://viaf.org/viaf/210276336
Preferred Forms
- 100 1 _ ‡a Laissue, Paul, ‡d 1975-
- 100 1 _ ‡a Laissue, Paul, ‡d 1975-....
- 100 0 _ ‡a Paul Laissue
4xx's: Alternate Name Forms (2)
Works
Title | Sources |
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Anomalies des récepteurs des bone morphogenic proteins : une nouvelle cause d’insuffisance ovarienne primaire | |
Biallelic HERC1 mutations in a syndromic form of overgrowth and intellectual disability. | |
BMP15 Mutations Associated With Primary Ovarian Insufficiency Reduce Expression, Activity, or Synergy With GDF9. | |
Candidate gene and QTL approaches in the research of factors related with premature ovarian failure and recurrent spontaneous abortion etiology : implication of BMP15, GDF9 and FOXD1 genes. | |
Centimorgan-range one-step mapping of fertility traits using interspecific recombinant congenic mice | |
Copy number variation profiling in pharmacogenetics CYP-450 and GST genes in Colombian population | |
Current needs for human and medical genomics research infrastructure in low and middle income countries | |
A de novo 14q12q13.3 interstitial deletion in a patient affected by a severe neurodevelopmental disorder of unknown origin | |
Differential functional effects of novel mutations of the transcription factor FOXL2 in BPES patients | |
Endothelial cell dysfunction and cardiac hypertrophy in the STOX1 model of preeclampsia | |
Exome sequencing is an efficient tool for variant late-infantile neuronal ceroid lipofuscinosis molecular diagnosis | |
Expressional and epigenetic alterations of placental serine protease inhibitors: SERPINA3 is a potential marker of preeclampsia. | |
A first description of the Colombian national registry for rare diseases | |
The forkhead-box family of transcription factors: key molecular players in colorectal cancer pathogenesis | |
FOXD1 mutations are related to repeated implantation failure, intra-uterine growth restriction and preeclampsia | |
Functional evidence implicating NOTCH2 missense mutations in primary ovarian insufficiency aetiology | |
[Genetic analysis of premature ovarian failure: role of forkhead and TGF-beta genes]. | |
Genome-wide linkage in a highly consanguineous pedigree reveals two novel loci on chromosome 7 for non-syndromic familial Premature Ovarian Failure | |
A high resolution map of mammalian X chromosome fragile regions assessed by large-scale comparative genomics | |
A homozygous donor splice-site mutation in the meiotic gene MSH4 causes primary ovarian insufficiency. | |
Identification and Functional Characterization of GAA Mutations in Colombian Patients Affected by Pompe Disease | |
Identification of 34 novel and 56 known FOXL2 mutations in patients with Blepharophimosis syndrome. | |
Identification of a New Candidate Locus for Ebstein Anomaly in 1p36.2 | |
Identification of Quantitative Trait Loci responsible for embryonic lethality in mice assessed by ultrasonography | |
Improving the evaluation of milestones for students completing a clinical genetics elective | |
Interspecific resources: a major tool for quantitative trait locus cloning and speciation research | |
The molecular complexity of primary ovarian insufficiency aetiology and the use of massively parallel sequencing | |
The multisystemic functions of FOXD1 in development and disease | |
Mutant GNLY is linked to Stevens-Johnson syndrome and toxic epidermal necrolysis | |
New mutations in non-syndromic primary ovarian insufficiency patients identified via whole-exome sequencing | |
Next generation sequencing in women affected by nonsyndromic premature ovarian failure displays new potential causative genes and mutations. | |
A novel BMP15 variant, potentially affecting the signal peptide, in a familial case of premature ovarian failure. | |
A novel familial case of diffuse leukodystrophy related to NDUFV1 compound heterozygous mutations | |
Novel genes and mutations in patients affected by recurrent pregnancy loss. | |
A novel method for quantified, superresolved, three-dimensional colocalisation of isotropic, fluorescent particles. | |
P-015: Association of FOXD1 variants with pregnancy failures in mice and humans | |
Partial defects in transcriptional activity of two novel DAX-1 mutations in childhood-onset adrenal hypoplasia congenita | |
A Pharmacogenomic Dissection of a Rosuvastatin-Induced Rhabdomyolysis Case Evokes the Polygenic Nature of Adverse Drug Reactions | |
Polymorphisms of human placental alkaline phosphatase are associated with in vitro fertilization success and recurrent pregnancy loss | |
Première mise en cause de l’autophagie dans l’étiologie de l’insuffisance ovarienne primaire | |
Prostaglandin transporter mutations cause pachydermoperiostosis with myelofibrosis | |
Quantified colocalization reveals heterotypic histocompatibility class I antigen associations on trophoblast cell membranes: relevance for human pregnancy | |
Recent advances in the study of genes involved in non-syndromic premature ovarian failure | |
Refined mapping of a quantitative trait locus on chromosome 1 responsible for mouse embryonic death. | |
Seminiferous tubule function in delayed-onset X-linked adrenal hypoplasia congenita associated with incomplete hypogonadotrophic hypogonadism | |
Sequence analysis of the ADRA2A coding region in children affected by attention deficit hyperactivity disorder. | |
Sequence analysis of the CDKN1B gene in patients with premature ovarian failure reveals a novel mutation potentially related to the phenotype. | |
Success stories in genomic medicine from resource-limited countries | |
THBD sequence variants potentially related to recurrent pregnancy loss | |
Transcriptomic analysis of FUCA1 knockdown in keratinocytes reveals new insights in the pathogenesis of fucosidosis skin lesions. | |
Transcriptomic analysis of skin in a case of ichthyosis Curth-Macklin caused by a KRT1 mutation. | |
Undertreatment strongly decreases prognosis of breast cancer in elderly women | |
Whole-exome sequencing enables rapid determination of xeroderma pigmentosum molecular etiology |