Human Genome Epidemiology Literature Finder
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Records 1 - 25 (of 25 Records) |
| Query Trace: Sickle cell[original query] |
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A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15.
Nature genetics 2007 Oct 39 (10): 1197-9. Menzel Stephan, Garner Chad, Gut Ivo, Matsuda Fumihiko, Yamaguchi Masao, Heath Simon, Foglio Mario, Zelenika Diana, Boland Anne, Rooks Helen, Best Steve, Spector Tim D, Farrall Martin, Lathrop Mark, Thein Swee L |
| 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 |
| 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 |
| Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients.
Journal of human genetics 2011 Apr 56 (4): 316-23. Bhatnagar Pallav, Purvis Shirley, Barron-Casella Emily, DeBaun Michael R, Casella James F, Arking Dan E, Keefer Jeffrey |
| Genome-wide association study indicates two novel resistance loci for severe malaria.
Nature 2012 Sep 489 (7416): 443-6. Timmann Christian, Thye Thorsten, Vens Maren, Evans Jennifer, May Jürgen, Ehmen Christa, Sievertsen Jürgen, Muntau Birgit, Ruge Gerd, Loag Wibke, Ansong Daniel, Antwi Sampson, Asafo-Adjei Emanuel, Nguah Samuel Blay, Kwakye Kingsley Osei, Akoto Alex Osei Yaw, Sylverken Justice, Brendel Michael, Schuldt Kathrin, Loley Christina, Franke Andre, Meyer Christian G, Agbenyega Tsiri, Ziegler Andreas, Horstmann Rolf |
| 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 meta-analysis of systolic blood pressure in children with sickle cell disease.
PloS one 2013 8 (9): e74193. Bhatnagar Pallav, Barron-Casella Emily, Bean Christopher J, Milton Jacqueline N, Baldwin Clinton T, Steinberg Martin H, Debaun Michael, Casella James F, Arking Dan |
| Genetic determinants of haemolysis in sickle cell anaemia.
British journal of haematology 2013 Apr 161 (2): 270-8. Milton Jacqueline N, Rooks Helen, Drasar Emma, McCabe Elizabeth L, Baldwin Clinton T, Melista Efi, Gordeuk Victor R, Nouraie Mehdi, Kato Gregory R, Kato Gregory J, Minniti Caterina, Taylor James, Campbell Andrew, Luchtman-Jones Lori, Rana Sohail, Castro Oswaldo, Zhang Yingze, Thein Swee Lay, Sebastiani Paola, Gladwin Mark T, , Steinberg Martin |
| 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 |
| A Genome-Wide Screen for Large-Effect Alloimmunization Susceptibility Loci among Red Blood Cell Transfusion Recipients with Sickle Cell Disease.
Transfusion medicine and hemotherapy : offizielles Organ der Deutschen Gesellschaft fur Transfusionsmedizin und Immunhamatologie 2014 Nov 41 (6): 453-61. Hanchard Neil A, Moulds Joann M, Belmont John W, Chen Ali |
| African Ancestry-Specific Alleles and Kidney Disease Risk in Hispanics/Latinos.
Journal of the American Society of Nephrology : JASN 2016 Sep . Kramer Holly J, Stilp Adrienne M, Laurie Cathy C, Reiner Alex P, Lash James, Daviglus Martha L, Rosas Sylvia E, Ricardo Ana C, Tayo Bamidele O, Flessner Michael F, Kerr Kathleen F, Peralta Carmen, Durazo-Arvizu Ramon, Conomos Matt, Thornton Timothy, Rotter Jerome, Taylor Kent D, Cai Jainwen, Eckfeldt John, Chen Han, Papanicolau George, Franceschini No |
| Original Research: A case-control genome-wide association study identifies genetic modifiers of fetal hemoglobin in sickle cell disease.
Experimental biology and medicine (Maywood, N.J.) 2016 04 241 (7): 706-18. Liu Li, Pertsemlidis Alexander, Ding Liang-Hao, Story Michael D, Steinberg Martin H, Sebastiani Paola, Hoppe Carolyn, Ballas Samir K, Pace Betty |
| 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 |
| Identification of unique venous thromboembolism-susceptibility variants in African-Americans.
Thrombosis and haemostasis 2017 Feb . Heit John A, Armasu Sebastian M, McCauley Bryan M, Kullo Iftikhar J, Sicotte Hugues, Pathak Jyotishman, Chute Christopher G, Gottesman Omri, Bottinger Erwin P, Denny Joshua C, Roden Dan M, Li Rongling, Ritchie Marylyn D, de Andrade Mari |
| A locus on chromosome 5 shows African ancestry-limited association with alloimmunization in sickle cell disease.
Blood advances 2018 Dec 2 (24): 3637-3647. Williams Lesedi M, Qi Zhihua, Batai Ken, Hooker Stanley, Hall Nancy J, Machado Roberto F, Chen Alice, Campbell-Lee Sally, Guan Yongtao, Kittles Rick, Hanchard Neil |
| Novel genetic polymorphisms associated with severe malaria and under selective pressure in North-eastern Tanzania.
PLoS genetics 2018 Jan 14 (1): e1007172. Ravenhall Matt, Campino Susana, Sepúlveda Nuno, Manjurano Alphaxard, Nadjm Behzad, Mtove George, Wangai Hannah, Maxwell Caroline, Olomi Raimos, Reyburn Hugh, Drakeley Christopher J, Riley Eleanor M, Clark Taane G, |
| Mapping eGFR loci to the renal transcriptome and phenome in the VA Million Veteran Program.
Nature communications 2019 Aug 10 (1): 3842. Hellwege Jacklyn N, Velez Edwards Digna R, Giri Ayush, Qiu Chengxiang, Park Jihwan, Torstenson Eric S, Keaton Jacob M, Wilson O D, Robinson-Cohen Cassianne, Chung Cecilia P, Roumie Christianne L, Klarin Derek, Damrauer Scott M, DuVall Scott L, Siew Edward, Akwo Elvis A, Wuttke Matthias, Gorski Mathias, Li Man, Li Yong, Gaziano J Michael, Wilson Peter W F, Tsao Philip S, O'Donnell Christopher J, Kovesdy Csaba P, Pattaro Cristian, Köttgen Anna, Susztak Katalin, Edwards Todd L, Hung Adriana |
| A Genome-Wide Association Study Identifies Blood Disorder-Related Variants Influencing Hemoglobin A With Implications for Glycemic Status in U.S. Hispanics/Latinos.
Diabetes care 2019 Jun . Moon Jee-Young, Louie Tin L, Jain Deepti, Sofer Tamar, Schurmann Claudia, Below Jennifer E, Lai Chao-Qiang, Aviles-Santa M Larissa, Talavera Gregory A, Smith Caren E, Petty Lauren E, Bottinger Erwin P, Chen Yii-Der Ida, Taylor Kent D, Daviglus Martha L, Cai Jianwen, Wang Tao, Tucker Katherine L, Ordovás José M, Hanis Craig L, Loos Ruth J F, Schneiderman Neil, Rotter Jerome I, Kaplan Robert C, Qi Qib |
| Clinical and Genetic Predictors of Priapism in Sickle Cell Disease: Results from the Recipient Epidemiology and Donor Evaluation Study III Brazil Cohort Study.
The journal of sexual medicine 2019 Oct . Cintho Ozahata Mina, Page Grier P, Guo Yuelong, Ferreira João Eduardo, Dinardo Carla Luana, Carneiro-Proietti Anna Bárbara F, Loureiro Paula, Mota Rosimere Afonso, Rodrigues Daniela O W, Belisario André Rolim, Maximo Claudia, Flor-Park Miriam V, Custer Brian, Kelly Shannon, Sabino Ester Cerdeira, |
| 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, |
| Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals.
Nature communications 2022 8 13 (1): 4923. Tahir Usman A, Katz Daniel H, Avila-Pachecho Julian, Bick Alexander G, Pampana Akhil, Robbins Jeremy M, Yu Zhi, Chen Zsu-Zsu, Benson Mark D, Cruz Daniel E, Ngo Debby, Deng Shuliang, Shi Xu, Zheng Shuning, Eisman Aaron S, Farrell Laurie, Hall Michael E, Correa Adolfo, Tracy Russell P, Durda Peter, Taylor Kent D, Liu Yongmei, Johnson W Craig, Guo Xiuqing, Yao Jie, Chen Yii-Der Ida, Manichaikul Ani W, Ruberg Frederick L, Blaner William S, Jain Deepti, , Bouchard Claude, Sarzynski Mark A, Rich Stephen S, Rotter Jerome I, Wang Thomas J, Wilson James G, Clish Clary B, Natarajan Pradeep, Gerszten Robert |
| Genome-wide meta-analysis identifies new candidate genes for sickle cell disease nephropathy.
Blood advances 2022 11 . Garrett Melanie E, Soldano Karen L, Erwin Kyle N, Zhang Yingze, Gordeuk Victor R, Gladwin Mark T, Telen Marilyn J, Ashley-Koch Allison |
| Sex-specific genetic modifiers identified susceptibility of cold stored red blood cells to osmotic hemolysis.
BMC genomics 2022 3 23 (1): 227. Fang Fang, Hazegh Kelsey, Mast Alan E, Triulzi Darrell J, Spencer Bryan R, Gladwin Mark T, Busch Michael P, Kanias Tamir, Page Grier |
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