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I Vater

Explore the profile of I Vater including associated specialties, affiliations and a list of published articles. Areas
Snapshot
Articles 7
Citations 164
Followers 0
Related Specialties
Oncology
Hematology
Gynecology & Obstetrics
Top 10 Co-Authors
R Siebert
J Richter
S Gesk
A Caliebe
O Ammerpohl
H Plendl
M Montesinos-Rongen
O D Wiestler
I Nagel
M Deckert
Published In
Leukemia
Eur J Med Genet
Mol Genet Metab
Prenat Diagn
Affiliations
Soon will be listed here.
Recent Articles
1.
The mutational pattern of primary lymphoma of the central nervous system determined by whole-exome sequencing
Vater I, Montesinos-Rongen M, Schlesner M, Haake A, Purschke F, Sprute R, et al.
Leukemia . 2014 Sep; 29(3):677-85. PMID: 25189415
To decipher the mutational pattern of primary CNS lymphoma (PCNSL), we performed whole-exome sequencing to a median coverage of 103 × followed by mutation verification in 9 PCNSL and validation...
2.
Base-pair resolution DNA methylome of the EBV-positive Endemic Burkitt lymphoma cell line DAUDI determined by SOLiD bisulfite-sequencing
Kreck B, Richter J, Ammerpohl O, Barann M, Esser D, Petersen B, et al.
Leukemia . 2013 Jan; 27(8):1751-3. PMID: 23307032
No abstract available.
3.
Bladder exstrophy and extreme genital anomaly in a patient with pure terminal 1q deletion: expansion of phenotypic spectrum
Zaki M, Gillessen-Kaesbach G, Vater I, Caliebe A, Siebert R, Kamel A, et al.
Eur J Med Genet . 2011 Nov; 55(1):43-8. PMID: 22061479
We describe a 5 2/12 years old male patient with a de novo deletion 1q43q44 of approximately 10.4 Mb in size. The boy presented with the classic features of chromosome...
4.
Maternal uniparental disomy 15 in a fetus resulting from a balanced familial translocation t(2;15)(p11;q11.2)
Heidemann S, Plendl H, Vater I, Gesk S, Exeler-Telker J, Grote W, et al.
Prenat Diagn . 2010 Jan; 30(2):183-5. PMID: 20063327
No abstract available.
5.
A 439 kb-sized homozygous deletion in 17p13.3 leading to biallelic loss of the ASPA as cause of Canavan disease detected by SNP-array analysis
Caliebe A, Vater I, Plendl H, Gesk S, Siebert R, Cremer F, et al.
Mol Genet Metab . 2009 Nov; 99(2):184-5. PMID: 19932039
No abstract available.
6.
Biallelic inactivation of TRAF3 in a subset of B-cell lymphomas with interstitial del(14)(q24.1q32.33)
Nagel I, Bug S, Tonnies H, Ammerpohl O, Richter J, Vater I, et al.
Leukemia . 2009 Aug; 23(11):2153-5. PMID: 19693093
No abstract available.
7.
Chromosomal imbalances and partial uniparental disomies in primary central nervous system lymphoma
Schwindt H, Vater I, Kreuz M, Montesinos-Rongen M, Brunn A, Richter J, et al.
Leukemia . 2009 Jun; 23(10):1875-84. PMID: 19494841
To determine the pattern of genetic alterations in primary central nervous system lymphomas (PCNSL), 19 PCNSL were studied by high-density single-nucleotide polymorphism arrays. Recurrent losses involved 6p21.32, 6q21, 8q12-12.2, 9p21.3,...