Hans Rudolf Lytchoff Eiberg
Associate Professor
Medical Genetics Program
Blegdamsvej 3, 2200 København N.
- 1998
- Published
Molecular genetic, clinical and psychiatric associations in nocturnal enuresis
Hollmann, E., Gontard, A. V., Eiberg, Hans Rudolf Lytchoff, Rittig, S. & Lemkuhl, G., 1998, In: British Journal of Urology. 81, suppl. 3, p. 37-39Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Molecular genetics of nocturnal enuresis: Clinical and genetic heterogeneity
Gontard, A. V., Eiberg, Hans Rudolf Lytchoff, Hollmann, E., Rittig, S. & Lehmkuhl, G., 1998, In: Acta Paediatrica. 87, p. 571-578Research output: Contribution to journal › Journal article › Research › peer-review
- Published
The Ala/Val98 Polymorphism of the Hepatocyte Nuclear Factor-1a Gene Contributes to the Interindividual Variation in Serum C-Peptide Response during an Oral Glucose Tolerance Test: Evidence from.....
Urhammer, S. A., Hansen, T., Ekstrøm, C. T., Eiberg, Hans Rudolf Lytchoff & Pedersen, O., 1998, In: Journal of Clinical Endocrinology and Metabolism. Vol. 83, No 12, p. 4506-4509Research output: Contribution to journal › Journal article › Research › peer-review
- Published
The effect of two frequent amino acid variant of the hepatocyte nuclear fact.-1a gene on estimates of pancr.ß-cell funct. in caucasian glucose-tolerant first-degree relatives of tp.2 diabetic ptt.
Urhammer, S. A., Møller, A. M., Nyholm, B., Ekstrøm, C. T., Eiberg, Hans Rudolf Lytchoff, Clausen, J. O., Hansen, T., Pedersen, O. & Schmitz, O., 1998, In: Journal of Clinical Endocrinology and Metabolism. Vol. 83, no. 11, p. 3992-3995Research output: Contribution to journal › Journal article › Research › peer-review
- Published
The g/a Nucleotide Variant at Position -30 in the *Gb-Cell-Specific Glucokinase Gene Promotor Has No Impact on the *Gb-Cell Function in Danish Caucasians
Urhammer, S. A., Hansen, T., Clausen, J. O., Eiberg, Hans Rudolf Lytchoff & Pedersen, O., 1998, In: Diabetes. 47, p. 1359-1361Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Total Genome Scan Analysis in a Single Extended Family for Primary Nocturnal Enuresis: Evidence for a New Locus (ENUR3) for Primary Nocturnal Enuresis on Chromosome 22q11
Eiberg, Hans Rudolf Lytchoff, 1998, In: European Urology. 33 (suppl 3), p. 34-36Research output: Contribution to journal › Journal article › Research › peer-review
- 1997
- Published
(1997) Clinical enuresis phenotypes in familial nocturnal enuresis
Gontard, A. V., Hollmann, E., Benden, B., Eiberg, Hans Rudolf Lytchoff, Rittig, S. & Lehmkuhl, G., 1997, In: Scandinavian Journal of Urology and Nephrology. 31 (suppl.183), p. 11-16Research output: Contribution to journal › Journal article › Research › peer-review
- Published
A Survey of the Newborn Populations in Belgium, Germany, Poland, Czech Republic, Hungary, Bulgaria, Spain, Turkey and Japan for the G985 Variant Allele with Haplotype Analysis at the Medium Chain Acyl-CoA Dehydrogenase Gene. Locus: Clinical and Evol.Con.
Tanaka, K., Gregersen, N., Ribes, A., Kim, J., Kølvraa, S., Winter, V. S., Eiberg, Hans Rudolf Lytchoff, Martinez, G., Deufel, T., Leifert, B., Santer, R., Francois, B., Pronicka, E., Laszlo, A., Kmoch, S., Kremensky, I., Kalaydjicva, L., Ozalp, I. & Ito, M., 1997, In: Pediatric Research. vol 41, 2, p. 201-209Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Assignment of human plasma methylumbelliferyl-tetra-N-acetylchitotetraoside hydrolase or chitinase to chromosome 1 q by a linkage study
Eiberg, Hans Rudolf Lytchoff & Tandt, W. R. D., 1997, In: Human Genetics. 101, p. 205-207Research output: Contribution to journal › Journal article › Research › peer-review
- Published
CAG repeat expansion in autosomal dominant pure spastic paraplegia linked to chromosome 2p21-p24
Nielsen, J. E., Koefoed, P., Abell, K., Eiberg, Hans Rudolf Lytchoff, Fenger, K., Niebuhr, E. & Sørensen, S. A., 1997, In: Human Molecular Genetics. Vol. 6, No. 11, p. 1811-1816Research output: Contribution to journal › Journal article › Research › peer-review
ID: 5291
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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
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1887
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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
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Sequencing and de novo assembly of 150 genomes from Denmark as a population reference
Research output: Contribution to journal › Letter › Research › peer-review
Published