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Whole-Genome Sequencing in Severe Chronic Obstructive Pulmonary Disease.
Prokopenko D, Sakornsakolpat P, Fier HL, Qiao D, Parker MM, McDonald MN, Manichaikul A, Rich SS, Barr RG, Williams CJ, Brantly ML, Lange C, Beaty TH, Crapo JD, Silverman EK, Cho MH. Prokopenko D, et al. Among authors: fier hl. Am J Respir Cell Mol Biol. 2018 Nov;59(5):614-622. doi: 10.1165/rcmb.2018-0088OC. Am J Respir Cell Mol Biol. 2018. PMID: 29949718 Free PMC article.
Reporting Correct p Values in VEGAS Analyses.
Hecker J, Maaser A, Prokopenko D, Fier HL, Lange C. Hecker J, et al. Among authors: fier hl. Twin Res Hum Genet. 2017 Jun;20(3):257-259. doi: 10.1017/thg.2017.16. Epub 2017 Mar 27. Twin Res Hum Genet. 2017. PMID: 28345502 Free PMC article.
Resequencing of VAX1 in patients with nonsyndromic cleft lip with or without cleft palate.
Nasser E, Mangold E, Tradowsky DC, Fier H, Becker J, Boehmer AC, Herberz R, Fricker N, Barth S, Wahle P, Nowak S, Reutter H, Reich RH, Lauster C, Braumann B, Kreusch T, Hemprich A, Pötzsch B, Hoffmann P, Kramer FJ, Knapp M, Lange C, Nöthen MM, Ludwig KU. Nasser E, et al. Birth Defects Res A Clin Mol Teratol. 2012 Nov;94(11):925-33. doi: 10.1002/bdra.23078. Epub 2012 Oct 18. Birth Defects Res A Clin Mol Teratol. 2012. PMID: 23081944
Investigation of the role of TCF4 rare sequence variants in schizophrenia.
Basmanav FB, Forstner AJ, Fier H, Herms S, Meier S, Degenhardt F, Hoffmann P, Barth S, Fricker N, Strohmaier J, Witt SH, Ludwig M, Schmael C, Moebus S, Maier W, Mössner R, Rujescu D, Rietschel M, Lange C, Nöthen MM, Cichon S. Basmanav FB, et al. Am J Med Genet B Neuropsychiatr Genet. 2015 Jul;168B(5):354-62. doi: 10.1002/ajmg.b.32318. Epub 2015 May 22. Am J Med Genet B Neuropsychiatr Genet. 2015. PMID: 26010163
17 results