1.
Susceptibility background for type 2 diabetes in eleven Mexican Indigenous populations: HNF4A gene analysis
by Granados-Silvestre, M. A
Molecular genetics and genomics : MGG, 2017-07-07, Vol.292 (6), p.1209-1219
2.
The association of glutathione-S-transferase gene polymorphisms (GSTM1, GSTT1, GSTP1) with idiopathic male infertility
by Safarinejad, Mohammad Reza
Journal of human genetics, 2010-09, Vol.55 (9), p.565-570
3.
MHC-DRB1 exon 2 polymorphism and its association with mycoplasma ovipneumonia resistance or susceptibility genotypes in sheep
by Wang, Kaisheng
Journal of genetics, 2020-03-06, Vol.99 (1)
4.
Novel mutation in UMPS gene leads to false positive result of DUMPS (genetic disorder) in buffaloes: need for gene sequencing before confirming results of RFLP in new species
by Sudhakar, A
Journal of genetics, 2021-07-27, Vol.100 (2)
5.
A novel study to examine the association of PCSK9 rs505151 polymorphism and coronary artery disease in north Indian population
by Reddy, S
Journal of genetics, 2018-11-29, Vol.97 (5), p.1371-1378
6.
Association of genetic polymorphisms in the RET-protooncogene and NRG1 with Hirschsprung disease in Thai patients
by Phusantisampan, Theerawut
Journal of human genetics, 2012-05, Vol.57 (5), p.286-293
7.
Association of genetic polymorphisms in MDM2, PTEN and P53 with risk of esophageal squamous cell carcinoma
by Ma, Juan
Journal of human genetics, 2012-04, Vol.57 (4), p.261-264
8.
Direct and accurate measurement of CAG repeat configuration in the ataxin-1 (ATXN-1) gene by "dual-fluorescence labeled PCR-restriction fragment length analysis"
by Lin, Jiang X
Journal of human genetics, 2008, Vol.53 (4), p.287-295
9.
An SNP in protamine 1: a possible genetic cause of male infertility?
by Iguchi, N
Journal of medical genetics, 2006-04, Vol.43 (4), p.382-384
10.
Absence of BRAF mutations in UV-protected mucosal melanomas
by Edwards, R H
Journal of medical genetics, 2004-04, Vol.41 (4), p.270-272
11.
Detection of c.139G>A (D47N) mutation in GJA8 gene in an extended family with inheritance of autosomal dominant zonular cataract without pulverulent opacities by exome sequencing
by Gunda, Padma
Journal of genetics, 2018-08-03, Vol.97 (4), p.879-885
12.
Frequencies of genotypes and alleles of the functional SNPs in CYP2C19 and CYP2E1 in mainland Chinese Kazakh, Uygur and Han populations
by Wang, Shu-Mei
Journal of human genetics, 2009-06, Vol.54 (6), p.372-375
13.
CHEK2 I157T associates with familial and sporadic colorectal cancer
by Kilpivaara, O
Journal of medical genetics, 2006-07, Vol.43 (7), p.e34-e34
14.
Association of polymorphisms in the RAGE gene with serum CRP levels and coronary artery disease in the Chinese Han population
by Gao, Jinxiong
Journal of human genetics, 2010-10, Vol.55 (10), p.668-675
15.
Genetic variation of genes for xenobiotic-metabolizing enzymes and risk of bronchial asthma: the importance of gene-gene and gene-environment interactions for disease susceptibilit...
by Polonikov, Alexey V
Journal of human genetics, 2009-08, Vol.54 (8), p.440-449
16.
Polymorphisms of the PTGDR and LTC4S influence responsiveness to leukotriene receptor antagonists in Korean children with asthma
by Kang, Mi-Jin
Journal of human genetics, 2011-04, Vol.56 (4), p.284-289
17.
Diversity of Mhc class I and IIB genes in house sparrows (Passer domesticus)
by Bonneaud, Camille
Immunogenetics (New York), 2004-03, Vol.55 (12), p.855-865
18.
CYP17 gene polymorphism and its association with high-risk north Indian breast cancer patients
by Chakraborty, Anurupa
Journal of human genetics, 2007-02, Vol.52 (2), p.159-165
19.
Sequence Variation of the Methylene Tetrahydrofolate Reductase Gene (677C>T and 1298 A>C) and Traditional Risk Factors in a South Indian Population
by Dayakar, Seetha
Genetic testing and molecular biomarkers, 2011-11-01, Vol.15 (11), p.765-769
20.
Human Genetic Affinities for Y-Chromosome P49a,f/ TaqI Haplotypes Show Strong Correspondence with Linguistics
by Poloni, E.S
American journal of human genetics, 1997, Vol.61 (5), p.1015-1035
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