Human Genome Epidemiology Literature Finder
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Records 1 - 25 (of 25 Records) |
| Query Trace: Anemia[original query] |
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Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study.
BMC medical genetics 2007 8 Suppl 1 S12. Yang Qiong, Kathiresan Sekar, Lin Jing-Ping, Tofler Geoffrey H, O'Donnell Christopher |
| Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia.
Proceedings of the National Academy of Sciences of the United States of America 2008 Feb 105 (5): 1620-5. Uda Manuela, Galanello Renzo, Sanna Serena, Lettre Guillaume, Sankaran Vijay G, Chen Weimin, Usala Gianluca, Busonero Fabio, Maschio Andrea, Albai Giuseppe, Piras Maria Grazia, Sestu Natascia, Lai Sandra, Dei Mariano, Mulas Antonella, Crisponi Laura, Naitza Silvia, Asunis Isadora, Deiana Manila, Nagaraja Ramaiah, Perseu Lucia, Satta Stefania, Cipollina Maria Dolores, Sollaino Carla, Moi Paolo, Hirschhorn Joel N, Orkin Stuart H, Abecasis Gonçalo R, Schlessinger David, Cao Anton |
| Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels.
American journal of human genetics 2009 Jan 84 (1): 60-5. Benyamin Beben, McRae Allan F, Zhu Gu, Gordon Scott, Henders Anjali K, Palotie Aarno, Peltonen Leena, Martin Nicholas G, Montgomery Grant W, Whitfield John B, Visscher Peter |
| Fetal hemoglobin in sickle cell anemia: genome-wide association studies suggest a regulatory region in the 5' olfactory receptor gene cluster.
Blood 2010 Mar 115 (9): 1815-22. Solovieff Nadia, Milton Jacqueline N, Hartley Stephen W, Sherva Richard, Sebastiani Paola, Dworkis Daniel A, Klings Elizabeth S, Farrer Lindsay A, Garrett Melanie E, Ashley-Koch Allison, Telen Marilyn J, Fucharoen Supan, Ha Shau Yin, Li Chi-Kong, Chui David H K, Baldwin Clinton T, Steinberg Martin |
| A genome-wide association analysis of serum iron concentrations.
Blood 2010 Jan 115 (1): 94-6. Tanaka Toshiko, Roy Cindy N, Yao Wenliang, Matteini Amy, Semba Richard D, Arking Dan, Walston Jeremy D, Fried Linda P, Singleton Andrew, Guralnik Jack, Abecasis Gonçalo R, Bandinelli Stefania, Longo Dan L, Ferrucci Lui |
| ITPA polymorphism affects ribavirin-induced anemia and outcomes of therapy--a genome-wide study of Japanese HCV virus patients.
Gastroenterology 2010 Oct 139 (4): 1190-7. Ochi Hidenori, Maekawa Toshiro, Abe Hiromi, Hayashida Yasufumi, Nakano Rikita, Kubo Michaki, Tsunoda Tatsuhiko, Hayes C Nelson, Kumada Hiromitsu, Nakamura Yusuke, Chayama Kazua |
| Genome-wide association identifies OBFC1 as a locus involved in human leukocyte telomere biology.
Proceedings of the National Academy of Sciences of the United States of America 2010 May 107 (20): 9293-8. Levy Daniel, Neuhausen Susan L, Hunt Steven C, Kimura Masayuki, Hwang Shih-Jen, Chen Wei, Bis Joshua C, Fitzpatrick Annette L, Smith Erin, Johnson Andrew D, Gardner Jeffrey P, Srinivasan Sathanur R, Schork Nicholas, Rotter Jerome I, Herbig Utz, Psaty Bruce M, Sastrasinh Malinee, Murray Sarah S, Vasan Ramachandran S, Province Michael A, Glazer Nicole L, Lu Xiaobin, Cao Xiaojian, Kronmal Richard, Mangino Massimo, Soranzo Nicole, Spector Tim D, Berenson Gerald S, Aviv Abrah |
| 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 |
| A genome-wide association study of total bilirubin and cholelithiasis risk in sickle cell anemia.
PloS one 2012 7 (4): e34741. Milton Jacqueline N, Sebastiani Paola, Solovieff Nadia, Hartley Stephen W, Bhatnagar Pallav, Arking Dan E, Dworkis Daniel A, Casella James F, Barron-Casella Emily, Bean Christopher J, Hooper W Craig, DeBaun Michael R, Garrett Melanie E, Soldano Karen, Telen Marilyn J, Ashley-Koch Allison, Gladwin Mark T, Baldwin Clinton T, Steinberg Martin H, Klings Elizabeth |
| Genome-wide association study identifies novel loci associated with serum level of vitamin B12 in Chinese men.
Human molecular genetics 2012 Jun 21 (11): 2610-7. Lin Xiaoling, Lu Daru, Gao Yong, Tao Sha, Yang Xiaobo, Feng Junjie, Tan Aihua, Zhang Haiying, Hu Yanling, Qin Xue, Kim Seong-Tae, Peng Tao, Li Li, Mo Linjian, Zhang Shijun, Trent Jeffrey M, Mo Zengnan, Zheng S Lilly, Xu Jianfeng, Sun Jiel |
| GWAS of blood cell traits identifies novel associated loci and epistatic interactions in Caucasian and African-American children.
Human molecular genetics 2013 Jan . Li J, Glessner JT, Zhang H, Hou C, Wei Z, Bradfield JP, Mentch FD, Guo Y, Kim C, Xia Q, Chiavacci RM, Thomas KA, Qiu H, Grant SF, Furth SL, Hakonarson H, Sleiman PM |
| The genetics of hemoglobin A2 regulation in sickle cell anemia.
American journal of hematology 2014 Nov 89 (11): 1019-23. Griffin Paula J, Sebastiani Paola, Edward Heather, Baldwin Clinton T, Gladwin Mark T, Gordeuk Victor R, Chui David H K, Steinberg Martin |
| Genome wide association study of fetal hemoglobin in sickle cell anemia in Tanzania.
PloS one 2014 9 (11): e111464. Mtatiro Siana Nkya, Singh Tarjinder, Rooks Helen, Mgaya Josephine, Mariki Harvest, Soka Deogratius, Mmbando Bruno, Msaki Evarist, Kolder Iris, Thein Swee Lay, Menzel Stephan, Cox Sharon E, Makani Julie, Barrett Jeffrey |
| Genome-wide association study to identify variants associated with acute severe vaso-occlusive pain in sickle cell anemia.
Blood 2017 08 130 (5): 686-688. Chaturvedi Shruti, Bhatnagar Pallav, Bean Christopher J, Steinberg Martin H, Milton Jaqueline N, Casella James F, Barron-Casella Emily, Arking Dan E, DeBaun Michael |
| Genome-wide association study of erythrocyte density in sickle cell disease patients.
Blood cells, molecules & diseases 2017 Jun 65 60-65. Ilboudo Yann, Bartolucci Pablo, Rivera Alicia, Sedzro Josepha-Clara, Beaudoin Mélissa, Trudel Marie, Alper Seth L, Brugnara Carlo, Galactéros Frédéric, Lettre Guillau |
| Interaction of iron status with single nucleotide polymorphisms on incidence of type 2 diabetes.
PloS one 2017 12 (4): e0175681. Kim Jihye, Kim Mi Kyung, Jung Sukyoung, Lim Ji Eun, Shin Myung-Hee, Kim Yeon-Jung, Oh Bermse |
| Circulating Chemerin Levels, but not the RARRES2 Polymorphisms, Predict the Long-Term Outcome of Angiographically Confirmed Coronary Artery Disease.
International journal of molecular sciences 2019 Mar 20 (5): . Er Leay Kiaw, Hsu Lung-An, Juang Jyh-Ming Jimmy, Chiang Fu-Tien, Teng Ming-Sheng, Tzeng I-Shiang, Wu Semon, Lin Jeng-Feng, Ko Yu-L |
| Genetic Variants Associated With Immunosuppressant Pharmacokinetics and Adverse Effects in the DeKAF Genomics Genome-wide Association Studies.
Transplantation 2019 Jun 103 (6): 1131-1139. Oetting William S, Wu Baolin, Schladt David P, Guan Weihua, van Setten Jessica, Keating Brendan J, Iklé David, Remmel Rory P, Dorr Casey R, Mannon Roslyn B, Matas Arthur J, Israni Ajay K, Jacobson Pamala A, |
| Predicted loss and gain of function mutations in ACO1 are associated with erythropoiesis.
Communications biology 2020 Apr 3 (1): 189. Oskarsson Gudjon R, Oddsson Asmundur, Magnusson Magnus K, Kristjansson Ragnar P, Halldorsson Gisli H, Ferkingstad Egil, Zink Florian, Helgadottir Anna, Ivarsdottir Erna V, Arnadottir Gudny A, Jensson Brynjar O, Katrinardottir Hildigunnur, Sveinbjornsson Gardar, Kristinsdottir Anna M, Lee Amy L, Saemundsdottir Jona, Stefansdottir Lilja, Sigurdsson Jon K, Davidsson Olafur B, Benonisdottir Stefania, Jonasdottir Aslaug, Jonasdottir Adalbjorg, Jonsson Stefan, Gudmundsson Reynir L, Asselbergs Folkert W, Tragante Vinicius, Gunnarsson Bjarni, Masson Gisli, Thorleifsson Gudmar, Rafnar Thorunn, Holm Hilma, Olafsson Isleifur, Onundarson Pall T, Gudbjartsson Daniel F, Norddahl Gudmundur L, Thorsteinsdottir Unnur, Sulem Patrick, Stefansson Ka |
| Genome-wide Association Study Identifies HLA-DPB1 as a Significant Risk Factor for Severe Aplastic Anemia.
American journal of human genetics 2020 Feb 106 (2): 264-271. Savage Sharon A, Viard Mathias, O'hUigin Colm, Zhou Weiyin, Yeager Meredith, Li Shengchao Alfred, Wang Tao, Ramsuran Veron, Vince Nicolas, Vogt Aurelie, Hicks Belynda, Burdett Laurie, Chung Charles, Dean Michael, de Andrade Kelvin C, Freedman Neal D, Berndt Sonja I, Rothman Nathaniel, Lan Qing, Cerhan James R, Slager Susan L, Zhang Yawei, Teras Lauren R, Haagenson Michael, Chanock Stephen J, Spellman Stephen R, Wang Youjin, Willis Amanda, Askar Medhat, Lee Stephanie J, Carrington Mary, Gadalla Shahinaz |
| Novel variant in glycophorin c gene protects against ribavirin-induced anemia during chronic hepatitis C treatment.
Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie 2021 Sep 143 112195. Lin Jennifer J, Loucks Catrina M, Trueman Jessica N, Drögemöller Britt I, Wright Galen E B, Yoshida Eric M, Ford Jo-Ann, Lee Samuel S, Kim Richard B, Al-Judaibi Bandar, Schwarz Ute I, Ramji Alnoor, Tam Edward, Ross Colin J, Carleton Bruce |
| GWAS of serum ALT and AST reveals an association of SLC30A10 Thr95Ile with hypermanganesemia symptoms.
Nature communications 2021 7 12 (1): 4571. Ward Lucas D, Tu Ho-Chou, Quenneville Chelsea B, Tsour Shira, Flynn-Carroll Alexander O, Parker Margaret M, Deaton Aimee M, Haslett Patrick A J, Lotta Luca A, Verweij Niek, Ferreira Manuel A R, , , Baras Aris, Hinkle Gregory, Nioi Pa |
| Multiple-ancestry genome-wide association study identifies 27 loci associated with measures of hemolysis following blood storage.
The Journal of clinical investigation 2021 May . Page Grier P, Kanias Tamir, Guo Yuelong J, Lanteri Marion C, Zhang Xu, Mast Alan E, Cable Ritchard G, Spencer Bryan R, Kiss Joseph E, Fang Fang, Endres-Dighe Stacy M, Brambilla Donald, Nouraie Mehdi, Gordeuk Victor R, Kleinman Steve, Busch Michael P, Gladwin Mark T, |
| A genome-wide meta-analysis yields 46 new loci associating with biomarkers of iron homeostasis.
Communications biology 2021 Feb 4 (1): 156. Bell Steven, Rigas Andreas S, Magnusson Magnus K, Ferkingstad Egil, Allara Elias, Bjornsdottir Gyda, Ramond Anna, Sørensen Erik, Halldorsson Gisli H, Paul Dirk S, Burgdorf Kristoffer S, Eggertsson Hannes P, Howson Joanna M M, Thørner Lise W, Kristmundsdottir Snaedis, Astle William J, Erikstrup Christian, Sigurdsson Jon K, Vuckovic Dragana, Dinh Khoa M, Tragante Vinicius, Surendran Praveen, Pedersen Ole B, Vidarsson Brynjar, Jiang Tao, Paarup Helene M, Onundarson Pall T, Akbari Parsa, Nielsen Kaspar R, Lund Sigrun H, Juliusson Kristinn, Magnusson Magnus I, Frigge Michael L, Oddsson Asmundur, Olafsson Isleifur, Kaptoge Stephen, Hjalgrim Henrik, Runarsson Gudmundur, Wood Angela M, Jonsdottir Ingileif, Hansen Thomas F, Sigurdardottir Olof, Stefansson Hreinn, Rye David, , Peters James E, Westergaard David, Holm Hilma, Soranzo Nicole, Banasik Karina, Thorleifsson Gudmar, Ouwehand Willem H, Thorsteinsdottir Unnur, Roberts David J, Sulem Patrick, Butterworth Adam S, Gudbjartsson Daniel F, Danesh John, Brunak Søren, Di Angelantonio Emanuele, Ullum Henrik, Stefansson Ka |
| Deep Learning of the Retina Enables Phenome- and Genome-Wide Analyses of the Microvasculature.
Circulation 2021 11 145 (2): 134-150. Zekavat Seyedeh Maryam, Raghu Vineet K, Trinder Mark, Ye Yixuan, Koyama Satoshi, Honigberg Michael C, Yu Zhi, Pampana Akhil, Urbut Sarah, Haidermota Sara, O'Regan Declan P, Zhao Hongyu, Ellinor Patrick T, Segrè Ayellet V, Elze Tobias, Wiggs Janey L, Martone James, Adelman Ron A, Zebardast Nazlee, Del Priore Lucian, Wang Jay C, Natarajan Prade |
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