Photo of Henrik Okkels
  • Denmark

20052020

Research output per year

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Research Output

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Conference abstract in journal
2020

Cell-based non-invasive prenatal testing (cbNIPT): an alternative to chorionic villus sampling to confirm diagnosis of unaffected fetuses following preimplantation genetic testing for monogenic disorders (PGT-M)

Toft, C. L. F., Ingerslev, H. J., Kesmodel, U. S., Hatt, L., Singh, R., Ravn, K., Hestbek, B., Christensen, I. B., Koelvraa, M., Jeppesen, L. D., Schelde, P., Vogel, I., Uldbjerg, N., Farlie, R., Sommer, S., Ostergaard, M. L. V., Jensen, A. N., Mogensen, H., Degn, B., Okkels, H. & 2 others, Ernst, A. & Pedersen, I. S., 1 Jul 2020, In : Human Reproduction. 35, suppl. 1, p. 79 1 p., O-182.

Research output: Contribution to journalConference abstract in journalResearchpeer-review

2019

Early experiences with screening for aneuploidy in preimplantation genetic testing for inherited disorders

Diemer, T., Toft, C. L. F., Hnida, C., Degn, B., Okkels, H., Ernst, A., Ingerslev, H. J. & Pedersen, I. S., 1 Oct 2019, In : European Journal of Human Genetics. 27, Suppl. 2, p. 1198-1199 2 p., P01.57A.

Research output: Contribution to journalConference abstract in journalResearchpeer-review

First reported Northern European with CABP2-related non-syndromic hearing loss

Hojland, A. T., Okkels, H. & Petersen, M. B., 2019, In : European Journal of Human Genetics. 27, Suppl. 2, p. 1225 1 p., P02.22D.

Research output: Contribution to journalConference abstract in journalResearchpeer-review

Open Access

Identification of a Novel Silent Exonic Point Mutation in the NF1 Gene Causing Partial Exon 9 Skipping

Hoejland, A. T., Lolas, I., Diemer, T., Okkels, H. & Petersen, M. B., 1 Jul 2019, In : European Journal of Human Genetics. 27, Suppl. 1, p. 291-292 2 p.

Research output: Contribution to journalConference abstract in journalResearchpeer-review

3 Citations (Scopus)
2013

Mother-to-offspring inheritance of MLH1 promotor hypermethylation

Højland, A. T., Okkels, H., Madsen, P. H., Jensen, T. D. & Petersen, M. B., Jun 2013, In : European Journal of Human Genetics. 21, s2, p. 309

Research output: Contribution to journalConference abstract in journalResearchpeer-review

Surgeons' query of family history are still crucial after implementation of MMR-screening with IHC in all CRC-patients

Lindberg, L. J., Holck, S., Okkels, H. & Bernstein, I., 2013, In : Familial Cancer. 12, 2 Suppl.

Research output: Contribution to journalConference abstract in journalResearchpeer-review

The utility of P16 in identifying Lynch Syndrome (LS)

Agander, T., Lindberg, L., Brixen, L., Okkels, H., Haska, M., Bernstein, I. & Holck, S., Mar 2013, In : APMIS - Journal of Pathology, Microbiology and Immunology. 121, Supl.135, p. 22 1 p., P2-3.

Research output: Contribution to journalConference abstract in journalResearchpeer-review

13 Citations (Scopus)
2008

In vitro functional analysis of missense mutations in hMLH1 and hMSH2 identified in Danish patients with colorectal cancer

Christensen, L. L., Kariola, R., Wikman, F., Sunde, L., Gerdes, A. M., Okkels, H., Brandt, C. A. & Bisgaard, M. L., 2008, In : European Journal of Cancer. p. 98 1 p.

Research output: Contribution to journalConference abstract in journalResearch