Human Genome Epidemiology Literature Finder
Records 1 - 14 (of 14 Records) |
Query Trace: EN1[original query] |
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Sudden infant death syndrome: case-control frequency differences at genes pertinent to early autonomic nervous system embryologic development. Pediatric research 2004 Sep 56 (3): 391-5. Weese-Mayer Debra E, Berry-Kravis Elizabeth M, Zhou Lili, Maher Brion S, Curran Mark E, Silvestri Jean M, Marazita Mary |
Polymorphisms of coding trinucleotide repeats of homeogenes in neurodevelopmental psychiatric disorders. Psychiatric genetics 2008 Dec 18 (6): 295-301. Laroche Fabrice, Ramoz Nicolas, Leroy Sophie, Fortin Célia, Rousselot-Paillet Bérangère, Philippe Anne, Colleaux Laurence, Bresson Jean-Louis, Mogenet Agnès, Golse Bernard, Mouren-Simeoni Marie-Christine, Gorwood Philip, Galli Thierry, Simonneau Michel, Krebs Marie-Odile, Robel Lauren |
Association of transcription factor polymorphisms PITX3 and EN1 with Parkinson's disease. Neurobiology of aging 2011 Feb 32 (2): 302-7. Haubenberger Dietrich, Reinthaler Eva, Mueller Jakob C, Pirker Walter, Katzenschlager Regina, Froehlich Roman, Bruecke Thomas, Daniel Gerhard, Auff Eduard, Zimprich Alexand |
Replication of top markers of a genome-wide association study in multiple sclerosis in Spain. Genes and immunity 2011 Mar 12 (2): 110-5. Cavanillas M L, Fernández O, Comabella M, Alcina A, Fedetz M, Izquierdo G, Lucas M, Cénit M C, Arroyo R, Vandenbroeck K, Alloza I, García-Barcina M, Antigüedad A, Leyva L, Gómez C L, Olascoaga J, Otaegui D, Blanco Y, Saiz A, Montalbán X, Matesanz F, Urcelay |
Evaluation of genes involved in limb development, angiogenesis, and coagulation as risk factors for congenital limb deficiencies. American journal of medical genetics. Part A 2012 Oct 158A (10): 2463-72. Browne Marilyn L, Carter Tonia C, Kay Denise M, Kuehn Devon, Brody Lawrence C, Romitti Paul A, Liu Aiyi, Caggana Michele, Druschel Charlotte M, Mills James |
Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture.
Nature 2015 Sep . Zheng Hou-Feng, Forgetta Vincenzo, Hsu Yi-Hsiang, Estrada Karol, Rosello-Diez Alberto, Leo Paul J, Dahia Chitra L, Park-Min Kyung Hyun, Tobias Jonathan H, Kooperberg Charles, Kleinman Aaron, Styrkarsdottir Unnur, Liu Ching-Ti, Uggla Charlotta, Evans Daniel S, Nielson Carrie M, Walter Klaudia, Pettersson-Kymmer Ulrika, McCarthy Shane, Eriksson Joel, Kwan Tony, Jhamai Mila, Trajanoska Katerina, Memari Yasin, Min Josine, Huang Jie, Danecek Petr, Wilmot Beth, Li Rui, Chou Wen-Chi, Mokry Lauren E, Moayyeri Alireza, Claussnitzer Melina, Cheng Chia-Ho, Cheung Warren, Medina-Gómez Carolina, Ge Bing, Chen Shu-Huang, Choi Kwangbom, Oei Ling, Fraser James, Kraaij Robert, Hibbs Matthew A, Gregson Celia L, Paquette Denis, Hofman Albert, Wibom Carl, Tranah Gregory J, Marshall Mhairi, Gardiner Brooke B, Cremin Katie, Auer Paul, Hsu Li, Ring Sue, Tung Joyce Y, Thorleifsson Gudmar, Enneman Anke W, van Schoor Natasja M, de Groot Lisette C P G M, van der Velde Nathalie, Melin Beatrice, Kemp John P, Christiansen Claus, Sayers Adrian, Zhou Yanhua, Calderari Sophie, van Rooij Jeroen, Carlson Chris, Peters Ulrike, Berlivet Soizik, Dostie Josée, Uitterlinden Andre G, Williams Stephen R, Farber Charles, Grinberg Daniel, LaCroix Andrea Z, Haessler Jeff, Chasman Daniel I, Giulianini Franco, Rose Lynda M, Ridker Paul M, Eisman John A, Nguyen Tuan V, Center Jacqueline R, Nogues Xavier, Garcia-Giralt Natalia, Launer Lenore L, Gudnason Vilmunder, Mellström Dan, Vandenput Liesbeth, Amin Najaf, van Duijn Cornelia M, Karlsson Magnus K, Ljunggren Östen, Svensson Olle, Hallmans Göran, Rousseau François, Giroux Sylvie, Bussière Johanne, Arp Pascal P, Koromani Fjorda, Prince Richard L, Lewis Joshua R, Langdahl Bente L, Pernille Hermann A, Jensen Jens-Erik B, Kaptoge Stephen, Khaw Kay-Tee, Reeve Jonathan, Formosa Melissa M, Xuereb-Anastasi Angela, Åkesson Kristina, McGuigan Fiona E, Garg Gaurav, Olmos Jose M, Zarrabeitia Maria T, Riancho Jose A, Ralston Stuart H, Alonso Nerea, Jiang Xi, Goltzman David, Pastinen Tomi, Grundberg Elin, Gauguier Dominique, Orwoll Eric S, Karasik David, Davey-Smith George, , Smith Albert V, Siggeirsdottir Kristin, Harris Tamara B, Carola Zillikens M, van Meurs Joyce B J, Thorsteinsdottir Unnur, Maurano Matthew T, Timpson Nicholas J, Soranzo Nicole, Durbin Richard, Wilson Scott G, Ntzani Evangelia E, Brown Matthew A, Stefansson Kari, Hinds David A, Spector Tim, Adrienne Cupples L, Ohlsson Claes, Greenwood Celia M T, , Jackson Rebecca D, Rowe David W, Loomis Cynthia A, Evans David M, Ackert-Bicknell Cheryl L, Joyner Alexandra L, Duncan Emma L, Kiel Douglas P, Rivadeneira Fernando, Richards J Bre |
Rare EN1 Variants and Pediatric Bone Mass. Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2016 Mar . Mitchell Jonathan A, Chesi Alessandra, McCormack Shana E, Roy Sani M, Cousminer Diana L, Kalkwarf Heidi J, Lappe Joan M, Gilsanz Vicente, Oberfield Sharon E, Shepherd John A, Kelly Andrea, Zemel Babette S, Grant Struan F |
Sequence variants in the PTCH1 gene associate with spine bone mineral density and osteoporotic fractures.
Nature communications 2016 Jan 7 10129. Styrkarsdottir Unnur, Thorleifsson Gudmar, Gudjonsson Sigurjon A, Sigurdsson Asgeir, Center Jacqueline R, Lee Seung Hun, Nguyen Tuan V, Kwok Timothy C Y, Lee Jenny S W, Ho Suzanne C, Woo Jean, Leung Ping-C, Kim Beom-Jun, Rafnar Thorunn, Kiemeney Lambertus A, Ingvarsson Thorvaldur, Koh Jung-Min, Tang Nelson L S, Eisman John A, Christiansen Claus, Sigurdsson Gunnar, Thorsteinsdottir Unnur, Stefansson Ka |
Association between EN1 rs4144782 and susceptibility of knee osteoarthritis: A case-control study. Oncotarget 2017 May 8 (22): 36650-36657. Li Haohuan, Zhang Xiaolong, Cao Yiping, Hu Song, Peng Fei, Zhou Jianlin, Li Jianpi |
Clinical Phenotypes Associated to Engrailed 2 Gene Alterations in a Series of Neuropediatric Patients. Frontiers in neuroanatomy 2018 8 12 61. Carratala-Marco Francisco, Andreo-Lillo Patricia, Martinez-Morga Marta, Escamez-Martínez Teresa, Botella-López Arancha, Bueno Carlos, Martinez Salvad |
Engrailed 1 overexpression as a potential prognostic marker in Lower Grade Glioma. PeerJ 2019 7 e7414. Zhu Jin, Zhang Yu- |
Homeobox transcription factor engrailed homeobox 1 is a possible diagnostic marker for adenoid cystic carcinoma and polymorphous adenocarcinoma. Pathology international 2020 12 71 (2): 113-123. Baba Shunichi, Akashi Takumi, Kayamori Kou, Ohuchi Tomoyuki, Ogawa Ikuko, Kubota Nobuhisa, Nakano Keisuke, Nagatsuka Hitoshi, Hasegawa Hiromasa, Matsuzaka Kenichi, Tomii Shohei, Uchida Keisuke, Katsuta Noriko, Sekiya Takahiro, Ando Noboru, Miura Keiko, Ishibashi Hironori, Ariizumi Yousuke, Asakage Takahiro, Michi Yasuyuki, Harada Hiroyuki, Sakamoto Kei, Eishi Yoshinobu, Okubo Kenichi, Ikeda Toh |
Increased gene expression variability in BRCA1-associated and basal-like breast tumours. Breast cancer research and treatment 2021 Jul . Wiggins George A R, Black Michael A, Dunbier Anita, Morley-Bunker Arthur E, , Pearson John F, Walker Logan |
An integrative approach toward identification and analysis of therapeutic targets involved in HPV pathogenesis with a focus on carcinomas. Cancer biomarkers : section A of Disease markers 2022 10 36 (1): 31-52. Gupta Amit Kumar, Kumar Man |
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