The nearly Newtonian regime in Non-Linear Theories of Gravity

The present paper reconsiders the Newtonian limit of models of modified gravity including higher order terms in the scalar curvature in the gravitational action. This was studied using the Palatini variational principle in [Meng X. and Wang P.: Gen. Rel. Grav. {\bf 36}, 1947 (2004)] and [Dom\'inguez A. E. and Barraco D. E.: Phys. Rev. D {\bf 70}, 043505 (2004)] with contradicting results. Here a different approach is used, and problems in the previous attempts are pointed out. It is shown that models with negative powers of the scalar curvature, like the ones used to explain the present accelerated expansion, as well as their generalization which include positive powers, can give the correct Newtonian limit, as long as the coefficients of these powers are reasonably small. Some consequences of the performed analysis seem to raise doubts for the way the Newtonian limit was derived in the purely metric approach of fourth order gravity [Dick R.: Gen. Rel. Grav. {\bf 36}, 217 (2004)]. Finally, we comment on a recent paper [Olmo G. J.: Phys. Rev. D {\bf 72}, 083505 (2005)] in which the problem of the Newtonian limit of both the purely metric and the Palatini formalism is discussed, using the equivalent Brans--Dicke theory, and with which our results partly disagree.Comment: typos corrected, replaced to match published versio

Accelerated Cosmological Models in First-Order Non-Linear Gravity

The evidence of the acceleration of universe at present time has lead to investigate modified theories of gravity and alternative theories of gravity, which are able to explain acceleration from a theoretical viewpoint without the need of introducing dark energy. In this paper we study alternative gravitational theories defined by Lagrangians which depend on general functions of the Ricci scalar invariant in minimal interaction with matter, in view of their possible cosmological applications. Structural equations for the spacetimes described by such theories are solved and the corresponding field equations are investigated in the Palatini formalism, which prevents instability problems. Particular examples of these theories are also shown to provide, under suitable hypotheses, a coherent theoretical explanation of earlier results concerning the present acceleration of the universe and cosmological inflation. We suggest moreover a new possible Lagrangian, depending on the inverse of sinh(R), which gives an explanation to the present acceleration of the universe.Comment: 23 pages, Revtex4 fil

Leptogenesis from a sneutrino condensate revisited

We re--examine leptogenesis from a right--handed sneutrino condensate, paying special attention to the $B-$term associated with the see--saw Majorana mass. This term generates a lepton asymmetry in the condensate whose time average vanishes. However, a net asymmetry will result if the sneutrino lifetime is not much longer than the period of oscillations. Supersymmetry breaking by thermal effects then yields a lepton asymmetry in the standard model sector after the condensate decays. We explore different possibilities by taking account of both the low--energy and Hubble $B-$terms. It will be shown that the desired baryon asymmetry of the Universe can be obtained for a wide range of Majorana mass.Comment: 17 revtex pages, 3 figures, 1 table. Slightly modified and references added. Final version accepted for publication in Phys. Rev.

Indications of Linkage and Association of Gilles de la Tourette Syndrome in Two Independent Family Samples: 17q25 Is a Putative Susceptibility Region

Gilles de la Tourette syndrome (GTS) is characterized by multiple motor and phonic tics and high comorbidity rates with other neurobehavioral disorders. It is hypothesized that frontal-subcortical pathways and a complex genetic background are involved in the etiopathogenesis of the disorder. The genetic basis of GTS remains elusive. However, several genomic regions have been implicated. Among them, 17q25 appears to be of special interest, as suggested by various independent investigators. In the present study, we explored the possibility that 17q25 contributes to the genetic component of GTS. The initial scan of chromosome 17 performed on two large pedigrees provided a nonparametric LOD score of 2.41 near D17S928. Fine mapping with 17 additional microsatellite markers increased the peak to 2.61 (P=.002). The original families, as well as two additional pedigrees, were genotyped for 25 single-nucleotide polymorphisms (SNPs), with a focus on three genes in the indicated region that could play a role in the development of GTS, on the basis of their function and expression profile. Multiple three-marker haplotypes spanning all three genes studied provided highly significant association results (P<.001). An independent sample of 96 small families with one or two children affected with GTS was also studied. Of the 25 SNPs, 3 were associated with GTS at a statistically significant level. The transmission/disequilibrium test for a three-site haplotype moving window again provided multiple positive results. The background linkage disequilibrium (LD) of the region was studied in eight populations of European origin. A complicated pattern was revealed, with the pairwise tests producing unexpectedly high LD values at the telomeric TBCD gene. In conclusion, our findings warrant the further investigation of 17q25 as a candidate susceptibility region for GTS

Novel genetic loci associated with hippocampal volume

The hippocampal formation is a brain structure integrally involved in episodic memory, spatial navigation, cognition and stress responsiveness. Structural abnormalities in hippocampal volume and shape are found in several common neuropsychiatric disorders. To identify the genetic underpinnings of hippocampal structure here we perform a genome-wide association study (GWAS) of 33,536 individuals and discover six independent loci significantly associated with hippocampal volume, four of them novel. Of the novel loci, three lie within genes (ASTN2, DPP4 and MAST4) and one is found 200 kb upstream of SHH. A hippocampal subfield analysis shows that a locus within the MSRB3 gene shows evidence of a localized effect along the dentate gyrus, subiculum, CA1 and fissure. Further, we show that genetic variants associated with decreased hippocampal volume are also associated with increased risk for Alzheimer's disease (rg =-0.155). Our findings suggest novel biological pathways through which human genetic variation influences hippocampal volume and risk for neuropsychiatric illness

New insights into the genetic etiology of Alzheimer's disease and related dementias

Characterization of the genetic landscape of Alzheimer's disease (AD) and related dementias (ADD) provides a unique opportunity for a better understanding of the associated pathophysiological processes. We performed a two-stage genome-wide association study totaling 111,326 clinically diagnosed/'proxy' AD cases and 677,663 controls. We found 75 risk loci, of which 42 were new at the time of analysis. Pathway enrichment analyses confirmed the involvement of amyloid/tau pathways and highlighted microglia implication. Gene prioritization in the new loci identified 31 genes that were suggestive of new genetically associated processes, including the tumor necrosis factor alpha pathway through the linear ubiquitin chain assembly complex. We also built a new genetic risk score associated with the risk of future AD/dementia or progression from mild cognitive impairment to AD/dementia. The improvement in prediction led to a 1.6- to 1.9-fold increase in AD risk from the lowest to the highest decile, in addition to effects of age and the APOE ε4 allele

Genome-wide association meta-analysis of corneal curvature identifies novel loci and shared genetic influences across axial length and refractive error.

Corneal curvature, a highly heritable trait, is a key clinical endophenotype for myopia - a major cause of visual impairment and blindness in the world. Here we present a trans-ethnic meta-analysis of corneal curvature GWAS in 44,042 individuals of Caucasian and Asian with replication in 88,218 UK Biobank data. We identified 47 loci (of which 26 are novel), with population-specific signals as well as shared signals across ethnicities. Some identified variants showed precise scaling in corneal curvature and eye elongation (i.e. axial length) to maintain eyes in emmetropia (i.e. HDAC11/FBLN2 rs2630445, RBP3 rs11204213); others exhibited association with myopia with little pleiotropic effects on eye elongation. Implicated genes are involved in extracellular matrix organization, developmental process for body and eye, connective tissue cartilage and glycosylation protein activities. Our study provides insights into population-specific novel genes for corneal curvature, and their pleiotropic effect in regulating eye size or conferring susceptibility to myopia