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Identifying latent genetic interactions in genome-wide association studies using multiple traits.
- Published in:
- Genome Medicine, 2024, v. 16, n. 1, p. 1, doi. 10.1186/s13073-024-01329-0
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- Article
The role of admixture in the rare variant contribution to inflammatory bowel disease.
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- Genome Medicine, 2023, v. 15, n. 1, p. 1, doi. 10.1186/s13073-023-01244-w
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- Article
Rare variant modifier analysis identifies variants in SEC24D associated with orofacial cleft subtypes.
- Published in:
- Human Genetics, 2023, v. 142, n. 10, p. 1531, doi. 10.1007/s00439-023-02596-4
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- Article
Evaluation of AQP4 functional variants and its association with fragile X-associated tremor/ataxia syndrome.
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- Frontiers in Aging Neuroscience, 2023, v. 14, p. 1, doi. 10.3389/fnagi.2022.1073258
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- Article
Longitudinal DNA methylation profiling of the rectal mucosa identifies cell-specific signatures of disease status, severity and clinical outcomes in ulcerative colitis cell-specific DNA methylation signatures of UC.
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- Clinical Epigenetics, 2023, v. 15, n. 1, p. 1, doi. 10.1186/s13148-023-01462-4
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- Article
Characterization of Intestinal Mesenchymal Stromal Cells From Patients With Inflammatory Bowel Disease for Autologous Cell Therapy.
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- Stem Cells Translational Medicine, 2023, v. 12, n. 2, p. 112, doi. 10.1093/stcltm/szad003
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- Article
Methylation quantitative trait loci are largely consistent across disease states in Crohn's disease.
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- G3: Genes | Genomes | Genetics, 2022, v. 12, n. 4, p. 1, doi. 10.1093/g3journal/jkac041
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- Article
Profiling non-coding RNA levels with clinical classifiers in pediatric Crohn's disease.
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- BMC Medical Genomics, 2021, v. 14, n. 1, p. 1, doi. 10.1186/s12920-021-01041-7
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- Article
Author Correction: Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome.
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- 2021
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- Correction Notice
Sex-specific recombination patterns predict parent of origin for recurrent genomic disorders.
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- BMC Medical Genomics, 2021, v. 14, n. 1, p. 1, doi. 10.1186/s12920-021-00999-8
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- Article
Identifying novel causal genes and proteins in Alzheimer's disease: Genetics/genetic factors of Alzheimer's disease.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2020, v. 16, n. 11, p. 1, doi. 10.1002/alz.043523
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- Article
Integrating human brain proteomes and genome‐wide association results implicates new genes in Alzheimer's disease: Functionalizing genetic variants in Alzheimer's disease.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2020, v. 16, n. 11, p. 1, doi. 10.1002/alz.043865
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- Article
Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome.
- Published in:
- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-74650-4
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- Article
Leveraging Family History in Case-Control Analyses of Rare Variation.
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- Genetics, 2020, v. 214, n. 2, p. 295, doi. 10.1534/genetics.119.302846
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- Article
Association of Early-Onset Alzheimer Disease With Elevated Low-Density Lipoprotein Cholesterol Levels and Rare Genetic Coding Variants of APOB.
- Published in:
- JAMA Neurology, 2019, v. 76, n. 7, p. 809, doi. 10.1001/jamaneurol.2019.0648
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- Article
Neutrophil GM-CSF signaling in inflammatory bowel disease patients is influenced by non-coding genetic variants.
- Published in:
- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-45701-2
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- Article
Bystro: rapid online variant annotation and natural-language filtering at whole-genome scale.
- Published in:
- Genome Biology, 2018, v. 19, p. 1, doi. 10.1186/s13059-018-1387-3
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- Article
Analysis of Copy Number Variants on Chromosome 21 in Down Syndrome-Associated Congenital Heart Defects.
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- G3: Genes | Genomes | Genetics, 2018, v. 8, n. 1, p. 105, doi. 10.1534/g3.117.300366
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- Article
Testing Two Evolutionary Theories of Human Aging with DNA Methylation Data.
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- Genetics, 2017, v. 207, n. 4, p. 1547, doi. 10.1534/genetics.117.300217
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- Publication type:
- Article
MPD: multiplex primer design for next-generation targeted sequencing.
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- BMC Bioinformatics, 2017, v. 18, p. 1, doi. 10.1186/s12859-016-1453-3
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- Article
Genome-Wide Association Study of Down Syndrome-Associated Atrioventricular Septal Defects.
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- G3: Genes | Genomes | Genetics, 2015, v. 5, n. 10, p. 1961, doi. 10.1534/g3.115.019943
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- Article
Dissecting Allele Architecture of Early Onset IBD Using High-Density Genotyping.
- Published in:
- PLoS ONE, 2015, v. 10, n. 6, p. 1, doi. 10.1371/journal.pone.0128074
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- Article
Population Genetics Identifies Challenges in Analyzing Rare Variants.
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- Genetic Epidemiology, 2015, v. 39, n. 3, p. 145, doi. 10.1002/gepi.21881
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- Article
A Comprehensive Search for Recombinogenic Motifs in the Human Genome.
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- PLoS ONE, 2013, v. 8, n. 4, p. 1, doi. 10.1371/journal.pone.0062920
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- Article
Excess variants in AFF2 detected by massively parallel sequencing of males with autism spectrum disorder.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 19, p. 4356, doi. 10.1093/hmg/dds267
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- Article
Genistein cooperates with the histone deacetylase inhibitor vorinostat to induce cell death in prostate cancer cells.
- Published in:
- BMC Cancer, 2012, v. 12, n. 1, p. 145, doi. 10.1186/1471-2407-12-145
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- Article
A model of binding on DNA microarrays: understanding the combined effect of probe synthesis failure, cross-hybridization, DNA fragmentation and other experimental details of affymetrix arrays.
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- BMC Genomics, 2012, v. 13, n. 1, p. 737, doi. 10.1186/1471-2164-13-737
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- Article
Identification of rare X-linked neuroligin variants by massively parallel sequencing in males with autism spectrum disorder.
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- Molecular Autism, 2012, v. 3, n. 1, p. 8, doi. 10.1186/2040-2392-3-8
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- Article
The Heritability of Amyotrophic Lateral Sclerosis in a Clinically Ascertained United States Research Registry.
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- PLoS ONE, 2011, v. 6, n. 11, p. 1, doi. 10.1371/journal.pone.0027985
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- Article
Pure drug nanoparticles in tablets: what are the dissolution limitations?
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- Journal of Nanoparticle Research, 2010, v. 12, n. 5, p. 1743, doi. 10.1007/s11051-009-9759-y
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- Article
Array-Based FMR1 Sequencing and Deletion Analysis in Patients with a Fragile X Syndrome-Like Phenotype.
- Published in:
- PLoS ONE, 2010, v. 5, n. 3, p. 1, doi. 10.1371/journal.pone.0009476
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- Article
Empirical Evaluation of Oligonucleotide Probe Selection for DNA Microarrays.
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- PLoS ONE, 2010, v. 5, n. 3, p. 1, doi. 10.1371/journal.pone.0009921
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- Article
SeqAnt: A web service to rapidly identify and annotate DNA sequence variations.
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- BMC Bioinformatics, 2010, v. 11, p. 471, doi. 10.1186/1471-2105-11-471
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- Article
Variation in the Lymphotoxin-α/Tumor Necrosis Factor Locus Modifies Risk of Erythema Nodosum in Sarcoidosis.
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- Journal of Investigative Dermatology, 2009, v. 129, n. 8, p. 1921, doi. 10.1038/jid.2008.456
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- Article
Origins, distribution and expression of the Duarte-2 (D2) allele of galactose-1-phosphate uridylyltransferase.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 9, p. 1624, doi. 10.1093/hmg/ddp080
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- Article
Interaction between a novel TGFB1 haplotype and CFTR genotype is associated with improved lung function in cystic fibrosis.
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- Human Molecular Genetics, 2008, v. 17, n. 14, p. 2228, doi. 10.1093/hmg/ddn123
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- Article
Microarray-based genomic selection for high-throughput resequencing.
- Published in:
- Nature Methods, 2007, v. 4, n. 11, p. 907, doi. 10.1038/nmeth1109
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- Article
Population Bottlenecks as a Potential Major Shaping Force of Human Genome Architecture.
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- PLoS Genetics, 2007, v. 3, n. 7, p. e119, doi. 10.1371/journal.pgen.0030119
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- Article
Genomic alterations in cultured human embryonic stem cells.
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- Nature Genetics, 2005, v. 37, n. 10, p. 1099, doi. 10.1038/ng1631
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- Article
A common sex-dependent mutation in a RET enhancer underlies Hirschsprung disease risk.
- Published in:
- Nature, 2005, v. 434, n. 7035, p. 857, doi. 10.1038/nature03467
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- Article
Exhaustive allelic transmission disequilibrium tests as a new approach to genome-wide association studies.
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- Nature Genetics, 2004, v. 36, n. 11, p. 1181, doi. 10.1038/ng1457
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- Article
Discrepancies in dbSNP confirmation rates and allele frequency distributions from varying genotyping error rates and patterns.
- Published in:
- Bioinformatics, 2004, v. 20, n. 7, p. 1022, doi. 10.1093/bioinformatics/bth034
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- Article
Aberrant Gating of Photic Input to the Suprachiasmatic Circadian Pacemaker of Mice Lacking the VPAC<sub>2</sub> Receptor.
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- Journal of Neuroscience, 2004, v. 24, n. 14, p. 3522, doi. 10.1523/JNEUROSCI.5345-03.2004
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- Article
Mometasone furoate degradation and metabolism in human biological fluids and tissues.
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- Biopharmaceutics & Drug Disposition, 2003, v. 24, n. 8, p. 321, doi. 10.1002/bdd.362
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- Article
Heterozygous mutations in BBS1, BBS2 and BBS6 have a potential epistatic effect on Bardet–Biedl patients with two mutations at a second BBS locus.
- Published in:
- Human Molecular Genetics, 2003, v. 12, n. 14, p. 1651, doi. 10.1093/hmg/ddg188
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- Article
Selective descriptor pruning for QSAR/QSPR studies using artificial neural networks.
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- Journal of Computational Chemistry, 2003, v. 24, n. 7, p. 891
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- Article
The mouse VPAC<sub>2</sub> receptor confers suprachiasmatic nuclei cellular rhythmicity and responsiveness to vasoactive intestinal polypeptide in vitro.
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- European Journal of Neuroscience, 2003, v. 17, n. 2, p. 197, doi. 10.1046/j.1460-9568.2003.02425.x
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- Publication type:
- Article
Distribution of substance P and neurokinin-1 receptor immunoreactivity in the suprachiasmatic nuclei and intergeniculate leaflet of hamster, mouse, and rat.
- Published in:
- Journal of Comparative Neurology, 2001, v. 438, n. 1, p. 50, doi. 10.1002/cne.1301
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- Article
Vasoactive intestinal polypeptide (VIP) phase-shifts the rat suprachiasmatic nucleus clock in vitro.
- Published in:
- European Journal of Neuroscience, 2001, v. 13, n. 4, p. 839, doi. 10.1046/j.0953-816X.2000.01437.x
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- Article
The hypothalamus and the regulation of energy homeostasis: lifting the lid on a black box.
- Published in:
- Proceedings of the Nutrition Society, 2000, v. 59, n. 3, p. 385, doi. 10.1017/S0029665100000434
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- Article