Human Genome Epidemiology Literature Finder
Records 1 - 19 (of 19 Records) |
Query Trace: Death and LDLR[original query] |
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Maternal apo E genotype is a modifier of the Smith-Lemli-Opitz syndrome. Journal of medical genetics 2004 Aug 41 (8): 577-84. Witsch-Baumgartner M, Gruber M, Kraft H G, Rossi M, Clayton P, Giros M, Haas D, Kelley R I, Krajewska-Walasek M, Utermann |
Familial hypercholesterolemia and coronary heart disease: a HuGE association review. American journal of epidemiology 2004 Sep 160 (5): 421-9. Austin Melissa A, Hutter Carolyn M, Zimmern Ron L, Humphries Steve |
Low density lipoprotein--receptor (LDL-R) gene mutations among Filipinos with familial hypercholesterolemia. Journal of atherosclerosis and thrombosis 2005 12 (5): 276-83. Punzalan Felix Eduardo R, Sy Rody G, Santos Ronald S, Cutiongco Eva Maria, Gosiengfiao Silver, Fadriguilan Erdie, George Peter, Laurie Andr |
Diagnosis of families with familial hypercholesterolaemia and/or Apo B-100 defect by means of DNA analysis of LDL-receptor gene mutations. Journal of inherited metabolic disease 2007 Apr 30 (2): 239-47. Widhalm K, Dirisamer A, Lindemayr A, Kostner |
Sudden cardiac death in young adults: environmental risk factors and genetic aspects of premature atherosclerosis. Journal of forensic sciences 2012 May 57 (3): 658-62. Larsen Maiken K, Nissen Peter H, Kristensen Ingrid B, Jensen Henrik K, Banner Jyt |
Prevalence and clinical correlates of familial hypercholesterolemia founder mutations in the general population. Atherosclerosis 2015 Jan 238 (1): 64-9. Lahtinen Annukka M, Havulinna Aki S, Jula Antti, Salomaa Veikko, Kontula Kim |
Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction. Nature 2015 Feb 518 (7537): 102-6. Do Ron, Stitziel Nathan O, Won Hong-Hee, Jørgensen Anders Berg, Duga Stefano, Angelica Merlini Pier, Kiezun Adam, Farrall Martin, Goel Anuj, Zuk Or, Guella Illaria, Asselta Rosanna, Lange Leslie A, Peloso Gina M, Auer Paul L, , Girelli Domenico, Martinelli Nicola, Farlow Deborah N, DePristo Mark A, Roberts Robert, Stewart Alexander F R, Saleheen Danish, Danesh John, Epstein Stephen E, Sivapalaratnam Suthesh, Hovingh G Kees, Kastelein John J, Samani Nilesh J, Schunkert Heribert, Erdmann Jeanette, Shah Svati H, Kraus William E, Davies Robert, Nikpay Majid, Johansen Christopher T, Wang Jian, Hegele Robert A, Hechter Eliana, Marz Winfried, Kleber Marcus E, Huang Jie, Johnson Andrew D, Li Mingyao, Burke Greg L, Gross Myron, Liu Yongmei, Assimes Themistocles L, Heiss Gerardo, Lange Ethan M, Folsom Aaron R, Taylor Herman A, Olivieri Oliviero, Hamsten Anders, Clarke Robert, Reilly Dermot F, Yin Wu, Rivas Manuel A, Donnelly Peter, Rossouw Jacques E, Psaty Bruce M, Herrington David M, Wilson James G, Rich Stephen S, Bamshad Michael J, Tracy Russell P, Cupples L Adrienne, Rader Daniel J, Reilly Muredach P, Spertus John A, Cresci Sharon, Hartiala Jaana, Tang W H Wilson, Hazen Stanley L, Allayee Hooman, Reiner Alex P, Carlson Christopher S, Kooperberg Charles, Jackson Rebecca D, Boerwinkle Eric, Lander Eric S, Schwartz Stephen M, Siscovick David S, McPherson Ruth, Tybjaerg-Hansen Anne, Abecasis Goncalo R, Watkins Hugh, Nickerson Deborah A, Ardissino Diego, Sunyaev Shamil R, O'Donnell Christopher J, Altshuler David, Gabriel Stacey, Kathiresan Sek |
Screening for genetic mutations in LDLR gene with familial hypercholesterolemia patients in the Saudi population. Acta biochimica Polonica 2015 62 (3): 559-62. Alharbi Khalid Khalaf, Kashour Tarek S, Al-Hussaini Wejdan, Nbaheen May Salem, Hasanato Rana M W, Mohamed Sarar, Tamimi Waleed, Khan Imran A |
Two-dye based arrayed primer extension for simultaneous multigene detection in lipid metabolism. Clinica chimica acta; international journal of clinical chemistry 2015 Mar 442 36-43. Jeenduang Nutjaree, Porntadavity Sureerut, von Nickisch-Rosenegk Markus, Bier Frank F, Promptmas Chamr |
Phenotype diversity among patients with homozygous familial hypercholesterolemia: A cohort study. Atherosclerosis 2016 Mar . Raal Frederick J, Sjouke Barbara, Hovingh G Kees, Isaac Barton |
Mutations causative of familial hypercholesterolaemia: screening of 98 098 individuals from the Copenhagen General Population Study estimated a prevalence of 1 in 217. European heart journal 2016 Feb . Benn Marianne, Watts Gerald F, Tybjærg-Hansen Anne, Nordestgaard Børge |
Molecular genetics of familial hypercholesterolemia in Israel-revisited. Atherosclerosis 2016 Dec 257 55-63. Durst Ronen, Ibe Uche Ken, Shpitzen Shoshi, Schurr Daniel, Eliav Osnat, Futema Marta, Whittall Ros, Szalat Auryan, Meiner Vardiella, Knobler Hilla, Gavish Dov, Henkin Yaakov, Ellis Avishay, Rubinstein Ardon, Harats Dror, Bitzur Rafael, Hershkovitz Bruno, Humphries Steve E, Leitersdorf Er |
LDLR Gene Polymorphisms (rs5925 and rs1529729) Are Associated with Susceptibility to Coronary Artery Disease in a South Indian Population. Medical sciences (Basel, Switzerland) 2019 Jul 7 (7): . K Jha Chandan, Mir Rashid, Elfaki Imadeldin, Banu Shaheena, Chahal S M |
A cross-national investigation of cardiovascular survival in homozygous familial hypercholesterolemia: The Sino-Roman Study. Journal of clinical lipidology 2019 7 13 (4): 608-617. Stefanutti Claudia, Pang Jing, Di Giacomo Serafina, Wu Xue, Wang Xumin, Morozzi Claudia, Watts Gerald F, Lin J |
Heterozygosity in LDLR rs2228671 and rs72658855 Gene is Associated with Increased Risk of Developing Coronary Artery Disease in India -A Case-Control Study. Endocrine, metabolic & immune disorders drug targets 2019 Oct . Jha Chandan K, Mir Rashid, Banu Shaheena, Elfaki Imadeldin, Chahal Sukh M |
Association of Triglyceride-Lowering LPL Variants and LDL-C-Lowering LDLR Variants With Risk of Coronary Heart Disease. JAMA 2019 Jan 321 (4): 364-373. Ference Brian A, Kastelein John J P, Ray Kausik K, Ginsberg Henry N, Chapman M John, Packard Chris J, Laufs Ulrich, Oliver-Williams Clare, Wood Angela M, Butterworth Adam S, Di Angelantonio Emanuele, Danesh John, Nicholls Stephen J, Bhatt Deepak L, Sabatine Marc S, Catapano Alberico |
Cholesterol-related gene variants are associated with diabetes in coronary artery disease patients. Molecular biology reports 2021 May . Ozuynuk Aybike Sena, Erkan Aycan Fahri, Ekici Berkay, Erginel-Unaltuna Nihan, Coban Neslih |
Long-term cancer risk in heterozygous familial hypercholesterolemia relatives: a 25-year cohort study. Lipids in health and disease 2022 7 21 (1): 56. Kjærgaard Kasper Aalbæk, Harborg Sixten, Jensen Henrik Kjærulf, Borgquist Sig |
Analysis of rare genetic variation underlying cardiometabolic diseases and traits among 200,000 individuals in the UK Biobank. Nature genetics 2022 Feb . Jurgens Sean J, Choi Seung Hoan, Morrill Valerie N, Chaffin Mark, Pirruccello James P, Halford Jennifer L, Weng Lu-Chen, Nauffal Victor, Roselli Carolina, Hall Amelia W, Oetjens Matthew T, Lagerman Braxton, vanMaanen David P, , Aragam Krishna G, Lunetta Kathryn L, Haggerty Christopher M, Lubitz Steven A, Ellinor Patrick |
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