Liran Carmel

Punic people were genetically diverse with almost no Levantine ancestors

RoAM: computational reconstruction of ancient methylomes and identification of differentially methylated regions

Maternal prenatal stress induces sex-dependent changes in tRNA fragment families and cholinergic pathways in newborns

Reconstructing DNA methylation maps of ancient populations

Improved detection of methylation in ancient DNA

Inferring DNA methylation in non-skeletal tissues of ancient specimens

Antisense oligonucleotide-based drug development for Cystic Fibrosis patients carrying the 3849+10 kb C-to-T splicing mutation

Lead in Archeological Human Bones Reflecting Historical Changes in Lead Production

SRCP: a comprehensive pipeline for accurate annotation and quantification of circRNAs

The Genomic History of the Bronze Age Southern Levant

Harnessing epigenetics to study human evolution

Assessing predictions of the impact of variants on splicing in CAGI5

Predicted Archaic 3D Genome Organization Reveals Genes Related to Head and Spinal Cord Separating Modern from Archaic Humans

Nucleotide composition affects codon usage toward the 3'-end

Evidence for convergent evolution of SINE-directed Staufen-mediated mRNA decay

Small RNA sequences derived from pre-microRNAs in the supraspliceosome

Alu exaptation enriches the human transcriptome by introducing new gene ends

Inferring Past Environments from Ancient Epigenomes

Gene ORGANizer: linking genes to the organs they affect

Identification of introns harboring functional sequence elements through positional conservation

A deep neural network witharestricted noisy channel for identification of functional introns

Archaic adaptive introgression in <i>TBX15/WARS2</i>

Epigenetics: It's Getting Old. Past Meets Future in Paleoepigenetics

Movement correlates of lizards’ dorsal pigmentation patterns

System-wide Analysis of the T Cell Response

Expanding the phenotype of <scp>CRB2</scp> mutations – A new ciliopathy syndrome?

Combined mineralocorticoid and glucocorticoid deficiency is caused by a novel founder nicotinamide nucleotide transhydrogenase mutation that alters mitochondrial morphology and increases oxidative stress

JuncDB: an exon–exon junction database

LEMONS – A Tool for the Identification of Splice Junctions in Transcriptomes of Organisms Lacking Reference Genomes

Reconstructing the DNA Methylation Maps of the Neandertal and the Denisovan