Hans Rudolf Lytchoff Eiberg
Associate Professor
Medical Genetics Program
Blegdamsvej 3, 2200 København N.
Born d. 8.4.45.
education
Cand. scient., Copenhagen University: Spring 1970 Biochemistry, Specialism: Plant physiology
professional experiences
- 1971-75 Adjunct Copenhagen University, Department of Medical Genetics since April 1, 1971
- 1975- Lecture; Assoc. professor
- 1980- Project leader, Family bank (RC-link), the Panum Institute.
- 1994- Group leader, Genome Group/RC-link, the Panum Institute.
areas of research interest
- Copenhagen Family Bank (RC-Link) 850 normal families (more than 3 children)
- Genetic and molecular mechanisms in developmental of inherited disorders and normal traits.
- Epidermologic research.
- Mapping, isolation and identifications of normal and disease genes.
- Eyes diseases, skin diseases, psykiatric diseases, normal traits.
- Computer programming.
organisations
- Member of the Human Genome Organization (HUGO)
- Member of the Danish Society of Medical Genetics
- Member of the European Society of Human Genetics
editorial
referee at Human Genetics, Clinical Genetics, Genomic
honours
Silver Medal 1972, University of Aarhus.
awards
1989: -Hede Nielsen Family Fondsi
invited speaker
- Speaker at Congresses, Courses and Workshops in Toronto, Oxford, London,
Verona. - Vice Chairman Human Genemapping 9 (chromosome
professor evaluation
Professor competance, University of Copenhagen 1994.
supervisor for
- Scolar-students: Marie-Louise Bisgaard, Ida Berendt, µslaug Jon sd¢ttir
- (Ph.D. Søren Eckwald, Ph.D Yang Huan Ming)
scientific activities
Prisopgave, Århus University 1972: Silver Medal, topic: Comparison and use of the new band differentiating techniques for human chromosomes. p. 1-165.
Invited speaker Toronto, Oxford, London, Verona. Vice Chairman: Human Gene Mapping 9 (chromosome 17-19) in Paris 1987.
Development of laboratory for mapping the human genome: Including collection of personal data and blood samples. Establishment of methods for antibody production, synthesis of ampholine, separation, storage, cultivation, transformation, thawing and typing of genetic polymorphisms in enzymes, proteins, chromosomes, DNA (RFLP and PCR), senses and various external traits. Programming in UNIX-Solaris, VAX-VMS, DOS, FORTRAN, DBASE4. Linkage analysis with the programs LIPED, SIMLINK, LINKAGE, EXCLUDE,
AUTOLIPED and drawprograms CYRILLIC and MEGABASE. Initiated establishment of a cDNA library from lenses.
Explored 22 diseases with the primary purpose of chromosomal localization of gene defects, including more than 10 diseases localized for the first time in our laboratory. Examined 80 "classical" marker systems, including 20 localized for the first time through linkage to another marker.
ID: 5291
Most downloads
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4563
downloads
Family and population-based studies of variation within the ghrelin receptor locus in relation to measures of obesity
Research output: Contribution to journal › Journal article › Research › peer-review
Published -
1887
downloads
A 3.2 Mb deletion on 18q12 in a patient with childhood autism and high-grade myopia.
Research output: Contribution to journal › Journal article › Research › peer-review
Published -
408
downloads
Sequencing and de novo assembly of 150 genomes from Denmark as a population reference
Research output: Contribution to journal › Letter › Research › peer-review
Published