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Primitive layered gabbros from fast-spreading lower oceanic crust.
Nature. 2014 Jan 9;505(7482):204-7. doi: 10.1038/nature12778. Epub 2013 Dec 1.
Nature. 2014.
PMID: 24291793
Free article.
Compositional boundary layers trigger liquid unmixing in a basaltic crystal mush.
Honour VC, Holness MB, Charlier B, Piazolo SC, Namur O, Prosa TJ, Martin I, Helz RT, Maclennan J, Jean MM.
Honour VC, et al. Among authors: jean mm.
Nat Commun. 2019 Oct 23;10(1):4821. doi: 10.1038/s41467-019-12694-5.
Nat Commun. 2019.
PMID: 31645560
Free PMC article.
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VARista: a free web platform for streamlined whole-genome variant analysis across T2T, hg38, and hg19.
Hadar N, Dolgin V, Oustinov K, Yogev Y, Poleg T, Safran A, Freund O, Agam N, Jean MM, Proskorovski-Ohayon R, Wormser O, Drabkin M, Halperin D, Eskin-Schwartz M, Narkis G, Sued-Hendrickson S, Aminov I, Gombosh M, Aharoni S, Birk OS.
Hadar N, et al. Among authors: jean mm.
Hum Genet. 2024 Apr 12. doi: 10.1007/s00439-024-02671-4. Online ahead of print.
Hum Genet. 2024.
PMID: 38607411
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A role of BPTF in viral oncogenicity delineated through studies of heritable Kaposi sarcoma.
Yogev Y, Schaffer M, Shlapobersky M, Jean MM, Wormser O, Drabkin M, Halperin D, Kassem R, Livoff A, Tsitrina AA, Asna N, Birk OS.
Yogev Y, et al. Among authors: jean mm.
J Med Virol. 2024 Feb;96(2):e29436. doi: 10.1002/jmv.29436.
J Med Virol. 2024.
PMID: 38380509
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Partial penetrance and phenotypic variability of aplasia of lacrimal and salivary glands caused by a novel FGF10 donor splice-site mutation.
Freund O, Elsana B, Agam N, Jean MM, Safran A, Poleg T, Roguin N, Gradstein L, Tsumi E, Birk OS.
Freund O, et al. Among authors: jean mm.
Am J Med Genet A. 2023 Nov;191(11):2768-2774. doi: 10.1002/ajmg.a.63359. Epub 2023 Aug 24.
Am J Med Genet A. 2023.
PMID: 37615310
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SMARCA4 mutation causes human otosclerosis and a similar phenotype in mice.
Drabkin M, Jean MM, Noy Y, Halperin D, Yogev Y, Wormser O, Proskorovski-Ohayon R, Dolgin V, Levaot N, Brumfeld V, Ovadia S, Kishner M, Kazenell U, Avraham KB, Shelef I, Birk OS.
Drabkin M, et al. Among authors: jean mm.
J Med Genet. 2024 Jan 19;61(2):117-124. doi: 10.1136/jmg-2023-109264.
J Med Genet. 2024.
PMID: 37399313
Free PMC article.
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Hyperinsulinism/hyperammonemia syndrome caused by biallelic SLC25A36 mutation.
Safran A, Proskorovski-Ohayon R, Eskin-Schwartz M, Yogev Y, Drabkin M, Eremenko E, Aharoni S, Freund O, Jean MM, Agam N, Hadar N, Loewenthal N, Staretz-Chacham O, Birk OS.
Safran A, et al. Among authors: jean mm.
J Inherit Metab Dis. 2023 Jul;46(4):744-755. doi: 10.1002/jimd.12594. Epub 2023 Feb 9.
J Inherit Metab Dis. 2023.
PMID: 36695547
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