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

Year Number of Results
1989 1
1991 1
1993 2
2005 1
2008 2
2009 2
2011 1
2013 2
2016 2
2017 2
2018 1
2019 3
2021 6
2024 4

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Page 1
Phenotype variability in Hajdu-Cheney syndrome.
Regev M, Pode-Shakked B, Jacobson JM, Raas-Rothschild A, Goldstein DB, Anikster Y. Regev M, et al. Eur J Med Genet. 2019 Jan;62(1):35-38. doi: 10.1016/j.ejmg.2018.04.015. Epub 2018 Apr 23. Eur J Med Genet. 2019. PMID: 29698804
The "Narratives" fMRI dataset for evaluating models of naturalistic language comprehension.
Nastase SA, Liu YF, Hillman H, Zadbood A, Hasenfratz L, Keshavarzian N, Chen J, Honey CJ, Yeshurun Y, Regev M, Nguyen M, Chang CHC, Baldassano C, Lositsky O, Simony E, Chow MA, Leong YC, Brooks PP, Micciche E, Choe G, Goldstein A, Vanderwal T, Halchenko YO, Norman KA, Hasson U. Nastase SA, et al. Among authors: regev m. Sci Data. 2021 Sep 28;8(1):250. doi: 10.1038/s41597-021-01033-3. Sci Data. 2021. PMID: 34584100 Free PMC article.
Fishing for Genes in Autoimmunity.
Regev M, Pras E. Regev M, et al. Isr Med Assoc J. 2016 Mar-Apr;18(3-4):209-11. Isr Med Assoc J. 2016. PMID: 27228645 Free article.
[Hemolytic uremic syndrome].
Bar-Oz B, Regev M. Bar-Oz B, et al. Among authors: regev m. Harefuah. 1993 Feb 15;124(4):226-30. Harefuah. 1993. PMID: 8495907 Review. Hebrew. No abstract available.
Congenital myopathy is caused by mutation of HACD1.
Muhammad E, Reish O, Ohno Y, Scheetz T, Deluca A, Searby C, Regev M, Benyamini L, Fellig Y, Kihara A, Sheffield VC, Parvari R. Muhammad E, et al. Among authors: regev m. Hum Mol Genet. 2013 Dec 20;22(25):5229-36. doi: 10.1093/hmg/ddt380. Epub 2013 Aug 9. Hum Mol Genet. 2013. PMID: 23933735 Free PMC article.
28 results