Peter L Nagy
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Explore the profile of Peter L Nagy including associated specialties, affiliations and a list of published articles.
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Articles
49
Citations
1238
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Recent Articles
1.
Rodriguez-Gil J, Nagy P, Francke U
Am J Med Genet A
. 2024 Jul;
194(12):e63814.
PMID: 39011850
We report a 17-year-old male with supravalvular stenosis, initial failure to thrive and delayed early development, short stature, acromelia, dysmorphic facial features, hypertelorism, macrocephaly, syringomyelia, hypertension, and anxiety disorder. Fluorescent...
2.
Broeckel U, Iqbal M, Levy B, Sahajpal N, Nagy P, Scharer G, et al.
J Mol Diagn
. 2024 Jan;
26(3):213-226.
PMID: 38211722
Optical genome mapping is a high-resolution technology that can detect all types of structural variations in the genome. This second phase of a multisite study compares the performance of optical...
3.
Iqbal M, Broeckel U, Levy B, Skinner S, Sahajpal N, Rodriguez V, et al.
J Mol Diagn
. 2023 Feb;
25(3):175-188.
PMID: 36828597
This study compares optical genome mapping (OGM) performed at multiple sites with current standard-of-care (SOC) methods used in clinical cytogenetics. This study included 50 negative controls and 359 samples from...
4.
Neparaczki E, Kis L, Maroti Z, Kovacs B, Varga G, Makoldi M, et al.
Heliyon
. 2022 Nov;
8(11):e11731.
PMID: 36425424
The Hunyadi family is one of the most influential families in the history of Central Europe in the 14th-16th centuries. The family's prestige was established by Johannes Hunyadi, a Turk-beater...
5.
Varga G, Kristof L, Maar K, Kis L, Schutz O, Varadi O, et al.
J Genet Genomics
. 2022 Jul;
50(1):58-61.
PMID: 35809778
No abstract available.
6.
Maroti Z, Neparaczki E, Schutz O, Maar K, Varga G, Kovacs B, et al.
Curr Biol
. 2022 May;
32(13):2858-2870.e7.
PMID: 35617951
Huns, Avars, and conquering Hungarians were migration-period nomadic tribal confederations that arrived in three successive waves in the Carpathian Basin between the 5 and 9 centuries. Based on the historical...
7.
Mikhail A, Nagy P, Manta K, Rouse N, Manta A, Ng S, et al.
J Clin Invest
. 2022 Mar;
132(10).
PMID: 35316212
BackgroundMyotonic dystrophy type 1 (DM1) is a complex life-limiting neuromuscular disorder characterized by severe skeletal muscle atrophy, weakness, and cardiorespiratory defects. Exercised DM1 mice exhibit numerous physiological benefits that are...
8.
Shan C, Kim J, Wang J, Bao K, Sun Y, Chen H, et al.
Cell Rep
. 2021 May;
35(7):109137.
PMID: 34010645
Oncogenic histone lysine-to-methionine mutations block the methylation of their corresponding lysine residues on wild-type histones. One attractive model is that these mutations sequester histone methyltransferases, but genome-wide studies show that...
9.
Pena-Padilla C, Romero-Valenzuela I, Baldomero-Lopez A, Sandoval-Talamantes A, Castellanos-Gonzalez A, Nagy P, et al.
Neuromuscul Disord
. 2021 Mar;
31(5):462-465.
PMID: 33741226
Duchenne muscular dystrophy is an X-Linked neuromuscular disorder, and the most common muscular dystrophy. Neuropsychiatric phenotype associated to DMD gene mutations include now low IQ scores, epilepsy, autism, and attention...
10.
Nagy P, Olasz J, Neparaczki E, Rouse N, Kapuria K, Cano S, et al.
Eur J Hum Genet
. 2021 Jan;
29(8):1317.
PMID: 33446829
No abstract available.