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Polymorphisms in Lysyl Oxidase Family Genes Are Associated With Intracranial Aneurysm Susceptibility in a Chinese Population

2021 . Luo, Chun | Hu, Chongyu | Li, Bingyang | Liu, Junyu | Hu, Liming | Dong, Rui | Liao, Xin | Zhou, Jilin | Xu, Lu | Liu, Songlin | Li, Yifeng | Yuan, Dun | Jiang, Weixi | Yan, Junxia

Discriminating the eight genotypes of the porcine circovirus type 2 with TaqMan-based real-time PCR

2021 . Link, Ellen Kathrin | Eddicks, Matthias | Nan, Liangliang | Ritzmann, Mathias | Sutter, Gerd | Fux, Robert

The association of heat shock protein genetic polymorphisms with age-related hearing impairment in Taiwan

2021 . Chang, Ning-Chia | Yang, Hua-Ling | Dai, Chia-Yen | Lin, Wen-Yi | Hsieh, Meng-Hsuen | Chien, Chen-Yu | Ho, Kuen-Yao

Mitochondrial nicotinamide adenine dinucleotide hydride dehydrogenase (NADH) subunit 4 (MTND4) polymorphisms and their association with male infertility

2021 . Dahadhah, Fatina | Jaweesh, Mayyas Saleh | Al Zoubi, Mazhar | Alarjah, Manal Issam Abu | Hammadeh, Mohamad Eid | Amor, Houda

Genetic polymorphism of CYP2C19 and subcortical variability in the human adult brain

2021 . Stingl, Julia | Scholl, Catharina | Bosch, Julia E. | Viviani, Roberto

Evidence for pathogenicity of variant ATM Val1729Leu in a family with ataxia telangiectasia

2021 . Shalash, Ali | Rösler, Thomas W. | Salama, Mohamed | Pendziwiat, Manuela | Müller, Stefanie H. | Hopfner, Franziska | Höglinger, Günter | Kuhlenbaeumer, Gregor

The association of the 5-HTTLPR polymorphism and the response to different stressors in healthy males

2021 . Kuhn, Leandra | Noack, Hannes | Skoluda, Nadine | Wagels, Lisa | Röhr, Ann-Kristin | Schulte, Christina | Eisenkolb, Sana | Nieratschker, Vanessa | Derntl, Birgit | Habel, Ute

Prevalence of human papillomavirus detection in ovarian cancer: a meta-analysis

2021 . CHERIF, Soumia | Amine, Abdessamad | Thies, Sarah | Taube, Eliane T. | Braicu, Elena Ioana | Sehouli, Jalid | Kaufmann, Andreas

NBAS Variants Are Associated with Quantitative and Qualitative NK and B Cell Deficiency

Sudden infant death syndrome revisited: serotonin transporter gene, polymorphisms and promoter methylation

2021 . Pfisterer, Nina | Meyer-Bockenkamp, Fiona | Qu, Dong | Preuss, Vanessa | Rothämel, Thomas | Geisenberger, Dorothee | Läer, Katharina | Vennemann, Benedikt | Albers, Anne | Engelmann, Theresa A. | Frieling, Helge | Rhein, Mathias | Klintschar, Michael

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