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Page 1
A complex immunodeficiency is based on U1 snRNP-mediated poly(A) site suppression.
Langemeier J, Schrom EM, Rabner A, Radtke M, Zychlinski D, Saborowski A, Bohn G, Mandel-Gutfreund Y, Bodem J, Klein C, Bohne J. Langemeier J, et al. Among authors: radtke m. EMBO J. 2012 Oct 17;31(20):4035-44. doi: 10.1038/emboj.2012.252. Epub 2012 Sep 11. EMBO J. 2012. PMID: 22968171 Free PMC article.
Genome Sequencing for Diagnosing Rare Diseases.
Wojcik MH, Lemire G, Berger E, Zaki MS, Wissmann M, Win W, White SM, Weisburd B, Wieczorek D, Waddell LB, Verboon JM, VanNoy GE, Töpf A, Tan TY, Syrbe S, Strehlow V, Straub V, Stenton SL, Snow H, Singer-Berk M, Silver J, Shril S, Seaby EG, Schneider R, Sankaran VG, Sanchis-Juan A, Russell KA, Reinson K, Ravenscroft G, Radtke M, Popp D, Polster T, Platzer K, Pierce EA, Place EM, Pajusalu S, Pais L, Õunap K, Osei-Owusu I, Opperman H, Okur V, Oja KT, O'Leary M, O'Heir E, Morel CF, Merkenschlager A, Marchant RG, Mangilog BE, Madden JA, MacArthur D, Lovgren A, Lerner-Ellis JP, Lin J, Laing N, Hildebrandt F, Hentschel J, Groopman E, Goodrich J, Gleeson JG, Ghaoui R, Genetti CA, Gburek-Augustat J, Gazda HT, Ganesh VS, Ganapathi M, Gallacher L, Fu JM, Evangelista E, England E, Donkervoort S, DiTroia S, Cooper ST, Chung WK, Christodoulou J, Chao KR, Cato LD, Bujakowska KM, Bryen SJ, Brand H, Bönnemann CG, Beggs AH, Baxter SM, Bartolomaeus T, Agrawal PB, Talkowski M, Austin-Tse C, Abou Jamra R, Rehm HL, O'Donnell-Luria A. Wojcik MH, et al. Among authors: radtke m. N Engl J Med. 2024 Jun 6;390(21):1985-1997. doi: 10.1056/NEJMoa2314761. N Engl J Med. 2024. PMID: 38838312 Free PMC article.
Exome sequencing in Nigerian children with early-onset epilepsy syndromes.
Ademuwagun IA, Adam Y, Rotimi SO, Syrbe S, Radtke M, Hentschel J, Lemke JR, Adebiyi E. Ademuwagun IA, et al. Among authors: radtke m. Epilepsia Open. 2024 Nov 21. doi: 10.1002/epi4.13106. Online ahead of print. Epilepsia Open. 2024. PMID: 39570184 Free article.
The Effectiveness of Recipe4Health: A Quasi-Experimental Evaluation.
Rosas LG, Chen S, Xiao L, Baiocchi M, Ng E, Emmert-Aronson BO, Chen WT, Thompson-Lastad A, Martinez E, Perez J, Melendez E, Markle E, Radtke MD, Tester J. Rosas LG, et al. Among authors: radtke md. Am J Prev Med. 2024 Nov 2:S0749-3797(24)00372-6. doi: 10.1016/j.amepre.2024.10.020. Online ahead of print. Am J Prev Med. 2024. PMID: 39491775
Addressing diabetes by elevating access to nutrition (ADELANTE) - A multi-level approach for improving household food insecurity and glycemic control among Latinos with diabetes: A randomized controlled trial.
Radtke MD, Chen WT, Xiao L, Rodriguez Espinosa P, Orizaga M, Thomas T, Venditti E, Yaroch AL, Zepada K, Rosas LG, Tester J. Radtke MD, et al. Contemp Clin Trials. 2024 Nov;146:107699. doi: 10.1016/j.cct.2024.107699. Epub 2024 Sep 23. Contemp Clin Trials. 2024. PMID: 39322114 Clinical Trial.
Automatized detection of uniparental disomies in a large cohort.
Moch J, Radtke M, Liehr T, Eggermann T, Gilissen C, Pfundt R, Astuti G, Hentschel J, Schumann I. Moch J, et al. Among authors: radtke m. Hum Genet. 2024 Aug;143(8):955-964. doi: 10.1007/s00439-024-02687-w. Epub 2024 Jul 16. Hum Genet. 2024. PMID: 39012485 Free PMC article.
Limitations in next-generation sequencing-based genotyping of breast cancer polygenic risk score loci.
Baumann A, Ruckert C, Meier C, Hutschenreiter T, Remy R, Schnur B, Döbel M, Fankep RCN, Skowronek D, Kutz O, Arnold N, Katzke AL, Forster M, Kobiela AL, Thiedig K, Zimmer A, Ritter J, Weber BHF, Honisch E, Hackmann K; Bioinformatics Working Group of the German Consortium for Hereditary Breast & Ovarian Cancer; Schmidt G, Sturm M, Ernst C. Baumann A, et al. Eur J Hum Genet. 2024 Aug;32(8):987-997. doi: 10.1038/s41431-024-01647-2. Epub 2024 Jun 21. Eur J Hum Genet. 2024. PMID: 38907004 Free PMC article.
259 results