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A beginners guide to SNP calling from high-throughput DNA-sequencing data.
- Published in:
- Human Genetics, 2012, v. 131, n. 10, p. 1541, doi. 10.1007/s00439-012-1213-z
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- Publication type:
- Article
Ian N.M. Day (ed) Molecular genetic epidemiology: a laboratory perspective: Springer, Berlin Heidelberg New York, 2002.
- Published in:
- 2003
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- Publication type:
- Book Review
Genetic markers for PTSD risk and resilience among survivors of the World Trade Center attacks.
- Published in:
- Disease Markers, 2011, v. 30, n. 2-3, p. 101
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- Publication type:
- Article
Multimodal workflows optimally predict response to repetitive transcranial magnetic stimulation in patients with schizophrenia: a multisite machine learning analysis.
- Published in:
- Translational Psychiatry, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41398-024-02903-1
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- Publication type:
- Article
HMG-CoA reductase is a potential therapeutic target for migraine: a mendelian randomization study.
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- Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-61628-9
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- Publication type:
- Article
Evaluation of the Performance of AmpliSeq and SureSelect Exome Sequencing Libraries for Ion Proton.
- Published in:
- Frontiers in Genetics, 2019, p. 1, doi. 10.3389/fgene.2019.00856
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- Publication type:
- Article
Identification of shared risk loci and pathways for bipolar disorder and schizophrenia.
- Published in:
- PLoS ONE, 2017, v. 12, n. 2, p. 1, doi. 10.1371/journal.pone.0171595
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- Publication type:
- Article
Sequence variants on chromosome 9p21.3 confer risk for atherosclerotic stroke.
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- Annals of Neurology, 2009, v. 65, n. 5, p. 531, doi. 10.1002/ana.21590
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- Publication type:
- Article
Inherited Myoclonus-dystonia syndrome: narrowing the 7q21-q31 locus in German families.
- Published in:
- 2001
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- Publication type:
- journal article
Treatment- and population-specific genetic risk factors for anti-drug antibodies against interferon-beta: a GWAS.
- Published in:
- 2020
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- Publication type:
- journal article
Mouse to human comparative genetics reveals a novel immunoglobulin E-controlling locus on Hsa8q12.
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- Immunogenetics, 2009, v. 61, n. 1, p. 15, doi. 10.1007/s00251-008-0343-x
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- Publication type:
- Article
A different view on fine-scale population structure in Western African populations.
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- Human Genetics, 2020, v. 139, n. 1, p. 45, doi. 10.1007/s00439-019-02069-7
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- Publication type:
- Article
Systematic Review of Functional MRI Applications for Psychiatric Disease Subtyping.
- Published in:
- Frontiers in Psychiatry, 2021, v. 12, p. 1, doi. 10.3389/fpsyt.2021.665536
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- Publication type:
- Article
SKP2 attenuates autophagy through Beclin1-ubiquitination and its inhibition reduces MERS-Coronavirus infection.
- Published in:
- Nature Communications, 2019, v. 10, n. 1, p. 1, doi. 10.1038/s41467-019-13659-4
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- Publication type:
- Article
Support for linkage of familial combined hyperlipidemia to chromosome 1q21–q23 in Chinese and German families.
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- Clinical Genetics, 2000, v. 57, n. 1, p. 29, doi. 10.1034/j.1399-0004.2000.570105.x
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- Publication type:
- Article
Commentary: The importance of exploring dose-dependent, subtype-specific, and age-related effects of maltreatment on the HPA axis and the mediating link to psychopathology. A response to Fisher (2017).
- Published in:
- Journal of Child Psychology, 2017, v. 58, n. 9, p. 1011, doi. 10.1111/jcpp.12770
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- Publication type:
- Article
Reduced hair cortisol after maltreatment mediates externalizing symptoms in middle childhood and adolescence.
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- Journal of Child Psychology, 2017, v. 58, n. 9, p. 998, doi. 10.1111/jcpp.12700
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- Publication type:
- Article
Burnout and secondary traumatic stress in staff working with people with intellectual disabilities: The role of adverse childhood experiences, resilience and trauma‐informed organisational climate.
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- Journal of Applied Research in Intellectual Disabilities, 2023, v. 36, n. 6, p. 1297, doi. 10.1111/jar.13148
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- Publication type:
- Article
Effect of HLA-DRB1 alleles and genetic variants on the development of neutralizing antibodies to interferon beta in the BEYOND and BENEFIT trials.
- Published in:
- Multiple Sclerosis Journal, 2019, v. 25, n. 4, p. 565, doi. 10.1177/1352458518763089
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- Publication type:
- Article
Dilution of candidates: the case of iron-related genes in restless legs syndrome.
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- European Journal of Human Genetics, 2013, v. 21, n. 4, p. 410, doi. 10.1038/ejhg.2012.193
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- Publication type:
- Article
Genome-wide linkage analysis is a powerful prenatal diagnostic tool in families with unknown genetic defects.
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- European Journal of Human Genetics, 2013, v. 21, n. 4, p. 367, doi. 10.1038/ejhg.2012.198
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- Publication type:
- Article
Imaging genetics of FOXP2 in dyslexia.
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- European Journal of Human Genetics, 2012, v. 20, n. 6, p. 714, doi. 10.1038/ejhg.2012.31
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- Publication type:
- Article
Determination of the real effect of genes identified in GWAS: the example of IL2RA in multiple sclerosis.
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- European Journal of Human Genetics, 2012, v. 20, n. 3, p. 321, doi. 10.1038/ejhg.2011.197
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- Publication type:
- Article
Imaging genetics of FOXP2 in dyslexia.
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- European Journal of Human Genetics, 2012, v. 20, n. 2, p. 224, doi. 10.1038/ejhg.2011.160
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- Publication type:
- Article
EPIBLASTER-fast exhaustive two-locus epistasis detection strategy using graphical processing units.
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- European Journal of Human Genetics, 2011, v. 19, n. 4, p. 465, doi. 10.1038/ejhg.2010.196
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- Publication type:
- Article
Talking hypotheses.
- Published in:
- 2007
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- Publication type:
- Book Review
PARK11 is not linked with Parkinson's disease in European families.
- Published in:
- European Journal of Human Genetics, 2005, v. 13, n. 2, p. 193, doi. 10.1038/sj.ejhg.5201317
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- Publication type:
- Article
Refinement of the PARK3 locus on chromosome 2p13 and the analysis of 14 candidate genes.
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- European Journal of Human Genetics, 2001, v. 9, n. 9, p. 659, doi. 10.1038/sj.ejhg.5200698
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- Publication type:
- Article
Polymorphisms in the FKBP5 gene region modulate recovery from psychosocial stress in healthy controls.
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- European Journal of Neuroscience, 2008, v. 28, n. 2, p. 389, doi. 10.1111/j.1460-9568.2008.06332.x
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- Publication type:
- Article
Approaches to the genetics of cardiovascular disease through genetic field work.
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- Kidney International, 1998, v. 53, n. 6, p. 1449, doi. 10.1046/j.1523-1755.1998.00928.x
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- Publication type:
- Article
Adapting the randomised controlled trial (RCT) for precision medicine: introducing the nested-precision RCT (npRCT).
- Published in:
- 2021
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- Publication type:
- letter
Identification of Restless Legs Syndrome Genes by Mutational Load Analysis.
- Published in:
- Annals of Neurology, 2020, v. 87, n. 2, p. 184, doi. 10.1002/ana.25658
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- Publication type:
- Article
Identification of Restless Legs Syndrome Genes by Mutational Load Analysis.
- Published in:
- 2019
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- Publication type:
- journal article
Dexamethasone Stimulated Gene Expression in Peripheral Blood is a Sensitive Marker for Glucocorticoid Receptor Resistance in Depressed Patients.
- Published in:
- Neuropsychopharmacology, 2012, v. 37, n. 8, p. 1972, doi. 10.1038/npp.2012.21
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- Publication type:
- Article
Dexamethasone Stimulated Gene Expression in Peripheral Blood is a Sensitive Marker for Glucocorticoid Receptor Resistance in Depressed Patients.
- Published in:
- Neuropsychopharmacology, 2012, v. 37, n. 6, p. 1455, doi. 10.1038/npp.2011.331
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- Publication type:
- Article
Genome-Wide Association Study of Antidepressant Treatment-Emergent Suicidal Ideation.
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- Neuropsychopharmacology, 2012, v. 37, n. 3, p. 797, doi. 10.1038/npp.2011.257
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- Publication type:
- Article
Gender-Specific Association of Galanin Polymorphisms with HPA-Axis Dysregulation, Symptom Severity, and Antidepressant Treatment Response.
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- Neuropsychopharmacology, 2010, v. 35, n. 7, p. 1583, doi. 10.1038/npp.2010.30
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- Publication type:
- Article
Polymorphisms in GRIK4, HTR2A, and FKBP5 Show Interactive Effects in Predicting Remission to Antidepressant Treatment.
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- Neuropsychopharmacology, 2010, v. 35, n. 3, p. 727, doi. 10.1038/npp.2009.180
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- Publication type:
- Article
netMUG: a novel network-guided multi-view clustering workflow for dissecting genetic and facial heterogeneity.
- Published in:
- Frontiers in Genetics, 2023, p. 1, doi. 10.3389/fgene.2023.1286800
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- Publication type:
- Article
Genome-wide association study reveals two new risk loci for bipolar disorder.
- Published in:
- Nature Communications, 2014, v. 5, n. 3, p. 3339, doi. 10.1038/ncomms4339
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- Publication type:
- Article
Investigation of gene-gene interactions in cardiac traits and serum fatty acid levels in the LURIC Health Study.
- Published in:
- PLoS ONE, 2020, v. 15, n. 9, p. 1, doi. 10.1371/journal.pone.0238304
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- Publication type:
- Article
Metabolic profiling of maternal serum of women at high-risk of spontaneous preterm birth using NMR and MGWAS approach.
- Published in:
- Bioscience Reports, 2021, v. 41, n. 9, p. 1, doi. 10.1042/BSR20210759
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- Publication type:
- Article
Analyzing pathways from childhood maltreatment to internalizing symptoms and disorders in children and adolescents (AMIS): a study protocol.
- Published in:
- BMC Psychiatry, 2015, v. 15, n. 1, p. 1, doi. 10.1186/s12888-015-0512-z
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- Publication type:
- Article
Polygenic risk scores outperform machine learning methods in predicting coronary artery disease status.
- Published in:
- Genetic Epidemiology, 2020, v. 44, n. 2, p. 125, doi. 10.1002/gepi.22279
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- Publication type:
- Article
Significant evidence for linkage of a simulated trait to D1G024-A conclusion reached using multiallelic transmission/disequilibrium tests.
- Published in:
- Genetic Epidemiology, 1999, v. 17, p. S785, doi. 10.1002/gepi.13701707129
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- Publication type:
- Article
Linkage Disequilibrium and Haplotype Analysis in German Friedreich Ataxia Families.
- Published in:
- Human Heredity, 1999, v. 49, n. 2, p. 90, doi. 10.1159/000022851
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- Publication type:
- Article
Mapping Undetected Mutations within a Gene - Evidence for Two Preferential Regions in the DMD Gene.
- Published in:
- Human Heredity, 1997, v. 47, n. 2, p. 61, doi. 10.1159/000154393
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- Publication type:
- Article
Epistasis detection on quantitative phenotypes by exhaustive enumeration using GPUs.
- Published in:
- Bioinformatics, 2011, v. 27, n. 13, p. i214, doi. 10.1093/bioinformatics/btr218
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- Publication type:
- Article
vipR: variant identification in pooled DNA using R.
- Published in:
- Bioinformatics, 2011, v. 27, n. 13, p. i77, doi. 10.1093/bioinformatics/btr205
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- Publication type:
- Article
Sleep disturbance by pramipexole is modified by Meis1 in mice.
- Published in:
- Journal of Sleep Research, 2018, v. 27, n. 4, p. 1, doi. 10.1111/jsr.12557
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- Publication type:
- Article