Human Genome Epidemiology Literature Finder
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Records 1 - 11 (of 11 Records) |
| Query Trace: Genetic testing[original query] |
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Genome-wide association study of interferon-related cytopenia in chronic hepatitis C patients.
Journal of hepatology 2012 Feb 56 (2): 313-9. Thompson Alexander J, Clark Paul J, Singh Abanish, Ge Dongliang, Fellay Jacques, Zhu Mingfu, Zhu Qianqian, Urban Thomas J, Patel Keyur, Tillmann Hans L, Naggie Susanna, Afdhal Nezam H, Jacobson Ira M, Esteban Rafael, Poordad Fred, Lawitz Eric J, McCone Jonathan, Shiffman Mitchell L, Galler Greg W, King John W, Kwo Paul Y, Shianna Kevin V, Noviello Stephanie, Pedicone Lisa D, Brass Clifford A, Albrecht Janice K, Sulkowski Mark S, Goldstein David B, McHutchison John G, Muir Andrew |
| Genome-wide association study of multiplex schizophrenia pedigrees.
The American journal of psychiatry 2012 Sep 169 (9): 963-73. Levinson Douglas F, Shi Jianxin, Wang Kai, Oh Sang, Riley Brien, Pulver Ann E, Wildenauer Dieter B, Laurent Claudine, Mowry Bryan J, Gejman Pablo V, Owen Michael J, Kendler Kenneth S, Nestadt Gerald, Schwab Sibylle G, Mallet Jacques, Nertney Deborah, Sanders Alan R, Williams Nigel M, Wormley Brandon, Lasseter Virginia K, Albus Margot, Godard-Bauché Stephanie, Alexander Madeline, Duan Jubao, O'Donovan Michael C, Walsh Dermot, O'Neill Anthony, Papadimitriou George N, Dikeos Dimitris, Maier Wolfgang, Lerer Bernard, Campion Dominique, Cohen David, Jay Maurice, Fanous Ayman, Eichhammer Peter, Silverman Jeremy M, Norton Nadine, Zhang Nancy, Hakonarson Hakon, Gao Cynthia, Citri Ami, Hansen Mark, Ripke Stephan, , Dudbridge Frank, Holmans Peter |
| Variants in the ATP-binding cassette transporter (ABCA7), apolipoprotein E ?4,and the risk of late-onset Alzheimer disease in African Americans.
JAMA 2013 Apr 309 (14): 1483-92. Reitz Christiane, Jun Gyungah, Naj Adam, Rajbhandary Ruchita, Vardarajan Badri Narayan, Wang Li-San, Valladares Otto, Lin Chiao-Feng, Larson Eric B, Graff-Radford Neill R, Evans Denis, De Jager Philip L, Crane Paul K, Buxbaum Joseph D, Murrell Jill R, Raj Towfique, Ertekin-Taner Nilufer, Logue Mark, Baldwin Clinton T, Green Robert C, Barnes Lisa L, Cantwell Laura B, Fallin M Daniele, Go Rodney C P, Griffith Patrick, Obisesan Thomas O, Manly Jennifer J, Lunetta Kathryn L, Kamboh M Ilyas, Lopez Oscar L, Bennett David A, Hendrie Hugh, Hall Kathleen S, Goate Alison M, Byrd Goldie S, Kukull Walter A, Foroud Tatiana M, Haines Jonathan L, Farrer Lindsay A, Pericak-Vance Margaret A, Schellenberg Gerard D, Mayeux Richard, |
| Genomewide Approach Validates Thiopurine Methyltransferase Activity Is a Monogenic Pharmacogenomic Trait.
Clinical pharmacology and therapeutics 2016 Aug . Liu Chengcheng, Yang Wenjian, Pei Deqing, Cheng Cheng, Smith Colton, Landier Wendy, Hageman Lindsey, Chen Yanjun, Yang Jun J, Crews Kristine R, Kornegay Nancy, Karol Seth E, Wong F Lennie, Jeha Sima, Sandlund John T, Ribeiro Raul R, Rubnitz Jeffrey E, Metzger Monika L, Pui Ching-Hon, Evans William E, Bhatia Smita, Relling Mary |
| Polymorphic variation in TPMT is the principal determinant of TPMT phenotype: A meta-analysis of three genome-wide association studies.
Clinical pharmacology and therapeutics 2016 Oct . Tamm Riin, Mägi Reedik, Tremmel Roman, Winter Stefan, Mihailov Evelin, Smid Alenka, Möricke Anja, Klein Kathrin, Schrappe Martin, Stanulla Martin, Houlston Richard, Weinshilboum Richard, Mlinari? Raš?an Irena, Metspalu Andres, Milani Lili, Schwab Matthias, Schaeffeler El |
| A Genome-Wide Association Study of Bisphosphonate-Associated Atypical Femoral Fracture.
Calcified tissue international 2019 Apr . Kharazmi Mohammad, Michaëlsson Karl, Schilcher Jörg, Eriksson Niclas, Melhus Håkan, Wadelius Mia, Hallberg P |
| Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome.
Circulation 2020 Jul 142 (4): 324-338. Lahrouchi Najim, Tadros Rafik, Crotti Lia, Mizusawa Yuka, Postema Pieter G, Beekman Leander, Walsh Roddy, Hasegawa Kanae, Barc Julien, Ernsting Marko, Turkowski Kari L, Mazzanti Andrea, Beckmann Britt M, Shimamoto Keiko, Diamant Ulla-Britt, Wijeyeratne Yanushi D, Kucho Yu, Robyns Tomas, Ishikawa Taisuke, Arbelo Elena, Christiansen Michael, Winbo Annika, Jabbari Reza, Lubitz Steven A, Steinfurt Johannes, Rudic Boris, Loeys Bart, Shoemaker M Ben, Weeke Peter E, Pfeiffer Ryan, Davies Brianna, Andorin Antoine, Hofman Nynke, Dagradi Federica, Pedrazzini Matteo, Tester David J, Bos J Martijn, Sarquella-Brugada Georgia, Campuzano Óscar, Platonov Pyotr G, Stallmeyer Birgit, Zumhagen Sven, Nannenberg Eline A, Veldink Jan H, van den Berg Leonard H, Al-Chalabi Ammar, Shaw Christopher E, Shaw Pamela J, Morrison Karen E, Andersen Peter M, Müller-Nurasyid Martina, Cusi Daniele, Barlassina Cristina, Galan Pilar, Lathrop Mark, Munter Markus, Werge Thomas, Ribasés Marta, Aung Tin, Khor Chiea C, Ozaki Mineo, Lichtner Peter, Meitinger Thomas, van Tintelen J Peter, Hoedemaekers Yvonne, Denjoy Isabelle, Leenhardt Antoine, Napolitano Carlo, Shimizu Wataru, Schott Jean-Jacques, Gourraud Jean-Baptiste, Makiyama Takeru, Ohno Seiko, Itoh Hideki, Krahn Andrew D, Antzelevitch Charles, Roden Dan M, Saenen Johan, Borggrefe Martin, Odening Katja E, Ellinor Patrick T, Tfelt-Hansen Jacob, Skinner Jonathan R, van den Berg Maarten P, Olesen Morten Salling, Brugada Josep, Brugada Ramón, Makita Naomasa, Breckpot Jeroen, Yoshinaga Masao, Behr Elijah R, Rydberg Annika, Aiba Takeshi, Kääb Stefan, Priori Silvia G, Guicheney Pascale, Tan Hanno L, Newton-Cheh Christopher, Ackerman Michael J, Schwartz Peter J, Schulze-Bahr Eric, Probst Vincent, Horie Minoru, Wilde Arthur A, Tanck Michael W T, Bezzina Connie |
| Monogenic and Polygenic Contributions to QTc Prolongation in the Population.
Circulation 2022 4 145 (20): 1524-1533. Nauffal Victor, Morrill Valerie N, Jurgens Sean J, Choi Seung Hoan, Hall Amelia W, Weng Lu-Chen, Halford Jennifer L, Austin-Tse Christina, Haggerty Christopher M, Harris Stephanie L, Wong Eugene K, Alonso Alvaro, Arking Dan E, Benjamin Emelia J, Boerwinkle Eric, Min Yuan-I, Correa Adolfo, Fornwalt Brandon K, Heckbert Susan R, , Kooperberg Charles, Lin Henry J, J F Loos Ruth, Rice Kenneth M, Gupta Namrata, Blackwell Thomas W, Mitchell Braxton D, Morrison Alanna C, Psaty Bruce M, Post Wendy S, Redline Susan, Rehm Heidi L, Rich Stephen S, Rotter Jerome I, Soliman Elsayed Z, Sotoodehnia Nona, Lunetta Kathryn L, Ellinor Patrick T, Lubitz Steven A, |
| Genome-wide association analysis identifies a susceptibility locus for sporadic vestibular schwannoma at 9p21.
Brain : a journal of neurology 2022 12 . Sadler Katherine V, Bowes John, Rowlands Charlie F, Perez-Becerril Cristina, van der Meer C Mwee, King Andrew T, Rutherford Scott A, Pathmanaban Omar N, Hammerbeck-Ward Charlotte, Lloyd Simon K W, Freeman Simon R, Williams Ricky, Hannan Cathal John, Lewis Daniel, Eyre Steve, Evans D Gareth, Smith Miriam |
| The Pharmacogenetics of Statin Therapy on Clinical Events: No Evidence that Genetic Variation Affects Statin Response on Myocardial Infarction.
Frontiers in pharmacology 2022 1 12 679857. Trompet Stella, Postmus Iris, Warren Helen R, Noordam Raymond, Smit Roelof A J, Theusch Elizabeth, Li Xiaohui, Arsenault Benoit, Chasman Daniel I, Hitman Graham A, Munroe Patricia B, Rotter Jerome I, Psaty Bruce M, Caulfield Mark J, Krauss Ron M, Cupples Adrienne L, Jukema Wouter |
| Ultra-low-coverage genome-wide association study-insights into gestational age using 17,844 embryo samples with preimplantation genetic testing.
Genome medicine 2023 2 15 (1): 10. Li Shumin, Yan Bin, Li Thomas K T, Lu Jianliang, Gu Yifan, Tan Yueqiu, Gong Fei, Lam Tak-Wah, Xie Pingyuan, Wang Yuexuan, Lin Ge, Luo Ruiba |
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