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BMC Medical Genetics

Most viewed

Editor-in-Chief
Melissa Norton, MD

Medical Editor
Jigisha Patel, MRCP PhD

In-house Editor
Scott Edmunds



BMC  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 (21April2008)
[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 (21April2008)
[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 (25April2008)
[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 Tmer, Helle Hjalgrim, Johanne Hahnemann, Birgitte Friis, Paal Ledaal, Vibeke Faurholt Pedersen, Peter Baekgaard, Niels Tommerup, Sultan Cingz, Morten Duno, Karen Brondum-Nielsen
BMC Medical Genetics 2005, 6:21 (17May2005)
[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 (22April2008)
[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 Gonzlez, Blanca Gener, Enrique Galn, Laura Toledo, Luis A Prez-Jurado
BMC Medical Genetics 2008, 9:27 (11April2008)
[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 (24April2008)
[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 (11February2005)
[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 (5December2006)
[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 (25March2008)
[Abstract] [Full text] [PDF] [PubMed] [Related articles]

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