Genetic role of CYP4A11 polymorphisms in the risk of developing cardiovascular and cerebrovascular diseases.
- Published in:
- Annals of Human Genetics, 2018, v. 82, n. 6, p. 370, doi. 10.1111/ahg.12280
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- Publication type:
- Article
Works matching IS 00034800 AND DT 2018 AND VI 82 AND IP 6
Results: 16
1
2
Deletion at 12q12 increases the risk of developmental delay and intellectual disability.
- Published in:
- Annals of Human Genetics, 2018, v. 82, n. 6, p. 482, doi. 10.1111/ahg.12279
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- Publication type:
- Article
3
Genotype–phenotype correlation and the size of microdeletion or microduplication of 7q11.23 region in patients with Williams‐Beuren syndrome.
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- Annals of Human Genetics, 2018, v. 82, n. 6, p. 469, doi. 10.1111/ahg.12278
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- Publication type:
- Article
4
Potential dysfunctional effects of synonymous variants: Insights from an exhaustive in silico analysis of the ABCB4 gene.
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- Annals of Human Genetics, 2018, v. 82, n. 6, p. 457, doi. 10.1111/ahg.12276
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- Publication type:
- Article
5
Uncommon IFITM5 mutation associated with severe skeletal deformity in osteogenesis imperfecta.
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- Annals of Human Genetics, 2018, v. 82, n. 6, p. 477, doi. 10.1111/ahg.12275
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- Publication type:
- Article
6
Genetic susceptibility of glutathione S‐transferase genes (GSTM1/T1 and P1) to coronary artery disease in Asian Indians.
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- Annals of Human Genetics, 2018, v. 82, n. 6, p. 448, doi. 10.1111/ahg.12274
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- Publication type:
- Article
7
Analysis of causal effect of APOA5 variants on premature coronary artery disease.
- Published in:
- Annals of Human Genetics, 2018, v. 82, n. 6, p. 437, doi. 10.1111/ahg.12273
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- Publication type:
- Article
8
Neurofibromatosis type I: mutation spectrum of NF1 in spanish patients.
- Published in:
- Annals of Human Genetics, 2018, v. 82, n. 6, p. 425, doi. 10.1111/ahg.12272
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- Publication type:
- Article
9
CRISPR‐Cas9: A cornerstone for the evolution of precision medicine.
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- Annals of Human Genetics, 2018, v. 82, n. 6, p. 331, doi. 10.1111/ahg.12271
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- Publication type:
- Article
10
CHRNA3 rs1051730 and CHRNA5 rs16969968 polymorphisms are associated with heavy smoking, lung cancer, and chronic obstructive pulmonary disease in a mexican population.
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- Annals of Human Genetics, 2018, v. 82, n. 6, p. 415, doi. 10.1111/ahg.12264
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- Publication type:
- Article
11
Polymorphisms of dopamine receptor genes DRD2 and DRD4 in African populations of Hadza and Datoga differing in the level of culturally permitted aggression.
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- Annals of Human Genetics, 2018, v. 82, n. 6, p. 407, doi. 10.1111/ahg.12263
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- Article
12
Association of CTLA‐4 polymorphisms with increased risks of myasthenia gravis.
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- Annals of Human Genetics, 2018, v. 82, n. 6, p. 358, doi. 10.1111/ahg.12262
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- Publication type:
- Article
13
An approach to estimate bidirectional mediation effects with application to body mass index and fasting glucose.
- Published in:
- Annals of Human Genetics, 2018, v. 82, n. 6, p. 396, doi. 10.1111/ahg.12261
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- Publication type:
- Article
14
Joint analysis of multiple phenotypes in association studies using allele‐based clustering approach for non‐normal distributions.
- Published in:
- Annals of Human Genetics, 2018, v. 82, n. 6, p. 389, doi. 10.1111/ahg.12260
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- Publication type:
- Article
15
The association of LRP6 rs2302685 (V1062I) polymorphism with the risk of hyperlipidemia in Iranian children and adolescents.
- Published in:
- Annals of Human Genetics, 2018, v. 82, n. 6, p. 382, doi. 10.1111/ahg.12254
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- Publication type:
- Article
16
Issue Information.
- Published in:
- Annals of Human Genetics, 2018, v. 82, n. 6, p. 1, doi. 10.1111/ahg.12219
- Publication type:
- Article