Welcome To The IGM Inside this site you will find information about the world renowned research, clinical and educational programs atthe Institute of Genetic Medicine, Johns Hopkins University.
This site is updated regularly to provide you with accurate information about our members, their research interests and contact information. We take great pride in our clinical services and are constantly striving to make them the very best. If you are a patient and need an appointment or information about a genetic disorder, we can help you.
We have outstanding predoctoral and postdoctoral training programs in medical and human genetics. The IGM is the home of the largest annotated database in medical genetics: 
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| Meet Our Director
David Valle, MD | Our Publication Corner | »NEW« Miller RA, Christoforou N, Pevsner J, McCallion AS*, Gearhart JD* Efficient Array-Based Identification of Novel Cardiac Genes through Differentiation of Mouse ESCs. PLoS One (2008)
*corresponding authors.
»NEW« Hans T. Bjornsson, Thomas J. Albert, Christine M. Ladd-Acosta, Roland D. Green, Michael A. Rongione, Christina M. Middle, Rafael A. Irizarry, Karl W. Broman,and Andrew P. Feinberg. SNP-specific array-based allele-specific expression analysis. Genome Research, May 2008.
»NEW« Emily C. Lisi , Ada Hamosh , Kimberly F. Doheny, Elizabeth Squibb, Barbara Jackson, Rebecca Galczynski, George H. Thomas, Denise Batista.3q29 interstitial microduplication: A new syndrome in a three-generation family.
Am J Med Genet A. 2008 Feb 1 [Epub ahead of print]
»NEW« Mathivanan, S., Ahmed, M., 157 coauthors and Pandey, A. Human Proteinpedia enables sharing of human protein data. Nature Biotechnology. 26, 6-9.
»NEW« Christoforou, N.,* Miller, R.A.,* Hill, C.M., Jie, C.C., McCallion, A.S., and Gearhart. J.D. The characterization of ES-derived cardiac precursor cells demonstrates their multipotentiality and identifies novel cardiac genes. J. Clin. Invest. 2/2008
»NEW« Dan E. Arking, David J. Cutler, Camille W. Brune, Tanya M. Teslovich, Kristen West, Morna Ikeda, Alexis Rea, Moltu Guy, Shin Lin,Edwin H. Cook Jr., and Aravinda Chakravarti
A Common Genetic Variant in the Neurexin Superfamily Member CNTNAP2 Increases Familial Risk of Autism. AJHG 1/2008
Read more»»»
»NEW« J. Michael Collaco, Lori Vanscoy, Lindsay Bremer, Kathryn McDougal, Scott Blackman, Amanda Bowers, Kathleen Naughton, Jacky Jennings, Jonathan Ellen and G. R. Cutting
Interactions Between Secondhand Smoke and Genes That Affect Cystic Fibrosis Lung Disease. JAMA 1/2008
Read more»»»» 
»NEW« Tina L. Cheng, MD, MPH, Ronald D. Cohn, MD George J. Dover, MD
The Genetics Revolution and Primary Care Pediatrics JAMA 2008
»NEW« Thomas E. Sussan, Annan Yang, Fu Li, Michael C. Ostrowski & Roger H. Reeves Trisomy represses Apc-mediated tumours in mouse models of Down's syndrome Trisomy represses ApcMin-mediated tumours in mouse models of Down syndrome Nature 451, 73-75 (3 January 2008) |
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