Scientific Publications Search Search Author Release Date Research Group Search Sort by RelevanceFrom A-ZAuthored onDate/Time RangeRelease date Order AscDesc Altmueller, Janine Dr.med. 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Hernáez G. Alonso J.M. Alonso-Lobo A. Rastrojo C. Fischer S. Sauer B. Aguado A. Alcamí August 24, 2017 / Nature Polylox barcoding reveals haematopoietic stem cell fates realized in vivo W. Pei T.B. Feyerabend J. Rössler X. Wang D. Postrach K. Busch I. Rode K. Klapproth N. Dietlein C. Quedenau W. Chen S. Sauer S. Wolf T. Höfer H.Re. Rodewald December 19, 2017 / Cold Spring Harb Mol Case Stud Late diagnosis of a truncating WISP3 mutation entails a severe phenotype of progressive pseudorheumatoid dysplasia S. Alawbathani A. Kawalia M. Karakaya J. Altmüller P. Nürnberg S. Cirak July 01, 2017 / Clin Genet Genetic heterogeneity in Pakistani microcephaly families revisited I. Ahmad S.M. Baig A.R. Abdulkareem M.S. Hussain I. Sur M.R. Toliat G. Nürnberg N. Dalibor A. Moawia S.S. Waseem M. Asif H. Nagra M. Sher M.M.A. Khan I. Hassan S.U. Rehman H. Thiele J. Altmüller A.A. Noegel P. Nürnberg June 01, 2017 / Immunogenetics Mutational profiling in the peripheral blood leukocytes of patients with systemic mast cell activation syndrome using next-generation sequencing J. Altmüller B. Haenisch A. Kawalia M. Menzen M.M. Nöthen H. Fier G.J. Molderings December 01, 2017 / Nat Med A microRNA screen reveals that elevated hepatic ectodysplasin A expression contributes to obesity-induced insulin resistance in skeletal muscle M. Awazawa P. Gabel E. Tsaousidou H. Nolte M. Krüger J. Schmitz P.J. Ackermann C. Brandt J. Altmüller S. Motameny F.T. Wunderlich J.W. Kornfeld M. Blüher J.C. Brüning July 01, 2017 / Hum Genet Heterozygous HNRNPU variants cause early onset epilepsy and severe intellectual disability N.C. Bramswig H.J. Lüdecke F.F. Hamdan J. Altmüller F. Beleggia N.H. Elcioglu C. Freyer E.H. Gerkes Y.K. Demirkol K.G. Knupp A. Kuechler Y. Li D.H. Lowenstein J.L. Michaud K. Park A.P.A. Stegmann H.E. Veenstra-Knol T. Wieland B. Wollnik H. Engels T.M. Strom T. Kleefstra D. Wieczorek September 26, 2017 / Mol Ecol Copy number increases of transposable elements and protein-coding genes in an invasive fish of hybrid origin S. Dennenmoser F.J. Sedlazeck E. Iwaszkiewicz X.Y. Li J. Altmüller A.W. Nolte November 02, 2017 / Am J Hum Genet De novo mutations in SLC25A24 cause a craniosynostosis syndrome with hypertrichosis, progeroid appearance, and mitochondrial dysfunction N. Ehmke L. Graul-Neumann L. Smorag R. Koenig L. Segebrecht P. Magoulas F. Scaglia E. Kilic A.F. Hennig N. Adolphs N. Saha B. Fauler V.M. Kalscheuer F. Hennig J. Altmüller C. Netzer H. Thiele P. Nürnberg G. Yigit M. Jäger J. Hecht U. Krüger T. Mielke P.M. Krawitz D. Horn M. Schuelke S. Mundlos C.A. Bacino P.E. Bonnen B. Wollnik B. Fischer-Zirnsak U. Kornak October 15, 2017 / Hum Mol Genet A TUBB6 mutation is associated with autosomal dominant non-progressive congenital facial palsy, bilateral ptosis and velopharyngeal dysfunction W. Fazeli P. Herkenrath B. Stiller A. Neugebauer J. Fricke R. Lang-Roth G. Nürnberg M. Thoenes J. Becker J. Altmüller A.E. Volk C. Kubisch R. Heller Pagination Current page 1 Page 2 Page 3 Page 4 Next page Next › Last page Last »
February 09, 2017 / J Immunol Res RNA-seq based transcriptome analysis of the type I interferon host response upon vaccinia virus infection of mouse cells B. Hernáez G. Alonso J.M. Alonso-Lobo A. Rastrojo C. Fischer S. Sauer B. Aguado A. Alcamí
August 24, 2017 / Nature Polylox barcoding reveals haematopoietic stem cell fates realized in vivo W. Pei T.B. Feyerabend J. Rössler X. Wang D. Postrach K. Busch I. Rode K. Klapproth N. Dietlein C. Quedenau W. Chen S. Sauer S. Wolf T. Höfer H.Re. Rodewald
December 19, 2017 / Cold Spring Harb Mol Case Stud Late diagnosis of a truncating WISP3 mutation entails a severe phenotype of progressive pseudorheumatoid dysplasia S. Alawbathani A. Kawalia M. Karakaya J. Altmüller P. Nürnberg S. Cirak
July 01, 2017 / Clin Genet Genetic heterogeneity in Pakistani microcephaly families revisited I. Ahmad S.M. Baig A.R. Abdulkareem M.S. Hussain I. Sur M.R. Toliat G. Nürnberg N. Dalibor A. Moawia S.S. Waseem M. Asif H. Nagra M. Sher M.M.A. Khan I. Hassan S.U. Rehman H. Thiele J. Altmüller A.A. Noegel P. Nürnberg
June 01, 2017 / Immunogenetics Mutational profiling in the peripheral blood leukocytes of patients with systemic mast cell activation syndrome using next-generation sequencing J. Altmüller B. Haenisch A. Kawalia M. Menzen M.M. Nöthen H. Fier G.J. Molderings
December 01, 2017 / Nat Med A microRNA screen reveals that elevated hepatic ectodysplasin A expression contributes to obesity-induced insulin resistance in skeletal muscle M. Awazawa P. Gabel E. Tsaousidou H. Nolte M. Krüger J. Schmitz P.J. Ackermann C. Brandt J. Altmüller S. Motameny F.T. Wunderlich J.W. Kornfeld M. Blüher J.C. Brüning
July 01, 2017 / Hum Genet Heterozygous HNRNPU variants cause early onset epilepsy and severe intellectual disability N.C. Bramswig H.J. Lüdecke F.F. Hamdan J. Altmüller F. Beleggia N.H. Elcioglu C. Freyer E.H. Gerkes Y.K. Demirkol K.G. Knupp A. Kuechler Y. Li D.H. Lowenstein J.L. Michaud K. Park A.P.A. Stegmann H.E. Veenstra-Knol T. Wieland B. Wollnik H. Engels T.M. Strom T. Kleefstra D. Wieczorek
September 26, 2017 / Mol Ecol Copy number increases of transposable elements and protein-coding genes in an invasive fish of hybrid origin S. Dennenmoser F.J. Sedlazeck E. Iwaszkiewicz X.Y. Li J. Altmüller A.W. Nolte
November 02, 2017 / Am J Hum Genet De novo mutations in SLC25A24 cause a craniosynostosis syndrome with hypertrichosis, progeroid appearance, and mitochondrial dysfunction N. Ehmke L. Graul-Neumann L. Smorag R. Koenig L. Segebrecht P. Magoulas F. Scaglia E. Kilic A.F. Hennig N. Adolphs N. Saha B. Fauler V.M. Kalscheuer F. Hennig J. Altmüller C. Netzer H. Thiele P. Nürnberg G. Yigit M. Jäger J. Hecht U. Krüger T. Mielke P.M. Krawitz D. Horn M. Schuelke S. Mundlos C.A. Bacino P.E. Bonnen B. Wollnik B. Fischer-Zirnsak U. Kornak
October 15, 2017 / Hum Mol Genet A TUBB6 mutation is associated with autosomal dominant non-progressive congenital facial palsy, bilateral ptosis and velopharyngeal dysfunction W. Fazeli P. Herkenrath B. Stiller A. Neugebauer J. Fricke R. Lang-Roth G. Nürnberg M. Thoenes J. Becker J. Altmüller A.E. Volk C. Kubisch R. Heller