Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 60 Records) |
| Query Trace: Disease and BTNL2[original query] |
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| Correction: Pooled sequencing of 531 genes in inflammatory bowel disease identifies an associated rare variant in BTNL2 and implicates other immune related genes. PLoS genetics 2015 Apr 11 (4): e1005172. Authors are not available |
| Deep resequencing of 131 Crohn's disease associated genes in pooled DNA confirmed three reported variants and identified eight novel variants. Gut 2015 Mar . Hong Sung Noh, Park Changho, Park Soo Jung, Lee Chang Kyun, Ye Byong Duk, Kim You Sun, Lee Seungbok, Chae Jeesoo, Kim Jong-Il, Kim Young-Ho, |
| Assessment of the genetic basis of rosacea by genome-wide association study. The Journal of investigative dermatology 2015 Jun 135 (6): 1548-55. Chang Anne Lynn S, Raber Inbar, Xu Jin, Li Rui, Spitale Robert, Chen Julia, Kiefer Amy K, Tian Chao, Eriksson Nicholas K, Hinds David A, Tung Joyce |
| Pooled sequencing of 531 genes in inflammatory bowel disease identifies an associated rare variant in BTNL2 and implicates other immune related genes. PLoS genetics 2015 Feb 11 (2): e1004955. Prescott Natalie J, Lehne Benjamin, Stone Kristina, Lee James C, Taylor Kirstin, Knight Jo, Papouli Efterpi, Mirza Muddassar M, Simpson Michael A, Spain Sarah L, Lu Grace, Fraternali Franca, Bumpstead Suzannah J, Gray Emma, Amar Ariella, Bye Hannah, Green Peter, Chung-Faye Guy, Hayee Bu'Hussain, Pollok Richard, Satsangi Jack, Parkes Miles, Barrett Jeffrey C, Mansfield John C, Sanderson Jeremy, Lewis Cathryn M, Weale Michael E, Schlitt Thomas, Mathew Christopher G, |
| Novel 6p21.3 Risk Haplotype Predisposes to Acute Coronary Syndrome. Circulation. Cardiovascular genetics 2015 Dec . Sinisalo Juha, Vlachopoulou Efthymia, Marchesani Marja, Nokelainen Johanna, Mäyränpää Mikko I, Lappalainen Jani, Paakkanen Riitta, Wennerström Annika, Salli Krista, Niemi Heikki J, Männistö Satu, Salo Perttu, Junttila Juhani, Eskola Markku, Nikus Kjell, Arstila T Petteri, Perola Markus, Huikuri Heikki, Karhunen Pekka J, Kovanen Petri T, Palotie Aarno, Havulinna Aki S, Lluís-Ganella Carla, Marrugat Jaume, Elosua Roberto, Salomaa Veikko, Nieminen Markku S, Lokki Marja-Lii |
| Association of genetic polymorphisms on BTNL2 with susceptibility to and prognosis of dilated cardiomyopathy in a Chinese population. International journal of clinical and experimental pathology 2015 8 (9): 10488-99. Cheng Liang, Zhao Rong, Jin ZhenXiao, Ren Kai, Deng Chao, Yu Shiqia |
| Genomic Study of Cardiovascular Continuum Comorbidity. Acta naturae 0 7 (3): 89-99. Makeeva O A, Sleptsov A A, Kulish E V, Barbarash O L, Mazur A M, Prokhorchuk E B, Chekanov N N, Stepanov V A, Puzyrev V |
| BTNL2 gene SNPs as a contributing factor to sarcoidosis pathogenesis in a cohort of Greek patients. Meta gene 2014 Dec 2 619-30. Delaveri Aikaterini, Rapti Aggeliki, Poulou Myrto, Fylaktou Eirini, Tsipi Maria, Roussos Charis, Makrythanasis Periklis, Kanavakis Emmanuel, Tzetis Mar |
| Associations between sarcoidosis clinical course and ANXA11 rs1049550 C/T, BTNL2 rs2076530 G/A, and HLA class I and II alleles. The clinical respiratory journal 2016 Sep . Morais Antonio, Lima Bruno, Alves Helena, Melo Natalia, Mota Patricia C, Marques Agostinho, Delgado Lu |
| Analysis of the Expression and Single-Nucleotide Variant Frequencies of the Butyrophilin-like 2 Gene in Patients With Uveal Melanoma. JAMA ophthalmology 2016 Oct 134 (10): 1125-1133. Amaro Adriana, Parodi Federica, Diedrich Konrad, Angelini Giovanna, Götz Cornelia, Viaggi Silvia, Maric Irena, Coviello Domenico, Pistillo Maria Pia, Morabito Anna, Mandalà Mario, Ghiorzo Paola, Visconti Paola, Gualco Marina, Anselmi Luca, Puzone Roberto, Lanza Francesco, Mosci Carlo, Raggi Federica, Bosco Maria Carla, Varesio Luigi, Zeschnigk Michael, Spano Laura, Queirolo Paola, Pfeffer Ulri |
Association of variations in HLA class II and other loci with susceptibility to EGFR-mutated lung adenocarcinoma.
Nature communications 2016 Aug 7 12451. Shiraishi Kouya, Okada Yukinori, Takahashi Atsushi, Kamatani Yoichiro, Momozawa Yukihide, Ashikawa Kyota, Kunitoh Hideo, Matsumoto Shingo, Takano Atsushi, Shimizu Kimihiro, Goto Akiteru, Tsuta Koji, Watanabe Shun-Ichi, Ohe Yuichiro, Watanabe Yukio, Goto Yasushi, Nokihara Hiroshi, Furuta Koh, Yoshida Akihiko, Goto Koichi, Hishida Tomoyuki, Tsuboi Masahiro, Tsuchihara Katsuya, Miyagi Yohei, Nakayama Haruhiko, Yokose Tomoyuki, Tanaka Kazumi, Nagashima Toshiteru, Ohtaki Yoichi, Maeda Daichi, Imai Kazuhiro, Minamiya Yoshihiro, Sakamoto Hiromi, Saito Akira, Shimada Yoko, Sunami Kuniko, Saito Motonobu, Inazawa Johji, Nakamura Yusuke, Yoshida Teruhiko, Yokota Jun, Matsuda Fumihiko, Matsuo Keitaro, Daigo Yataro, Kubo Michiaki, Kohno Takas |
| The BTNL2 G16071A gene polymorphism increases granulomatous disease susceptibility: A meta-analysis including FPRP test of 8710 participants. Medicine 2016 Jul 95 (30): e4325. Tong Xiang, Ma Yao, Niu Xundong, Yan Zhipeng, Liu Sitong, Peng Bo, Peng Shifeng, Fan Ho |
| Genetic Association Analysis Reveals Differences in the Contribution of NOD2 Variants to the Clinical Phenotypes of Orofacial Granulomatosis. Inflammatory bowel diseases 2016 Jul 22 (7): 1552-8. Mentzer Alexander, Nayee Shalini, Omar Yasmin, Hullah Esther, Taylor Kirstin, Goel Rishi, Bye Hannah, Shembesh Tarik, Elliott Timothy R, Campbell Helen, Patel Pritash, Nolan Anita, Mansfield John, Challacombe Stephen, Escudier Michael, Mathew Christopher G, Sanderson Jeremy D, Prescott Natalie |
| Association of Frontotemporal Dementia GWAS Loci with Late-Onset Alzheimer's Disease in a Northern Han Chinese Population. Journal of Alzheimer's disease : JAD 2016 Feb . Tan Chen-Chen, Wan Yu, Tan Meng-Shan, Zhang Wei, Wang Zi-Xuan, Sun Fu-Rong, Miao Dan, Tan Lan, Yu Jin-T |
| Familial vs. sporadic sarcoidosis: BTNL2 polymorphisms, clinical presentations, and outcomes in a French cohort. Orphanet journal of rare diseases 2016 Dec 11 (1): 165. Pacheco Yves, Calender Alain, Israël-Biet Dominique, Roy Pascal, Lebecque Serge, Cottin Vincent, Bouvry Diane, Nunes Hilario, Sève Pascal, Pérard Laurent, Devouassoux Gilles, Freymond Nathalie, Khouatra Chahira, Wallaert Benoît, Lamy Raphaelle, Elsensohn Mad-Hélénie, Bardel Claire, Valeyre Dominique, |
| TNFA, ANXA11 and BTNL2 Polymorphisms in CVID Patients with Granulomatous Disease. Journal of clinical immunology 2016 Jan . Boutboul David, Vince Nicolas, Mahevas Matthieu, Bories Jean-Christophe, Fieschi Claire, |
| SNP Variants in Major Histocompatibility Complex Are Associated with Sarcoidosis Susceptibility-A Joint Analysis in Four European Populations. Frontiers in immunology 2017 8 422. Wolin Annika, Lahtela Elisa Laura, Anttila Verneri, Petrek Martin, Grunewald Johan, van Moorsel Coline H M, Eklund Anders, Grutters Jan C, Kolek Vitezslav, Mrazek Frantisek, Kishore Amit, Padyukov Leonid, Pietinalho Anne, Ronninger Marcus, Seppänen Mikko, Selroos Olof, Lokki Marja-Lii |
| Atopobium and Fusobacterium as novel candidates for sarcoidosis-associated microbiota. The European respiratory journal 2017 12 50 (6): . Zimmermann Alexandra, Knecht Henrik, Häsler Robert, Zissel Gernot, Gaede Karoline I, Hofmann Sylvia, Nebel Almut, Müller-Quernheim Joachim, Schreiber Stefan, Fischer Annegr |
| The Roles of Genetic Factors in Kawasaki Disease: A Systematic Review and Meta-analysis of Genetic Association Studies. Pediatric cardiology 2017 Nov . Xie Xiaochuan, Shi Xiaohan, Liu Meil |
| HLA-DRA/HLA-DRB5 polymorphism affects risk of sporadic ALS and survival in a southwest Chinese cohort. Journal of the neurological sciences 2017 Feb 373 124-128. Yang Xinglong, Zheng JinHua, Tian Sijia, Chen Yalan, An Ran, Zhao Quanzhen, Xu Yanmi |
| Transethnic, Genome-Wide Analysis Reveals Immune-Related Risk Alleles and Phenotypic Correlates in Pediatric Steroid-Sensitive Nephrotic Syndrome.
Journal of the American Society of Nephrology : JASN 2018 Jun . Debiec Hanna, Dossier Claire, Letouzé Eric, Gillies Christopher E, Vivarelli Marina, Putler Rosemary K, Ars Elisabet, Jacqz-Aigrain Evelyne, Elie Valery, Colucci Manuela, Debette Stéphanie, Amouyel Philippe, Elalaoui Siham C, Sefiani Abdelaziz, Dubois Valérie, Simon Tabassome, Kretzler Matthias, Ballarin Jose, Emma Francesco, Sampson Matthew G, Deschênes Georges, Ronco Pier |
| Deep Resequencing of Ulcerative Colitis-Associated Genes Identifies Novel Variants in Candidate Genes in the Korean Population. Inflammatory bowel diseases 2018 May . Moon Chang Mo, Kim Seung Won, Ahn Jae Bum, Ma Hyun Woo, Che Xiumei, Kim Tae Il, Kim Won Ho, Cheon Jae H |
| Genetic Predisposition to Rosacea. Dermatologic clinics 2018 Apr 36 (2): 87-92. Awosika Olabola, Oussedik Eli |
| Two Variants in the NOTCH4 and HLA-C Genes Contribute to Familial Clustering of Psoriasis. International journal of genomics 2020 11 2020 6907378. Cai Minglong, Huang He, Hu Zhulin, Yuan Tao, Li Weiran, Liu Yaoguang, Zheng Lijun, Zhang Yan, Sheng Yujun, Zhang Xuej |
| Genome-wide association study identifies BTNL2 associated with atopic asthma in children.
Medicine 2021 Nov 100 (44): e27626. Kim Soo Yeon, Kim Eun Gyul, Kim Mina, Hong Jung Yeon, Kim Ga Eun, Jung Jae Hwa, Park Mireu, Kim Min Jung, Kim Yoon Hee, Sohn Myung Hyun, Kim Kyung W |
| Missense Variant rs28362680 in BTNL2 Reduces Risk of Coronary Heart Disease. Pharmacogenomics and personalized medicine 2022 5 15 449-464. Zhuo Jian, Wu Yingchun, Li Wei, Li Zerong, Ding Yipeng, Jin Tian |
| Exome variants associated with asthma and allergy. Scientific reports 2022 12 12 (1): 21028. Wjst Matthi |
| A human leukocyte antigen imputation study uncovers possible genetic interplay between gut inflammatory processes and autism spectrum disorders. Translational psychiatry 2023 7 13 (1): 244. Laura Lombardi, Sigrid Le Clerc, Ching-Lien Wu, Jihène Bouassida, Wahid Boukouaci, Sobika Sugusabesan, Jean-Romain Richard, Mohamed Lajnef, Maxime Tison, Philippe Le Corvoisier, Caroline Barau, Tobias Banaschewski, Rosemary Holt, Sarah Durston, Antonio M Persico, Bethany Oakley, Eva Loth, Jan Buitelaar, Declan Murphy, Marion Leboyer, Jean-François Zagury, Ryad Tamou |
| Germline variants of the genes involved in NF-kB activation are associated with the risk of COPD and lung cancer development. Acta pharmaceutica (Zagreb, Croatia) 2023 6 73 (2): 243-256. Jurica Baranasic, Yasmeen Niazi, Subhayan Chattopadhyay, Lada Rumora, Lorna ?orak, Andrea Vuki? Dugac, Marko Jakopovi?, Miroslav Samaržija, Asta Försti, Jelena Knežev |
| Impact of missense TSBP1 variants on the susceptibility to coronary heart disease. Gene 2023 12 896 148042. Wei Yang, Xuguang Li, Xuemei Li, Baoping Hu, Shilin Xu, Hengxun Zhang, Yuhe Wang, Tianbo Jin, Yongjun |
- Page last reviewed:Feb 1, 2024
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