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Year Number of Results
2014 2
2016 1
2017 1
2018 2
2020 2
2021 2
2022 2
2023 2
2024 2

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Page 1
The phenotypic and genotypic spectrum of epilepsy and intellectual disability in adults: Implications for genetic testing.
von Brauchitsch S, Haslinger D, Lindlar S, Thiele H, Bernsen N, Zahnert F, Reif PS, Balcik Y, Au PYB, Josephson CB, Altmüller J, Strzelczyk A, Knake S, Rosenow F, Chiocchetti A, Klein KM. von Brauchitsch S, et al. Among authors: haslinger d. Epilepsia Open. 2023 Jun;8(2):497-508. doi: 10.1002/epi4.12719. Epub 2023 Mar 17. Epilepsia Open. 2023. PMID: 36896643 Free PMC article.
Interferon regulatory factor 4 plays a pivotal role in the development of aGVHD-associated colitis.
Frueh JT, Campe J, Sunaga-Franze DY, Verheyden NA, Ghimire S, Meedt E, Haslinger D, Harenkamp S, Staudenraus D, Sauer S, Kreft A, Schubert R, Lohoff M, Krueger A, Bonig H, Chiocchetti AG, Zeiser R, Holler E, Ullrich E. Frueh JT, et al. Among authors: haslinger d. Oncoimmunology. 2023 Dec 27;13(1):2296712. doi: 10.1080/2162402X.2023.2296712. eCollection 2024. Oncoimmunology. 2023. PMID: 38170159 Free PMC article.
The methylome in females with adolescent Conduct Disorder: Neural pathomechanisms and environmental risk factors.
Chiocchetti AG, Yousaf A, Waltes R, Bernhard A, Martinelli A, Ackermann K, Haslinger D, Rotter B, Krezdorn N, Konrad K, Kohls G, Vetro A, Hervas A, Fernández-Rivas A, Freitag CM. Chiocchetti AG, et al. Among authors: haslinger d. PLoS One. 2022 Jan 28;17(1):e0261691. doi: 10.1371/journal.pone.0261691. eCollection 2022. PLoS One. 2022. PMID: 35089926 Free PMC article. Clinical Trial.
Energy Metabolism Disturbances in Cell Models of PARK2 CNV Carriers with ADHD.
Palladino VS, Chiocchetti AG, Frank L, Haslinger D, McNeill R, Radtke F, Till A, Haupt S, Brüstle O, Günther K, Edenhofer F, Hoffmann P, Reif A, Kittel-Schneider S. Palladino VS, et al. Among authors: haslinger d. J Clin Med. 2020 Dec 18;9(12):4092. doi: 10.3390/jcm9124092. J Clin Med. 2020. PMID: 33353000 Free PMC article.
ADHD-associated PARK2 copy number variants: A pilot study on gene expression and effects of supplementary deprivation in patient-derived cell lines.
Radtke F, Palladino VS, McNeill RV, Chiocchetti AG, Haslinger D, Leyh M, Gersic D, Frank M, Grünewald L, Klebe S, Brüstle O, Günther K, Edenhofer F, Kranz TM, Reif A, Kittel-Schneider S. Radtke F, et al. Among authors: haslinger d. Am J Med Genet B Neuropsychiatr Genet. 2022 Oct;189(7-8):257-270. doi: 10.1002/ajmg.b.32918. Epub 2022 Aug 16. Am J Med Genet B Neuropsychiatr Genet. 2022. PMID: 35971782
Quantitative genome-wide association study of six phenotypic subdomains identifies novel genome-wide significant variants in autism spectrum disorder.
Yousaf A, Waltes R, Haslinger D, Klauck SM, Duketis E, Sachse M, Voran A, Biscaldi M, Schulte-Rüther M, Cichon S, Nöthen M, Ackermann J, Koch I, Freitag CM, Chiocchetti AG. Yousaf A, et al. Among authors: haslinger d. Transl Psychiatry. 2020 Jul 5;10(1):215. doi: 10.1038/s41398-020-00906-2. Transl Psychiatry. 2020. PMID: 32624584 Free PMC article.
Common functional variants of the glutamatergic system in Autism spectrum disorder with high and low intellectual abilities.
Chiocchetti AG, Yousaf A, Bour HS, Haslinger D, Waltes R, Duketis E, Jarczok T, Sachse M, Biscaldi M, Degenhardt F, Herms S, Cichon S, Ackermann J, Koch I, Klauck SM, Freitag CM. Chiocchetti AG, et al. Among authors: haslinger d. J Neural Transm (Vienna). 2018 Feb;125(2):259-271. doi: 10.1007/s00702-017-1813-9. Epub 2017 Nov 16. J Neural Transm (Vienna). 2018. PMID: 29147782
14 results