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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2007 1
2009 2
2010 5
2012 1
2013 3
2014 4
2015 1
2016 2
2017 2
2018 4
2019 3
2020 3
2021 3
2023 1
2024 0

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31 results

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Page 1
Disruption of RFX family transcription factors causes autism, attention-deficit/hyperactivity disorder, intellectual disability, and dysregulated behavior.
Harris HK, Nakayama T, Lai J, Zhao B, Argyrou N, Gubbels CS, Soucy A, Genetti CA, Suslovitch V, Rodan LH, Tiller GE, Lesca G, Gripp KW, Asadollahi R, Hamosh A, Applegate CD, Turnpenny PD, Simon MEH, Volker-Touw CML, Gassen KLIV, Binsbergen EV, Pfundt R, Gardeitchik T, Vries BBA, Immken LL, Buchanan C, Willing M, Toler TL, Fassi E, Baker L, Vansenne F, Wang X, Ambrus JL Jr, Fannemel M, Posey JE, Agolini E, Novelli A, Rauch A, Boonsawat P, Fagerberg CR, Larsen MJ, Kibaek M, Labalme A, Poisson A, Payne KK, Walsh LE, Aldinger KA, Balciuniene J, Skraban C, Gray C, Murrell J, Bupp CP, Pascolini G, Grammatico P, Broly M, Küry S, Nizon M, Rasool IG, Zahoor MY, Kraus C, Reis A, Iqbal M, Uguen K, Audebert-Bellanger S, Ferec C, Redon S, Baker J, Wu Y, Zampino G, Syrbe S, Brosse I, Jamra RA, Dobyns WB, Cohen LL, Blomhoff A, Mignot C, Keren B, Courtin T, Agrawal PB, Beggs AH, Yu TW. Harris HK, et al. Among authors: asadollahi r. Genet Med. 2021 Jun;23(6):1028-1040. doi: 10.1038/s41436-021-01114-z. Epub 2021 Mar 3. Genet Med. 2021. PMID: 33658631 Free PMC article.
Pathogenic SCN2A variants cause early-stage dysfunction in patient-derived neurons.
Asadollahi R, Delvendahl I, Muff R, Tan G, Rodríguez DG, Turan S, Russo M, Oneda B, Joset P, Boonsawat P, Masood R, Mocera M, Ivanovski I, Baumer A, Bachmann-Gagescu R, Schlapbach R, Rehrauer H, Steindl K, Begemann A, Reis A, Winkler J, Winner B, Müller M, Rauch A. Asadollahi R, et al. Hum Mol Genet. 2023 Jun 19;32(13):2192-2204. doi: 10.1093/hmg/ddad048. Hum Mol Genet. 2023. PMID: 37010102 Free PMC article.
Proteomics and biomarkers for ovarian cancer diagnosis.
Zhang B, Barekati Z, Kohler C, Radpour R, Asadollahi R, Holzgreve W, Zhong XY. Zhang B, et al. Among authors: asadollahi r. Ann Clin Lab Sci. 2010 Summer;40(3):218-25. Ann Clin Lab Sci. 2010. PMID: 20689132 Review.
Umbilical cord blood stem cells: what to expect.
Zhong XY, Zhang B, Asadollahi R, Low SH, Holzgreve W. Zhong XY, et al. Among authors: asadollahi r. Ann N Y Acad Sci. 2010 Sep;1205:17-22. doi: 10.1111/j.1749-6632.2010.05659.x. Ann N Y Acad Sci. 2010. PMID: 20840248 Review.
Low-Level Chromosomal Mosaicism in Neurodevelopmental Disorders.
Oneda B, Asadollahi R, Azzarello-Burri S, Niedrist D, Baldinger R, Masood R, Schinzel A, Latal B, Jenni OG, Rauch A. Oneda B, et al. Among authors: asadollahi r. Mol Syndromol. 2017 Aug;8(5):266-271. doi: 10.1159/000477189. Epub 2017 Jun 13. Mol Syndromol. 2017. PMID: 28878611 Free PMC article.
Inspirations in medical genetics.
Asadollahi R. Asadollahi R. J Med Biogr. 2016 Feb;24(1):138-40. doi: 10.1177/0967772014525097. Epub 2014 Mar 21. J Med Biogr. 2016. PMID: 24658215
Avicenna's view on medical genetics.
Asadollahi R, Asadollahi H. Asadollahi R, et al. Genet Med. 2013 May;15(5):410-1. doi: 10.1038/gim.2013.27. Genet Med. 2013. PMID: 23649382 Free article. No abstract available.
Elucidation of the phenotypic spectrum and genetic landscape in primary and secondary microcephaly.
Boonsawat P, Joset P, Steindl K, Oneda B, Gogoll L, Azzarello-Burri S, Sheth F, Datar C, Verma IC, Puri RD, Zollino M, Bachmann-Gagescu R, Niedrist D, Papik M, Figueiro-Silva J, Masood R, Zweier M, Kraemer D, Lincoln S, Rodan L; Undiagnosed Diseases Network (UDN); Passemard S, Drunat S, Verloes A, Horn AHC, Sticht H, Steinfeld R, Plecko B, Latal B, Jenni O, Asadollahi R, Rauch A. Boonsawat P, et al. Among authors: asadollahi r. Genet Med. 2019 Sep;21(9):2043-2058. doi: 10.1038/s41436-019-0464-7. Epub 2019 Mar 7. Genet Med. 2019. PMID: 30842647 Free PMC article.
31 results