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Enrichment of B cell receptor signaling and epidermal growth factor receptor pathways in monoclonal gammopathy of undetermined significance: a genome-wide genetic interaction study.
- Published in:
- Molecular Medicine, 2018, v. 24, n. 1, p. N.PAG, doi. 10.1186/s10020-018-0031-8
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- Article
Familial occurrence of the VATER/VACTERL association.
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- 2012
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- Publication type:
- Report
Exome-Wide Association Study Identifies FN3KRP and PGP as New Candidate Longevity Genes.
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- Journals of Gerontology Series A: Biological Sciences & Medical Sciences, 2021, v. 76, n. 5, p. 786, doi. 10.1093/gerona/glab023
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- Article
Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia.
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- Translational Psychiatry, 2019, v. 9, n. 1, p. 1, doi. 10.1038/s41398-019-0402-0
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- Article
Transethnic meta-analysis of rare coding variants in PLCG2, ABI3, and TREM2 supports their general contribution to Alzheimer's disease.
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- Translational Psychiatry, 2019, v. 9, n. 1, p. 1, doi. 10.1038/s41398-019-0394-9
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- Article
Elevated expression of a minor isoform of ANK3 is a risk factor for bipolar disorder.
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- Translational Psychiatry, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41398-018-0175-x
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- Article
Inbreeding and homozygosity in breast cancer survival.
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- Scientific Reports, 2015, p. 16467, doi. 10.1038/srep16467
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- Article
Novel genetic variants in differentiated thyroid cancer and assessment of the cumulative risk.
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- Scientific Reports, 2015, p. 8922, doi. 10.1038/srep08922
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- Article
Population structure and linkage disequilibrium in diploid and tetraploid potato revealed by genome-wide high-density genotyping using the SolCAP SNP array.
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- Plant Breeding, 2013, v. 132, n. 6, p. 718, doi. 10.1111/pbr.12102
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- Article
Complete homozygous deletion of CTSC in an Iranian family with Papillon- Lefèvre syndrome.
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- International Journal of Dermatology, 2014, v. 53, n. 7, p. 885, doi. 10.1111/j.1365-4632.2012.05769.x
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- Article
Advanced paternal age as a risk factor for neurodevelopmental disorders: a translational study.
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- Molecular Autism, 2020, v. 11, n. 1, p. 1, doi. 10.1186/s13229-020-00345-2
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- Article
Mendelian Randomization Study on Amino Acid Metabolism Suggests Tyrosine as Causal Trait for Type 2 Diabetes.
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- Nutrients, 2020, v. 12, n. 12, p. 3890, doi. 10.3390/nu12123890
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- Article
Desaturase Activity and the Risk of Type 2 Diabetes and Coronary Artery Disease: A Mendelian Randomization Study.
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- Nutrients, 2020, v. 12, n. 8, p. 2261, doi. 10.3390/nu12082261
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- Article
Genomewide association study on monoclonal gammopathy of unknown significance (MGUS).
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- European Journal of Haematology, 2017, v. 99, n. 1, p. 70, doi. 10.1111/ejh.12892
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- Article
Exome sequencing in large, multiplex bipolar disorder families from Cuba.
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- PLoS ONE, 2018, v. 13, n. 10, p. 1, doi. 10.1371/journal.pone.0205895
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- Article
Primary Osteoporosis Is Not Reflected by Disease‐Specific DNA Methylation or Accelerated Epigenetic Age in Blood.
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- Journal of Bone & Mineral Research, 2018, v. 33, n. 2, p. 356, doi. 10.1002/jbmr.3298
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- Article
Addressing Global Environmental Challenges to Mental Health Using Population Neuroscience: A Review.
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- JAMA Psychiatry, 2023, v. 80, n. 10, p. 1066, doi. 10.1001/jamapsychiatry.2023.2996
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- Publication type:
- Article
Multi-omics signatures of alcohol use disorder in the dorsal and ventral striatum.
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- Translational Psychiatry, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41398-022-01959-1
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- Publication type:
- Article
Polygenic risk scores across the extended psychosis spectrum.
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- Translational Psychiatry, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41398-021-01720-0
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- Article
Identification of pleiotropy at the gene level between psychiatric disorders and related traits.
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- Translational Psychiatry, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41398-021-01530-4
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- Article
Mendelian randomization provides support for obesity as a risk factor for meningioma.
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- Scientific Reports, 2019, v. 9, n. 1, p. 1, doi. 10.1038/s41598-018-36186-6
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- Article
SUCLG2 identified as both a determinator of CSF Aβ1–42 levels and an attenuator of cognitive decline in Alzheimer's disease.
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- Human Molecular Genetics, 2014, v. 23, n. 24, p. 6644
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- Article
16p11.2 600 kb Duplications confer risk for typical and atypical Rolandic epilepsy.
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- Human Molecular Genetics, 2014, v. 23, n. 22, p. 6069, doi. 10.1093/hmg/ddu306
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- Article
The DISC locus and schizophrenia: evidence from an association study in a central European sample and from a meta-analysis across different European populations.
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- Human Molecular Genetics, 2009, v. 18, n. 14, p. 2719, doi. 10.1093/hmg/ddp204
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- Article
A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia.
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- Human Molecular Genetics, 2007, v. 16, n. 6, p. 667, doi. 10.1093/hmg/ddm009
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- Article
Genome-wide mapping of genetic determinants influencing DNA methylation and gene expression in human hippocampus.
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- Nature Communications, 2017, v. 8, n. 1, p. 1, doi. 10.1038/s41467-017-01818-4
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- Article
Large scale meta-analysis characterizes genetic architecture for common psoriasis associated variants.
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- Nature Communications, 2017, v. 8, n. 5, p. 15382, doi. 10.1038/ncomms15382
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- Article
Genome-wide association study identifies variation at 6q25.1 associated with survival in multiple myeloma.
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- Nature Communications, 2016, v. 7, n. 1, p. 10290, doi. 10.1038/ncomms10290
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- Article
Genome-wide association study reveals two new risk loci for bipolar disorder.
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- Nature Communications, 2014, v. 5, n. 3, p. 3339, doi. 10.1038/ncomms4339
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- Article
Variation at 3p24.1 and 6q23.3 influences the risk of Hodgkin's lymphoma.
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- Nature Communications, 2013, v. 4, n. 10, p. 2549, doi. 10.1038/ncomms3549
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- Article
DNA methylation signature in peripheral blood reveals distinct characteristics of human X chromosome numerical aberrations.
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- Clinical Epigenetics, 2015, v. 7, n. 1, p. 1, doi. 10.1186/s13148-015-0112-2
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- Article
Brief Report: No Association Between Premorbid Adjustment in Adult-Onset Schizophrenia and Genetic Variation in Dysbindin.
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- Journal of Autism & Developmental Disorders, 2008, v. 38, n. 10, p. 1977, doi. 10.1007/s10803-008-0582-6
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- Article
Differential DNA methylation and mRNA transcription in gingival tissues in periodontal health and disease.
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- Journal of Clinical Periodontology, 2021, v. 48, n. 9, p. 1152, doi. 10.1111/jcpe.13504
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- Article
The severity of human peri‐implantitis lesions correlates with the level of submucosal microbial dysbiosis.
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- Journal of Clinical Periodontology, 2018, v. 45, n. 12, p. 1498, doi. 10.1111/jcpe.13023
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- Publication type:
- Article
Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort.
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- European Journal of Human Genetics, 2014, v. 22, n. 5, p. 675, doi. 10.1038/ejhg.2013.199
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- Article
Combating the SARS-CoV-2 pandemic: How can the field of Human Genetics contribute?
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- Medizinische Genetik, 2020, p. 163, doi. 10.1515/medgen-2020-2027
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- Article
Hepatic Expression of the Na + -Taurocholate Cotransporting Polypeptide Is Independent from Genetic Variation.
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- International Journal of Molecular Sciences, 2022, v. 23, n. 13, p. 7468, doi. 10.3390/ijms23137468
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- Article
Excitation-induced ataxin-3 aggregation in neurons from patients with Machado-Joseph disease.
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- Nature, 2011, v. 480, n. 7378, p. 543, doi. 10.1038/nature10671
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- Article
Distinct pathways associated with chromosomal aberration frequency in a cohort exposed to genotoxic compounds compared to general population.
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- Mutagenesis, 2019, v. 34, n. 4, p. 323, doi. 10.1093/mutage/gez024
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- 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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- 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
Genetics and Neuroscience in Dyslexia: Perspectives for Education and Remediation.
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- Mind, Brain & Education, 2007, v. 1, n. 4, p. 162, doi. 10.1111/j.1751-228X.2007.00017.x
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- Article
Defining the role of common variation in the genomic and biological architecture of adult human height.
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- Nature Genetics, 2014, v. 46, n. 11, p. 1173, doi. 10.1038/ng.3097
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- Article
The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.
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- Nature Genetics, 2013, v. 45, n. 5, p. 522, doi. 10.1038/ng.2583
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- Article
Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk.
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- Nature Genetics, 2012, v. 44, n. 1, p. 58, doi. 10.1038/ng.993
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- Article
Common variation at 10p12.31 near MLLT10 influences meningioma risk.
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- Nature Genetics, 2011, v. 43, n. 9, p. 825, doi. 10.1038/ng.879
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- Article
A statistical model for the analysis of beta values in DNA methylation studies.
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- BMC Bioinformatics, 2016, v. 17, p. 1, doi. 10.1186/s12859-016-1347-4
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- Article
BMP Inhibition in Seminomas Initiates Acquisition of Pluripotency via NODAL Signaling Resulting in Reprogramming to an Embryonal Carcinoma.
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- PLoS Genetics, 2015, v. 11, n. 7, p. 1, doi. 10.1371/journal.pgen.1005415
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- Article
Zur Bleiche von Fichten-BisulfitzellstofFen mit Wasserstoffperoxid und Chlordioxid.
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- Holzforschung: International Journal of the Biology, Chemistry, Physics, & Technology of Wood, 1979, v. 33, n. 5, p. 167
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- Article
Some investigations into the suitability of young Pinus caribaea (Morelet) from plantations in Venezuelan Guayana for pulp production.
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- Holzforschung: International Journal of the Biology, Chemistry, Physics, & Technology of Wood, 1978, v. 32, n. 4, p. 138
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- Article