S. Haas

发表

Disruptions of Topological Chromatin Domains Cause Pathogenic Rewiring of Gene-Enhancer Interactions

A. Visel, J. Opitz, D. Horn, 2015, Cell.

Integrative genome analyses identify key somatic driver mutations of small-cell lung cancer

K. Cibulskis, J. Shendure, G. Getz, 2012, Nature Genetics.

THOC2 Mutations Implicate mRNA-Export Pathway in X-Linked Intellectual Disability.

B. V. van Bon, K. Friend, M. Shaw, 2015, American journal of human genetics.

CD74-NRG1 fusions in lung adenocarcinoma.

I. Petersen, S. Haas, M. Vingron, 2014, Cancer discovery.

A Global View of Gene Activity and Alternative Splicing by Deep Sequencing of the Human Transcriptome

Marcel H. Schulz, S. Haas, H. Lehrach, 2008, Science.

Frequent mutations in chromatin-remodeling genes in pulmonary carcinoids

Martin Vingron, Thomas Zander, Viktor Achter, 2014, Nature Communications.

Genome-wide analysis of LXRα activation reveals new transcriptional networks in human atherosclerotic foam cells

S. Haas, M. Vingron, S. Sauer, 2013, Nucleic acids research.

Genome-Wide RNAi Analysis of Growth and Viability in Drosophila Cells

N. Perrimon, M. Boutros, A. Kiger, 2004, Science.

Deep sequencing reveals 50 novel genes for recessive cognitive disorders

Wei Chen, Reinhard Ullmann, Dagmar Wieczorek, 2011, Nature.

Involvement of the kinesin family members KIF4A and KIF5C in intellectual disability and synaptic function

L. Vissers, S. Haas, T. Kleefstra, 2014, Journal of Medical Genetics.

Mutations in RAB39B cause X-linked intellectual disability and early-onset Parkinson disease with α-synuclein pathology.

P. Lockhart, S. Haas, K. Hogan, 2014, American journal of human genetics.

Intellectual Disability and Early-Onset Parkinson Disease with a-Synuclein Pathology

P. Lockhart, S. Haas, K. Hogan, 2014 .

Variants in CUL4B are Associated with Cerebral Malformations

A. V. Vulto-van Silfhout, L. Vissers, S. Haas, 2015, Human mutation.

Induction of kidney-related gene programs through co-option of SALL1 in mole ovotestes

Athanasia C. Tzika, A. Visel, S. Haas, 2023, Development.

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

Marcel H. Schulz, S. Haas, H. Lehrach, 2010, Nucleic acids research.

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

Martin Vingron, Boris Lenhard, Helge G. Roider, 2009, Nucleic acids research.

Comprehensive genomic profiles of small cell lung cancer

Martin Vingron, Jan O. Korbel, Lucia Anna Muscarella, 2015, Nature.

Identification of novel fusion genes in lung cancer using breakpoint assembly of transcriptome sequencing data

I. Petersen, S. Haas, M. Vingron, 2015, Genome Biology.

Identification of novel transcriptional regulators involved in macrophage differentiation and activation in U937 cells

S. Haas, H. Lehrach, S. Sauer, 2009, BMC Immunology.

Repression and 3D-restructuring resolves regulatory conflicts in evolutionarily rearranged genomes

S. Mundlos, S. Haas, M. Vingron, 2022, Cell.

Promoter repression and 3D-restructuring resolves divergent developmental gene expression in TADs

S. Mundlos, S. Haas, M. Vingron, 2021, bioRxiv.

Characterization of hundreds of regulatory landscapes in developing limbs reveals two regimes of chromatin folding

Martin Vingron, Stefan Mundlos, Verena Heinrich, 2017, Genome research.

Statistical Applications in Genetics and Molecular Biology Modeling Read Counts for CNV Detection in Exome Sequencing Data

Martin Vingron, Michael I Love, Alena Myšičková, 2011 .

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

S. Haas, H. Van Esch, I. Järvelä, 2014, Orphanet Journal of Rare Diseases.

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

S. Haas, M. Topf, V. Kalscheuer, 2016, Front. Mol. Neurosci..

X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes

K. Friend, M. Shaw, E. Haan, 2015, Molecular Psychiatry.

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

Monika Heiner, Albrecht Bindereif, Jingyi Hui, 2005, The EMBO journal.

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

Martin Vingron, Shobhit Gupta, Stefan A. Haas, 2005, Nucleic Acids Res..

Integrative genomic profiling of large-cell neuroendocrine carcinomas reveals distinct subtypes of high-grade neuroendocrine lung tumors

Martin Vingron, Thomas Zander, Yupeng Cun, 2018, Nature Communications.

Integrative genomic profiling of large-cell neuroendocrine carcinomas reveals distinct subtypes of high-grade neuroendocrine lung tumors

I. Petersen, D. Hayes, M. Wilkerson, 2018, Nature Communications.

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

Martin Vingron, Thomas Manke, Helge G. Roider, 2008, Bioinform..

Customized oligonucleotide microarray gene expression-based classification of neuroblastoma patients outperforms current clinical risk stratification.

Patrick Warnat, R. Eils, S. Haas, 2006, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Mutations in the polyglutamine binding protein 1 gene cause X-linked mental retardation

Steffen Lenzner, Constance Scharff, Kirsten Hoffmann, 2003, Nature Genetics.

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

P. Robinson, Sebastian Bauer, S. Mundlos, 2006, BMC Genomics.

Haplotype-resolved sweet potato genome traces back its hexaploidization history

Martin Vingron, Jianli Zheng, M-Hossein Moeinzadeh, 2017, Nature Plants.

SpliceNest: visualizing gene structure and alternative splicing based on EST clusters

Martin Vingron, Eivind Coward, Stefan A. Haas, 2002 .

Genome wide identification and classification of alternative splicing based on EST data

Martin Vingron, Bernhard Korn, Shobhit Gupta, 2004, Bioinform..

Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling.

Michael J Parker, Katrina Tatton-Brown, Christian Gilissen, 2015, American journal of human genetics.

EIF2S3 Mutations Associated with Severe X‐Linked Intellectual Disability Syndrome MEHMO

S. Haas, E. Leshinsky‐Silver, M. Skopkova, 2017, Human mutation.

Tentative clinical diagnosis of Lujan‐Fryns syndrome—A conglomeration of different genetic entities?

S. Haas, A. Rump, D. Wieczorek, 2016, American journal of medical genetics. Part A.

Genomic and Functional Fidelity of Small Cell Lung Cancer Patient-Derived Xenografts.

Roman K. Thomas, M. Mino‐Kenudson, D. Haber, 2018, Cancer discovery.

Identification and classification of differentially expressed genes in renal cell carcinoma by expression profiling on a global human 31,500-element cDNA array.

A. Poustka, S. Haas, W. Huber, 2001, Genome research.

Identification and Classification of Differentially Expressed Genes in Renal Cell Carcinoma by Expression Profiling on a Global Human 31 , 500-Element cDNA Array

M Vingron, A. Poustka, S. Haas, 2001 .

Genome-wide comparison of cyanobacterial transposable elements, potential genetic diversity indicators.

M. Vingron, T. Żemojtel, Renhui Li, 2010, Gene.

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

S. Haas, V. Kalscheuer, R. Harvey, 2019, Front. Mol. Neurosci..

Pathogenic variants in E3 ubiquitin ligase RLIM/RNF12 lead to a syndromic X-linked intellectual disability and behavior disorder

K. Friend, M. Shaw, E. Haan, 2019, Molecular Psychiatry.

Preformed chromatin topology assists transcriptional robustness of Shh during limb development

S. Mundlos, M. Vingron, M. Nicodemi, 2019, Proceedings of the National Academy of Sciences.

An integrated gene annotation and transcriptional profiling approach towards the full gene content of the Drosophila genome

M Vingron, K Fellenberg, M. Boutros, 2003, Genome Biology.

Analysis of Genes Involved in Body Weight Regulation by Targeted Re-Sequencing

S. Haas, H. Grallert, J. Hebebrand, 2016, PloS one.

A Novel Mutation in RPL10 (Ribosomal Protein L10) Causes X‐Linked Intellectual Disability, Cerebellar Hypoplasia, and Spondylo‐Epiphyseal Dysplasia

S. Klauck, E. Bertini, S. Haas, 2015, Human mutation.

Mutations in SLC33A1 cause a lethal autosomal-recessive disorder with congenital cataracts, hearing loss, and low serum copper and ceruloplasmin.

P. Huppke, S. Kaler, J. Christodoulou, 2012, American journal of human genetics.

The mole genome reveals regulatory rearrangements associated with adaptive intersexuality

A. Meyer, A. Visel, S. Mundlos, 2020, Science.

A DNA microarray for fission yeast: minimal changes in global gene expression after temperature shift

S. Haas, M. Vingron, A. Gusnanto, 2004, Yeast.

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

S. Haas, Wei Chen, H. Richard, 2009, The HUGO Journal.

Rare GABRA3 variants are associated with epileptic seizures, encephalopathy and dysmorphic features

P. May, R. Krause, S. Haas, 2017, Brain : a journal of neurology.

Survey of brain-expressed genes in a 7.3 mb region on proximal xp involved in non-syndromic X-linked mental retardation

J. Gécz, C. Scharff, S. Haas, 2003 .