J. Hecht

J. Hecht, C. Harms, Sophie Schweizer, 2015, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

FGFR3 is a target of the homeobox transcription factor SHOX in limb development.

C. Rödelsperger, G. Rappold, J. Hecht, 2011, Human molecular genetics.

Saturation analysis of ChIP-seq data for reproducible identification of binding peaks

Matthias Truss, Peter Hansen, P. Robinson, 2015, Genome research.

The allele distribution in next-generation sequencing data sets is accurately described as the result of a stochastic branching process

Sebastian Bauer, Thorsten Dickhaus, Peter M. Krawitz, 2011, Nucleic acids research.

Efficient CRISPR/Cas9 genome editing with low off-target effects in zebrafish

Peter Krawitz, Verena Heinrich, Christian Haass, 2013, Development.

Homeobox genes d11-d13 and a13 control mouse autopod cortical bone and joint formation.

S. Mundlos, D. Duboule, J. Hecht, 2010, The Journal of clinical investigation.

Q-nexus: a comprehensive and efficient analysis pipeline designed for ChIP-nexus

P. Robinson, J. Hecht, Jonas Ibn-Salem, 2016, BMC Genomics.

IMSEQ - a fast and error aware approach to immunogenetic sequence analysis

Peter N. Robinson, Knut Reinert, Jochen Hecht, 2015, Bioinform..

An inversion involving the mouse Shh locus results in brachydactyly through dysregulation of Shh expression.

S. Mundlos, A. Helmrich, J. Hecht, 2005, The Journal of clinical investigation.

Mutational spectrum of adult T-ALL

S. Bohlander, H. Blum, P. Greif, 2014, Oncotarget.

Composite transcriptome assembly of RNA-seq data in a sheep model for delayed bone healing

Georg N Duda, Marten Jäger, Stefan Mundlos, 2011, BMC Genomics.

G6PC3 Deficiency Associated with Congenital Neutropenia and Enterocolitis

A. Schäffer, P. Robinson, S. Mundlos, 2011 .

An inversion involving the mouse Shh locus results in brachydactyly through dysregulation of Shh expression

S. Mundlos, A. Helmrich, E. Schröck, 2005 .

Whole-exome sequencing in adult ETP-ALL reveals a high rate of DNMT 3 A mutations

S. Bohlander, H. Blum, P. Greif, 2013 .

Missense variant in CCDC22 causes X-linked recessive intellectual disability with features of Ritscher-Schinzel/3C syndrome

P. Robinson, D. Horn, S. Mundlos, 2014, European Journal of Human Genetics.

A homozygous HOXD13 missense mutation causes a severe form of synpolydactyly with metacarpal to carpal transformation

S. Mundlos, M. Spielmann, Alexej Knaus, 2016, American Journal of Medical Genetics. Part A.

Estimating exome genotyping accuracy by comparing to data from large scale sequencing projects

T. Dickhaus, P. Robinson, D. Parkhomchuk, 2013 .

TCR Repertoire Analysis by Next Generation Sequencing Allows Complex Differential Diagnosis of T Cell–Related Pathology

P. Robinson, S. Mundlos, C. Rödelsperger, 2013, American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons.

Identification of a Novel Missense Mutation in EDAR Causing Autosomal Recessive Hypohidrotic Ectodermal Dysplasia with Bilateral Amastia and Palmoplantar Hyperkeratosis

S. Mundlos, P. Krawitz, J. Hecht, 2013 .

Extension of the sheep sequence space using composite transcriptome assembly of RNA-Seq data in a sheep model for delayed bone healing

P. Robinson, S. Mundlos, G. Duda, 2011 .

Whole‐exome sequencing identifies a novel missense mutation in EDAR causing autosomal recessive hypohidrotic ectodermal dysplasia with bilateral amastia and palmoplantar hyperkeratosis

S. Mundlos, P. Krawitz, J. Hecht, 2013, The British journal of dermatology.

Missense variant in CCDC22 causes X-linked recessive intellectual disability with features of Ritscher-Schinzel/3C syndrome

P. Robinson, D. Horn, S. Mundlos, 2015, European Journal of Human Genetics.

Strategies to improve the performance of rare variant association studies by optimizing the selection of controls

Peter N. Robinson, Tom Kamphans, Thorsten Dickhaus, 2015, Bioinform..

Copy-number variations involving the IHH locus are associated with syndactyly and craniosynostosis.

S. Mundlos, F. Garaci, Mahim Jain, 2011, American journal of human genetics.

Molecular mechanism of CHRDL1-mediated X-linked megalocornea in humans and in Xenopus model.

B. Seliger, P. Krawitz, E. Klopocki, 2015, Human molecular genetics.

PAX5 biallelic genomic alterations define a novel subgroup of B-cell precursor acute lymphoblastic leukemia

Michael P. Schroeder, H. Blum, P. Greif, 2019, Leukemia.

PGAP2 mutations, affecting the GPI-anchor-synthesis pathway, cause hyperphosphatasia with mental retardation syndrome.

P. Robinson, D. Horn, S. Mundlos, 2013, American journal of human genetics.