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

di Gupta, Shobhit, Vingron, Martin, Haas, Stefan A.
Pubblicazione 2005

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

di Krause, Antje, Haas, Stefan A., Coward, Eivind, Vingron, Martin
Pubblicazione 2002

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

di Gupta, Shobhit, Zink, Dorothea, Korn, Bernhard, Vingron, Martin, Haas, Stefan A
Pubblicazione 2004

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

di Roider, Helge G., Lenhard, Boris, Kanhere, Aditi, Haas, Stefan A., Vingron, Martin
Pubblicazione 2009

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

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

Modeling Read Counts for CNV Detection in Exome Sequencing Data

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

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

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

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

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

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

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

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

di 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
Pubblicazione 2010

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

di 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.
Pubblicato in 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

di 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
Pubblicazione 2010

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

di 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
Pubblicazione 2010

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

di 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
Pubblicazione 2010

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

di 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
Pubblicazione 2006-07-01

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

di 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
Pubblicazione 2006

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

di 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
Pubblicazione 2014

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

di 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.
Pubblicato in 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

di 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
Pubblicazione 2011

A Noncoding, Regulatory Mutation Implicates HCFC1 in Nonsyndromic Intellectual Disability

di 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
Pubblicazione 2012