Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Carina Quast"'
Autor:
Carina Quast, Serena Cuboni, Daniel Bader, André Altmann, Peter Weber, Janine Arloth, Simone Röh, Tanja Brückl, Marcus Ising, Anna Kopczak, Angelika Erhardt, Felix Hausch, Susanne Lucae, Elisabeth B Binder
Publikováno v:
PLoS ONE, Vol 8, Iss 7, p e68645 (2013)
SLC6A15 is a neuron-specific neutral amino acid transporter that belongs to the solute carrier 6 gene family. This gene family is responsible for presynaptic re-uptake of the majority of neurotransmitters. Convergent data from human studies, animal m
Externí odkaz:
https://doaj.org/article/f8ebdc48182f4e458543972384420fb7
Autor:
Sarah Kittel-Schneider, Lena Grünewald, Heike Weber, Elisabeth B. Binder, Carina Quast, Simone Röh, Andreas Reif, Klaus-Peter Lesch, Marcel Romanos, C. Schartner, Julia Geissler, E.T. Landaas
Publikováno v:
ResearcherID
The DIRAS2 gene is coding for a small Ras GTPase with so far unknown function. In a previous study, we described the association of DIRAS2 rs1412005, as well as a haplotype containing this polymorphism and located in the promoter region of this gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::197b27db6cbc696c61733a2dea41e973
https://doi.org/10.1038/npp.2016.113
https://doi.org/10.1038/npp.2016.113
Autor:
Marianne B. Müller, Felix Hausch, Elisabeth B. Binder, Florian Holsboer, Rainer Landgraf, Julia Brenndörfer, L. Czibere, Peter Weber, Mathias V. Schmidt, Carina Quast, Christiana Labermaier, Andre Altmann, Jakob Hartmann, Sebastian H. Scharf, Christian Devigny, Janine Arloth, Manfred Uhr, Klaus V. Wagner, Christine Kohl, Regina Widner-Andrä, Kenneth A. Jones
Publikováno v:
Endocrinology. 155:2500-2510
Chronic stress is a risk factor for psychiatric disorders but does not necessarily lead to uniform long-term effects on mental health, suggesting modulating factors such as genetic predispositions. Here we address the question whether natural genetic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a35283946006c87df906179d25e6496d
https://doi.org/10.1210/en.2013-1986
https://doi.org/10.1210/en.2013-1986
Autor:
Sven Cichon, Tanja Brückl, Alexander L. Gerlach, Heike Weber, Hans-Ulrich Wittchen, Alfons Hamm, Angelika Erhardt, Andreas Reif, Paul Pauli, Georg W. Alpers, Elisabeth B. Binder, Manuel Mattheisen, Hildegard Pfister, Tilo Kircher, Volker Arolt, Lydia Fehm, Andreas Ströhle, Carina Quast, Jürgen Deckert, Katharina Domschke, Thomas Lang, Rainer Rupprecht
Publikováno v:
Depression and Anxiety. 31:843-850
Background: Neurosteroids are synthesized both in brain and peripheral steroidogenic tissue from cholesterol or steroidal precursors. Neurosteroids have been shown to be implicated in neural proliferation, differentiation, and activity. Preclinical a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0b2f76d9cda489e394cdc010b04b91d5
https://doi.org/10.1002/da.22229
https://doi.org/10.1002/da.22229
Autor:
Peter Weber, Hildegard Pfister, Bertram Müller-Myhsok, Carina Quast, Angelika Erhardt, Angela Heck, Daniel M. Bader, Andre Altmann, Elisabeth B. Binder, Janine Arloth
Publikováno v:
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. :896-907
Genome-wide association studies have identified common variants associated with common diseases. Most variants, however, explain only a small proportion of the estimated heritability, suggesting that rare variants might contribute to a larger extent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::322dbe1755f6a2a5d0c677c78b97ff64
https://doi.org/10.1002/ajmg.b.32096
https://doi.org/10.1002/ajmg.b.32096
Autor:
Peter Weber, Elisabeth B. Binder, Carina Quast, Monika Rex-Haffner, Bertram Müller-Myhsok, Andre Altmann
Publikováno v:
Bioinformatics
Motivation: High-throughput-sequencing (HTS) technologies are the method of choice for screening the human genome for rare sequence variants causing susceptibility to complex diseases. Unfortunately, preparation of samples for a large number of indiv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f2da11bb913c215887b082854bc761c6
http://europepmc.org/articles/PMC3117388
http://europepmc.org/articles/PMC3117388
Autor:
Carina Quast
Publikováno v:
PPH. 22:229-229
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8d7813133b47afa88b8edf72051d0bf2
https://doi.org/10.1055/s-0042-107403
https://doi.org/10.1055/s-0042-107403
Detecting Rare Variants for Psychiatric Disorders Using Next Generation Sequencing: A Methods Primer
Publikováno v:
Current Psychiatry Reports. 15
Recent advances in massively parallel sequencing (MPS) have had an extensive impact on research in medical genomics. In particular, the analysis of rare variants using MPS promises to lead to a better understanding of complex disorders. Nevertheless,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b7632c42ef8e0357096a573b26d0685
https://doi.org/10.1007/s11920-012-0333-4
https://doi.org/10.1007/s11920-012-0333-4
Autor:
Pascal Burger, Franziska Voigt, Carina Quast, Divya Mehta, Anna Seifert, Arif B. Ekici, Matthias W. Beckmann, Peter A. Fasching, Elisabeth B. Binder, Tamme W. Goecke, Florian Faschingbauer, Johannes Kornhuber
Publikováno v:
Journal of affective disorders. 136(3)
Background: Maternal depression during the peripartum period has an incidence of about 13%. Individuals with specific genetic predispositions are more vulnerable to stressful life events suggesting that exploration of gene-environmental pathways migh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::37a915d314eb57431becd090e8cb3823
https://pubmed.ncbi.nlm.nih.gov/22209125
https://pubmed.ncbi.nlm.nih.gov/22209125
Autor:
Bertram Müller-Myhsok, Peter Weber, Angelika Erhardt, Elisabeth B. Binder, Monika Rex-Haffner, Carina Quast, Andre Altmann
Publikováno v:
European Neuropsychopharmacology. 21:S6-S7
The aetiology of anxiety disorders is known to be influenced by genetic factors. Genome-wide association studies revealed common intronic SNPs within the 831942 bp long transmembrane protein 132D gene (TMEM132D) located on chromosome 12 to be associa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::df34fa6a2620644bec7c7b16010d857b
https://doi.org/10.1016/s0924-977x(11)70007-4
https://doi.org/10.1016/s0924-977x(11)70007-4