J. Ramser

Decreased expression of angiogenesis antagonist EFEMP1 in sporadic breast cancer is caused by aberrant promoter methylation and points to an impact of EFEMP1 as molecular biomarker (2009)

Sadr-Nabavi, A., Ramser, J., Volkmann, J., Naehrig, J., Wiesmann, F., Betz, B., ...

Classification of Non-Bacterial Osteitis: Retrospective study of clinical, immunological and genetic aspects in 89 patients (2007)

Jansson, A., Renner, E. D., Ramser, J., Mayer, A., Haban, M., Meindl, A., ...

Objective. To define non-bacterial osteitis (NBO) as a clinical entity possibly associated with autoimmune manifestations. Patients with sterile osteitis were analysed to develop diagnostic criteria....

Classification of Non-Bacterial Osteitis: Retrospective study of clinical, immunological and genetic aspects in 89 patients (2006)

Jansson, A., Renner, E. D., Ramser, J., Mayer, A., Haban, M., Meindl, A., ...

Objective. To define non-bacterial osteitis (NBO) as a clinical entity possibly associated with autoimmune manifestations. Patients with sterile osteitis were analysed to develop diagnostic criteria....

Classification of Non-Bacterial Osteitis: Retrospective study of clinical, immunological and genetic aspects in 89 patients (2006)

Jansson, A., Renner, E. D., Ramser, J., Mayer, A., Haban, M., Meindl, A., ...

Objective. To define non-bacterial osteitis (NBO) as a clinical entity possibly associated with autoimmune manifestations. Patients with sterile osteitis were analysed to develop diagnostic criteria....

The DNA sequence of the human X chromosome. (2005)

Ross, MT., Grafham, DV., Coffey, AJ, Scherer, S., McLay, K., Muzny, D., ...

An integrated, functionally annotated gene map of the DXS8026- ELK1 interval on human Xp11.3-Xp11.23: Potential hotspot for neurogenetic disorders (2002)

Thiselton,D. L., McDowall,J., Brandau,O., Ramser,J., D'Esposito,F., Bhattacharya,S. S., ...

Human chromosome Xp11.3-Xp11.23 encompasses the map location for a growing number of diseases with a genetic basis or genetic component. These include several eye disorders, syndromic and...

An integrated, functionally annotated gene map of the DXS8026- ELK1 interval on human Xp11.3-Xp11.23: Potential hotspot for neurogenetic disorders (2002)

Thiselton, D. L., McDowall, J., Brandau, O., Ramser, J., D'Esposito, F., Bhattacharya, S. S., ...

Human chromosome Xp11.3-Xp11.23 encompasses the map location for a growing number of diseases with a genetic basis or genetic component. These include several eye disorders, syndromic and...

Initial sequencing and analysis of the human genome (2001)

Lander, ES, Linton, LM, Birren, B, Nusbaum, C, Zody, MC, Baldwin, J, ...

The human genome holds an extraordinary trove of information about human development, physiology, medicine and evolution. Here we report the results of an international collaboration to produce and...

Preselection of shotgun clones by oligonucleotide fingerprinting: an efficient and high throughput strategy to reduce redundancy in large- scale sequencing projects (1998)

Radelof, U, Hennig, S, Seranski, P, Steinfath, M, Ramser, J, Reinhardt, R, ...

Hybridization of microsatellites to RAPD: a new source of polymorphic markers (1995)

Richardson, T., Cato, S., Ramser, J., Kahl, G., Weising, K.

Preselection of shotgun clones by oligonucleotide fingerprinting: an efficient and high throughput strategy to reduce redundancy in large-scale sequencing projects.

Radelof, U, Hennig, S, Seranski, P, Steinfath, M, Ramser, J, Reinhardt, R, ...

Large-scale genomic sequencing projects generally rely on random sequencing of shotgun clones, followed by different gap closing strategies. To reduce the overall effort and cost of those projects...

Hybridization of microsatellites to RAPD: a new source of polymorphic markers.

Richardson, T, Cato, S, Ramser, J, Kahl, G, Weising, K

Preselection of shotgun clones by oligonucleotide fingerprinting: an efficient and high throughput strategy to reduce redundancy in large-scale sequencing projects.

Radelof, U, Hennig, S, Seranski, P, Steinfath, M, Ramser, J, Reinhardt, R, ...

Large-scale genomic sequencing projects generally rely on random sequencing of shotgun clones, followed by different gap closing strategies. To reduce the overall effort and cost of those projects...

Hybridization of microsatellites to RAPD: a new source of polymorphic markers.

Richardson, T, Cato, S, Ramser, J, Kahl, G, Weising, K

A splice site mutation in the methyltransferase gene FTSJ1 in Xp11.23 is associated with non-syndromic mental retardation in a large Belgian family (MRX9)

Ramser, J, Winnepenninckx, B, Lenski, C, Errijgers, V, Platzer, M, Schwartz, C, ...

Mental retardation is the most frequent cause of serious handicap in children and young adults. The underlying causes of this heterogeneous condition are both acquired and genetically based. A...