Molecular genetics & genomic medicine

ISSNs: 2324-9269

Additional searchable ISSN (electronic): 2324-9269

John Wiley and Sons Inc.

Scopus rating (2024): CiteScore 3 SJR 0.611 SNIP 0.804

Indexed in DOAJ

Journal

Titles	Molecular genetics & genomic medicine Molecular genetics & genomic medicine Molecular Genetics and Genomic Medicine
Additional searchable titles	Molecular Genetics and Genomic Medicine
ISSNs	2324-9269
Additional searchable ISSN (electronic)	2324-9269
Publisher	John Wiley and Sons Inc.
ZDB-ID	2734884-2

Keywords

ASJC Scopus subject areas

Library keywords

610 Medicine and health

A rare PALB2 germline variant causing G2/M cell cycle arrest is associated with isolated myelosarcoma in infancy

Beer, A., Beck, R., Schedel, A., von Bonin, M., Meinel, J., Friedrich, U. A. & Menzel, M. & 7 others, Suttorp, M., Brenner, S., Fitze, G., Lange, B., Knöfler, R., Hauer, J. & Auer, F., Aug 2021, In: Molecular genetics & genomic medicine. 9, 9, p. e1746 e1746.

Research output: Contribution to journal › Research article › Contributed › peer-review

Constitutional de novo and postzygotic mutations in isolated cases of cerebral cavernous malformations.

Rath, M., Spiegler, S., Nath, N., Schwefel, K., Di Donato, N., Gerber, J. & Korenke, G. C. & 8 others, Hellenbroich, Y., Hehr, U., Gross, S., Sure, U., Zoll, B., Gilberg, E., Kaderali, L. & Felbor, U., 2017, In: Molecular genetics & genomic medicine. 5, 1, p. 21-27 7 p.

Research output: Contribution to journal › Research article › Contributed › peer-review

High mutation detection rates in cerebral cavernous malformation upon stringent inclusion criteria: One-third of probands are minors

Spiegler, S., Najm, J., Liu, J., Gkalympoudis, S., Schrëoder, W., Borck, G. & Brockmann, K. & 24 others, Elbracht, M., Fauth, C., Ferbert, A., Freudenberg, L., Grasshoff, U., Hellenbroich, Y., Henn, W., Hoffjan, S., Hëuning, I., Korenke, G. C., Kroisel, P. M., Kunstmann, E., Mair, M., Munk-Schulenburg, S., Nikoubashman, O., Pauli, S., Rudnik-Schëoneborn, S., Sudholt, I., Sure, U., Tinschert, S., Wiednig, M., Zoll, B., Ginsberg, M. H. & Felbor, U., Mar 2014, In: Molecular Genetics and Genomic Medicine. 2, 2, p. 176-185 10 p.

Research output: Contribution to journal › Research article › Contributed › peer-review

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Research Portal of the TU Dresden

Molecular genetics & genomic medicine

Keywords

ASJC Scopus subject areas

Library keywords

Related content

A rare PALB2 germline variant causing G2/M cell cycle arrest is associated with isolated myelosarcoma in infancy

Constitutional de novo and postzygotic mutations in isolated cases of cerebral cavernous malformations.

High mutation detection rates in cerebral cavernous malformation upon stringent inclusion criteria: One-third of probands are minors