Found: 22
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A high-throughput real-time PCR tissue-of-origin test to distinguish blood from lymphoblastoid cell line DNA for (epi)genomic studies.
- Published in:
- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-08663-6
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- Publication type:
- Article
Germline loss-of-function mutations in SPRED1 cause a neurofibromatosis 1–like phenotype.
- Published in:
- Nature Genetics, 2007, v. 39, n. 9, p. 1120, doi. 10.1038/ng2113
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- Publication type:
- Article
High level of inbreeding in final phase of 1000 Genomes Project.
- Published in:
- Scientific Reports, 2015, v. 5, n. 1, p. 17453, doi. 10.1038/srep17453
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- Publication type:
- Article
Genome-wide inbreeding estimation within Lebanese communities using SNP arrays.
- Published in:
- European Journal of Human Genetics, 2015, v. 23, n. 10, p. 1364, doi. 10.1038/ejhg.2014.246
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- Publication type:
- Article
Genome-wide inbreeding estimation within Lebanese communities using SNP arrays.
- Published in:
- European Journal of Human Genetics, 2015, v. 23, n. 10, p. 1434, doi. 10.1038/ejhg.2015.17
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- Publication type:
- Article
Consanguinity around the world: what do the genomic data of the HGDP-CEPH diversity panel tell us?
- Published in:
- European Journal of Human Genetics, 2011, v. 19, n. 5, p. 583, doi. 10.1038/ejhg.2010.205
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- Publication type:
- Article
Human longevity and 11p15.5: a study in 1321 centenarians.
- Published in:
- European Journal of Human Genetics, 2009, v. 17, n. 11, p. 1515, doi. 10.1038/ejhg.2009.54
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- Publication type:
- Article
Estimating the odds ratios of Crohn disease for the main CARD15/NOD2 mutations using a conditional maximum likelihood method in pedigrees collected via affected family members.
- Published in:
- European Journal of Human Genetics, 2007, v. 15, n. 8, p. 864, doi. 10.1038/sj.ejhg.5201839
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- Publication type:
- Article
Correction to: The CEPH aging cohort and biobank: a valuable collection of biological samples from exceptionally long‑lived French individuals and their offspring for longevity studies.
- Published in:
- 2024
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- Publication type:
- Correction Notice
The CEPH aging cohort and biobank: a valuable collection of biological samples from exceptionally long-lived French individuals and their offspring for longevity studies.
- Published in:
- GeroScience, 2024, v. 46, n. 2, p. 2681, doi. 10.1007/s11357-023-01037-4
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- Publication type:
- Article
Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease.
- Published in:
- Nature, 2001, v. 411, n. 6837, p. 599, doi. 10.1038/35079107
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- Publication type:
- Article
Improvements and inter-laboratory implementation and optimization of blood-based single-locus age prediction models using DNA methylation of the ELOVL2 promoter.
- Published in:
- Scientific Reports, 2020, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41598-020-72567-6
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- Publication type:
- Article
Constitutional DNA Polymorphisms Associated with the Plasma Imatinib Concentration in Chronic Myeloid Leukemia Patients.
- Published in:
- Pharmaceutics, 2024, v. 16, n. 6, p. 834, doi. 10.3390/pharmaceutics16060834
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- Publication type:
- Article
SREBF-1 gene polymorphisms are associated with obesity and type 2 diabetes in French obese and diabetic cohorts.
- Published in:
- 2004
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- Publication type:
- journal article
Major improvement in the detection of microsatellite instability in colorectal cancer using HSP110 T17 E‐<italic>ice</italic>‐COLD‐PCR.
- Published in:
- Human Mutation, 2018, v. 39, n. 3, p. 441, doi. 10.1002/humu.23379
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- Publication type:
- Article
Tumor DNA hypomethylation of LINE-1 is associated with low tumor grade of breast cancer in Tunisian patients.
- Published in:
- Oncology Letters, 2020, v. 20, n. 2, p. 1999, doi. 10.3892/ol.2020.11745
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- Publication type:
- Article
Significant linkage to spondyloarthropathy on 9q31–34.
- Published in:
- Human Molecular Genetics, 2004, v. 13, n. 15, p. 1641, doi. 10.1093/hmg/ddh179
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- Publication type:
- Article
Comparative Power of Family-Based Association Strategies to Detect Disease-Causing Variants Under Two-Locus Models.
- Published in:
- Genetic Epidemiology, 2012, v. 36, n. 8, p. 848, doi. 10.1002/gepi.21672
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- Publication type:
- Article
A new F-box protein 7 gene mutation causing typical Parkinson's disease.
- Published in:
- Movement Disorders, 2015, v. 30, n. 8, p. 1130, doi. 10.1002/mds.26266
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- Publication type:
- Article
Inbreeding Coefficient Estimation with Dense SNP Data: Comparison of Strategies and Application to HapMap III.
- Published in:
- Human Heredity, 2014, v. 77, n. 1-4, p. 49, doi. 10.1159/000358224
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- Publication type:
- Article
Could Inbred Cases Identified in GWAS Data Succeed in Detecting Rare Recessive Variants Where Affected Sib-Pairs Have Failed?
- Published in:
- Human Heredity, 2013, v. 74, n. 3/4, p. 142, doi. 10.1159/000346790
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- Publication type:
- Article
FSuite: exploiting inbreeding in dense SNP chip and exome data.
- Published in:
- Bioinformatics, 2014, v. 30, n. 13, p. 1940, doi. 10.1093/bioinformatics/btu149
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- Publication type:
- Article