Search Results - "Burmeister, Margit"

β‐Arrestin 2 (ARRB2) Polymorphism is Associated With Adverse Consequences of Chronic Heroin Use.

Authors: Karavidha, Klevis K. Burmeister, Margit Greenwald, Mark K.

Source: American Journal on Addictions. Jul2021, Vol. 30 Issue 4, p351-357.

Genetic interactions with stressful environments in depression and addiction.

Authors: Burmeister, Margit Sen, Srijan

Source: BJPsych Advances. May2021, Vol. 27 Issue 3, p153-157. 5p.

Functional mu opioid receptor polymorphism ( OPRM1 A¹¹⁸G) associated with heroin use outcomes in Caucasian males: A pilot study.

Authors: Woodcock, Eric A. Lundahl, Leslie H. Burmeister, Margit et al.

Source: American Journal on Addictions. Jun2015, Vol. 24 Issue 4, p329-335.

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Heroin delay discounting and impulsivity: Modulation by DRD1 genetic variation.

Authors: Moses, Tabitha E.H. Burmeister, Margit Greenwald, Mark K.

Source: Addiction Biology. May2020, Vol. 25 Issue 3, p1-8. 8p.

Why Public Scholarship Needs Research on Religion for Religious Leaders: H. Paul Douglass Lecture, Religious Research Association.

Authors: Ecklund, Elaine Howard¹ (AUTHOR) ehe@rice.edu

Source: Review of Religious Research. Jun2025, Vol. 67 Issue 2, p163-174. 12p.

Prevalence and risk factors for depression among training physicians in China and the United States.

Authors: Chen, Lihong Zhao, Zhuo Wang, Zhen et al.

Source: Scientific Reports. 5/17/2022, Vol. 12 Issue 1, p1-7. 7p.

Functional Study of TMEM163 Gene Variants Associated with Hypomyelination Leukodystrophy.

Authors: Yan, Huifang Yang, Shuyan Hou, Yiming et al.

Source: Cells (2073-4409). Apr2022, Vol. 11 Issue 8, p1285. 17p.

recurrent mutation in RNF220 also causes hypomyelination in China and is a CpG hot spot.

Authors: Yan, Huifang Kubisiak, Thomas Gao, Kai et al.

Source: Brain: A Journal of Neurology; Dec2022, Vol. 145 Issue 12, pe122-e124, 3p

Exome-wide association study of treatment-resistant depression suggests novel treatment targets.

Authors: Shah, Shrey B. Peddada, Teja N. Song, Christopher et al.

Source: Scientific Reports. 8/1/2023, Vol. 13 Issue 1, p1-9. 9p.

Pathways to Youth Behavior: The Role of Genetic, Neural, and Behavioral Markers.

Authors: Trucco, Elisa M. Cope, Lora M. Burmeister, Margit et al.

Source: Journal of Research on Adolescence (Wiley-Blackwell). Mar2018, Vol. 28 Issue 1, p26-39. 14p.

Subjects: Youths' attitudes, Adolescent psychology, Psychological resilience, Cerebellum, Aggression (Psychology) in adolescence

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Rule breaking mediates the developmental association between GABRA2 and adolescent substance abuse.

Authors: Trucco, Elisa M. Villafuerte, Sandra Heitzeg, Mary M. et al.

Source: Journal of Child Psychology & Psychiatry. Dec2014, Vol. 55 Issue 12, p1372-1379. 8p. 3 Diagrams, 2 Charts.

Subjects: Alleles, Cell receptors, Chi-squared test, Confidence intervals, Statistical correlation, Genetic polymorphisms, Longitudinal method, Questionnaires, Research evaluation, Research funding, Risk-taking behavior, Scale analysis (Psychology), Self-evaluation, Substance abuse, Data analysis software, Genotypes, Symptoms

Diaphanous homolog 3 (Diap3) Overexpression Causes Progressive Hearing Loss and Inner Hair Cell Defects in a Transgenic Mouse Model of Human Deafness.

Authors: Schoen, Cynthia J. Burmeister, Margit Lesperance, Marci M.

Source: PLoS ONE. Feb2013, Vol. 8 Issue 2, p1-11. 11p.

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New insights into the genetics of addiction.

Authors: Li, Ming D. Burmeister, Margit

Source: Nature Reviews Genetics. Apr2009, Vol. 10 Issue 4, p225-231. 7p. 3 Charts, 1 Graph.

Psychiatric genetics: progress amid controversy.

Authors: Burmeister, Margit McInnis, Melvin G. Zöllner, Sebastian

Source: Nature Reviews Genetics. Jul2008, Vol. 9 Issue 7, p527-540. 14p. 1 Diagram, 7 Charts.

Referees for Volume 4.

Authors: Crusio, Wim E.

Source: Genes, Brain & Behavior. Feb2006, Vol. 5 Issue 1, p112-112. 1p.

Deletion of Chromosome 2 q37 and Autism: A Distinct Subtype?

Authors: Ghaziuddin, Mohammad Burmeister, Margit

Source: Journal of Autism & Developmental Disorders. Jun1999, Vol. 29 Issue 3, p259-263. 5p.

Subjects: Autism, Chromosome abnormalities

Family-based association analysis to finemap bipolar linkage peak on chromosome 8q24 using 2,500 genotyped SNPs and 15,000 imputed SNPs.

Authors: Zhang, Peng Xiang, Nan Chen, Yi et al.

Source: Bipolar Disorders. Dec2010, Vol. 12 Issue 8, p786-792. 7p. 1 Chart, 2 Graphs.