Connection
Co-Authors
This is a "connection" page, showing publications co-authored by Dagmar Wieczorek and Arndt Borkhardt.
Connection Strength
0,633
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Family-based germline sequencing in children with cancer. Oncogene. 2019 02; 38(9):1367-1380.
Score: 0,169
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Autism spectrum disorder and Li-Fraumeni syndrome: purely coincidental or mechanistically associated? Mol Cell Pediatr. 2017 Oct 05; 4(1):8.
Score: 0,158
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C2orf69 mutations disrupt mitochondrial function and cause a multisystem human disorder with recurring autoinflammation. J Clin Invest. 2021 06 15; 131(12).
Score: 0,051
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QRICH1 variants in Ververi-Brady syndrome-delineation of the genotypic and phenotypic spectrum. Clin Genet. 2021 01; 99(1):199-207.
Score: 0,049
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Fragile X mental retardation protein protects against tumour necrosis factor-mediated cell death and liver injury. Gut. 2020 01; 69(1):133-145.
Score: 0,045
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Penetrance and Expressivity in Inherited Cancer Predisposing Syndromes. Trends Cancer. 2018 11; 4(11):718-728.
Score: 0,042
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Correction to: Genetic predisposition in children with cancer - affected families' acceptance of Trio-WES. Eur J Pediatr. 2018 01; 177(1):61.
Score: 0,040
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Genetic predisposition in children with cancer - affected families' acceptance of Trio-WES. Eur J Pediatr. 2018 Jan; 177(1):53-60.
Score: 0,039
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Hematopoietic Stem Cell Transplantation in an Infant with Immunodeficiency, Centromeric Instability, and Facial Anomaly Syndrome. Front Immunol. 2017; 8:773.
Score: 0,039
