Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 71 Records) |
Query Trace: REL[original query] |
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Common Genetic Polymorphisms within NF?B-Related Genes and the Risk of Developing Invasive Aspergillosis. Frontiers in microbiology 2016 7 1243. Lupiañez Carmen B, Villaescusa María T, Carvalho Agostinho, Springer Jan, Lackner Michaela, Sánchez-Maldonado José M, Canet Luz M, Cunha Cristina, Segura-Catena Juana, Alcazar-Fuoli Laura, Solano Carlos, Fianchi Luana, Pagano Livio, Potenza Leonardo, Aguado José M, Luppi Mario, Cuenca-Estrella Manuel, Lass-Flörl Cornelia, Einsele Hermann, Vázquez Lourdes, , Ríos-Tamayo Rafael, Loeffler Jurgen, Jurado Manuel, Sainz Ju |
Investigation of the genetic overlap between rheumatoid arthritis and psoriatic arthritis in a Greek population. Scandinavian journal of rheumatology 2017 May 46 (3): 180-186. Myrthianou E, Zervou M I, Budu-Aggrey A, Eliopoulos E, Kardassis D, Boumpas D T, Kougkas N, Barton A, Sidiropoulos P, Goulielmos G |
Association of REL polymorphisms and outcome of patients with septic shock. Annals of intensive care 2016 Dec 6 (1): 28. Toubiana Julie, Courtine Emilie, Tores Frederic, Asfar Pierre, Daubin Cédric, Rousseau Christophe, Ouaaz Fatah, Marin Nathalie, Cariou Alain, Chiche Jean-Daniel, Mira Jean-Pa |
Impact of CTLA4 genotype and other immune response gene polymorphisms on outcomes after single umbilical cord blood transplantation. Blood 2016 Nov . Cunha Renato, Zago Marco A, Querol Sergio, Volt Fernanda, Ruggeri Annalisa, Sanz Guillermo, Pouthier Fabienne, Kogler Gesine, Vicario José L, Bergamaschi Paola, Saccardi Riccardo, Lamas Carmen H, Díaz-de-Heredia Cristina, Michel Gerard, Bittencourt Henrique, Tavella Marli, Panepucci Rodrigo A, Fernandes Francisco, Pavan Julia, Gluckman Eliane, Rocha Vanders |
Genetic Variation in the REL Gene Increases Risk of Behcet's Disease in a Chinese Han Population but That of PRKCQ Does Not. PloS one 2016 11 (1): e0147350. Chen Feilan, Xu Lei, Zhao Tingting, Xiao Xiang, Pan Yongquan, Hou Shengpi |
Genomic Landscape of Atypical Adenomatous Hyperplasia Reveals Divergent Modes to Lung Adenocarcinoma. Cancer research 2017 9 77 (22): 6119-6130. Sivakumar Smruthy, Lucas F Anthony San, McDowell Tina L, Lang Wenhua, Xu Li, Fujimoto Junya, Zhang Jianjun, Futreal P Andrew, Fukuoka Junya, Yatabe Yasushi, Dubinett Steven M, Spira Avrum E, Fowler Jerry, Hawk Ernest T, Wistuba Ignacio I, Scheet Paul, Kadara Hum |
The association between MICA/MICB polymorphism and respiratory syncytial virus infection in children. International journal of immunogenetics 2017 Sep . Luo Q, Guo X, Peng S, Luo W, Tian F, Yu P, Zou |
High-depth, high-accuracy microsatellite genotyping enables precision lung cancer risk classification. Oncogene 2017 8 36 (46): 6383-6390. Velmurugan K R, Varghese R T, Fonville N C, Garner H |
TNF-a Genetic Predisposition and Higher Expression of Inflammatory Pathway Components in Keratoconus. Investigative ophthalmology & visual science 2017 Jul 58 (9): 3481-3487. Arbab Muneeza, Tahir Saira, Niazi Muhammad Khizar, Ishaq Mazhar, Hussain Alamdar, Siddique Pir Muhammad, Saeed Sadia, Khan Wajid Ali, Qamar Raheel, Butt Azeem Mehmood, Azam Malee |
The association between 38 previously reported polymorphisms and psoriasis in a Polish population: High predicative accuracy of a genetic risk score combining 16 loci. PloS one 2017 12 (6): e0179348. Kisiel Bart?omiej, Kisiel Katarzyna, Szyma?ski Konrad, Mackiewicz Wojciech, Bia?o-Wójcicka Ewelina, Uczniak Sebastian, Fogtman Anna, Iwanicka-Nowicka Roksana, Koblowska Marta, Kossowska Helena, Placha Grzegorz, Sykulski Maciej, Bachta Artur, T?ustochowicz Witold, P?oski Rafa?, Kaszuba Andrz |
Anaplastic Variant of Diffuse Large B-cell Lymphoma Displays Intricate Genetic Alterations and Distinct Biological Features. The American journal of surgical pathology 2017 Mar . Li Mingyang, Liu Yixiong, Wang Yingmei, Chen Gang, Chen Qiongrong, Xiao Hualiang, Liu Fang, Qi Chubo, Yu Zhou, Li Xia, Fan Linni, Guo Ying, Yan Qingguo, Guo Shuangping, Wang Z |
Analysis of the GCK gene in 79 MODY type 2 patients: A multicenter Turkish study, mutation profile and description of twenty novel mutations. Gene 2017 10 641 186-189. Aykut Ayça, Karaca Emin, Onay Hüseyin, Gök?en Damla, Çetinkalp ?evki, Eren Erdal, Ersoy Betül, Çak?r Esra Papatya, Büyükinan Muammer, Kara Cengiz, An?k Ahmet, K?rel Birgül, Özen Samim, Atik Tahir, Darcan ?ükran, Özk?nay Fer |
[Association between nuclear factor kappa-light-chain-enhancer of activated B cells genetic polymorphisms and HCV susceptibility among the Chinese population under high-risk]. Zhonghua liu xing bing xue za zhi = Zhonghua liuxingbingxue zazhi 2018 Sep 39 (9): 1261-1264. Fan Y Y, Shao J G, Huang P, Tian T, Li J, Han Y P, Yue M, Zhang L |
Association of REL Polymorphism with Cow's Milk Proteins Allergy in Pediatric Algerian Population. Fetal and pediatric pathology 2018 Jan 1-10. Rahmoun Nesrine, El Mecherfi Kamel Eddine, Bouchetara Assia, Lardjem Hetraf Sara, Dahmani Amira Chahinez, Adda Neggaz Leila, Boudjema Abdallah, Zemani-Fodil Faouzia, Kheroua Om |
Clinical and molecular characteristics of lymphoplasmacytic lymphoma not associated with an IgM monoclonal protein: A multicentric study of the Rete Ematologica Lombarda (REL) network. American journal of hematology 2019 Aug . Varettoni Marzia, Boveri Emanuela, Zibellini Silvia, Tedeschi Alessandra, Candido Chiara, Ferretti Virginia Valeria, Rizzo Ettore, Doni Elisa, Merli Michele, Farina Lucia, Goldaniga Maria, Gallì Anna, Rattotti Sara, Frustaci Anna Maria, Deodato Marina, Bandiera Laura, Isimbaldi Giuseppe, Uccella Silvia, Cabras Antonello Domenico, Gianelli Umberto, Baldini Luca, Paulli Marco, Arcaini Lu |
Genetic mutations in NF-?B pathway genes were associated with the protection from hepatitis C virus infection among Chinese Han population. Scientific reports 2019 Jul 9 (1): 10830. Yue Ming, Tian Ting, Wang Chunhui, Fan Haozhi, Wu Jingjing, Wang Jinke, Li Jun, Xia Xueshan, Zhang Amei, Yu Rongbin, Zhang Yun, Huang Pe |
Distinct molecular profile of IRF4-rearranged large B-cell lymphoma. Blood 2019 11 135 (4): 274-286. Ramis-Zaldivar Joan Enric, Gonzalez-Farré Blanca, Balagué Olga, Celis Verónica, Nadeu Ferran, Salmerón-Villalobos Julia, Andrés Mara, Martin-Guerrero Idoia, Garrido-Pontnou Marta, Gaafar Ayman, Suñol Mariona, Bárcena Carmen, Garcia-Bragado Federico, Andión Maitane, Azorín Daniel, Astigarraga Itziar, Sagaseta de Ilurdoz Maria, Sábado Constantino, Gallego Soledad, Verdú-Amorós Jaime, Fernandez-Delgado Rafael, Perez Vanesa, Tapia Gustavo, Mozos Anna, Torrent Montserrat, Solano-Páez Palma, Rivas-Delgado Alfredo, Dlouhy Ivan, Clot Guillem, Enjuanes Anna, López-Guillermo Armando, Galera Pallavi, Oberley Matthew J, Maguire Alanna, Ramsower Colleen, Rimsza Lisa M, Quintanilla-Martinez Leticia, Jaffe Elaine S, Campo Elías, Salaverria Itzi |
Genome-Wide Association Study of Susceptibility Loci for TCF3-PBX1 Acute Lymphoblastic Leukemia in Children.
Journal of the National Cancer Institute 2020 9 113 (7): 933-937. Lee Shawn H R, Qian Maoxiang, Yang Wentao, Diedrich Jonathan D, Raetz Elizabeth, Yang Wenjian, Dong Qian, Devidas Meenakshi, Pei Deqing, Yeoh Allen, Cheng Cheng, Pui Ching-Hon, Evans William E, Mullighan Charles G, Hunger Stephen P, Savic Daniel, Relling Mary V, Loh Mignon L, Yang Jun |
The impact of cytogenetic risk on the outcomes of allogeneic hematopoietic cell transplantation in patients with relapsed/refractory acute myeloid leukemia: On behalf of the acute leukemia working party (ALWP) of the European group for blood and marrow transplantation (EBMT). American journal of hematology 2020 9 96 (1): 40-50. Poiani Monica, Labopin Myriam, Battipaglia Giorgia, Beelen Dietrich W, Tischer Johanna, Finke Jürgen, Brecht Arne, Forcade Edouard, Ganser Arnold, Passweg Jakob R, Labussiere-Wallet Helene, Yakoub-Agha Ibrahim, Schäfer-Eckart Kerstin, Kroeger Nicolaus, Guffroy Blandine, Ruggeri Annalisa, Esteve Jordi, Nagler Arnon, Mohty Moham |
Genomic alterations in chronic lymphocytic leukemia and their correlation with clinico-hematological parameters and disease progression. Blood research 2020 8 55 (3): 131-138. Srinivasan Vishrut K, Naseem Shano, Varma Neelam, Lad Deepesh P, Malhotra Pank |
Genetic Polymorphisms of Cytokines Might Affect Postoperative Sufentanil Dosage for Analgesia in Patients. Journal of pain research 2020 7 13 1461-1470. Guo Jian, Yuan Fei, Yang Yixin, Li Yunze, Bao Fangping, Guo Xuejiao, Feng Zhiyi |
Association study between vitiligo and autoimmune-related genes CYP27B1, REL, TNFAIP3, IL2 and IL21. Experimental dermatology 2020 Apr . Martins Laysa Toschi, Frigeri Henrique Ravanhol, de Castro Caio Cesar Silva, Mira Marcelo Távo |
PRKCQ rs4750316 is associated with Vogt-Koyanagi-Harada syndrome in a Han Chinese population. Molecular vision 2019 25 834-842. Xu Lei, Zhao Tingting, Yuan Gangxiang, Hou Shengping, Zeng Wenxin, Chen Feil |
Genome-wide association meta-analysis identifies pleiotropic risk loci for aerodigestive squamous cell cancers.
PLoS genetics 2021 Mar 17 (3): e1009254. Lesseur Corina, Ferreiro-Iglesias Aida, McKay James D, Bossé Yohan, Johansson Mattias, Gaborieau Valerie, Landi Maria Teresa, Christiani David C, Caporaso Neil C, Bojesen Stig E, Amos Christopher I, Shete Sanjay, Liu Geoffrey, Rennert Gadi, Albanes Demetrius, Aldrich Melinda C, Tardon Adonina, Chen Chu, Triantafillos Liloglou, Field John K, Teare Marion Dawn, Kiemeney Lambertus A, Diergaarde Brenda, Ferris Robert L, Zienolddiny Shanbeh, Lam Stephen, Olshan Andrew F, Weissler Mark C, Lacko Martin, Risch Angela, Bickeböller Heike, Ness Andy R, Thomas Steve, Le Marchand Loic, Schabath Matthew B, Wünsch-Filho Victor, Tajara Eloiza H, Andrew Angeline S, Clifford Gary M, Lazarus Philip, Grankvist Kjell, Johansson Mikael, Arnold Susanne, Melander Olle, Brunnström Hans, Boccia Stefania, Cadoni Gabriella, Timens Wim, Obeidat Ma'en, Xiao Xiangjun, Houlston Richard S, Hung Rayjean J, Brennan Pa |
Association of Single-Nucleotide Variants in the Human Leukocyte Antigen and Other Loci With Childhood Hodgkin Lymphoma.
JAMA network open 2022 08 5 (8): e2225647. Chen Cheng, Song Nan, Dong Qian, Sun Xiaojun, Mulder Heather L, Easton John, Zhang Jinghui, Yasui Yutaka, Bhatia Smita, Armstrong Gregory T, Wang Hui, Ness Kirsten K, Hudson Melissa M, Robison Leslie L, Wang Zhaomi |
Genomic analysis of paired IDHwt glioblastomas reveals recurrent alterations of MPDZ at relapse after radiotherapy and chemotherapy. Journal of the neurological sciences 2022 3 436 120207. Chanez Brice, Appay Romain, Guille Arnaud, Lagarde Arnaud, Colin Carole, Adelaide José, Denicolai Emilie, Jiguet-Jiglaire Carine, Bequet Céline, Graillon Thomas, Boissonneau Sébastien, Nanni-Metellus Isabelle, Dufour Henry, Figarella-Branger Dominique, Chinot Olivier, Tabouret Emeli |
REL and BHLHE40 Variants Are Associated with IL-12 and IL-10 Responses and Tuberculosis Risk. Journal of immunology (Baltimore, Md. : 1950) 2022 Feb . Shah Javeed A, Warr Alex J, Graustein Andrew D, Saha Aparajita, Dunstan Sarah J, Thuong Nguyen T T, Thwaites Guy E, Caws Maxine, Thai Phan V K, Bang Nguyen D, Chau Tran T H, Khor Chiea Chuen, Li Zheng, Hibberd Martin, Chang Xuling, Nguyen Felicia K, Hernandez Carlo A, Jones Madison A, Sassetti Christopher M, Fitzgerald Katherine A, Musvosvi Munyaradzi, Gela Anele, Hanekom Willem A, Hatherill Mark, Scriba Thomas J, Hawn Thomas |
Mutations Associated with Progression in Follicular Lymphoma Predict Inferior Outcomes at Diagnosis (Alliance A151303). Blood advances 2023 7 . David A Russler-Germain, Kilannin Krysiak, Cody Ramirez, Matthew Mosior, Marcus P Watkins, Felicia Gomez, Zachary L Skidmore, Lee Trani, Feng Gao, Susan Geyer, Amanda F Cashen, Neha Mehta-Shah, Brad S Kahl, Nancy L Bartlett, Juan Pablo Alderuccio, Izidore S Lossos, Sarah L Ondrejka, Eric D Hsi, Peter Martin, John P Leonard, Malachi Griffith, Obi L Griffith, Todd A Fehnig |
Ultra-Rare Genetic Variation in Relapsing Polychondritis: A Whole-Exome Sequencing Study. medRxiv : the preprint server for health sciences 2023 6 . Yiming Luo, Marcela A Ferrada, Keith A Sikora, Cameron Rankin, Hugh Alessi, Daniel L Kastner, Zuoming Deng, Mengqi Zhang, Peter A Merkel, Virginia B Kraus, Andrew S Allen, Peter C Grays |
Ultra-rare genetic variation in relapsing polychondritis: a whole-exome sequencing study. Annals of the rheumatic diseases 2023 11 . Yiming Luo, Marcela A Ferrada, Keith A Sikora, Cameron Rankin, Hugh D Alessi, Daniel L Kastner, Zuoming Deng, Mengqi Zhang, Peter A Merkel, Virginia B Kraus, Andrew S Allen, Peter C Grays |
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- Page last updated:Apr 16, 2024
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