Latest Publications

Coordinated responses to individual tumor antigens by IgG antibody and CD8+ T cells following cancer vaccination

Novel compound heterozygous mutations in the GPR98 (USH2C) gene identified by whole exome sequencing in a Moroccan deaf family

The Fungal bZIP Transcription Factor AtfB Controls Virulence-Associated Processes in Aspergillus parasiticus

SIRT1/HERC4 locus associated with Bisphosphonate-induced osteonecrosis of the jaw: an exome-wide association analysis

BRCA1-mimetic compound NSC35446.HCL inhibits IKKBexpression by reducing estrogen receptor-a occupancy in the IKKB promoter and inhibits NF-kB activity in antiestrogen resistant human breast cancer cells

Autosomal recessive chondrodysplasia with severe short stature caused by a biallelic COL10A1 variant

Mutations in SCAPER cause autosomal recessive retinitis pigmentosa with intellectual disability

Differentially expressed genes in PPARg-deficient MSCs

Homozygous mutations in PJVK and MYO15A genes associated with nonsyndromic hearing loss in Moroccan families

Exome sequencing identifies targets in the treatment-resistant phathalmoplegic subphenotype of Myasthenia Gravis

Digenic inheritance of mutations in the cardiac troponin (TNNT2) and cardiac beta myosin heavy chain (MYH7) as the cause of severe dilated cardiomyopathy

Familial epilepsy with anterior polymicrogyria as a presentation of COL18A1 mutations