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153 results

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Page 1
Exome sequencing identifies ACAD9 mutations as a cause of complex I deficiency.
Haack TB, Danhauser K, Haberberger B, Hoser J, Strecker V, Boehm D, Uziel G, Lamantea E, Invernizzi F, Poulton J, Rolinski B, Iuso A, Biskup S, Schmidt T, Mewes HW, Wittig I, Meitinger T, Zeviani M, Prokisch H. Haack TB, et al. Among authors: mewes hw. Nat Genet. 2010 Dec;42(12):1131-4. doi: 10.1038/ng.706. Epub 2010 Nov 7. Nat Genet. 2010. PMID: 21057504
A novel putative miRNA target enhancer signal.
Schmidt T, Mewes HW, Stümpflen V. Schmidt T, et al. Among authors: mewes hw. PLoS One. 2009 Jul 31;4(7):e6473. doi: 10.1371/journal.pone.0006473. PLoS One. 2009. PMID: 19649282 Free PMC article.
A genome-wide perspective of genetic variation in human metabolism.
Illig T, Gieger C, Zhai G, Römisch-Margl W, Wang-Sattler R, Prehn C, Altmaier E, Kastenmüller G, Kato BS, Mewes HW, Meitinger T, de Angelis MH, Kronenberg F, Soranzo N, Wichmann HE, Spector TD, Adamski J, Suhre K. Illig T, et al. Among authors: mewes hw. Nat Genet. 2010 Feb;42(2):137-41. doi: 10.1038/ng.507. Epub 2009 Dec 27. Nat Genet. 2010. PMID: 20037589 Free PMC article.
The PEDANT genome database in 2005.
Riley ML, Schmidt T, Wagner C, Mewes HW, Frishman D. Riley ML, et al. Among authors: mewes hw. Nucleic Acids Res. 2005 Jan 1;33(Database issue):D308-10. doi: 10.1093/nar/gki019. Nucleic Acids Res. 2005. PMID: 15608204 Free PMC article.
Human metabolic individuality in biomedical and pharmaceutical research.
Suhre K, Shin SY, Petersen AK, Mohney RP, Meredith D, Wägele B, Altmaier E; CARDIoGRAM; Deloukas P, Erdmann J, Grundberg E, Hammond CJ, de Angelis MH, Kastenmüller G, Köttgen A, Kronenberg F, Mangino M, Meisinger C, Meitinger T, Mewes HW, Milburn MV, Prehn C, Raffler J, Ried JS, Römisch-Margl W, Samani NJ, Small KS, Wichmann HE, Zhai G, Illig T, Spector TD, Adamski J, Soranzo N, Gieger C. Suhre K, et al. Among authors: mewes hw. Nature. 2011 Aug 31;477(7362):54-60. doi: 10.1038/nature10354. Nature. 2011. PMID: 21886157 Free PMC article.
PEDANT genome database: 10 years online.
Riley ML, Schmidt T, Artamonova II, Wagner C, Volz A, Heumann K, Mewes HW, Frishman D. Riley ML, et al. Among authors: mewes hw. Nucleic Acids Res. 2007 Jan;35(Database issue):D354-7. doi: 10.1093/nar/gkl1005. Epub 2006 Dec 5. Nucleic Acids Res. 2007. PMID: 17148486 Free PMC article.
Rare variants in LRRK1 and Parkinson's disease.
Schulte EC, Ellwanger DC, Dihanich S, Manzoni C, Stangl K, Schormair B, Graf E, Eck S, Mollenhauer B, Haubenberger D, Pirker W, Zimprich A, Brücke T, Lichtner P, Peters A, Gieger C, Trenkwalder C, Mewes HW, Meitinger T, Lewis PA, Klünemann HH, Winkelmann J. Schulte EC, et al. Among authors: mewes hw. Neurogenetics. 2014 Mar;15(1):49-57. doi: 10.1007/s10048-013-0383-8. Epub 2013 Nov 16. Neurogenetics. 2014. PMID: 24241507 Free PMC article.
153 results