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Year | Number of Results |
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2013 | 2 |
2019 | 2 |
2020 | 3 |
2024 | 0 |
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HDAC4 mutations cause diabetes and induce β-cell FoxO1 nuclear exclusion.
Mol Genet Genomic Med. 2019 May;7(5):e602. doi: 10.1002/mgg3.602. Epub 2019 Apr 9.
Mol Genet Genomic Med. 2019.
PMID: 30968599
Free PMC article.
Phosphatidylinositol 4-kinase β mutations cause nonsyndromic sensorineural deafness and inner ear malformation.
Su X, Feng Y, Rahman SA, Wu S, Li G, Rüschendorf F, Zhao L, Cui H, Liang J, Fang L, Hu H, Froehler S, Yu Y, Patone G, Hummel O, Chen Q, Raile K, Luft FC, Bähring S, Hussain K, Chen W, Zhang J, Gong M.
Su X, et al. Among authors: froehler s.
J Genet Genomics. 2020 Oct 20;47(10):618-626. doi: 10.1016/j.jgg.2020.07.008. Epub 2020 Oct 28.
J Genet Genomics. 2020.
PMID: 33358777
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Concordance of Genomic Alterations by Next-Generation Sequencing in Tumor Tissue versus Cell-Free DNA in Stage I-IV Non-Small Cell Lung Cancer.
Jiang J, Adams HP, Yao L, Yaung S, Lal P, Balasubramanyam A, Fuhlbrück F, Tikoo N, Lovejoy AF, Froehler S, Fang LT, Achenbach HJ, Floegel R, Krügel R, Palma JF.
Jiang J, et al. Among authors: froehler s.
J Mol Diagn. 2020 Feb;22(2):228-235. doi: 10.1016/j.jmoldx.2019.10.013. Epub 2019 Dec 16.
J Mol Diagn. 2020.
PMID: 31837429
Free article.
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Plasma-based longitudinal mutation monitoring as a potential predictor of disease progression in subjects with adenocarcinoma in advanced non-small cell lung cancer.
Jiang J, Adams HP, Lange M, Siemann S, Feldkamp M, McNamara S, Froehler S, Yaung SJ, Yao L, Balasubramanyam A, Tikoo N, Ju C, Achenbach HJ, Krügel R, Palma JF.
Jiang J, et al. Among authors: froehler s.
BMC Cancer. 2020 Sep 15;20(1):885. doi: 10.1186/s12885-020-07340-z.
BMC Cancer. 2020.
PMID: 32933495
Free PMC article.
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A systematic evaluation of hybridization-based mouse exome capture system.
Gao Q, Sun W, You X, Froehler S, Chen W.
Gao Q, et al. Among authors: froehler s.
BMC Genomics. 2013 Jul 21;14:492. doi: 10.1186/1471-2164-14-492.
BMC Genomics. 2013.
PMID: 23870319
Free PMC article.
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Abnormal centrosome and spindle morphology in a patient with autosomal recessive primary microcephaly type 2 due to compound heterozygous WDR62 gene mutation.
Farag HG, Froehler S, Oexle K, Ravindran E, Schindler D, Staab T, Huebner A, Kraemer N, Chen W, Kaindl AM.
Farag HG, et al. Among authors: froehler s.
Orphanet J Rare Dis. 2013 Nov 14;8:178. doi: 10.1186/1750-1172-8-178.
Orphanet J Rare Dis. 2013.
PMID: 24228726
Free PMC article.
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