Glucose feeds the TCA cycle via circulating lactate S Hui, JM Ghergurovich, RJ Morscher, C Jang, X Teng, W Lu, LA Esparza, ... Nature 551 (7678), 115-118, 2017 | 1386 | 2017 |
The small intestine converts dietary fructose into glucose and organic acids C Jang, S Hui, W Lu, AJ Cowan, RJ Morscher, G Lee, W Liu, GJ Tesz, ... Cell metabolism 27 (2), 351-361. e3, 2018 | 573 | 2018 |
Reversal of cytosolic one-carbon flux compensates for loss of the mitochondrial folate pathway GS Ducker, L Chen, RJ Morscher, JM Ghergurovich, M Esposito, X Teng, ... Cell metabolism 23 (6), 1140-1153, 2016 | 415 | 2016 |
Quantitative analysis of the whole-body metabolic fate of branched-chain amino acids MD Neinast, C Jang, S Hui, DS Murashige, Q Chu, RJ Morscher, X Li, ... Cell metabolism 29 (2), 417-429. e4, 2019 | 383 | 2019 |
Mitochondrial translation requires folate-dependent tRNA methylation RJ Morscher, GS Ducker, SHJ Li, JA Mayer, Z Gitai, W Sperl, ... Nature 554 (7690), 128-132, 2018 | 240 | 2018 |
Metabolite exchange between mammalian organs quantified in pigs C Jang, S Hui, X Zeng, AJ Cowan, L Wang, L Chen, RJ Morscher, ... Cell metabolism 30 (3), 594-606. e3, 2019 | 199 | 2019 |
Serine catabolism feeds NADH when respiration is impaired L Yang, JCG Canaveras, Z Chen, L Wang, L Liang, C Jang, JA Mayr, ... Cell metabolism 31 (4), 809-821. e6, 2020 | 160 | 2020 |
Inhibition of neuroblastoma tumor growth by ketogenic diet and/or calorie restriction in a CD1-Nu mouse model RJ Morscher, S Aminzadeh-Gohari, RG Feichtinger, JA Mayr, R Lang, ... PloS one 10 (6), e0129802, 2015 | 134 | 2015 |
3-methylcrotonyl-CoA carboxylase deficiency: clinical, biochemical, enzymatic and molecular studies in 88 individuals SC Grünert, M Stucki, RJ Morscher, T Suormala, C Bürer, P Burda, ... Orphanet journal of rare diseases 7, 1-24, 2012 | 92 | 2012 |
Clinical, biochemical and genetic spectrum of 70 patients with ACAD9 deficiency: is riboflavin supplementation effective? BM Repp, E Mastantuono, CL Alston, M Schiff, TB Haack, A Rötig, ... Orphanet journal of rare diseases 13, 1-10, 2018 | 80 | 2018 |
Combination of metronomic cyclophosphamide and dietary intervention inhibits neuroblastoma growth in a CD1-nu mouse model RJ Morscher, S Aminzadeh-Gohari, C Hauser-Kronberger, ... Oncotarget 7 (13), 17060, 2016 | 45 | 2016 |
A single mutation in MCCC1 or MCCC2 as a potential cause of positive screening for 3-methylcrotonyl-CoA carboxylase deficiency RJ Morscher, SC Grünert, C Bürer, P Burda, T Suormala, B Fowler, ... Molecular Genetics and Metabolism 105 (4), 602-606, 2012 | 35 | 2012 |
First-in-child phase I/II study of the dual mTORC1/2 inhibitor vistusertib (AZD2014) as monotherapy and in combination with topotecan-temozolomide in children with advanced … RJ Morscher, C Brard, P Berlanga, LV Marshall, N André, J Rubino, ... European Journal of Cancer 157, 268-277, 2021 | 28 | 2021 |
Phase I or II study of ribociclib in combination with topotecan-temozolomide or everolimus in children with advanced malignancies: arms A and B of the AcSé-ESMART trial F Bautista, X Paoletti, J Rubino, C Brard, K Rezai, S Nebchi, N Andre, ... Journal of Clinical Oncology 39 (32), 3546-3560, 2021 | 27 | 2021 |
Psychosocial outcomes and counselee satisfaction following genetic counseling for hereditary breast and ovarian cancer: A patient-reported outcome study A Oberguggenberger, M Sztankay, RJ Morscher, B Sperner-Unterweger, ... Journal of psychosomatic research 89, 39-45, 2016 | 27 | 2016 |
Integrated multi-omics reveals anaplerotic rewiring in methylmalonyl-CoA mutase deficiency P Forny, X Bonilla, D Lamparter, W Shao, T Plessl, C Frei, A Bingisser, ... Nature Metabolism 5 (1), 80-95, 2023 | 21 | 2023 |
A biobank of pediatric patient-derived-xenograft models in cancer precision medicine trial MAPPYACTS for relapsed and refractory tumors ME Marques Da Costa, S Zaidi, JY Scoazec, R Droit, WC Lim, A Marchais, ... Communications Biology 6 (1), 949, 2023 | 6 | 2023 |
Seizures, enamel defects and psychomotor developmental delay: The first patient with Kohlschütter-Tönz syndrome caused by a ROGDI-gene deletion RJ Morscher, C Rauscher, W Sperl, O Rittinger Seizure-European Journal of Epilepsy 50, 118-120, 2017 | 6 | 2017 |
High prevalence of BRCA1 stop mutation c. 4183C> T in the Tyrolean population: implications for genetic testing L Pölsler, H Fiegl, K Wimmer, W Oberaigner, A Amberger, P Traunfellner, ... European journal of human genetics 24 (2), 258-262, 2016 | 5 | 2016 |
Cancer in children with biallelic BRCA1 variants and Fanconi anemia-like features: Report of a malignant brain tumor in a young child PR Borlin, P Brazzola, K Frontzek, P Zanoni, RJ Morscher, J Hench, ... Pediatric blood & cancer 69 (10), e29680, 2022 | 2 | 2022 |