Thomas Eggermann
Overview
Explore the profile of Thomas Eggermann including associated specialties, affiliations and a list of published articles.
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257
Citations
4211
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Recent Articles
1.
David S, Costa A, Hohenfeld C, Romanzetti S, Mirzazade S, Pahl J, et al.
J Alzheimers Dis
. 2025 Jan;
103(2):552-569.
PMID: 39814521
Background: Physical activity and fitness are major targets in Alzheimer's disease (AD) preventive research. However, current research is heterogeneous and often disregards the relationship between these parameters and disease outcomes....
2.
Schmidt A, Casadei N, Brand F, Demidov G, Vojgani E, Abolhassani A, et al.
PLoS Pathog
. 2024 Dec;
20(12):e1012786.
PMID: 39715278
Courses of SARS-CoV-2 infections are highly variable, ranging from asymptomatic to lethal COVID-19. Though research has shown that host genetic factors contribute to this variability, cohort-based joint analyses of variants...
3.
Krause J, Classen C, Dey D, Lausberg E, Kessler L, Eggermann T, et al.
BMC Bioinformatics
. 2024 Dec;
25(1):376.
PMID: 39690401
Background: Methods to call, analyze and visualize copy number variations (CNVs) from massive parallel sequencing data have been widely adopted in clinical practice and genetic research. To enable a streamlined...
4.
Kessler L, Krause J, Kraft F, Amin A, Fekete G, Lengyel A, et al.
Clin Genet
. 2024 Dec;
107(3):278-291.
PMID: 39663844
To assess the suitability of genome sequencing (GS) as the second step in the diagnostics of patients with the features of 11p15.5-associated imprinting disorders (ImpDis: Silver-Russell syndrome [SRS], Beckwith-Wiedemann syndrome...
5.
Kraft F, Rodriguez-Aliaga P, Yuan W, Franken L, Zajt K, Hasan D, et al.
Science
. 2024 Oct;
386(6721):516-525.
PMID: 39480921
Malformations of the brain are common and vary in severity, from negligible to potentially fatal. Their causes have not been fully elucidated. Here, we report pathogenic variants in the core...
6.
Krug A, Markov V, Sheldrick A, Krach S, Jansen A, Zerres K, et al.
Eur Arch Psychiatry Clin Neurosci
. 2024 Sep;
275(2):589.
PMID: 39349685
No abstract available.
7.
Mackay D, Gazdagh G, Monk D, Brioude F, Giabicani E, Krzyzewska I, et al.
Clin Epigenetics
. 2024 Aug;
16(1):99.
PMID: 39090763
Background: Imprinting disorders are rare diseases resulting from altered expression of imprinted genes, which exhibit parent-of-origin-specific expression patterns regulated through differential DNA methylation. A subgroup of patients with imprinting disorders...
8.
Krug A, Nieratschker V, Markov V, Krach S, Jansen A, Zerres K, et al.
Neuroimage
. 2024 Jul;
297:120741.
PMID: 39048493
No abstract available.
9.
Moch J, Radtke M, Liehr T, Eggermann T, Gilissen C, Pfundt R, et al.
Hum Genet
. 2024 Jul;
143(8):955-964.
PMID: 39012485
Uniparental disomy (UPD) is the inheritance of both homologues of a chromosome from only one parent. The detection of UPDs in sequencing data is not well established and a common...
10.
Prawitt D, Eggermann T
Front Genet
. 2024 Jun;
15:1382371.
PMID: 38894719
Overgrowth disorders comprise a group of entities with a variable phenotypic spectrum ranging from tall stature to isolated or lateralized overgrowth of body parts and or organs. Depending on the...