Reinhard Ullmann

发表

CGHPRO – A comprehensive data analysis tool for array CGH

Wei Chen, Fikret Erdogan, H.-Hilger Ropers, 2005, BMC Bioinformatics.

GenomeCAT: a versatile tool for the analysis and integrative visualization of DNA copy number variants

Reinhard Ullmann, Katrin Tebel, Vivien Boldt, 2017, BMC Bioinformatics.

Mapping translocation breakpoints by next-generation sequencing.

Martin Vingron, Marcel H. Schulz, Fikret Erdogan, 2008, Genome research.

Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia.

Fikret Erdogan, Reinhard Ullmann, Wei Chen, 2007, Human molecular genetics.

Complex inheritance pattern resembling autosomal recessive inheritance involving a microdeletion in thrombocytopenia-absent radius syndrome.

Reinhard Ullmann, Stefan Mundlos, Lynn Greenhalgh, 2007, American journal of human genetics.

Gene amplification as double minutes or homogeneously staining regions in solid tumors: origin and structure.

Domenico Trombetta, Reinhard Ullmann, Peter F Ambros, 2010, Genome research.

The position of pulmonary carcinoids within the spectrum of neuroendocrine tumors of the lung and other tissues

Reinhard Ullmann, Helmut H Popper, P. Hasleton, 2002, Genes, chromosomes & cancer.

Truncation of the Down syndrome candidate gene DYRK1A in two unrelated patients with microcephaly.

Reinhard Ullmann, Zeynep Tümer, Niels Tommerup, 2008, American journal of human genetics.

Array CGH identifies reciprocal 16p13.1 duplications and deletions that predispose to autism and/or mental retardation

Fikret Erdogan, Reinhard Ullmann, Wei Chen, 2007, Human mutation.

Breakpoint analysis of balanced chromosome rearrangements by next-generation paired-end sequencing

Reinhard Ullmann, Wei Chen, Hao Hu, 2010, European Journal of Human Genetics.

A balanced chromosomal translocation disrupting ARHGEF9 is associated with epilepsy, anxiety, aggression, and mental retardation

Reinhard Ullmann, Cheng Fang, Kirsten Harvey, 2009, Human mutation.

Deep sequencing reveals 50 novel genes for recessive cognitive disorders

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

A Cohort of Balanced Reciprocal Translocations Associated with Dyslexia: Identification of Two Putative Candidate Genes at DYX1

Carsten Elbro, Reinhard Ullmann, Asli Silahtaroglu, 2010, Behavior genetics.

Amplification and translocation of 3q26 with overexpression of EVI1 in Fanconi anemia‐derived childhood acute myeloid leukemia with biallelic FANCD1/BRCA2 disruption

Reinhard Ullmann, Crispin Miller, Crispin J. Miller, 2007, Genes, chromosomes & cancer.

Deletion of 7q34–q36.2 in two siblings with mental retardation, language delay, primary amenorrhea, and dysmorphic features

Reinhard Ullmann, Zeynep Tümer, Niels Tommerup, 2010, American journal of medical genetics. Part A.

Expanding the clinical spectrum associated with defects in CNTNAP2 and NRXN1

Reinhard Ullmann, Juliane Hoyer, Arif B Ekici, 2011, BMC Medical Genetics.