Human Genome Epidemiology Literature Finder
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Records 1 - 9 (of 9 Records) |
| Query Trace: Disease and RARB[original query] |
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Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association study.
The Lancet. Neurology 2009 Jan 8 (1): 57-66. Mead Simon, Poulter Mark, Uphill James, Beck John, Whitfield Jerome, Webb Thomas E F, Campbell Tracy, Adamson Gary, Deriziotis Pelagia, Tabrizi Sarah J, Hummerich Holger, Verzilli Claudio, Alpers Michael P, Whittaker John C, Collinge Jo |
| Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function.
Nature genetics 2011 Sep 43 (11): 1082-90. Soler Artigas María, Loth Daan W, Wain Louise V, Gharib Sina A, Obeidat Ma'en, Tang Wenbo, Zhai Guangju, Zhao Jing Hua, Smith Albert Vernon, Huffman Jennifer E, Albrecht Eva, Jackson Catherine M, Evans David M, Cadby Gemma, Fornage Myriam, Manichaikul Ani, Lopez Lorna M, Johnson Toby, Aldrich Melinda C, Aspelund Thor, Barroso Inês, Campbell Harry, Cassano Patricia A, Couper David J, Eiriksdottir Gudny, Franceschini Nora, Garcia Melissa, Gieger Christian, Gislason Gauti Kjartan, Grkovic Ivica, Hammond Christopher J, Hancock Dana B, Harris Tamara B, Ramasamy Adaikalavan, Heckbert Susan R, Heliövaara Markku, Homuth Georg, Hysi Pirro G, James Alan L, Jankovic Stipan, Joubert Bonnie R, Karrasch Stefan, Klopp Norman, Koch Beate, Kritchevsky Stephen B, Launer Lenore J, Liu Yongmei, Loehr Laura R, Lohman Kurt, Loos Ruth J F, Lumley Thomas, Al Balushi Khalid A, Ang Wei Q, Barr R Graham, Beilby John, Blakey John D, Boban Mladen, Boraska Vesna, Brisman Jonas, Britton John R, Brusselle Guy G, Cooper Cyrus, Curjuric Ivan, Dahgam Santosh, Deary Ian J, Ebrahim Shah, Eijgelsheim Mark, Francks Clyde, Gaysina Darya, Granell Raquel, Gu Xiangjun, Hankinson John L, Hardy Rebecca, Harris Sarah E, Henderson John, Henry Amanda, Hingorani Aroon D, Hofman Albert, Holt Patrick G, Hui Jennie, Hunter Michael L, Imboden Medea, Jameson Karen A, Kerr Shona M, Kolcic Ivana, Kronenberg Florian, Liu Jason Z, Marchini Jonathan, McKeever Tricia, Morris Andrew D, Olin Anna-Carin, Porteous David J, Postma Dirkje S, Rich Stephen S, Ring Susan M, Rivadeneira Fernando, Rochat Thierry, Sayer Avan Aihie, Sayers Ian, Sly Peter D, Smith George Davey, Sood Akshay, Starr John M, Uitterlinden André G, Vonk Judith M, Wannamethee S Goya, Whincup Peter H, Wijmenga Cisca, Williams O Dale, Wong Andrew, Mangino Massimo, Marciante Kristin D, McArdle Wendy L, Meibohm Bernd, Morrison Alanna C, North Kari E, Omenaas Ernst, Palmer Lyle J, Pietiläinen Kirsi H, Pin Isabelle, Pola Sbreve Ek Ozren, Pouta Anneli, Psaty Bruce M, Hartikainen Anna-Liisa, Rantanen Taina, Ripatti Samuli, Rotter Jerome I, Rudan Igor, Rudnicka Alicja R, Schulz Holger, Shin So-Youn, Spector Tim D, Surakka Ida, Vitart Veronique, Völzke Henry, Wareham Nicholas J, Warrington Nicole M, Wichmann H-Erich, Wild Sarah H, Wilk Jemma B, Wjst Matthias, Wright Alan F, Zgaga Lina, Zemunik Tatijana, Pennell Craig E, Nyberg Fredrik, Kuh Diana, Holloway John W, Boezen H Marike, Lawlor Debbie A, Morris Richard W, Probst-Hensch Nicole, , , Kaprio Jaakko, Wilson James F, Hayward Caroline, Kähönen Mika, Heinrich Joachim, Musk Arthur W, Jarvis Deborah L, Gläser Sven, Järvelin Marjo-Riitta, Ch Stricker Bruno H, Elliott Paul, O'Connor George T, Strachan David P, London Stephanie J, Hall Ian P, Gudnason Vilmundur, Tobin Martin |
| Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction.
American journal of respiratory and critical care medicine 2012 Oct 186 (7): 622-32. Wilk Jemma B, Shrine Nick R G, Loehr Laura R, Zhao Jing Hua, Manichaikul Ani, Lopez Lorna M, Smith Albert Vernon, Heckbert Susan R, Smolonska Joanna, Tang Wenbo, Loth Daan W, Curjuric Ivan, Hui Jennie, Cho Michael H, Latourelle Jeanne C, Henry Amanda P, Aldrich Melinda, Bakke Per, Beaty Terri H, Bentley Amy R, Borecki Ingrid B, Brusselle Guy G, Burkart Kristin M, Chen Ting-hsu, Couper David, Crapo James D, Davies Gail, Dupuis Josée, Franceschini Nora, Gulsvik Amund, Hancock Dana B, Harris Tamara B, Hofman Albert, Imboden Medea, James Alan L, Khaw Kay-Tee, Lahousse Lies, Launer Lenore J, Litonjua Augusto, Liu Yongmei, Lohman Kurt K, Lomas David A, Lumley Thomas, Marciante Kristin D, McArdle Wendy L, Meibohm Bernd, Morrison Alanna C, Musk Arthur W, Myers Richard H, North Kari E, Postma Dirkje S, Psaty Bruce M, Rich Stephen S, Rivadeneira Fernando, Rochat Thierry, Rotter Jerome I, Artigas María Soler, Starr John M, Uitterlinden André G, Wareham Nicholas J, Wijmenga Cisca, Zanen Pieter, Province Michael A, Silverman Edwin K, Deary Ian J, Palmer Lyle J, Cassano Patricia A, Gudnason Vilmundur, Barr R Graham, Loos Ruth J F, Strachan David P, London Stephanie J, Boezen H Marike, Probst-Hensch Nicole, Gharib Sina A, Hall Ian P, O'Connor George T, Tobin Martin D, Stricker Bruno |
| RARB and STMN2 polymorphisms are not associated with sporadic Creutzfeldt-Jakob disease (CJD) in the Korean population. Molecular biology reports 2014 41 (4): 2389-95. Jeong Byung-Hoon, Kim Hae-Jung, Lee Kyung-Hee, Carp Richard I, Kim Yong-S |
| Aberrant DNA methylation is associated with aggressive clinicopathological features and poor survival in cutaneous melanoma. The British journal of dermatology 2017 Dec . de Unamuno Bustos B, Murria Estal R, Pérez Simó G, Simarro Farinos J, Pujol Marco C, Navarro Mira M, Alegre de Miquel V, Ballester Sánchez R, Sabater Marco V, Llavador Ros M, Palanca Suela S, Botella Estrada |
| Identification of a 3'-Untranslated Genetic Variant of RARB Associated With Carotid Intima-Media Thickness in Rheumatoid Arthritis: A Genome-Wide Association Study.
Arthritis & rheumatology (Hoboken, N.J.) 2018 Sep . López-Mejías Raquel, Carmona F David, Genre Fernanda, Remuzgo-Martínez Sara, González-Juanatey Carlos, Corrales Alfonso, Vicente Esther F, Pulito-Cueto Verónica, Miranda-Filloy José A, Ramírez Huaranga Marco A, Blanco Ricardo, Robustillo-Villarino Montserrat, Rodríguez-Carrio Javier, Alperi-López Mercedes, Alegre-Sancho Juan J, Mijares Verónica, Lera-Gómez Leticia, Pérez-Pampín Eva, González Antonio, Ortega-Castro Rafaela, López-Pedrera Chary, García Vivar Mari L, Gómez-Arango Catalina, Raya Enrique, Narvaez Javier, Balsa Alejandro, López-Longo Francisco J, Carreira Patricia, González-Álvaro Isidoro, Rodríguez-Rodríguez Luis, Fernández-Gutiérrez Benjamín, Ferraz-Amaro Iván, Gualillo Oreste, Castañeda Santos, Martín Javier, Llorca Javier, González-Gay Miguel |
| Hydroa vacciniforme-like lymphoproliferative disorder: A study of clinicopathology and whole-exome sequencing in Chinese patients. Journal of dermatological science 2020 7 99 (2): 128-134. Xie Yao, Wang Tingting, Wang L |
| Polymorphisms in Vitamin A-Related Genes and Their Functions in Autoimmune Thyroid Disease. Thyroid : official journal of the American Thyroid Association 2021 9 31 (11): 1749-1756. Homma Hinako, Watanabe Mikio, Inoue Naoya, Isono Moeko, Hidaka Yoh, Iwatani Yoshino |
| RARB genetic variants might contribute to the risk of chronic obstructive pulmonary disease based on a case-control study. Annals of medicine 2024 12 57 (1): 2445195. Linhui Huang, Wenya Xu, Yihui Fu, Zehua Yang, Rubing Mo, Yipeng Ding, Tian X |
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