Genetic analysis of hsCRP in American Indians: The Strong Heart Family Study.
Plos One
Best, Lyle G LG; Balakrishnan, Poojitha P; Cole, Shelley A SA; Haack, Karin K; Kocarnik, Jonathan M JM; Pankratz, Nathan N; Anderson, Matthew Z MZ; Franceschini, Nora N; Howard, Barbara V BV; Lee, Elisa T ET; North, Kari E KE; Umans, Jason G JG; Yracheta, Joseph M JM; Navas-Acien, Ana A; Voruganti, V Saroja VS
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
Serotonin transporter gene, depressive symptoms, and interleukin-6.
Circulation. Cardiovascular Genetics
Su, Shaoyong S; Zhao, Jinying J; Bremner, J Douglas JD; Miller, Andrew H AH; Tang, Weining W; Bouzyk, Mark M; Snieder, Harold H; Novik, Olga O; Afzal, Nadeem N; Goldberg, Jack J; Vaccarino, Viola V
Variants of the serotonin transporter gene and NEO-PI-R Neuroticism: No association in the BLSA and SardiNIA samples.
American Journal Of Medical Genetics. Part B, Neuropsychiatric Genetics : The Official Publication Of The International Society Of Psychiatric Genetics
Terracciano, Antonio A; Balaci, Lenuta L; Thayer, Jason J; Scally, Matthew M; Kokinos, Sarah S; Ferrucci, Luigi L; Tanaka, Toshiko T; Zonderman, Alan B AB; Sanna, Serena S; Olla, Nazario N; Zuncheddu, Maria Antonietta MA; Naitza, Silvia S; Busonero, Fabio F; Uda, Manuela M; Schlessinger, David D; Abecasis, Gonçalo R GR; Costa, Paul T PT
Examination of association of genes in the serotonin system to autism.
Neurogenetics
Anderson, B M BM; Schnetz-Boutaud, N C NC; Bartlett, J J; Wotawa, A M AM; Wright, H H HH; Abramson, R K RK; Cuccaro, M L ML; Gilbert, J R JR; Pericak-Vance, M A MA; Haines, J L JL
SNPs in dopamine D2 receptor gene (DRD2) and norepinephrine transporter gene (NET) are associated with continuous performance task (CPT) phenotypes in ADHD children and their families.
American Journal Of Medical Genetics. Part B, Neuropsychiatric Genetics : The Official Publication Of The International Society Of Psychiatric Genetics
Kollins, S H SH; Anastopoulos, A D AD; Lachiewicz, A M AM; FitzGerald, D D; Morrissey-Kane, E E; Garrett, M E ME; Keatts, S L SL; Ashley-Koch, A E AE