| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
African vs. Caucasian and Asian difference for the association of interleukin-10 promotor polymorphisms with type 2 diabetes mellitus (a meta-analysis study)
|
Tarabay, Mohammad
|
|
2016
|
9 |
C |
p. 10-17
8 p.
|
artikel
|
| 2 |
An enhanced version of Cochran-Armitage trend test for genome-wide association studies
|
Ghodsi, Mansi
|
|
2016
|
9 |
C |
p. 225-229
5 p.
|
artikel
|
| 3 |
A novel de novo mutation in DYNC1H1 gene underlying malformation of cortical development and cataract
|
Hertecant, Jozef
|
|
2016
|
9 |
C |
p. 124-127
4 p.
|
artikel
|
| 4 |
Apolipoprotein C3 gene variants and the risk of coronary heart disease: A meta-analysis
|
Li, Yan
|
|
2016
|
9 |
C |
p. 104-109
6 p.
|
artikel
|
| 5 |
Association between GNB3 c.825C>T polymorphism and the risk of overweight and obesity: A meta-analysis
|
Li, Hui-Lan
|
|
2016
|
9 |
C |
p. 18-25
8 p.
|
artikel
|
| 6 |
Association of adiponectin receptor 1 gene −106 C>T variant with susceptibility to colorectal cancer
|
Mahmoudi, Touraj
|
|
2016
|
9 |
C |
p. 210-214
5 p.
|
artikel
|
| 7 |
Association of EVI5 rs11808092, CD58 rs2300747, and CIITA rs3087456 polymorphisms with multiple sclerosis risk: A meta-analysis
|
Liu, Jiahe
|
|
2016
|
9 |
C |
p. 97-103
7 p.
|
artikel
|
| 8 |
Association of G894T eNOS, 4G/5G PAI and T1131C APOA5 polymorphisms with susceptibility to myocardial infarction in Morocco
|
Hassani Idrissi, Hind
|
|
2016
|
9 |
C |
p. 56-61
6 p.
|
artikel
|
| 9 |
Association of TFAP2A gene polymorphism with susceptibility to non-syndromic cleft lip with or without palate risk in south Indian population
|
Babu Gurramkonda, Venkatesh
|
|
2016
|
9 |
C |
p. 181-184
4 p.
|
artikel
|
| 10 |
Association of TLR and TREM-1 gene polymorphisms with atherosclerosis severity in a Russian population
|
Kutikhin, Anton G.
|
|
2016
|
9 |
C |
p. 76-89
14 p.
|
artikel
|
| 11 |
Combined sequence and sequence-structure based methods for analyzing FGF23, CYP24A1 and VDR genes
|
Nagamani, Selvaraman
|
|
2016
|
9 |
C |
p. 26-36
11 p.
|
artikel
|
| 12 |
Editorial Board
|
|
|
2016
|
9 |
C |
p. i-
1 p.
|
artikel
|
| 13 |
Effect of RAS status on anti-EGFR monoclonal antibodies+5-FU infusion-based chemotherapy in first-line treatment of metastatic colorectal cancer: A meta-analysis
|
Zhou, Mingyi
|
|
2016
|
9 |
C |
p. 110-119
10 p.
|
artikel
|
| 14 |
ERBB3-rs2292239 as primary type 1 diabetes association locus among non-HLA genes in Chinese
|
Sun, Chengjun
|
|
2016
|
9 |
C |
p. 120-123
4 p.
|
artikel
|
| 15 |
Identification of a novel WFS1 homozygous nonsense mutation in Jordanian children with Wolfram syndrome
|
Bodoor, Khaldon
|
|
2016
|
9 |
C |
p. 219-224
6 p.
|
artikel
|
| 16 |
Identification of novel splice site mutation IVS9+1(G>A) and novel complex allele G355R/R359X in Type 1 Gaucher patients heterozygous for mutation N370S
|
Hoitsema, Kourtnee
|
|
2016
|
9 |
C |
p. 47-51
5 p.
|
artikel
|
| 17 |
Identification of TRPCs genetic variants that modify risk for lung cancer based on the pathway and two-stage study
|
Zhang, Zili
|
|
2016
|
9 |
C |
p. 191-196
6 p.
|
artikel
|
| 18 |
Impact of CYP2C9, VKORC1 and CYP4F2 genetic polymorphisms on maintenance warfarin dosage in Han-Chinese patients: A systematic review and meta-analysis
|
Zhang, Jinhua
|
|
2016
|
9 |
C |
p. 197-209
13 p.
|
artikel
|
| 19 |
Influence of cytokine and cytokine receptor gene polymorphisms on the degree of liver damage in patients with chronic hepatitis C
|
Moreira, Sara Tatiana
|
|
2016
|
9 |
C |
p. 90-96
7 p.
|
artikel
|
| 20 |
Inherited Xq13.2-q21.31 duplication in a boy with recurrent seizures and pubertal gynecomastia: Clinical, chromosomal and aCGH characterization
|
Linhares, Natália D.
|
|
2016
|
9 |
C |
p. 185-190
6 p.
|
artikel
|
| 21 |
In silico analysis of deleterious single nucleotide polymorphisms in human BUB1 mitotic checkpoint serine/threonine kinase B gene
|
Akhoundi, Fatemeh
|
|
2016
|
9 |
C |
p. 142-150
9 p.
|
artikel
|
| 22 |
Interleukin 10 (−1082 G/A) and (−819 C/T) gene polymorphisms in Egyptian women with polycystic ovary syndrome (PCOS)
|
Talaat, Roba M.
|
|
2016
|
9 |
C |
p. 254-258
5 p.
|
artikel
|
| 23 |
Interleukin-18 gene promoter 607A polymorphism, but not 137C polymorphism, is a protective factor for ischemic stroke in the Chinese population: A meta-analysis
|
Zhang, Ming-Jie
|
|
2016
|
9 |
C |
p. 165-172
8 p.
|
artikel
|
| 24 |
Investigating regulatory signatures of human autophagy related gene 5 (ATG5) through functional in silico analysis
|
Vij, Avni
|
|
2016
|
9 |
C |
p. 237-248
12 p.
|
artikel
|
| 25 |
MMP3 and TIMP2 gene variants as predisposing factors for Achilles tendon pathologies: Attempted replication study in a British case–control cohort
|
El Khoury, Louis
|
|
2016
|
9 |
C |
p. 52-55
4 p.
|
artikel
|
| 26 |
Molecular evolution of WDR62, a gene that regulates neocorticogenesis
|
Pervaiz, Nashaiman
|
|
2016
|
9 |
C |
p. 1-9
9 p.
|
artikel
|
| 27 |
Nucleotide polymorphisms and protein structure changes in the Fg16 gene of Fusarium graminearum sensu stricto
|
Abedi-Tizaki, Mostafa
|
|
2016
|
9 |
C |
p. 62-69
8 p.
|
artikel
|
| 28 |
Polymorphisms of apolipoprotein E and aneurysmal subarachnoid haemorrhage: A meta-analysis
|
Arati, S.
|
|
2016
|
9 |
C |
p. 151-158
8 p.
|
artikel
|
| 29 |
Rapid and ultra-rapid metabolizers with CYP2C19*17 polymorphism do not respond to standard therapy with proton pump inhibitors
|
Deshpande, Neha
|
|
2016
|
9 |
C |
p. 159-164
6 p.
|
artikel
|
| 30 |
Relationship between MTHFR C677T and A1298C gene polymorphisms and complications of type 2 diabetes mellitus in an Emirati population
|
El Hajj Chehadeh, Sarah W.
|
|
2016
|
9 |
C |
p. 70-75
6 p.
|
artikel
|
| 31 |
Sequence analysis of Meq oncogene among Indian isolates of Marek's disease herpesvirus
|
Gupta, Mridula
|
|
2016
|
9 |
C |
p. 230-236
7 p.
|
artikel
|
| 32 |
TNF-α − 308 G > A and IFN-γ + 874 A>T gene polymorphisms in Egyptian patients with lupus erythematosus
|
Al-Kholy, Wfaa
|
|
2016
|
9 |
C |
p. 137-141
5 p.
|
artikel
|
| 33 |
Tumor necrosis factor-α (TNF-α)-308G/A promoter polymorphism in colorectal cancer in ethnic Kashmiri population — A case control study in a detailed perspective
|
Banday, Mujeeb Zafar
|
|
2016
|
9 |
C |
p. 128-136
9 p.
|
artikel
|
| 34 |
Two gene polymorphisms (rs4977756 and rs11515) in CDKN2A/B and glioma risk in South Indian population
|
Sibin, M.K.
|
|
2016
|
9 |
C |
p. 215-218
4 p.
|
artikel
|
| 35 |
Variants of resistin gene and the risk of idiopathic dilated cardiomyopathy in Pakistan
|
Hussain, Sabir
|
|
2016
|
9 |
C |
p. 37-41
5 p.
|
artikel
|
| 36 |
Vascular endothelial growth factor gene polymorphisms and association with age related macular degeneration in Indian patients
|
Gupta, Divya
|
|
2016
|
9 |
C |
p. 249-253
5 p.
|
artikel
|
| 37 |
Vitamin D receptor gene polymorphism in Egyptian pediatric acute lymphoblastic leukemia correlation with BMD
|
Tantawy, Maha
|
|
2016
|
9 |
C |
p. 42-46
5 p.
|
artikel
|
| 38 |
Vitellogenin knockdown strongly affects cotton boll weevil egg viability but not the number of eggs laid by females
|
Coelho, Roberta R.
|
|
2016
|
9 |
C |
p. 173-180
8 p.
|
artikel
|
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