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Results 1 to 25 of 164

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Variant Creutzfeldt-Jakob diseaseCROES, Esther A; VAN DUIJN, Cornelia M.European journal of epidemiology. 2003, Vol 18, Num 6, pp 473-477, issn 0393-2990, 5 p.Article

Prospects of genetic epidemiology in the 21st centuryDEKKER, Marieke C. J; VAN DUIJN, Cornelia M.European journal of epidemiology. 2003, Vol 18, Num 7, pp 607-616, issn 0393-2990, 10 p.Article

Opportunities for population-based studies of complex genetic disorders after the human genome projectVAESSEN, Norbert; VAN DUIJN, Cornelia M.Epidemiology (Cambridge, Mass.). 2001, Vol 12, Num 3, pp 360-364, issn 1044-3983Article

Is genetic screening for hemochromatosis worthwhile?NJAJOU, Omer T; ALIZADEH, Behrooz Z; VAN DUIJN, Cornelia M et al.European journal of epidemiology. 2004, Vol 19, Num 2, pp 101-108, issn 0393-2990, 8 p.Article

PredictABEL: an R package for the assessment of risk prediction modelsKUNDU, Suman; AULCHENKO, Yurii S; VAN DUIJN, Cornelia M et al.European journal of epidemiology. 2011, Vol 26, Num 4, pp 261-264, issn 0393-2990, 4 p.Article

Mutation analysis of candidate genes within the 2q33.3 linkage area for familial early-onset generalised osteoarthritisMIN, Josine L; MEULENBELT, Ingrid; KLOPPENBURG, Margreet et al.European journal of human genetics. 2007, Vol 15, Num 7, pp 791-799, issn 1018-4813, 9 p.Article

Infectious mononucleosis-linked HLA class I single nucleotide polymorphism is associated with multiple sclerosisJAFARI, Naghmeh; BROER, Linda; HOPPENBROUWERS, Ilse A et al.Multiple sclerosis. 2010, Vol 16, Num 11, pp 1303-1307, issn 1352-4585, 5 p.Article

An approach for cutting large and complex pedigrees for linkage analysisFAN LIU; KIRICHENKO, Anatoliy; AXENOVICH, Tatiana I et al.European journal of human genetics. 2008, Vol 16, Num 7, pp 854-860, issn 1018-4813, 7 p.Article

CYP2E1PstI/RsaI polymorphism and interaction with tobacco, alcohol and GSTs in gastric cancer susceptibility : a meta-analysis of the literatureBOCCIA, Stefania; DE LAURETIS, Angelo; GIANFAGNA, Francesco et al.Carcinogenesis (New York. Print). 2007, Vol 28, Num 1, pp 101-106, issn 0143-3334, 6 p.Article

Strengthening the reporting of Genetic RIsk Prediction Studies: the GRIPS StatementJANSSENS, A. Cecile J. W; IOANNIDIS, John P. A; VAN DUIJN, Cornelia M et al.Journal of clinical epidemiology. 2011, Vol 64, Num 8, pp 843-847, issn 0895-4356, 5 p.Article

The association between angiotensin-converting enzyme gene polymorphism and coronary calcification The Rotterdam Coronary Calcification StudyOEI, Hok-Hay S; SAYED-TABATABAEI, Fakhredin A; HOFMAN, Albert et al.Atherosclerosis. 2005, Vol 182, Num 1, pp 169-173, issn 0021-9150, 5 p.Article

The dopamine D4 receptor gene 48-base-pair-repeat polymorphism and mood disorders : A meta-analysisLOPEZ LEON, Sandra; CROES, Esther A; SAYED-TABATABAEI, Fakhredin A et al.Biological psychiatry (1969). 2005, Vol 57, Num 9, pp 999-1003, issn 0006-3223, 5 p.Article

Angiotensin-converting enzyme gene polymorphism and carotid artery wall thickness: A meta-analysisSAYED-TABATABAEI, Fakhredin A; HOUWING-DUISTERMAAT, Jeanine J; VAN DUIJN, Cornelia M et al.Stroke (1970). 2003, Vol 34, Num 7, pp 1634-1639, issn 0039-2499, 6 p.Article

CYP2D6 polymorphism in Parkinson's disease : The Rotterdam studySANJAY HARHANGI, B; OOSTRA, Ben A; HEUTINK, Peter et al.Movement disorders. 2001, Vol 16, Num 2, pp 290-293, issn 0885-3185Article

Strengthening the reporting of genetic risk prediction studies: the GRIPS statementJANSSENS, A. Cecile J. W; IOANNIDIS, John P. A; VAN DUIJN, Cornelia M et al.European journal of human genetics. 2011, Vol 19, Num 8, pp 833-836, issn 1018-4813, 4 p.Article

The GAB2 Gene and the Risk of Alzheimer's Disease: Replication and Meta-AnalysisARFAN IKRAM, M; FAN LIU; OOSTRA, Ben A et al.Biological psychiatry (1969). 2009, Vol 65, Num 11, pp 995-999, issn 0006-3223, 5 p.Article

Rapid variance components―based method for whole-genome association analysisSVISHCHEVA, Gulnara R; AXENOVICH, Tatiana I; BELONOGOVA, Nadezhda M et al.Nature genetics. 2012, Vol 44, Num 10, pp 1166-1170, issn 1061-4036, 5 p.Article

Strengthening the Reporting of Genetic Risk Prediction Studies: The GRIPS StatementJANSSENS, A. Cecile J. W; LOANNIDIS, John P. A; VAN DUIJN, Cornelia M et al.Annals of internal medicine. 2011, Vol 154, Num 6, pp 421-425, issn 0003-4819, 5 p.Article

Strengthening the reporting of genetic risk prediction studies: the GRIPS statementJANSSENS, A. Cecile J. W; IOANNIDIS, John P. A; VAN DUIJN, Cornelia M et al.BMJ (Overseas and retired doctors ed.). 2011, Vol 342, Num 7798, pp 640-643, issn 1759-2151, 4 p.Article

Strengthening the reporting of genetic risk prediction studies: the GRIPS statementJANSSENS, A. Cecile J. W; IOANNIDIS, John P. A; VAN DUIJN, Cornelia M et al.European journal of epidemiology. 2011, Vol 26, Num 4, pp 255-259, issn 0393-2990, 5 p.Article

A Critical Appraisal of the Scientific Basis of Commercial Genomic Profiles Used to Assess Health Risks and Personalize Health InterventionsCECILE, A; JANSSENS, J. W; GWINN, Marta et al.American journal of human genetics. 2008, Vol 82, Num 3, pp 593-599, issn 0002-9297, 7 p.Article

Strong linkage on 2q33.3 to familial early-onset generalized osteoarthritis and a consideration of two positional candidate genesMEULENBELT, Ingrid; MIN, Josine L; VAN DUIJN, Cornelia M et al.European journal of human genetics. 2006, Vol 14, Num 12, pp 1280-1287, issn 1018-4813, 8 p.Article

Apolipoprotein E ε4 allele is associated with left ventricular systolic dysfunctionBLEUMINK, Gysèle S; VAN DUIJN, Cornelia M; KINGMA, J. Herre et al.The American heart journal. 2004, Vol 147, Num 4, pp 685-689, issn 0002-8703, 5 p.Article

Neopterin and the risk of dementia in persons with Down syndromeCOPPUS, Antonia M. W; FEKKES, Durk; VERHOEVEN, Willem M. A et al.Neuroscience letters. 2009, Vol 458, Num 2, pp 60-64, issn 0304-3940, 5 p.Article

Renin-Angiotensin System Inhibitors, Angiotensin I-converting Enzyme Gene Insertion/Deletion Polymorphism, and Cancer : The Rotterdam StudyVAN DER KNAAP, Ronald; SIEMES, Claire; COEBERGH, Jan-Willem W et al.Cancer. 2008, Vol 112, Num 4, pp 748-757, issn 0008-543X, 10 p.Article

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