Altered Cerebral Curvature in Preterm Infants Is Associated with the Common Genetic Variation Related to Autism Spectrum Disorder and Lipid Metabolism.
Journal Of Clinical Medicine
Kim, Hyuna H; Ahn, Ja-Hye JH; Lee, Joo Young JY; Jang, Yong Hun YH; Kim, Young-Eun YE; Kim, Johanna Inhyang JI; Kim, Bung-Nyun BN; Lee, Hyun Ju HJ
Genetic variants and cognitive functions in patients with brain tumors.
Neuro-Oncology
Correa, Denise D DD; Satagopan, Jaya J; Martin, Axel A; Braun, Erica E; Kryza-Lacombe, Maria M; Cheung, Kenneth K; Sharma, Ajay A; Dimitriadoy, Sofia S; O'Connell, Kelli K; Leong, Siok S; Karimi, Sasan S; Lyo, John J; DeAngelis, Lisa M LM; Orlow, Irene I
Candidate gene analyses for acute pain and morphine analgesia after pediatric day surgery: African American versus European Caucasian ancestry and dose prediction limits.
The Pharmacogenomics Journal
Li, Jin J; Wei, Zhi Z; Zhang, Jie J; Hakonarson, Hakon H; Cook-Sather, Scott D SD
A gene-environment interaction analysis of plasma selenium with prevalent and incident diabetes: The Hortega study.
Redox Biology
Galan-Chilet, Inmaculada I; Grau-Perez, Maria M; De Marco, Griselda G; Guallar, Eliseo E; Martin-Escudero, Juan Carlos JC; Dominguez-Lucas, Alejandro A; Gonzalez-Manzano, Isabel I; Lopez-Izquierdo, Raul R; Briongos-Figuero, Laisa Socorro LS; Redon, Josep J; Chaves, Felipe Javier FJ; Tellez-Plaza, Maria M
Association of maternal and infant variants in PNOC and COMT genes with neonatal abstinence syndrome severity.
The American Journal On Addictions
Wachman, Elisha M EM; Hayes, Marie J MJ; Sherva, Richard R; Brown, Mark S MS; Shrestha, Hira H; Logan, Beth A BA; Heller, Nicole A NA; Nielsen, David A DA; Farrer, Lindsay A LA
A human neurodevelopmental model for Williams syndrome.
Nature
Chailangkarn, Thanathom T; Trujillo, Cleber A CA; Freitas, Beatriz C BC; Hrvoj-Mihic, Branka B; Herai, Roberto H RH; Yu, Diana X DX; Brown, Timothy T TT; Marchetto, Maria C MC; Bardy, Cedric C; McHenry, Lauren L; Stefanacci, Lisa L; Järvinen, Anna A; Searcy, Yvonne M YM; DeWitt, Michelle M; Wong, Wenny W; Lai, Philip P; Ard, M Colin MC; Hanson, Kari L KL; Romero, Sarah S; Jacobs, Bob B; Dale, Anders M AM; Dai, Li L; Korenberg, Julie R JR; Gage, Fred H FH; Bellugi, Ursula U; Halgren, Eric E; Semendeferi, Katerina K; Muotri, Alysson R AR
COMT, BDNF, and DTNBP1 polymorphisms and cognitive functions in patients with brain tumors.
Neuro-Oncology
Correa, Denise D DD; Satagopan, Jaya J; Cheung, Kenneth K; Arora, Arshi K AK; Kryza-Lacombe, Maria M; Xu, Youming Y; Karimi, Sasan S; Lyo, John J; DeAngelis, Lisa M LM; Orlow, Irene I
The nutrigenetic influence of the interaction between dietary vitamin E and TXN and COMT gene polymorphisms on waist circumference: a case control study.
Journal Of Translational Medicine
Mansego, Maria L ML; De Marco, Griselda G; Ivorra, Carmen C; Lopez-Izquierdo, Raúl R; Morcillo, Sonsoles S; Rojo-Martínez, Gemma G; González-Albert, Verónica V; Martinez, Fernando F; Soriguer, Federico F; Martín-Escudero, Juan C JC; Redon, Josep J; Chaves, F Javier FJ
COMT and MAO-A polymorphisms and obsessive-compulsive disorder: a family-based association study.
Plos One
Sampaio, Aline Santos AS; Hounie, Ana Gabriela AG; Petribú, Kátia K; Cappi, Carolina C; Morais, Ivanil I; Vallada, Homero H; do Rosário, Maria Conceição MC; Stewart, S Evelyn SE; Fargeness, Jesen J; Mathews, Carol C; Arnold, Paul P; Hanna, Gregory L GL; Richter, Margaret M; Kennedy, James J; Fontenelle, Leonardo L; de Bragança Pereira, Carlos Alberto CA; Pauls, David L DL; Miguel, Eurípedes Constantino EC
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
No association between germline variation in catechol-O-methyltransferase and colorectal cancer survival in postmenopausal women.
Menopause (New York, N.Y.)
Passarelli, Michael N MN; Newcomb, Polly A PA; Makar, Karen W KW; Burnett-Hartman, Andrea N AN; Phipps, Amanda I AI; David, Sean P SP; Hsu, Li L; Harrison, Tabitha A TA; Hutter, Carolyn M CM; Duggan, David J DJ; White, Emily E; Chan, Andrew T AT; Peters, Ulrike U
The associations between OPRM 1 and COMT genotypes and postoperative pain, opioid use, and opioid-induced sedation.
Biological Research For Nursing
Henker, Richard A RA; Lewis, Allison A; Dai, Feng F; Lariviere, William R WR; Meng, Li L; Gruen, Gary S GS; Sereika, Susan M SM; Pape, Hans H; Tarkin, Ivan S IS; Gowda, Indira I; Conley, Yvette P YP
Is ethnicity associated with morphine's side effects in children? Morphine pharmacokinetics, analgesic response, and side effects in children having tonsillectomy.
Paediatric Anaesthesia
Jimenez, Nathalia N; Anderson, Gail D GD; Shen, Danny D DD; Nielsen, Susan S SS; Farin, Federico M FM; Seidel, Kristy K; Lynn, Anne M AM
Association of catechol-O-methyltransferase gene polymorphisms with schizophrenia and negative symptoms in a Chinese population.
American Journal Of Medical Genetics. Part B, Neuropsychiatric Genetics : The Official Publication Of The International Society Of Psychiatric Genetics
Li, Wen Jun WJ; Kou, Chang Gui CG; Yu, Yaqin Y; Sun, Shilong S; Zhang, Xuan X; Kosten, Thomas R TR; Zhang, Xiang Yang XY
Association between polymorphisms in catechol-O-methyltransferase (COMT) and cocaine-induced paranoia in European-American and African-American populations.
American Journal Of Medical Genetics. Part B, Neuropsychiatric Genetics : The Official Publication Of The International Society Of Psychiatric Genetics
Ittiwut, Rungnapa R; Listman, Jennifer B JB; Ittiwut, Chupong C; Cubells, Joseph F JF; Weiss, Roger D RD; Brady, Kathleen K; Oslin, David D; Farrer, Lindsay A LA; Kranzler, Henry R HR; Gelernter, Joel J
A reappraisal of the association between Dysbindin (DTNBP1) and schizophrenia in a large combined case-control and family-based sample of German ancestry.
Schizophrenia Research
Strohmaier, Jana J; Frank, Josef J; Wendland, Jens R JR; Schumacher, Johannes J; Jamra, Rami Abou RA; Treutlein, Jens J; Nieratschker, Vanessa V; Breuer, René R; Mattheisen, Manuel M; Herms, Stefan S; Mühleisen, Thomas W TW; Maier, Wolfgang W; Nöthen, Markus M MM; Cichon, Sven S; Rietschel, Marcella M; Schulze, Thomas G TG
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