Elisabeth B. Binder

ORCID: 0000-0001-7088-6618
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About
Contact & Profiles
Research Areas
  • Stress Responses and Cortisol
  • Birth, Development, and Health
  • Epigenetics and DNA Methylation
  • Tryptophan and brain disorders
  • Genetic Associations and Epidemiology
  • Hormonal Regulation and Hypertension
  • Child and Adolescent Psychosocial and Emotional Development
  • Neuroendocrine regulation and behavior
  • Mental Health Research Topics
  • Neonatal Respiratory Health Research
  • Genetics and Neurodevelopmental Disorders
  • Maternal Mental Health During Pregnancy and Postpartum
  • Bipolar Disorder and Treatment
  • Treatment of Major Depression
  • Functional Brain Connectivity Studies
  • Cognitive Abilities and Testing
  • Childhood Cancer Survivors' Quality of Life
  • Adolescent and Pediatric Healthcare
  • Child Abuse and Trauma
  • Pregnancy and preeclampsia studies
  • Early Childhood Education and Development
  • Health, Environment, Cognitive Aging
  • Resilience and Mental Health
  • Identity, Memory, and Therapy
  • Receptor Mechanisms and Signaling

Max Planck Institute of Psychiatry
2016-2025

Emory University
2016-2025

VA Connecticut Healthcare System
2017-2024

Yale University
2017-2024

Universität Innsbruck
2015-2024

California Department of Education
2023-2024

Technical University of Munich
2021-2024

Innsbruck Medical University
2009-2024

LMU Klinikum
2024

Ludwig-Maximilians-Universität München
2009-2024

<h3>Context</h3>In addition to trauma exposure, other factors contribute risk for development of posttraumatic stress disorder (PTSD) in adulthood. Both genetic and environmental are contributory, with child abuse providing significant liability.<h3>Objective</h3>To increase understanding as well their interaction the PTSD by gene × environment interactions abuse, level non–child polymorphisms at stress-related FKBP5.<h3>Design, Setting, Participants</h3>A cross-sectional study examining...

10.1001/jama.299.11.1291 article EN JAMA 2008-03-18
Colm Ó'Dúshláine Lizzy Rossin Susan J. Lee Laramie E. Duncan Neelroop Parikshak and 95 more Stephen Newhouse Stephan Ripke Benjamin M. Neale Shaun Purcell Daniëlle Posthuma John I. Nürnberger Sang Lee Stephen V. Faraone Roy H. Perlis Bryan Mowry Anita Thapar Michael E. Goddard John S. Witte Devin Absher Ingrid Agartz Huda Akil Farooq Amin Ole A. Andreassen Adebayo Anjorin Richard Anney Verneri Anttila Dan E. Arking Philip Asherson Maria H. Azevedo Lena Backlund Judith A. Badner Anthony Bailey Tobias Banaschewski Jack D. Barchas Michael R. Barnes Thomas B. Barrett Nicholas Bass Agatino Battaglia Michael Bauer Mónica Bayés Frank Bellivier Sarah E. Bergen Wade H. Berrettini Catalina Betancur Thomas Bettecken Joseph Biederman Elisabeth B. Binder Donald W. Black Douglas H. R. Blackwood Cinnamon S. Bloss Michael Boehnke Dorret I. Boomsma René Breuer Richard Bruggeman Paul Cormican Nancy G. Buccola Jan K. Buitelaar William E. Bunney Joseph D. Buxbaum William Byerley Enda M. Byrne Sian Caesar Wiepke Cahn Rita M. Cantor Miguel Casas Aravinda Chakravarti Kimberly Chambert Khalid Choudhury Sven Cichon Manuel Mattheisen C. Robert Cloninger David Collier Edwin H. Cook Hilary Coon Bru Cormand Aiden Corvin William Coryell David W. Craig Ian W. Craig Jennifer Crosbie Michael L. Cuccaro David Curtis Darina Czamara Susmita Datta Géraldine Dawson Richard Day Eco J. C. de Geus Franziska Degenhardt Srdjan Djurovic Gary Donohoe Alysa E. Doyle Jubao Duan Frank Dudbridge Eftichia Duketis Richard P. Ebstein Howard J. Edenberg Josephine Elia Sean Ennis Bruno Étain Ayman Fanous

10.1038/nn.3922 article EN Nature Neuroscience 2015-01-19
Jason L. Stein Sarah E. Medland Alejandro Arias Väsquez Derrek P. Hibar Rudy E Senstad and 95 more Anderson M. Winkler Roberto Toro Katja Appel Richard Barteček Ørjan Bergmann Manon Bernard Andrew Brown Dara M. Cannon M. Mallar Chakravarty Andrea Christoforou Martin Domín O. Grimm Marisa O. Hollinshead Avram J. Holmes Georg Homuth Jouke‐Jan Hottenga Camilla Langan Lorna M. Lopez Narelle K. Hansell Kristy Hwang Sungeun Kim Gonzalo Laje Phil H. Lee Xinmin Liu Eva Loth Anbarasu Lourdusamy Morten Mattingsdal Sebastian Mohnke Susana Muñoz Maniega Kwangsik Nho Allison C. Nugent Carol O’Brien Martina Papmeyer Benno Pütz Adaikalavan Ramasamy Jerod M. Rasmussen Mark Rijpkema Shannon L. Risacher J. Cooper Roddey Emma J. Rose Mina Ryten Li Shen Emma Sprooten Eric Strengman Alexander Teumer Daniah Trabzuni Jessica A. Turner Kristel van Eijk Theo G.M. van Erp Marie‐José van Tol Katharina Wittfeld Christiane Wolf Saskia Woudstra André Alemán Saud Alhusaini Laura Almasy Elisabeth B. Binder David G. Brohawn Rita M. Cantor Melanie A. Carless Aiden Corvin Michael Czisch Joanne E. Curran Gail Davies Marcio Almeida Norman Delanty Chantal Depondt Ravi Duggirala Thomas D. Dyer Susanne Erk Jesen Fagerness Peter T. Fox Nelson B. Freimer Michael Gill Harald H.H. Göring Donald J. Hagler David Hoehn Herta Flor Martine Hoogman Norbert Hosten Neda Jahanshad Matthew P. Johnson Dalia Kasperavičiūtė Jack W. Kent Peter Kochunov Jack L. Lancaster Stephen M. Lawrie David C. Liewald René C.W. Mandl Mar Matarín Manuel Mattheisen Eva Meisenzahl Ingrid Melle Eric K. Moses Thomas W. Mühleisen

10.1038/ng.2250 article EN Nature Genetics 2012-04-15

<h3>Context</h3> Genetic inheritance and developmental life stress both contribute to major depressive disorder in adults. Child abuse trauma alter the endogenous response, principally corticotropin-releasing hormone its downstream effectors, suggesting that a gene × environment interaction at this locus may be important depression. <h3>Objective</h3> To examine whether effects of child on adult symptoms are moderated by genetic polymorphisms within type 1 receptor (<i>CRHR1</i>) gene....

10.1001/archgenpsychiatry.2007.26 article EN Archives of General Psychiatry 2008-02-01

Childhood maltreatment is likely to influence fundamental biological processes and engrave long-lasting epigenetic marks, leading adverse health outcomes in adulthood. We aimed elucidate the impact of different early environment on disease-related genome-wide gene expression DNA methylation peripheral blood cells patients with posttraumatic stress disorder (PTSD). Compared same trauma-exposed controls (n = 108), gene-expression profiles PTSD similar clinical symptoms matched adult trauma...

10.1073/pnas.1217750110 article EN Proceedings of the National Academy of Sciences 2013-04-29

Chronic psychological stress is associated with accelerated aging and increased risk for aging-related diseases, but the underlying molecular mechanisms are unclear. We examined effect of lifetime stressors on a DNA methylation-based age predictor, epigenetic clock. After controlling blood cell-type composition lifestyle parameters, cumulative stress, not childhood maltreatment or current alone, predicted in an urban, African American cohort (n = 392). This was primarily driven by personal...

10.1186/s13059-015-0828-5 article EN cc-by Genome biology 2015-11-27

Insulin pump therapy may improve metabolic control in young patients with type 1 diabetes, but the association short-term diabetes complications is unclear.To determine whether rates of severe hypoglycemia and diabetic ketoacidosis are lower insulin compared injection children, adolescents, adults diabetes.Population-based cohort study conducted between January 2011 December 2015 446 centers participating Diabetes Prospective Follow-up Initiative Germany, Austria, Luxembourg. Patients...

10.1001/jama.2017.13994 article EN JAMA 2017-10-10

Highlights•m6A/m mRNA methylation in the adult mouse brain is regulated by stress•m6A/m regulation region, time, and gene specific•Mettl3 Fto cKO alter m6A/m, fear memory, expression, synaptic plasticity•The m6A/m glucocorticoid response impaired major depressive disorder patientsSummaryN6-methyladenosine (m6A) N6,2′-O-dimethyladenosine (m6Am) are abundant modifications that regulate transcript processing translation. The role of both, here termed stress vivo currently unknown. Here, we...

10.1016/j.neuron.2018.07.009 article EN cc-by-nc-nd Neuron 2018-07-01

Abstract Background Gene expression profiling from peripheral blood is a valuable tool for biomarker discovery in clinical studies. Different whole RNA collection and processing methods are highly variable might confound comparisons of results across The main aim the study was to compare genome-wide gene profiles obtained two widely used commercially available systems - PAXgene™ Tempus™ tubes. Comparisons present call rates, variances, correlations influence globin reduction performed using...

10.1186/1756-0500-5-1 article EN cc-by BMC Research Notes 2012-01-04
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