Found: 27
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National data on the early clinical use of non‐invasive prenatal testing in public and private healthcare in Denmark 2013–2017.
- Published in:
- Acta Obstetricia et Gynecologica Scandinavica, 2021, v. 100, n. 5, p. 884, doi. 10.1111/aogs.14052
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- Publication type:
- Article
Total number of reads affects the accuracy of fetal fraction estimates in NIPT.
- Published in:
- Molecular Genetics & Genomic Medicine, 2021, v. 9, n. 4, p. 1, doi. 10.1002/mgg3.1653
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- Publication type:
- Article
17q12 deletion and duplication syndrome in Denmark-A clinical cohort of 38 patients and review of the literature.
- Published in:
- American Journal of Medical Genetics. Part A, 2016, v. 170A, n. 11, p. 2934, doi. 10.1002/ajmg.a.37848
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- Publication type:
- Article
Prostaglandin E<sub>2</sub>‐EP<sub>3</sub> receptor subtype gene deletion in mother and son impairs platelet aggregation.
- Published in:
- British Journal of Haematology, 2019, v. 184, n. 5, p. 851, doi. 10.1111/bjh.15196
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- Publication type:
- Article
Genomic Analyses of Breast Cancer Progression Reveal Distinct Routes of Metastasis Emergence.
- Published in:
- Scientific Reports, 2017, p. 43813, doi. 10.1038/srep43813
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- Publication type:
- Article
Linkage of atopic dermatitis to chromosomes 4q22, 3p24 and 3q21.
- Published in:
- Human Genetics, 2009, v. 126, n. 4, p. 549, doi. 10.1007/s00439-009-0692-z
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- Publication type:
- Article
The relationship of glutathione-S-transferases copy number variation and indoor air pollution to symptoms and markers of respiratory disease.
- Published in:
- Clinical Respiratory Journal, 2012, v. 6, n. 3, p. 175, doi. 10.1111/j.1752-699X.2011.00258.x
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- Publication type:
- Article
Genetic polymorphisms in antioxidative enzymes are associated to forced expiratory volume in 1 s (FEV<sub>1</sub>) in smokers independently of asthma.
- Published in:
- Clinical Respiratory Journal, 2012, v. 6, n. 1, p. 46, doi. 10.1111/j.1752-699X.2011.00245.x
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- Publication type:
- Article
A BRCA2 mutation incorrectly mapped in the original BRCA2 reference sequence, is a common West Danish founder mutation disrupting mRNA splicing.
- Published in:
- Breast Cancer Research & Treatment, 2011, v. 128, n. 1, p. 179, doi. 10.1007/s10549-010-1272-6
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- Publication type:
- Article
Deletion of T-type calcium channels Ca3.1 or Ca3.2 attenuates endothelial dysfunction in aging mice.
- Published in:
- Pflügers Archiv: European Journal of Physiology, 2018, v. 470, n. 2, p. 355, doi. 10.1007/s00424-017-2068-x
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- Publication type:
- Article
Heme oxygenase 1 polymorphism, occupational vapor, gas, dust, and fume exposure and chronic obstructive pulmonary disease in a Danish population-based study.
- Published in:
- Scandinavian Journal of Work, Environment & Health, 2020, v. 46, n. 1, p. 96, doi. 10.5271/sjweh.3846
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- Publication type:
- Article
Quantification of morphine, morphine 6-glucuronide, buprenorphine, and the enantiomers of methadone by enantioselective mass spectrometric chromatography in whole blood.
- Published in:
- Forensic Science, Medicine & Pathology, 2015, v. 11, n. 2, p. 193, doi. 10.1007/s12024-015-9673-9
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- Publication type:
- Article
Mono‐allelic loss of YTHDF3 and neurodevelopmental disorder: clinical features of four individuals with 8q12.3 deletions.
- Published in:
- Clinical Genetics, 2022, v. 101, n. 2, p. 208, doi. 10.1111/cge.14083
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- Publication type:
- Article
ZMYND11 variants are a novel cause of centrotemporal and generalised epilepsies with neurodevelopmental disorder.
- Published in:
- Clinical Genetics, 2021, v. 100, n. 4, p. 412, doi. 10.1111/cge.14023
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- Publication type:
- Article
A new 1p36.13‐1p36.12 microdeletion syndrome characterized by learning disability, behavioral abnormalities, and ptosis.
- Published in:
- Clinical Genetics, 2020, v. 97, n. 6, p. 927, doi. 10.1111/cge.13739
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- Publication type:
- Article
A candidate gene study of serotonergic pathway genes and pain relief during treatment with escitalopram in patients with neuropathic pain shows significant association to serotonin receptor2C (HTR2C)
- Published in:
- 2011
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- Publication type:
- Journal Article
A candidate gene study of serotonergic pathway genes and pain relief during treatment with escitalopram in patients with neuropathic pain shows significant association to serotonin receptor2C (HTR2C).
- Published in:
- European Journal of Clinical Pharmacology, 2011, v. 67, n. 11, p. 1131, doi. 10.1007/s00228-011-1056-x
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- Publication type:
- Article
Retrospective study of the impact of pharmacogenetic variants on paclitaxel toxicity and survival in patients with ovarian cancer.
- Published in:
- European Journal of Clinical Pharmacology, 2011, v. 67, n. 7, p. 693, doi. 10.1007/s00228-011-1007-6
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- Publication type:
- Article
Linkage disequilibrium between the CYP2C19*17 allele and wildtype CYP2C8 and CYP2C9 alleles: identification of CYP2C haplotypes in healthy Nordic populations.
- Published in:
- European Journal of Clinical Pharmacology, 2010, v. 66, n. 12, p. 1199, doi. 10.1007/s00228-010-0864-8
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- Publication type:
- Article
Impact of ABCB1 Variants on Neutrophil Depression: A Pharmacogenomic Study of Paclitaxel in 92 Women with Ovarian Cancer.
- Published in:
- Basic & Clinical Pharmacology & Toxicology, 2012, v. 110, n. 2, p. 199, doi. 10.1111/j.1742-7843.2011.00802.x
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- Publication type:
- Article
Association of serum surfactant protein D and SFTPD gene variants with asthma in Danish children, adolescents, and young adults.
- Published in:
- Immunity, Inflammation & Disease, 2022, v. 10, n. 2, p. 189, doi. 10.1002/iid3.560
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- Publication type:
- Article
S100A14 is a novel independent prognostic biomarker in the triple-negative breast cancer subtype.
- Published in:
- International Journal of Cancer, 2015, v. 137, n. 9, p. 2093, doi. 10.1002/ijc.29582
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- Publication type:
- Article
Comprehensive prenatal diagnostics: Exome versus genome sequencing.
- Published in:
- Prenatal Diagnosis, 2023, v. 43, n. 9, p. 1132, doi. 10.1002/pd.6402
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- Publication type:
- Article
Possible gene dosage effect of glutathione-S-transferases on atopic asthma: Using real-time PCR for quantification of GSTM1 and GSTT1 gene copy numbers.
- Published in:
- Human Mutation, 2004, v. 24, n. 3, p. 208, doi. 10.1002/humu.20074
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- Publication type:
- Article
CD18 is redundant for the response to multiple vaccines: A case study.
- Published in:
- 2019
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- Publication type:
- Case Study
Genotype-Phenotype Comparison in POGZ-Related Neurodevelopmental Disorders by Using Clinical Scoring.
- Published in:
- Genes, 2022, v. 13, n. 1, p. 154, doi. 10.3390/genes13010154
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- Publication type:
- Article
The ABCB1, rs9282564, AG and TT Genotypes and the COMT, rs4680, AA Genotype are Less Frequent in Deceased Patients with Opioid Addiction than in Living Patients with Opioid Addiction.
- Published in:
- Basic & Clinical Pharmacology & Toxicology, 2016, v. 119, n. 4, p. 381, doi. 10.1111/bcpt.12602
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- Publication type:
- Article