Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

16 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
Author Correction: GPR15-mediated T cell recruitment during acute viral myocarditis facilitated virus elimination and improved outcome.
Stoffers B, Wolf H, Bacmeister L, Kupsch S, Vico T, Marchini T, Brehm MA, Yan I, Becher PM, Ardeshirdavani A, Escher F, Kim SV, Klingel K, Kirchhof P, Blankenberg S, Zeller T, Wolf D, Hilgendorf I, Westermann D, Lindner D. Stoffers B, et al. Among authors: ardeshirdavani a. Nat Cardiovasc Res. 2024 Sep;3(9):1177. doi: 10.1038/s44161-024-00540-x. Nat Cardiovasc Res. 2024. PMID: 39271820 Free PMC article. No abstract available.
GPR15-mediated T cell recruitment during acute viral myocarditis facilitated virus elimination and improved outcome.
Stoffers B, Wolf H, Bacmeister L, Kupsch S, Vico T, Marchini T, Brehm MA, Yan I, Becher PM, Ardeshirdavani A, Escher F, Kim SV, Klingel K, Kirchhof P, Blankenberg S, Zeller T, Wolf D, Hilgendorf I, Westermann D, Lindner D. Stoffers B, et al. Among authors: ardeshirdavani a. Nat Cardiovasc Res. 2024 Jan;3(1):76-93. doi: 10.1038/s44161-023-00401-z. Epub 2023 Dec 27. Nat Cardiovasc Res. 2024. PMID: 39195892 Free PMC article.
Identification of a Novel Homozygous Mutation in PRDM12 Gene in a Patient with Hereditary Sensory and Autonomic Neuropathy Type VIII.
Ebrahimi AH, Bolhassani M, Zarei MR, Heidari M, ArdeshirDavani A, Mehrtash AH, Shiri Z, Heidari M, Soleyman-Nejad M, Taskhiri MH, Norouzbeigi A, Heidari M. Ebrahimi AH, et al. Among authors: ardeshirdavani a. Arch Iran Med. 2024 Apr 1;27(4):223-226. doi: 10.34172/aim.2024.32. Arch Iran Med. 2024. PMID: 38685849 Free PMC article.
Towards solving the genetic diagnosis odyssey in Iranian patients with congenital anomalies.
Vaseghi P, Habibi L, Neidich JA, Cao Y, Fattahi N, Rashidi-Nezhad R, Salehnezhad T, Dalili H, Rahimi Sharbaf F, Zarkesh MR, Malekian M, Mokhberdezfuli M, Mehrtash A, Ardeshirdavani A, Kariminejad R, Ghorbansabagh V, Sadeghimoghadam P, Naddaf A, Esmaeilnia Shirvany T, Mosayebi Z, Sahebdel B, Golshahi F, Shirazi M, Shamel S, Moeini R, Heidari A, Daneshmand MA, Ghasemi R, Akrami SM, Rashidi-Nezhad A. Vaseghi P, et al. Among authors: ardeshirdavani a. Eur J Hum Genet. 2024 Oct;32(10):1238-1249. doi: 10.1038/s41431-024-01533-x. Epub 2024 Jan 26. Eur J Hum Genet. 2024. PMID: 38278869
Clinical whole-exome sequencing analysis reveals a novel missense COL11A1 mutation resulting in an 18-week Iranian male aborted fetus with Fibrochondrogenesis 1: A case report.
Mirtavoos-Mahyari H, Ajami S, Mehrtash A, Marashiyan SM, Bahreini F, Sheikhy K, Ghanbari S, Ardeshirdavani A. Mirtavoos-Mahyari H, et al. Among authors: ardeshirdavani a. Clin Case Rep. 2022 Nov 15;10(11):e6574. doi: 10.1002/ccr3.6574. eCollection 2022 Nov. Clin Case Rep. 2022. PMID: 36397853 Free PMC article.
Recommendations for whole genome sequencing in diagnostics for rare diseases.
Souche E, Beltran S, Brosens E, Belmont JW, Fossum M, Riess O, Gilissen C, Ardeshirdavani A, Houge G, van Gijn M, Clayton-Smith J, Synofzik M, de Leeuw N, Deans ZC, Dincer Y, Eck SH, van der Crabben S, Balasubramanian M, Graessner H, Sturm M, Firth H, Ferlini A, Nabbout R, De Baere E, Liehr T, Macek M, Matthijs G, Scheffer H, Bauer P, Yntema HG, Weiss MM. Souche E, et al. Among authors: ardeshirdavani a. Eur J Hum Genet. 2022 Sep;30(9):1017-1021. doi: 10.1038/s41431-022-01113-x. Epub 2022 May 16. Eur J Hum Genet. 2022. PMID: 35577938 Free PMC article.
Multiple Sclerosis Data Alliance - A global multi-stakeholder collaboration to scale-up real world data research.
Peeters LM, Parciak T, Kalra D, Moreau Y, Kasilingam E, van Galen P, Thalheim C, Uitdehaag B, Vermersch P, Hellings N, Stinissen P, Van Wijmeersch B, Ardeshirdavani A, Pirmani A, De Brouwer E, Bauer CR, Krefting D, Ribbe S, Middleton R, Stahmann A, Comi G. Peeters LM, et al. Among authors: ardeshirdavani a. Mult Scler Relat Disord. 2021 Jan;47:102634. doi: 10.1016/j.msard.2020.102634. Epub 2020 Nov 21. Mult Scler Relat Disord. 2021. PMID: 33278741 Free article.
Towards practical privacy-preserving genome-wide association study.
Bonte C, Makri E, Ardeshirdavani A, Simm J, Moreau Y, Vercauteren F. Bonte C, et al. Among authors: ardeshirdavani a. BMC Bioinformatics. 2018 Dec 20;19(1):537. doi: 10.1186/s12859-018-2541-3. BMC Bioinformatics. 2018. PMID: 30572817 Free PMC article.
16 results