Han Brunner

Research activity per year

146 Article
8 Erratum / corrigendum / retractions
6 Editorial
3 (Systematic) Review article
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2021
Liquid biopsy: state of reproductive medicine and beyond
Schobers, G., Koeck, R., Pellaers, D., Stevens, S. J. C., Macville, M. V. E., Paulussen, A. D. C., Coonen, E., van den Wijngaard, A., de Die-Smulders, C., de Wert, G., Brunner, H. G. & Zamani Esteki, M., 18 Oct 2021, In: Human Reproduction. 36, 11, p. 2824-2839 16 p.
Research output: Contribution to journal › (Systematic) Review article › peer-review

Open Access
2019
Meta-analysis and multidisciplinary consensus statement: exome sequencing is a first-tier clinical diagnostic test for individuals with neurodevelopmental disorders
Srivastava, S., Love-Nichols, J. A., Dies, K. A., Ledbetter, D. H., Martin, C. L., Chung, W. K., Firth, H., Frazier, T., Hansen, R. L., Prock, L., Brunner, H., Hoang, N., Scherer, S. W., Sahin, M., Miller, D. T., Restrepo, B., Shankar, S., Riggs, E. R., Constantinou, P. & Reed-Weston, A. & 6 others, Tong, R. S., Howe, J., Buchanan, J., Fisher, R., Mahida, S. & NDD Exome Scoping Review Work Group, Nov 2019, In: Genetics in Medicine. 21, 11, p. 2413-2421 9 p.
Research output: Contribution to journal › (Systematic) Review article › peer-review

Open Access
2018
PURA syndrome: clinical delineation and genotype-phenotype study in 32 individuals with review of published literature
Reijnders, M. R. F., Janowski, R., Alvi, M., Self, J. E., van Essen, T. J., Vreeburg, M., Rouhl, R. P. W., Stevens, S. J. C., Stegmann, A. P. A., Schieving, J., Pfundt, R., Dijk, K., Smeets, E., Stumpel, C. T. R. M., Bok, L. A., Cobben, J. M., Engelen, M., Mansour, S., Whiteford, M. & Chandler, K. E. & 32 others, Douzgou, S., Cooper, N. S., Tan, E.-C., Foo, R., Lai, A. H. M., Rankin, J., Green, A., Lonnqvist, T., Isohanni, P., Williams, S., Ruhoy, I., Carvalho, K. S., Dowling, J. J., Lev, D. L., Sterbova, K., Lassuthova, P., Neupauerova, J., Waugh, J. L., Keros, S., Clayton-Smith, J., Smithson, S. F., Brunner, H. G., van Hoeckel, C., Anderson, M., Clowes, V. E., Siu, V. M., Selber, P., Leventer, R. J., Nellaker, C., Niessing, D., DDD Study & Baralle, D., 1 Feb 2018, In: Journal of Medical Genetics. 55, 2, p. 104-113 10 p.
Research output: Contribution to journal › (Systematic) Review article › peer-review

Open Access

Han Brunner

Research output

Search results

Liquid biopsy: state of reproductive medicine and beyond

Meta-analysis and multidisciplinary consensus statement: exome sequencing is a first-tier clinical diagnostic test for individuals with neurodevelopmental disorders

PURA syndrome: clinical delineation and genotype-phenotype study in 32 individuals with review of published literature