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Author Correction: Somatic mosaicism and common genetic variation contribute to the risk of very-early-onset inflammatory bowel disease.
- Published in:
- 2022
- By:
- Publication type:
- Correction Notice
No association between typical European mitochondrial variation and prostate cancer risk in a Spanish cohort.
- Published in:
- Journal of Human Genetics, 2014, v. 59, n. 7, p. 411, doi. 10.1038/jhg.2014.46
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- Publication type:
- Article
No evidence of association between common European mitochondrial DNA variants in Alzheimer, Parkinson, and migraine in the Spanish population.
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2015, v. 168B, n. 1, p. 54, doi. 10.1002/ajmg.b.32276
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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
Natural resistance to Meningococcal Disease related to CFH loci: Meta-analysis of genome-wide association studies.
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- Scientific Reports, 2016, p. 35842, doi. 10.1038/srep35842
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- Publication type:
- Article
Large Genomic Rearrangements of <i>BRCA1</i> and <i>BRCA2</i> among Patients Referred for Genetic Analysis in Galicia (NW Spain): Delimitation and Mechanism of Three Novel <i>BRCA1</i> Rearrangements.
- Published in:
- PLoS ONE, 2014, v. 9, n. 3, p. 1, doi. 10.1371/journal.pone.0093306
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- Publication type:
- Article
Indian Signatures in the Westernmost Edge of the European Romani Diaspora: New Insight from Mitogenomes.
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- PLoS ONE, 2013, v. 8, n. 10, p. 1, doi. 10.1371/journal.pone.0075397
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- Article
Multiple Local and Recent Founder Effects of TGM1 in Spanish Families.
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- PLoS ONE, 2012, v. 7, n. 4, p. 1, doi. 10.1371/journal.pone.0033580
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- Publication type:
- Article
Investigating the Role of Mitochondrial Haplogroups in Genetic Predisposition to Meningococcal Disease.
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- PLoS ONE, 2009, v. 4, n. 12, p. 1, doi. 10.1371/journal.pone.0008347
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- Publication type:
- Article
Large-scale meta–genome-wide association study reveals common genetic factors linked to radiation-induced acute toxicities across cancer types.
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- JNCI Cancer Spectrum, 2023, v. 7, n. 6, p. 1, doi. 10.1093/jncics/pkad088
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- Publication type:
- Article
Characterization of TGM1 c.984+1G>A mutation identified in a homozygous carrier of lamellar ichthyosis.
- Published in:
- 2012
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- Publication type:
- Case Study
Candidate Causal Variants at the 8p12 Breast Cancer Risk Locus Regulate DUSP4.
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- Cancers, 2020, v. 12, n. 1, p. 170, doi. 10.3390/cancers12010170
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- Publication type:
- Article
Limited family structure and triple-negative breast cancer (TNBC) subtype as predictors of BRCA mutations in a genetic counseling cohort of early-onset sporadic breast cancers.
- Published in:
- Breast Cancer Research & Treatment, 2014, v. 148, n. 2, p. 415, doi. 10.1007/s10549-014-3167-4
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- Publication type:
- Article
Characterization of BRCA1 and BRCA2 splicing variants: a collaborative report by ENIGMA consortium members.
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- Breast Cancer Research & Treatment, 2012, v. 132, n. 3, p. 1009, doi. 10.1007/s10549-011-1674-0
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- Publication type:
- Article
Novel CYP4F22 mutations associated with autosomal recessive congenital ichthyosis (ARCI). Study of the CYP4F22 c.1303C>T founder mutation.
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- PLoS ONE, 2020, v. 15, n. 2, p. 1, doi. 10.1371/journal.pone.0229025
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- Publication type:
- Article
Novel and Recurrent PNPLA1 Mutations in Spanish Patients with Autosomal Recessive Congenital Ichthyosis; Evidence of a Founder Effect.
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- Acta Dermato-Venereologica, 2019, v. 99, n. 10, p. 894, doi. 10.2340/00015555-3227
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- Publication type:
- Article
Common genetic variation associated with increased susceptibility to prostate cancer does not increase risk of radiotherapy toxicity.
- Published in:
- 2016
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- Publication type:
- journal article
BRCA1 mutations do not increase prostate cancer risk: Results from a meta-analysis including new data.
- Published in:
- Prostate, 2011, v. 71, n. 16, p. 1768, doi. 10.1002/pros.21394
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- Publication type:
- Article
A novel ABCA12 pathologic variant identified in an Ecuadorian harlequin ichthyosis patient: A step forward in genotype‐phenotype correlations.
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- Molecular Genetics & Genomic Medicine, 2019, v. 7, n. 5, p. N.PAG, doi. 10.1002/mgg3.608
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- Publication type:
- Article
Genome-wide association study and functional follow-up identify 14q12 as a candidate risk locus for cervical cancer.
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- Human Molecular Genetics, 2022, v. 31, n. 15, p. 2483, doi. 10.1093/hmg/ddac031
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- Publication type:
- Article
A genome-wide association study of radiotherapy induced toxicity in head and neck cancer patients identifies a susceptibility locus associated with mucositis.
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- British Journal of Cancer, 2022, v. 126, n. 7, p. 1082, doi. 10.1038/s41416-021-01670-w
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- Publication type:
- Article
A genome-wide association study of radiotherapy induced toxicity in head and neck cancer patients identifies a susceptibility locus associated with mucositis.
- Published in:
- 2022
- By:
- Publication type:
- journal article
EGFR testing and clinical management of advanced NSCLC: a Galician Lung Cancer Group study (GGCP 048-10).
- Published in:
- Cancer Management & Research, 2016, v. 8, p. 11, doi. 10.2147/CMAR.S85173
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- Publication type:
- Article
Evaluation of a 5-Tier Scheme Proposed for Classification of Sequence Variants Using Bioinformatic and Splicing Assay Data: Inter-Reviewer Variability and Promotion of Minimum Reporting Guidelines.
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- Human Mutation, 2013, v. 34, n. 10, p. 1424, doi. 10.1002/humu.22388
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- Publication type:
- Article
Chromatin interactome mapping at 139 independent breast cancer risk signals.
- Published in:
- Genome Biology, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s13059-019-1877-y
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- Publication type:
- Article
Non-coding RNAs underlie genetic predisposition to breast cancer.
- Published in:
- Genome Biology, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s13059-019-1876-z
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- Publication type:
- Article
Radiogenomics Consortium Genome-Wide Association Study Meta-Analysis of Late Toxicity After Prostate Cancer Radiotherapy.
- Published in:
- 2020
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- Publication type:
- journal article
Somatic mosaicism and common genetic variation contribute to the risk of very-early-onset inflammatory bowel disease.
- Published in:
- Nature Communications, 2020, v. 11, n. 1, p. 1, doi. 10.1038/s41467-019-14275-y
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- Publication type:
- Article