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Henrik Okkels

  • Denmark

20052019
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  • 19 Similar Profiles
Hereditary Nonpolyposis Colorectal Neoplasms Medicine & Life Sciences
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Mutation Medicine & Life Sciences
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Research Output 2005 2019

Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database

Dominguez-Valentin, M., Sampson, J. R., Seppälä, T. T., Ten Broeke, S. W., Plazzer, J-P., Nakken, S., Engel, C., Aretz, S., Jenkins, M. A., Sunde, L., Bernstein, I., Capella, G., Balaguer, F., Thomas, H., Evans, D. G., Burn, J., Greenblatt, M., Hovig, E., de Vos Tot Nederveen Cappel, W. H., Sijmons, R. H. & 68 others, Bertario, L., Tibiletti, M. G., Cavestro, G. M., Lindblom, A., Della Valle, A., Lopez-Köstner, F., Gluck, N., Katz, L. H., Heinimann, K., Vaccaro, C. A., Büttner, R., Görgens, H., Holinski-Feder, E., Morak, M., Holzapfel, S., Hüneburg, R., Knebel Doeberitz, M. V., Loeffler, M., Rahner, N., Schackert, H. K., Steinke-Lange, V., Schmiegel, W., Vangala, D., Pylvänäinen, K., Renkonen-Sinisalo, L., Hopper, J. L., Win, A. K., Haile, R. W., Lindor, N. M., Gallinger, S., Le Marchand, L., Newcomb, P. A., Figueiredo, J. C., Thibodeau, S. N., Wadt, K., Therkildsen, C., Okkels, H., Ketabi, Z., Moreira, L., Sánchez, A., Serra-Burriel, M., Pineda, M., Navarro, M., Blanco, I., Green, K., Lalloo, F., Crosbie, E. J., Hill, J., Denton, O. G., Frayling, I. M., Rødland, E. A., Vasen, H., Mints, M., Neffa, F., Esperon, P., Alvarez, K., Kariv, R., Rosner, G., Pinero, T. A., Gonzalez, M. L., Kalfayan, P., Tjandra, D., Winship, I. M., Macrae, F., Möslein, G., Mecklin, J-P., Nielsen, M. & Møller, P., 24 Jul 2019, In : Genetics in Medicine.

Research output: Contribution to journalJournal articleResearchpeer-review

Open Access
Hereditary Nonpolyposis Colorectal Neoplasms
DNA Mismatch Repair
Neoplasm Genes
Databases
Endometrial Neoplasms

Detection of PMS2 mutations by screening hereditary nonpolyposis colon cancer families from Denmark and Sweden

Okkels, H., Lagerstedt-Robinsson, K., Wikman, F. P., Hansen, T. V. O., Lolas, I., Lindberg, L. J. & Krarup, H. B., 1 Sep 2019, In : Genetic Testing and Molecular Biomarkers. 23, 9, p. 688-695 8 p.

Research output: Contribution to journalJournal articleResearchpeer-review

Hereditary Nonpolyposis Colorectal Neoplasms
Denmark
Sweden
DNA Mismatch Repair
Mutation

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
115 Downloads (Pure)

First reported adult patient with TARP syndrome: A case report

Højland, A. T., Lolas, I., Okkels, H., Lautrup, C. K., Diness, B. R., Petersen, M. B. & Nielsen, I. K., Dec 2018, In : American Journal of Medical Genetics. Part A. 176, 12, p. 2915-2918 4 p.

Research output: Contribution to journalJournal articleResearchpeer-review

Open Access
File
Pierre Robin Syndrome
Nose
Intellectual Disability
Micrognathism
Siblings

Activities 2005 2014

Ion Torrent Complete Workflow - from Design to Interpretation.

Henrik Okkels (Lecturer)
28 Oct 2014

Activity: Talks and presentationsTalks and presentations in private or public companies

DSMOME - Current Status on the Clinical Use of NGS in Denmark

Henrik Okkels (Participant)
28 Oct 2014

Activity: Attending an eventOrganisation or participation in workshops, courses, or seminars

HNPCC-registrets årsmøde

Henrik Okkels (Participant)
2014

Activity: Attending an eventOrganisation or participation in workshops, courses, or seminars

Ion Torrent™ user group meeting

Henrik Okkels (Participant)
2014

Activity: Attending an eventOrganisation or participation in workshops, courses, or seminars

The 5th TECHGENE Meeting

Henrik Okkels (Participant)
21 Nov 2013

Activity: Attending an eventOrganisation or participation in workshops, courses, or seminars