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

Year Number of Results
1990 1
1992 1
1994 3
1997 3
1998 4
1999 3
2000 4
2001 3
2002 2
2003 1
2004 2
2005 2
2006 4
2007 3
2008 3
2009 1
2010 2
2011 3
2012 1
2013 1
2014 2
2015 3
2016 1
2017 4
2018 4
2019 2
2020 2
2021 5
2022 8
2023 3
2024 0

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69 results

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Page 1
Bi-allelic variants in INTS11 are associated with a complex neurological disorder.
Tepe B, Macke EL, Niceta M, Weisz Hubshman M, Kanca O, Schultz-Rogers L, Zarate YA, Schaefer GB, Granadillo De Luque JL, Wegner DJ, Cogne B, Gilbert-Dussardier B, Le Guillou X, Wagner EJ, Pais LS, Neil JE, Mochida GH, Walsh CA, Magal N, Drasinover V, Shohat M, Schwab T, Schmitz C, Clark K, Fine A, Lanpher B, Gavrilova R, Blanc P, Burglen L, Afenjar A, Steel D, Kurian MA, Prabhakar P, Gößwein S, Di Donato N, Bertini ES; Undiagnosed Diseases Network; Wangler MF, Yamamoto S, Tartaglia M, Klee EW, Bellen HJ. Tepe B, et al. Among authors: magal n. Am J Hum Genet. 2023 May 4;110(5):774-789. doi: 10.1016/j.ajhg.2023.03.012. Epub 2023 Apr 12. Am J Hum Genet. 2023. PMID: 37054711 Free PMC article.
Toward multimode-fiber shape sensing.
Hadad B, Marima D, Magal N, Eyal A, Bahabad A. Hadad B, et al. Among authors: magal n. Opt Lett. 2023 Mar 1;48(5):1160-1163. doi: 10.1364/OL.479876. Opt Lett. 2023. PMID: 36857238
Homozygous MED25 mutation implicated in eye-intellectual disability syndrome.
Basel-Vanagaite L, Smirin-Yosef P, Essakow JL, Tzur S, Lagovsky I, Maya I, Pasmanik-Chor M, Yeheskel A, Konen O, Orenstein N, Weisz Hubshman M, Drasinover V, Magal N, Peretz Amit G, Zalzstein Y, Zeharia A, Shohat M, Straussberg R, Monté D, Salmon-Divon M, Behar DM. Basel-Vanagaite L, et al. Among authors: magal n. Hum Genet. 2015 Jun;134(6):577-87. doi: 10.1007/s00439-015-1541-x. Epub 2015 Mar 20. Hum Genet. 2015. PMID: 25792360 Clinical Trial.
69 results