Human Genome Epidemiology Literature Finder
Records 1 - 10 (of 10 Records) |
Query Trace: CHRNE[original query] |
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Genetic variants in epidermal growth factor receptor pathway genes and risk of esophageal squamous cell carcinoma and gastric cancer in a Chinese population. PloS one 2013 8 (7): e68999. Li Wen-Qing, Hu Nan, Wang Zhaoming, Yu Kai, Su Hua, Wang Lemin, Wang Chaoyu, Chanock Stephen J, Burdett Laurie, Ding Ti, Qiao You-Lin, Fan Jin-Hu, Wang Yuan, Xu Yi, Giffen Carol, Xiong Xiaoqin, Murphy Gwen, Tucker Margaret A, Dawsey Sanford M, Freedman Neal D, Abnet Christian C, Goldstein Alisa M, Taylor Philip |
Natural killer cells and single nucleotide polymorphisms of specific ion channels and receptor genes in myalgic encephalomyelitis/chronic fatigue syndrome. The application of clinical genetics 2016 9 39-47. Marshall-Gradisnik Sonya, Huth Teilah, Chacko Anu, Johnston Samantha, Smith Pete, Staines Dona |
Evidence for Association Between Low Frequency Variants in CHRNA6/CHRNB3 and Antisocial Drug Dependence. Behavior genetics 2016 Apr . Kamens Helen M, Corley Robin P, Richmond Phillip A, Darlington Todd M, Dowell Robin, Hopfer Christian J, Stallings Michael C, Hewitt John K, Brown Sandra A, Ehringer Marissa |
Congenital myasthenic syndrome in Israel: Genetic and clinical characterization. Neuromuscular disorders : NMD 2016 12 27 (2): 136-140. Aharoni Sharon, Sadeh Menachem, Shapira Yehuda, Edvardson Simon, Daana Muhannad, Dor-Wollman Talia, Mimouni-Bloch Aviva, Halevy Ayelet, Cohen Rony, Sagie Liora, Argov Zohar, Rabie Malcolm, Spiegel Ronen, Chervinsky Ilana, Orenstein Naama, Engel Andrew G, Nevo Yor |
Congenital Myasthenic Syndrome: Spectrum of Mutations in an Indian Cohort. Journal of clinical neuromuscular disease 2018 Sep 20 (1): 14-27. Selvam Pavalan, Arunachal Gautham, Danda Sumita, Chapla Aaron, Sivadasan Ajith, Alexander Mathew, Thomas Maya Mary, Thomas Nihal |
A common CHRNE mutation in Brazilian patients with congenital myasthenic syndrome. Journal of neurology 2018 2 265 (3): 708-713. Estephan Eduardo de Paula, Sobreira Cláudia Ferreira da Rosa, Dos Santos André Clériston José, Tomaselli Pedro José, Marques Wilson, Ortega Roberta Paiva Magalhães, Costa Marcela Câmara Machado, da Silva André Macedo Serafim, Mendonça Rodrigo Holanda, Caldas Vitor Marques, Zambon Antonio Alberto, Abath Neto Osório, Marchiori Paulo Eurípedes, Heise Carlos Otto, Reed Umbertina Conti, Azuma Yoshiteru, Töpf Ana, Lochmüller Hanns, Zanoteli Edm |
No Hot Spot Mutations CHRNE c.1327 delG, CHAT c.914T>C, and RAPSN c.264C>A in Iranian Patients with Congenital Myasthenic Syndrome. Iranian journal of child neurology 2019 5 13 (2): 135-143. Parvizi Omran Sima, Houshmand Massod, Dominic Donkor, Farjami Zahra, Karimzadeh Parvan |
Common variants in Alzheimer's disease and risk stratification by polygenic risk scores.
Nature communications 2021 6 12 (1): 3417. de Rojas Itziar, Moreno-Grau Sonia, Tesi Niccolo, Grenier-Boley Benjamin, Andrade Victor, Jansen Iris E, Pedersen Nancy L, Stringa Najada, Zettergren Anna, Hernández Isabel, Montrreal Laura, Antúnez Carmen, Antonell Anna, Tankard Rick M, Bis Joshua C, Sims Rebecca, Bellenguez Céline, Quintela Inés, González-Perez Antonio, Calero Miguel, Franco-Macías Emilio, Macías Juan, Blesa Rafael, Cervera-Carles Laura, Menéndez-González Manuel, Frank-García Ana, Royo Jose Luís, Moreno Fermin, Huerto Vilas Raquel, Baquero Miquel, Diez-Fairen Mónica, Lage Carmen, García-Madrona Sebastián, García-González Pablo, Alarcón-Martín Emilio, Valero Sergi, Sotolongo-Grau Oscar, Ullgren Abbe, Naj Adam C, Lemstra Afina W, Benaque Alba, Pérez-Cordón Alba, Benussi Alberto, Rábano Alberto, Padovani Alessandro, Squassina Alessio, de Mendonça Alexandre, Arias Pastor Alfonso, Kok Almar A L, Meggy Alun, Pastor Ana Belén, Espinosa Ana, Corma-Gómez Anaïs, Martín Montes Angel, Sanabria Ángela, DeStefano Anita L, Schneider Anja, Haapasalo Annakaisa, Kinhult Ståhlbom Anne, Tybjærg-Hansen Anne, Hartmann Annette M, Spottke Annika, Corbatón-Anchuelo Arturo, Rongve Arvid, Borroni Barbara, Arosio Beatrice, Nacmias Benedetta, Nordestgaard Børge G, Kunkle Brian W, Charbonnier Camille, Abdelnour Carla, Masullo Carlo, Martínez Rodríguez Carmen, Muñoz-Fernandez Carmen, Dufouil Carole, Graff Caroline, Ferreira Catarina B, Chillotti Caterina, Reynolds Chandra A, Fenoglio Chiara, Van Broeckhoven Christine, Clark Christopher, Pisanu Claudia, Satizabal Claudia L, Holmes Clive, Buiza-Rueda Dolores, Aarsland Dag, Rujescu Dan, Alcolea Daniel, Galimberti Daniela, Wallon David, Seripa Davide, Grünblatt Edna, Dardiotis Efthimios, Düzel Emrah, Scarpini Elio, Conti Elisa, Rubino Elisa, Gelpi Ellen, Rodriguez-Rodriguez Eloy, Duron Emmanuelle, Boerwinkle Eric, Ferri Evelyn, Tagliavini Fabrizio, Küçükali Fahri, Pasquier Florence, Sanchez-Garcia Florentino, Mangialasche Francesca, Jessen Frank, Nicolas Gaël, Selbæk Geir, Ortega Gemma, Chêne Geneviève, Hadjigeorgiou Georgios, Rossi Giacomina, Spalletta Gianfranco, Giaccone Giorgio, Grande Giulia, Binetti Giuliano, Papenberg Goran, Hampel Harald, Bailly Henri, Zetterberg Henrik, Soininen Hilkka, Karlsson Ida K, Alvarez Ignacio, Appollonio Ildebrando, Giegling Ina, Skoog Ingmar, Saltvedt Ingvild, Rainero Innocenzo, Rosas Allende Irene, Hort Jakub, Diehl-Schmid Janine, Van Dongen Jasper, Vidal Jean-Sebastien, Lehtisalo Jenni, Wiltfang Jens, Thomassen Jesper Qvist, Kornhuber Johannes, Haines Jonathan L, Vogelgsang Jonathan, Pineda Juan A, Fortea Juan, Popp Julius, Deckert Jürgen, Buerger Katharina, Morgan Kevin, Fließbach Klaus, Sleegers Kristel, Molina-Porcel Laura, Kilander Lena, Weinhold Leonie, Farrer Lindsay A, Wang Li-San, Kleineidam Luca, Farotti Lucia, Parnetti Lucilla, Tremolizzo Lucio, Hausner Lucrezia, Benussi Luisa, Froelich Lutz, Ikram M Arfan, Deniz-Naranjo M Candida, Tsolaki Magda, Rosende-Roca Maitée, Löwenmark Malin, Hulsman Marc, Spallazzi Marco, Pericak-Vance Margaret A, Esiri Margaret, Bernal Sánchez-Arjona María, Dalmasso Maria Carolina, Martínez-Larrad María Teresa, Arcaro Marina, Nöthen Markus M, Fernández-Fuertes Marta, Dichgans Martin, Ingelsson Martin, Herrmann Martin J, Scherer Martin, Vyhnalek Martin, Kosmidis Mary H, Yannakoulia Mary, Schmid Matthias, Ewers Michael, Heneka Michael T, Wagner Michael, Scamosci Michela, Kivipelto Miia, Hiltunen Mikko, Zulaica Miren, Alegret Montserrat, Fornage Myriam, Roberto Natalia, van Schoor Natasja M, Seidu Nazib M, Banaj Nerisa, Armstrong Nicola J, Scarmeas Nikolaos, Scherbaum Norbert, Goldhardt Oliver, Hanon Oliver, Peters Oliver, Skrobot Olivia Anna, Quenez Olivier, Lerch Ondrej, Bossù Paola, Caffarra Paolo, Dionigi Rossi Paolo, Sakka Paraskevi, Mecocci Patrizia, Hoffmann Per, Holmans Peter A, Fischer Peter, Riederer Peter, Yang Qiong, Marshall Rachel, Kalaria Rajesh N, Mayeux Richard, Vandenberghe Rik, Cecchetti Roberta, Ghidoni Roberta, Frikke-Schmidt Ruth, Sorbi Sandro, Hägg Sara, Engelborghs Sebastiaan, Helisalmi Seppo, Botne Sando Sigrid, Kern Silke, Archetti Silvana, Boschi Silvia, Fostinelli Silvia, Gil Silvia, Mendoza Silvia, Mead Simon, Ciccone Simona, Djurovic Srdjan, Heilmann-Heimbach Stefanie, Riedel-Heller Steffi, Kuulasmaa Teemu, Del Ser Teodoro, Lebouvier Thibaud, Polak Thomas, Ngandu Tiia, Grimmer Timo, Bessi Valentina, Escott-Price Valentina, Giedraitis Vilmantas, Deramecourt Vincent, Maier Wolfgang, Jian Xueqiu, Pijnenburg Yolande A L, , , , , , Kehoe Patrick Gavin, Garcia-Ribas Guillermo, Sánchez-Juan Pascual, Pastor Pau, Pérez-Tur Jordi, Piñol-Ripoll Gerard, Lopez de Munain Adolfo, García-Alberca Jose María, Bullido María J, Álvarez Victoria, Lleó Alberto, Real Luis M, Mir Pablo, Medina Miguel, Scheltens Philip, Holstege Henne, Marquié Marta, Sáez María Eugenia, Carracedo Ángel, Amouyel Philippe, Schellenberg Gerard D, Williams Julie, Seshadri Sudha, van Duijn Cornelia M, Mather Karen A, Sánchez-Valle Raquel, Serrano-Ríos Manuel, Orellana Adelina, Tárraga Lluís, Blennow Kaj, Huisman Martijn, Andreassen Ole A, Posthuma Danielle, Clarimón Jordi, Boada Mercè, van der Flier Wiesje M, Ramirez Alfredo, Lambert Jean-Charles, van der Lee Sven J, Ruiz Agust |
Congenital myasthenic syndrome in a cohort of patients with 'double' seronegative myasthenia gravis. Arquivos de neuro-psiquiatria 2021 12 80 (1): 69-74. Lorenzoni Paulo José, Ducci Renata Dal-Pra, Arndt Raquel Cristina, Hrysay Nyvia Milicio Coblinski, Fustes Otto Jesus Hernandez, Töpf Ana, Lochmüller Hanns, Werneck Lineu Cesar, Kay Cláudia Suemi Kamoi, Scola Rosana Hermin |
The clinical and molecular landscape of congenital myasthenic syndromes in Austria: a nationwide study. Journal of neurology 2022 10 270 (2): 909-916. Krenn Martin, Sener Merve, Rath Jakob, Zulehner Gudrun, Keritam Omar, Wagner Matias, Laccone Franco, Iglseder Stephan, Marte Sonja, Baumgartner Manuela, Eisenkölbl Astrid, Liechtenstein Christian, Rudnik Sabine, Quasthoff Stefan, Grinzinger Susanne, Spenger Johannes, Wortmann Saskia B, Löscher Wolfgang N, Zimprich Fritz, Kellersmann Anna, Rappold Mika, Bernert Günther, Freilinger Michael, Cetin Hak |
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- Page last updated:Apr 16, 2024
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