Human Genome Epidemiology Literature Finder
Records 1 - 26 (of 26 Records) |
Query Trace: DOCK8[original query] |
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Diagnostic approach to the hyper-IgE syndromes: immunologic and clinical key findings to differentiate hyper-IgE syndromes from atopic dermatitis. The Journal of allergy and clinical immunology 2010 Sep 126 (3): 611-7.e1. Schimke Lena F, Sawalle-Belohradsky Julie, Roesler Joachim, Wollenberg Andreas, Rack Anita, Borte Michael, Rieber Nikolaus, Cremer Reinhold, Maass Eberhart, Dopfer Roland, Reichenbach Janine, Wahn Volker, Hoenig Manfred, Jansson Annette F, Roesen-Wolff Angela, Schaub Bianca, Seger Reinhard, Hill Harry R, Ochs Hans D, Torgerson Troy R, Belohradsky Bernd H, Renner Ellen |
A novel Dock8 gene mutation confers diabetogenic susceptibility in the LEW.1AR1/Ztm-iddm rat, an animal model of human type 1 diabetes. Diabetologia 2015 Sep . Arndt Tanja, Wedekind Dirk, Jörns Anne, Tsiavaliaris Georgios, Cuppen Edwin, Hedrich Hans-Jürgen, Lenzen Sigu |
De novo genic mutations among a Chinese autism spectrum disorder cohort. Nature communications 2016 Nov 7 13316. Wang Tianyun, Guo Hui, Xiong Bo, Stessman Holly A F, Wu Huidan, Coe Bradley P, Turner Tychele N, Liu Yanling, Zhao Wenjing, Hoekzema Kendra, Vives Laura, Xia Lu, Tang Meina, Ou Jianjun, Chen Biyuan, Shen Yidong, Xun Guanglei, Long Min, Lin Janice, Kronenberg Zev N, Peng Yu, Bai Ting, Li Honghui, Ke Xiaoyan, Hu Zhengmao, Zhao Jingping, Zou Xiaobing, Xia Kun, Eichler Evan |
Copy number variation meta-analysis reveals a novel duplication at 9p24 associated with multiple neurodevelopmental disorders. Genome medicine 2017 Nov 9 (1): 106. Glessner Joseph T, Li Jin, Wang Dai, March Michael, Lima Leandro, Desai Akshatha, Hadley Dexter, Kao Charlly, Gur Raquel E, Cohen Nadine, Sleiman Patrick M A, Li Qingqin, Hakonarson Hakon, |
Evaluating the Genetics of Common Variable Immunodeficiency: Monogenetic Model and Beyond. Frontiers in immunology 2018 6 9 636. de Valles-Ibáñez Guillem, Esteve-Solé Ana, Piquer Mònica, González-Navarro E Azucena, Hernandez-Rodriguez Jessica, Laayouni Hafid, González-Roca Eva, Plaza-Martin Ana María, Deyà-Martínez Ángela, Martín-Nalda Andrea, Martínez-Gallo Mónica, García-Prat Marina, Del Pino-Molina Lucía, Cuscó Ivón, Codina-Solà Marta, Batlle-Masó Laura, Solís-Moruno Manuel, Marquès-Bonet Tomàs, Bosch Elena, López-Granados Eduardo, Aróstegui Juan Ignacio, Soler-Palacín Pere, Colobran Roger, Yagüe Jordi, Alsina Laia, Juan Manel, Casals Ferr |
Rare structural variants in the DOCK8 gene identified in a cohort of 439 patients with neurodevelopmental disorders. Scientific reports 2018 6 8 (1): 9449. Krgovic Danijela, Kokalj Vokac Nadja, Zagorac Andreja, Gregoric Kumperscak Hoj |
Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways.
Nature communications 2018 11 9 (1): 4774. Duffy David L, Zhu Gu, Li Xin, Sanna Marianna, Iles Mark M, Jacobs Leonie C, Evans David M, Yazar Seyhan, Beesley Jonathan, Law Matthew H, Kraft Peter, Visconti Alessia, Taylor John C, Liu Fan, Wright Margaret J, Henders Anjali K, Bowdler Lisa, Glass Dan, Ikram M Arfan, Uitterlinden André G, Madden Pamela A, Heath Andrew C, Nelson Elliot C, Green Adele C, Chanock Stephen, Barrett Jennifer H, Brown Matthew A, Hayward Nicholas K, MacGregor Stuart, Sturm Richard A, Hewitt Alex W, , Kayser Manfred, Hunter David J, Newton Bishop Julia A, Spector Timothy D, Montgomery Grant W, Mackey David A, Smith George Davey, Nijsten Tamar E, Bishop D Timothy, Bataille Veronique, Falchi Mario, Han Jiali, Martin Nicholas |
The first cohort of Iranian patients with hyper immunoglobulin E syndrome: A long-term follow-up and genetic analysis. Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology 2019 2 30 (4): 469-478. Tavassoli Mahmood, Abolhassani Hassan, Yazdani Reza, Ghadami Mohsen, Azizi Gholamreza, Abdolrahim Poor Heravi Sina, Moeini Shad Tannaz, Kokabee Mostafa, Movahedi Masoud, Abdshahzadeh Hormoz, Gharagozlou Mohammad, Rezaei Nima, Esmaeilzadeh Hossein, Aleyasin Soheila, Aghamohammadi Asgh |
Genes and variants in hematopoiesis-related pathways are associated with gemcitabine/carboplatin-induced thrombocytopenia. The pharmacogenomics journal 2019 10 20 (2): 179-191. Björn Niclas, Sigurgeirsson Benjamín, Svedberg Anna, Pradhananga Sailendra, Brandén Eva, Koyi Hirsh, Lewensohn Rolf, de Petris Luigi, Apellániz-Ruiz Maria, Rodríguez-Antona Cristina, Lundeberg Joakim, Gréen Henr |
MLPA is a practical and complementary alternative to CMA for diagnostic testing in patients with autism spectrum disorders and identifying new candidate CNVs associated with autism. PeerJ 2019 6 e6183. Capkova Pavlina, Srovnal Josef, Capkova Zuzana, Staffova Katerina, Becvarova Vera, Trkova Marie, Adamova Katerina, Santava Alena, Curtisova Vaclava, Hajduch Marian, Prochazka Mart |
Identifying Genetic Lesions in Ocular Adnexal Extranodal Marginal Zone Lymphomas of the MALT Subtype by Whole Genome, Whole Exome and Targeted Sequencing. Cancers 2020 4 12 (4): . Johansson Patricia, Klein-Hitpass Ludger, Budeus Bettina, Kuhn Matthias, Lauber Chris, Seifert Michael, Roeder Ingo, Pförtner Roman, Stuschke Martin, Dührsen Ulrich, Eckstein Anja, Dürig Jan, Küppers Ra |
New Gene Variants Associated with the Risk of Chronic HBV Infection. Virologica Sinica 2020 4 35 (4): 378-387. Fan Mengjie, Wang Jing, Wang Sa, Li Tengyan, Pan Hong, Liu Hankui, Xu Huifang, Zhernakova Daria V, O'Brien Stephen J, Feng Zhenru, Chang Le, Dai Erhei, Lu Jianhua, Xi Hongli, Yu Yanyan, Zhang Jianguo, Wang Binbin, Zeng Zhe |
Prevalence and Clinical Features of Inflammatory Bowel Diseases Associated With Monogenic Variants, Identified by Whole-Exome Sequencing in 1000 Children at a Single Center. Gastroenterology 2020 2 158 (8): 2208-2220. Crowley Eileen, Warner Neil, Pan Jie, Khalouei Sam, Elkadri Abdul, Fiedler Karoline, Foong Justin, Turinsky Andrei L, Bronte-Tinkew Dana, Zhang Shiqi, Hu Jamie, Tian David, Li Dalin, Horowitz Julie, Siddiqui Iram, Upton Julia, Roifman Chaim M, Church Peter C, Wall Donna A, Ramani Arun K, Kotlarz Daniel, Klein Christoph, Uhlig Holm, Snapper Scott B, Gonzaga-Jauregui Claudia, Paterson Andrew D, McGovern Dermot P B, Brudno Michael, Walters Thomas D, Griffiths Anne M, Muise Aleixo |
Association of DOCK8, IL17RA, and KLK12 Polymorphisms with Atopic Dermatitis in Koreans. Annals of dermatology 2020 Jun 32 (3): 197-205. Heo Won Il, Park Kui Young, Lee Mi-Kyung, Bae Yu Jeong, Moon Nam Ju, Seo Seong J |
Corrigendum: Association of DOCK8, IL17RA, and KLK12 Polymorphisms with Atopic Dermatitis in Koreans. Annals of dermatology 2021 4 32 (6): 538. Heo Won Il, Park Kui Young, Lee Mi-Kyung, Bae Yu Jeong, Moon Nam Ju, Seo Seong J |
Prenatal detection of terminal 9p24.3 microduplication encompassing DOCK8 gene: A variant of likely benign. Medicine 2021 2 100 (3): e23967. Yue Fagui, Yu Yang, Zhang Xinyue, Jiang Yuting, Li Leilei, Liu Ruizhi, Zhang Hongg |
Germline copy number variations in BRCA1/2 negative families: Role in the molecular etiology of hereditary breast cancer in Tunisia. PloS one 2021 16 (1): e0245362. Boujemaa Maroua, Hamdi Yosr, Mejri Nesrine, Romdhane Lilia, Ghedira Kais, Bouaziz Hanen, El Benna Houda, Labidi Soumaya, Dallali Hamza, Jaidane Olfa, Ben Nasr Sonia, Haddaoui Abderrazek, Rahal Khaled, Abdelhak Sonia, Boussen Hamouda, Boubaker Mohamed Sam |
Duplication of 9p24.3 in three unrelated patients and their phenotypes, considering affected genes, and similar recurrent variants. Molecular genetics & genomic medicine 2021 1 9 (3): e1592. Capkova Zuzana, Capkova Pavlina, Srovnal Josef, Adamova Katerina, Prochazka Martin, Hajduch Mari |
Identification of a functional DOCK8 gene polymorphism associated with atopic dermatitis. Allergy 2022 Jul . Kunimura Kazufumi, Yamamura Kazuhiko, Nakahara Takeshi, Kido-Nakahara Makiko, Uruno Takehito, Fukui Yoshino |
Confirmation of Hyperimmunoglobulin E Syndrome in Two Patients with an Ocular Problem: Detection of Two New DOCK8 Mutations. Iranian journal of allergy, asthma, and immunology 2022 7 21 (3): 355-363. Saghafi Shiva, Zandieh Fariborz, Fazlollahi Mohammad Reza, Glocker Cristina, Frede Natalie, Buchta Mary, Yang Linlin, Mahmoudi Amir Hossein, Houshmand Massoud, Pourpak Zahra, Grimbacher Bodo, Moin Mosta |
Relevance of Coding Variation in FLG And DOCK8 in Finnish Pediatric Patients with Early-Onset Moderate-To-Severe Atopic Dermatitis. JID innovations : skin science from molecules to population health 2023 8 3 (4): 100203. Miia Perälä, Meri Kaustio, Alexander Salava, Eveliina Jakkula, Anna S Pelkonen, Janna Saarela, Anita Remitz, Mika J Mäke |
Gene-Smoking Interaction Analysis for the Identification of Novel Asthma-Associated Genetic Factors. International journal of molecular sciences 2023 8 24 (15): . Junho Cha, Sungkyoung Ch |
LRP2 and DOCK8 Are Potential Antigens for mRNA Vaccine Development in Immunologically 'Cold' KIRC Tumours. Vaccines 2023 2 11 (2): . Zhang Shichao, Xia Kaide, Chang Yue, Wei Yimei, Xiong Yu, Tang Fuzhou, Peng Jian, Ouyang Y |
The Autoimmune Manifestations in Patients with Genetic Defects in the B Cell Development and Differentiation Stages. Journal of clinical immunology 2023 2 . Azizi Gholamreza, Hesari Mina Fattah, Sharifinejad Niusha, Fayyaz Farimah, Chavoshzadeh Zahra, Mahdaviani Seyed Alireza, Alan Mahnaz Seifi, Jamee Mahnaz, Tavakol Marzieh, Sadri Homa, Shahrestanaki Ehsan, Nabavi Mohammad, Ebrahimi Sareh Sadat, Shirkani Afshin, Vosughi Motlagh Ahmad, Delavari Samaneh, Rasouli Seyed Erfan, Esmaeili Marzie, Salami Fereshte, Yazdani Reza, Rezaei Nima, Abolhassani Hass |
Genetic Characterization of Primary Mediastinal B-Cell Lymphoma: Pathogenesis and Patient Outcomes. Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2023 12 JCO2301053. Daniel Noerenberg, Franziska Briest, Cornelius Hennch, Kenichi Yoshida, Raphael Hablesreiter, Yasuhide Takeuchi, Hiroo Ueno, Annette M Staiger, Marita Ziepert, Fazila Asmar, Benjamin N Locher, Erika Toth, Thomas Weber, Rose-Marie Amini, Wolfram Klapper, Maria Bouzani, Viola Poeschel, Andreas Rosenwald, Gerhard Held, Elías Campo, Naveed Ishaque, Kostas Stamatopoulos, George Kanellis, Ioannis Anagnostopoulos, Lars Bullinger, Neta Goldschmidt, Pier Luigi Zinzani, Csaba Bödör, Richard Rosenquist, Theodoros P Vassilakopoulos, German Ott, Seishi Ogawa, Frederik Da |
DNA Copy Number Alterations and Copy Neutral Loss of Heterozygosity in Adult Ph-Negative Acute B-Lymphoblastic Leukemia: Focus on the Genes Involved. International journal of molecular sciences 2023 12 24 (24): . Natalya Risinskaya, Maria Gladysheva, Abdulpatakh Abdulpatakhov, Yulia Chabaeva, Valeriya Surimova, Olga Aleshina, Anna Yushkova, Olga Dubova, Nikolay Kapranov, Irina Galtseva, Sergey Kulikov, Tatiana Obukhova, Andrey Sudarikov, Elena Parovichniko |
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- Page last updated:Mar 25, 2024
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