Literature DB >> 11061733

Single gene disorders or complex traits: lessons from the thalassaemias and other monogenic diseases.

D J Weatherall1.   

Abstract

Mesh:

Year:  2000        PMID: 11061733      PMCID: PMC1118897          DOI: 10.1136/bmj.321.7269.1117

Source DB:  PubMed          Journal:  BMJ        ISSN: 0959-8138


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  12 in total

Review 1.  Integrated regional genetic services: current and future provision.

Authors:  D Donnai; R Elles
Journal:  BMJ       Date:  2001-04-28

Review 2.  Genetics 101: detecting mutations in human genes.

Authors:  Alison Sinclair
Journal:  CMAJ       Date:  2002-08-06       Impact factor: 8.262

3.  Navigating the road to personalized medicine: can we believe?

Authors:  Gideon M Hirschfield; Christopher I Amos; Katherine A Siminovitch
Journal:  CMAJ       Date:  2010-04-06       Impact factor: 8.262

Review 4.  Anemia, ineffective erythropoiesis, and hepcidin: interacting factors in abnormal iron metabolism leading to iron overload in β-thalassemia.

Authors:  Sara Gardenghi; Robert W Grady; Stefano Rivella
Journal:  Hematol Oncol Clin North Am       Date:  2010-10-15       Impact factor: 3.722

Review 5.  Identifying genetic risk factors for serious adverse drug reactions: current progress and challenges.

Authors:  Russell A Wilke; Debbie W Lin; Dan M Roden; Paul B Watkins; David Flockhart; Issam Zineh; Kathleen M Giacomini; Ronald M Krauss
Journal:  Nat Rev Drug Discov       Date:  2007-11       Impact factor: 84.694

6.  Decreased differentiation of erythroid cells exacerbates ineffective erythropoiesis in beta-thalassemia.

Authors:  Ilaria V Libani; Ella C Guy; Luca Melchiori; Raffaella Schiro; Pedro Ramos; Laura Breda; Thomas Scholzen; Amy Chadburn; YiFang Liu; Margrit Kernbach; Bettina Baron-Lühr; Matteo Porotto; Maria de Sousa; Eliezer A Rachmilewitz; John D Hood; M Domenica Cappellini; Patricia J Giardina; Robert W Grady; Johannes Gerdes; Stefano Rivella
Journal:  Blood       Date:  2008-05-14       Impact factor: 22.113

7.  Genetic heterogeneity in autosomal recessive dyskeratosis congenita with one subtype due to mutations in the telomerase-associated protein NOP10.

Authors:  Amanda J Walne; Tom Vulliamy; Anna Marrone; Richard Beswick; Michael Kirwan; Yuka Masunari; Fat-Hia Al-Qurashi; Mahmoud Aljurf; Inderjeet Dokal
Journal:  Hum Mol Genet       Date:  2007-05-16       Impact factor: 6.150

8.  Saturation of the human phenome.

Authors:  Mark E Samuels
Journal:  Curr Genomics       Date:  2010-11       Impact factor: 2.236

Review 9.  Genetic epidemiology, hematological and clinical features of hemoglobinopathies in Iran.

Authors:  Zohreh Rahimi
Journal:  Biomed Res Int       Date:  2013-06-18       Impact factor: 3.411

Review 10.  New insights from monogenic diabetes for "common" type 2 diabetes.

Authors:  Divya Sri Priyanka Tallapragada; Seema Bhaskar; Giriraj R Chandak
Journal:  Front Genet       Date:  2015-08-07       Impact factor: 4.599

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