Genetic Polymorphisms in Serotonin Transporter (5HTT) and Catechol-O-Methyltransferase (COMT) On Dental Implant Loss-Pilot Project.
Iranian Journal Of Public Health
Chaves, Thais Mariana Neves TMN; Spada, Paula Cruz Porto PCP; Meger, Michelle Nascimento MN; Gabardo, Marilisa Carneiro Leão MCL; Zielak, João Cézar JC; Deliberador, Tatiana Miranda TM; Brancher, João Armando JA
Genetic variations in catechol-O-methyltransferase gene are associated with levodopa response variability in Chinese patients with Parkinson's disease.
Replication and exploratory analysis of 24 candidate risk polymorphisms for neural tube defects.
Bmc Medical Genetics
Pangilinan, Faith F; Molloy, Anne M AM; Mills, James L JL; Troendle, James F JF; Parle-McDermott, Anne A; Kay, Denise M DM; Browne, Marilyn L ML; McGrath, Emily C EC; Abaan, Hatice Ozel HO; Sutton, Marie M; Kirke, Peadar N PN; Caggana, Michele M; Shane, Barry B; Scott, John M JM; Brody, Lawrence C LC
Effect of catechol-o-methyltransferase-gene (COMT) variants on experimental and acute postoperative pain in 1,000 women undergoing surgery for breast cancer.
Anesthesiology
Kambur, Oleg O; Kaunisto, Mari A MA; Tikkanen, Emmi E; Leal, Suzanne M SM; Ripatti, Samuli S; Kalso, Eija A EA
Associations between maternal genotypes and metabolites implicated in congenital heart defects.
Molecular Genetics And Metabolism
Chowdhury, Shimul S; Hobbs, Charlotte A CA; MacLeod, Stewart L SL; Cleves, Mario A MA; Melnyk, Stepan S; James, S Jill SJ; Hu, Ping P; Erickson, Stephen W SW
Evaluation of common genetic variants in 82 candidate genes as risk factors for neural tube defects.
Bmc Medical Genetics
Pangilinan, Faith F; Molloy, Anne M AM; Mills, James L JL; Troendle, James F JF; Parle-McDermott, Anne A; Signore, Caroline C; O'Leary, Valerie B VB; Chines, Peter P; Seay, Jessica M JM; Geiler-Samerotte, Kerry K; Mitchell, Adam A; VanderMeer, Julia E JE; Krebs, Kristine M KM; Sanchez, Angelica A; Cornman-Homonoff, Joshua J; Stone, Nicole N; Conley, Mary M; Kirke, Peadar N PN; Shane, Barry B; Scott, John M JM; Brody, Lawrence C LC
Interaction of early environment, gender and genes of monoamine neurotransmission in the aetiology of depression in a large population-based Finnish birth cohort.
Bmj Open
Nyman, Emma S ES; Sulkava, Sonja S; Soronen, Pia P; Miettunen, Jouko J; Loukola, Anu A; Leppä, Virpi V; Joukamaa, Matti M; Mäki, Pirjo P; Järvelin, Marjo-Riitta MR; Freimer, Nelson N; Peltonen, Leena L; Veijola, Juha J; Paunio, Tiina T
Sexually dimorphic effects of four genes (COMT, SLC6A2, MAOA, SLC6A4) in genetic associations of ADHD: a preliminary study.
American Journal Of Medical Genetics. Part B, Neuropsychiatric Genetics : The Official Publication Of The International Society Of Psychiatric Genetics
Biederman, Joseph J; Kim, Jang Woo JW; Doyle, Alysa E AE; Mick, Eric E; Fagerness, Jesen J; Smoller, Jordan W JW; Faraone, Stephen V SV