Most viewed
Editor-in-Chief Melissa Norton, MD
Medical Editor Jigisha Patel, MRCP PhD
In-house Editor Scott Edmunds
BMC Medical Genetics: Most viewed articles in past 30 days [more info ]
Figures given indicate the abstract, full text and PDF accesses on BioMed Central for each article, over the last 30 days. All research articles are also available via the PubMed Central archive, so the total number of accesses to each article is significantly higher. Lists of
most-viewed articles in the past year and
all time most-viewed articles are also available
most viewed articles over the last 30 days from all BioMed Central Journals
1. Accesses 756
Research article
Gene polymorphisms of superoxide dismutases and catalase in diabetes mellitus Milan Flekac, Jan Skrha, Jirina Hilgertova, Zdena Lacinova, Marcela Jarolimkova BMC Medical Genetics 2008, 9 :30 (21 April 2008) [Abstract ] [Full text ] [PDF ] [PubMed ] [Related articles ]
2. Accesses 699
Research article
Cathepsin D SNP associated with increased risk of variant Creutzfeldt-Jakob disease Matthew T Bishop, Gabor G Kovacs, Pascual Sanchez-Juan, Richard SG Knight BMC Medical Genetics 2008, 9 :31 (21 April 2008) [Abstract ] [Full text ] [PDF ] [PubMed ] [Related articles ]
3. Accesses 466
Research article
A luteinizing hormone receptor intronic variant is significantly associated with decreased risk of Alzheimer's disease in males carrying an apolipoprotein E epsilon4 allele Ryan J Haasl, M. Reza Ahmadi, Sivan Vadakkadath Meethal, Carey E Gleason, Sterling C Johnson, Richard L Bowen, Sanjay Asthana, Craig S Atwood BMC Medical Genetics 2008, 9 :37 (25 April 2008) [Abstract ] [Provisional PDF ] [PubMed ] [Related articles ]
4. Accesses 461
Research article
Subtelomeric study of 132 patients with mental retardation reveals 9 chromosomal anomalies and contributes to the delineation of submicroscopic deletions of 1pter, 2qter, 4pter, 5qter and 9qter Marie Sogaard, Zeynep T mer, Helle Hjalgrim, Johanne Hahnemann, Birgitte Friis, Paal Ledaal, Vibeke Faurholt Pedersen, Peter Baekgaard, Niels Tommerup, Sultan Cing z, Morten Duno, Karen Brondum-Nielsen BMC Medical Genetics 2005, 6 :21 (17 May 2005) [Abstract ] [Full text ] [PDF ] [PubMed ] [Related articles ]
5. Accesses 452
Research article
Genetic and functional association of FAM5C with myocardial infarction Jessica J Connelly, Svati H Shah, Jennifer F Doss, Shera Gadson, Sarah Nelson, David R Crosslin, A Brent Hale, Xuemei Lou, Ty Wang, Carol Haynes, David Seo, David C Crossman, Vincent Mooser, Christopher B Granger, Christopher JH Jones, William E Kraus, Elizabeth R Hauser, Simon G Gregory BMC Medical Genetics 2008, 9 :33 (22 April 2008) [Abstract ] [Full text ] [PDF ] [PubMed ] [Related articles ]
6. Accesses 399
Research article
Array-CGH in patients with Kabuki-like phenotype: Identification of two patients with complex rearrangements including 2q37 deletions and no other recurrent aberration Ivon Cusc , Miguel del Campo, Mireia Vilardell, Eva Gonz lez, Blanca Gener, Enrique Gal n, Laura Toledo, Luis A P rez-Jurado BMC Medical Genetics 2008, 9 :27 (11 April 2008) [Abstract ] [Full text ] [PDF ] [PubMed ] [Related articles ]
7. Accesses 374
Research article
Effects of interacting networks of cardiovascular risk genes on the risk of type 2 diabetes mellitus (the CODAM study) Marleen MJ van Greevenbroek, Jian Zhang, Carla JH van der Kallen, Paul MH Schiffers, Edith JM Feskens, Tjerk WA de Bruin BMC Medical Genetics 2008, 9 :36 (24 April 2008) [Abstract ] [Provisional PDF ] [PubMed ] [Related articles ]
8. Accesses 357
Debate
Theories of schizophrenia: a genetic-inflammatory-vascular synthesis Daniel R Hanson, Irving I Gottesman BMC Medical Genetics 2005, 6 :7 (11 February 2005) [Abstract ] [Full text ] [PDF ] [PubMed ] [Related articles ] [Cited on BioMed Central ]
9. Accesses 343
Case report
A novel mutation in the SH3BP2 gene causes cherubism: case report Cui-Ying Li, Shi-Feng Yu BMC Medical Genetics 2006, 7 :84 (5 December 2006) [Abstract ] [Full text ] [PDF ] [PubMed ] [Related articles ]
10. Accesses 340
Database
The FH mutation database: an online database of fumarate hydratase mutations involved in the MCUL (HLRCC) tumor syndrome and congenital fumarase deficiency Jean-Pierre Bayley, Virpi Launonen, Ian PM Tomlinson BMC Medical Genetics 2008, 9 :20 (25 March 2008) [Abstract ] [Full text ] [PDF ] [PubMed ] [Related articles ]