Human Genome Epidemiology Literature Finder
Heart, Lung, Blood and Sleep Disorders
Records 1 - 30 (of 44 Records) |
Query Trace: Blood Disorders[original query] |
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Heme oxygenase-1 gene promoter polymorphism is associated with reduced incidence of acute chest syndrome among children with sickle cell disease. Blood 2012 Nov 120 (18): 3822-8. Bean Christopher J, Boulet Sheree L, Ellingsen Dorothy, Pyle Meredith E, Barron-Casella Emily A, Casella James F, Payne Amanda B, Driggers Jennifer, Trau Heidi A, Yang Genyan, Jones Kimberly, Ofori-Acquah Solomon F, Hooper W Craig, DeBaun Michael |
Increased risk of venous thromboembolism is associated with genetic variation in heme oxygenase-1 in Blacks. Thrombosis research 2012 Dec 130 (6): 942-7. Bean Christopher J, Boulet Sheree L, Ellingsen Dorothy, Trau Heidi, Ghaji Nafisa, Hooper W Craig, Austin Harla |
Thrombophilias and adverse pregnancy outcomes: results from the Danish National Birth Cohort. Journal of thrombosis and haemostasis : JTH 2012 Jul 10 (7): 1320-5. Lykke J A, Bare L A, Olsen J, Lagier R, Arellano A R, Tong C, Paidas M J, Langhoff-Roos |
Three most common nonsynonymous UGT1A6*2 polymorphisms (Thr181Ala, Arg184Ser and Ser7Ala) and therapeutic response to deferiprone in ß-thalassemia major patients. Gene 2013 Dec 531 (2): 301-5. Dadheech Sneha, Rao A Venkateswara, Shaheen Uzma, Hussien Mohammed Dyia, Jain Suman, Jyothy A, Munshi Anja |
Acute chest syndrome is associated with single nucleotide polymorphism-defined beta globin cluster haplotype in children with sickle cell anaemia. British journal of haematology 2013 Oct 163 (2): 268-76. Bean Christopher J, Boulet Sheree L, Yang Genyan, Payne Amanda B, Ghaji Nafisa, Pyle Meredith E, Hooper W Craig, Bhatnagar Pallav, Keefer Jeffrey, Barron-Casella Emily A, Casella James F, Debaun Michael |
Microsomal epoxide hydrolase (EPHX1) polymorphisms are associated with aberrant promoter methylation of ERCC3 and hematotoxicity in benzene-exposed workers. Environmental and molecular mutagenesis 2013 Jul 54 (6): 397-405. Xing Caihong, Chen Qi, Li Guilan, Zhang Linyuan, Zheng Min, Zou Zhengyong, Hou Lifang, Wang Qian-Fei, Liu Xin, Guo Xinbi |
Cytochrome P450 2D6 polymorphisms and predicted opioid metabolism in African American children with sickle cell disease. Journal of pediatric hematology/oncology 2013 Oct 35 (7): e301-5. Yee Marianne M, Josephson Cassandra, Hill Charles E, Harrington Rosiland, Castillejo Marta-Inés, Ramjit Ruan, Osunkwo Ifeyin |
Single nucleotide polymorphism array analysis of bone marrow failure patients reveals characteristic patterns of genetic changes. British journal of haematology 2014 Jan 164 (1): 73-82. Babushok Daria V, Xie Hongbo M, Roth Jacquelyn J, Perdigones Nieves, Olson Timothy S, Cockroft Joshua D, Gai Xiaowu, Perin Juan C, Li Yimei, Paessler Michele E, Hakonarson Hakon, Podsakoff Gregory M, Mason Philip J, Biegel Jaclyn A, Bessler Moni |
[Strokes and hemoglobinopathies in Burkina Faso]. Medecine et sante tropicales 2013 Jan . Napon C, Kaboré A, Ouédraogo M, Dravé A, Lompo L, Kaboré J |
High HLA-DP Expression and Graft-versus-Host Disease. The New England journal of medicine 2015 Aug 373 (7): 599-609. Petersdorf Effie W, Malkki Mari, O'hUigin Colm, Carrington Mary, Gooley Ted, Haagenson Michael D, Horowitz Mary M, Spellman Stephen R, Wang Tao, Stevenson Phil |
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 |
Prevalence and genetic analysis of a- and ß-thalassemia in Baise region, a multi-ethnic region in southern China. Gene 2016 Feb . He Sheng, Qin Qian, Yi Shang, Wei Yuan, Lin Li, Chen Shaoke, Deng Jianping, Xu Xianmin, Zheng Chenguang, Chen Biy |
Serum Soluble Transferrin Receptor Concentrations Are Elevated in Congolese Children with Glucose-6-Phosphate Dehydrogenase Variants, but Not Sickle Cell Variants or ?-Thalassemia. The Journal of nutrition 2017 8 147 (9): 1785-1794. Barker Mikaela K, Henderson Amanda M, Naguib Karimah, Vercauteren Suzanne M, Devlin Angela M, Albert Arianne Y, Bahizire Esto, Tugirimana Pierrot L, Akilimali Pierre Z, Boy Erick, Green Tim J, Karakochuk Crystal |
Prevalence of Thalassemia and Glucose-6-Phosphate Dehydrogenase Deficiency in Newborns and Adults at the Ramathibodi Hospital, Bangkok, Thailand. Hemoglobin 2017 12 41 (4-6): 260-266. Banyatsuppasin Wansa, Jindadamrongwech Sumalee, Limrungsikul Anchalee, Butthep Punn |
Mutational Profiles of F8 and F9 in a Cohort of Haemophilia A and Haemophilia B Patients in the Multi-ethnic Malaysian Population. Mediterranean journal of hematology and infectious diseases 2018 9 10 (1): e2018056. Zahari Maimiza, Sulaiman Siti Aishah, Othman Zulhabri, Ayob Yasmin, Karim Faraizah Abd, Jamal Rahm |
Molecular characterization of ?- and ?-thalassemia in the Yulin region of Southern China. Gene 2018 Feb . He Sheng, Li Jihui, Li Dong Ming, Yi Shang, Lu Xiongcai, Luo Yudi, Liang Yi, Feng Chunfeng, Chen Biyan, Zheng Chenguang, Qiu Xiaox |
Macrothrombocytopenia associated with a rare GFI1B missense variant confounding the presentation of immune thrombocytopenia. Pediatric blood & cancer 2019 6 66 (9): e27874. Cheng Aaron N, Bao Erik L, Fiorini Claudia, Sankaran Vijay |
HLA-B leader and survivorship after HLA-mismatched unrelated donor transplantation. Blood 2020 6 136 (3): 362-369. Petersdorf Effie W, Stevenson Philip, Bengtsson Mats, De Santis Dianne, Dubois Valerie, Gooley Ted, Horowitz Mary, Hsu Katharine, Madrigal J Alejandro, Malkki Mari, McKallor Caroline, Morishima Yasuo, Oudshoorn Machteld, Spellman Stephen R, Villard Jean, Carrington Ma |
Use of the HLA-B leader to optimize cord blood transplantation. Haematologica 2020 10 106 (12): 3107-3114. Petersdorf Effie W, Gooley Ted, Volt Fernanda, Kenzey Chantal, Madrigal Alejandro, McKallor Caroline, Querol Sergio, Rafii Hanadi, Rocha Vanderson, Tamouza Ryad, Chabannon Christian, Ruggeri Annalisa, Gluckman Elia |
Human mutational constraint as a tool to understand biology of rare and emerging bone marrow failure syndromes. Blood advances 2020 10 4 (20): 5232-5245. Oved Joseph H, Babushok Daria V, Lambert Michele P, Wolfset Nicole, Kowalska M Anna, Poncz Mortimer, Karczewski Konrad J, Olson Timothy |
Nationwide carrier detection and molecular characterization of ?-thalassemia and hemoglobin E variants in Bangladeshi population. Orphanet journal of rare diseases 2020 1 15 (1): 15. Noor Farjana Akther, Sultana Nusrat, Bhuyan Golam Sarower, Islam Md Tarikul, Hossain Mohabbat, Sarker Suprovath Kumar, Islam Khaleda, Khan Waqar Ahmed, Rahman Mujahida, Qadri Syeda Kashfi, Shekhar Hossain Uddin, Qadri Firdausi, Qadri Syed Saleheen, Mannoor Kaiiss |
Analysis of Relationships between Immune Checkpoint and Methylase Gene Polymorphisms and Outcomes after Unrelated Bone Marrow Transplantation. Cancers 2021 Jun 13 (11): . Takahashi Hidekazu, Okayama Naoko, Yamaguchi Natsu, Nomura Moe, Miyahara Yuta, Mahbub M H, Hase Ryosuke, Morishima Yasuo, Suehiro Yutaka, Yamasaki Takahiro, Tamada Koji, Takahashi Satoshi, Tojo Arinobu, Tanabe Tsuyos |
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 |
Genotype-Guided Prescription of Azathioprine Reduces the Incidence of Adverse Drug Reactions in TPMT Intermediate Metabolizers to a Similar Incidence as Normal Metabolizers. Advances in therapy 2022 2 39 (4): 1743-1753. Casajús Ana, Zubiaur Pablo, Méndez Marta, Campodónico Diana, Gómez Antía, Navares-Gómez Marcos, Villapalos-García Gonzalo, Soria-Chacartegui Paula, Novalbos Jesús, Román Manuel, Mejía-Abril Gina, Ochoa Dolores, Abad-Santos Francis |
Schizophrenia-associated somatic copy-number variants from 12,834 cases reveal recurrent NRXN1 and ABCB11 disruptions. Cell genomics 2023 8 3 (8): 100356. Eduardo A Maury, Maxwell A Sherman, Giulio Genovese, Thomas G Gilgenast, Tushar Kamath, S J Burris, Prashanth Rajarajan, Erin Flaherty, Schahram Akbarian, Andrew Chess, Steven A McCarroll, Po-Ru Loh, Jennifer E Phillips-Cremins, Kristen J Brennand, Evan Z Macosko, James T R Walters, Michael O'Donovan, Patrick Sullivan, , , Jonathan Sebat, Eunjung A Lee, Christopher A Wal |
Exploration of KIR genes and hematological-related diseases in Chinese Han population. Scientific reports 2023 6 13 (1): 9773. Ye-Mo Li, Yu-Xia Li, Xiao-Zhuang Hu, Dai-Yang Li, Lin An, Zhi-Yang Yuan, Zhong-Liang Liu, Ke-Ming Du, Zhong-Zheng Zhe |
?- and ?-Globin Gene Mutations in Individuals with Hemoglobinopathies in the Chattogram and Sylhet Regions of Bangladesh. Hemoglobin 2023 3 1-8. Kabir Tamanna, Anwar Saeed, Mourosi Jarin Taslem, Akter Shanjida, Hosen Mohammad Jak |
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- Page last updated:Apr 22, 2024
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