Wanda Maria Gerding - Search Results

Year	Number of Results
2009	1
2013	1
2015	1
2018	1
2019	1
2022	1
2023	2
2024	0

1

Optical Genome Mapping Reveals and Characterizes Recurrent Aberrations and New Fusion Genes in Adult ALL.

Vieler LM, Nilius-Eliliwi V, Schroers R, Vangala DB, Nguyen HP, Gerding WM. Vieler LM, et al. Among authors: gerding wm. Genes (Basel). 2023 Mar 9;14(3):686. doi: 10.3390/genes14030686. Genes (Basel). 2023. PMID: 36980958 Free PMC article.

2

Novel NUP98::ASH1L Gene Fusion in Acute Myeloid Leukemia Detected by Optical Genome Mapping.

Tembrink M, Gerding WM, Wieczorek S, Mika T, Schroers R, Nguyen HP, Vangala DB, Nilius-Eliliwi V. Tembrink M, et al. Among authors: gerding wm. Cancers (Basel). 2023 May 27;15(11):2942. doi: 10.3390/cancers15112942. Cancers (Basel). 2023. PMID: 37296904 Free PMC article.

3

bHLH Transcription Factor Math6 Antagonizes TGF-β Signalling in Reprogramming, Pluripotency and Early Cell Fate Decisions.

Divvela SSK, Nell P, Napirei M, Zaehres H, Chen J, Gerding WM, Nguyen HP, Gao S, Brand-Saberi B. Divvela SSK, et al. Among authors: gerding wm. Cells. 2019 Jun 2;8(6):529. doi: 10.3390/cells8060529. Cells. 2019. PMID: 31159500 Free PMC article.

4

Excessive brain iron accumulation in spinocerebellar ataxia type 17.

Claassen J, Gerding WM, Kastrup O, Uslar E, Goericke S, Timmann D. Claassen J, et al. Among authors: gerding wm. Neurology. 2015 Jan 13;84(2):212-3. doi: 10.1212/WNL.0000000000001141. Neurology. 2015. PMID: 25583826 No abstract available.

5

Broad genomic workup including optical genome mapping uncovers a DDX3X: MLLT10 gene fusion in acute myeloid leukemia.

Nilius-Eliliwi V, Tembrink M, Gerding WM, Lubieniecki KP, Lubieniecka JM, Kankel S, Liehr T, Mika T, Dimopoulos F, Döhner K, Schroers R, Nguyen HHP, Vangala DB. Nilius-Eliliwi V, et al. Among authors: gerding wm. Front Oncol. 2022 Sep 9;12:959243. doi: 10.3389/fonc.2022.959243. eCollection 2022. Front Oncol. 2022. PMID: 36158701 Free PMC article.

6

Hereditary motor and sensory neuropathy (HMSN) type X1 in an Argentinean family reveals independent GJB1/Cx32 mutations at the identical nucleotide position.

Gerding WM, Koetting J, Rey LP, Bibas Bonet H, Abdala ME, Mazzeo A, Mostacciuolo ML, Arning L, Carrero-Valenzuela R. Gerding WM, et al. Mol Cell Probes. 2013 Jun-Aug;27(3-4):118-21. doi: 10.1016/j.mcp.2013.01.002. Epub 2013 Feb 4. Mol Cell Probes. 2013. PMID: 23384994

7

Frequency of SCA8, SCA10, SCA12, SCA36, FXTAS and C9orf72 repeat expansions in SCA patients negative for the most common SCA subtypes.

Aydin G, Dekomien G, Hoffjan S, Gerding WM, Epplen JT, Arning L. Aydin G, et al. Among authors: gerding wm. BMC Neurol. 2018 Jan 9;18(1):3. doi: 10.1186/s12883-017-1009-9. BMC Neurol. 2018. PMID: 29316893 Free PMC article.

8

Hereditary motor and sensory neuropathy caused by a novel mutation in LITAF.

Gerding WM, Koetting J, Epplen JT, Neusch C. Gerding WM, et al. Neuromuscul Disord. 2009 Oct;19(10):701-3. doi: 10.1016/j.nmd.2009.05.006. Epub 2009 Jun 21. Neuromuscul Disord. 2009. PMID: 19541485

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