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

Year Number of Results
2010 3
2011 3
2012 3
2013 8
2014 9
2015 13
2016 8
2017 5
2018 10
2019 1
2020 4
2021 2
2022 1
2023 1
2024 0

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63 results

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Page 1
Rare variants in SOS2 and LZTR1 are associated with Noonan syndrome.
Yamamoto GL, Aguena M, Gos M, Hung C, Pilch J, Fahiminiya S, Abramowicz A, Cristian I, Buscarilli M, Naslavsky MS, Malaquias AC, Zatz M, Bodamer O, Majewski J, Jorge AA, Pereira AC, Kim CA, Passos-Bueno MR, Bertola DR. Yamamoto GL, et al. Among authors: fahiminiya s. J Med Genet. 2015 Jun;52(6):413-21. doi: 10.1136/jmedgenet-2015-103018. Epub 2015 Mar 20. J Med Genet. 2015. PMID: 25795793
Methodologies for Transcript Profiling Using Long-Read Technologies.
Oikonomopoulos S, Bayega A, Fahiminiya S, Djambazian H, Berube P, Ragoussis J. Oikonomopoulos S, et al. Among authors: fahiminiya s. Front Genet. 2020 Jul 7;11:606. doi: 10.3389/fgene.2020.00606. eCollection 2020. Front Genet. 2020. PMID: 32733532 Free PMC article. Review.
Infantile Pulmonary Teratoid Tumor.
de Kock L, Fahiminiya S, Fiset PO, Astigarraga I, Nguyen VH, Albrecht S, Foulkes WD. de Kock L, et al. Among authors: fahiminiya s. N Engl J Med. 2018 Jun 7;378(23):2238-2240. doi: 10.1056/NEJMc1803354. N Engl J Med. 2018. PMID: 29874541 No abstract available.
[Follicular fluid in mammals].
Fahiminiya S, Gérard N. Fahiminiya S, et al. Gynecol Obstet Fertil. 2010 Jun;38(6):402-4. doi: 10.1016/j.gyobfe.2010.04.010. Epub 2010 Jun 4. Gynecol Obstet Fertil. 2010. PMID: 20576551 Review. French.
Transcript Profiling Using Long-Read Sequencing Technologies.
Bayega A, Wang YC, Oikonomopoulos S, Djambazian H, Fahiminiya S, Ragoussis J. Bayega A, et al. Among authors: fahiminiya s. Methods Mol Biol. 2018;1783:121-147. doi: 10.1007/978-1-4939-7834-2_6. Methods Mol Biol. 2018. PMID: 29767360
Biologic and Clinical Perspectives on Thyroid Cancer.
Fahiminiya S, de Kock L, Foulkes WD. Fahiminiya S, et al. N Engl J Med. 2016 Dec 8;375(23):2306-2307. doi: 10.1056/NEJMc1613118. N Engl J Med. 2016. PMID: 27959678 No abstract available.
Germline Missense Variants in CDC20 Result in Aberrant Mitotic Progression and Familial Cancer.
Chen OJ, Castellsagué E, Moustafa-Kamal M, Nadaf J, Rivera B, Fahiminiya S, Wang Y, Gamache I, Pacifico C, Jiang L, Carrot-Zhang J, Witkowski L, Berghuis AM, Schönberger S, Schneider D, Hillmer M, Bens S, Siebert R, Stewart CJR, Zhang Z, Chao WCH, Greenwood CMT, Barford D, Tischkowitz M, Majewski J, Foulkes WD, Teodoro JG. Chen OJ, et al. Among authors: fahiminiya s. Cancer Res. 2022 Oct 4;82(19):3499-3515. doi: 10.1158/0008-5472.CAN-21-3956. Cancer Res. 2022. PMID: 35913887
Causative Mutations and Mechanism of Androgenetic Hydatidiform Moles.
Nguyen NMP, Ge ZJ, Reddy R, Fahiminiya S, Sauthier P, Bagga R, Sahin FI, Mahadevan S, Osmond M, Breguet M, Rahimi K, Lapensee L, Hovanes K, Srinivasan R, Van den Veyver IB, Sahoo T, Ao A, Majewski J, Taketo T, Slim R. Nguyen NMP, et al. Among authors: fahiminiya s. Am J Hum Genet. 2018 Nov 1;103(5):740-751. doi: 10.1016/j.ajhg.2018.10.007. Am J Hum Genet. 2018. PMID: 30388401 Free PMC article.
63 results