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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 7 (of 7 Records)

Query Trace: Disease and ADCY2[original query]
Identification of KIF3A as a novel candidate gene for childhood asthma using RNA expression and population allelic frequencies differences.
PloS one 2011 6 (8): e23714.
Kovacic Melinda Butsch, Myers Jocelyn M Biagini, Wang Ning, Martin Lisa J, Lindsey Mark, Ericksen Mark B, He Hua, Patterson Tia L, Baye Tesfaye M, Torgerson Dara, Roth Lindsey A, Gupta Jayanta, Sivaprasad Umasundari, Gibson Aaron M, Tsoras Anna M, Hu Donglei, Eng Celeste, Chapela Rocío, Rodríguez-Santana José R, Rodríguez-Cintrón William, Avila Pedro C, Beckman Kenneth, Seibold Max A, Gignoux Chris, Musaad Salma M, Chen Weiguo, Burchard Esteban González, Hershey Gurjit K Khura
CHRNA3/5, IREB2, and ADCY2 are associated with severe chronic obstructive pulmonary disease in Poland.
American journal of respiratory cell and molecular biology 2012 Mar .
Hardin M, Zielinski J, Wan ES, Hersh CP, Castaldi PJ, Schwinder E, Hawrylkiewicz I, Sliwinski P, Cho MH, Silverman EK
Genome-wide association study reveals two new risk loci for bipolar disorder. GWAS Catalog
Nature communications 2014 5 3339.
Mühleisen Thomas W, Leber Markus, Schulze Thomas G, Strohmaier Jana, Degenhardt Franziska, Treutlein Jens, Mattheisen Manuel, Forstner Andreas J, Schumacher Johannes, Breuer René, Meier Sandra, Herms Stefan, Hoffmann Per, Lacour André, Witt Stephanie H, Reif Andreas, Müller-Myhsok Bertram, Lucae Susanne, Maier Wolfgang, Schwarz Markus, Vedder Helmut, Kammerer-Ciernioch Jutta, Pfennig Andrea, Bauer Michael, Hautzinger Martin, Moebus Susanne, Priebe Lutz, Czerski Piotr M, Hauser Joanna, Lissowska Jolanta, Szeszenia-Dabrowska Neonila, Brennan Paul, McKay James D, Wright Adam, Mitchell Philip B, Fullerton Janice M, Schofield Peter R, Montgomery Grant W, Medland Sarah E, Gordon Scott D, Martin Nicholas G, Krasnow Valery, Chuchalin Alexander, Babadjanova Gulja, Pantelejeva Galina, Abramova Lilia I, Tiganov Alexander S, Polonikov Alexey, Khusnutdinova Elza, Alda Martin, Grof Paul, Rouleau Guy A, Turecki Gustavo, Laprise Catherine, Rivas Fabio, Mayoral Fermin, Kogevinas Manolis, Grigoroiu-Serbanescu Maria, Propping Peter, Becker Tim, Rietschel Marcella, Nöthen Markus M, Cichon Sv
Evaluation of genetic association of neurodevelopment and neuroimmunological genes with antipsychotic treatment response in schizophrenia in Indian populations.
Molecular genetics & genomic medicine 2016 Jan 4 (1): 18-27.
Jajodia Ajay, Kaur Harpreet, Kumari Kalpana, Kanojia Neha, Gupta Meenal, Baghel Ruchi, Sood Mamta, Jain Sanjeev, Chadda Rakesh K, Kukreti Ritushr
Systems-level differential gene expression analysis reveals new genetic variants of oral cancer.
Scientific reports 2020 9 10 (1): 14667.
Abbas Syeda Zahra, Qadir Muhammad Imran, Muhammad Syed A
Systems genetics analysis identifies calcium-signaling defects as novel cause of congenital heart disease.
Genome medicine 2020 8 12 (1): 76.
Izarzugaza Jose M G, Ellesøe Sabrina G, Doganli Canan, Ehlers Natasja Spring, Dalgaard Marlene D, Audain Enrique, Dombrowsky Gregor, Banasik Karina, Sifrim Alejandro, Wilsdon Anna, Thienpont Bernard, Breckpot Jeroen, Gewillig Marc, , Brook J David, Hitz Marc-Phillip, Larsen Lars A, Brunak Sør
Timing of chronic obstructive pulmonary disease diagnosis in lung cancer prognosis: a clinical and genomic-based study.
Translational lung cancer research 2021 Mar 10 (3): 1209-1220.
Dai Jie, He Yanqi, Maneenil Kunlatida, Liu Han, Liu Ming, Guo Qian, Bennett Amy C, Stoddard Shawn M, Wampfler Jason A, Jiang Gening, Yang Pi
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