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Liquid Biopsy Biomarkers for Immunotherapy in Non-Small Cell Lung Carcinoma: Lessons Learned and the Road Ahead.
- Published in:
- Journal of Personalized Medicine, 2021, v. 11, n. 10, p. 971, doi. 10.3390/jpm11100971
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- Publication type:
- Article
The Road so Far in Colorectal Cancer Pharmacogenomics: Are We Closer to Individualised Treatment?
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- Journal of Personalized Medicine, 2020, v. 10, n. 4, p. 237, doi. 10.3390/jpm10040237
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- Publication type:
- Article
Broadening the Applicability of a Custom Multi-Platform Panel of Microhaplotypes: Bio-Geographical Ancestry Inference and Expanded Reference Data.
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- Frontiers in Genetics, 2020, v. 11, p. N.PAG, doi. 10.3389/fgene.2020.581041
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- Publication type:
- Article
A Comparison of Forensic Age Prediction Models Using Data From Four DNA Methylation Technologies.
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- Frontiers in Genetics, 2020, v. 11, p. N.PAG, doi. 10.3389/fgene.2020.00932
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- Publication type:
- Article
Review of Pharmacokinetics and Pharmacogenetics in Atypical Long-Acting Injectable Antipsychotics.
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- Pharmaceutics, 2021, v. 13, n. 7, p. 935, doi. 10.3390/pharmaceutics13070935
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- Publication type:
- Article
Viability Study of Machine Learning-Based Prediction of COVID-19 Pandemic Impact in Obsessive-Compulsive Disorder Patients.
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- Frontiers in Neuroinformatics, 2022, v. 15, p. 1, doi. 10.3389/fninf.2022.807584
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- Publication type:
- Article
Finding genes that underlie cancer using genetic tools.
- Published in:
- 2006
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- Publication type:
- Editorial
Genetic dissection of Hippocampal sclerosis MRI surrogates.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2023, v. 19, p. 1, doi. 10.1002/alz.074598
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- Publication type:
- Article
Rare copy number variation in the GR@ACE/DEGESCO dementia dataset of spanish population.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2023, v. 19, p. 1, doi. 10.1002/alz.074012
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- Publication type:
- Article
Genetic dissection of Hippocampal sclerosis MRI surrogates.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2023, v. 19, p. 1, doi. 10.1002/alz.074598
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- Publication type:
- Article
Rare copy number variation in the GR@ACE/DEGESCO dementia dataset of spanish population.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2023, v. 19, p. 1, doi. 10.1002/alz.074012
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- Publication type:
- Article
Meta‐GWAS of amyloid burden endophenotype combining PET and CSF results.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2021, v. 17, n. 3, p. 1, doi. 10.1002/alz.052333
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- Publication type:
- Article
P2‐139: GENOME‐WIDE ASSOCIATION STUDY OF ALZHEIMER'S DISEASE (AD) SUSCEPTIBILITY USING THE FUNDACIO ACE GENOME REPOSITORY: THE GR@ACE PROJECT.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2018, v. 14, p. P721, doi. 10.1016/j.jalz.2018.06.825
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- Publication type:
- Article
Genetic Susceptibility to Periodontal Disease in Down Syndrome: A Case-Control Study.
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- International Journal of Molecular Sciences, 2021, v. 22, n. 12, p. 6274, doi. 10.3390/ijms22126274
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- Publication type:
- Article
The molecular characterization of a depurinated trial DNA sample can be a model to understand the reliability of the results in forensic genetics.
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- Electrophoresis, 2014, v. 35, n. 21/22, p. 3134, doi. 10.1002/elps.201400141
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- Publication type:
- Article
'New turns from old STaRs': Enhancing the capabilities of forensic short tandem repeat analysis.
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- Electrophoresis, 2014, v. 35, n. 21/22, p. 3173, doi. 10.1002/elps.201400095
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- Publication type:
- Article
Next generation sequencing challenges in the analysis of cardiac sudden death due to arrhythmogenic disorders.
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- Electrophoresis, 2014, v. 35, n. 21/22, p. 3111, doi. 10.1002/elps.201400148
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- Publication type:
- Article
Development of a novel forensic STR multiplex for ancestry analysis and extended identity testing.
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- Electrophoresis, 2013, v. 34, n. 8, p. 1151, doi. 10.1002/elps.201200621
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- Publication type:
- Article
A new approach to long QT syndrome mutation detection by Sequenom MassARRAY<sup>®</sup> system.
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- Electrophoresis, 2010, v. 31, n. 10, p. 1648, doi. 10.1002/elps.201000022
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- Publication type:
- Article
Applications of MALDI-TOF MS to large-scale human mtDNA population-based studies.
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- Electrophoresis, 2009, v. 30, n. 21, p. 3665, doi. 10.1002/elps.200900294
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- Publication type:
- Article
A new multiplex for human identification using insertion/deletion polymorphisms.
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- Electrophoresis, 2009, v. 30, n. 21, p. 3682, doi. 10.1002/elps.200900274
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- Publication type:
- Article
Dissection of mitochondrial superhaplogroup H using coding region SNPs.
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- Electrophoresis, 2006, v. 27, n. 13, p. 2541
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- Publication type:
- Article
A multiplex assay with 52 single nucleotide polymorphisms for human identification.
- Published in:
- Electrophoresis, 2006, v. 27, n. 9, p. 1713, doi. 10.1002/elps.200500671
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- Publication type:
- Article
Introduction of an single nucleodite polymorphism-based “Major Y-chromosome haplogroup typing kit” suitable for predicting the geographical origin of male lineages.
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- Electrophoresis, 2005, v. 26, n. 23, p. 4411
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- Publication type:
- Article
The early-life exposome modulates the effect of polymorphic inversions on DNA methylation.
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- Communications Biology, 2022, v. 5, n. 1, p. 1, doi. 10.1038/s42003-022-03380-2
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- Publication type:
- Article
Prevalence of CYP2C9 polymorphisms in the south of Europe.
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- Pharmacogenomics Journal, 2009, v. 9, n. 5, p. 306, doi. 10.1038/tpj.2009.16
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- Publication type:
- Article
UTMOST, a single and cross-tissue TWAS (Transcriptome Wide Association Study), reveals new ASD (Autism Spectrum Disorder) associated genes.
- Published in:
- Translational Psychiatry, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41398-021-01378-8
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- Publication type:
- Article
Association between DNA methylation and ADHD symptoms from birth to school age: a prospective meta-analysis.
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- Translational Psychiatry, 2020, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41398-020-01058-z
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- Publication type:
- Article
Psychiatric comorbidities in Asperger syndrome are related with polygenic overlap and differ from other Autism subtypes.
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- Translational Psychiatry, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41398-020-00939-7
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- Publication type:
- Article
Looking into the genetic bases of OCD dimensions: a pilot genome-wide association study.
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- Translational Psychiatry, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41398-020-0804-z
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- Publication type:
- Article
Genetic Diversity of Drug-Related Genes in Native Americans of the Brazilian Amazon.
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- Pharmacogenomics & Personalized Medicine, 2021, v. 14, p. 117, doi. 10.2147/PGPM.S274741
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- Publication type:
- Article
Novel truncating variants expand the phenotypic spectrum of KAT6B‐related disorders.
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- American Journal of Medical Genetics. Part A, 2019, v. 179, n. 2, p. 290, doi. 10.1002/ajmg.a.60689
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- Publication type:
- Article
Interstitial Microdeletions Including the Chromosome Band 4q13.2 and the UBA6 Gene as Possible Causes of Intellectual Disability and Behavior Disorder.
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- American Journal of Medical Genetics. Part A, 2015, v. 167A, n. 12, p. 3113, doi. 10.1002/ajmg.a.37291
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- Publication type:
- Article
Female Patient with Autistic Disorder, Intellectual Disability, and Co-Morbid Anxiety Disorder: Expanding the Phenotype Associated with the Recurrent 3q13.2-q13.31 Microdeletion.
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- American Journal of Medical Genetics. Part A, 2015, v. 167A, n. 12, p. 3121, doi. 10.1002/ajmg.a.37292
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- Publication type:
- Article
Clinical characterization of a male patient with the recently described 8q21.11 microdeletion syndrome.
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- American Journal of Medical Genetics. Part A, 2015, v. 167A, n. 6, p. 1369, doi. 10.1002/ajmg.a.37038
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- Publication type:
- Article
A maternally inherited 16p13.11-p12.3 duplication concomitant with a de novo SOX5 deletion in a male patient with global developmental delay, disruptive and obsessive behaviors and minor dysmorphic features.
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- American Journal of Medical Genetics. Part A, 2015, v. 167A, n. 6, p. 1315, doi. 10.1002/ajmg.a.36909
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- Publication type:
- Article
A three-stage genome-wide association study identifies a susceptibility locus for late radiotherapy toxicity at 2q24.1.
- Published in:
- Nature Genetics, 2014, v. 46, n. 8, p. 891, doi. 10.1038/ng.3020
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- Publication type:
- Article
Mutations in the gene encoding PDGF-B cause brain calcifications in humans and mice.
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- Nature Genetics, 2013, v. 45, n. 9, p. 1077, doi. 10.1038/ng.2723
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- Publication type:
- Article
Common variants at 2q37.3, 8q24.21, 15q21.3 and 16q24.1 influence chronic lymphocytic leukemia risk.
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- Nature Genetics, 2010, v. 42, n. 2, p. 132, doi. 10.1038/ng.510
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- Publication type:
- Article
In utero and childhood exposure to tobacco smoke and multi-layer molecular signatures in children.
- Published in:
- 2020
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- Publication type:
- journal article
A new panel of SNPs to assess thyroid carcinoma risk: a pilot study in a Brazilian admixture population.
- Published in:
- BMC Medical Genetics, 2017, v. 18, p. 1, doi. 10.1186/s12881-017-0502-8
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- Publication type:
- Article
SNPs as Supplements in Simple Kinship Analysis or as Core Markers in Distant Pairwise Relationship Tests: When Do SNPs Add Value or Replace Well-Established and Powerful STR Tests?
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- Transfusion Medicine & Hemotherapy, 2012, v. 39, n. 3, p. 202, doi. 10.1159/000338857
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- Publication type:
- Article
Forensic genetics and genomics: Much more than just a human affair.
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- PLoS Genetics, 2017, v. 13, n. 9, p. 1, doi. 10.1371/journal.pgen.1006960
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- Publication type:
- Article
CYP2D6 genotyping by liquid chromatography-electrospray ionization mass spectrometry.
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- Analytical & Bioanalytical Chemistry, 2011, v. 400, n. 8, p. 2361, doi. 10.1007/s00216-010-4597-4
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- Publication type:
- Article
DNA REWRITING OUR MEMORY: Recovering missing people through their genetic profile.
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- Mètode Science Studies Journal, 2020, n. 10, p. 119, doi. 10.7203/metode.10.13691
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- Publication type:
- Article
BEYOND THE CSI EFFECT: THE KEYS TO GOOD FORENSIC GENETICS COMMUNICATION.
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- Mètode Science Studies Journal, 2019, n. 9, p. 31, doi. 10.7203/metode.9.10628
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- Publication type:
- Article
Clinical and molecular characterization of Wilson disease in Spanish patients.
- Published in:
- Hepatology Research, 2007, v. 37, n. 1, p. 18, doi. 10.1111/j.1872-034X.2007.00010.x
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- Publication type:
- Article
Patterns of Default Mode Network Deactivation in Obsessive Compulsive Disorder.
- Published in:
- Scientific Reports, 2017, p. 44468, doi. 10.1038/srep44468
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- Publication type:
- Article
Natural resistance to Meningococcal Disease related to CFH loci: Meta-analysis of genome-wide association studies.
- Published in:
- Scientific Reports, 2016, p. 35842, doi. 10.1038/srep35842
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- Publication type:
- Article
Incertidumbre en la interpretación de variantes genéticas detectadas mediante secuenciación masiva.
- Published in:
- CorSalud, 2017, v. 9, n. 3, p. 183
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- Publication type:
- Article