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Megan Truitt Cho
National Human Genome Research Institute - Bethesda / United States
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AD Scientific Index ID: 4387252
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Megan Truitt Cho's MOST POPULAR ARTICLES
1-)
Clinical application of whole-exome sequencing across clinical indicationsK Retterer, J Juusola, MT Cho, P Vitazka, F Millan, F Gibellini, ...Genetics in Medicine 18 (7), 696-704, 20167882016
2-)
High rate of recurrent de novo mutations in developmental and epileptic encephalopathiesFF Hamdan, CT Myers, P Cossette, P Lemay, D Spiegelman, AD Laporte, ...The American Journal of Human Genetics 101 (5), 664-685, 20173122017
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Mutations in DDX3X are a common cause of unexplained intellectual disability with gender-specific effects on Wnt signalingLS Blok, E Madsen, J Juusola, C Gilissen, D Baralle, MRF Reijnders, ...The American Journal of Human Genetics 97 (2), 343-352, 20152482015
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The usefulness of whole-exome sequencing in routine clinical practiceA Iglesias, K Anyane-Yeboa, J Wynn, A Wilson, M Truitt Cho, E Guzman, ...Genetics in Medicine 16 (12), 922-931, 20142622014
5-)
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disordersV Salpietro, CL Dixon, H Guo, OD Bello, J Vandrovcova, S Efthymiou, ...Nature communications 10 (1), 3094, 20192102019
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