Children's Hospital of Philadelphia

The MAGIC Algorithm Probability (MAP): A Novel Laboratory Biomarker for the Response to Treatment of Acute Graft-Versus-Host Disease (2019) Srinagesh H, Ozbek U, Kapoor U, Ayuk FA, Aziz MD, Ben-David K, Choe HK, et al. Conference contribution De novo missense variants in RHOBTB2 cause a developmental and epileptic encephalopathy in humans, and altered levels cause neurological defects in Drosophila (2019) Straub J, Konrad E, Grüner J, Toutain A, Bok LA, Cho MT, Crawford HP, et al. Conference contribution Blood pressure in chronic kidney disease: conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference (2019) Cheung AK, Chang TI, Cushman WC, Furth SL, Ix JH, Pecoits-Filho R, Perkovic V, et al. Journal article SMARCA4 loss is synthetic lethal with CDK4/6 inhibition in non-small cell lung cancer (2019) Xue Y, Meehan B, Fu Z, Wang XQD, Fiset PO, Rieker R, Levins C, et al. Journal article Spherical Harmonic Residual Network for Diffusion Signal Harmonization (2019) Koppers S, Bloy L, Berman J, Tax CMW, Edgar JC, Merhof D Conference contribution Trial of Fingolimod versus Interferon Beta-1a in Pediatric Multiple Sclerosis. (2018) Chitnis T, Arnold DL, Banwell B, Brueck W, Ghezzi A, Giovannoni G, Greenberg B, et al. Journal article Autosomal recessive Noonan syndrome associated with biallelic LZTR1 variants (2018) Johnston JJ, Van Der Smagt JJ, Rosenfeld JA, Pagnamenta AT, Alswaid A, Baker EH, Blair E, et al. Journal article De Novo Variants in the F-Box Protein FBXO11 in 20 Individuals with a Variable Neurodevelopmental Disorder (2018) Gregor A, Sadleir LG, Asadollahi R, Azzarello-Burri S, Battaglia A, Ousager LB, Boonsawat P, et al. Journal article Missense Variants in RHOBTB2 Cause a Developmental and Epileptic Encephalopathy in Humans, and Altered Levels Cause Neurological Defects in Drosophila (2018) Straub J, Konrad E, Grüner J, Toutain A, Bok LA, Cho MT, Crawford HP, et al. Journal article The Phenotypic Spectrum of Nephropathies Associated with Mutations in Diacylglycerol Kinase? (2017) Azukaitis K, Simkova E, Majid MA, Galiano M, Benz K, Amann KU, Bockmeyer C, et al. Journal article