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: 4.471
ISI Journal Citation Reports © Ranking: 2015: 31/166 (Genetics & Heredity)
Online ISSN: 1552-4876
Recently Published Issues
Current Issue:March 2017
Volume 175, Issue 1
Special Issue: The Ehlers-Danlos Syndromes: Report...
Volume 172, Issue 4
Special Issue: Treatment of Non-metabolic Genetic ...
Volume 172, Issue 3
Special Issue: Perspectives on the Care and Advanc...
Volume 172, Issue 2
Special Issue: Laird G. Jackson, M.D. - Celebrator...
Volume 172, Issue 1
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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
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.
Editor in Chief News
We are pleased to announce that Dr. John C. Carey (Utah, USA) will continue to serve as the Editor in Chief of AJMG Part C in 2017. Dr. Carey has expertly guided the journal through 16 years and maintained it’s status as a major publication in medical genetics.
2017 John M. Opitz Award Nominations
In honor of Dr. Opitz, Founding Editor-in-Chief of the American Journal of Medical Geneics, Wiley 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 2016. 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 5, 2017
More details for the 2017 John M. Opitz Award
Congratulations to Esra Dikoglu, the winner of the 2016 John M. Opitz Young Investigator Award, for her paper: Mutations in LONP1, a mitochondrial matrix protease, cause CODAS syndrome.
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.