“…We refer to [73 ▪▪ ,123] for recent overviews. We cite recent reviews addressing these complex, multifacted processes involving: mother-fetus-placenta unit [78]; HPA axis and cortisol [120,124 ▪ ,125]; autonomic nervous system [125]; iron deficiency [126]; maternal inflammation and offspring microglial activity [127]; mitochondria [128]; microbiome [10,129–131]; maternal metabolic risk factors including diabetes, obesity, undernutrition, specific macro- and micronutrient intake (e.g., long-chain polyunsaturated fatty acids (PUFAs) [132–135]; epigenetic changes, epigenome wide associations studies, relevant for e.g., the HPA axis or oxytocin system [136] including DNA methylation, histone modification, microRNA and other-non coding RNA [73 ▪▪ ,135,137–139] or multiomics data (transcriptomics, proteomics, metabolomics, and microbiomics [140]); telomere length [57]; paternal mediated effects [141,142]; oxidative stress [143], breast milk composition [78]; oxytocin system [73 ▪▪ ]; serotonin functions (e.g., SCL6A4) [73 ▪▪ ]; brain-derived neurotrophic factor (BDNF) [73 ▪▪ ]; structural and functional brain alterations beyond regions previously identified as relevant (i.e., prefrontal cortex, hippocampus, amygdala (limbic system)) additionally including basal ganglia, anterior cingulate cortex, thalamus, middle and superior frontal gyri, occipital gyrus and precentral gyrus [9,31,108].…”