1552-4876/asset/olbannerleft.gif?v=1&s=3c2729cd895954452a2250238f60958c09d9935e)
1552-4876/asset/olbannerright.gif?v=1&s=7ce70917c1cb0516996ebc295be736c5e1434422)
American Journal of Medical Genetics Part C: Seminars in Medical Genetics
Copyright © 2012 Wiley-Liss, Inc., A Wiley Company
Edited By: John C. Carey
Impact Factor: 4.058
ISI Journal Citation Reports © Ranking: 2011: 35/157 (Genetics & Heredity)
Online ISSN: 1552-4876
Associated Title(s): American Journal of Medical Genetics Part A, American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
Recently Published Issues
Current Issue:May 2013
Volume 163, Issue 2
Special Issue: Molecular Mechanisms of Childhood O...
Volume 163, Issue 1
Special Issue: Medical and Neurodevelopmental Aspe...
Volume 160C, Issue 4
Special Issue: Smith-Lemli-Opitz Syndrome and Rela...
Volume 160C, Issue 3
Special Issue: New Topics in the Skeletal Dysplasi...
Volume 160C, Issue 2
Special Issue: Autism and Intellectual Disability:...
Top Downloads
1552-4876/asset/homepages/AJMGCarticles.gif?v=1&s=d0c3b57d3121986626ba4439be1b98016d993b67)
Access these top downloaded articles for FREE online:
The new era of Pompe disease: Advances in the detection, understanding of the phenotypic spectrum, pathophysiology, and management
The genotype–phenotype correlation in Pompe disease
Autophagy and mitochondria in Pompe disease: Nothing is so new as what has long been forgotten
Network- and attribute-based classifiers can prioritize genes and pathways for autism spectrum disorders and intellectual disability
Autism and intellectual disability: Two sides of the same coin
Centers for Mendelian Genomics
1552-4876/asset/homepages/Centers_for_Medelian_Genomics_image_45_.gif?v=1&s=689dfdf952038d4cd8294ac432481a4652f8249b)
The National Human Genome Research Institute and the National Heart, Lung, and Blood Institute have partnered to support the discovery of variant genes underlying Mendelian disorders at three Centers for Mendelian Genomics. Click here for more information. See also the article Bamshad et al., “The Centers for Mendelian Genomics: A new large-scale initiative to identify the genes underlying rare Mendelian conditions” in AJMG Part A.
2012 John M. Opitz Award Winner
1552-4876/asset/homepages/OPITZ-logo.gif?v=1&s=d5a597b149945bd0ecbc4b739d6541a1b44d3d9a){kind=logo}
In honor of Dr. Opitz, Founding Editor-in-Chief of the American Journal of Medical Geneics, Wiley-Blackwell is seeking nominations for its annual John M. Opitz Young Investigator Award.
The recipient of this award is selected on the basis of significant research published in AJMG in 2012. The paper must cover one of the following areas of research: congenital anomalies, mechanisms of morphogenesis and malformations, developmental biology, or genes involved in development.
NOMINATIONS DEADLINE: June 10, 2013
More details for the 2013 John M. Opitz Award
Congratulations to Dr. Rubén Cabanillas, the winner of the 2012 John M. Opitz Young Investigator Award for his paper, Néstor-Guillermo Progeria Syndrome: A Novel Premature Aging Condition With Early Onset and Chronic Development Caused by BANF1 Mutations .
Autism research in AJMG
1552-4876/asset/homepages/AJMG_Autism.gif?v=1&s=68d26b9c40abd047443b6af7cb41e43f92a2a959)
Read these ground-breaking new reports on Autism Spectrum Disorder published in the journal:
- Autism and epistemology III: Child development, behavioral stability, and reliability of measurement
Gene S. Fisch, in AJMG Part A - Virtual Issue: Genetics of Autism Spectrum Disorders
(A virtual issue on AJMG Part B: Neuropsychiatric Genetics) - Special Issue: Autism and Intellectual Disability: Two Sides of the Same Coin
(A full issue of AJMG Part C: Seminars in Medical Genetics)
Getting Your Scientific Paper Written & Published When English Is Your Second Language
AJMG sponsored the workshop, “Getting Your Scientific Paper Written & Published When English Is Your Second Language", at the 2011 Annual Meeting for ASHG (Montreal). Access the program and most of the presentations online now.