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Results 1 to 25 of 135

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Melanoma etiology: where are we?TUCKER, Margaret A; GOLDSTEIN, Alisa M.Oncogene (Basingstoke). 2003, Vol 22, Num 20, pp 3042-3052, issn 0950-9232, 11 p.Article

Linkage analysis of glomerular filtration rate in American Indians. CommentaryKIRYLUK, Krzysztof; MOTTL, Amy K; LEE, Elisa T et al.Kidney international. 2008, Vol 74, Num 9, issn 0085-2538, 1109-1112, 1185-1191 [11 p.]Article

Statistical genetics concepts and approaches in schizophrenia and related neuropsychiatric research : The use of endophenotypes to deconstruct and understand the genetic architecture, neurobiology, and guide future treatments of the group of schizophreniasSCHORK, Nicholas J; GREENWOOD, Tiffany A; BRAFF, David L et al.Schizophrenia bulletin. 2007, Vol 33, Num 1, pp 95-104, issn 0586-7614, 10 p.Article

From candidate gene to genome-wide association studies in cardiovascular diseaseGIANFAGNA, Francesco; CUGINO, Daniela; SANTIMONE, Iolanda et al.Thrombosis research. 2012, Vol 129, Num 3, pp 320-324, issn 0049-3848, 5 p.Conference Paper

Family, twin, and adoption studies of bipolar disorderSMOLLER, Jordan W; FINN, Christine T.American journal of medical genetics. 2003, Vol 123C, Num 1, pp 48-58, issn 0148-7299, 11 p.Article

Toward a Road Map for Global -Omics: A Primer on -Omic TechnologiesCOUGHLIN, Steven S.American journal of epidemiology. 2014, Vol 180, Num 12, pp 1188-1195, issn 0002-9262, 8 p.Article

Is obsessive―compulsive disorder an anxiety disorder, and what, if any, are spectrum conditions? A family study perspectiveBIENVENU, O. J; SAMUELS, J. F; FYER, A. J et al.Psychological medicine (Print). 2012, Vol 42, Num 1, pp 1-13, issn 0033-2917, 13 p.Article

A Phenotype for Genetic Studies of Successful Cognitive AgingSILVERMAN, Jeremy M; SCHNAIDER-BEERI, Michal; GROSSMAN, Hillel T et al.American journal of medical genetics. Part B, Neuropsychiatric genetics. 2008, Vol 147, Num 2, pp 167-173, issn 1552-4841, 7 p.Article

MORGAM (an international pooling of cardiovascular cohorts)EVANS, Alun; SALOMAA, Veikko; KUULASMAA, Kari et al.International journal of epidemiology. 2005, Vol 34, Num 1, pp 21-27, issn 0300-5771, 7 p.Article

Evidence for an association between the Leu162Val polymorphism of the PPARα gene and decreased fasting serum triglyceride levels in glucose tolerant subjectsNIELSEN, Eva-Maria D; HANSEN, Lars; ECHWALD, Søren M et al.Pharmacogenetics (London). 2003, Vol 13, Num 7, pp 417-423, issn 0960-314X, 7 p.Article

The FTO gene polymorphism is associated with end-stage renal disease: two large independent case―control studies in a general populationHUBACEK, Jaroslav A; VIKLICKY, Ondrej; BOBAK, Martin et al.Nephrology, dialysis, transplantation (Print). 2012, Vol 27, Num 3, pp 1030-1035, issn 0931-0509, 6 p.Article

Recent progress in the genetics of common obesity : ObesityLOOS, Ruth J. F.British journal of clinical pharmacology. 2009, Vol 68, Num 6, issn 0306-5251, 811-829, 966 [20 p.]Article

Genetic epidemiology, endophenotypes, and eating disorder classification. CommentariesBULIK, Cynthia M; HEBEBRAND, Johannes; KESKI-RAHKONEN, Anna et al.The International journal of eating disorders (Print). 2007, Vol 40, issn 0276-3478, S52-S60, S76-S78 [12 p.], SUPArticle

Unraveling a complex genetic disease : Age-related macular degenerationCHAMBERLAIN, Matt; BAIRD, Paul; DIRANI, Mohamed et al.Survey of ophthalmology. 2006, Vol 51, Num 6, pp 576-586, issn 0039-6257, 11 p.Article

Familial aggregation of endometriosis in a large pedigree of rhesus macaquesZONDERVAN, Krina T; WEEKS, Daniel E; COLMAN, Ricki et al.Human reproduction (Oxford. Print). 2004, Vol 19, Num 2, pp 448-455, issn 0268-1161, 8 p.Article

A Major Gene Effect Controls Resistance to CariesWERNECK, R. I; LAZARO, F. P; COBAT, A et al.Journal of dental research. 2011, Vol 90, Num 6, pp 735-739, issn 0022-0345, 5 p.Article

Finding genes underlying human diseaseSTEIN, C. M; ELSTON, R. C.Clinical genetics. 2009, Vol 75, Num 2, pp 101-106, issn 0009-9163, 6 p.Article

Molecular genetic studies of schizophreniaRILEY, Brien; KENDLER, Kenneth S.European journal of human genetics. 2006, Vol 14, Num 6, pp 669-680, issn 1018-4813, 12 p.Article

Mapping genes of complex psychiatric diseases in daghestan genetic isolatesBULAYEVA, Kazima B; LEAL, Suzanne M; PAVLOVA, Tatiana A et al.American journal of medical genetics. 2005, Vol 132B, Num 1, pp 76-84, issn 0148-7299, 9 p.Article

An integrated approach to the meta-analysis of genetic association studies using Mendelian randomizationMINELLI, Cosetta; THOMPSON, John R; TOBIN, Martin D et al.American journal of epidemiology. 2004, Vol 160, Num 5, pp 445-452, issn 0002-9262, 8 p.Article

Confounding, ascertainment bias, and the blind quest for a genetic 'fountain of youth'TERWILLIGER, Joseph D; WEISS, Kenneth M.Annals of medicine (Helsinki). 2003, Vol 35, Num 7, pp 532-544, issn 0785-3890, 13 p.Article

Quantitative genetic analysis of blood pressure reactivity to orthostatic tilt using principal components analysisCHOH, A. C; CZERWINSKI, S. A; LEE, M et al.Journal of human hypertension. 2006, Vol 20, Num 4, pp 281-289, issn 0950-9240, 9 p.Article

Population frequency of HLA haplotypes contributes to the prevalence difference of multiple sclerosis in IrelandMCGUIGAN, Christopher; DUNNE, Ciaran; CROWLEY, John et al.Journal of neurology. 2005, Vol 252, Num 10, pp 1245-1248, issn 0340-5354, 4 p.Article

Studies of relationships between the GLUT10 Ala206Thr polymorphism and impaired insulin secretionROSE, C. S; ANDERSEN, G; HAMID, Y. H et al.Diabetic medicine. 2005, Vol 22, Num 7, pp 946-949, issn 0742-3071, 4 p.Article

Predicting Stroke Through Genetic Risk Functions The CHARGE Risk Score ProjectIBRAHIM-VERBAAS, Carla A; FORNAGE, Myriam; KATHIRESAN, Sekar et al.Stroke (1970). 2014, Vol 45, Num 2, pp 403-412, issn 0039-2499, 10 p.Article

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