Human Genome Epidemiology Literature Finder
Records 1 - 22 (of 22 Records) |
Query Trace: Syndrome and LMNA[original query] |
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Subcutaneous abdominal adipocyte size, a predictor of type 2 diabetes, is linked to chromosome 1q21--q23 and is associated with a common polymorphism in LMNA in Pima Indians. Molecular genetics and metabolism 2001 Mar 72 (3): 231-8. Weyer C, Wolford J K, Hanson R L, Foley J E, Tataranni P A, Bogardus C, Pratley R |
An LMNA variant is associated with dyslipidemia and insulin resistance in the Japanese. Metabolism: clinical and experimental 2002 Aug 51 (8): 1017-21. Murase Yuko, Yagi Kunimasa, Katsuda Yuko, Asano Akimichi, Koizumi Junji, Mabuchi Hiros |
Variation in the lamin A/C gene: associations with metabolic syndrome. Arteriosclerosis, thrombosis, and vascular biology 2004 Sep 24 (9): 1708-13. Steinle Nanette I, Kazlauskaite Rasa, Imumorin Ikhide G, Hsueh Wen-Chi, Pollin Toni I, O'Connell Jeffrey R, Mitchell Braxton D, Shuldiner Alan |
Association of LMNA 1908C/T polymorphism with cerebral vascular disease and diabetic nephropathy in Japanese men with type 2 diabetes. Clinical endocrinology 2005 Sep 63 (3): 317-22. Liang H, Murase Y, Katuta Y, Asano A, Kobayashi J, Mabuchi H |
Aging syndrome genes and premature coronary artery disease. BMC medical genetics 2005 Oct 6 (): 38. Low Adrian F, O'Donnell Christopher J, Kathiresan Sekar, Everett Brendan, Chae Claudia U, Shaw Stanley Y, Ellinor Patrick T, MacRae Calum |
Common variation in the LMNA gene (encoding lamin A/C) and type 2 diabetes: association analyses in 9,518 subjects. Diabetes 2007 Mar 56 (3): 879-83. Owen Katharine R, Groves Christopher J, Hanson Robert L, Knowler William C, Shuldiner Alan R, Elbein Steven C, Mitchell Braxton D, Froguel Philippe, Ng Maggie C Y, Chan Juliana C, Jia Weiping, Deloukas Panos, Hitman Graham A, Walker Mark, Frayling Timothy M, Hattersley Andrew T, Zeggini Eleftheria, McCarthy Mark |
Lamin A/C polymorphisms, type 2 diabetes, and the metabolic syndrome: case-control and quantitative trait studies. Diabetes 2007 Mar 56 (3): 884-9. Mesa José L, Loos Ruth J F, Franks Paul W, Ong Ken K, Luan Jian'an, O'Rahilly Stephen, Wareham Nicholas J, Barroso In |
Comprehensive mutation scanning of LMNA in 268 patients with lone atrial fibrillation. The American journal of cardiology 2009 May 103 (10): 1426-8. Brauch Katharine M, Chen Lin Y, Olson Timothy |
The role of genetic variation in the lamin a/c gene in the etiology of polycystic ovary syndrome. The Journal of clinical endocrinology and metabolism 2009 Jul 94 (7): 2665-9. Urbanek Margrit, Nampiaparampil Geetha, D'Souza Janine, Sefton Elizabeth, Ackerman Christine, Legro Richard S, Dunaif Andr |
Polymorphisms of the lamina maturation pathway and their association with the metabolic syndrome: the DESIR prospective study. Journal of molecular medicine (Berlin, Germany) 2010 Feb 88 (2): 193-201. Fontaine-Bisson Benedicte, Alessi Marie-Christine, Saut Noemie, Fumeron Frederic, Marre Michel, Dutour Anne, Badens Catherine, Levy Nicolas, Tichet Jean, Juhan-Vague Irene, Trégouët David-Alexandre, Balkau Beverly, Morange Pierre-Emmanu |
C1824T mutation in the LMNA gene has no association with senile cataract. Neurobiology of aging 2012 Jul 33 (7): 1487.e15-9. Sadikov Tamilla, Simon Amos J, Avraham-Lubin Bat-Chen R, Dratviman-Storobinsky Olga, Cohen Yoram, Goldenberg-Cohen Nit |
Human longevity and common variations in the LMNA gene: a meta-analysis. Aging cell 2012 Jun 11 (3): 475-81. Conneely Karen N, Capell Brian C, Erdos Michael R, Sebastiani Paola, Solovieff Nadia, Swift Amy J, Baldwin Clinton T, Budagov Temuri, Barzilai Nir, Atzmon Gil, Puca Annibale A, Perls Thomas T, Geesaman Bard J, Boehnke Michael, Collins Francis |
A Novel Generalized Lipodystrophy-Associated Progeroid Syndrome Due to Recurrent Heterozygous LMNA p.T10I Mutation. The Journal of clinical endocrinology and metabolism 2017 12 103 (3): 1005-1014. Hussain Iram, Patni Nivedita, Ueda Masako, Sorkina Ekaterina, Valerio Cynthia M, Cochran Elaine, Brown Rebecca J, Peeden Joseph, Tikhonovich Yulia, Tiulpakov Anatoly, Stender Sarah R S, Klouda Elisabeth, Tayeh Marwan K, Innis Jeffrey W, Meyer Anders, Lal Priti, Godoy-Matos Amelio F, Teles Milena G, Adams-Huet Beverley, Rader Daniel J, Hegele Robert A, Oral Elif A, Garg Abhiman |
Genetic mutation of familial dilated cardiomyopathy based on next?generation semiconductor sequencing. Molecular medicine reports 2018 9 18 (5): 4271-4280. Lin Xin-Fu, Luo Jie-Wei, Liu Gui, Zhu Yao-Bin, Jin Zhao, Lin Xi |
Association of Lonafarnib Treatment vs No Treatment With Mortality Rate in Patients With Hutchinson-Gilford Progeria Syndrome. JAMA 2018 5 319 (16): 1687-1695. Gordon Leslie B, Shappell Heather, Massaro Joe, D'Agostino Ralph B, Brazier Joan, Campbell Susan E, Kleinman Monica E, Kieran Mark |
Genetic basis of channelopathies and cardiomyopathies in Hong Kong Chinese patients: a 10-year regional laboratory experience. Hong Kong medical journal = Xianggang yi xue za zhi 2018 3 24 (4): 340-349. Mak C M, Chen S Pl, Mok N S, Siu W K, Lee H Hc, Ching C K, Tsui P T, Fong N C, Yuen Y P, Poon W T, Law C Y, Chong Y K, Chan Y W, Yung T C, Fan K Yy, Lam C |
Pathogenic Variants Associated With Dilated Cardiomyopathy Predict Outcome in Pediatric Myocarditis. Circulation. Genomic and precision medicine 2021 7 14 (4): e003250. Seidel Franziska, Holtgrewe Manuel, Al-Wakeel-Marquard Nadya, Opgen-Rhein Bernd, Dartsch Josephine, Herbst Christopher, Beule Dieter, Pickardt Thomas, Klingel Karin, Messroghli Daniel, Berger Felix, Schubert Stephan, Kühnisch Jirko, Klaassen Sabi |
Genetic Evaluation of A Nation-Wide Dutch Pediatric DCM Cohort: The Use of Genetic Testing in Risk Stratification. Circulation. Genomic and precision medicine 2022 Sep 101161CIRCGEN120002981. van der Meulen Marijke H, Herkert Johanna C, den Boer Susanna L, du Marchie Sarvaas Gideon J, Blom Nico A, Ten Harkel Arend D J, Breur Hans M P J, Rammeloo Lukas A J, Tanke Ronald B, Marcelis Carlo, van de Laar Ingrid M B H, Verhagen Judith M A, Lekanne Dit Deprez Ronald H, Barge-Schaapveld Daniela Q C M, Baas Annette F, Sammani Arjan, Christiaans Imke, van Tintelen J Peter, Dalinghaus Michi |
Prevalence and Phenotypic Burden of Monogenic Arrhythmias Using Integration of Electronic Health Records With Genetics. Circulation. Genomic and precision medicine 2022 9 15 (5): e003675. Nafissi Navid A, Abdulrahim Jawan W, Kwee Lydia Coulter, Coniglio Amanda C, Kraus William E, Piccini Jonathan P, Daubert James P, Sun Albert Y, Shah Svati |
Role of genetic testing in young patients with idiopathic atrioventricular conduction disease. Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology 2022 11 25 (2): 643-650. Auricchio Angelo, Demarchi Andrea, Özkartal Tardu, Campanale Daniela, Caputo Maria Luce, di Valentino Marcello, Menafoglio Andrea, Regoli Francois, Facchini Marco, Del Bufalo Alessandro, Foglia Pietro, Ferrari Nicola, Bomio Fulvio, Medeiros-Domingo Argelia, Moccetti Tiziano, Pedrazzini Giovanni B, Klersy Catherine, Conte Giul |
Familial Partial Lipodystrophy: Clinical Features, Genetics and Treatment in a Greek Referral Center. International journal of molecular sciences 2023 8 24 (15): . Aikaterini Kountouri, Emmanouil Korakas, Eirini Maratou, Ignatios Ikonomidis, Konstantinos Balampanis, Stavros Liatis, Nikolaos Tentolouris, Panagiotis Toulas, Foteini Kousathana, Christophoros Giatzakis, George D Dimitriadis, Vaia Lambadia |
Epidemiological characteristics of patients with Hutchinson-Gilford progeria syndrome and progeroid laminopathies in China. Pediatric research 2024 1 . Jingjing Wang, Qinmei Yu, Xiaoxiao Tang, Leslie B Gordon, Junyi Chen, Buchun Jiang, Guoping Huang, Haidong Fu, Jianqin Qian, Zhihong Liu, Jianhua M |
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