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Author/Creator Carmel, Miri

1. Differential methylation of imprinting genes and MHC locus in 22q11.2 deletion syndrome-related schizophrenia spectrum disorders. (2nd January 2021)

Authors:
Carmel, Miri; Michaelovsky, Elena; Weinberger, Ronnie; Frisch, Amos; Mekori-Domachevsky, Ehud; Gothelf, Doron; Weizman, Abraham
Journal:
World journal of biological psychiatry
Issue:
Volume 22:Number 1(2021)
Page Start:
46
Record Type:
Journal Article
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3. Genome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the GPR98 Locus on 5q14.3. (October 2017)

Authors:
Guo, Tingwei; Repetto, Gabriela M.; McDonald McGinn, Donna M.; Chung, Jonathan H.; Nomaru, Hiroko; Campbell, Christopher L.; Blonska, Anna; Bassett, Anne S.; Chow, Eva W.C.; Mlynarski, Elisabeth E.; Swillen, Ann; Vermeesch, Joris; Devriendt, Koen; Gothelf, Doron; Carmel, Miri; Michaelovsky, Elena...
Journal:
Circulation
Issue:
Volume 10:Number 5(2017)
Page Start:
Record Type:
Journal Article
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6. Runs of homozygosity, copy number variation, and risk for depression and suicidal behavior in an Arab Bedouin kindred. (October 2017)

Authors:
Melhem, Nadine M.; Hamdan, Sami; Klei, Lambertus; Wood, Shawn; Zelazny, Jamie; Frisch, Amos; Weizman, Abraham; Carmel, Miri; Michaelovsky, Elena; Farbstein, Ilana; Wasserman, Danuta; El-Heib, Muhammad; Ferrell, Robert; Apter, Alan; Devlin, Bernie; Brent, David
Journal:
Psychiatric genetics
Issue:
Volume 27:Number 5(2017:Oct.)
Page Start:
Record Type:
Journal Article
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