Human Genome Epidemiology Literature Finder
Records 1 - 19 (of 19 Records) |
Query Trace: DNM3[original query] |
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Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution.
Nature genetics 2010 Oct . Heid IM, Jackson AU, Randall JC, Winkler TW, Qi L, Steinthorsdottir V, Thorleifsson G, Zillikens MC, Speliotes EK, Mägi R, Workalemahu T, White CC, Bouatia-Naji N, Harris TB, Berndt SI, Ingelsson E, Willer CJ, Weedon MN, Luan J, Vedantam S, Esko T, Kilpeläinen TO, Kutalik Z, Li S, Monda KL, Dixon AL, Holmes CC, Kaplan LM, Liang L, Min JL, Moffatt MF, Molony C, Nicholson G, Schadt EE, Zondervan KT, Feitosa MF, Ferreira T, Allen HL, Weyant RJ, Wheeler E, Wood AR, Estrada K, Goddard ME, Lettre G, Mangino M, Nyholt DR, Purcell S, Smith AV, Visscher PM, Yang J, McCarroll SA, Nemesh J, Voight BF, Absher D, Amin N, Aspelund T, Coin L, Glazer NL, Hayward C, Heard-Costa NL, Hottenga JJ, Johansson A, Johnson T, Kaakinen M, Kapur K, Ketkar S, Knowles JW, Kraft P, Kraja AT, Lamina C, Leitzmann MF, McKnight B, Morris AP, Ong KK, Perry JR, Peters MJ, Polasek O, Prokopenko I, Rayner NW, Ripatti S, Rivadeneira F, Robertson NR, Sanna S, Sovio U, Surakka I, Teumer A, van Wingerden S, Vitart V, Zhao JH, Cavalcanti-Proença C, Chines PS, Fisher E, Kulzer JR, Lecoeur C, Narisu N, Sandholt C, Scott LJ, Silander K, Stark K, Tammesoo ML, Teslovich TM, Timpson NJ, Watanabe RM, Welch R, Chasman DI, Cooper MN, Jansson JO, Kettunen J, Lawrence RW, Pellikka N, Perola M, Vandenput L, Alavere H, Almgren P, Atwood LD, Bennett AJ, Biffar R, Bonnycastle LL, Bornstein SR, Buchanan TA, Campbell H, Day IN, Dei M, Dörr M, Elliott P, Erdos MR, Eriksson JG, Freimer NB, Fu M, Gaget S, Geus EJ, Gjesing AP, Grallert H, Gräßler J, Groves CJ, Guiducci C, Hartikainen AL, Hassanali N, Havulinna AS, Herzig KH, Hicks AA, Hui J, Igl W, Jousilahti P, Jula A, Kajantie E, Kinnunen L, Kolcic I, Koskinen S, Kovacs P, Kroemer HK, Krzelj V, Kuusisto J, Kvaloy K, Laitinen J, Lantieri O, Lathrop GM, Lokki ML, Luben RN, Ludwig B, McArdle WL, McCarthy A, Morken MA, Nelis M, Neville MJ, Paré G, Parker AN, Peden JF, Pichler I, Pietiläinen KH, Platou CG, Pouta A, Ridderstråle M, Samani NJ, Saramies J, Sinisalo J, Smit JH, Strawbridge RJ, Stringham HM, Swift AJ, Teder-Laving M, Thomson B, Usala G, van Meurs JB, van Ommen GJ, Vatin V, Volpato CB, Wallaschofski H, Walters GB, Widen E, Wild SH, Willemsen G, Witte DR, Zgaga L, Zitting P, Beilby JP, James AL, Kähönen M, Lehtimäki T, Nieminen MS, Ohlsson C, Palmer LJ, Raitakari O, Ridker PM, Stumvoll M, Tönjes A, Viikari J, Balkau B, Ben-Shlomo Y, Bergman RN, Boeing H, Smith GD, Ebrahim S, Froguel P, Hansen T, Hengstenberg C, Hveem K, Isomaa B, Jørgensen T, Karpe F, Khaw KT, Laakso M, Lawlor DA, Marre M, Meitinger T, Metspalu A, Midthjell K, Pedersen O, Salomaa V, Schwarz PE, Tuomi T, Tuomilehto J, Valle TT, Wareham NJ, Arnold AM, Beckmann JS, Bergmann S, Boerwinkle E, Boomsma DI, Caulfield MJ, Collins FS, Eiriksdottir G, Gudnason V, Gyllensten U, Hamsten A, Hattersley AT, Hofman A, Hu FB, Illig T, Iribarren C, Jarvelin MR, Kao WH, Kaprio J, Launer LJ, Munroe PB, Oostra B, Penninx BW, Pramstaller PP, Psaty BM, Quertermous T, Rissanen A, Rudan I, Shuldiner AR, Soranzo N, Spector TD, Syvanen AC, Uda M, Uitterlinden A, Völzke H, Vollenweider P, Wilson JF, Witteman JC, Wright AF, Abecasis GR, Boehnke M, Borecki IB, Deloukas P, Frayling TM, Groop LC, Haritunians T, Hunter DJ, Kaplan RC, North KE, O'Connell JR, Peltonen L, Schlessinger D, Strachan DP, Hirschhorn JN, Assimes TL, Wichmann HE, Thorsteinsdottir U, van Duijn CM, Stefansson K, Cupples LA, Loos RJ, Barroso I, McCarthy MI, Fox CS, Mohlke KL, Lindgren CM |
A gene-centric study of common carotid artery remodelling. Atherosclerosis 2012 Nov . Harrison SC, Zabaneh D, Asselbergs FW, Drenos F, Jones GT, Shah S, Gertow K, Sennblad B, Strawbridge RJ, Gigante B, Holewijn S, De Graaf J, Vermeulen S, Folkersen L, van Rij AM, Baldassarre D, Veglia F, Talmud PJ, Deanfield JE, Agu O, Kivimaki M, Kumari M, Bown MJ, Nyyssönen K, Rauramaa R, Smit AJ, Franco-Cereceda A, Giral P, Mannarino E, Silveira A, Syvänen AC, de Borst GJ, van der Graaf Y, de Faire U, Baas AF, Blankensteijn JD, Wareham NJ, Fowkes G, Tzoulaki I, Price JF, Tremoli E, Hingorani AD, Eriksson P, Hamsten A, Humphries SE |
Replication study of 15 recently published Loci for body fat distribution in the Japanese population. Journal of atherosclerosis and thrombosis 2012 Dec . Hotta K, Kitamoto A, Kitamoto T, Mizusawa S, Teranishi H, So R, Matsuo T, Nakata Y, Hyogo H, Ochi H, Nakamura T, Kamohara S, Miyatake N, Kotani K, Itoh N, Mineo I, Wada J, Yoneda M, Nakajima A, Funahashi T, Miyazaki S, Tokunaga K, Masuzaki H, Ueno T, Chayama K, Hamaguchi K, Yamada K, Hanafusa T, Oikawa S, Sakata T, Tanaka K, Matsuzawa Y, Nakao K, Sekine A |
Generalization of adiposity genetic loci to US Hispanic women. Nutrition & diabetes 2013 3 e85. Graff M, Fernández-Rhodes L, Liu S, Carlson C, Wassertheil-Smoller S, Neuhouser M, Reiner A, Kooperberg C, Rampersaud E, Manson J E, Kuller L H, Howard B V, Ochs-Balcom H M, Johnson K C, Vitolins M Z, Sucheston L, Monda K, North K |
Assessment of copy number variations in the brain genome of schizophrenia patients. Molecular cytogenetics 2015 8 46. Sakai Miwako, Watanabe Yuichiro, Someya Toshiyuki, Araki Kazuaki, Shibuya Masako, Niizato Kazuhiro, Oshima Kenichi, Kunii Yasuto, Yabe Hirooki, Matsumoto Junya, Wada Akira, Hino Mizuki, Hashimoto Takeshi, Hishimoto Akitoyo, Kitamura Noboru, Iritani Shuji, Shirakawa Osamu, Maeda Kiyoshi, Miyashita Akinori, Niwa Shin-Ichi, Takahashi Hitoshi, Kakita Akiyoshi, Kuwano Ryozo, Nawa Hiroyu |
Exon-focused genome-wide association study of obsessive-compulsive disorder and shared polygenic risk with schizophrenia. Translational psychiatry 2016 6 e768. Costas J, Carrera N, Alonso P, Gurriarán X, Segalàs C, Real E, López-Solà C, Mas S, Gassó P, Domènech L, Morell M, Quintela I, Lázaro L, Menchón J M, Estivill X, Carracedo |
A Genetic Risk Score Is Associated with Weight Loss Following Roux-en Y Gastric Bypass Surgery. Obesity surgery 2016 09 26 (9): 2183-2189. Bandstein Marcus, Voisin Sarah, Nilsson Emil K, Schultes Bernd, Ernst Barbara, Thurnheer Martin, Benedict Christian, Mwinyi Jessica, Schiöth Helgi |
DNM3 and genetic modifiers of age of onset in LRRK2 Gly2019Ser parkinsonism: a genome-wide linkage and association study. The Lancet. Neurology 2016 Sep . Trinh Joanne, Gustavsson Emil K, Vilariño-Güell Carles, Bortnick Stephanie, Latourelle Jeanne, McKenzie Marna B, Tu Chelsea Szu, Nosova Ekaterina, Khinda Jaskaran, Milnerwood Austen, Lesage Suzanne, Brice Alexis, Tazir Meriem, Aasly Jan O, Parkkinen Laura, Haytural Hazal, Foroud Tatiana, Myers Richard H, Sassi Samia Ben, Hentati Emna, Nabli Fatma, Farhat Emna, Amouri Rim, Hentati Fayçal, Farrer Matthew |
No association of DNM3 with age of onset in Asian Parkinson's disease. European journal of neurology 2018 Aug . Foo Jia Nee, Tan Louis C, Au Wing-Lok, Prakash Kumar-M, Liu Jianjun, Tan Eng-Ki |
Waist-hip ratio related genetic loci are associated with risk of impaired fasting glucose in Chinese children: a case control study. Nutrition & metabolism 2018 15 34. Song Qi-Ying, Meng Xiang-Rui, Hinney Anke, Song Jie-Yun, Huang Tao, Ma Jun, Wang Hai-J |
?-synuclein (SNCA) but not dynamin 3 (DNM3) influences age at onset of leucine-rich repeat kinase 2 (LRRK2) Parkinson's disease in Spain. Movement disorders : official journal of the Movement Disorder Society 2018 Feb . Fernández-Santiago Rubén, Garrido Alicia, Infante Jon, González-Aramburu Isabel, Sierra María, Fernández Manel, Valldeoriola Francesc, Muñoz Esteban, Compta Yaroslau, Martí María-José, Ríos José, Tolosa Eduardo, Ezquerra Mario, |
No evidence for DNM3 as genetic modifier of age at onset in idiopathic Parkinson's disease. Neurobiology of aging 2019 02 74 236.e1-236.e5. Berge-Seidl Victoria, Pihlstrøm Lasse, Wszolek Zbigniew K, Ross Owen A, Toft Mathi |
SNCA but not DNM3 and GAK modifies age at onset of LRRK2-related Parkinson's disease in Chinese population. Journal of neurology 2019 Apr . Yang Zhi-Hua, Li Yu-Sheng, Shi Meng-Meng, Yang Jing, Liu Yu-Tao, Mao Cheng-Yuan, Fan Yu, Hu Xin-Chao, Shi Chang-He, Xu Yu-Mi |
Analysis of DNM3 and VAMP4 as genetic modifiers of LRRK2 Parkinson's disease. Neurobiology of aging 2020 Jul . Brown Emmeline E, Blauwendraat Cornelis, Trinh Joanne, Rizig Mie, Nalls Mike A, Leveille Etienne, Ruskey Jennifer A, Jonvik Hallgeir, Tan Manuela M X, Bandres-Ciga Sara, Hassin-Baer Sharon, Brockmann Kathrin, Infante Jon, Tolosa Eduardo, Ezquerra Mario, Ben Romdhan Sawssan, Benmahdjoub Mustapha, Arezki Mohamed, Mhiri Chokri, Hardy John, Singleton Andrew B, Alcalay Roy N, Gasser Thomas, Grosset Donald G, Williams Nigel M, Pittman Alan, Gan-Or Ziv, Fernandez-Santiago Ruben, Brice Alexis, Lesage Suzanne, Farrer Matthew, Wood Nicholas, Morris Huw R, |
Role of LRRK2 variant p.Gly2019Ser in patients with Parkinsonism. The Indian journal of medical research 2020 Jun 151 (6): 592-597. Sadhukhan Dipanwita, Biswas Arindam, Bhaduri Arunima, Sarkar Neelanjana, Biswas Atanu, Das Shyamal K, Banerjee Tapas K, Ray Kunal, Ray Jhar |
TBX15 rs98422, DNM3 rs1011731, RAD51B rs8017304, and rs2588809 Gene Polymorphisms and Associations With Pituitary Adenoma. In vivo (Athens, Greece) 2021 2 35 (2): 815-826. Juknyt? Gabija, Laurinaityt? Inga, Vilkevi?i?t? Alvita, Gedvilait? Greta, Glebauskien? Brigita, Kriau?i?nien? Loresa, Liutkevi?ien? Ra |
Integrated multi-omic analysis of low-grade ovarian serous carcinoma collected from short and long-term survivors. Journal of translational medicine 2022 12 20 (1): 606. Wong Kwong-Kwok, Bateman Nicholas W, Ng Chun Wai, Tsang Yvonne T M, Sun Charlotte S, Celestino Joseph, Nguyen Tri V, Malpica Anais, Hillman R Tyler, Zhang Jianhua, Futreal P Andrew, Rojas Christine, Conrads Kelly A, Hood Brian L, Dalgard Clifton L, Wilkerson Matthew D, Phippen Neil T, Conrads Thomas P, Maxwell George L, Sood Anil K, Gershenson David |
Locus for severity implicates CNS resilience in progression of multiple sclerosis. Nature 2023 6 . , |
Decoding the genetic relationship between Alzheimer's disease and type 2 diabetes: potential risk variants and future direction for North Africa. Frontiers in aging neuroscience 2023 6 15 1114810. Wided Boukhalfa, Haifa Jmel, Nadia Kheriji, Ismail Gouiza, Hamza Dallali, Mariem Hechmi, Rym Ke |
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