Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder

Attention deficit hyperactivity disorder (ADHD) is a common, heritable neuropsychiatric disorder of unknown etiology. We performed a whole-genome copy number variation (CNV) study on 1,013 cases with ADHD and 4,105 healthy children of European ancestry using 550,000 SNPs. We evaluated statistically significant findings in multiple independent cohorts, with a total of 2,493 cases with ADHD and 9,222 controls of European ancestry, using matched platforms. CNVs affecting metabotropic glutamate receptor genes were enriched across all cohorts (P = 2.1 × 10(-9)). We saw GRM5 (encoding glutamate receptor, metabotropic 5) deletions in ten cases and one control (P = 1.36 × 10(-6)). We saw GRM7 deletions in six cases, and we saw GRM8 deletions in eight cases and no controls. GRM1 was duplicated in eight cases. We experimentally validated the observed variants using quantitative RT-PCR. A gene network analysis showed that genes interacting with the genes in the GRM family are enriched for CNVs in ～10% of the cases (P = 4.38 × 10(-10)) after correction for occurrence in the controls. We identified rare recurrent CNVs affecting glutamatergic neurotransmission genes that were overrepresented in multiple ADHD cohorts.     

Predicting the signs of forecast errors

The signs of forecast errors can be predicted using the difference between individuals' forecasts and the average of earlier forecasts of the same variable. It is possible to improve forecasts without worsening any. It is difficult to reconcile this result with the rational expectations hypothesis because the average of earlier forecasts is in the information set of the forecasters. Copyright © 2009 John Wiley & Sons, Ltd.     

A bibliographical study of the introduction of Lavoisier's Traité élémentaire de chimie into Great Britain and America

As the most famous woman scientist of the twentieth century, there has been no shortage of books and articles on the life and career of Marie Curie (1867–1934). Her role as a director of a laboratory-based research school in the new scientific field of radioactivity, a field which embraced both chemistry and physics, however, has never been examined. In recent years, there has been a growing interest in the question of research schools, and Morrell, Ravetz, Geison, and Klosterman, amongst others, have written on this subject. Using, in part, the methodology of Morrell, this paper investigates the role of Marie Curie as a school director in the Paris Faculty in the years 1907–14, examining the work and characteristics of her school and assessing her effectiveness as a director.     

Default Priors for Neural Network Classification

Feedforward neural networks are a popular tool for classification, offering a method for fully flexible modeling. This paper looks at the underlying probability model, so as to understand statistically what is going on in order to facilitate an intelligent choice of prior for a fully Bayesian analysis. The parameters turn out to be difficult or impossible to interpret, and yet a coherent prior requires a quantification of this inherent uncertainty. Several approaches are discussed, including flat priors, Jeffreys priors and reference priors.     

Human gamma-chain genes are rearranged in leukaemic T cells and map to the short arm of chromosome 7

Three gene families that rearrange during the somatic development of T cells have been identified in the murine genome. Two of these gene families (alpha and beta) encode subunits of the antigen-specific T-cell receptor and are also present in the human genome. The third gene family, designated here as the gamma-chain gene family, is rearranged in murine cytolytic T cells but not in most helper T cells. Here we present evidence that the human genome also contains gamma-chain genes that undergo somatic rearrangement in leukaemia-derived T cells. Murine gamma-chain genes appear to be encoded in gene segments that are analogous to the immunoglobulin gene variable, constant and joining segments. There are two closely related constant-region gene segments in the human genome. One of the constant-region genes is deleted in all three T-cell leukaemias that we have studied. The two constant-region gamma-chain genes reside on the short arm of chromosome 7 (7p15); this region is involved in chromosomal rearrangements identified in T cells from individuals with the immunodeficiency syndrome ataxia telangiectasia and observed only rarely in routine cytogenetic analyses of normal individuals. This region is also a secondary site of beta-chain gene hybridization.     

土壤质量及其评价指标

在提出土壤质量概念的共性中，重要的是土壤在现今和将来均能有效地挥功能，在这种能力的基础上，认为土壤质量评价指标不要简化，要多层次，应满足5个标准，并对现有的物理，化学，生物评价指标的实用性有其优缺点进行了分析。参24。     

Applications of a generalized data-management language in medicine: Some recent experience at Stanford university

Zusammenfassung Um den Zugang zum Computer auch für den Nichtfachmann möglichst einfach und effektiv zu gestalten, müssen neue Programmiertechniken entwickelt werden. Ein Teil dieser Neuentwicklungen beschäftigt sich mit dem Aufbau und dem Gebrauch von Computer-Dateien. Zu diesem Zwecke wurde DIRAC an der Stanford-University entwickelt und getestet. Diese Sprache ist die erste einer ganzen Familie von Prototypen, welche eingesetzt werden, um die organisatorischen Probleme der Speicherung und Wiederauffindung wissenschaftlicher Information zu lösen. Die Sprache ist so konstruiert, dass die Benützer via einen Fernschreiber, der weit von der Computer-Zentrale entfernt aufgestellt sein kann, mit Hilfe einfacher Schlüsselwörter ihren Zwecken angepasste Kartotheken aufbauen können («create»), die einmal gespeicherte Information ergänzen, zerstören oder modifizieren können («up date»), die Kartothek nach fast beliebigen Kriterien abfragen und gesuchte Informationen heraussortieren können («query») sowie den Inhalt der ganzen Kartothek herausdrucken und einfach statistisch bearbeiten lassen können («status»). Ein kurzer Überblick über den Sprachaufbau von DIRAC und Beispiele für den Gebrauch von DIRAC durch verschiedene medizinische Abteilungen der Stanford-University sind beschrieben.     

The signature of hot hydrogen in the atmosphere of the extrasolar planet HD 209458b

About ten per cent of the known extrasolar planets are gas giants that orbit very close to their parent stars. The atmospheres of these 'hot Jupiters' are heated by the immense stellar irradiation. In the case of the planet HD 209458b, this energy deposition results in a hydrodynamic state in the upper atmosphere, allowing for sizeable expansion and escape of neutral hydrogen gas. HD 209458b was the first extrasolar planet discovered that transits in front of its parent star. The size of the planet can be measured using the total optical obscuration of the stellar disk during an observed transit, and the structure and composition of the planetary atmosphere can be studied using additional planetary absorption signatures in the stellar spectrum. Here we report the detection of absorption by hot hydrogen in the atmosphere of HD 209458b. Previously, the lower atmosphere and the full extended upper atmosphere of HD 209458b have been observed, whereas here we probe a layer where the escaping gas forms in the upper atmosphere of HD 209458b.