Publications by authors named "Madeline Graf"

3Publications

De novo EIF2AK1 and EIF2AK2 Variants Are Associated with Developmental Delay, Leukoencephalopathy, and Neurologic Decompensation.

Am J Hum Genet 2020 04 19;106(4):570-583. Epub 2020 Mar 19.

Department of Pediatrics, Baylor College of Medicine (BCM), Houston, TX 77030, USA; Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, Houston, TX 77030, USA; Division of Neurology and Developmental Neuroscience, Department of Pediatrics, BCM, Houston, TX 77030, USA; Department of Molecular and Human Genetics, BCM, Houston, TX 77030, USA; Texas Children's Hospital, Houston, TX 77030, USA; Program in Development, Disease Models, and Therapeutics, BCM, Houston, TX 77030, USA; Department of Neuroscience, BCM, Houston, TX 77030, USA; McNair Medical Institute, The Robert and Janice McNair Foundation, Houston, TX 77030, USA. Electronic address:

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http://dx.doi.org/10.1016/j.ajhg.2020.02.016DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7118694PMC
April 2020

Genetics and Precision Medicine: Heritable Thoracic Aortic Disease.

Med Clin North Am 2019 Nov 31;103(6):1005-1019. Epub 2019 Aug 31.

Johns Hopkins School of Medicine, Blalock 1008, 600 North Wolfe Street, Baltimore, MD 21287, USA. Electronic address:

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http://dx.doi.org/10.1016/j.mcna.2019.08.001DOI Listing
November 2019

Use of genetic risks in pediatric organ transplantation listing decisions: A national survey.

Pediatr Transplant 2019 06 23;23(4):e13402. Epub 2019 Apr 23.

Stanford Center for Biomedical Ethics, Stanford University School of Medicine, Stanford University, Stanford, California.

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http://dx.doi.org/10.1111/petr.13402DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6836721PMC
June 2019