Human Genome Epidemiology Literature Finder
Records 1 - 12 (of 12 Records) |
Query Trace: PDE7B[original query] |
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Identification of novel candidate genes for treatment response to risperidone and susceptibility for schizophrenia: integrated analysis among pharmacogenomics, mouse expression, and genetic case-control association approaches. Biological psychiatry 2010 Feb 67 (3): 263-9. Ikeda Masashi, Tomita Yasuyuki, Mouri Akihiro, Koga Minori, Okochi Tomo, Yoshimura Reiji, Yamanouchi Yoshio, Kinoshita Yoko, Hashimoto Ryota, Williams Hywel J, Takeda Masatoshi, Nakamura Jun, Nabeshima Toshitaka, Owen Michael J, O'Donovan Michael C, Honda Hiroyuki, Arinami Tadao, Ozaki Norio, Iwata Nak |
Fine mapping of AHI1 as a schizophrenia susceptibility gene: from association to evolutionary evidence. FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2010 Aug 24 (8): 3066-82. Torri Federica, Akelai Anna, Lupoli Sara, Sironi Manuela, Amann-Zalcenstein Daniela, Fumagalli Matteo, Dal Fiume Chiara, Ben-Asher Edna, Kanyas Kyra, Cagliani Rachele, Cozzi Paolo, Trombetti Gabriele, Strik Lievers Luisa, Salvi Erika, Orro Alessandro, Beckmann Jacques S, Lancet Doron, Kohn Yoav, Milanesi Luciano, Ebstein Richard B, Lerer Bernard, Macciardi Fab |
A large replication study and meta-analysis in European samples provides further support for association of AHI1 markers with schizophrenia. Human molecular genetics 2010 Apr 19 (7): 1379-86. Ingason Andrés, Giegling Ina, Cichon Sven, Hansen Thomas, Rasmussen Henrik B, Nielsen Jimmi, Jürgens Gesche, Muglia Pierandrea, Hartmann Annette M, Strengman Eric, Vasilescu Catalina, Mühleisen Thomas W, Djurovic Srdjan, Melle Ingrid, Lerer Bernard, Möller Hans-Jürgen, Francks Clyde, Pietiläinen Olli P H, Lonnqvist Jouko, Suvisaari Jaana, Tuulio-Henriksson Annamari, Walshe Muriel, Vassos Evangelos, Di Forti Marta, Murray Robin, Bonetto Chiara, Tosato Sarah, , Cantor Rita M, Rietschel Marcella, Craddock Nick, Owen Michael J, Peltonen Leena, Andreassen Ole A, Nöthen Markus M, St Clair David, Ophoff Roel A, O'Donovan Michael C, Collier David A, Werge Thomas, Rujescu D |
Genetic variation in phosphodiesterase (PDE) 7B in chronic lymphocytic leukemia: overview of genetic variants of cyclic nucleotide PDEs in human disease. Journal of human genetics 2011 Sep 56 (9): 676-81. Peiró Ana M, Tang Chih-Min, Murray Fiona, Zhang Lingzhi, Brown Loren M, Chou Daisy, Rassenti Laura, Kipps Thomas J, Kipps Thomas A, Insel Paul |
Bioavailability of testosterone enanthate dependent on genetic variation in the phosphodiesterase 7B but not on the uridine 5'-diphospho-glucuronosyltransferase (UGT2B17) gene. Pharmacogenetics and genomics 2011 Jun 21 (6): 325-32. Ekström Lena, Schulze Jenny J, Guillemette Chantal, Belanger Alain, Rane Ande |
Genomic variation in the MAP3K5 gene is associated with ß-thalassemia disease severity and hydroxyurea treatment efficacy. Pharmacogenomics 2013 Apr 14 (5): 469-83. Tafrali Christina, Paizi Arsinoi, Borg Joseph, Radmilovic Milena, Bartsakoulia Marina, Giannopoulou Emily, Giannakopoulou Olga, Stojiljkovic-Petrovic Maja, Zukic Branka, Poulas Konstantinos, Stavrou Eleana F, Lambropoulou Polyxeni, Kourakli Alexandra, Felice Alexander E, Papachatzopoulou Adamantia, Philipsen Sjaak, Pavlovic Sonja, Georgitsi Marianthi, Patrinos George |
Phosphodiesterase sequence variants may predispose to prostate cancer. Endocrine-related cancer 2015 Aug 22 (4): 519-30. de Alexandre Rodrigo B, Horvath Anelia D, Szarek Eva, Manning Allison D, Leal Leticia F, Kardauke Fabio, Epstein Jonathan A, Carraro Dirce M, Soares Fernando A, Apanasovich Tatiyana V, Stratakis Constantine A, Faucz Fabio |
PDE7B, NMBR and EPM2A Variants and Schizophrenia: A Case-Control and Pharmacogenetics Study. Neuropsychobiology 2016 Apr 73 (3): 160-168. Porcelli Stefano, Balzarro Beatrice, Lee Soo-Jung, Han Changsu, Patkar Ashwin A, Pae Chi-Un, Serretti Alessand |
A multiethnic genome-wide association study of primary open-angle glaucoma identifies novel risk loci.
Nature communications 2018 Jun 9 (1): 2278. Choquet Hélène, Paylakhi Seyyedhassan, Kneeland Stephen C, Thai Khanh K, Hoffmann Thomas J, Yin Jie, Kvale Mark N, Banda Yambazi, Tolman Nicholas G, Williams Pete A, Schaefer Catherine, Melles Ronald B, Risch Neil, John Simon W M, Nair K Saidas, Jorgenson Er |
BRCA1/2-negative, high-risk breast cancers (BRCAX) for Asian women: genetic susceptibility loci and their potential impacts.
Scientific reports 2018 Oct 8 (1): 15263. Lee Joo-Yeon, Kim Jisun, Kim Sung-Won, Park Sue K, Ahn Sei Hyun, Lee Min Hyuk, Suh Young Jin, Noh Dong-Young, Son Byung Ho, Cho Young Up, Lee Sae Byul, Lee Jong Won, Hopper John L, Sung Jooh |
Role of Genomic Biomarkers in Increasing Fetal Hemoglobin Levels Upon Hydroxyurea Therapy and in ?-Thalassemia Intermedia: A Validation Cohort Study. Hemoglobin 2019 5 43 (1): 27-33. Kolliopoulou Alexandra, Siamoglou Stavroula, John Anne, Sgourou Argyro, Kourakli Alexandra, Symeonidis Argiris, Vlachaki Efthymia, Chalkia Panagiota, Theodoridou Stamatia, Ali Bassam R, Katsila Theodora, Patrinos George P, Papachatzopoulou Adamant |
Novel insights into genetic susceptibility for colorectal cancer from transcriptome-wide association and functional investigation. Journal of the National Cancer Institute 2023 8 . Zhishan Chen, Wenqiang Song, Xiao-Ou Shu, Wanqing Wen, Matthew Devall, Christopher Dampier, Ferran Moratalla-Navarro, Qiuyin Cai, Jirong Long, Luc Van Kaer, Lan Wu, Jeroen R Huyghe, Minta Thomas, Li Hsu, Michael O Woods, Demetrius Albanes, Daniel D Buchanan, Andrea Gsur, Michael Hoffmeister, Pavel Vodicka, Alicja Wolk, Loic Le Marchand, Anna H Wu, Amanda I Phipps, Victor Moreno, Peters Ulrike, Wei Zheng, Graham Casey, Xingyi G |
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