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Schizophrenia Research|December 14, 2020
Psychotic experiences in seven-year-old children with familial high risk of schizophrenia or bipolar disorder in: The Danish High Risk and Resilience Study - VIA 7; A population-based cohort studyDitte Ellersgaard, Maja Gregersen, Katrine Soeborg Spang, et al.
Scientific Reports|August 1, 2018
Exploring Cuba's population structure and demographic history using genome-wide dataCesar Fortes-Lima, Jonas Bybjerg-Grauholm, Lilia Caridad Marin-Padrón, et al.
Journal of Medicinal Chemistry|October 10, 2019
Design, Synthesis, and Pharmacological Evaluation of Potent Positive Allosteric Modulators of the Glucagon-like Peptide-1 Receptor (GLP-1R)María Méndez, Hans Matter, Elisabeth Defossa, et al.
Depression and Anxiety|October 16, 2007
Sex differences in symptom patterns of recurrent major depression in siblingsValentina Moskvina, Anne Farmer, Ian Richard Jones, et al.
Psychiatric Genetics|August 24, 2013
An association study between the norepinephrine transporter gene and depressionHenriette N Buttenschøn, Iben S Jacobsen, Matias B Grynderup, et al.
The Journal of Clinical Psychiatry|July 19, 2019
Trajectories of Suicidal Ideation During 12 Weeks of Escitalopram or Nortriptyline Antidepressant Treatment Among 811 Patients With Major Depressive DisorderTrine Madsen, Henriette N Buttenschøn, Rudolf Uher, et al.
BMC Psychiatry|December 14, 2004
The Depression Network (DeNT) Study: methodology and sociodemographic characteristics of the first 470 affected sibling pairs from a large multi-site linkage genetic studyAnne Farmer, Gerome Breen, Shyama Brewster, et al.
Translational Psychiatry|October 29, 2014
Investigation of blood mRNA biomarkers for suicidality in an independent sampleN Mullins, K Hodgson, K E Tansey, et al.
Frontiers in Microbiology|June 12, 2018
Microscale Biosignatures and Abiotic Mineral Authigenesis in Little Hot Creek, CaliforniaEmily A Kraus, Scott R Beeler, R Agustin Mors, et al.
European Journal of Human Genetics : EJHG|August 4, 2011
A genome-wide study of panic disorder suggests the amiloride-sensitive cation channel 1 as a candidate geneNoomi Gregersen, Hans A Dahl, Henriette N Buttenschøn, et al.
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