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References (6)

Title : A COLQ Missense Mutation in Sphynx and Devon Rex Cats with Congenital Myasthenic Syndrome - Abitbol_2015_PLoS.One_10_e0137019
Author(s) : Abitbol M , Hitte C , Bosse P , Blanchard-Gutton N , Thomas A , Martignat L , Blot S , Tiret L
Ref : PLoS ONE , 10 :e0137019 , 2015
Abstract : Abitbol_2015_PLoS.One_10_e0137019
ESTHER : Abitbol_2015_PLoS.One_10_e0137019
PubMedSearch : Abitbol_2015_PLoS.One_10_e0137019
PubMedID: 26327126

Title : A genome-wide association study identifies LIPA as a susceptibility gene for coronary artery disease - Wild_2011_Circ.Cardiovasc.Genet_4_403
Author(s) : Wild PS , Zeller T , Schillert A , Szymczak S , Sinning CR , Deiseroth A , Schnabel RB , Lubos E , Keller T , Eleftheriadis MS , Bickel C , Rupprecht HJ , Wilde S , Rossmann H , Diemert P , Cupples LA , Perret C , Erdmann J , Stark K , Kleber ME , Epstein SE , Voight BF , Kuulasmaa K , Li M , Schafer AS , Klopp N , Braund PS , Sager HB , Demissie S , Proust C , Konig IR , Wichmann HE , Reinhard W , Hoffmann MM , Virtamo J , Burnett MS , Siscovick D , Wiklund PG , Qu L , El Mokthari NE , Thompson JR , Peters A , Smith AV , Yon E , Baumert J , Hengstenberg C , Marz W , Amouyel P , Devaney J , Schwartz SM , Saarela O , Mehta NN , Rubin D , Silander K , Hall AS , Ferrieres J , Harris TB , Melander O , Kee F , Hakonarson H , Schrezenmeir J , Gudnason V , Elosua R , Arveiler D , Evans A , Rader DJ , Illig T , Schreiber S , Bis JC , Altshuler D , Kavousi M , Witteman JC , Uitterlinden AG , Hofman A , Folsom AR , Barbalic M , Boerwinkle E , Kathiresan S , Reilly MP , O'Donnell CJ , Samani NJ , Schunkert H , Cambien F , Lackner KJ , Tiret L , Salomaa V , Munzel T , Ziegler A , Blankenberg S
Ref : Circ Cardiovasc Genet , 4 :403 , 2011
Abstract : Wild_2011_Circ.Cardiovasc.Genet_4_403
ESTHER : Wild_2011_Circ.Cardiovasc.Genet_4_403
PubMedSearch : Wild_2011_Circ.Cardiovasc.Genet_4_403
PubMedID: 21606135
Gene_locus related to this paper: human-LIPA

Title : Platelet-activating factor-acetylhydrolase and PAF-receptor gene haplotypes in relation to future cardiovascular event in patients with coronary artery disease - Ninio_2004_Hum.Mol.Genet_13_1341
Author(s) : Ninio E , Tregouet D , Carrier JL , Stengel D , Bickel C , Perret C , Rupprecht HJ , Cambien F , Blankenberg S , Tiret L
Ref : Hum Mol Genet , 13 :1341 , 2004
Abstract : Ninio_2004_Hum.Mol.Genet_13_1341
ESTHER : Ninio_2004_Hum.Mol.Genet_13_1341
PubMedSearch : Ninio_2004_Hum.Mol.Genet_13_1341
PubMedID: 15115767
Gene_locus related to this paper: human-PLA2G7

Title : Paraoxonase-1 L55M polymorphism is associated with an abnormal oral glucose tolerance test and differentiates high risk coronary disease families - Deakin_2002_J.Clin.Endocrinol.Metab_87_1268
Author(s) : Deakin S , Leviev I , Nicaud V , Brulhart Meynet MC , Tiret L , James RW
Ref : J Clinical Endocrinology Metab , 87 :1268 , 2002
Abstract : Deakin_2002_J.Clin.Endocrinol.Metab_87_1268
ESTHER : Deakin_2002_J.Clin.Endocrinol.Metab_87_1268
PubMedSearch : Deakin_2002_J.Clin.Endocrinol.Metab_87_1268
PubMedID: 11889198

Title : Lipoprotein lipase gene variation is associated with a paternal history of premature coronary artery disease and fasting and postprandial plasma triglycerides: the European Atherosclerosis Research Study (EARS) - Humphries_1998_Arterioscler.Thromb.Vasc.Biol_18_526
Author(s) : Humphries SE , Nicaud V , Margalef J , Tiret L , Talmud PJ
Ref : Arterioscler Thromb Vasc Biol , 18 :526 , 1998
Abstract : Humphries_1998_Arterioscler.Thromb.Vasc.Biol_18_526
ESTHER : Humphries_1998_Arterioscler.Thromb.Vasc.Biol_18_526
PubMedSearch : Humphries_1998_Arterioscler.Thromb.Vasc.Biol_18_526
PubMedID: 9555857

Title : Family study of lipoprotein lipase gene polymorphisms and plasma triglyceride levels - Georges_1996_Genet.Epidemiol_13_179
Author(s) : Georges JL , Regis-Bailly A , Salah D , Rakotovao R , Siest G , Visvikis S , Tiret L
Ref : Genet Epidemiol , 13 :179 , 1996
Abstract : Georges_1996_Genet.Epidemiol_13_179
ESTHER : Georges_1996_Genet.Epidemiol_13_179
PubMedSearch : Georges_1996_Genet.Epidemiol_13_179
PubMedID: 8722745