Laura Crisponi
Researcher Next ID · RN-029791
Researcher · Biochemistry, Genetics and Molecular Biology
Institute of Genetic and Biomedical Research
Monserrato, Romania
- Works count
- 110
- Citation count
- 14,233
- H-index
- 41
- i10-index
- 66
Research interests
Publications
Genetic insights into biological mechanisms governing human ovarian ageing
Nature · 2021 · https://doi.org/10.1038/s41586-021-03779-7
Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk
Nature Genetics · 2017 · https://doi.org/10.1038/ng.3841
A Genome-Wide Association Scan on the Levels of Markers of Inflammation in Sardinians Reveals Associations That Underpin Its Complex Regulation
PLoS Genetics · 2012 · https://doi.org/10.1371/journal.pgen.1002480
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk
Nature Genetics · 2010 · https://doi.org/10.1038/ng.520
Common variants in the SLCO1B3 locus are associated with bilirubin levels and unconjugated hyperbilirubinemia
Human Molecular Genetics · 2009 · https://doi.org/10.1093/hmg/ddp203
Common variants at ten loci modulate the QT interval duration in the QTSCD Study
Nature Genetics · 2009 · https://doi.org/10.1038/ng.362
Phosphodiesterase 8B Gene Variants Are Associated with Serum TSH Levels and Thyroid Function
The American Journal of Human Genetics · 2008 · https://doi.org/10.1016/j.ajhg.2008.04.019
Common variants in the GDF5-UQCC region are associated with variation in human height
Nature Genetics · 2008 · https://doi.org/10.1038/ng.74
Variants in MTNR1B influence fasting glucose levels
Nature Genetics · 2008 · https://doi.org/10.1038/ng.290
Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of β-thalassemia
Proceedings of the National Academy of Sciences · 2008 · https://doi.org/10.1073/pnas.0711566105
The GLUT9 Gene Is Associated with Serum Uric Acid Levels in Sardinia and Chianti Cohorts
PLoS Genetics · 2007 · https://doi.org/10.1371/journal.pgen.0030194
IRAK-M Is Involved in the Pathogenesis of Early-Onset Persistent Asthma
The American Journal of Human Genetics · 2007 · https://doi.org/10.1086/518259
Foxl2 is required for commitment to ovary differentiation
Human Molecular Genetics · 2005 · https://doi.org/10.1093/hmg/ddi210
Foxl2 disruption causes mouse ovarian failure by pervasive blockage of follicle development
Human Molecular Genetics · 2004 · https://doi.org/10.1093/hmg/ddh124
Genes and translocations involved in POF
American Journal of Medical Genetics · 2002 · https://doi.org/10.1002/ajmg.10565
The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome
Nature Genetics · 2001 · https://doi.org/10.1038/84781
Current projects
No projects listed.