Human Genome Epidemiology Literature Finder
Heart, Lung, Blood and Sleep Disorders
Records 1 - 30 (of 59 Records) |
Query Trace: Blood Diseases |
---|
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 association study of platelet factor 4/heparin antibodies in heparin-induced thrombocytopenia.
Blood advances 2022 May . Giles Jason B, Steiner Heidi E, Rollin Jerome, Shaffer Christian M, Momozawa Yukihide, Mushiroda Taisei, Inai Chihiro, Selleng Kathleen, Thiele Thomas, Pouplard Claire, Heddle Nancy M, Kubo Michiaki, Miller Elise C, Martinez Kiana L, Phillips Elizabeth J, Warkentin Theodore E, Gruel Yves, Greinacher Andreas, Roden Dan M, Karnes Jason |
ABO O blood group as a risk factor for platelet reactivity in heparin-induced thrombocytopenia.
Blood 2022 4 140 (3): 274-284. Karnes Jason H, Rollin Jerome, Giles Jason B, Martinez Kiana L, Steiner Heidi E, Shaffer Christian M, Momozawa Yukihide, Inai Chihiro, Bombin Andrei, Shi Mingjian, Mosley Jonathan D, Stanaway Ian, Selleng Kathleen, Thiele Thomas, Mushiroda Taisei, Pouplard Claire, Heddle Nancy M, Kubo Michiaki, Phillips Elizabeth J, Warkentin Theodore E, Gruel Yves, Greinacher Andreas, Roden Dan |
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 |
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 |
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 |
Genetic Profile of Endotoxemia Reveals an Association With Thromboembolism and Stroke.
Journal of the American Heart Association 2021 Oct e022482. Leskelä Jaakko, Toppila Iiro, Härma Mari-Anne, Palviainen Teemu, Salminen Aino, Sandholm Niina, Pietiäinen Milla, Kopra Elisa, Pais de Barros Jean-Paul, , Lassenius Mariann I, Kumar Anmol, Harjutsalo Valma, Roslund Kajsa, Forsblom Carol, Loukola Anu, Havulinna Aki S, Lagrost Laurent, Salomaa Veikko, Groop Per-Henrik, Perola Markus, Kaprio Jaakko, Lehto Markku, Pussinen Pirkko |
Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiative.
Human molecular genetics 2021 9 31 (3): 347-361. Little Amarise, Hu Yao, Sun Quan, Jain Deepti, Broome Jai, Chen Ming-Huei, Thibord Florian, McHugh Caitlin, Surendran Praveen, Blackwell Thomas W, Brody Jennifer A, Bhan Arunoday, Chami Nathalie, de Vries Paul S, Ekunwe Lynette, Heard-Costa Nancy, Hobbs Brian D, Manichaikul Ani, Moon Jee-Young, Preuss Michael H, Ryan Kathleen, Wang Zhe, Wheeler Marsha, Yanek Lisa R, Abecasis Goncalo R, Almasy Laura, Beaty Terri H, Becker Lewis C, Blangero John, Boerwinkle Eric, Butterworth Adam S, Choquet Hélène, Correa Adolfo, Curran Joanne E, Faraday Nauder, Fornage Myriam, Glahn David C, Hou Lifang, Jorgenson Eric, Kooperberg Charles, Lewis Joshua P, Lloyd-Jones Donald M, Loos Ruth J F, Min Yuan-I, Mitchell Braxton D, Morrison Alanna C, Nickerson Deborah A, North Kari E, O'Connell Jeffrey R, Pankratz Nathan, Psaty Bruce M, Vasan Ramachandran S, Rich Stephen S, Rotter Jerome I, Smith Albert V, Smith Nicholas L, Tang Hua, Tracy Russell P, Conomos Matthew P, Laurie Cecelia A, Mathias Rasika A, Li Yun, Auer Paul L, , Thornton Timothy, Reiner Alexander P, Johnson Andrew D, Raffield Laura |
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 |
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 |
Dissecting genetic factors affecting phenylephrine infusion rates during anesthesia: a genome-wide association study employing EHR data.
BMC medicine 2019 08 17 (1): 168. Zhang Yanfei, Poler S Mark, Li Jiang, Abedi Vida, Pendergrass Sarah A, Williams Marc S, Lee Ming Ta Micha |
LRRTM4 and PCSK5 Genetic Polymorphisms as Markers for Cognitive Impairment in A Hypotensive Aging Population: A Genome-Wide Association Study in Taiwan.
Journal of clinical medicine 2019 Jul 8 (8): . Chen Yi-Chun, Liu Yu-Li, Tsai Shih-Jen, Kuo Po-Hsiu, Huang Shih-Sin, Lee Yun-Shi |
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 |
GWAS and PheWAS of red blood cell components in a Northern Nevadan cohort.
PloS one 2019 14 (6): e0218078. Read Robert W, Schlauch Karen A, Elhanan Gai, Metcalf William J, Slonim Anthony D, Aweti Ramsey, Borkowski Robert, Grzymski Joseph |
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, |
Genetic Study of Severe Prolonged Lymphopenia in Multiple Sclerosis Patients Treated With Dimethyl Fumarate.
Frontiers in genetics 2019 10 1039. Sangurdekar Dipen, Sun Chao, McLaughlin Helen, Ayling-Rouse Katherine, Allaire Normand E, Penny Michelle A, Bronson Paola |
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, |
Genome-Wide Association Study Links Receptor Tyrosine Kinase Inhibitor Sprouty 2 to Thrombocytopenia after Coronary Artery Bypass Surgery.
Thrombosis and haemostasis 2018 Aug . Karhausen Jörn A, Qi Wenjing, Smeltz Alan M, Li Yi-Ju, Shah Svati H, Kraus William E, Mathew Joseph P, Podgoreanu Mihai V, Kertai Miklos D, |
Targeted resequencing of a locus for heparin-induced thrombocytopenia on chromosome 5 identified in a genome-wide association study.
Journal of molecular medicine (Berlin, Germany) 2018 Jun . Witten Anika, Bolbrinker Juliane, Barysenka Andrei, Huber Matthias, Rühle Frank, Nowak-Göttl Ulrike, Garbe Edeltraut, Kreutz Reinhold, Stoll Moni |
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 |
Clinical and Genetic Determinants of Varicose Veins.
Circulation 2018 Dec 138 (25): 2869-2880. Fukaya Eri, Flores Alyssa M, Lindholm Daniel, Gustafsson Stefan, Zanetti Daniela, Ingelsson Erik, Leeper Nicholas |
Genetic association with B-cell acute lymphoblastic leukemia in allogeneic transplant patients differs by age and sex.
Blood advances 2017 Sep 1 (20): 1717-1728. Clay-Gilmour Alyssa I, Hahn Theresa, Preus Leah M, Onel Kenan, Skol Andrew, Hungate Eric, Zhu Qianqian, Haiman Christopher A, Stram Daniel O, Pooler Loreall, Sheng Xin, Yan Li, Liu Qian, Hu Qiang, Liu Song, Battaglia Sebastiano, Zhu Xiaochun, Block AnneMarie W, Sait Sheila N J, Karaesmen Ezgi, Rizvi Abbas, Weisdorf Daniel J, Ambrosone Christine B, Tritchler David, Ellinghaus Eva, Ellinghaus David, Stanulla Martin, Clavel Jacqueline, Orsi Laurent, Spellman Stephen, Pasquini Marcelo C, McCarthy Philip L, Sucheston-Campbell Lara |
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 |
Genome-wide Association Studies of Retinal Vessel Tortuosity Identify Numerous Novel Loci Revealing Genes and Pathways Associated With Ocular and Cardiometabolic Diseases.
Ophthalmology science 2023 5 3 (3): 100288. Tomasoni Mattia, Beyeler Michael Johannes, Vela Sofia Ortin, Mounier Ninon, Porcu Eleonora, Corre Tanguy, Krefl Daniel, Button Alexander Luke, Abouzeid Hana, Lazaros Konstantinidis, Bochud Murielle, Schlingemann Reinier, Bergin Ciara, Bergmann Sv |
- Page last reviewed:Feb 1, 2024
- Page last updated:May 06, 2024
- Content source: