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Rare Variant Testing of Imputed Data: An Analysis Pipeline Typified.
- Published in:
- Human Heredity, 2015, v. 78, n. 3/4, p. 164, doi. 10.1159/000368676
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- Article
Integrated Genome-Wide Pathway Association Analysis with INTERSNP.
- Published in:
- Human Heredity, 2012, v. 73, n. 2, p. 63, doi. 10.1159/000336196
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- Article
Selected variants of the steroid-5-alpha-reductase isoforms SRD5A1 and SRD5A2 and the sex steroid hormone receptors ESR1, ESR2 and PGR: No association with female pattern hair loss identified.
- Published in:
- Experimental Dermatology, 2012, v. 21, n. 5, p. 390, doi. 10.1111/j.1600-0625.2012.01469.x
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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.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 24, p. 6644
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- Article
Publisher Correction: Identification and characterization of two functional variants in the human longevity gene FOXO3.
- Published in:
- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-02842-8
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- Article
Identification and characterization of two functional variants in the human longevity gene FOXO3.
- Published in:
- Nature Communications, 2017, v. 8, n. 1, p. 1, doi. 10.1038/s41467-017-02183-y
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- Article
Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness.
- Published in:
- Nature Communications, 2017, v. 8, n. 3, p. 14694, doi. 10.1038/ncomms14694
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- Article
Novel genetic matching methods for handling population stratification in genome-wide association studies.
- Published in:
- BMC Bioinformatics, 2015, v. 16, n. 1, p. 1, doi. 10.1186/s12859-015-0521-4
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- Article
Novel genetic matching methods for handling population stratification in genome-wide association studies.
- Published in:
- BMC Bioinformatics, 2015, v. 16, n. 1, p. 1, doi. 10.1186/s12859-015-0521-4
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- Publication type:
- Article
Quick, "Imputation-free" meta-analysis with proxy-SNPs.
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- BMC Bioinformatics, 2012, v. 13, n. 1, p. 231, doi. 10.1186/1471-2105-13-231
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- Article
Ancient DNA study reveals HLA susceptibility locus for leprosy in medieval Europeans.
- Published in:
- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-03857-x
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- Article
Genome-wide association study using cerebrospinal fluid biomarkers beta-amyloid-42 and pTau181 in German samples of Alzheimer's disease
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- 2012
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- Abstract
Exome sequencing identifies potential novel candidate genes in patients with unexplained colorectal adenomatous polyposis.
- Published in:
- Familial Cancer, 2016, v. 15, n. 2, p. 281, doi. 10.1007/s10689-016-9870-z
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- Article
Expanding the genetic architecture of nicotine dependence and its shared genetics with multiple traits.
- Published in:
- Nature Communications, 2020, v. 11, n. 1, p. N.PAG, doi. 10.1038/s41467-020-19265-z
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- Article
A One-Degree-of-Freedom Test for Supra-Multiplicativity of SNP Effects.
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- PLoS ONE, 2013, v. 8, n. 10, p. 1, doi. 10.1371/journal.pone.0078038
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- Article
High-Throughput miRNA and mRNA Sequencing of Paired Colorectal Normal, Tumor and Metastasis Tissues and Bioinformatic Modeling of miRNA-1 Therapeutic Applications.
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- PLoS ONE, 2013, v. 8, n. 7, p. 1, doi. 10.1371/journal.pone.0067461
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- Publication type:
- Article
PLD3 in non-familial Alzheimer's disease.
- Published in:
- Nature, 2015, v. 520, n. 7545, p. E3, doi. 10.1038/nature14039
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- Article
A genome-wide association meta-analysis implicates Hedgehog and Notch signaling in Dupuytren's disease.
- Published in:
- Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-023-44451-0
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- Publication type:
- Article
METAINTER: meta-analysis of multiple regression models in genome-wide association studies.
- Published in:
- Bioinformatics, 2015, v. 31, n. 2, p. 151, doi. 10.1093/bioinformatics/btu629
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- Article
Androgenetic Alopecia: Identification of Four Genetic Risk Loci and Evidence for the Contribution of WNT Signaling to Its Etiology.
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- Journal of Investigative Dermatology, 2013, v. 133, n. 6, p. 1489, doi. 10.1038/jid.2013.43
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- Article
Investigation of four novel male androgenetic alopecia susceptibility loci: no association with female pattern hair loss.
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- Archives of Dermatological Research, 2014, v. 306, n. 4, p. 413, doi. 10.1007/s00403-013-1436-4
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- Article
Selected variants of the melanocortin 4 receptor gene ( MC4R) do not confer susceptibility to female pattern hair loss.
- Published in:
- Archives of Dermatological Research, 2013, v. 305, n. 3, p. 249, doi. 10.1007/s00403-012-1296-3
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- Article
Identification of de novo variants in nonsyndromic cleft lip with/without cleft palate patients with low polygenic risk scores.
- Published in:
- Molecular Genetics & Genomic Medicine, 2023, v. 11, n. 3, p. 1, doi. 10.1002/mgg3.2109
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- Article
Exome sequencing characterizes the somatic mutation spectrum of early serrated lesions in a patient with serrated polyposis syndrome (SPS).
- Published in:
- Hereditary Cancer in Clinical Practice, 2017, v. 15, p. 1, doi. 10.1186/s13053-017-0082-9
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- Article