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Transmission disequilibrium of polymorphic variants in the tryptophan hydroxylase-2 gene in children and adolescents with obsessive–compulsive disorder.
- Published in:
- International Journal of Neuropsychopharmacology, 2006, v. 9, n. 4, p. 437, doi. 10.1017/S1461145705005997
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- Publication type:
- Article
Brain-derived neurotrophic factor V66M polymorphism in childhood-onset obsessivecompulsive disorder.
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- International Journal of Neuropsychopharmacology, 2005, v. 8, n. 1, p. 133, doi. 10.1017/s146114570400495x
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- Publication type:
- Article
Evidence for correlations between BMI-associated SNPs and circRNAs.
- Published in:
- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-16495-7
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- Publication type:
- Article
Subjective reward processing and catechol-Omethyltransferase Val158Met polymorphism as potential research domain criteria in addiction: A pilot study.
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- Frontiers in Psychiatry, 2022, v. 13, p. 1, doi. 10.3389/fpsyt.2022.992657
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- Publication type:
- Article
Expression of CXCR4 on CD4C<sup>+</sup> T cells predicts body composition parameters in female adolescents with anorexia nervosa.
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- Frontiers in Psychiatry, 2022, v. 13, p. 1, doi. 10.3389/fpsyt.2022.960905
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- Publication type:
- Article
Suggestive Evidence for Causal Effect of Leptin Levels on Risk for Anorexia Nervosa: Results of a Mendelian Randomization Study.
- Published in:
- Frontiers in Genetics, 2021, v. 12, p. 1, doi. 10.3389/fgene.2021.733606
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- Article
Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies.
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- 2021
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- Publication type:
- journal article
Short-term metreleptin treatment of patients with anorexia nervosa: rapid on-set of beneficial cognitive, emotional, and behavioral effects.
- Published in:
- Translational Psychiatry, 2020, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41398-020-00977-1
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- Publication type:
- Article
Evaluation of Metabolic Profiles of Patients with Anorexia Nervosa at Inpatient Admission, Short- and Long-Term Weight Regain—Descriptive and Pattern Analysis.
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- Metabolites (2218-1989), 2021, v. 11, n. 1, p. 7, doi. 10.3390/metabo11010007
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- Publication type:
- Article
Size Matters: The CAG Repeat Length of the Androgen Receptor Gene, Testosterone, and Male Adolescent Depression Severity.
- Published in:
- Frontiers in Psychiatry, 2021, v. 12, p. 1, doi. 10.3389/fpsyt.2021.732759
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- Publication type:
- Article
The involvement of the canonical Wnt‐signaling receptor LRP5 and LRP6 gene variants with ADHD and sexual dimorphism: Association study and meta‐analysis.
- Published in:
- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2019, v. 180, n. 6, p. 365, doi. 10.1002/ajmg.b.32695
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- Publication type:
- Article
Cover Image, Volume 171B, Number 6, September 2016.
- Published in:
- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 6, p. i, doi. 10.1002/ajmg.b.32490
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- Publication type:
- Article
Pathway analysis in attention deficit hyperactivity disorder: An ensemble approach.
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 6, p. 815, doi. 10.1002/ajmg.b.32446
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- Publication type:
- Article
Genetic variation at the CELF1 (CUGBP, elav-like family member 1 gene) locus is genome-wide associated with Alzheimer's disease and obesity.
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2014, v. 165B, n. 4, p. 283, doi. 10.1002/ajmg.b.32234
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- Publication type:
- Article
Refining the impact of TCF7L2 gene variants on type 2 diabetes and adaptive evolution.
- Published in:
- Nature Genetics, 2007, v. 39, n. 2, p. 218, doi. 10.1038/ng1960
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- Publication type:
- Article
Genetic Association and Gene Expression Analysis Identify FGFR1 as a New Susceptibility Gene for Human Obesity.
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- Journal of Clinical Endocrinology & Metabolism, 2011, v. 96, n. 6, p. E962, doi. 10.1210/jc.2010-2639
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- Publication type:
- Article
Association of common variants identified by recent genome-wide association studies with obesity in Chinese children: a case-control study.
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- BMC Medical Genetics, 2016, v. 17, p. 1, doi. 10.1186/s12881-016-0268-4
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- Publication type:
- Article
Estimated prevalence of potentially damaging variants in the leptin gene.
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- Molecular & Cellular Pediatrics, 2017, v. 4, n. 1, p. 1, doi. 10.1186/s40348-017-0074-x
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- Publication type:
- Article
Food Addiction in Gambling Disorder: Frequency and Clinical Outcomes.
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- Frontiers in Psychology, 2017, v. 8, p. 1, doi. 10.3389/fpsyg.2017.00473
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- Publication type:
- Article
Rapid amelioration of anorexia nervosa in a male adolescent during metreleptin treatment including recovery from hypogonadotropic hypogonadism.
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- European Child & Adolescent Psychiatry, 2022, v. 31, n. 10, p. 1573, doi. 10.1007/s00787-021-01778-7
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- Publication type:
- Article
Eating disorders: the current status of molecular genetic research.
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- European Child & Adolescent Psychiatry, 2010, v. 19, n. 3, p. 211, doi. 10.1007/s00787-009-0085-9
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- Publication type:
- Article
Child and adolescent psychiatric genetics.
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- European Child & Adolescent Psychiatry, 2010, v. 19, n. 3, p. 259, doi. 10.1007/s00787-010-0091-y
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- Publication type:
- Article
From monogenic to polygenic obesity: recent advances.
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- European Child & Adolescent Psychiatry, 2010, v. 19, n. 3, p. 297, doi. 10.1007/s00787-010-0096-6
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- Publication type:
- Article
No Effect of Thyroid Dysfunction and Autoimmunity on Health-Related Quality of Life and Mental Health in Children and Adolescents: Results From a Nationwide Cross-Sectional Study.
- Published in:
- Frontiers in Endocrinology, 2020, v. 11, p. N.PAG, doi. 10.3389/fendo.2020.00454
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- Publication type:
- Article
The Effect of SH2B1 Variants on Expression of Leptin- and Insulin-Induced Pathways in Murine Hypothalamus.
- Published in:
- Obesity Facts: The European Journal of Obesity, 2018, v. 11, n. 2, p. 93, doi. 10.1159/000486962
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- Publication type:
- Article
Successful Treatment with Atomoxetine of an Adolescent Boy with Attention Deficit/Hyperactivity Disorder, Extreme Obesity, and Reduced Melanocortin 4 Receptor Function.
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- Obesity Facts: The European Journal of Obesity, 2013, v. 6, n. 1, p. 109, doi. 10.1159/000348792
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- Publication type:
- Article
Association of the rs10830963 Polymorphism in MTNR1B with Fasting Glucose Levels in Chinese Children and Adolescents.
- Published in:
- Obesity Facts: The European Journal of Obesity, 2011, v. 4, n. 3, p. 197, doi. 10.1159/000329306
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- Publication type:
- Article
Evaluation of the Obesity Genes FTO and MC4R and the Type 2 Diabetes Mellitus Gene TCF7L2 for Contribution to Stroke Risk: The Mannheim-Heidelberg Stroke Study.
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- Obesity Facts: The European Journal of Obesity, 2011, v. 4, n. 4, p. 290, doi. 10.1159/000330881
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- Publication type:
- Article
Common Variants Near MC4R: Exploring Gender Effects in Overweight and Obese Children and Adolescents Participating in a Lifestyle Intervention.
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- Obesity Facts: The European Journal of Obesity, 2011, v. 4, n. 1, p. 67, doi. 10.1159/000324557
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- Publication type:
- Article
Chipping Away the 'Missing Heritability': GIANT Steps Forward in the Molecular Elucidation of Obesity - but Still Lots to Go.
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- Obesity Facts: The European Journal of Obesity, 2010, v. 3, n. 5, p. 294, doi. 10.1159/000321537
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- Article
Three at One Swoop!
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- Obesity Facts: The European Journal of Obesity, 2009, v. 2, n. 1, p. 3, doi. 10.1159/000200020
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- Publication type:
- Article
Procolipase Gene: No Association with Early-Onset Obesity or Fat Intake.
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- Obesity Facts: The European Journal of Obesity, 2009, v. 2, n. 1, p. 40, doi. 10.1159/000196379
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- Publication type:
- Article
A Heterozygous Mutation in the Third Transmembrane Domain Causes a Dominant-Negative Effect on Signalling Capability of the MC4R.
- Published in:
- Obesity Facts: The European Journal of Obesity, 2008, v. 1, n. 3, p. 155, doi. 10.1159/000138251
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- Article
Polygenic Obesity in Humans.
- Published in:
- Obesity Facts: The European Journal of Obesity, 2008, v. 1, n. 1, p. 35, doi. 10.1159/000113935
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- Publication type:
- Article
Fine Mapping of a GWAS-Derived Obesity Candidate Region on Chromosome 16p11.2.
- Published in:
- PLoS ONE, 2015, v. 10, n. 5, p. 1, doi. 10.1371/journal.pone.0125660
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- Publication type:
- Article
Indications for Potential Parent-of-Origin Effects within the FTO Gene.
- Published in:
- PLoS ONE, 2015, v. 10, n. 3, p. 1, doi. 10.1371/journal.pone.0119206
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- Publication type:
- Article
Catechol-O-Methyltransferase Val158Met Polymorphism Is Associated with Somatosensory Amplification and Nocebo Responses.
- Published in:
- PLoS ONE, 2014, v. 9, n. 9, p. 1, doi. 10.1371/journal.pone.0107665
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- Publication type:
- Article
A Novel SP1/SP3 Dependent Intronic Enhancer Governing Transcription of the UCP3 Gene in Brown Adipocytes.
- Published in:
- PLoS ONE, 2013, v. 8, n. 12, p. 1, doi. 10.1371/journal.pone.0083426
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- Publication type:
- Article
Gene Set of Nuclear-Encoded Mitochondrial Regulators Is Enriched for Common Inherited Variation in Obesity.
- Published in:
- PLoS ONE, 2013, v. 8, n. 2, p. 1, doi. 10.1371/journal.pone.0055884
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- Publication type:
- Article
DCLK1 Variants Are Associated across Schizophrenia and Attention Deficit/Hyperactivity Disorder.
- Published in:
- PLoS ONE, 2012, v. 7, n. 4, p. 1, doi. 10.1371/journal.pone.0035424
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- Publication type:
- Article
Investigation of a Genome Wide Association Signal for Obesity: Synthetic Association and Haplotype Analyses at the Melanocortin 4 Receptor Gene Locus.
- Published in:
- PLoS ONE, 2010, v. 5, n. 11, p. 1, doi. 10.1371/journal.pone.0013967
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- Publication type:
- Article
Lifelong Reduction of LDL-Cholesterol Related to a Common Variant in the LDL-Receptor Gene Decreases the Risk of Coronary Artery Disease--A Mendelian Randomisation Study.
- Published in:
- PLoS ONE, 2008, v. 3, n. 8, p. 1, doi. 10.1371/journal.pone.0002986
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- Publication type:
- Article
Molecular Genetic Aspects of Weight Regulation.
- Published in:
- Deutsches Ärzteblatt International, 2013, v. 110, n. 19, p. 338, doi. 10.3238/arztebl.2013.0338
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- Publication type:
- Article
Sympathetic Function in Human Carriers of Melanocortin-4 Receptor Gene Mutations.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2010, v. 95, n. 4, p. 1998, doi. 10.1210/jc.2009-2297
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- Publication type:
- Article
Prevalence, Spectrum, and Functional Characterization of Melanocortin-4 Receptor Gene Mutations in a Representative Population-Based Sample and Obese Adults from Germany.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2006, v. 91, n. 5, p. 1761, doi. 10.1210/jc.2005-2056
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- Publication type:
- Article
The 103I Variant of the Melanocortin 4 Receptor Is Associated with Low Serum Triglyceride Levels.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2006, v. 91, n. 2, p. 535, doi. 10.1210/jc.2005-0919
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- Publication type:
- Article
Ghrelin Receptor Gene: Identification of Several Sequence Variants in Extremely Obese Children and Adolescents, Healthy Normal-Weight and Underweight Students, and Children with Short Normal Stature.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2004, v. 89, n. 1, p. 157, doi. 10.1210/jc.2003-031395
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- Publication type:
- Article
Melanocortin-4 Receptor Gene: Case-Control Study and Transmission Disequilibrium Test Confirm that Functionally Relevant Mutations Are Compatible with a Major Gene Effect for Extreme Obesity.
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- Journal of Clinical Endocrinology & Metabolism, 2003, v. 88, n. 9, p. 4258, doi. 10.1210/jc.2003-030233
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- Publication type:
- Article
Ghrelin gene: identification of missense variants and a frameshift mutation in extremely obese children and adolescents and healthy normal weight students.
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- Journal of Clinical Endocrinology & Metabolism, 2002, v. 87, n. 6, p. 2716, doi. 10.1210/jcem.87.6.8672
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- Publication type:
- Article
Ghrelin Receptor Gene: Identification of Several Sequence Variants in Extremely Obese Children and Adolescents, Healthy Normal-Weight and Underweight Students, and Children with Short Normal Stature.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 1996, v. 81, n. 1, p. 157, doi. 10.1210/jc.2003-031395
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- Publication type:
- Article