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MTHFR Gene C677T polymorphism (rs1801133) and susceptibility to colorectal polyps in an Azerbaijani population by Aslanov, Hazi (Author) , Bayramov, Bayram (Author) , Reißfelder, Christoph (Author) , Abdullayeva, Shams (Author) , Mammadova, Zeynab (Author) , Aliyev, Fikrat (Author) , Keese, Michael (Author) , Hajibabazade, Javahir (Author) , Yagublu, Vugar (Author) ,

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Common variants increase risk for congenital diaphragmatic hernia within the context of de novo variants by Qiao, Lu (Author) , Welch, Carrie L. (Author) , Hernan, Rebecca (Author) , Wynn, Julia (Author) , Krishnan, Usha S. (Author) , Zalieckas, Jill M. (Author) , Buchmiller, Terry (Author) , Khlevner, Julie (Author) , De, Aliva (Author) , Farkouh-Karoleski, Christiana (Author) , Wagner, Amy J. (Author) , Heydweiller, Andreas (Author) , Mueller, Andreas C. (Author) , de Klein, Annelies (Author) , Warner, Brad W. (Author) , Maj, Carlo (Author) , Chung, Dai (Author) , McCulley, David J. (Author) , Schindel, David (Author) , Potoka, Douglas (Author) , Fialkowski, Elizabeth (Author) , Schulz, Felicitas (Author) , Kipfmuller, Florian (Author) , Lim, Foong-Yen (Author) , Magielsen, Frank (Author) , Mychaliska, George B. (Author) , Aspelund, Gudrun (Author) , Reutter, Heiko Martin (Author) , Needelman, Howard (Author) , Schnater, J. Marco (Author) , Fisher, Jason C. (Author) , Azarow, Kenneth (Author) , Elfiky, Mahmoud (Author) , Nöthen, Markus M. (Author) , Danko, Melissa E. (Author) , Li, Mindy (Author) , Kosiński, Przemyslaw (Author) , Wijnen, Rene M. H. (Author) , Cusick, Robert A. (Author) , Soffer, Samuel Z. (Author) , Cochius-Den Otter, Suzan C. M. (Author) , Schaible, Thomas (Author) , Crombleholme, Timothy (Author) , Duron, Vincent P. (Author) , Donahoe, Patricia K. (Author) , Sun, Xin (Author) , High, Frances A. (Author) , Bendixen, Charlotte (Author) , Brosens, Erwin (Author) , Shen, Yufeng (Author) , Chung, Wendy K. (Author) ,

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Functional consequences of TCF4 missense substitutions associated with Pitt-Hopkins syndrome, mild intellectual disability, and schizophrenia by Sirp, Alex (Author) , Roots, Kaisa (Author) , Nurm, Kaja (Author) , Tuvikene, Jürgen (Author) , Sepp, Mari (Author) , Timmusk, Tõnis (Author) ,

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Genetic variation associated with chromosomal aberration frequency: a genome-wide association study by Niazi, Yasmeen (Author) , Thomsen, Hauke (Author) , Hemminki, Kari (Author) , Försti, Asta (Author) ,

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ANGPT2 and NOS3 polymorphisms and clinical outcome in advanced hepatocellular carcinoma patients receiving sorafenib by Marisi, Giorgia (Author) , Raimondi, Francesco (Author) ,

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FGFR4 Arg388 genotype is associated with pathological complete response to neoadjuvant chemotherapy for primary breast cancer by Marmé, Frederik (Author) , Werft, Wiebke (Author) , Benner, Axel (Author) , Burwinkel, Barbara (Author) , Sinn, Peter (Author) , Sohn, Christof (Author) , Lichter, Peter (Author) , Hahn, Meinhard (Author) , Schneeweiss, Andreas (Author) ,

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