Human Genome Epidemiology Literature Finder
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Records 1 - 13 (of 13 Records) |
| Query Trace: Disease and BMP6[original query] |
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| Association of polymorphisms of IGF1R and genes in the transforming growth factor- beta /bone morphogenetic protein pathway with bacteremia in sickle cell anemia. Clinical infectious diseases : an official publication of the Infectious Diseases Society of America 2006 Sep 43 (5): 593-8. Adewoye Adeboye H, Nolan Vikki G, Ma Qianli, Baldwin Clinton, Wyszynski Diego F, Farrell John J, Farrer Lindsay A, Steinberg Martin |
| Identification of genetic polymorphisms associated with risk for pulmonary hypertension in sickle cell disease. Blood 2008 Jun 111 (12): 5721-6. Ashley-Koch Allison E, Elliott Laine, Kail Melanie E, De Castro Laura M, Jonassaint Jude, Jackson Terry L, Price Jennifer, Ataga Kenneth I, Levesque Marc C, Weinberg J Brice, Orringer Eugene P, Collins Ann, Vance Jeffery M, Telen Marilyn |
| Bone morphogenetic protein 6 polymorphisms are associated with radiographic progression in ankylosing spondylitis. PloS one 2014 9 (8): e104966. Joo Young Bin, Bang So-Young, Kim Tae-Hwan, Shim Seung-Cheol, Lee Seunghun, Joo Kyung Bin, Kim Jong Heon, Min Hye Joon, Rahman Proton, Inman Robert |
Genome-wide association analysis identifies six new loci associated with forced vital capacity.
Nature genetics 2014 Jul 46 (7): 669-77. Loth Daan W, Artigas María Soler, Gharib Sina A, Wain Louise V, Franceschini Nora, Koch Beate, Pottinger Tess D, Smith Albert Vernon, Duan Qing, Oldmeadow Chris, Lee Mi Kyeong, Strachan David P, James Alan L, Huffman Jennifer E, Vitart Veronique, Ramasamy Adaikalavan, Wareham Nicholas J, Kaprio Jaakko, Wang Xin-Qun, Trochet Holly, Kähönen Mika, Flexeder Claudia, Albrecht Eva, Lopez Lorna M, de Jong Kim, Thyagarajan Bharat, Alves Alexessander Couto, Enroth Stefan, Omenaas Ernst, Joshi Peter K, Fall Tove, Viñuela Ana, Launer Lenore J, Loehr Laura R, Fornage Myriam, Li Guo, Wilk Jemma B, Tang Wenbo, Manichaikul Ani, Lahousse Lies, Harris Tamara B, North Kari E, Rudnicka Alicja R, Hui Jennie, Gu Xiangjun, Lumley Thomas, Wright Alan F, Hastie Nicholas D, Campbell Susan, Kumar Rajesh, Pin Isabelle, Scott Robert A, Pietiläinen Kirsi H, Surakka Ida, Liu Yongmei, Holliday Elizabeth G, Schulz Holger, Heinrich Joachim, Davies Gail, Vonk Judith M, Wojczynski Mary, Pouta Anneli, Johansson Asa, Wild Sarah H, Ingelsson Erik, Rivadeneira Fernando, Völzke Henry, Hysi Pirro G, Eiriksdottir Gudny, Morrison Alanna C, Rotter Jerome I, Gao Wei, Postma Dirkje S, White Wendy B, Rich Stephen S, Hofman Albert, Aspelund Thor, Couper David, Smith Lewis J, Psaty Bruce M, Lohman Kurt, Burchard Esteban G, Uitterlinden André G, Garcia Melissa, Joubert Bonnie R, McArdle Wendy L, Musk A Bill, Hansel Nadia, Heckbert Susan R, Zgaga Lina, van Meurs Joyce B J, Navarro Pau, Rudan Igor, Oh Yeon-Mok, Redline Susan, Jarvis Deborah L, Zhao Jing Hua, Rantanen Taina, O'Connor George T, Ripatti Samuli, Scott Rodney J, Karrasch Stefan, Grallert Harald, Gaddis Nathan C, Starr John M, Wijmenga Cisca, Minster Ryan L, Lederer David J, Pekkanen Juha, Gyllensten Ulf, Campbell Harry, Morris Andrew P, Gläser Sven, Hammond Christopher J, Burkart Kristin M, Beilby John, Kritchevsky Stephen B, Gudnason Vilmundur, Hancock Dana B, Williams O Dale, Polasek Ozren, Zemunik Tatijana, Kolcic Ivana, Petrini Marcy F, Wjst Matthias, Kim Woo Jin, Porteous David J, Scotland Generation, Smith Blair H, Viljanen Anne, Heliövaara Markku, Attia John R, Sayers Ian, Hampel Regina, Gieger Christian, Deary Ian J, Boezen H Marike, Newman Anne, Jarvelin Marjo-Riitta, Wilson James F, Lind Lars, Stricker Bruno H, Teumer Alexander, Spector Timothy D, Melén Erik, Peters Marjolein J, Lange Leslie A, Barr R Graham, Bracke Ken R, Verhamme Fien M, Sung Joohon, Hiemstra Pieter S, Cassano Patricia A, Sood Akshay, Hayward Caroline, Dupuis Josée, Hall Ian P, Brusselle Guy G, Tobin Martin D, London Stephanie |
| Evaluation of a bone morphogenetic protein 6 variant as a cause of iron loading. Human genomics 2018 4 12 (1): 23. McDonald Cameron J, Rishi Gautam, Secondes Eriza S, Ostini Lesa, Wallace Daniel F, Crawford Darrell H G, Sia Hanlon, Clark Paul, Subramaniam V Nath |
| Association analysis of polymorphisms rs12997 in ACVR1 and rs1043784 in BMP6 genes involved in bone morphogenic protein signaling pathway in primary angle-closure and pseudoexfoliation glaucoma patients of Saudi origin. BMC medical genetics 2020 Jul 21 (1): 145. Kondkar Altaf A, Sultan Tahira, Azad Taif A, Osman Essam A, Almobarak Faisal A, Al-Obeidan Saleh |
| Genome-wide Association Analysis Across 16,956 Patients Identifies a Novel Genetic Association Between BMP6, NIPAL1, CNGA1 and Spondylosis.
Spine 2020 Dec Publish Ahead of Print . Zhang Yanfei, Grant Ryan A, Shivakumar Manu K, Zaleski Michael, Sofoluke Nelson, Slotkin Jonathan R, Williams Marc S, Lee Ming Ta Micha |
| Polymorphisms and avascular necrosis in patients with sickle cell disease - A systematic review. Revista paulista de pediatria : orgao oficial da Sociedade de Pediatria de Sao Paulo 2022 5 40 e2021013. Leandro Márcio Passos, Almeida Natália Damasceno, Hocevar Lara Santana, Sá Cloud Kennedy Couto de, Souza Amâncio José de, Matos Marcos Almei |
| Blood BMP6 Associated with Cognitive Performance and Alzheimer's Disease Diagnosis: A Longitudinal Study of Elders. Journal of Alzheimer's disease : JAD 2022 Jun . Sun Lin, Guo Chunni, Song Yan, Sheng Jianhua, Xiao Shifu, |
| Identification of Genetic Markers Linked to The Activity of Indoleamine 2,3-Dioxygenase and Kidney Function. Metabolites 2023 4 13 (4): . Hye-Rim Kim, Hyun-Seok Jin, Yong-Bin E |
| Genetic association and transferability for urinary albumin-creatinine ratio as a marker of kidney disease in four Sub-Saharan African populations and non-continental individuals of African ancestry. Frontiers in genetics 2024 5 15 1372042. Jean-Tristan Brandenburg, Wenlong Carl Chen, Palwende Romuald Boua, Melanie A Govender, Godfred Agongo, Lisa K Micklesfield, Hermann Sorgho, Stephen Tollman, Gershim Asiki, Felistas Mashinya, Scott Hazelhurst, Andrew P Morris, June Fabian, Michèle Rams |
| Unveiling therapeutic targets for spinal stenosis from genetic insights: a Mendelian randomization analysis. Scientific reports 2024 11 14 (1): 29118. Zhaopeng Fan, Bohong Chen, Le Ding, Hua G |
| Genetic Association and Transferability for Urinary Albumin-Creatinine Ratio as a Marker of Kidney Function in four Sub-Saharan African Populations and non-continental Individuals of African Ancestry. medRxiv : the preprint server for health sciences 2024 1 . Jean-Tristan Brandenburg, Wenlong Carl Chen, Palwende Romuald Boua, Melanie Ann Govender, Godfred Agongo, Lisa K Micklesfield, Hermann Sorgho, Stephen Tollman, Gershim Asiki, Felistas Mashinya, Scott Hazelhurst, Andrew P Morris, June Fabian, Michèle Ramsay, |
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