| human | Q5 |
| P496 | ORCID iD | 0000-0001-7854-0267 |
| P735 | given name | Karine | Q13365966 |
| Karine | Q13365966 | ||
| P106 | occupation | researcher | Q1650915 |
| P21 | sex or gender | female | Q6581072 |
| Q36585045 | A nonsense variant in HERC1 is associated with intellectual disability, megalencephaly, thick corpus callosum and cerebellar atrophy |
| Q44385992 | A novel mutation in STXBP1 causing epileptic encephalopathy (late onset infantile spasms) with partial respiratory chain complex IV deficiency |
| Q35648078 | Contiguous mutation syndrome in the era of high-throughput sequencing |
| Q39574159 | Differential expression of the 18 kDa translocator protein (TSPO) by neoplastic and inflammatory cells in mouse tumors of breast cancer. |
| Q54012004 | Effect of dexamethasone on adipocyte differentiation markers and tumour necrosis factor-alpha expression in human PAZ6 cells. |
| Q45303655 | Genotype specific age related changes in a transgenic rat model of Huntington's disease |
| Q34503914 | Multimodal In Vivo Imaging of Tumorigenesis and Response to Chemotherapy in a Transgenic Mouse Model of Mammary Cancer |
| Q41931653 | Mutation in TTI2 reveals a role for triple T complex in human brain development |
| Q30845425 | Mutations in NONO lead to syndromic intellectual disability and inhibitory synaptic defects |
| Q36803093 | Mutations in TBCK, Encoding TBC1-Domain-Containing Kinase, Lead to a Recognizable Syndrome of Intellectual Disability and Hypotonia |
| Q36443544 | Profiling olfactory stem cells from living patients identifies miRNAs relevant for autism pathophysiology |
| Q39417013 | Refining the phenotype associated with CASC5 mutation |
| Q36865263 | Utility of whole exome sequencing for the early diagnosis of pediatric-onset cerebellar atrophy associated with developmental delay in an inbred population |
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