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| Open AccessThe Genetics of POAG in Black South Africans: A Candidate Gene Association Study
- Susan E. I. Williams
- , Trevor R. Carmichael
- & Michele Ramsay
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| Open AccessHandedness and the X chromosome: The role of androgen receptor CAG-repeat length
- Larissa Arning
- , Sebastian Ocklenburg
- & Christian Beste
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| Open AccessAssociation of genetic variants of GRIN2B with autism
- Yongcheng Pan
- , Jingjing Chen
- & Kun Xia
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| Open AccessSystematic Confirmation Study of GWAS-Identified Genetic Variants for Kawasaki Disease in A Chinese Population
- Jiao Lou
- , Rong Zhong
- & Xiao-ping Miao
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| Open AccessT2DM GWAS in the Lebanese population confirms the role of TCF7L2 and CDKAL1 in disease susceptibility
- Michella Ghassibe-Sabbagh
- , Marc Haber
- & Pierre A. Zalloua
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| Open AccessSEPP1 gene variants and abdominal aortic aneurysm: gene association in relation to metabolic risk factors and peripheral arterial disease coexistence
- Ewa Strauss
- , Grzegorz Oszkinis
- & Ryszard Staniszewski
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| Open AccessThe common functional FKBP5 variant rs1360780 is associated with altered cognitive function in aged individuals
- Takashi Fujii
- , Miho Ota
- & Hiroshi Kunugi
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Article
| Open AccessScreening of Clock Gene Polymorphisms Demonstrates Association of a PER3 Polymorphism with Morningness–Eveningness Preference and Circadian Rhythm Sleep Disorder
- Akiko Hida
- , Shingo Kitamura
- & Kazuo Mishima
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| Open AccessEstimating heritability of drug-induced liver injury from common variants and implications for future study designs
- Casey Lynnette Overby
- , George Hripcsak
- & Yufeng Shen
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| Open AccessNovel common variants and susceptible haplotype for exfoliation glaucoma specific to Asian population
- Masakazu Nakano
- , Yoko Ikeda
- & Kei Tashiro
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| Open AccessThe Roles of Ca2+/NFAT Signaling Genes in Kawasaki Disease: Single- and Multiple-Risk Genetic Variants
- Wei Wang
- , Jiao Lou
- & Fang-qi Gong
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Article
| Open AccessUpstream Transcription Factor 1 (USF1) allelic variants regulate lipoprotein metabolism in women and USF1 expression in atherosclerotic plaque
- Yue-Mei Fan
- , Jussi Hernesniemi
- & Terho Lehtimäki
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Article
| Open AccessVariants near CHRNB3-CHRNA6 are associated with DSM-5 cocaine use disorder: evidence for pleiotropy
- Brooke Sadler
- , Gabe Haller
- & Alison Goate
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Article
| Open Access8p22–23-rs2254546 as a Susceptibility Locus for Kawasaki Disease: a Case-control Study and a Meta-analysis
- Wei Wang
- , Jiao Lou
- & Fang-qi Gong
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Article
| Open AccessGenetic variant in SWI/SNF complexes influences hepatocellular carcinoma risk: a new clue for the contribution of chromatin remodeling in carcinogenesis
- Rong Zhong
- , Li Liu
- & Xiao-ping Miao
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Article
| Open AccessContribution of NKX2-3 Polymorphisms to Inflammatory Bowel Diseases: A Meta-Analysis of 35358 subjects
- XiaoCheng Lu
- , Linjun Tang
- & Li-Xin Li
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Article
| Open AccessABCG2 dysfunction causes hyperuricemia due to both renal urate underexcretion and renal urate overload
- Hirotaka Matsuo
- , Akiyoshi Nakayama
- & Nariyoshi Shinomiya
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Article
| Open AccessGWAS meta analysis identifies TSNARE1 as a novel Schizophrenia / Bipolar susceptibility locus
- Patrick Sleiman
- , Dai Wang
- & Qingqin Li
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Article
| Open AccessGSTM1 and GSTT1 null polymorphisms and male infertility risk: an updated meta-analysis encompassing 6934 subjects
- Wei Wu
- , Jing Lu
- & Xinru Wang
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Article
| Open AccessIdentification of Two Maternal Transmission Ratio Distortion Loci in Pedigrees of the Framingham Heart Study
- Yang Liu
- , Liangliang Zhang
- & Xiangyin Kong
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Article
| Open AccessA splice variant in KRT71 is associated with curly coat phenotype of Selkirk Rex cats
- Barbara Gandolfi
- , Hasan Alhaddad
- & Leslie A. Lyons
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Article
| Open AccessDrug addiction is associated with leukocyte telomere length
- Zhaoyang Yang
- , Junyi Ye
- & Yun Liu
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Article
| Open AccessEstimating the proportion of variation in susceptibility to multiple sclerosis captured by common SNPs
- Corey T. Watson
- , Giulio Disanto
- & Sreeram V. Ramagopalan
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Article
| Open AccessCOMT Val158Met polymorphism interacts with stressful life events and parental warmth to influence decision making
- Qinghua He
- , Gui Xue
- & Antoine Bechara
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Article
| Open AccessRare coding SNP in DZIP1 gene associated with late-onset sporadic Parkinson's disease
- André X. C. N. Valente
- , Joo H. Shin
- & Yuan Gao
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| Open AccessAn SNP selection strategy identified IL-22 associating with susceptibility to tuberculosis in Chinese
- Guoliang Zhang
- , Xinchun Chen
- & Junwen Wang