Publikationen von J. Hecht
Alle Typen
Zeitschriftenartikel (38)
21.
Zeitschriftenartikel
The allele distribution in next-generation sequencing data sets is accurately described as the result of a stochastic branching process. Nucleic Acids Res (2011)
22.
Zeitschriftenartikel
12, S. 158 (2011)
Composite transcriptome assembly of RNA-seq data in a sheep model for delayed bone healing. BMC Genomics 23.
Zeitschriftenartikel
88 (1), S. 70 - 5 (2011)
Copy-number variations involving the IHH locus are associated with syndactyly and craniosynostosis. Am J Hum Genet 24.
Zeitschriftenartikel
10 (17), S. 2967 - 77 (2011)
Misregulation of mitotic chromosome segregation in a new type of autosomal recessive primary microcephaly. Cell Cycle 25.
Zeitschriftenartikel
27 (6), S. 829 - 36 (2011)
Identity-by-descent filtering of exome sequence data for disease-gene identification in autosomal recessive disorders. Bioinformatics 26.
Zeitschriftenartikel
27 (6), S. 829 - 36 (2011)
Identity-by-descent filtering of exome sequence data for disease-gene identification in autosomal recessive disorders. Bioinformatics 27.
Zeitschriftenartikel
42 (10), S. 827 - 829 (2010)
Identity-by-descent filtering of exome sequence data identifies PIGV mutations in hyperphosphatasia mental retardation syndrome. Nature Genetics 28.
Zeitschriftenartikel
42 (10), S. 827 - 829 (2010)
Identity-by-descent filtering of exome sequence data identifies PIGV mutations in hyperphosphatasia mental retardation syndrome. Nature Genetics 29.
Zeitschriftenartikel
42 (10), S. 827 - 829 (2010)
Identity-by-descent filtering of exome sequence data identifies PIGV mutations in hyperphosphatasia mental retardation syndrome. Nature Genetics 30.
Zeitschriftenartikel
120 (6), S. 1994 - 2004 (2010)
Homeobox genes d11-d13 and a13 control mouse autopod cortical bone and joint formation. Journal of Clinical Investigation 31.
Zeitschriftenartikel
45 (5-6), S. 252 - 263 (2009)
PBX1 is dispensable for neural commitment of RA-treated murine ES cells. In Vitro Cellular & Developmental Biology - Animal 32.
Zeitschriftenartikel
119 (1), S. 146 - 156 (2009)
Mutant Hoxd13 induces extra digits in a mouse model of synpolydactyly directly and by decreasing retinoic acid synthesis. Journal of Clinical Investigation 33.
Zeitschriftenartikel
40 (4), S. 638 - 650 (2008)
A short ultraconserved sequence drives transcription from an alternate FBN1 promoter. The International Journal of Biochemistry & Cell Biology 34.
Zeitschriftenartikel
4 (3), S. e1000025 - e1000025 (2008)
Evolution of a core gene network for skeletogenesis in chordates. PLoS Genetics 35.
Zeitschriftenartikel
7 (1 - 2), S. 102 - 112 (2007)
Detection of novel skeletogenesis target genes by comprehensive analysis of a Runx2−/− mouse model. Gene Expression Patterns: A Section of Brain Research Devoted to Patterns of Expression of Genes during the Development, Maturity and Aging of the Central Nervous System 36.
Zeitschriftenartikel
17, S. 1855 - 1862 (2006)
Induction of Macrophage Chemotaxis by Aortic Extracts of the mgR Marfan Mouse Model and a GxxPG-Containing Fibrillin-1 Fragment. Circulation 37.
Zeitschriftenartikel
7, S. 172 - 192 (2006)
Gene identification and analysis of transcripts differentially regulated in fracture healing by EST sequencing in the domestic sheep. BMC Genomics 38.
Zeitschriftenartikel
27 (8), S. 673 - 684 (2003)
A single amphioxus and sea urchin runt-gene suggests that runt-gene duplications occurred in early chordate evolution. Developmental and Comparative Immunology Hochschulschrift - Doktorarbeit (1)
39.
Hochschulschrift - Doktorarbeit
Gene-Expression analysis in bone development and fracture healing Genexpressionsanalysen zum besseren Verständnis von Knochenheilung und -entwicklung. Dissertation, Freie Universität Berlin, Berlin (2007)