نتایج جستجو برای: endophenotypes

تعداد نتایج: 1086  

2017
Molly Losh Gary E Martin Michelle Lee Jessica Klusek John Sideris Sheila Barron Thomas Wassink

Genetic liability to autism spectrum disorder (ASD) can be expressed in unaffected relatives through subclinical, genetically meaningful traits, or endophenotypes. This study aimed to identify developmental endophenotypes in parents of individuals with ASD by examining parents' childhood academic development over the school-age period. A cohort of 139 parents of individuals with ASD were studie...

Journal: :Annals of General Psychiatry 2008

Journal: :Alzheimer's & Dementia 2016
Eva Louwersheimer Steffen Wolfsgruber Ana Espinosa André Lacour Stefanie Heilmann-Heimbach Montserrat Alegret Isabel Hernández Maitée Rosende-Roca Lluís Tárraga Mercè Boada Johannes Kornhuber Oliver Peters Lutz Frölich Michael Hüll Eckart Rüther Jens Wiltfang Martin Scherer Steffi Riedel-Heller Frank Jessen Markus M. Nöthen Wolfgang Maier Ted Koene Philip Scheltens Henne Holstege Michael Wagner Agustín Ruiz Wiesje M. van der Flier Tim Becker Alfredo Ramirez

INTRODUCTION We evaluated the effect of Alzheimer's disease (AD) susceptibility loci on endophenotypes closely related with AD pathology in patients with mild cognitive impairment (MCI). METHODS We selected 1730 MCI patients from four independent data sets. Weighted polygenic risk scores (PGS) were constructed of 18 non-apolipoprotein E (APOE) AD risk variants. In addition, we determined APOE...

Journal: :Psychophysiology 2014
Scott I Vrieze Stephen M Malone Uma Vaidyanathan Alan Kwong Hyun Min Kang Xiaowei Zhan Matthew Flickinger Daniel Irons Goo Jun Adam E Locke Giorgio Pistis Eleonora Porcu Shawn Levy Richard M Myers William Oetting Matt McGue Goncalo Abecasis William G Iacono

Whole genome sequencing was completed on 1,325 individuals from 602 families, identifying 27 million autosomal variants. Genetic association tests were conducted for those individuals who had been assessed for one or more of 17 endophenotypes (N range = 802-1,185). No significant associations were found. These 27 million variants were then imputed into the full sample of individuals with psycho...

Journal: :Biological psychiatry 2009
J John Mann Victoria A Arango Shelli Avenevoli David A Brent Frances A Champagne Paula Clayton Dianne Currier Donald M Dougherty Fatemah Haghighi Susan E Hodge Joel Kleinman Thomas Lehner Francis McMahon Eve K Mościcki Maria A Oquendo Ganshayam N Pandey Jane Pearson Barbara Stanley Joseph Terwilliger Amy Wenzel

Twin, adoption, and family studies have established the heritability of suicide attempts and suicide. Identifying specific suicide diathesis-related genes has proven more difficult. As with psychiatric disorders in general, methodological difficulties include complexity of the phenotype for suicidal behavior and distinguishing suicide diathesis-related genes from genes associated with mood diso...

Journal: :Canadian journal of psychiatry. Revue canadienne de psychiatrie 2007
Janet L Treasure

Treatment for anorexia nervosa has changed little from that described by Gull over a century ago. To focus merely on symptomatic relief from "not eating," as occurs with some forms of hospital care, is primitive. The evidence base to guide treatment is thin. Nevertheless, there is hope that better understanding of the causes and maintaining factors may translate into more sophisticated treatmen...

Journal: :Psychophysiology 2014
William G Iacono Uma Vaidyanathan Scott I Vrieze Stephen M Malone

We review and summarize seven molecular genetic studies of 17 psychophysiological endophenotypes that comprise this special issue of Psychophysiology, address criticisms raised in accompanying Perspective and Commentary pieces, and offer suggestions for future research. Endophenotypes are polygenic, and possibly influenced by rare genetic variants. Because they are not simpler genetically than ...

Journal: :Annual review of clinical psychology 2013
Gregory A Miller Brigitte Rockstroh

Endophenotypes for psychopathology have been conceived as latent, unobserved, but measureable manifestations of phenomena that causally connect genetic liability to clinical disorder. Several decades of research have led to refinement of the construct and identification of some candidate endophenotypes, but rather limited progress on finding the genes involved or the mechanisms by which endophe...

Journal: :Biological psychiatry 2012
David C Glahn Joanne E Curran Anderson M Winkler Melanie A Carless Jack W Kent Jac C Charlesworth Matthew P Johnson Harald H H Göring Shelley A Cole Thomas D Dyer Eric K Moses Rene L Olvera Peter Kochunov Ravi Duggirala Peter T Fox Laura Almasy John Blangero

BACKGROUND Despite overwhelming evidence that major depression is highly heritable, recent studies have localized only a single depression-related locus reaching genome-wide significance and have yet to identify a causal gene. Focusing on family-based studies of quantitative intermediate phenotypes or endophenotypes, in tandem with studies of unrelated individuals using categorical diagnoses, s...

2015
Juliana de Lima Muller Kamilla Irigaray Torquato Gisele Gus Manfro Clarissa Marceli Trentini

Evidence in the literature indicates that neurocognitive impairments may represent endophenotypes in psychiatric disorders. Objective This study aimed to conduct a systematic review on executive functions as a potential neurocognitive endophenotype in anxiety disorder diagnosis according to the DSM-IV and DSM-5 classifications. Methods A literature search of the LILACS, Cochrane Library, In...

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