Azzedine Aboura
Assistance Publique – Hôpitaux de Paris(FR)Hôpital Robert-Debré(FR)
Publications by Year
Research Areas
Genomic variations and chromosomal abnormalities, Prenatal Screening and Diagnostics, Chromosomal and Genetic Variations, Congenital heart defects research, Genetics and Neurodevelopmental Disorders
Most-Cited Works
- → Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus(2011)475 cited
- → Duplication of the 15q11-q13 region: Clinical and genetic study of 30 new cases(2013)134 cited
- → Cytogenetic, molecular and testicular tissue studies in an infertile 45,X male carrying an unbalanced (Y;22) translocation: Case report(2005)107 cited
- → Array Comparative Genomic Hybridization Profiling Analysis Reveals Deoxyribonucleic Acid Copy Number Variations Associated with Premature Ovarian Failure(2009)97 cited
- → 2q23.1 microdeletion identified by array comparative genomic hybridisation: an emerging phenotype with Angelman-like features?(2008)88 cited
- → Discordant prenatal diagnosis of trisomy 21 due to mosaic structural rearrangements of chromosome 21(2003)87 cited
- → First cryptic balanced reciprocal translocation mosaicism and familial transmission(2008)72 cited
- → Complex nature of apparently balanced chromosomal rearrangements in patients with autism spectrum disorder(2015)70 cited
- → Pre‐ and postnatal phenotype of 6p25 deletions involving the FOXC1 gene(2012)67 cited
- → Common 4q24 deletion in four cases of hematopoietic malignancy: early stem cell involvement?(2005)66 cited