Thomas Haaf

发表

Genome-wide quantitative analysis of DNA methylation from bisulfite sequencing data

Achim Tresch, Kemal Akman, Thomas Haaf, 2014, Bioinform..

Erratum: The DNA sequence of human chromosome 21: The chromosome 21 mapping and sequencing consortium (Nature (2000) 405 (311-319))

Shinsei Minoshima, Susumu Mitsuyama, Yoshiyuki Sakaki, 2000 .

Chromosome-specific α-satellite DNA from the centromere of chimpanzee chromosome 4

Huntington F. Willard, Thomas Haaf, H. Willard, 1997, Chromosoma.

De novo mutations in HCN1 cause early infantile epileptic encephalopathy

Oriane Trouillard, Christel Depienne, Emmanuel Roze, 2014, Nature Genetics.

Disruption of CNTNAP2 and additional structural genome changes in a boy with speech delay and autism spectrum disorder

Thomas Haaf, Martin Poot, M. Poot, 2010, neurogenetics.

Gene panel testing of 5589 BRCA1/2‐negative index patients with breast cancer in a routine diagnostic setting: results of the German Consortium for Hereditary Breast and Ovarian Cancer

Nina Ditsch, Peter Nürnberg, Dieter Niederacher, 2018, Cancer medicine.

Analyses of the extent of shared synteny and conserved gene orders between the genome of Fugu rubripes and human 20q.

Thomas Haaf, Anthony R Green, Sarah F. Smith, 2002, Genome research.

Novel form of X-linked nonsyndromic hearing loss with cochlear malformation caused by a mutation in the type IV collagen gene COL4A6

Thomas Haaf, Clemens R Müller, T. Haaf, 2013, European Journal of Human Genetics.

Spatial, temporal and interindividual epigenetic variation of functionally important DNA methylation patterns

Achim Tresch, Thomas Haaf, K. Frauenknecht, 2010, Nucleic acids research.

Expression profiling of uniparental mouse embryos is inefficient in identifying novel imprinted genes.

Peter Nürnberg, Thomas Haaf, T. Haaf, 2006, Genomics.

Non-syndromic hearing loss gene identification: A brief history and glimpse into the future.

Thomas Haaf, T. Haaf, W. Shehata-Dieler, 2015, Molecular and cellular probes.