Author / Editor

• Antonarakis, Stylianos (16)
• Borel, Christelle (11)
• Gehrig, Corinne (9)
• Dermitzakis, Emmanouil (7)
• Falconnet, Emilie (5)
• Letourneau, Audrey (5)
• Deutsch, Samuel (4)
• Guipponi, Michel (4)
• Migliavacca Voeffray, Eugenia Linda (4)
• Montgomery, Stephen (4)
• Attar Cohen, Homa (3)
• Deutsch Escalante, Samuel (3)
• Gutierrez Arcelus, Maria (3)
• Lyle, Robert (3)
• Bryois, Julien (2)
• Buil Demur, Alfonso Alberto (2)
• Descombes, Patrick (2)
• Dupre, Yann (2)
• Giger, Thomas (2)
• Lappalainen, Tuuli Emilia (2)
• Makrythanasis, Periklis (2)
• Ongen, Halit (2)
• Padioleau, Ismael (2)
• Planchon, Alexandra (2)
• Romano, Luciana (2)
• Sailani, Mohammad Reza (2)
• Sharp, Andrew James (2)
• Sloan Bena, Frédérique (2)
• Yurovsky, Alisa (2)

Document type

• Article scientifique (15)
• Article professionnel (1)

Full text accessibility

• Restricted access (11)
• Free access (5)

Full text version

• Published version (11)
• Unknown (3)
• Accepted version (2)

Licence

• CC BY (2)

Subject

• Humans (14)
• Polymorphism, single nucleotide (5)
• Cell line (4)
• Gene expression profiling (4)
• Female (3)
• Fibroblasts (3)
• Gene expression regulation (3)
• Genetic variation (3)
• Genome-wide association study (3)
• Infant, newborn (3)
• Base sequence (2)
• Cell line, tumor (2)
• Chromosome mapping (2)
• Chromosomes, human, pair 21 (2)
• Chromosomes, human, pair 21/genetics (2)
• Cohort studies (2)
• Down syndrome/genetics (2)
• Enhancer elements, genetic (2)
• Gene expression regulation/genetics (2)
• Gene frequency (2)
• Genetic linkage (2)
• Genetic markers (2)
• Genome, human/genetics (2)
• Genotype (2)
• Karyotyping (2)
• Male (2)
• Molecular sequence data (2)
• Phenotype (2)
• Quantitative trait loci (2)
• Quantitative trait loci/genetics (2)