Human Genome Epidemiology Literature Finder
Records 1 - 9 (of 9 Records) |
Query Trace: SH3PXD2A[original query] |
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A study of the association between the ADAM12 and SH3PXD2A (SH3MD1) genes and Alzheimer's disease. Neuroscience letters 2010 Jan 468 (1): 1-2. Laumet Geoffroy, Petitprez Vincent, Sillaire Adeline, Ayral Anne-Marie, Hansmannel Franck, Chapuis Julien, Hannequin Didier, Pasquier Florence, Scarpini Elio, Galimberti Daniela, Lendon Corinne, Campion Dominique, Amouyel Philippe, Lambert Jean-Charl |
Investigation of the involvement of MIR185 and its target genes in the development of schizophrenia. Journal of psychiatry & neuroscience : JPN 2014 Nov 39 (6): 386-96. Forstner Andreas J, Basmanav F B, Mattheisen Manuel, Böhmer Anne C, Hollegaard Mads V, Janson Esther, Strengman Eric, Priebe Lutz, Degenhardt Franziska, Hoffmann Per, Herms Stefan, Maier Wolfgang, Mössner Rainald, Rujescu Dan, Ophoff Roel A, Moebus Susanne, Mortensen Preben B, Børglum Anders D, Hougaard David M, Frank Josef, Witt Stephanie H, Rietschel Marcella, Zimmer Andreas, Nöthen Markus M, Miró Xavier, Cichon Sv |
Identification of six new genetic loci associated with atrial fibrillation in the Japanese population.
Nature genetics 2017 Apr . Low Siew-Kee, Takahashi Atsushi, Ebana Yusuke, Ozaki Kouichi, Christophersen Ingrid E, Ellinor Patrick T, , Ogishima Soichi, Yamamoto Masayuki, Satoh Mamoru, Sasaki Makoto, Yamaji Taiki, Iwasaki Motoki, Tsugane Shoichiro, Tanaka Keitaro, Naito Mariko, Wakai Kenji, Tanaka Hideo, Furukawa Tetsushi, Kubo Michiaki, Ito Kaoru, Kamatani Yoichiro, Tanaka Toshihi |
Non-Syndromic Cleft Lip with or without Cleft Palate: Genome-Wide Association Study in Europeans Identifies a Suggestive Risk Locus at 16p12.1 and Supports SH3PXD2A as a Clefting Susceptibility Gene. Genes 2019 Dec 10 (12): . van Rooij Iris Alm, Ludwig Kerstin U, Welzenbach Julia, Ishorst Nina, Thonissen Michelle, Galesloot Tessel E, Ongkosuwito Edwin, Bergé Stefaan J, Aldhorae Khalid, Rojas-Martinez Augusto, Kiemeney Lambertus Alm, Vermeesch Joris Robert, Brunner Han, Roeleveld Nel, Devriendt Koen, Dormaar Titiaan, Hens Greet, Knapp Michael, Carels Carine, Mangold Elisabe |
Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities.
Stroke 2020 07 51 (7): 2111-2121. Armstrong Nicola J, Mather Karen A, Sargurupremraj Muralidharan, Knol Maria J, Malik Rainer, Satizabal Claudia L, Yanek Lisa R, Wen Wei, Gudnason Vilmundur G, Dueker Nicole D, Elliott Lloyd T, Hofer Edith, Bis Joshua, Jahanshad Neda, Li Shuo, Logue Mark A, Luciano Michelle, Scholz Markus, Smith Albert V, Trompet Stella, Vojinovic Dina, Xia Rui, Alfaro-Almagro Fidel, Ames David, Amin Najaf, Amouyel Philippe, Beiser Alexa S, Brodaty Henry, Deary Ian J, Fennema-Notestine Christine, Gampawar Piyush G, Gottesman Rebecca, Griffanti Ludovica, Jack Clifford R, Jenkinson Mark, Jiang Jiyang, Kral Brian G, Kwok John B, Lampe Leonie, C M Liewald David, Maillard Pauline, Marchini Jonathan, Bastin Mark E, Mazoyer Bernard, Pirpamer Lukas, Rafael Romero José, Roshchupkin Gennady V, Schofield Peter R, Schroeter Matthias L, Stott David J, Thalamuthu Anbupalam, Trollor Julian, Tzourio Christophe, van der Grond Jeroen, Vernooij Meike W, Witte Veronica A, Wright Margaret J, Yang Qiong, Morris Zoe, Siggurdsson Siggi, Psaty Bruce, Villringer Arno, Schmidt Helena, Haberg Asta K, van Duijn Cornelia M, Jukema J Wouter, Dichgans Martin, Sacco Ralph L, Wright Clinton B, Kremen William S, Becker Lewis C, Thompson Paul M, Mosley Thomas H, Wardlaw Joanna M, Ikram M Arfan, Adams Hieab H H, Seshadri Sudha, Sachdev Perminder S, Smith Stephen M, Launer Lenore, Longstreth William, DeCarli Charles, Schmidt Reinhold, Fornage Myriam, Debette Stephanie, Nyquist Paul |
Genetic basis of lacunar stroke: a pooled analysis of individual patient data and genome-wide association studies.
The Lancet. Neurology 2021 (5): 351-361. Traylor Matthew, Persyn Elodie, Tomppo Liisa, Klasson Sofia, Abedi Vida, Bakker Mark K, Torres Nuria, Li Linxin, Bell Steven, Rutten-Jacobs Loes, Tozer Daniel J, Griessenauer Christoph J, Zhang Yanfei, Pedersen Annie, Sharma Pankaj, Jimenez-Conde Jordi, Rundek Tatjana, Grewal Raji P, Lindgren Arne, Meschia James F, Salomaa Veikko, Havulinna Aki, Kourkoulis Christina, Crawford Katherine, Marini Sandro, Mitchell Braxton D, Kittner Steven J, Rosand Jonathan, Dichgans Martin, Jern Christina, Strbian Daniel, Fernandez-Cadenas Israel, Zand Ramin, Ruigrok Ynte, Rost Natalia, Lemmens Robin, Rothwell Peter M, Anderson Christopher D, Wardlaw Joanna, Lewis Cathryn M, Markus Hugh S, , , , |
A novel senescence-related lncRNA signature that predicts prognosis and the tumor microenvironment in patients with lung adenocarcinoma. Frontiers in genetics 2022 11 13 951311. Fang Xueying, Huang Enmin, Xie Xiaopeng, Yang Kai, Wang Shuqian, Huang Xiaoqing, Song M |
Stroke genetics informs drug discovery and risk prediction across ancestries.
Nature 2022 10 611 (7934): 115-123. Mishra Aniket, Malik Rainer, Hachiya Tsuyoshi, Jürgenson Tuuli, Namba Shinichi, Posner Daniel C, Kamanu Frederick K, Koido Masaru, Le Grand Quentin, Shi Mingyang, He Yunye, Georgakis Marios K, Caro Ilana, Krebs Kristi, Liaw Yi-Ching, Vaura Felix C, Lin Kuang, Winsvold Bendik Slagsvold, Srinivasasainagendra Vinodh, Parodi Livia, Bae Hee-Joon, Chauhan Ganesh, Chong Michael R, Tomppo Liisa, Akinyemi Rufus, Roshchupkin Gennady V, Habib Naomi, Jee Yon Ho, Thomassen Jesper Qvist, Abedi Vida, Cárcel-Márquez Jara, Nygaard Marianne, Leonard Hampton L, Yang Chaojie, Yonova-Doing Ekaterina, Knol Maria J, Lewis Adam J, Judy Renae L, Ago Tetsuro, Amouyel Philippe, Armstrong Nicole D, Bakker Mark K, Bartz Traci M, Bennett David A, Bis Joshua C, Bordes Constance, Børte Sigrid, Cain Anael, Ridker Paul M, Cho Kelly, Chen Zhengming, Cruchaga Carlos, Cole John W, de Jager Phil L, de Cid Rafael, Endres Matthias, Ferreira Leslie E, Geerlings Mirjam I, Gasca Natalie C, Gudnason Vilmundur, Hata Jun, He Jing, Heath Alicia K, Ho Yuk-Lam, Havulinna Aki S, Hopewell Jemma C, Hyacinth Hyacinth I, Inouye Michael, Jacob Mina A, Jeon Christina E, Jern Christina, Kamouchi Masahiro, Keene Keith L, Kitazono Takanari, Kittner Steven J, Konuma Takahiro, Kumar Amit, Lacaze Paul, Launer Lenore J, Lee Keon-Joo, Lepik Kaido, Li Jiang, Li Liming, Manichaikul Ani, Markus Hugh S, Marston Nicholas A, Meitinger Thomas, Mitchell Braxton D, Montellano Felipe A, Morisaki Takayuki, Mosley Thomas H, Nalls Mike A, Nordestgaard Børge G, O'Donnell Martin J, Okada Yukinori, Onland-Moret N Charlotte, Ovbiagele Bruce, Peters Annette, Psaty Bruce M, Rich Stephen S, Rosand Jonathan, Sabatine Marc S, Sacco Ralph L, Saleheen Danish, Sandset Else Charlotte, Salomaa Veikko, Sargurupremraj Muralidharan, Sasaki Makoto, Satizabal Claudia L, Schmidt Carsten O, Shimizu Atsushi, Smith Nicholas L, Sloane Kelly L, Sutoh Yoichi, Sun Yan V, Tanno Kozo, Tiedt Steffen, Tatlisumak Turgut, Torres-Aguila Nuria P, Tiwari Hemant K, Trégouët David-Alexandre, Trompet Stella, Tuladhar Anil Man, Tybjærg-Hansen Anne, van Vugt Marion, Vibo Riina, Verma Shefali S, Wiggins Kerri L, Wennberg Patrik, Woo Daniel, Wilson Peter W F, Xu Huichun, Yang Qiong, Yoon Kyungheon, , , , , , , , , , , , , , , , Millwood Iona Y, Gieger Christian, Ninomiya Toshiharu, Grabe Hans J, Jukema J Wouter, Rissanen Ina L, Strbian Daniel, Kim Young Jin, Chen Pei-Hsin, Mayerhofer Ernst, Howson Joanna M M, Irvin Marguerite R, Adams Hieab, Wassertheil-Smoller Sylvia, Christensen Kaare, Ikram Mohammad A, Rundek Tatjana, Worrall Bradford B, Lathrop G Mark, Riaz Moeen, Simonsick Eleanor M, Kõrv Janika, França Paulo H C, Zand Ramin, Prasad Kameshwar, Frikke-Schmidt Ruth, de Leeuw Frank-Erik, Liman Thomas, Haeusler Karl Georg, Ruigrok Ynte M, Heuschmann Peter Ulrich, Longstreth W T, Jung Keum Ji, Bastarache Lisa, Paré Guillaume, Damrauer Scott M, Chasman Daniel I, Rotter Jerome I, Anderson Christopher D, Zwart John-Anker, Niiranen Teemu J, Fornage Myriam, Liaw Yung-Po, Seshadri Sudha, Fernández-Cadenas Israel, Walters Robin G, Ruff Christian T, Owolabi Mayowa O, Huffman Jennifer E, Milani Lili, Kamatani Yoichiro, Dichgans Martin, Debette Stephan |
[Classification and Molecular Diagnosis of Benign Brain Tumors]. No shinkei geka. Neurological surgery 2023 9 51 (5): 771-777. Koji Yoshimo |
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- Page last updated:Mar 25, 2024
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