PM Kroisel

Medical University of Graz — Austria

Biochemistry, Genetics and Molecular Biology · Life Sciences

8h-index255citations14works0.02yr avg
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Research Topics

Genomic variations and chromosomal abnormalities(9), RNA modifications and cancer(3), Advanced biosensing and bioanalysis techniques(2), Genomics and Chromatin Dynamics(2), Chromosomal and Genetic Variations(2)

Publications14 total

Predictive diagnosis of the cancer prone Li–Fraumeni syndrome by accident: new challenges through whole genome array testing
Journal of Medical Genetics·2009· 74 citedOpen Access
Mental retardation in a girl with a subtelomeric deletion on chromosome 20q and complete deletion of the <i>myelin transcription factor 1</i> gene (<i>MYT1</i>)
Clinical Genetics·2008· 59 cited
3p25-Deletionssyndrom mit atrioventrikulärem Septumdefekt. Eine Genotyp-Phänotyp-Korrelation
Zeitschrift für Geburtshilfe und Neonatologie·2006
3p25-Deletionssyndrom mit atrioventrikulärem Septumdefekt. Eine Genotyp-Phänotyp-Korrelation
Neuropediatrics·2006
Breakage of the ERBB4-gene in a girl with reciprocal translocation t(1;2) (p22.3;q34) – Is there a relation to severe infantile epilepsy?
Neuropediatrics·2005
Molecular characterization of a unique <i>de novo</i> 15q deletion associated with Prader–Willi syndrome and central visual impairment
Clinical Genetics·2003· 17 cited
Characterisation of a 19-year-old "long-term survivor" with Edwards syndrome.
PubMed·2003· 21 cited
Chromosomal localization and genomic organization of the human Linker for Activation of T cells (LAT) gene
Cytogenetic and Genome Research·2002· 1 cited
Terminal tandem duplication of 16p: a case with "pure" partial trisomy (16)(pter-->p13).
PubMed·2002· 10 cited
Localization&lt;footref rid="foot01"&gt;&lt;sup&gt;1&lt;/sup&gt;&lt;/footref&gt; of the human anterior gradient-2 gene (AGR2) to chromosome band 7p21.3 by radiation hybrid mapping and fluorescencein situ hybridisation
Cytogenetic and Genome Research·2000· 32 cited
Assignment&lt;footref rid="foot01"&gt;&lt;sup&gt;1&lt;/sup&gt;&lt;/footref&gt; of STAC to human chromosome band 3p22.3 between D3S3718 and D3S1611
Cytogenetic and Genome Research·1999
Complete coding sequence, exon/intron arrangement and chromosome location of ZNF45, a KRAB-domain-containing gene
Cytogenetic and Genome Research·1996· 11 cited
Microdissection of a human marker chromosome reveals its origin and a new family of centromeric repetitive DNA
Human Molecular Genetics·1992· 28 cited
Simultaneous production of R-bands and either replication patterns or sister chromatid differentiation
Human Genetics·1985· 2 cited

Frequent Co-authors

Erwin Petek(8), Klaus Wagner(5), Christian Windpassinger(3), Thomas Schwarzbraun(2), A. Langmann(2), Barbara Plecko(2), W Rosenkranz(2), M Tschernigg(2), A Kaufhold(2), Johannes‐Peter Haas(2), H Tomczak(2), S Armbrust(2), H Tönnies(2), B Stiller(2), C Fusch(2), Anna C. Obenauf(1), U Gruber‐Sedlmayr(1), Michael R. Speicher(1), T Kroepfl(1), H. Egger(1)