Ute Moog
Overview
Explore the profile of Ute Moog including associated specialties, affiliations and a list of published articles.
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Snapshot
Articles
76
Citations
2526
Followers
0
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Recent Articles
1.
Paneque M, Serra Juhe C, Melegh B, Carreira I, Moog U, Liehr T
Med Genet
. 2024 Jun;
34(1):81-83.
PMID: 38836018
No abstract available.
2.
Paneque M, Serra Juhe C, Melegh B, Carreira I, Moog U, Liehr T
Med Genet
. 2024 Jun;
34(2):189-191.
PMID: 38835907
[This corrects the article DOI: 10.1515/medgen-2022-2116.].
3.
Kolvenbach C, Felger T, Schierbaum L, Thiffault I, Pastinen T, Szczepanska M, et al.
J Med Genet
. 2022 Nov;
60(6):587-596.
PMID: 36379543
Background: is thought to play an important role in cytoskeletal modification and development of the early nervous system. Previously, single-nucleotide variants (SNVs) or copy number variations (CNVs) in have been...
4.
Morison L, Meffert E, Stampfer M, Steiner-Wilke I, Vollmer B, Schulze K, et al.
J Med Genet
. 2022 Nov;
60(6):597-607.
PMID: 36328423
Background: Heterozygous disruptions of were the first identified molecular cause for severe speech disorder: childhood apraxia of speech (CAS), and yet few cases have been reported, limiting knowledge of the...
5.
Paneque M, Liehr T, Serra Juhe C, Moog U, Melegh B, Carreira I
Eur J Hum Genet
. 2022 Mar;
30(6):639-640.
PMID: 35283482
No abstract available.
6.
Gieldon L, Jauch A, Obeid K, Kaufmann L, Hinderhofer K, Haug U, et al.
Am J Med Genet A
. 2021 Feb;
185(4):1261-1265.
PMID: 33577136
Haploinsufficiency of AUTS2 has been associated with neurodevelopmental disorders and dysmorphic features (MIM # 615834). More than 50 patients have been described, mostly carrying de novo deletions of one or...
7.
Schwaibold E, Beygo J, Obeid K, Jauch A, Hinderhofer K, Moog U
Am J Med Genet A
. 2020 Nov;
185(2):549-554.
PMID: 33191647
Silver-Russell syndrome (SRS) is characterized by pre- and postnatal growth deficiency. It is most often caused by hypomethylation of the paternal imprinting center 1 of chromosome 11p15.5. In contrast, Sotos...
8.
Essinger C, Karch S, Moog U, Fekete G, Lengyel A, Pinti E, et al.
Clin Epigenetics
. 2020 May;
12(1):63.
PMID: 32393365
Background: Beckwith-Wiedemann syndrome (BWS) is an imprinting disorder caused by disturbances of the chromosomal region 11p15.5. The most frequent molecular finding in BWS is loss of methylation (LOM) of the...
9.
Moog U, Felbor U, Has C, Zirn B
Dtsch Arztebl Int
. 2020 Mar;
116(8):119-125.
PMID: 32181732
Background: Genetic mosaics arise through new mutations occurring after fertiliza- tion (i.e., postzygotic mutations). Mosaics have been described in recent years as the cause of many different disorders; many of...
10.
Toberer F, Moog U, Enk A, Hartschuh W
J Dtsch Dermatol Ges
. 2020 Mar;
18(3):247-250.
PMID: 32130766
No abstract available.