Bernd Wollnik

Has grant

Germany

Research Interests

Explore related searches

Professors in Germany Professors in Medical Science Medical Science professors in Germany

Contact this professor

Get a free first email built on one of their papers, ready for you to edit and send yourself.

Recent Grants

Grant: Close

Clinical Research Unit 5002 Deciphering genome dynamics for subtype-specific therapy in pancreatic cancer / CP 1 Translational platform for PDAC models and drug response validation

Open Date:

Close Date:

Grant: Close

SFB1002 Modulatory Units in Heart Failure / D02 Novel mechanisms of genome instability in the failing heart

Open Date:

Close Date:

Grant: Close

Excellence Cluster: Multiscale Bioimaging: from Molecular Machines to Networks of Excitable Cells (MBExC 2067/1)

Open Date:

Close Date:

Grant: Close

FOR 2800 Chromosome Instability: Cross-talk of DNA replication stress and mitotic dysfunction / SP 5 Impaired chromosome integrity caused by mutations in members of the BTR complex

Open Date:

Close Date:

Grant: Close

FOR 2800 Chromosome Instability: Cross-talk of DNA replication stress and mitotic dysfunction / SP Z NGS-based approaches for systematic analysis of genomic and chromosome instability

Open Date:

Close Date:

Articles (11)

Year:

2023

Year:

2023

Year:

2023

Year:

2022

Year:

2022

Year:

2022

Year:

2022

Year:

2022

Year:

2022

Year:

2022

Year:

2022

Collaborators (2)

Hauke Hillen

Assistant Professor

University Medical Center Göttingen

GERMANY

View details

Barbara Vona

GERMANY

View details

ApplyKite TwinLearns as you apply

Make your next move.

Prepare your application

Review drafts before you send them.

Bernd Wollnik

Research Interests

Explore related searches

Contact this professor

Recent Grants

Articles (11)

Expanding the spectrum of EEF1D neurodevelopmental disorders: Biallelic variants in the guanine exchange domain

Homozygous loss-of-function variants in FILIP1 cause autosomal recessive arthrogryposis multiplex congenita with microcephaly

The genetic spectrum of congenital ocular motor apraxia type Cogan: an observational study, continued

<i>WARS1</i> and <i>SARS1</i> : Two tRNA synthetases implicated in autosomal recessive microcephaly

Evaluation of growth, puberty, osteoporosis, and the response to long-term bisphosphonate therapy in four patients with osteoporosis-pseudoglioma syndrome.

A novel single-cell RNA-sequencing approach and its applicability connecting genotype to phenotype in ageing disease

Doxorubicin induces cardiotoxicity in a pluripotent stem cell model of aggressive B cell lymphoma cancer patients

GJB2-RELATED NON-SYNDROMIC HEARING LOSS VARIANTS' SPECTRUM AND THEIR FREQUENCY IN TURKISH POPULATION

Mutations in PYCR1 cause cutis laxa with progeroid features (vol 41, pg 1016, 2009)

Phenotypic spectrum of BLM- and RMI1-related Bloom syndrome

Progressive frontal intraosseous lipoma: Detection of the mosaic AKT1 variant discloses Proteus syndrome

Collaborators (2)

Hauke Hillen

Barbara Vona

Make your next move.