Literature DB >> 16154023

Key concepts in genetic epidemiology.

Paul R Burton1, Martin D Tobin, John L Hopper.   

Abstract

This article is the first in a series of seven that will provide an overview of central concepts and topical issues in modern genetic epidemiology. In this article, we provide an overall framework for investigating the role of familial factors, especially genetic determinants, in the causation of complex diseases such as diabetes. The discrete steps of the framework to be outlined integrate the biological science underlying modern genetics and the population science underpinning mainstream epidemiology. In keeping with the broad readership of The Lancet and the diverse background of today's genetic epidemiologists, we provide introductory sections to equip readers with basic concepts and vocabulary. We anticipate that, depending on their professional background and specialist knowledge, some readers will wish to skip some of this article.

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Year:  2005        PMID: 16154023     DOI: 10.1016/S0140-6736(05)67322-9

Source DB:  PubMed          Journal:  Lancet        ISSN: 0140-6736            Impact factor:   79.321


  51 in total

1.  [Genetics of common chronic inflammatory skin diseases : An update on atopic dermatitis and psoriasis].

Authors:  E Rodríguez; K Eyerich; S Weidinger
Journal:  Hautarzt       Date:  2011-02       Impact factor: 0.751

2.  Familial aggregation of irritable bowel syndrome: a family case-control study.

Authors:  Yuri A Saito; Gloria M Petersen; Joseph J Larson; Elizabeth J Atkinson; Brooke L Fridley; Mariza de Andrade; G Richard Locke; Janice M Zimmerman; Ann E Almazar-Elder; Nicholas J Talley
Journal:  Am J Gastroenterol       Date:  2010-03-16       Impact factor: 10.864

Review 3.  Infantile hypertrophic pyloric stenosis--genetics and syndromes.

Authors:  Babette Peeters; Marc A Benninga; Raoul C M Hennekam
Journal:  Nat Rev Gastroenterol Hepatol       Date:  2012-07-10       Impact factor: 46.802

Review 4.  Genetics in child and adolescent psychiatry: methodological advances and conceptual issues.

Authors:  Sarah Hohmann; Nicoletta Adamo; Benjamin B Lahey; Stephen V Faraone; Tobias Banaschewski
Journal:  Eur Child Adolesc Psychiatry       Date:  2015-04-08       Impact factor: 4.785

5.  Familial risks for nerve, nerve root and plexus disorders in siblings based on hospitalisations in Sweden.

Authors:  Kari Hemminki; Xinjun Li; Kristina Sundquist
Journal:  J Epidemiol Community Health       Date:  2007-01       Impact factor: 3.710

6.  Family history of hematopoietic malignancies and risk of non-Hodgkin lymphoma (NHL): a pooled analysis of 10 211 cases and 11 905 controls from the International Lymphoma Epidemiology Consortium (InterLymph).

Authors:  Sophia S Wang; Susan L Slager; Paul Brennan; Elizabeth A Holly; Silvia De Sanjose; Leslie Bernstein; Paolo Boffetta; James R Cerhan; Marc Maynadie; John J Spinelli; Brian C H Chiu; Pier Luigi Cocco; Fiona Mensah; Yawei Zhang; Alexandra Nieters; Luigino Dal Maso; Paige M Bracci; Adele Seniori Costantini; Paolo Vineis; Richard K Severson; Eve Roman; Wendy Cozen; Dennis Weisenburger; Scott Davis; Silvia Franceschi; Carlo La Vecchia; Lenka Foretova; Nikolaus Becker; Anthony Staines; Martine Vornanen; Tongzhang Zheng; Patricia Hartge
Journal:  Blood       Date:  2006-12-21       Impact factor: 22.113

7.  A direct assessment of genetic contribution to the incidence of coronary infarct in the general population Greek EPIC cohort.

Authors:  Nikos Yiannakouris; Antonia Trichopoulou; Vassiliki Benetou; Theodora Psaltopoulou; Jose M Ordovas; Dimitrios Trichopoulos
Journal:  Eur J Epidemiol       Date:  2006-11-22       Impact factor: 8.082

8.  Optimal screening for promising genes in 2-stage designs.

Authors:  B Moerkerke; E Goetghebeur
Journal:  Biostatistics       Date:  2008-03-18       Impact factor: 5.899

Review 9.  Impact of common genetic variation on neonatal disease and outcome.

Authors:  David Harding
Journal:  Arch Dis Child Fetal Neonatal Ed       Date:  2007-09       Impact factor: 5.747

10.  The novel genetic variant predisposing to coronary artery disease in the region of the PSRC1 and CELSR2 genes on chromosome 1 associates with serum cholesterol.

Authors:  Nilesh J Samani; Peter S Braund; Jeanette Erdmann; Anika Götz; Maciej Tomaszewski; Patrick Linsel-Nitschke; Cother Hajat; Massimo Mangino; Christian Hengstenberg; Klaus Stark; Andreas Ziegler; Mark Caulfield; Paul R Burton; Heribert Schunkert; Martin D Tobin
Journal:  J Mol Med (Berl)       Date:  2008-07-23       Impact factor: 4.599

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