Found: 31
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Association of the BANK1 R61H variant with systemic lupus erythematosus in Americans of European and African ancestry.
- Published in:
- Application of Clinical Genetics, 2009, v. 2, p. 1
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- Publication type:
- Article
Early Infantile Epileptic Encephalopathy in an STXBP1 Patient with Lactic Acidemia and Normal Mitochondrial Respiratory Chain Function.
- Published in:
- Case Reports in Genetics, 2016, p. 1, doi. 10.1155/2016/4140780
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- Publication type:
- Article
Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder.
- Published in:
- Nature Genetics, 2012, v. 44, n. 1, p. 78, doi. 10.1038/ng.1013
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- Publication type:
- Article
Common variants at 5q22 associate with pediatric eosinophilic esophagitis.
- Published in:
- Nature Genetics, 2010, v. 42, n. 4, p. 289, doi. 10.1038/ng.547
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- Publication type:
- Article
Body mass index (BMI) trajectories in infancy differ by population ancestry and may presage disparities in early childhood obesity.
- Published in:
- 2015
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- Publication type:
- journal article
Gene Network Analysis in a Pediatric Cohort Identifies Novel Lung Function Genes.
- Published in:
- PLoS ONE, 2013, v. 8, n. 9, p. 1, doi. 10.1371/journal.pone.0072899
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- Publication type:
- Article
Association Analysis of the FTO Gene with Obesity in Children of Caucasian and African Ancestry Reveals a Common Tagging SNP.
- Published in:
- PLoS ONE, 2008, v. 3, n. 3, p. 1, doi. 10.1371/journal.pone.0001746
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- Publication type:
- Article
Genomic copy number variation association study in Caucasian patients with nonsyndromic cryptorchidism.
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- BMC Urology, 2016, v. 16, p. 1, doi. 10.1186/s12894-016-0180-4
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- Publication type:
- Article
Integrative genomics identifies LMO1 as a neuroblastoma oncogene.
- Published in:
- Nature, 2011, v. 469, n. 7329, p. 216, doi. 10.1038/nature09609
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- Publication type:
- Article
Common genetic variants on 5p14.1 associate with autism spectrum disorders.
- Published in:
- Nature, 2009, v. 459, n. 7246, p. 528, doi. 10.1038/nature07999
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- Publication type:
- Article
Autism genome-wide copy number variation reveals ubiquitin and neuronal genes.
- Published in:
- Nature, 2009, v. 459, n. 7246, p. 569, doi. 10.1038/nature07953
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- Publication type:
- Article
A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene.
- Published in:
- 2007
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- Publication type:
- Letter
Pathway analysis supports association of nonsyndromic cryptorchidism with genetic loci linked to cytoskeleton-dependent functions.
- Published in:
- 2015
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- Publication type:
- journal article
Genetic sharing and heritability of paediatric age of onset autoimmune diseases.
- Published in:
- Nature Communications, 2015, v. 6, n. 10, p. 8442, doi. 10.1038/ncomms9442
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- Publication type:
- Article
GWAS of blood cell traits identifies novel associated loci and epistatic interactions in Caucasian and African-American children.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 7, p. 1457, doi. 10.1093/hmg/dds534
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- Publication type:
- Article
Follow-Up Analysis of Genome-Wide Association Data Identifies Novel Loci for Type 1 Diabetes.
- Published in:
- Diabetes, 2009, v. 58, n. 1, p. 290, doi. 10.2337/db08-1022
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- Publication type:
- Article
A Novel Susceptibility Locus for Type 1 Diabetes on Chr12q13 Identified by a Genome-Wide Association Study.
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- Diabetes, 2008, v. 57, n. 4, p. 1143, doi. 10.2337/db07-1305
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- Publication type:
- Article
Fasoracetam in adolescents with ADHD and glutamatergic gene network variants disrupting mGluR neurotransmitter signaling.
- Published in:
- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-017-02244-2
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- Publication type:
- Article
Association of a rare NOTCH4 coding variant with systemic sclerosis: a family-based whole exome sequencing study.
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- BMC Musculoskeletal Disorders, 2016, v. 17, p. 1, doi. 10.1186/s12891-016-1320-4
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- Publication type:
- Article
A Genome-Wide Meta-Analysis of Six Type 1 Diabetes Cohorts Identifies Multiple Associated Loci.
- Published in:
- PLoS Genetics, 2011, v. 7, n. 9, p. 1, doi. 10.1371/journal.pgen.1002293
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- Publication type:
- Article
From Disease Association to Risk Assessment: An Optimistic View from Genome-Wide Association Studies on Type 1 Diabetes.
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- PLoS Genetics, 2009, v. 5, n. 10, p. 1, doi. 10.1371/journal.pgen.1000678
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- Publication type:
- Article
The Philadelphia Neurodevelopmental Cohort: constructing a deep phenotyping collaborative.
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- Journal of Child Psychology, 2015, v. 56, n. 12, p. 1356, doi. 10.1111/jcpp.12416
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- Publication type:
- Article
Systematic data-querying of large pediatric biorepository identifies novel Ehlers-Danlos Syndrome variant.
- Published in:
- 2016
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- Publication type:
- journal 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
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
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- Publication type:
- Article
Examination of All Type 2 Diabetes GWAS Loci Reveals HHEX-IDE as a Locus Influencing Pediatric BMI.
- Published in:
- Diabetes, 2010, v. 59, n. 3, p. 751, doi. 10.2337/db09-0972
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- Publication type:
- Article
Examination of Type 2 Diabetes Loci Implicates CDKAL1 as a Birth Weight Gene.
- Published in:
- Diabetes, 2009, v. 58, n. 10, p. 2414, doi. 10.2337/db09-0506
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- Publication type:
- Article
The role of height-associated loci identified in genome wide association studies in the determination of pediatric stature.
- Published in:
- BMC Medical Genetics, 2010, v. 11, p. 96, doi. 10.1186/1471-2350-11-96
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- Publication type:
- Article