Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucoma.
Scientific Reports
Rauf, Bushra B; Khan, Shahid Y SY; Jiao, Xiaodong X; Irum, Bushra B; Ashfaq, Ramla R; Zehra, Mubashra M; Khan, Asma A AA; Naeem, Muhammad Asif MA; Shahzad, Mohsin M; Riazuddin, Sheikh S; Hejtmancik, J Fielding JF; Riazuddin, S Amer SA
Pharmacogenetic Predictors of Cannabidiol Response and Tolerability in Treatment-Resistant Epilepsy.
Clinical Pharmacology And Therapeutics
Davis, Brittney H BH; Beasley, T Mark TM; Amaral, Michelle M; Szaflarski, Jerzy P JP; Gaston, Tyler T; Perry Grayson, Leslie L; Standaert, David G DG; Bebin, E Martina EM; Limdi, Nita A NA; ,
Association between the APOA2 rs3813627 Single Nucleotide Polymorphism and HDL and APOA1 Levels Through BMI.
Biomedicines
Boughanem, Hatim H; Bandera-Merchán, Borja B; Hernández-Alonso, Pablo P; Moreno-Morales, Noelia N; Tinahones, Francisco José FJ; Lozano, José J; Morcillo, Sonsoles S; Macias-Gonzalez, Manuel M
Investigation of DNA repair-related SNPs underlying susceptibility to papillary thyroid carcinoma reveals MGMT as a novel candidate gene in Belarusian children exposed to radiation.
Bmc Cancer
Lonjou, Christine C; Damiola, Francesca F; Moissonnier, Monika M; Durand, Geoffroy G; Malakhova, Irina I; Masyakin, Vladimir V; Le Calvez-Kelm, Florence F; Cardis, Elisabeth E; Byrnes, Graham G; Kesminiene, Ausrele A; Lesueur, Fabienne F
The Affymetrix DMET Plus platform reveals unique distribution of ADME-related variants in ethnic Arabs.
Disease Markers
Wakil, Salma M SM; Nguyen, Cao C; Muiya, Nzioka P NP; Andres, Editha E; Lykowska-Tarnowska, Agnieszka A; Baz, Batoul B; Tahir, Asma I AI; Meyer, Brian F BF; Morahan, Grant G; Dzimiri, Nduna N
Evaluating the association of common APOA2 variants with type 2 diabetes.
Bmc Medical Genetics
Duesing, Konsta K; Charpentier, Guillaume G; Marre, Michel M; Tichet, Jean J; Hercberg, Serge S; Balkau, Beverley B; Froguel, Philippe P; Gibson, Fernando F