T-STAG: resource and web-interface for tissue-specific transcripts and genes

по Gupta, Shobhit, Vingron, Martin, Haas, Stefan A.
Опубликовано 2005

SYSTERS, GeneNest, SpliceNest: exploring sequence space from genome to protein

по Krause, Antje, Haas, Stefan A., Coward, Eivind, Vingron, Martin
Опубликовано 2002

Strengths and weaknesses of EST-based prediction of tissue-specific alternative splicing

по Gupta, Shobhit, Zink, Dorothea, Korn, Bernhard, Vingron, Martin, Haas, Stefan A
Опубликовано 2004

CpG-depleted promoters harbor tissue-specific transcription factor binding signals—implications for motif overrepresentation analyses

по Roider, Helge G., Lenhard, Boris, Kanhere, Aditi, Haas, Stefan A., Vingron, Martin
Опубликовано 2009

PASTAA: identifying transcription factors associated with sets of co-regulated genes

по Roider, Helge G., Manke, Thomas, O'Keeffe, Sean, Vingron, Martin, Haas, Stefan A.
Опубликовано 2009

Modeling Read Counts for CNV Detection in Exome Sequencing Data

по Love, Michael I., Myšičková, Alena, Sun, Ruping, Kalscheuer, Vera, Vingron, Martin, Haas, Stefan A.
Опубликовано 2011

Genome-scale design of PCR primers and long oligomers for DNA microarrays

по Haas, Stefan A., Hild, Marc, Wright, Anthony P. H., Hain, Torsten, Talibi, Driss, Vingron, Martin
Опубликовано 2003

Intronic CA-repeat and CA-rich elements: a new class of regulators of mammalian alternative splicing

по Hui, Jingyi, Hung, Lee-Hsueh, Heiner, Monika, Schreiner, Silke, Neumüller, Norma, Reither, Gregor, Haas, Stefan A, Bindereif, Albrecht
Опубликовано 2005

Comparing active and repressed expression states of genes controlled by the Polycomb/Trithorax group proteins

по Beisel, Christian, Buness, Andreas, Roustan-Espinosa, Ian M., Koch, Britta, Schmitt, Sabine, Haas, Stefan A., Hild, Marc, Katsuyama, Tomonori, Paro, Renato
Опубликовано 2007

Prediction of alternative isoforms from exon expression levels in RNA-Seq experiments

по Richard, Hugues, Schulz, Marcel H., Sultan, Marc, Nürnberger, Asja, Schrinner, Sabine, Balzereit, Daniela, Dagand, Emilie, Rasche, Axel, Lehrach, Hans, Vingron, Martin, Haas, Stefan A., Yaspo, Marie-Laure
Опубликовано 2010

Mutation p.R356Q in the Collybistin Phosphoinositide Binding Site Is Associated With Mild Intellectual Disability

по Chiou, Tzu-Ting, Long, Philip, Schumann-Gillett, Alexandra, Kanamarlapudi, Venkateswarlu, Haas, Stefan A., Harvey, Kirsten, O’Mara, Megan L., De Blas, Angel L., Kalscheuer, Vera M., Harvey, Robert J.
Опубликовано в: Front Mol Neurosci (2019)

Erratum to: Mutation screening in 86 known X-linked mental retardation genes by droplet-based multiplex PCR and massive parallel sequencing

по Hu, Hao, Wrogemann, Klaus, Kalscheuer, Vera, Tzschach, Andreas, Richard, Hugues, Haas, Stefan A., Menzel, Corinna, Bienek, Melanie, Froyen, Guy, Raynaud, Martine, Van Bokhoven, Hans, Chelly, Jamel, Ropers, Hilger, Chen, Wei
Опубликовано 2010

Mutation screening in 86 known X-linked mental retardation genes by droplet-based multiplex PCR and massive parallel sequencing

по Hu, Hao, Wrogemann, Klaus, Kalscheuer, Vera, Tzschach, Andreas, Richard, Hugues, Haas, Stefan A., Menzel, Corinna, Bienek, Melanie, Froyen, Guy, Raynaud, Martine, Van Bokhoven, Hans, Chelly, Jamel, Ropers, Hilger, Chen, Wei
Опубликовано 2010

Functional analysis and identification of cis-regulatory elements of human chromosome 21 gene promoters

по Warnatz, Hans-Jörg, Querfurth, Robert, Guerasimova, Anna, Cheng, Xi, Haas, Stefan A., Hufton, Andrew L., Manke, Thomas, Vanhecke, Dominique, Nietfeld, Wilfried, Vingron, Martin, Janitz, Michal, Lehrach, Hans, Yaspo, Marie-Laure
Опубликовано 2010

Gene identification and analysis of transcripts differentially regulated in fracture healing by EST sequencing in the domestic sheep

по Hecht Jochen, Kuhl Heiner, Haas Stefan A, Bauer Sebastian, Poustka Albert J, Lienau Jasmin, Schell Hanna, Stiege Asita C, Seitz Volkhard, Reinhardt Richard, Duda Georg N, Mundlos Stefan, Robinson Peter N
Опубликовано 2006-07-01

Gene identification and analysis of transcripts differentially regulated in fracture healing by EST sequencing in the domestic sheep

по Hecht, Jochen, Kuhl, Heiner, Haas, Stefan A, Bauer, Sebastian, Poustka, Albert J, Lienau, Jasmin, Schell, Hanna, Stiege, Asita C, Seitz, Volkhard, Reinhardt, Richard, Duda, Georg N, Mundlos, Stefan, Robinson, Peter N
Опубликовано 2006

X-exome sequencing in Finnish families with Intellectual Disability - four novel mutations and two novel syndromic phenotypes

по Philips, Anju K, Sirén, Auli, Avela, Kristiina, Somer, Mirja, Peippo, Maarit, Ahvenainen, Minna, Doagu, Fatma, Arvio, Maria, Kääriäinen, Helena, Van Esch, Hilde, Froyen, Guy, Haas, Stefan A, Hu, Hao, Kalscheuer, Vera M, Järvelä, Irma
Опубликовано 2014

Novel Missense Mutation A789V in IQSEC2 Underlies X-Linked Intellectual Disability in the MRX78 Family

по Kalscheuer, Vera M., James, Victoria M., Himelright, Miranda L., Long, Philip, Oegema, Renske, Jensen, Corinna, Bienek, Melanie, Hu, Hao, Haas, Stefan A., Topf, Maya, Hoogeboom, A. Jeannette M., Harvey, Kirsten, Walikonis, Randall, Harvey, Robert J.
Опубликовано в: Front Mol Neurosci (2016)

Next-Generation Sequencing Identifies Mutations of SMPX, which Encodes the Small Muscle Protein, X-Linked, as a Cause of Progressive Hearing Impairment

по Schraders, Margit, Haas, Stefan A., Weegerink, Nicole J.D., Oostrik, Jaap, Hu, Hao, Hoefsloot, Lies H., Kannan, Sriram, Huygen, Patrick L.M., Pennings, Ronald J.E., Admiraal, Ronald J.C., Kalscheuer, Vera M., Kunst, Henricus P.M., Kremer, Hannie
Опубликовано 2011

A Noncoding, Regulatory Mutation Implicates HCFC1 in Nonsyndromic Intellectual Disability

по Huang, Lingli, Jolly, Lachlan A., Willis-Owen, Saffron, Gardner, Alison, Kumar, Raman, Douglas, Evelyn, Shoubridge, Cheryl, Wieczorek, Dagmar, Tzschach, Andreas, Cohen, Monika, Hackett, Anna, Field, Michael, Froyen, Guy, Hu, Hao, Haas, Stefan A., Ropers, Hans-Hilger, Kalscheuer, Vera M., Corbett, Mark A., Gecz, Jozef
Опубликовано 2012