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Genetics of BAG3: A Paradigm for Developing Precision Therapies for Dilated Cardiomyopathies.
- Published in:
- 2022
- By:
- Publication type:
- journal article
Implications of the non‐neuronal cholinergic system for therapeutic interventions of inflammatory skin diseases.
- Published in:
- Experimental Dermatology, 2024, v. 33, n. 10, p. 1, doi. 10.1111/exd.15181
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- Publication type:
- Article
The Role of BAG3 Protein Interactions in Cardiomyopathies.
- Published in:
- International Journal of Molecular Sciences, 2024, v. 25, n. 20, p. 11308, doi. 10.3390/ijms252011308
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- Publication type:
- Article
Erratum to: Heritability and genome-wide analyses of problematic peer relationships during childhood and adolescence.
- Published in:
- 2016
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- Publication type:
- Erratum
Heritability and genome-wide analyses of problematic peer relationships during childhood and adolescence.
- Published in:
- Human Genetics, 2015, v. 134, n. 6, p. 539, doi. 10.1007/s00439-014-1514-5
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- Publication type:
- Article
Replication of a GWAS signal in a Caucasian population implicates ADD3 in susceptibility to biliary atresia.
- Published in:
- Human Genetics, 2014, v. 133, n. 2, p. 235, doi. 10.1007/s00439-013-1368-2
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- Publication type:
- Article
Dynamic Bayesian Testing of Sets of Variants in Complex Diseases.
- Published in:
- Genetics, 2014, v. 198, n. 3, p. 867, doi. 10.1534/genetics.114.167403
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- Publication type:
- Article
Genetic predisposition to longer telomere length and risk of childhood, adolescent and adult-onset ependymoma.
- Published in:
- Acta Neuropathologica Communications, 2020, v. 8, n. 1, p. N.PAG, doi. 10.1186/s40478-020-01038-w
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- Publication type:
- Article
Phenotype wide association study links bronchopulmonary dysplasia with eosinophilia in children.
- Published in:
- Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-72348-5
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- Publication type:
- Article
Identification of genetic variants associated with clinical features of sickle cell disease.
- Published in:
- Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-70922-5
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- Publication type:
- Article
The Tehran longitudinal family-based cardiometabolic cohort study sheds new light on dyslipidemia transmission patterns.
- Published in:
- Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-53504-3
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- Publication type:
- Article
Attitudes among Parents towards Return of Disease-Related Polygenic Risk Scores (PRS) for Their Children.
- Published in:
- Journal of Personalized Medicine, 2022, v. 12, n. 12, p. 1945, doi. 10.3390/jpm12121945
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- Publication type:
- Article
Outcomes of Returning Medically Actionable Genomic Results in Pediatric Research.
- Published in:
- Journal of Personalized Medicine, 2022, v. 12, n. 11, p. 1910, doi. 10.3390/jpm12111910
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- Publication type:
- Article
Implementing Pharmacogenetic Testing in Gastrointestinal Cancers (IMPACT-GI): Study Protocol for a Pragmatic Implementation Trial for Establishing DPYD and UGT1A1 Screening to Guide Chemotherapy Dosing.
- Published in:
- Frontiers in Oncology, 2022, v. 12, p. 1, doi. 10.3389/fonc.2022.859846
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- Publication type:
- Article
SOCS-JAK-STAT inhibitors and SOCS mimetics as treatment options for autoimmune uveitis, psoriasis, lupus, and autoimmune encephalitis.
- Published in:
- Frontiers in Immunology, 2023, p. 1, doi. 10.3389/fimmu.2023.1271102
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- Publication type:
- Article
Genome-wide association study of the age of onset of type 1 diabetes reveals HTATIP2 as a novel T cell regulator.
- Published in:
- Frontiers in Immunology, 2023, v. 14, p. 1, doi. 10.3389/fimmu.2023.1101488
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- Publication type:
- Article
Association of Rare Recurrent Copy Number Variants With Congenital Heart Defects Based on Next-Generation Sequencing Data From Family Trios.
- Published in:
- Frontiers in Genetics, 2019, p. 1, doi. 10.3389/fgene.2019.00819
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- Publication type:
- Article
Target Genes of Autism Risk Loci in Brain Frontal Cortex.
- Published in:
- Frontiers in Genetics, 2019, p. 1, doi. 10.3389/fgene.2019.00707
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- Publication type:
- Article
Multiple Epistasis Interactions Within MHC Are Associated With Ulcerative Colitis.
- Published in:
- Frontiers in Genetics, 2019, p. N.PAG, doi. 10.3389/fgene.2019.00257
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- Publication type:
- Article
Identification of Target Genes at Juvenile Idiopathic Arthritis GWAS Loci in Human Neutrophils.
- Published in:
- Frontiers in Genetics, 2019, p. N.PAG, doi. 10.3389/fgene.2019.00181
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- Publication type:
- Article
Dominant Form of Congenital Hyperinsulinism Maps to HK1 Region on 10q.
- Published in:
- Hormone Research in Paediatrics, 2013, v. 80, n. 1, p. 18, doi. 10.1159/000351943
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- Publication type:
- Article
Learning-dependent chromatin remodeling highlights noncoding regulatory regions linked to autism.
- Published in:
- Science Signaling, 2018, v. 11, n. 513, p. 1, doi. 10.1126/scisignal.aan6500
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- Publication type:
- Article
Interstitial deletion 4p15.32p16.1 and complex chromoplexy in a female proband with severe neurodevelopmental delay, growth failure and dysmorphism.
- Published in:
- Molecular Cytogenetics (17558166), 2022, v. 15, n. 1, p. 1, doi. 10.1186/s13039-022-00610-4
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- Publication type:
- Article
High prevalence of elevated serum liver enzymes in Chinese children suggests metabolic syndrome as a common risk factor.
- Published in:
- 2020
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- Publication type:
- journal article
Role of the ADCY9 gene in cardiac abnormalities of the Rubinstein-Taybi syndrome.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Heterozygous Mutations in TBX1 as a Cause of Isolated Hypoparathyroidism.
- Published in:
- 2018
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- Publication type:
- journal article
CYP3A4 Induction by Rifampin: An Alternative Pathway for Vitamin D Inactivation in Patients With CYP24A1 Mutations.
- Published in:
- 2017
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- Publication type:
- journal article
Exome Sequencing Reveals Mutations in AIRE as a Cause of Isolated Hypoparathyroidism.
- Published in:
- 2017
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- Publication type:
- journal article
Genetic Discrimination Between LADA and Childhood-Onset Type 1 Diabetes Within the MHC.
- Published in:
- 2020
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- Publication type:
- journal article
DENND1B gene variants associate with elevated exhaled nitric oxide in healthy high-risk neonates.
- Published in:
- Pediatric Pulmonology, 2015, v. 50, n. 2, p. 109, doi. 10.1002/ppul.22958
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- Publication type:
- Article
Genome-wide association studies (GWAS): impact on elucidating the aetiology of diabetes.
- Published in:
- 2011
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- Publication type:
- Journal Article
Genome-wide association studies (GWAS): impact on elucidating the aetiology of diabetes.
- Published in:
- Diabetes/Metabolism Research & Reviews, 2011, v. 27, n. 7, p. 685, doi. 10.1002/dmrr.1221
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- Publication type:
- Article
Genetic Determinants of Pediatric Inflammatory Bowel Disease: Is Age of Onset Genetically Determined?
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- Digestive Diseases, 2009, v. 27, n. 3, p. 236, doi. 10.1159/000228555
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- Publication type:
- Article
Analysing biological pathways in genome-wide association studies.
- Published in:
- 2010
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- Publication type:
- journal article
Evaluating sequence data quality from the Swift Accel-Amplicon CFTR Panel.
- Published in:
- Scientific Data, 2020, v. 7, n. 1, p. 1, doi. 10.1038/s41597-019-0339-4
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- Publication type:
- Article
Genes Associated with Cancer, Schizophrenia and Type 2 Diabetes in the Circassian and Chechen Populations in Jordan.
- Published in:
- Jordan Medical Journal, 2018, v. 52, n. 1, p. 59
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- Publication type:
- Article
A genome wide association study of plasma uric acid levels in obese cases and never-overweight controls.
- Published in:
- Obesity (19307381), 2013, v. 21, n. 9, p. E490, doi. 10.1002/oby.20303
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- Publication type:
- Article
Obesity-susceptibility loci and the tails of the pediatric BMI distribution.
- Published in:
- Obesity (19307381), 2013, v. 21, n. 6, p. 1256, doi. 10.1002/oby.20319
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- Publication type:
- Article
The missense variation landscape of FTO, MC4R, and TMEM18 in obese children of African Ancestry.
- Published in:
- Obesity (19307381), 2013, v. 21, n. 1, p. 159, doi. 10.1002/oby.20147
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- Publication type:
- Article
Association of Type 2 Diabetes Susceptibility Loci With One-Year Weight Loss in the Look AHEAD Clinical Trial.
- Published in:
- Obesity (19307381), 2012, v. 20, n. 8, p. 1675, doi. 10.1038/oby.2012.11
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- Publication type:
- Article
Role of BMI-Associated Loci Identified in GWAS Meta-Analyses in the Context of Common Childhood Obesity in European Americans.
- Published in:
- Obesity (19307381), 2011, v. 19, n. 12, p. 2436, doi. 10.1038/oby.2011.237
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- Publication type:
- Article
BMD-Associated Variation at the Osterix Locus Is Correlated With Childhood Obesity in Females.
- Published in:
- Obesity (19307381), 2011, v. 19, n. 6, p. 1311, doi. 10.1038/oby.2010.324
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- Publication type:
- Article
The Role of Obesity-associated Loci Identified in Genome-wide Association Studies in the Determination of Pediatric BMI.
- Published in:
- Obesity (19307381), 2009, v. 17, n. 12, p. 2254, doi. 10.1038/oby.2009.159
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- Publication type:
- Article
Investigation of the Locus Near MC4R With Childhood Obesity in Americans of European and African Ancestry.
- Published in:
- Obesity (19307381), 2009, v. 17, n. 7, p. 1461, doi. 10.1038/oby.2009.53
- By:
- Publication type:
- Article
Association Between a Common, Benign Genotype and Unnecessary Bone Marrow Biopsies Among African American Patients.
- Published in:
- 2021
- By:
- Publication type:
- journal article
Integrative analysis of genome-wide association studies identifies novel loci associated with neuropsychiatric disorders.
- Published in:
- Translational Psychiatry, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41398-020-01195-5
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- Publication type:
- Article
Mitochondrial DNA haplogroups and risk of attention deficit and hyperactivity disorder in European Americans.
- Published in:
- Translational Psychiatry, 2020, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41398-020-01064-1
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- Publication type:
- Article
Food allergen triggers are increased in children with the TSLP risk allele and eosinophilic esophagitis.
- Published in:
- Clinical & Translational Gastroenterology, 2018, v. 9, n. 3, p. 1, doi. 10.1038/s41424-018-0003-x
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- Publication type:
- Article
GWAS meta analysis identifies TSNARE1 as a novel Schizophrenia / Bipolar susceptibility locus.
- Published in:
- Scientific Reports, 2013, p. 1, doi. 10.1038/srep03075
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- Publication type:
- Article
Expansion of Schizophrenia Gene Network Knowledge Using Machine Learning Selected Signals From Dorsolateral Prefrontal Cortex and Amygdala RNA-seq Data.
- Published in:
- Frontiers in Psychiatry, 2022, v. 13, p. 1, doi. 10.3389/fpsyt.2022.797329
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- Publication type:
- Article